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    Outpatient Registered Nurse - RN  

    - Baltimore
    PURPOSE AND SCOPE: The professional registered nurse Outpatient RN CA... Read More

    PURPOSE AND SCOPE:

    The professional registered nurse Outpatient RN CAP 2 may be an entry level designation into the Clinical Advancement Program (CAP) for new employees who meet the RN CAP 2 criteria or attained through advancement from RN CAP 1. This position is accountable and responsible for the provision and coordination of clinically competent care including assessment, planning, intervention, and evaluation for an assigned group of patients. This may include delegation of appropriate tasks to direct patient care staff including but not limited to RNs, LVN/LPNs, and Patient Care Technicians. As a member of the End Stage Kidney Disease (ESKD) health care team, this position participates in decision-making, teaching, leadership functions, and quality improvement activities that enhance patient care outcomes and facility operations.

    PRINCIPAL DUTIES AND RESPONSIBILITIES:

    All duties and responsibilities are expected to be performed in accordance with Fresenius Kidney Care policy, procedures, standards of nursing practice, state, and federal regulations.

    Performs all essential functions under the direction of the Supervisor and with guidance from the Clinical Educator, Preceptor or in collaboration with other Registered Nurses.Performs ongoing, systematic collection and analysis of patient data pre - during - post hemodialysis treatment for assigned patients and documents in the patient medical record, makes adjustments or modifications to treatment plan as indicated and notifies Team Leader, Charge Nurse, Supervisor or Physician as needed.Assesses, collaborates, and documents patient/family's basic learning needs to provide initial and ongoing education to patients and family.Directs and provides, in collaboration with direct and ancillary patient care staff, all aspects of the daily provision of safe and effective delivery of hemodialysis therapy to assigned patients.Administers medications as prescribed or in accordance with approved algorithm(s), and documents appropriate medical justification and effectiveness.Initiates or assists with emergency response measures.Serves as a resource, leader, coach, mentor and role model for new and incumbent employees by setting examples of appropriate behavior, work habits and attitudes towards patients, co-workers, supervisors and the company at the facility, and area level. Ensures correct laboratory collection, processing and shipping procedures are performed and reschedules missed or insufficient laboratory collections.Identifies expected outcomes, documents, and updates the nursing assessment and plan of care for assigned patients through collaboration with the Interdisciplinary Team.Ensures patient awareness related to transplant and treatment modality options.Participates in education and quality improvement projects at the facility and area level as directed by Supervisor.May serve as a Preceptor to new employees.Required to complete CAP requirements to maintain or advance.Performs all other duties as assigned by Supervisor.

    PHYSICAL DEMANDS AND WORKING CONDITIONS:

    The physical demands and work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

    The position provides direct patient care that regularly involves heavy lifting, moving of patients and assisting with ambulation. Equipment aids and/or coworkers may provide assistance. This position requires frequent, prolonged periods of standing and the employee must be able to bend over.The employee may occasionally be required to move, with assistance, machines, and equipment of up to 200 lbs., and may lift chemical and water solutions of up to 30 lbs. as high as 5 feet. The work environment is characteristic of a health care facility with air temperature control and moderate noise levels. May be exposed to infectious and contagious diseases/materials.Day to day work includes desk work, computer work and interaction with patients, facility/hospital staff and physicians.The position may require travel to training sites or other facilities.May be asked to provide essential functions of this position in other locations with the same physical demands and working conditions as described above.

    SUPERVISION:

    Assigned oversight of Patient Care Technicians LVN/LPNs/RNs as a Team Leader or designated Nurse in Charge, after meeting all the following: Successful completion of all FKC education and training requirements for new employees. Must have a minimum of 3 months experience in chronic/acute hemodialysis as a RN.

    EDUCATION and LICENSURE:

    Graduate of an accredited School of Nursing.Current appropriate state licensure.Current or successful completion of CPR BLS CertificationMust meet the practice requirements in the state in which he or she is employed.

    EXPERIENCE AND REQUIRED SKILLS:

    Entry level for RNs with minimum of 2 years of Nephrology Nursing experience

    "The rate of pay for this position will depend on the successful candidate's work location and qualifications, including relevant education, work 17perience, skills, and competencies.

    Hourly Rate: $33 - $56

    Non-Bonus Eligible Positions: include language below.
    Benefit Overview: This position offers a comprehensive benefits package including medical, dental, and vision insurance, a 401(k) with company match, paid time off, parental leave.

    Bonus Eligible Positions - include language below.
    Benefit Overview: This position offers a comprehensive benefits package including medical, dental, and vision insurance, a 401(k) with company match, paid time off, parental leave and potential for performance-based bonuses depending on company and individual performance."

    Fresenius Medical Care maintains a drug-free workplace in accordance with applicable federal and state laws.

    "

    EOE, disability/veterans

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    Dialysis Clinical Manager Registered Nurse - RN  

    - Baltimore
    Sign-on Bonus Available About this role: As a Clinical Manager with Fr... Read More
    Sign-on Bonus Available

    About this role: As a Clinical Manager with Fresenius Medical Care, you will ensure that quality patient care is delivered while maintaining clinical operations. As the facility leader, you will be part of a close-knit, collaborative team responsible for delivering unique care plans and providing dialysis treatment to patients facing end stage renal disease or chronic kidney disease.

    Training and advancement: You will enter our Clinical Leadership Program that creates and supports a culture of continuous learning for our managers. The curriculum will cover onboarding, essential functions, leading your business, and advanced leadership. As a Clinical Manager, you may advance your career into an Area Team Lead or Director of Operations role.

    Our culture: We believe our employees are our most important asset - we value, care about, and support our people. We are there when you may need us most, from tuition reimbursement to support your education goals, granting scholarships to family members, delivering relief when natural disasters strike, or providing financial support when personal hardship hits, we take care of our people.

    Our focus on diversity: We have built a nurturing environment that welcomes every age, race, gender, sexual orientation, background, and cultural tradition. We have a diverse range of employee resource groups (ERGs) to encourage employees with similar interests, goals, social and cultural backgrounds, or experiences to come together for professional and personal development, discussion, activities, and peer support. Our diverse workforce and culture encourage opportunity, equity, and inclusion for all, which is a tremendous asset that sets us apart.

    At Fresenius Medical Care, you will truly make a difference in the lives of people living with kidney disease. If this sounds like the career and company you have been looking for, and you want to be a vital part of the future of healthcare, apply today.

    PURPOSE AND SCOPE:
    Manage and oversee the daily operations of the facility, ensuring cost-effective facility operations in accordance with all legal, compliance and regulatory requirements and programs. Collaborates with the Medical Director and the Clinical Manager/Charge Nurse regarding the provision of quality patient care in the dialysis facility incorporating all activities from admission through to discharge. As the clinic leader, has the authority to make daily decisions to ensure the appropriate continuity of care and patient and staff safety. Markets available services through presentations to physicians and dialysis facilities.

    You will ensure that quality patient care is delivered while maintaining clinical operations. As the facility leader, you will be part of a close-knit, collaborative team responsible for delivering unique care plans and providing dialysis treatment to patients facing end stage renal disease or chronic kidney disease.

    PRINCIPAL DUTIES AND RESPONSIBILITIES:
    Clinic Operations:
    • Provides leadership, coaching, and development plans for all direct reports.
    • Partners with internal Human Resources, Quality, Education, and Technical Services departments.
    • Collaborates with the Home Therapies Program Manager to oversee the facility's Home Therapies Program.
    • Maintains integrity of medical and operations records and complies with all data collections and auditing activities.
    • Accountable for completion of the Internal Classification of Disease (ICD) coding.
    • Responsible for all required network reporting and on-site state or federal surveys.
    • Manages the tactical execution of short- and long-term objectives through the coordination of activities with a direct responsibility for results, including costs, methods, and staffing.
    • Responsible for the administration of the daily business operations of the dialysis clinics including managing the functions and actions related to the center staff, quality of overall provision of patient care, maintenance of the physical plant and center equipment, and inventory control.
    • Manages the profit and loss and other related financial aspects for the center, ensuring optimal facility operations to achieve or exceed the budget and key performance indicators.
    Patient Care:
    • Coordinates all aspects of patient care with the appropriate staff members, from admission through discharge of the patient.
    • Acts as a resource for the patient and family to address concerns and questions.
    • Oversee the timely completion of patient care assessments and care plans.
    • Manages timely patient schedules to ensure facility efficiency and develop action plans for missed treatments.
    • Reports changes in patient status regarding any clinical, insurance, or travel and transportation issues.
    Staff:
    • Participates in the selection and hiring of new team members and ensures completion of new hiring orientation and mandatory training.
    • Responsible for all patient care employees completing appropriate training courses and that licensures/certifications are current.
    • Provides support for all clinical staff members at regular intervals and encourages professional growth.
    • Maintains current knowledge regarding company benefits, policies, procedures, and processes.
    • Obtains clinical feedback for employee evaluations and establishes annual goals and conducts employee evaluations.
    • Documents any disciplinary actions and confers with the clinic Director of Operations and Human Resources when needed.
    • Manages staff scheduling and payroll.

    Physicians:
    • Facilitates the application process for physician privileges and compliance with Fresenius Medical Care Medical Staff By-Laws.
    • Responsible for strong physician relationships and ensures regular and effective communication.
    • Participates in Governing Body, an interdisciplinary team for each region including MDs, DOs etc. that governs policies.
    Other:
    • Collaborates closely with, providing oversight as needed to, the Clinical Manager/Charge RN acting as nurse manager, the Medical Director, and the physicians regarding the direct patient care responsibilities within the facility to ensure the provision of outstanding quality of patient care, as defined by the FMS quality goals, and compliance with the pertinent company policies and procedures. Collaboration activities include:
    • Coordinating all aspects of patient care from admission through discharge of the patient.
    • Addressing patient concerns, issues, and questions including the review of patient satisfaction surveys.
    • Developing and communicating efficient and timely patient schedules to ensure maximization of facility efficiency.
    • Assisting as needed with patient workflow.
    • Implementing and maintaining a Continuous Quality Improvement (CQI) Process and Quality Assessment and Improvement Program (QAPI) Improvement Team that involves staff and pertinent physicians in problem solving activities meeting on a regular basis to address identified issues.
    • Continually review Center operations to ensure compliance with Federal and State laws.
    • Develops and maintains strong Medical Director and physician relationships, facilitating staff relationships with physicians, and ensuring regular and effective communication with all physicians including participating in regular meetings with Medical Directors.
    • Supports and drives FMS quality standards through meeting regulatory requirements and the practice of CQI, including the use of the appropriate company CQI tools.
    • Works with the Charge RN and Medical Director to implement FMS quality FKC goals and develop facility specific action plans to achieve FMS quality standards.
    • Oversees and monitors the provision of the appropriate training according to FMS policy to ensure ongoing compliance with all company and FMS risk management initiatives.
    • Collaborates with the Charge RN to ensure the aggressive treatment of, and actions taken, regarding adverse safety events and action thresholds.
    • Ensures all Quality policies and procedures are communicated to and implemented by the facility staff.
    • Maintains integrity of medical records and other FMS administrative and operational records.
    • Complies and assists with all data collection and auditing activities.
    • Manages the day-to-day activities and workload of the facility staff providing guidance and leadership as appropriate to ensure the effective, efficient and timely execution of duties and tasks.
    • Creates, maintains, and communicates efficient and timely employee schedules according to the staffing needs of the facility to ensure adequate staffing daily. Consults with Charge RN and Medical Director to optimize clinical staffing.
    • Provides informal feedback to staff on an ongoing basis and formal feedback in the form of the annual performance evaluation during the focal merit review process. Obtains feedback and input regarding the staff performance from the Medical Director and Charge RN and acts on the feedback as appropriate. Collaborates with staff and Charge RN and Medical Director to set annual goals for staff.
    • Manages the department staffing through the appropriate hiring, firing and disciplinary actions.
    • Maintains written documentation of all disciplinary meetings in accordance with the established personnel policies and confers with Human Resources and Director of Operations regarding the nature of the disciplinary decisions.
    • Ensures successful execution of new hire orientation and training, and ICD-9 code training when ICD-10 applicable for new hires and works with Medical Director to ensure mandatory in-services are completed.
    • Ensures appropriate documentation is completed for current licensure . click apply for full job details Read Less
  • SALES ASSOCIATE in HALETHORPE, MD S04579  

    - Baltimore
    Work Where You MatterAt Dollar General, our mission is Serving Others!... Read More
    Work Where You MatterAt Dollar General, our mission is Serving Others! We value each and every one of our employees. Whether you are looking to launch a new career in one of our many convenient Store locations, Distribution Centers, Store Support... Read Less
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    Judaics Coordinator  

    - Baltimore
    Job DescriptionJob DescriptionJudaics CoordinatorLev HaTorah Academy o... Read More
    Job DescriptionJob Description

    Judaics Coordinator
    Lev HaTorah Academy of Baltimore will open in the 2026–2027 school year with a Preschool, a Girls’ Elementary and Middle School, and a separate Boys’ Elementary and Middle School. Our school is founded on the belief that every child is valued for who they are, with a commitment to nurturing each student’s individual path in Torah and academics. We honor every child’s unique strengths and support their growth through differentiated instruction and individualized multiple modality learning.

    Lev HaTorah Academy is seeking a dynamic, organized, and thoughtful Judaics Coordinator to work alongside the Head of School in supervising teachers and curriculum. This educational leader will combine instructional expertise, coaching skills, curriculum development, and a strong commitment to the school’s hashkafa and educational philosophy. The ideal candidate will inspire staff to guide every child with warmth, respect, and a deep belief in their individual value and potential.

    The Judaics Coordinator will oversee all aspects of the Judaic Studies program, ensuring alignment with Baltimore community Torah values, multiple-modality instruction, and the school’s mission and vision. The role includes developing curriculum, scope, and sequence for the preschool, elementary, and middle school divisions, while supporting students, faculty, and families in fostering Torah values, academic excellence, and joyful learning.

    Responsibilities

    Curriculum & Program Leadership

    Design, implement, and refine Judaic Studies curriculum aligned with school goals, student needs, and differentiated learning. 

    Collaborate with the Head of School, Operations Manager, and faculty on curriculum and school-wide initiatives.

    Ensure consistency and excellence across all Judaic Studies divisions.

    Faculty Development & Instructional Leadership

    Mentor, supervise, and support Judaic Studies teachers in instructional practices, classroom management, and experiential learning.

    Conduct classroom observations and provide feedback to strengthen teaching effectiveness and student engagement.

    Lead ongoing professional development and collaborate on staff meetings related to Judaic Studies.

    Promote differentiated instruction and integration of Torah values throughout learning.

    Student Support & Religious Growth

    Foster a warm, spiritually rich environment rooted in Torah, Mitzvos, and Derech Eretz.

    Serve as a role model through active engagement in tefillah, limudei kodesh, and school life.

    Support students’ social-emotional and religious growth, including discipline aligned with school values.

    Strategic Leadership & School Culture

    Partner with school leadership on strategic planning and school improvement.

    Help cultivate an inclusive, collaborative, and mission-driven school culture.

    Parent & Community Engagement

    Serve as a visible and approachable liaison for families regarding Judaic programming and student progress.

    Build strong partnerships with parents and represent the school’s Judaic vision within the broader community.

    Attend and contribute to monthly meet-ups and school programs.

    Operational Support

    Assist with scheduling, planning, and logistics related to Judaic programming.

    Strengthen communication between General and Judaic Studies faculty and support daily school operations.

    Required Qualifications

    Strong background in Judaic curriculum design, pedagogy, and differentiated instruction

    Experience in educational leadership

    Excellent organizational, communication, and leadership skills

    Ability to mentor teachers with warmth and professionalism

    Commitment to the school’s hashkafa and educational vision

    Preferred Qualifications

    Leadership experience in an Orthodox Jewish day school or similar environment

    Experience developing and leading professional development

    Strong data-informed decision-making skills

    What We’re Looking For

    A leader who values both excellence and heart

    A collaborative partner committed to shared vision and growth in this 12 month position. 

    An instructional leader who supports teachers while maintaining high standards

    A thoughtful builder excited to help shape the future of the school


    To Apply: Send resume and cover letter to careers@levbaltimore.com


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  • V
    Job DescriptionJob DescriptionDegree in Speech-Language Pathology, act... Read More
    Job DescriptionJob DescriptionDegree in Speech-Language Pathology, active SLP license and 1+ year of Speech-Language Pathology experience required. Applicants who do not meet these qualifications will not be considered.

    Sunbelt Staffing is seeking a dedicated Speech-Language Pathologist (SLP) licensed in Maryland to provide virtual services to students in a school-based setting. This remote opportunity offers flexibility, competitive hourly compensation, and the chance to make a meaningful impact on students' communication and academic success.

    Position Details

    Fully Remote1099 Independent ContractorCompetitive Hourly Pay - direct and indirect servicesWeekly CompensationFlexible SchedulingSchool-Based Assignment

    Responsibilities

    Provide virtual speech and language therapy services to K-12 students.Conduct evaluations and assessments to determine student needs.Develop and implement individualized treatment plans and IEP goals.Collaborate with teachers, parents, and school teams to support student progress.Maintain accurate documentation and complete required reporting.Participate in virtual IEP meetings and multidisciplinary team discussions.

    Qualifications

    Active Maryland Speech-Language Pathologist license required.Maryland Department of Education (MSDE) certification, if required by the district.ASHA Certificate of Clinical Competence (CCC-SLP) required.Previous school-based experience preferred.Strong communication, organizational, and technology skills.Ability to effectively deliver services through a virtual platform.Compensation for this position ranges from $34.00 to $50.00. This posting is open for 60 days after the posting date.

    #p34

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    Quality Control Analyst  

    - Baltimore
    Job DescriptionJob DescriptionJob Title: Quality Control AnalystJob De... Read More
    Job DescriptionJob Description

    Job Title: Quality Control Analyst

    Job Description

    The Quality Control Analyst will serve as a hands-on analyst and specialist within the Quality Control (QC) unit at a large molecule manufacturing facility. This role focuses on utility and environmental monitoring sample collection, basic QC testing, and analytical support to ensure inspection readiness and timely release of results. The analyst will work within the QC Analytical group and collaborate closely with QC Micro, Manufacturing, Quality Assurance, Regulatory Affairs, Supply Chain, and Biologics Process Development teams to support drug substance development, manufacturing, and regulatory compliance.

    Responsibilities

    Work in Quality Control operations, focusing on taking samples of utilities such as water and gas, performing Environmental Monitoring (EM), and conducting basic QC testing on collected samples.Serve as the primary point for sample collection activities, ensuring accurate, timely, and compliant sampling of utilities and environmental conditions.Compile and organize test results to support qualification reports and other quality documentation.Review test records to ensure accuracy, completeness, and compliance with internal procedures and regulatory expectations.Support testing of QC samples as needed, including basic analytical and microbiological testing within the QC Analytical laboratory.Collaborate with the Biologics Process Development team to execute testing activities that support drug substance development and manufacturing for large molecule products.Support laboratory incidents, out-of-specification (OOS) results, deviations, out-of-trend (OOT) results, and client complaints related to QC testing, contributing to timely and thorough resolution.Ensure all documentation, including SOPs, IOPs, EOPs, and STPs, is periodically reviewed, updated, and maintained according to the documentation control system.Ensure timely completion of QC activities in line with project timelines and update work plans periodically to accommodate changes in project scope, priorities, or schedules.Adhere to ALCOA principles of data integrity and promote compliance with data integrity standards among team members.Participate in functional working teams to perform self-assessments of compliance with SOPs and data integrity requirements.Support and contribute to investigations related to QC testing, analytical issues, or quality events as needed.Ensure laboratory safety protocols are followed at all times and help resolve technical issues in the QC Analytical lab efficiently.Support QC Analytical documentation in regulatory filings, including prior approval submissions, renewals, updates, and supplements, as required.Support monitoring of QC analytical trends, complaints, failures, deviations, and changes to identify opportunities for process, system, and product improvements.Plan and help manage resources to support smooth operations within the QC laboratory.

    Essential Skills

    2–4 years of progressively responsible experience in Quality Control within biologics or pharmaceutical manufacturing environments, specifically supporting large molecule products.Bachelor’s degree in Chemistry, Biochemistry, Chemical Engineering, or a related scientific discipline.Experience in basic QC testing within a laboratory environment.Working knowledge of biologic analytical techniques and validation of analytical methods.Experience working within quality systems, including qualifications, validations, and product lifecycle quality management.Experience with biologics and biopharmaceutical manufacturing processes.Experience in environmental monitoring and utility sampling, including water sampling and gas sampling.Knowledge of Good Manufacturing Practices (GMP) in biopharmaceutical, pharmaceutical, biotechnology, or biotech production settings.Familiarity with microbiology laboratory practices and aseptic technique.Experience working in cleanroom environments and following gowning procedures.Understanding and application of ALCOA principles of data integrity.Knowledge of change control processes related to QC activities and laboratory operations.Ability to support investigations of OOS, OOT, deviations, and complaints related to QC testing.Understanding of regulatory expectations from USDA and USFDA, ICH, EU, and Health Canada for biologics manufacturing.Familiarity with USP and other pharmacopeial standards relevant to biologics.

    Additional Skills & Qualifications

    Experience supporting QC Analytical documentation for regulatory filings, including prior approval submissions, renewals, updates, and supplements.Experience monitoring QC analytical trends, complaints, failures, deviations, and changes to drive process and system improvements.Experience collaborating with cross-functional teams such as QC Micro, Manufacturing, Quality Assurance, Regulatory Affairs, Supply Chain, and Process Development.Experience in bioprocess or production environments within biologics or biotechnology.Experience in laboratory operations planning and resource management.Strong attention to detail and ability to maintain accurate and compliant documentation.Ability to work in a fast-paced, innovation-focused organization serving pharmaceutical, biotechnology, nutrition, animal health, consumer goods, and specialty chemical industries.Comfort working in an environment that emphasizes safety, shared responsibility, and adherence to SOPs and safety guidelines.Strong communication and collaboration skills to support clients and internal stakeholders in resolving scientific and quality challenges.

    Work Environment

    This role is based in a large molecule manufacturing environment, with work performed both on the manufacturing floor and in the QC laboratory. The position involves regular utility sampling (such as water and gas), environmental monitoring, and work in cleanroom and controlled environments where aseptic technique and gowning procedures are required. The organization operates within a GMP-compliant biopharmaceutical and biotechnology setting, using established laboratory equipment and analytical technologies to support biologics production. The culture emphasizes innovation, scientific problem-solving, and close collaboration with global clients across pharmaceutical, biotechnology, nutrition, animal health, consumer goods, and specialty chemical industries. Safety is a core value, with shared accountability for following safety guidelines, procedures, and SOPs at all times. The work environment supports cross-functional teamwork, continuous improvement, and adherence to data integrity principles and regulatory standar

    Job Type & Location

    This is a Contract position based out of Baltimore, MD.

    Pay and Benefits

    The pay range for this position is $32.00 - $32.00/hr.

    Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:
    • Medical, dental & vision
    • Critical Illness, Accident, and Hospital
    • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
    • Life Insurance (Voluntary Life & AD&D for the employee and dependents)
    • Short and long-term disability
    • Health Spending Account (HSA)
    • Transportation benefits
    • Employee Assistance Program
    • Time Off/Leave (PTO, Vacation or Sick Leave)

    Workplace Type

    This is a fully onsite position in Baltimore,MD.

    Application Deadline

    This position is anticipated to close on Jul 30, 2026.

    About Actalent

    Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.

    The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

    If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

    San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records.

    Massachusetts Lie Detector: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

    Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.

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    Warehouse Worker  

    - Baltimore
    Job DescriptionJob DescriptionJob Title: Warehouse WorkerJob Descripti... Read More
    Job DescriptionJob DescriptionJob Title: Warehouse WorkerJob Description

    This role focuses on material handling and general warehouse duties, including the accurate picking and packing of products using an RF scanner and various material handling equipment. You will support daily warehouse operations by safely moving, organizing, and preparing products for shipment in a small, collaborative warehouse environment.

    ResponsibilitiesPerform material handling and general warehouse duties to support daily operations.Pick and pack products accurately using an RF scanner for tracking and inventory control.Operate an electric pallet jack and sit-down forklift to move, load, and unload materials, once trained and certified as required.Manually pick and pack orders, ensuring correct items, quantities, and packaging standards.Load and unload trucks and pallets safely and efficiently.Support inventory activities by handling products carefully and maintaining accurate counts.Maintain a clean, organized, and safe work area by performing regular cleaning and housekeeping tasks.Handle physical labor tasks, including lifting, moving, and stacking products as needed.Follow all warehouse procedures and safety guidelines while working with equipment and materials.Collaborate with team members and communicate effectively to complete orders and meet deadlines.Assist with general labor tasks and other warehouse duties as assigned.Essential SkillsPrevious warehouse experience.Experience with RF scanners for picking, packing, and tracking products.Ability to perform physical labor, including lifting, carrying, and standing for extended periods.Experience with general labor tasks such as loading, unloading, and material handling.Strong attendance, reliability, and punctuality.Ability to follow instructions and warehouse procedures accurately.Comfort working with equipment such as pallet jacks and forklifts (training provided if needed).Additional Skills & QualificationsExperience operating an electric pallet jack.Experience operating a sit-down forklift.Background in order picking and packing in a warehouse environment.Familiarity with inventory processes and basic material handling practices.Ability to contribute to warehouse cleanliness and organization.Willingness to learn and be trained on forklift operation if not already experienced.Why Work Here?

    You will join a stable logistics organization with multiple branches and locations, offering opportunities to learn, grow, and expand your skills. The company supports on-the-job training, including forklift training for those with warehouse experience, helping you build valuable, transferable skills. You will work in a small, close-knit team where reliability and teamwork are appreciated and recognized, with the potential for ongoing development within a broader logistics network.

    Work Environment

    This position is based in a small warehouse environment with approximately 7–10 team members on site, fostering a collaborative and supportive atmosphere. The standard schedule is a first shift from 8:30 a.m. to 5:00 p.m., with some occasional overtime as business needs require. You will work around typical warehouse equipment such as RF scanners, electric pallet jacks, and sit-down forklifts, as well as engage in physical tasks like loading, unloading, and general material handling. The environment emphasizes cleanliness, organization, and safety while maintaining a steady workflow throughout the day.

    Job Type & Location

    This is a Contract position based out of Baltimore, MD.

    Pay and Benefits

    The pay range for this position is $18.00 - $23.00/hr.

    Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)

    Workplace Type

    This is a fully onsite position in Baltimore,MD.

    Application Deadline

    This position is anticipated to close on Jul 31, 2026.

    About Aerotek

    Aerotek® Inc. provides staffing and services solutions in manufacturing, logistics, construction, aviation, facilities and maintenance. We provide the expertise, solutions and people required to rise to the challenges of North American industry. Headquartered in Hanover, Md., Aerotek operates a unified network of over 200 offices across North America, supporting more than 18,000 clients each year. Aerotek is an Allegis Group company, the global leader in workforce and business solutions. To learn more, visit: Aerotek.com | 1-888-AEROTEK.

    Aerotek offers weekly pay, employee benefits including medical, dental & vision, life insurance, health advocacy and employee assistance programs, a 401(k) plan, and employee discounts.

    The company is an equal opportunity employer and will consider all applications without regards to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

    San Francisco Fair Chance Ordinance:
    Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records.

    Massachusetts Lie Detector:
    It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

    Use of Artificial Intelligence (AI):
    We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.

    Company DescriptionWe know that finding work is hard, and finding meaningful work is harder. Aerotek connects 180,000+ light industrial and skilled trades workers with 14,000+ employers each year, helping our workers navigate an evolving labor market and find jobs that meet their goals, skills, and interests. Since 1983, we have provided a variety of career opportunities across North American industry – from short-term assignments at Fortune 500 companies where you can build your skills, to long-term opportunities where you can play a vital role in solving companies’ construction, manufacturing, and maintenance challenges. Our 1,500+ experienced recruiters across 250+ offices work relentlessly to put our workforce in a position to thrive. Let us rise to meet your challenges and put our people-are-everything spirit to the test as your career continues to grow.Company DescriptionWe know that finding work is hard, and finding meaningful work is harder. Aerotek connects 180,000+ light industrial and skilled trades workers with 14,000+ employers each year, helping our workers navigate an evolving labor market and find jobs that meet their goals, skills, and interests. Since 1983, we have provided a variety of career opportunities across North American industry – from short-term assignments at Fortune 500 companies where you can build your skills, to long-term opportunities where you can play a vital role in solving companies’ construction, manufacturing, and maintenance challenges. Our 1,500+ experienced recruiters across 250+ offices work relentlessly to put our workforce in a position to thrive. Let us rise to meet your challenges and put our people-are-everything spirit to the test as your career continues to grow. Read Less
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    Superintendent  

    - Baltimore
    Job DescriptionJob DescriptionJob Title: SuperintendentJob Description... Read More
    Job DescriptionJob Description

    Job Title: Superintendent

    Job Description

    This Superintendent role supports a large, multifamily construction program in Baltimore that uses pre-fabricated wall panel construction. The Superintendent oversees multiple ongoing commercial and residential projects, managing scheduling and coordination with subcontractors while ensuring work is completed according to plans, specifications, and safety standards. The position involves daily use of technology, regular reporting, and interaction with institutional personnel and city officials, offering significant growth potential and performance-based bonus opportunities as part of a cutting-edge program.

    Responsibilities

    Manage multiple ongoing commercial and residential construction projects within a large multifamily program that uses pre-fabricated wall panel construction.Develop, maintain, and regularly update detailed project schedules to ensure timely completion of all phases of work.Oversee all daily on-site activities, including monitoring subcontractor actions and ensuring work progresses according to plan.Coordinate and communicate effectively with subcontractors to align resources, resolve issues, and maintain project timelines.Conduct daily toolbox talks and lead all on-site safety initiatives to promote a safe working environment.Ensure compliance with safety standards and regulations, including adherence to OSHA-related requirements.Review, read, and interpret blueprints, engineering plans, and specifications to ensure construction meets design intent and quality expectations.Manage RFIs and submittals to clarify design details, obtain approvals, and keep documentation organized and current.Prepare accurate daily reports documenting site activities, progress, issues, and safety observations using technology tools.Collaborate and communicate professionally with institutional personnel and city officials to coordinate inspections, approvals, and project requirements.Use construction management software to track project progress, documentation, and communication.Support a small project team by providing leadership, direction, and clear communication on site.

    Essential Skills

    Proven experience as a construction superintendent managing commercial and residential construction projects.Strong experience in subcontractor management, including coordination, oversight, and performance monitoring.Demonstrated ability to create, maintain, and adjust construction project schedules.Hands-on experience overseeing on-site safety programs and conducting regular toolbox talks.Ability to read and interpret blueprints, engineering plans, and specifications accurately.Experience managing RFIs and submittals within a construction project environment.Proficiency with construction technology and daily use of digital tools for reporting and communication.Knowledge of OSHA safety standards and practices applicable to construction sites.Strong organizational skills with the ability to manage multiple ongoing projects simultaneously.Effective communication skills for working with subcontractors, institutional personnel, and city officials.

    Additional Skills & Qualifications

    OSHA 30 certification.Experience using Procore or similar construction management software.Familiarity with pre-fabricated wall panel construction methods.Ability to interpret plans and specifications to ensure projects are completed according to engineering requirements.Interest in contributing to an innovative, cutting-edge construction program with significant growth potential.Motivation to perform at a high level in an environment that offers substantial bonus opportunities tied to project success.

    Work Environment

    This role is primarily field-based, working on site as part of a small project team. The Superintendent spends most of the day on active construction sites, overseeing daily activities and coordinating subcontractors. The environment involves regular interaction with institutional personnel and city officials, use of construction technology such as Procore and digital reporting tools, and adherence to established safety protocols. Attire is typical for a professional field construction setting, including appropriate safety gear and site-appropriate clothing.

    Job Type & Location

    This is a Contract to Hire position based out of Baltimore, MD.

    Pay and Benefits

    The pay range for this position is $77.00 - $85.00/hr.

    Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)

    Workplace Type

    This is a fully onsite position in Baltimore,MD.

    Application Deadline

    This position is anticipated to close on Jul 31, 2026.

    About Actalent

    Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.

    The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

    If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

    San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records.

    Massachusetts Lie Detector: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

    Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.

    Read Less
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    Quality Control Specialist  

    - Baltimore
    Job DescriptionJob DescriptionJob Title: Quality Control Specialist –... Read More
    Job DescriptionJob Description

    Job Title: Quality Control Specialist – Sample Management and Technical Writer

    Job Description

    This Quality Control Specialist role focuses on sample management and technical writing within a large molecule manufacturing plant. The specialist works hands-on in the Quality Control unit, coordinating QC samples for routine and qualification testing, supporting qualification studies through detailed report writing, and providing backup testing as needed. The role collaborates closely with QC Microbiology, Manufacturing, Quality Assurance, Regulatory Affairs, Supply Chain, and Biologics Process Development teams to ensure timely analysis, inspection readiness, and robust data integrity across all QC activities.

    Responsibilities

    Work in Quality Control operations, performing hands-on activities including handling QC samples for routine and qualification testing, technical documentation, and backup testing of QC samples.Coordinate QC sample management, including receipt, verification, labeling, storage, and distribution of samples to relevant testing laboratories and functions.Compile, organize, and trend test results to support qualification reports and other technical documentation required for large molecule manufacturing.Review test records and associated documentation to ensure they are accurate, complete, and compliant with internal procedures and regulatory expectations.Support and perform testing of QC samples as needed to meet project timelines and manufacturing schedules.Collaborate with the Biologics Process Development team to plan and execute testing activities that support drug substance development and manufacturing.Ensure that laboratory incidents, out-of-specification (OOS) results, out-of-trend (OOT) results, deviations, and client complaints related to QC testing are thoroughly investigated and documented.Identify root causes for QC-related issues and implement effective corrective and preventive actions (CAPA) within agreed timelines.Maintain and periodically review all QC documentation, including SOPs, IOPs, EOPs, STPs, and other controlled documents, in alignment with the documentation control system.Ensure timely completion of QC activities according to project plans, and update work plans to accommodate changes in project scope, priorities, or timelines.Adhere to ALCOA principles of data integrity and promote compliance with these standards among team members.Participate in functional working teams to perform self-assessments of compliance with SOPs, Good Manufacturing Practice (GMP), and data integrity standards.Support preparation, execution, and timely closure of audit action plans, escalating concerns and risks as appropriate.Support investigations and closure of client and regulatory audit observations related to Quality Control activities.Ensure laboratory safety protocols are followed at all times, including aseptic techniques, cleanroom practices, and gowning procedures, and resolve technical issues in the QC lab effectively.Support preparation and maintenance of QC documentation used in regulatory filings, including prior approval submissions, renewals, updates, and supplements.Monitor QC analytical trends, complaints, failures, deviations, and changes to identify opportunities for process, system, and product improvements.Plan and manage QC analytical lab resources to support smooth day-to-day operations and meet business needs.Contribute to a culture of quality, compliance, safety, and continuous improvement within the QC organization.

    Essential Skills

    Bachelor’s degree in Chemistry, Biochemistry, Chemical Engineering, or a related scientific discipline.5–8 years of progressively responsible experience in Quality Control within biologics or pharmaceutical manufacturing environments, specifically supporting large molecule products.Hands-on experience in Quality Control operations, including sample management, routine and qualification testing, and technical documentation.Strong understanding of USDA and USFDA regulations, as well as ICH, EU, and Health Canada regulatory frameworks relevant to biologics manufacturing.Knowledge of USP and other pharmacopeial standards applicable to biologics and large molecule products.Working knowledge of biologic analytical techniques and validation of analytical methods.Experience with GMP environments, including adherence to Good Manufacturing Practice and data integrity standards such as ALCOA.Proficiency in deviation management, OOS/OOT investigations, CAPA development, and change control processes.Experience in technical writing for qualification reports, SOPs, and other regulated documents.Demonstrated ability to support regulatory inspections and third-party audits from a QC perspective.Experience working within established quality systems, including qualifications, validations, and product lifecycle quality management.Proven ability to lead or coordinate cross-functional teams and build strong working relationships across departments.Track record of driving continuous improvement initiatives to enhance efficiency, reduce deviations, and improve product quality.Strong organizational skills with the ability to manage multiple projects and timelines in a fast-paced environment.Excellent attention to detail, documentation accuracy, and commitment to data integrity.

    Additional Skills & Qualifications

    Experience in bioanalytical and bioassay methods for monoclonal antibodies and other biologic molecules.Experience in biopharmaceutical, pharmaceutical, or biotechnology manufacturing, particularly in large molecule and bioprocess environments.Familiarity with aseptic techniques, cleanroom operations, and gowning procedures in a regulated manufacturing or laboratory setting.Experience with document control systems and structured management of SOPs, IOPs, EOPs, STPs, and other controlled documents.Exposure to production and bioprocess operations and an understanding of how QC supports end-to-end manufacturing.Experience supporting or authoring documentation for regulatory submissions, including prior approval supplements, renewals, and updates.Ability to analyze QC trends and metrics to identify systemic issues and propose process or system enhancements.Strong problem-solving skills with the ability to resolve technical issues in the laboratory and support troubleshooting of analytical methods.Experience working in or with global organizations and comfort operating within complex, matrixed environments.Interest in contributing to an innovation-focused culture that emphasizes scientific excellence, client service, and operational efficiency.

    Work Environment

    The role is based in a large molecule manufacturing environment that includes both the manufacturing floor and Quality Control laboratories. You work closely with biologics process development and production teams in a GMP-regulated setting, supporting biopharmaceutical and biotechnology operations. The QC lab operates under strict safety protocols, including aseptic techniques, cleanroom practices, and gowning procedures, with a strong emphasis on data integrity and compliance. The organization maintains a culture driven by passionate scientists focused on solving complex scientific problems, improving R&D productivity, accelerating time to market, and reducing innovation costs. Safety is central to operations, with shared responsibility and accountability for following safety guidelines, procedures, and SOPs. The environment offers exposure to advanced biologic analytical techniques, qualification and validation activities, and regulatory inspections, providing opportunities for professional growth in a dynamic and innovation-oriented setting.

    Job Type & Location

    This is a Contract position based out of Baltimore, MD.

    Pay and Benefits

    The pay range for this position is $36.00 - $36.00/hr.

    Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)

    Workplace Type

    This is a fully onsite position in Baltimore,MD.

    Application Deadline

    This position is anticipated to close on Jul 31, 2026.

    About Actalent

    Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.

    The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

    If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

    San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records.

    Massachusetts Lie Detector: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

    Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.

    Read Less
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    Quality Control Analyst  

    - Baltimore
    Job DescriptionJob DescriptionJob Title: Quality Control AnalystJob De... Read More
    Job DescriptionJob Description

    Job Title: Quality Control Analyst

    Job Description

    The Quality Control Analyst will serve as a hands-on analyst and specialist within the Quality Control (QC) unit at a large molecule manufacturing facility. This role focuses on utility and environmental monitoring sample collection, basic QC testing, and analytical support to ensure inspection readiness and timely release of results. The analyst will work within the QC Analytical group and collaborate closely with QC Micro, Manufacturing, Quality Assurance, Regulatory Affairs, Supply Chain, and Biologics Process Development teams to support drug substance development, manufacturing, and regulatory compliance.

    Responsibilities

    Work in Quality Control operations, focusing on taking samples of utilities such as water and gas, performing Environmental Monitoring (EM), and conducting basic QC testing on collected samples.Serve as the primary point for sample collection activities, ensuring accurate, timely, and compliant sampling of utilities and environmental conditions.Compile and organize test results to support qualification reports and other quality documentation.Review test records to ensure accuracy, completeness, and compliance with internal procedures and regulatory expectations.Support testing of QC samples as needed, including basic analytical and microbiological testing within the QC Analytical laboratory.Collaborate with the Biologics Process Development team to execute testing activities that support drug substance development and manufacturing for large molecule products.Support laboratory incidents, out-of-specification (OOS) results, deviations, out-of-trend (OOT) results, and client complaints related to QC testing, contributing to timely and thorough resolution.Ensure all documentation, including SOPs, IOPs, EOPs, and STPs, is periodically reviewed, updated, and maintained according to the documentation control system.Ensure timely completion of QC activities in line with project timelines and update work plans periodically to accommodate changes in project scope, priorities, or schedules.Adhere to ALCOA principles of data integrity and promote compliance with data integrity standards among team members.Participate in functional working teams to perform self-assessments of compliance with SOPs and data integrity requirements.Support and contribute to investigations related to QC testing, analytical issues, or quality events as needed.Ensure laboratory safety protocols are followed at all times and help resolve technical issues in the QC Analytical lab efficiently.Support QC Analytical documentation in regulatory filings, including prior approval submissions, renewals, updates, and supplements, as required.Support monitoring of QC analytical trends, complaints, failures, deviations, and changes to identify opportunities for process, system, and product improvements.Plan and help manage resources to support smooth operations within the QC laboratory.

    Essential Skills

    2–4 years of progressively responsible experience in Quality Control within biologics or pharmaceutical manufacturing environments, specifically supporting large molecule products.Bachelor’s degree in Chemistry, Biochemistry, Chemical Engineering, or a related scientific discipline.Experience in basic QC testing within a laboratory environment.Working knowledge of biologic analytical techniques and validation of analytical methods.Experience working within quality systems, including qualifications, validations, and product lifecycle quality management.Experience with biologics and biopharmaceutical manufacturing processes.Experience in environmental monitoring and utility sampling, including water sampling and gas sampling.Knowledge of Good Manufacturing Practices (GMP) in biopharmaceutical, pharmaceutical, biotechnology, or biotech production settings.Familiarity with microbiology laboratory practices and aseptic technique.Experience working in cleanroom environments and following gowning procedures.Understanding and application of ALCOA principles of data integrity.Knowledge of change control processes related to QC activities and laboratory operations.Ability to support investigations of OOS, OOT, deviations, and complaints related to QC testing.Understanding of regulatory expectations from USDA and USFDA, ICH, EU, and Health Canada for biologics manufacturing.Familiarity with USP and other pharmacopeial standards relevant to biologics.

    Additional Skills & Qualifications

    Experience supporting QC Analytical documentation for regulatory filings, including prior approval submissions, renewals, updates, and supplements.Experience monitoring QC analytical trends, complaints, failures, deviations, and changes to drive process and system improvements.Experience collaborating with cross-functional teams such as QC Micro, Manufacturing, Quality Assurance, Regulatory Affairs, Supply Chain, and Process Development.Experience in bioprocess or production environments within biologics or biotechnology.Experience in laboratory operations planning and resource management.Strong attention to detail and ability to maintain accurate and compliant documentation.Ability to work in a fast-paced, innovation-focused organization serving pharmaceutical, biotechnology, nutrition, animal health, consumer goods, and specialty chemical industries.Comfort working in an environment that emphasizes safety, shared responsibility, and adherence to SOPs and safety guidelines.Strong communication and collaboration skills to support clients and internal stakeholders in resolving scientific and quality challenges.

    Work Environment

    This role is based in a large molecule manufacturing environment, with work performed both on the manufacturing floor and in the QC laboratory. The position involves regular utility sampling (such as water and gas), environmental monitoring, and work in cleanroom and controlled environments where aseptic technique and gowning procedures are required. The organization operates within a GMP-compliant biopharmaceutical and biotechnology setting, using established laboratory equipment and analytical technologies to support biologics production. The culture emphasizes innovation, scientific problem-solving, and close collaboration with global clients across pharmaceutical, biotechnology, nutrition, animal health, consumer goods, and specialty chemical industries. Safety is a core value, with shared accountability for following safety guidelines, procedures, and SOPs at all times. The work environment supports cross-functional teamwork, continuous improvement, and adherence to data integrity principles and regulatory standar

    Job Type & Location

    This is a Contract position based out of Baltimore, MD.

    Pay and Benefits

    The pay range for this position is $32.00 - $32.00/hr.

    Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)

    Workplace Type

    This is a fully onsite position in Baltimore,MD.

    Application Deadline

    This position is anticipated to close on Jul 31, 2026.

    About Actalent

    Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.

    The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

    If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

    San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records.

    Massachusetts Lie Detector: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

    Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.

    Read Less
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    Job DescriptionJob DescriptionElectrical AssemblerJob Responsibilities... Read More
    Job DescriptionJob DescriptionElectrical AssemblerJob ResponsibilitiesAssemble wire harnesses, cable assemblies, and related electrical components following blueprints, wiring diagrams, schematics, and work instructions.Cut and prepare wires to specified lengths, working with wire sizes ranging from 2 AWG to 22 AWG.Crimp, pin, and terminate wires using appropriate hand tools, connectors, and terminals.Build complete harnesses and cable assemblies by connecting terminals, connectors, and electrical components.Perform soldering on electrical and electronic components as required.Read and interpret technical drawings, schematics, and assembly instructions to ensure accurate production.Assemble and support production of printed circuit boards (PCBs) and electronic assemblies.Utilize hand tools and production equipment to complete electrical and mechanical assembly tasks.Inspect, test, and verify wire harnesses, cable assemblies, and electrical products for functionality and quality.Adhere to safety standards, production procedures, and housekeeping requirements in the work area.Required Skills & QualificationsMinimum 3 years of electrical assembly experience preferred.Strong electrical wiring experience, including handling wire sizes from 2 AWG to 22 AWG.Proficiency in crimping and pinning terminals and connectors.Hands-on soldering experience with electrical and electronic components.Experience assembling electronic components and printed circuit boards (PCBs).Ability to read and interpret blueprints, wiring diagrams, schematics, and technical instructions.Skilled in the use of hand tools and basic production equipment.Strong attention to detail and commitment to quality workmanship.Ability to follow established assembly procedures and work instructions.Preferred QualificationsExperience with both electrical and mechanical assembly.BG working in a manufacturing or production environment.Knowledge of testing and troubleshooting wire harnesses and cable assemblies.Familiarity with electrical and electronic components and assemblies.Why Join Us?Positive and team-oriented work culture.Opportunity for long-term employment and permanent hire.Performance-based pay increases after conversion to a permanent role.Clean, modern facility with a strong focus on quality and continuous improvement.Work EnvironmentFirst-shift schedule: Monday through Thursday, 5:00 AM to 3:15 PM.Four-day workweek with extended weekends.Work in a modern manufacturing facility opened within the last two years.Hands-on production environment using hand tools and standard assembly equipment.Focus on building and testing high-quality electrical and electronic products.Job Type & Location

    This is a Contract to Hire position based out of Baltimore, MD.

    Pay and Benefits

    The pay range for this position is $20.00 - $30.00/hr.

    Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)

    Workplace Type

    This is a fully onsite position in Baltimore,MD.

    Application Deadline

    This position is anticipated to close on Jul 24, 2026.

    About Aerotek

    Aerotek® Inc. provides staffing and services solutions in manufacturing, logistics, construction, aviation, facilities and maintenance. We provide the expertise, solutions and people required to rise to the challenges of North American industry. Headquartered in Hanover, Md., Aerotek operates a unified network of over 200 offices across North America, supporting more than 18,000 clients each year. Aerotek is an Allegis Group company, the global leader in workforce and business solutions. To learn more, visit: Aerotek.com | 1-888-AEROTEK.

    Aerotek offers weekly pay, employee benefits including medical, dental & vision, life insurance, health advocacy and employee assistance programs, a 401(k) plan, and employee discounts.

    The company is an equal opportunity employer and will consider all applications without regards to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

    San Francisco Fair Chance Ordinance:
    Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records.

    Massachusetts Lie Detector:
    It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

    Use of Artificial Intelligence (AI):
    We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.

    Company DescriptionWe know that finding work is hard, and finding meaningful work is harder. Aerotek connects 180,000+ light industrial and skilled trades workers with 14,000+ employers each year, helping our workers navigate an evolving labor market and find jobs that meet their goals, skills, and interests. Since 1983, we have provided a variety of career opportunities across North American industry – from short-term assignments at Fortune 500 companies where you can build your skills, to long-term opportunities where you can play a vital role in solving companies’ construction, manufacturing, and maintenance challenges. Our 1,500+ experienced recruiters across 250+ offices work relentlessly to put our workforce in a position to thrive. Let us rise to meet your challenges and put our people-are-everything spirit to the test as your career continues to grow.Company DescriptionWe know that finding work is hard, and finding meaningful work is harder. Aerotek connects 180,000+ light industrial and skilled trades workers with 14,000+ employers each year, helping our workers navigate an evolving labor market and find jobs that meet their goals, skills, and interests. Since 1983, we have provided a variety of career opportunities across North American industry – from short-term assignments at Fortune 500 companies where you can build your skills, to long-term opportunities where you can play a vital role in solving companies’ construction, manufacturing, and maintenance challenges. Our 1,500+ experienced recruiters across 250+ offices work relentlessly to put our workforce in a position to thrive. Let us rise to meet your challenges and put our people-are-everything spirit to the test as your career continues to grow. Read Less
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    Quality Control Analyst  

    - Baltimore
    Job DescriptionJob DescriptionJob Title: Quality Control AnalystJob De... Read More
    Job DescriptionJob Description

    Job Title: Quality Control Analyst

    Job Description

    The Quality Control Analyst will serve as a hands-on analyst and specialist within the Quality Control (QC) unit at a large molecule manufacturing facility. This role focuses on utility and environmental monitoring sample collection, basic QC testing, and analytical support to ensure inspection readiness and timely release of results. The analyst will work within the QC Analytical group and collaborate closely with QC Micro, Manufacturing, Quality Assurance, Regulatory Affairs, Supply Chain, and Biologics Process Development teams to support drug substance development, manufacturing, and regulatory compliance.

    Responsibilities

    Work in Quality Control operations, focusing on taking samples of utilities such as water and gas, performing Environmental Monitoring (EM), and conducting basic QC testing on collected samples.Serve as the primary point for sample collection activities, ensuring accurate, timely, and compliant sampling of utilities and environmental conditions.Compile and organize test results to support qualification reports and other quality documentation.Review test records to ensure accuracy, completeness, and compliance with internal procedures and regulatory expectations.Support testing of QC samples as needed, including basic analytical and microbiological testing within the QC Analytical laboratory.Collaborate with the Biologics Process Development team to execute testing activities that support drug substance development and manufacturing for large molecule products.Support laboratory incidents, out-of-specification (OOS) results, deviations, out-of-trend (OOT) results, and client complaints related to QC testing, contributing to timely and thorough resolution.Ensure all documentation, including SOPs, IOPs, EOPs, and STPs, is periodically reviewed, updated, and maintained according to the documentation control system.Ensure timely completion of QC activities in line with project timelines and update work plans periodically to accommodate changes in project scope, priorities, or schedules.Adhere to ALCOA principles of data integrity and promote compliance with data integrity standards among team members.Participate in functional working teams to perform self-assessments of compliance with SOPs and data integrity requirements.Support and contribute to investigations related to QC testing, analytical issues, or quality events as needed.Ensure laboratory safety protocols are followed at all times and help resolve technical issues in the QC Analytical lab efficiently.Support QC Analytical documentation in regulatory filings, including prior approval submissions, renewals, updates, and supplements, as required.Support monitoring of QC analytical trends, complaints, failures, deviations, and changes to identify opportunities for process, system, and product improvements.Plan and help manage resources to support smooth operations within the QC laboratory.

    Essential Skills

    2–4 years of progressively responsible experience in Quality Control within biologics or pharmaceutical manufacturing environments, specifically supporting large molecule products.Bachelor’s degree in Chemistry, Biochemistry, Chemical Engineering, or a related scientific discipline.Experience in basic QC testing within a laboratory environment.Working knowledge of biologic analytical techniques and validation of analytical methods.Experience working within quality systems, including qualifications, validations, and product lifecycle quality management.Experience with biologics and biopharmaceutical manufacturing processes.Experience in environmental monitoring and utility sampling, including water sampling and gas sampling.Knowledge of Good Manufacturing Practices (GMP) in biopharmaceutical, pharmaceutical, biotechnology, or biotech production settings.Familiarity with microbiology laboratory practices and aseptic technique.Experience working in cleanroom environments and following gowning procedures.Understanding and application of ALCOA principles of data integrity.Knowledge of change control processes related to QC activities and laboratory operations.Ability to support investigations of OOS, OOT, deviations, and complaints related to QC testing.Understanding of regulatory expectations from USDA and USFDA, ICH, EU, and Health Canada for biologics manufacturing.Familiarity with USP and other pharmacopeial standards relevant to biologics.

    Additional Skills & Qualifications

    Experience supporting QC Analytical documentation for regulatory filings, including prior approval submissions, renewals, updates, and supplements.Experience monitoring QC analytical trends, complaints, failures, deviations, and changes to drive process and system improvements.Experience collaborating with cross-functional teams such as QC Micro, Manufacturing, Quality Assurance, Regulatory Affairs, Supply Chain, and Process Development.Experience in bioprocess or production environments within biologics or biotechnology.Experience in laboratory operations planning and resource management.Strong attention to detail and ability to maintain accurate and compliant documentation.Ability to work in a fast-paced, innovation-focused organization serving pharmaceutical, biotechnology, nutrition, animal health, consumer goods, and specialty chemical industries.Comfort working in an environment that emphasizes safety, shared responsibility, and adherence to SOPs and safety guidelines.Strong communication and collaboration skills to support clients and internal stakeholders in resolving scientific and quality challenges.

    Work Environment

    This role is based in a large molecule manufacturing environment, with work performed both on the manufacturing floor and in the QC laboratory. The position involves regular utility sampling (such as water and gas), environmental monitoring, and work in cleanroom and controlled environments where aseptic technique and gowning procedures are required. The organization operates within a GMP-compliant biopharmaceutical and biotechnology setting, using established laboratory equipment and analytical technologies to support biologics production. The culture emphasizes innovation, scientific problem-solving, and close collaboration with global clients across pharmaceutical, biotechnology, nutrition, animal health, consumer goods, and specialty chemical industries. Safety is a core value, with shared accountability for following safety guidelines, procedures, and SOPs at all times. The work environment supports cross-functional teamwork, continuous improvement, and adherence to data integrity principles and regulatory standar

    Job Type & Location

    This is a Contract position based out of Baltimore, MD.

    Pay and Benefits

    The pay range for this position is $32.00 - $32.00/hr.

    Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)

    Workplace Type

    This is a fully onsite position in Baltimore,MD.

    Application Deadline

    This position is anticipated to close on Jul 31, 2026.

    About Actalent

    Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.

    The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

    If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

    San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records.

    Massachusetts Lie Detector: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

    Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.

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    Contracts Specialist  

    - Baltimore
    Job DescriptionJob DescriptionContracts SpecialistJob DescriptionThe C... Read More
    Job DescriptionJob Description

    Contracts Specialist

    Job Description

    The Contracts Specialist reviews client contracts and issues insurance certificates in accordance with contractual requirements. This role ensures that insurance terms and documentation comply with client-specific conditions, manages a high volume of time-sensitive requests, and maintains accurate records. You work in a fast-paced environment where strong attention to detail, solid contract comprehension, and clear communication are essential to supporting risk management and client service.

    Responsibilities

    Review and interpret client contracts to identify insurance requirements and compliance obligations.Issue insurance certificates that accurately reflect contractual insurance terms and conditions.Ensure all insurance documentation complies with client-specific contractual requirements and internal standards.Manage a high volume of time-sensitive contract and certificate requests while maintaining accuracy and completeness.Work within spreadsheets to track, organize, and update contract and insurance certificate information.Create and maintain simple formulas in Excel to support reporting, data validation, and documentation control.Maintain accurate records of contracts, insurance certificates, and related correspondence.Communicate clearly and professionally with internal stakeholders and external clients regarding insurance terms, certificate requests, and compliance matters.Identify discrepancies or gaps in insurance requirements and escalate or resolve them in line with established procedures.Support continuous improvement of contract review and insurance certificate issuance processes in a fast-paced, remote environment.

    Essential Skills

    At least 3 years of experience reviewing and interpreting client contracts.At least 3 years of experience issuing insurance certificates.At least 3 years of experience ensuring compliance with contractual insurance requirements.Proficiency working within spreadsheets and creating simple formulas in Excel.Strong attention to detail and accuracy in contract and insurance documentation.Ability to manage a high volume of time-sensitive requests in a fast-paced environment.Solid contract comprehension and ability to interpret insurance-related clauses.Effective written and verbal communication skills for interacting with clients and internal teams.Organizational skills to maintain structured and complete records of contracts and certificates.

    Additional Skills & Qualifications

    Experience in the architecture, engineering, and construction (AEC) industry.Experience in data entry with a focus on accuracy and consistency.Exposure to finance or insurance environments and terminology.Prior experience with contract review beyond insurance requirements.Familiarity with insurance practices and documentation processes.Ability to work independently in a remote setting across various time zones.Job Type & Location

    This is a Contract to Hire position based out of Baltimore, MD.

    Pay and Benefits

    The pay range for this position is $24.00 - $28.50/hr.

    Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)

    Workplace Type

    This is a fully remote position.

    Application Deadline

    This position is anticipated to close on Jul 24, 2026.

    About Aston Carter

    Aston Carter provides world-class corporate talent solutions to thousands of clients across the globe. Specialized in accounting, finance, human resources, talent acquisition, procurement, supply chain and select administrative professions, we extend the capabilities of industry-leading companies. We draw on our deep recruiting expertise and expansive network to meet the evolving needs of our clients and talent community with agility and excellence. With offices across the U.S., Canada, Asia Pacific and Europe, Aston Carter serves many of the Fortune 500. We are proud to be a ClearlyRated Best of Staffing® Platinum Award winner for both client and talent service.

    The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

    If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email astoncarteraccommodation@astoncarter.com for other accommodation options.

    San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records.

    Massachusetts Lie Detector: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

    Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.

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    Senior Architect  

    - Baltimore
    Job DescriptionJob DescriptionJob DescriptionThis Sr. Architect role l... Read More
    Job DescriptionJob Description

    Job Description

    This Sr. Architect role leads and manages complex architectural projects from initial concept through construction administration, with a focus on high-end hospitality and private club environments. You will oversee project schedules, budgets, staffing, and deliverables while managing client expectations and ensuring high-quality, refined design solutions. Partnering closely with firm leadership, you will develop master plans, building designs, presentations, drawing sets, specifications, and construction documents, coordinating closely with clients, consultants, contractors, and internal multidisciplinary teams. The position emphasizes advanced Revit production, strong design sensibilities, and robust project management skills, offering a clear path for career growth within a collaborative and dynamic studio environment.

    Responsibilities

    Lead and manage architectural projects from master planning through all phases, including conceptual design, schematic design, design development, construction documentation, and construction administration.Oversee project schedules, budgets, staffing, and deliverables to ensure projects are completed on time and within budget.Develop and refine design concepts for planning, architecture, and interior design projects, with a focus on highly refined architectural design solutions.Produce and coordinate architectural drawing sets, project schedules, and design specifications in Revit, following established firm guidelines and standards.Review design and construction documentation for quality, accuracy, and conformity with project design concepts and client requirements.Lead site planning, space planning, and massing studies to create compelling and functional design solutions.Manage architectural projects under the supervision of firmwide leadership, including scheduling within project fee structures and overseeing architectural staff.Mentor and support architectural staff, providing guidance on design, technical detailing, and project delivery best practices.Ensure project designers and architects adhere to internal policies, procedures, and quality standards.Review staffing and scheduling projections for architecture projects and participate in weekly office-wide scheduling meetings.Manage work plans to deliver high-quality presentations and construction documents that clearly communicate design intent.Evaluate project progress, performance, and design goals, adjusting strategies as needed to maintain quality and schedule.Engage directly with high-end private club clientele and other key stakeholders to understand their needs and maintain strong client relationships.Coordinate efforts with all associated technical disciplines and consultants to ensure integrated and timely project deliverables.Assist the production team in preparing and reviewing design and construction documents, ensuring consistency with firm standards.Apply strong knowledge of building codes and technical qualifications to ensure code-compliant and constructible designs.Participate in contract administration activities and utilize AIA documents, CSI specifications, and established project procedures.Collaborate closely with multidisciplinary project teams, including engineering consultants, general contractors, subcontractors, vendors, and other partners.Represent the firm in a professional, client-facing capacity, including periodic travel to project sites for meetings, reviews, and construction-related activities.

    Essential Skills

    Bachelor’s or Master’s degree in architecture.15–20 years of professional architectural experience.Proven experience leading and developing architectural designs, supported by a strong portfolio demonstrating creative and refined project solutions.Demonstrated ability to manage the full design process from pre-design and programming through construction administration.Significant experience managing architectural projects, including scheduling, budgeting, staffing, and coordination with multidisciplinary teams.Strong client-facing skills with the ability to build and maintain long-term client relationships.Advanced proficiency in Revit for production of architectural drawing sets, schedules, and design specifications.Proficiency in Bluebeam, AutoCAD, and other BIM software tools.Proficiency in Adobe Photoshop for design presentations and visual communication.Demonstrated contract administration capabilities and working knowledge of building codes.Working knowledge of CSI specifications, AIA documents, and standard project procedures.Ability to interpret and apply technical qualifications and codes to design and construction documents.Capability to lead conceptual master planning, site planning, and space planning efforts.Strong organizational and time-management skills to oversee multiple projects and deadlines.Ability to mentor and guide architectural staff in design, technical detailing, and project management.

    Additional Skills & Qualifications

    Architectural license and/or NCARB certification preferred.Hospitality design experience, particularly with private clubs, clubhouses, restaurants, and aquatic centers, preferred.Experience engaging with high-end clientele and delivering projects with a high level of design refinement.Active involvement or interest in professional organizations such as AIA, ULI, or USGBC is desirable.Experience working within established firm design standards and guidelines.Comfort working in a hybrid environment and collaborating closely with firm leadership across locations.Strong communication and presentation skills, both verbal and written.Ability to travel approximately once a month, typically for local day trips with occasional overnight stays.

    Work Environment

    leadership roles. The work environment also features a range of social and wellness-oriented activities such as happy hours, holiday events, seasonal celebrations, sporting outings, free parking, and complimentary workout classes, alongside a comprehensive benefits package, a 401(k) match, and flexible time off.

    Job Type & Location

    This is a Permanent position based out of Baltimore, MD.

    Pay and Benefits

    The pay range for this position is $100000.00 - $136500.00/yr.

    Chambers offers competitive compensation commensurate with experience and a welcoming environment that encourages and supports professional development. Unlimited PTO Paid Holiday 401K Paid Healthcare Insurance Plans

    Workplace Type

    This is a hybrid position in Baltimore,MD.

    Application Deadline

    This position is anticipated to close on Aug 3, 2026.

    About Actalent

    Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.

    The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

    If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

    San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records.

    Massachusetts Lie Detector: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

    Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.

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    Excavator Operator  

    - Baltimore
    Job DescriptionJob DescriptionJob Title: Excavator OperatorJob Descrip... Read More
    Job DescriptionJob DescriptionJob Title: Excavator OperatorJob Description

    This role operates heavy equipment to safely and efficiently load a high volume of trucks with dirt at a busy site in Curtis Bay, Maryland. You will use excavators and other heavy equipment to support daily operations and help maintain a productive, safety-focused work environment.

    ResponsibilitiesOperate excavators to load approximately 150–200 trucks per day with dirt in a safe and efficient manner.Use heavy equipment such as excavators, loaders, front-end loaders, and dozers to support daily site operations as needed.Perform pre-operation inspections of equipment to ensure safe and proper functioning.Follow all site safety procedures and best practices while operating heavy equipment.Coordinate with truck drivers and site personnel to maintain a steady and organized flow of loading activity.Monitor material quality and loading accuracy to meet site and project requirements.Report any equipment issues, safety concerns, or operational delays to site leadership promptly.Maintain a clean and orderly work area around loading and operating zones.Essential SkillsAt least 5 years of experience operating excavators, specifically in loading trucks.Proven heavy equipment operation experience, including excavators, loaders, front-end loaders, and dozers.Ability to safely and consistently load a high volume of trucks each day.Strong awareness of safety practices and procedures in a heavy equipment environment.Capability to work efficiently in a fast-paced, production-oriented setting.Additional Skills & QualificationsAny additional heavy equipment experience beyond excavators, such as loaders, front-end loaders, or dozers, is a plus.Experience working in industrial, construction, or environmental plant settings is beneficial.Ability to communicate clearly with drivers and team members to coordinate loading activities.Why Work Here?

    You join a company that offers steady work with the potential for ongoing opportunities beyond the initial 6‑month contract. The organization operates multiple plants in the area, creating room for internal mobility and growth. Promotion from within is a core part of the culture, giving motivated operators a clear path to advance their careers while working with an experienced and supportive team.

    Work Environment

    This position is based at a plant facility in Curtis Bay, Maryland, where you will primarily work outdoors or in an industrial yard environment. You will operate heavy equipment such as excavators, loaders, front-end loaders, and dozers to support daily operations. The standard schedule runs from 6:45 AM to 3:30 PM. The role involves working around trucks, dirt, and other site materials, requiring consistent attention to safety and situational awareness in a busy, production-focused setting.

    Job Type & Location

    This is a Contract position based out of Baltimore, MD.

    Pay and Benefits

    The pay range for this position is $25.00 - $30.00/hr.

    Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)

    Workplace Type

    This is a fully onsite position in Baltimore,MD.

    Application Deadline

    This position is anticipated to close on Aug 3, 2026.

    About Aerotek

    Aerotek® Inc. provides staffing and services solutions in manufacturing, logistics, construction, aviation, facilities and maintenance. We provide the expertise, solutions and people required to rise to the challenges of North American industry. Headquartered in Hanover, Md., Aerotek operates a unified network of over 200 offices across North America, supporting more than 18,000 clients each year. Aerotek is an Allegis Group company, the global leader in workforce and business solutions. To learn more, visit: Aerotek.com | 1-888-AEROTEK.

    Aerotek offers weekly pay, employee benefits including medical, dental & vision, life insurance, health advocacy and employee assistance programs, a 401(k) plan, and employee discounts.

    The company is an equal opportunity employer and will consider all applications without regards to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

    San Francisco Fair Chance Ordinance:
    Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records.

    Massachusetts Lie Detector:
    It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

    Use of Artificial Intelligence (AI):
    We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.

    Company DescriptionWe know that finding work is hard, and finding meaningful work is harder. Aerotek connects 180,000+ light industrial and skilled trades workers with 14,000+ employers each year, helping our workers navigate an evolving labor market and find jobs that meet their goals, skills, and interests. Since 1983, we have provided a variety of career opportunities across North American industry – from short-term assignments at Fortune 500 companies where you can build your skills, to long-term opportunities where you can play a vital role in solving companies’ construction, manufacturing, and maintenance challenges. Our 1,500+ experienced recruiters across 250+ offices work relentlessly to put our workforce in a position to thrive. Let us rise to meet your challenges and put our people-are-everything spirit to the test as your career continues to grow.Company DescriptionWe know that finding work is hard, and finding meaningful work is harder. Aerotek connects 180,000+ light industrial and skilled trades workers with 14,000+ employers each year, helping our workers navigate an evolving labor market and find jobs that meet their goals, skills, and interests. Since 1983, we have provided a variety of career opportunities across North American industry – from short-term assignments at Fortune 500 companies where you can build your skills, to long-term opportunities where you can play a vital role in solving companies’ construction, manufacturing, and maintenance challenges. Our 1,500+ experienced recruiters across 250+ offices work relentlessly to put our workforce in a position to thrive. Let us rise to meet your challenges and put our people-are-everything spirit to the test as your career continues to grow. Read Less
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    Controls Engineer 4  

    - Baltimore
    Job DescriptionJob DescriptionJob Title: Controls Engineer 4Job Descri... Read More
    Job DescriptionJob Description

    Job Title: Controls Engineer 4

    Job Description

    As a Controls Engineer, you will be responsible for the design, development, installation, and maintenance of equipment used to monitor and control systems, machinery, and processes. Your expertise will be applied across various applications such as industrial controls, cybersecurity, building automation, water and wastewater management, power controls and protection, energy management, and transportation systems. You will leverage your technical skills in advanced process control, instrumentation, distributed control systems, PLCs, and SCADA systems to design and implement solutions for complex customer needs.

    Responsibilities

    Design and originate documents for small projects and support large programs.Conduct requirements analysis, subsystem designs, and prepare specifications.Perform QA/QC and technical reviews of designs.Lead programming and configuration efforts for complex automation and SCADA applications.Program, configure, and troubleshoot PLCs, RTUs, and HMI systems with protocols like DNP3, Modbus, SEL Fast Messaging, or Mirrored Bits.Author testing and commissioning procedures and prepare test reports.Commission deployed systems and develop test fixtures and simulation devices.Perform factory and field testing.Troubleshoot service calls and perform hardware/software upgrades on existing systems.Conduct surveys, inspections, and prepare cost estimates for projects.Assist expereinced engineers with bids and proposals.Assign and coordinate tasks with entry-level engineers and technical staff.

    Essential Skills

    Proficiency in PLC programming, SCADA, switchgear, SEL, RTAC, generator controls, and substations.Bachelor's degree with 7+ years or Master's degree with 5+ years in electrical, automation, or other engineering fields.At least 5 years of hands-on experience in the electric utilities sector.Minimum of 5 years specializing in solution architecture.Proficiency in real-time grid management with systems like ADMS, DERMS, SCADA, and EMS.Experience with vendor software systems such as Aspen, Siemens, ABB, General Electric, Schneider Electric, OSIsoft, Honeywell, Oracle Utilities, Eaton, PcVue, Inductive Ignition, or similar products.

    Additional Skills & Qualifications

    Experience in reading electrical and control schematics and plans.Experience in control system startup, configuration, and calibration.Proficiency in testing and troubleshooting control systems.Experience using basic electrical and machinist hand tools, as well as industry-specific tools.

    Work Environment

    This position is based in Baltimore, MD, with support required in Frederick and Ft Meade, necessitating travel as needed. You will be part of the PCS (power control systems) group within a large and reputable company. The standard work shift is Monday through Friday, from 7:00 AM to 4:00 PM.

    Job Type & Location

    This is a Permanent position based out of Baltimore, MD.

    Pay and Benefits

    The pay range for this position is $125120.00 - $187680.00/yr.

    A competitive salary Medical, dental, vision, life, and disability insurance Paid time off Tuition reimbursement 401k Retirement Plan Military Reserve pay offset Paid maternity leave

    Workplace Type

    This is a fully onsite position in Baltimore,MD.

    Application Deadline

    This position is anticipated to close on Aug 3, 2026.

    About Actalent

    Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.

    The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

    If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

    San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records.

    Massachusetts Lie Detector: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

    Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.

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    Project Architect  

    - Baltimore
    Job DescriptionJob DescriptionJob Title: Project ArchitectJob Descript... Read More
    Job DescriptionJob DescriptionJob Title: Project ArchitectJob Description

    We are seeking a highly skilled Project Architect with over three years of experience to lead and manage commercial projects. This position offers a unique opportunity to work in a collaborative environment alongside a talented team of designers, planners, and architects. The ideal candidate will have experience in the design and documentation of complex projects, including ground-up construction, adaptive reuse, and significant renovations. Our studios specialize in the housing, commercial, and hospitality sectors, often with overlapping mixed-uses. Knowledge of these areas is highly beneficial. You will be responsible for leading the production of deliverables through all project phases, from schematic design to construction administration, ensuring design quality and compliance with building codes and zoning regulations.

    ResponsibilitiesLead the production of project deliverables from schematic design to construction administration.Demonstrate strong technical leadership and coordinate project documentation.Ensure design quality and compliance with building codes and zoning regulations.Engage directly with clients and contractors to facilitate project success.Mentor junior staff and collaborate closely with Principals, project design leaders, and project managers.Uphold the integrity of the design vision throughout the project process.Essential SkillsProficiency in Revit and AutoCAD.Registered Architect with an accredited degree in Architecture.Minimum of 3 years of experience in commercial projects.Expertise in ground-up construction, renovation, and adaptive reuse.Strong knowledge of construction documents and technical detailing.Familiarity with building codes and zoning regulations.Ability to lead projects through all phases.Experience in client and contractor coordination.Strong communication and organizational skills.Additional Skills & QualificationsExperience in construction administration and project management.Proficiency in design development and schematic design.Ability to manage multiple projects and meet deadlines.Strong problem-solving and decision-making skills.Detail-oriented with excellent written and verbal communication skills.Experience mentoring junior staff and a collaborative, team-focused mindset.Knowledge of sustainable design principles is a plus.Preferred experience in hospitality, residential, and mixed-use projects.Strong client presentation and relationship management skills.Work Environment

    Our firm operates five studios with approximately 75 employees in the Baltimore office. The work is divided across focus areas including commercial projects such as retail, shell buildings, interiors, and restaurants, as well as housing with an emphasis on multifamily and senior living. We have a specialized interiors team and a focus on graphics and signage. The office is located in a recently renovated, modern workspace on the 18th floor of a prime downtown location. Employees have the flexibility to work remotely one day per week, while being part of a dynamic team with opportunities for professional growth across different studios and project types.

    Job Type & Location

    This is a Contract to Hire position based out of Baltimore, MD.

    Pay and Benefits

    The pay range for this position is $90000.00 - $125000.00/hr.

    Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)

    Workplace Type

    This is a hybrid position in Baltimore,MD.

    Application Deadline

    This position is anticipated to close on Aug 3, 2026.

    About Actalent

    Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.

    The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

    If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

    San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records.

    Massachusetts Lie Detector: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

    Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.

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    Quality Control Specialist  

    - Baltimore
    Job DescriptionJob DescriptionJob Title: Quality Control Specialist –... Read More
    Job DescriptionJob Description

    Job Title: Quality Control Specialist – Sample Management and Technical Writer

    Job Description

    This Quality Control Specialist role focuses on sample management and technical writing within a large molecule manufacturing plant. The specialist works hands-on in the Quality Control unit, coordinating QC samples for routine and qualification testing, supporting qualification studies through detailed report writing, and providing backup testing as needed. The role collaborates closely with QC Microbiology, Manufacturing, Quality Assurance, Regulatory Affairs, Supply Chain, and Biologics Process Development teams to ensure timely analysis, inspection readiness, and robust data integrity across all QC activities.

    Responsibilities

    Work in Quality Control operations, performing hands-on activities including handling QC samples for routine and qualification testing, technical documentation, and backup testing of QC samples.Coordinate QC sample management, including receipt, verification, labeling, storage, and distribution of samples to relevant testing laboratories and functions.Compile, organize, and trend test results to support qualification reports and other technical documentation required for large molecule manufacturing.Review test records and associated documentation to ensure they are accurate, complete, and compliant with internal procedures and regulatory expectations.Support and perform testing of QC samples as needed to meet project timelines and manufacturing schedules.Collaborate with the Biologics Process Development team to plan and execute testing activities that support drug substance development and manufacturing.Ensure that laboratory incidents, out-of-specification (OOS) results, out-of-trend (OOT) results, deviations, and client complaints related to QC testing are thoroughly investigated and documented.Identify root causes for QC-related issues and implement effective corrective and preventive actions (CAPA) within agreed timelines.Maintain and periodically review all QC documentation, including SOPs, IOPs, EOPs, STPs, and other controlled documents, in alignment with the documentation control system.Ensure timely completion of QC activities according to project plans, and update work plans to accommodate changes in project scope, priorities, or timelines.Adhere to ALCOA principles of data integrity and promote compliance with these standards among team members.Participate in functional working teams to perform self-assessments of compliance with SOPs, Good Manufacturing Practice (GMP), and data integrity standards.Support preparation, execution, and timely closure of audit action plans, escalating concerns and risks as appropriate.Support investigations and closure of client and regulatory audit observations related to Quality Control activities.Ensure laboratory safety protocols are followed at all times, including aseptic techniques, cleanroom practices, and gowning procedures, and resolve technical issues in the QC lab effectively.Support preparation and maintenance of QC documentation used in regulatory filings, including prior approval submissions, renewals, updates, and supplements.Monitor QC analytical trends, complaints, failures, deviations, and changes to identify opportunities for process, system, and product improvements.Plan and manage QC analytical lab resources to support smooth day-to-day operations and meet business needs.Contribute to a culture of quality, compliance, safety, and continuous improvement within the QC organization.

    Essential Skills

    Bachelor’s degree in Chemistry, Biochemistry, Chemical Engineering, or a related scientific discipline.5–8 years of progressively responsible experience in Quality Control within biologics or pharmaceutical manufacturing environments, specifically supporting large molecule products.Hands-on experience in Quality Control operations, including sample management, routine and qualification testing, and technical documentation.Strong understanding of USDA and USFDA regulations, as well as ICH, EU, and Health Canada regulatory frameworks relevant to biologics manufacturing.Knowledge of USP and other pharmacopeial standards applicable to biologics and large molecule products.Working knowledge of biologic analytical techniques and validation of analytical methods.Experience with GMP environments, including adherence to Good Manufacturing Practice and data integrity standards such as ALCOA.Proficiency in deviation management, OOS/OOT investigations, CAPA development, and change control processes.Experience in technical writing for qualification reports, SOPs, and other regulated documents.Demonstrated ability to support regulatory inspections and third-party audits from a QC perspective.Experience working within established quality systems, including qualifications, validations, and product lifecycle quality management.Proven ability to lead or coordinate cross-functional teams and build strong working relationships across departments.Track record of driving continuous improvement initiatives to enhance efficiency, reduce deviations, and improve product quality.Strong organizational skills with the ability to manage multiple projects and timelines in a fast-paced environment.Excellent attention to detail, documentation accuracy, and commitment to data integrity.

    Additional Skills & Qualifications

    Experience in bioanalytical and bioassay methods for monoclonal antibodies and other biologic molecules.Experience in biopharmaceutical, pharmaceutical, or biotechnology manufacturing, particularly in large molecule and bioprocess environments.Familiarity with aseptic techniques, cleanroom operations, and gowning procedures in a regulated manufacturing or laboratory setting.Experience with document control systems and structured management of SOPs, IOPs, EOPs, STPs, and other controlled documents.Exposure to production and bioprocess operations and an understanding of how QC supports end-to-end manufacturing.Experience supporting or authoring documentation for regulatory submissions, including prior approval supplements, renewals, and updates.Ability to analyze QC trends and metrics to identify systemic issues and propose process or system enhancements.Strong problem-solving skills with the ability to resolve technical issues in the laboratory and support troubleshooting of analytical methods.Experience working in or with global organizations and comfort operating within complex, matrixed environments.Interest in contributing to an innovation-focused culture that emphasizes scientific excellence, client service, and operational efficiency.

    Work Environment

    The role is based in a large molecule manufacturing environment that includes both the manufacturing floor and Quality Control laboratories. You work closely with biologics process development and production teams in a GMP-regulated setting, supporting biopharmaceutical and biotechnology operations. The QC lab operates under strict safety protocols, including aseptic techniques, cleanroom practices, and gowning procedures, with a strong emphasis on data integrity and compliance. The organization maintains a culture driven by passionate scientists focused on solving complex scientific problems, improving R&D productivity, accelerating time to market, and reducing innovation costs. Safety is central to operations, with shared responsibility and accountability for following safety guidelines, procedures, and SOPs. The environment offers exposure to advanced biologic analytical techniques, qualification and validation activities, and regulatory inspections, providing opportunities for professional growth in a dynamic and innovation-oriented setting.

    Job Type & Location

    This is a Contract position based out of Baltimore, MD.

    Pay and Benefits

    The pay range for this position is $36.00 - $36.00/hr.

    Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)

    Workplace Type

    This is a fully onsite position in Baltimore,MD.

    Application Deadline

    This position is anticipated to close on Aug 3, 2026.

    About Actalent

    Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.

    The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

    If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

    San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records.

    Massachusetts Lie Detector: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

    Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.

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    Architectural Designer  

    - Baltimore
    Job DescriptionJob DescriptionJob Title: Architectural DesignerJob Des... Read More
    Job DescriptionJob DescriptionJob Title: Architectural DesignerJob Description

    This role offers an excellent opportunity for an Architectural Designer with 3–5 years of experience to contribute to an award‑winning, full‑service design practice. You will work on a wide variety of commercial and related project types, gaining exposure from schematic design through construction documents while collaborating with energetic, highly skilled design professionals. The position provides strong potential for professional growth, cross‑studio collaboration, and long‑term career advancement in a modern, design‑focused environment.

    ResponsibilitiesParticipate in all phases of the design process, from schematic design through construction documents, for a variety of commercial and related projects.Develop, manage, and maintain Revit BIM models across all project phases, ensuring accuracy, consistency, and adherence to office standards.Produce coordinated, detailed, and code‑compliant construction drawing sets, including plans, elevations, sections, details, and schedules.Create, modify, and manage Revit families to support project‑specific design and documentation needs.Use Revit for space planning, detailing, and documentation, ensuring constructability and alignment with project requirements, timelines, and commercial building codes.Collaborate closely with internal design teams and external consultants, including MEP and structural engineers, to coordinate and integrate all disciplines into cohesive project documents.Support design development by preparing diagrams, 3D views, and visualizations using Revit, SketchUp, and Adobe Suite tools as needed.Assist in the production and refinement of design presentations and documentation for client reviews and internal design critiques.Contribute to the production of drawing sets for commercial projects such as retail, shell buildings, interiors, restaurants, multifamily housing, senior living, and related work.Maintain model and documentation standards, helping to improve workflows and quality across project teams.Work across different studios as project needs require, supporting various project types and teams to balance workload and broaden experience.Essential Skills3–5 years of professional experience as an Architectural Designer or in a closely related architectural role.Strong Revit experience on commercial architectural projects, with the ability to develop and manage BIM models across all project phases from schematic design through construction documents.Proven ability to produce coordinated, detailed construction drawing sets for commercial projects.Experience using Revit for space planning, detailing, and documentation, with a focus on accuracy, constructability, and alignment with project requirements and timelines.Demonstrated experience working with commercial building codes and incorporating them into design and documentation.Experience collaborating with internal design teams and external consultants, including MEP and structural engineers, within a BIM workflow.Proficiency in Revit for creating and modifying families and maintaining model standards.Experience with production of drawing sets for commercial projects.Ability to work effectively from schematic design through construction documents while managing multiple tasks and deadlines.Additional Skills & QualificationsExperience with SketchUp for 3D modeling and design visualization.Proficiency with Adobe Suite (such as Photoshop, InDesign, Illustrator) to support presentations and graphic communication.Background in commercial project types such as retail, shell buildings, interiors, restaurants, multifamily housing, or senior living.Interest in working within different studios and project types, including commercial, housing, interiors, and graphics/signage.Strong communication and collaboration skills, with a desire to learn and grow within a multidisciplinary design environment.Motivated, detail‑oriented, and eager to expand experience across all phases of design and documentation.Work Environment

    This role is based in a recently renovated, modern office located on a high floor in a prime downtown setting, offering a bright, contemporary workspace with city views. The firm operates as an award‑winning, full‑service design practice with about 75 employees in the local office, organized into multiple studios that focus on commercial projects (including retail, shell buildings, interiors, and restaurants), housing with an emphasis on multifamily and senior living, a specialized interiors team, and graphics and signage. Architectural staff are not limited to a single studio; while each person has a home base, they have the opportunity to work across different studios depending on project needs and workload, providing exposure to a wide range of project types and teams. The commercial studio maintains an extensive backlog of projects, offering consistent, engaging work and strong opportunities for professional growth. The environment emphasizes collaboration, coordinated use of Revit and other digital design tools, and close interaction with consultants. Dress expectations align with a professional design office in a downtown commercial setting.

    Job Type & Location

    This is a Contract to Hire position based out of Baltimore, MD.

    Pay and Benefits

    The pay range for this position is $26.44 - $40.87/hr.

    Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)

    Workplace Type

    This is a hybrid position in Baltimore,MD.

    Application Deadline

    This position is anticipated to close on Aug 3, 2026.

    About Actalent

    Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.

    The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

    If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

    San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records.

    Massachusetts Lie Detector: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

    Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.

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    Dump Truck Driver  

    - Baltimore
    Job DescriptionJob DescriptionJob Title: Dump Truck DriverJob Descript... Read More
    Job DescriptionJob DescriptionJob Title: Dump Truck DriverJob Description

    This role involves safely operating an on-site dump truck at a wastewater facility, transporting materials between a feeder and designated dumping areas on a structured night shift schedule. You will support consistent plant operations by performing regular hauls throughout the shift with minimal physical labor.

    ResponsibilitiesOperate an on-site dump truck safely and efficiently within the wastewater facility.Drive the dump truck from the loading feeder to the designated dumping area and return for the next load.Complete approximately 12–13 dump truck loads per night, averaging about one dump per hour.Perform pre-trip and post-trip inspections of the dump truck to ensure safe operating condition.Follow all site safety protocols, traffic patterns, and operational procedures within the plant.Coordinate with plant personnel and equipment operators to ensure smooth material flow.Operate in a consistent, repetitive route within the facility, maintaining focus and attention to detail.Report any mechanical issues, hazards, or incidents promptly to site supervision.Maintain cleanliness and organization of the cab and work area as required by site standards.Essential Skills4+ years of experience operating dump trucks or heavy equipment.Proficiency in operating dump trucks in an industrial or construction environment.Experience operating heavy equipment such as front-end loaders, excavators, or dozers.Ability to safely maneuver large vehicles in confined or busy industrial areas.Strong awareness of safety practices and adherence to site-specific safety protocols.Willingness and ability to work night shifts on a rotating schedule.Comfort working in a wastewater plant environment.Additional Skills & QualificationsCommercial Driver’s License (CDL) is a plus.Experience working in wastewater, industrial, or similar heavy industrial facilities is beneficial.Ability to follow a structured schedule and maintain consistent performance throughout the shift.Strong communication skills to coordinate with plant operators and team members.Why Work Here?

    You can enjoy the stability of reporting to the same site each shift, with a predictable route and routine that reduces the physical demands often associated with similar roles. The position offers overtime opportunities for those who want to increase their earnings, while the structured Dupont schedule provides regular, planned days off to support work-life balance.

    Work Environment

    You will work on-site at a wastewater plant and must be comfortable with the associated sights, sounds, and odors of this type of facility. The role is based on a night shift using a Dupont schedule, which includes working every other weekend and a repeating pattern of on and off days: first week working Saturday, Sunday, and Monday, off Tuesday and Wednesday, working Thursday and Friday; second week off Saturday, Sunday, and Monday, working Tuesday and Wednesday, off Thursday and Friday, and working Saturday and Sunday. The work focuses on operating a dump truck and coordinating with other heavy equipment such as front-end loaders, excavators, and dozers in an industrial setting, with minimal manual labor required.

    Job Type & Location

    This is a Contract position based out of Baltimore, MD.

    Pay and Benefits

    The pay range for this position is $24.00 - $24.00/hr.

    Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)

    Workplace Type

    This is a fully onsite position in Baltimore,MD.

    Application Deadline

    This position is anticipated to close on Aug 3, 2026.

    About Aerotek

    Aerotek® Inc. provides staffing and services solutions in manufacturing, logistics, construction, aviation, facilities and maintenance. We provide the expertise, solutions and people required to rise to the challenges of North American industry. Headquartered in Hanover, Md., Aerotek operates a unified network of over 200 offices across North America, supporting more than 18,000 clients each year. Aerotek is an Allegis Group company, the global leader in workforce and business solutions. To learn more, visit: Aerotek.com | 1-888-AEROTEK.

    Aerotek offers weekly pay, employee benefits including medical, dental & vision, life insurance, health advocacy and employee assistance programs, a 401(k) plan, and employee discounts.

    The company is an equal opportunity employer and will consider all applications without regards to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

    San Francisco Fair Chance Ordinance:
    Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records.

    Massachusetts Lie Detector:
    It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

    Use of Artificial Intelligence (AI):
    We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.

    Company DescriptionWe know that finding work is hard, and finding meaningful work is harder. Aerotek connects 180,000+ light industrial and skilled trades workers with 14,000+ employers each year, helping our workers navigate an evolving labor market and find jobs that meet their goals, skills, and interests. Since 1983, we have provided a variety of career opportunities across North American industry – from short-term assignments at Fortune 500 companies where you can build your skills, to long-term opportunities where you can play a vital role in solving companies’ construction, manufacturing, and maintenance challenges. Our 1,500+ experienced recruiters across 250+ offices work relentlessly to put our workforce in a position to thrive. Let us rise to meet your challenges and put our people-are-everything spirit to the test as your career continues to grow.Company DescriptionWe know that finding work is hard, and finding meaningful work is harder. Aerotek connects 180,000+ light industrial and skilled trades workers with 14,000+ employers each year, helping our workers navigate an evolving labor market and find jobs that meet their goals, skills, and interests. Since 1983, we have provided a variety of career opportunities across North American industry – from short-term assignments at Fortune 500 companies where you can build your skills, to long-term opportunities where you can play a vital role in solving companies’ construction, manufacturing, and maintenance challenges. Our 1,500+ experienced recruiters across 250+ offices work relentlessly to put our workforce in a position to thrive. Let us rise to meet your challenges and put our people-are-everything spirit to the test as your career continues to grow. Read Less

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