Job Title: Pharmacist
Job Description
We are seeking a skilled and dedicated Pharmacist to join our team in an onsite position, working Monday through Friday from 10 am to 7 pm CST. This role requires counseling patients and verifying prescriptions, with 8-10 shifts on Saturdays per year, for which you will receive a weekday off. You will primarily be on the phone, counseling patients about their medication and verifying prescriptions. This is a contract-to-hire position.
Responsibilities
Oversee pharmacy technicians.Conduct comprehensive clinical reviews of pharmacotherapy for each patient, including drug utilization, counseling, compliance, drug interaction screening, side effect profiling, and drug administration support.Document results of pharmacotherapy reviews in patient charts to educate the nursing team performing follow-up assessments.Counsel patients on new drug therapy in accordance with clinical management models.Complete REMS training and follow program SOPs.Coordinate patient care with the referring clinician, addressing social, psychological, and physical needs.Serve as a liaison between patients, caregivers, home health agency nurses, hospice nurses, and the prescribing physician/clinician.Provide subcutaneous teaching support for patients and caregivers and coordinate nursing services if necessary.Offer on-call coverage as directed by the Pharmacist-in-Charge.Process prescriptions accurately and timely.Verify discontinuation of service for each patient and deactivate their charts, prescriptions, and software profiles.Implement clinical management models for products and disease states.Conduct primary intake for all new team referrals initiated by telephone.Commit to providing 'outrageous customer service' as defined by internal policies.Build relationships with patients and clinicians.Ensure strict adherence to company policy regarding government-funded payers, specifically Medicaid and Medicare.Dispense all medications pursuant to a physician’s order and in accordance with all state, federal, and board of pharmacy laws.Verify accuracy of prescription order entries and final prescription products dispensed.Assist pharmacy technicians in adjudicating pharmacy claims.Monitor hazardous waste material management within the pharmacy.Supervise the aseptic technique of pharmacy personnel.Utilize patient education materials effectively.Perform intake of and ensure appropriate reporting of adverse events and product quality complaints.Meet or exceed current CE requirements pursuant to Board of Pharmacy Laws.Support professional development goals of staff within the assigned patient care team.Maintain an attitude of constant learning and ensure self-education within the pharmacy arena.Attend conferences and report topics discussed at staff meetings.Essential Skills
At least 2 years of experience counseling patients and verifying prescriptions.Strong background in counseling and ability to be on the phone for most of the shift.Experience in pharmacy operations, including retail or independent settings.Familiarity with hospital settings is acceptable but not required.Additional Skills & Qualifications
PharmD or equivalent degree.Experience in pharmaceutical and healthcare settings.Work Environment
The pharmacist will work onsite in a dynamic environment, primarily engaged in phone-based patient counseling for 6-8 hours a day. The role involves a supportive team atmosphere with opportunities for long-term career growth. The work schedule includes weekdays and occasional Saturdays, with advanced notice provided for weekend shifts. The dress code is professional attire appropriate for a clinical setting.
Job Type & Location
This is a Contract position based out of NA, Texas.
Pay and Benefits
The pay range for this position is $60.00 - $60.00/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 Fort Worth,TX.
Application Deadline
This position is anticipated to close on Oct 28, 2025.
About ActalentActalent 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 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
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 due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.
Read LessJob Description
The Quality Control Lead will oversee food safety, product quality, and documentation processes within our fast-paced Retail Ready department. This role is ideal for someone with a strong background in a food manufacturing setting, quality assurance testing, and communication with production. Bilingual candidates (English/Spanish) are encouraged to apply.
Responsibilities
Monitor and enforce quality standards across all Retail Ready departments.Conduct regular quality control checks of raw materials, in-process products, and finished goods to ensure compliance with company and regulatory standards.Lead documentation efforts including batch records, quality logs, corrective actions, and audit preparation.Train and mentor staff on food safety protocols, GMPs, and quality procedures.Collaborate with production supervisors to resolve quality issues and implement process improvements.Ensure proper labeling, packaging, and storage of Retail Ready products.Support internal and external audits and maintain readiness for inspections.Essential Skills
Quality assuranceQuality controlGMPQuality inspectionFood manufacturingFood safetyAdditional Skills & Qualifications
Experience in bakery or food qualityStrong documentation skills (GDP & GMP)Bilingual in English/Spanish is a plusPay and Benefits
The pay range for this position is $23.00 - $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 Saint Paul,MN.
Application Deadline
This position is anticipated to close on Oct 31, 2025.
About ActalentActalent 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 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
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 due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.
Read LessJob Title: Chemistry Lab Technician
Job Description
We are seeking a dedicated and detail-oriented Lab Technician to execute written laboratory experiments testing prototype sensors, meters, methodologies, and reagents. The role involves documenting all work meticulously in laboratory notebooks and performing basic data graphic and analysis under senior staff guidance. The successful candidate will manage scheduled and long-term experiments, maintain the laboratory by ensuring it is well-stocked with consumables, and perform routine maintenance and inspection of equipment.
Responsibilities
Execute written laboratory experiments for testing prototype sensors, meters, methodologies, and reagents.Document all experimental work in laboratory notebooks.Perform basic data graphic and analysis.Manage scheduled and long-term experiments effectively.Maintain laboratory stocks and ensure equipment and work areas are clean.Conduct routine maintenance and inspection of laboratory equipment.Essential Skills
1-2 years of experience in a professional laboratory setting.Associate’s Degree or higher in Chemistry or a similar field.Completion of 2 years of college-level chemistry coursework and laboratory courses.Proficiency in writing laboratory reports.Strong skills in data manipulation and graphing using Excel.Exceptional attention to detail.Effective and professional communication skills.Additional Skills & Qualifications
Experience with UV Spectroscopy.Experience in reagent stocking and laboratory maintenance.Work Environment
Join a global leader in analytical instrumentation, committed to innovation, quality, and service in electrochemistry, photometry, and chemical analysis across various industries. This position offers the opportunity to be part of a team dedicated to advancing scientific progress in a supportive and resourceful environment.
Job Type & Location
This is a Contract to Hire position
Pay and Benefits
The pay range for this position is $24.00 - $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 Woonsocket,RI.
Application Deadline
This position is anticipated to close on Oct 31, 2025.
About ActalentActalent 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 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
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 due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.
Read LessJob Title: Quality Deviation Investigator
Job Description
We are seeking a Quality Deviation Investigator to support the Compliance branch. This role requires a proactive communicator who can efficiently organize and manage a workload of at least two to three deviations simultaneously, including two significant and one non-significant deviation. The successful candidate will be responsible for closing non-significant deviations within five days and significant deviations within thirty days. This position involves managing deviations across all critical utilities, automation/MES, facilities, maintenance, EMS, and BMS systems for twelve sites.
Responsibilities
Investigate and manage deviations related to critical utilities, automation/MES, facilities, maintenance, EMS, and BMS systems.Ensure timely closure of non-significant deviations within five days and significant deviations within thirty days.Utilize Root Cause Analysis tools such as fishbone diagrams and 5 Whys to identify and resolve issues.Maintain a track record of Right First Time performance in closing out deviations.Communicate effectively with team members and stakeholders to ensure compliance with organizational standards.Essential Skills
Proven experience in deviation investigation and technical writing.Strong Root Cause Analysis skills, including the use of fishbone diagrams and 5 Whys.Demonstrated ability to manage multiple deviations concurrently.Experience in maintaining Right First Time performance with deviations.Additional Skills & Qualifications
Six Sigma Green/Black Belt certification is preferred.Ability to work proactively and communicate effectively in a compliance environment.Work Environment
This is a full-time, onsite position with first shift hours, working five days a week. The role involves managing deviations across twelve sites, requiring a hands-on approach and proactive communication.
Job Type & Location
This is a Contract position based out of Framingham, Massachusetts.
Pay and Benefits
The pay range for this position is $60.00 - $70.00/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 Framingham,MA.
Application Deadline
This position is anticipated to close on Oct 31, 2025.
About ActalentActalent 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 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
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 due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.
Read LessAs a QA Technician, you will conduct general food micro testing, including generic pathogenic micro testing, under the guidance of the Quality Assurance Supervisor or as outlined in the protocol. You will revise, edit, and create quality documents, count and record micro plate counts, and assist in processing samples from receipt through testing. Your role includes ensuring thorough and timely completion of all steps as outlined in the protocol, communicating promptly with the Quality Assurance Supervisor, and adhering to GMP/GLP guidelines.
ResponsibilitiesConduct general food micro testing, including generic pathogenic micro testing under guidance.Revise, edit, and create quality documents.Count and record micro plate counts.Assist in processing samples from receipt through testing, including documentation and recordkeeping.Ensure all steps are completed thoroughly and in a timely manner as outlined in the protocol.Communicate promptly with the Quality Assurance Supervisor.Follow GMP/GLP guidelines.Essential SkillsFood chemistryQuality assuranceQC testingSample preparationMedia preparationQA testingMicrobiology testingFood analysis testingFood scienceBiologicsAdditional Skills & Qualifications1-2 years of experience in micro testing or food analysis lab.Prior QA/QC experience in food manufacturing.Associate or B.S. degree in food, chemistry, microbiology, biology, or a related field is preferred.Work Environment
This is a fully onsite role where you will help lead a team of 10 individuals and report to the QA Supervisor. The position is available on the 3rd shift, from 12 am to 8:30 am. You may be required to work some weekends occasionally, depending on the volume of samples.
Job Type & Location
This is a Contract to Hire position based out of Ayer, Massachusetts.
Pay and Benefits
The pay range for this position is $25.00 - $25.00/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 Ayer,MA.
Application Deadline
This position is anticipated to close on Oct 31, 2025.
About ActalentActalent 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 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
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 due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.
Read LessDescription
Contract Length: 1 Year Location: Onsite - Cambridge MA no remote option - Please ensure candidates live near the Amgen site. Work Hours: Standard 8-hour day flex start between 7-9 AM Must-Have Requirements Please vet candidates well on their chromatography experience and analytical techniques. they need to be able to speak technically. Education: Bachelors degree in Chemistry Biochemistry or Biotechnology no advanced degrees. Industry Experience: Minimum 6 months of hands-on experience in the pharmaceutical or biotech industry academic lab/internship acceptable only if candidate has strong chromatography skills. Technical Skills: - Hands-on experience with chromatography HPLC strongly preferred. - Basic sample preparation and testing in a regulated lab environment. - Familiarity with analytical techniques used in late-stage drug development. Work Environment: Must be comfortable working onsite daily and following strict safety and procedural guidelines. Job Summary Amgens Attribute Sciences AS department within the Process Development PD organization defines the favorable quality characteristics of the therapies it produces and optimizes state-of-the-art analytical tools to guide that development. The Pivotal PD organizations focus is developing and commercializing robust manufacturing processes across a wide range of therapeutic modalities including but not limited to monoclonal and bispecific antibodies bispecific T-cell engagers BiTEs live oncolytic viruses and synthetic medicines. Located in our Cambridge MA office the PD Associate Scientist Process Analytics will work to provide testing support for commercial process development and process characterization studies for clinical candidate molecules in the pivotal stage of development. Responsibilities: - Transition of analytical methods from our early-stage development teams to the pivotal testing laboratory. This will include interfacing with attribute sciences team leads and early stage development teams performing method assessment / qualification method optimization and formatting chromatography data software methods. - Performing high-sample volume testing by High Performance Liquid Chromatography HPLC Ultra High-Performance Liquid Chromatography UHPLC Capillary Electrophoresis CE and Tecan in support of Drug Substance Drug Product and Attribute Sciences process development teams under prescribed timelines. Full documentation of analyses in electronic lab notebook. Performing tracking and trend analysis of method performance. - Hand-off/transfer of testing to our Rapid Analytics teams. - Evaluation of novel platform methodologies to improve testing efficiencies in the Process Analytics and Rapid Analytics teams. - Performing HPLC/UHPLC and CE method qualification studies to support transfer of methods to pivotal Quality Control teams. - Perform forced degradation studies to support product characterization understanding of product stability and evaluation of product comparability. - Closely collaborate with partner organizations during commercial process development process characterization and process validation studies to support marketing applications. Preferred Qualifications - B.S. in Chemistry or Biochemistry - 1-2 years of experience in a pharmaceutical/biotech analytical lab. - Good general biochemistry laboratory skills - Working knowledge of chromatography including HPLC UPLC and CE - Working knowledge of compendial methods testing such as Karl Fischer Color/Clarity and UV/VIS spectroscopy - Strong desire to learn and interest in science - Demonstrated proficiency in execution of test methodology following a defined procedure. - Background in chromatography data software Waters Empower Thermo Agilent softwares and/or automation software Tecan - Understanding of phase-appropriate GMP compliance and documentation - Well-organized ability to multitask effectively plan and follow through on complex projects and to work both independently and in teams
Pay and Benefits
The pay range for this position is $23.00 - $25.00/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 Cambridge,MA.
Application Deadline
This position is anticipated to close on Oct 31, 2025.
About ActalentActalent 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 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
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 due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.
Read LessJob Title: Quality Deviation Investigator
Job Description
We are seeking a Quality Deviation Investigator to support the Compliance branch. This role requires a proactive communicator who can efficiently organize and manage a workload of at least two to three deviations simultaneously, including two significant and one non-significant deviation. The successful candidate will be responsible for closing non-significant deviations within five days and significant deviations within thirty days. This position involves managing deviations across all critical utilities, automation/MES, facilities, maintenance, EMS, and BMS systems for twelve sites.
Responsibilities
Investigate and manage deviations related to critical utilities, automation/MES, facilities, maintenance, EMS, and BMS systems.Ensure timely closure of non-significant deviations within five days and significant deviations within thirty days.Utilize Root Cause Analysis tools such as fishbone diagrams and 5 Whys to identify and resolve issues.Maintain a track record of Right First Time performance in closing out deviations.Communicate effectively with team members and stakeholders to ensure compliance with organizational standards.Essential Skills
Proven experience in deviation investigation and technical writing.Strong Root Cause Analysis skills, including the use of fishbone diagrams and 5 Whys.Demonstrated ability to manage multiple deviations concurrently.Experience in maintaining Right First Time performance with deviations.Additional Skills & Qualifications
Six Sigma Green/Black Belt certification is preferred.Ability to work proactively and communicate effectively in a compliance environment.Work Environment
This is a full-time, onsite position with first shift hours, working five days a week. The role involves managing deviations across twelve sites, requiring a hands-on approach and proactive communication.
Job Type & Location
This is a Contract position based out of Framingham, Massachusetts.
Pay and Benefits
The pay range for this position is $60.00 - $70.00/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 Framingham,MA.
Application Deadline
This position is anticipated to close on Oct 31, 2025.
About ActalentActalent 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 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
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 due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.
Read LessWe are seeking a Quality Deviation Investigator to support the Compliance branch. This role requires a proactive communicator who can efficiently organize and manage a workload of at least two to three deviations simultaneously, including two significant and one non-significant deviation. The successful candidate will be responsible for closing non-significant deviations within five days and significant deviations within thirty days. This position involves managing deviations across all critical utilities, automation/MES, facilities, maintenance, EMS, and BMS systems for twelve sites.
ResponsibilitiesInvestigate and manage deviations related to critical utilities, automation/MES, facilities, maintenance, EMS, and BMS systems.Ensure timely closure of non-significant deviations within five days and significant deviations within thirty days.Utilize Root Cause Analysis tools such as fishbone diagrams and 5 Whys to identify and resolve issues.Maintain a track record of Right First Time performance in closing out deviations.Communicate effectively with team members and stakeholders to ensure compliance with organizational standards.Essential SkillsProven experience in deviation investigation and technical writing.Strong Root Cause Analysis skills, including the use of fishbone diagrams and 5 Whys.Demonstrated ability to manage multiple deviations concurrently.Experience in maintaining Right First Time performance with deviations.Additional Skills & QualificationsSix Sigma Green/Black Belt certification is preferred.Ability to work proactively and communicate effectively in a compliance environment.Work Environment
This is a full-time, onsite position with first shift hours, working five days a week. The role involves managing deviations across twelve sites, requiring a hands-on approach and proactive communication.
Job Type & Location
This is a Contract position based out of Framingham, Massachusetts.
Pay and Benefits
The pay range for this position is $60.00 - $70.00/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 Framingham,MA.
Application Deadline
This position is anticipated to close on Oct 24, 2025.
About ActalentActalent 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 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
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 due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.
Read LessDescription
Hybrid Through End of Year Top 3-5 Skills Needed: 1. Strong programming and data engineering skills Python SQL R 2. Experience with large-scale omics data management and integration 3. Knowledge of metadata standards and ontologies for biological data 4. Experience designing or maintaining bioinformatics data pipelines or repositories 5. Understanding of data governance permissions and FAIR data principles Job Description: We are seeking a highly motivated Data Scientist to design and implement an internal GEO-like system for managing the Immune Discovery omics data assets. The successful candidate will build a centralized platform that integrates raw processed and metadata layers of multi-omics datasets e.g. bulk and single-cell RNA-seq spatial omics CyTOF and ensures that they are findable accessible well-documented and permission-controlled. This role bridges bioinformatics data engineering and data governance enabling researchers to efficiently submit query and reuse internal datasets while maintaining data quality and compliance. Key Responsibilities: - Design and implement scalable pipelines for ingestion curation and storage of raw and processed omics data. - Build and maintain a searchable data catalog or portal to enable dataset discovery and visualization of metadata and QC metrics. - Implement access controls and permission management systems to ensure appropriate data security and compliance. - Work closely with Immunology Discovery and IR teams to integrate the system with existing compute and storage infrastructure. - Develop and enforce metadata standards ontologies and schema to ensure consistency and interoperability across studies. Impact: By developing this internal data platform the candidate will transform how omics data are organized and shared across AbbVie. The system will improve data visibility and reuse enhance reproducibility and accelerate scientific insights by enabling streamlined access to all relevant data layers raw processed and annotated. Qualifications: - BS 5 years or MS 0-3 years in Bioinformatics Computational Biology Data Science Computer Science or related field. - Proficiency in Python and SQL with experience in data wrangling ETL pipelines and automation. - Hands-on experience managing large omics datasets. - Strong understanding of metadata models data provenance and FAIR data principles. - Excellent communication skills and ability to collaborate with cross-functional teams. Preferred Technical Skills: - Experience with cloud storage or compute environments AWS GCP or on-prem HPC. - Experience with workflow orchestration tools Nextflow Snakemake. - Familiarity with relational and NoSQL databases PostgreSQL. - Familiarity with public repositories such as GEO or SRA and their metadata standards. - Proficiency with Git for version control and collaboration. Additional Technical Skills a plus: - Experience with containerization Docker/Singularity and CI/CD workflows. - Understanding of web application frameworks or dashboarding tools for data portals. - Exposure to single-cell or multi-omics integration workflows. - Experience implementing data access and permission systems integrated with organizational identity management.
Pay and Benefits
The pay range for this position is $90.00 - $95.00/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 Cambridge,MA.
Application Deadline
This position is anticipated to close on Oct 31, 2025.
About ActalentActalent 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 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
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 due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.
Read LessDescription
Perform analyses using PSX products within routine Clinical Sample Analysis in compliance with PSX internal regulations. • Handle, analyze and process laboratory samples (small to large sample sets) with high quality and per established protocols. • Work independently within the Clinical Sample Analysis team and collaborate effectively • Understand and work according to established methods, processes and techniques concerning Clinical Sample Analysis. • Actively maintain documentation and systems within the unit’s quality system. • Communicate with internal and external customers and provide a customer service-focus on all aspects of the work. • Collaborate with more experienced Clinical Sample Analysis Specialist to solve technical or sample-related issues, customer or general problems
Skills
sample prep, Sample analysis, quality management system, media prep, patient samples, microbiology, molecular biology
Top Skills Details
sample prep,Sample analysis,quality management system,media prep
Additional Skills & Qualifications
• Bachelor’s degree or higher within the Life Sciences field or similar. Experience • One or more years of documented laboratory experience, preferentially routine work with large sample sets and service organizations.
Experience Level
Entry Level
Pay and Benefits
The pay range for this position is $20.00 - $26.00/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 Waltham,MA.
Application Deadline
This position is anticipated to close on Oct 31, 2025.
About ActalentActalent 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 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
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 due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.
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