Job DescriptionJob DescriptionJob Title: Scientist – Microbiology
Job Description

This role supports a Quality Control (QC) team in a GMP-regulated pharmaceutical environment, with a primary focus on validation and qualification of microbiological methods. The scientist ensures that microbiological testing methods are compliant, robust, and aligned with regulatory expectations, while actively contributing to quality systems, validation activities, and laboratory operations. This position is ideal for a microbiology professional who wants to deepen expertise in QC method validation and advance their career in a biomanufacturing setting.

ResponsibilitiesPlan, execute, and support validation and qualification of microbiological methods in alignment with GMP and applicable regulatory requirements.Assist with the development, review, and execution of method validation protocols, including Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ).Perform and support routine and non-routine microbiological testing, including bioburden, endotoxin, sterility, and related assays, in a Quality Control laboratory.Accurately record, analyze, and document validation and testing results in accordance with quality standards and data integrity expectations.Use electronic systems, such as Laboratory Information Management Systems (LIMS), to manage test data, documentation, and method validation records.Partner with cross-functional teams, including Quality Control (QC), Quality Assurance (QA), and operations, to coordinate and support method validation and transfer activities.Contribute to continuous improvement initiatives for microbiology methods, laboratory workflows, and QC processes to enhance robustness, efficiency, and compliance.Support QC method validation or transfer activities by providing microbiology expertise and ensuring methods are appropriately qualified for intended use.Adhere to Good Manufacturing Practice (GMP) guidelines, laboratory procedures, and safety requirements while working in a pharmaceutical biomanufacturing facility.Essential SkillsBachelor’s degree in Microbiology, Biology, or a closely related scientific field.2–5+ years of experience working in a GMP-regulated microbiology laboratory.At least 2 years of hands-on experience with endotoxin and bioburden methods.Strong understanding of GMP principles, regulatory compliance requirements, and method qualification practices.Practical experience performing microbiological testing such as bioburden, endotoxin, and sterility in a Quality Control environment.Experience supporting QC method validation or method transfer activities.Ability to develop, execute, and interpret method validation protocols, including IQ/OQ/PQ.Strong documentation skills with a clear understanding of data integrity expectations in a regulated environment.Ability to collaborate effectively with QC, QA, and operations teams to support validation and routine testing activities.Additional Skills & QualificationsExperience using electronic systems and documentation tools, such as Laboratory Information Management Systems (LIMS).Familiarity with validation lifecycle concepts and continuous improvement of laboratory methods and processes.Demonstrated interest in quality systems, validation, and laboratory operations within a pharmaceutical or biomanufacturing setting.Ability to work independently in a fast-paced QC laboratory while managing multiple validation and testing priorities.Strong problem-solving skills and attention to detail when troubleshooting microbiological methods and test results.Work Environment

The role is based in a Quality Control testing laboratory within a pharmaceutical biomanufacturing facility. Approximately 80% of the time is spent in the lab performing microbiological testing on samples, with the remaining time spent in an office area located down the hallway due to ongoing renovations in the lab. The environment is GMP-regulated and highly focused on compliance, data integrity, and safety. Work is performed using standard microbiology laboratory equipment and electronic systems such as LIMS. The position follows a 4x10 schedule, with shifts available Sunday through Wednesday or Wednesday through Saturday, and candidate shift preference is taken into consideration. The workplace culture emphasizes professional growth, competitive compensation and benefits, and opportunities for QC professionals to gain substantial experience in method validation and advance their careers.

Job Type & Location

This is a Contract position based out of Raleigh, NC.

Pay and Benefits

The pay range for this position is $30.00 - $45.00/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 Raleigh,NC.

Application Deadline

This position is anticipated to close on Jul 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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Job DescriptionJob DescriptionJob Title: Scientist – Microbiology
Job Description

This role supports a Quality Control (QC) team in a GMP-regulated pharmaceutical environment, with a primary focus on validation and qualification of microbiological methods. The scientist ensures that microbiological testing methods are compliant, robust, and aligned with regulatory expectations, while actively contributing to quality systems, validation activities, and laboratory operations. This position is ideal for a microbiology professional who wants to deepen expertise in QC method validation and advance their career in a biomanufacturing setting.

ResponsibilitiesPlan, execute, and support validation and qualification of microbiological methods in alignment with GMP and applicable regulatory requirements.Assist with the development, review, and execution of method validation protocols, including Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ).Perform and support routine and non-routine microbiological testing, including bioburden, endotoxin, sterility, and related assays, in a Quality Control laboratory.Accurately record, analyze, and document validation and testing results in accordance with quality standards and data integrity expectations.Use electronic systems, such as Laboratory Information Management Systems (LIMS), to manage test data, documentation, and method validation records.Partner with cross-functional teams, including Quality Control (QC), Quality Assurance (QA), and operations, to coordinate and support method validation and transfer activities.Contribute to continuous improvement initiatives for microbiology methods, laboratory workflows, and QC processes to enhance robustness, efficiency, and compliance.Support QC method validation or transfer activities by providing microbiology expertise and ensuring methods are appropriately qualified for intended use.Adhere to Good Manufacturing Practice (GMP) guidelines, laboratory procedures, and safety requirements while working in a pharmaceutical biomanufacturing facility.Essential SkillsBachelor’s degree in Microbiology, Biology, or a closely related scientific field.2–5+ years of experience working in a GMP-regulated microbiology laboratory.At least 2 years of hands-on experience with endotoxin and bioburden methods.Strong understanding of GMP principles, regulatory compliance requirements, and method qualification practices.Practical experience performing microbiological testing such as bioburden, endotoxin, and sterility in a Quality Control environment.Experience supporting QC method validation or method transfer activities.Ability to develop, execute, and interpret method validation protocols, including IQ/OQ/PQ.Strong documentation skills with a clear understanding of data integrity expectations in a regulated environment.Ability to collaborate effectively with QC, QA, and operations teams to support validation and routine testing activities.Additional Skills & QualificationsExperience using electronic systems and documentation tools, such as Laboratory Information Management Systems (LIMS).Familiarity with validation lifecycle concepts and continuous improvement of laboratory methods and processes.Demonstrated interest in quality systems, validation, and laboratory operations within a pharmaceutical or biomanufacturing setting.Ability to work independently in a fast-paced QC laboratory while managing multiple validation and testing priorities.Strong problem-solving skills and attention to detail when troubleshooting microbiological methods and test results.Work Environment

The role is based in a Quality Control testing laboratory within a pharmaceutical biomanufacturing facility. Approximately 80% of the time is spent in the lab performing microbiological testing on samples, with the remaining time spent in an office area located down the hallway due to ongoing renovations in the lab. The environment is GMP-regulated and highly focused on compliance, data integrity, and safety. Work is performed using standard microbiology laboratory equipment and electronic systems such as LIMS. The position follows a 4x10 schedule, with shifts available Sunday through Wednesday or Wednesday through Saturday, and candidate shift preference is taken into consideration. The workplace culture emphasizes professional growth, competitive compensation and benefits, and opportunities for QC professionals to gain substantial experience in method validation and advance their careers.

Job Type & Location

This is a Contract position based out of Sanford, NC.

Pay and Benefits

The pay range for this position is $30.00 - $45.00/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 Sanford,NC.

Application Deadline

This position is anticipated to close on Jun 24, 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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Job DescriptionJob Description

Job Title: QC Microbiology Analyst

Schedule: Wednesday thru Saturday from 3:30 PM to 2:00 AM

Job Description

The QC Microbiology Analyst performs environmental monitoring and microbiological testing in a cleanroom and Good Manufacturing Practice (GMP) environment to support advanced cell therapy and biotechnology manufacturing. This role focuses on aseptic techniques, environmental and personnel monitoring, and accurate documentation of results using specialized databases. The position offers extensive training in environmental monitoring and the opportunity to contribute to a rapidly growing organization in the CAR-T and cell therapy industry.

Responsibilities

Perform routine environmental monitoring in cleanroom and GMP areas, including active air, passive air, and surface viable testing.Conduct micro sampling, personnel monitoring, and surface plating to assess contamination levels in classified areas.Monitor and document equipment conditions as part of the environmental monitoring program.Analyze and read microbiological plates after incubation, accurately interpreting results and documenting findings.Collect and process air and water samples using aseptic techniques to ensure compliance with environmental and quality standards.Perform bioburden testing and other microbiological assays as required to support quality control activities.Use and maintain the MODA database or similar systems to document environmental monitoring data and test results in a timely and accurate manner.Follow standard operating procedures (SOPs) for all microbiological and environmental monitoring activities, ensuring adherence to GMP and ISO standards.Perform aseptic technique consistently, including proper pipetting, plating, swabbing, and handling of microorganisms.Prepare, incubate, and subculture microbiological samples, including performing cell counts and gram stains as needed.Support equipment monitoring activities by documenting environmental conditions and reporting deviations or abnormal results.Participate in extensive environmental monitoring training and apply learned techniques to daily operations.Complete gowning qualification and maintain proper gowning practices to work effectively in cleanroom and aseptic environments.Contribute to maintaining a clean and controlled environment by performing cleaning tasks related to microbiological and environmental monitoring activities.Collaborate with cross-functional teams in quality control and manufacturing to ensure accurate communication of environmental monitoring results.Adhere to all safety, quality, and regulatory requirements while working with microorganisms and within cleanroom facilities.

Essential Skills

At least 1 year of environmental monitoring experience in a cleanroom or GMP environment.1–3 years of experience with sampling, personnel monitoring, and surface plating.Demonstrated experience working within an aseptic environment and applying aseptic techniques.Basic microbiology knowledge, including microbiology techniques and working with microorganisms.Hands-on experience with environmental monitoring, including air and water sampling and surface monitoring.Proficiency in aseptic technique, pipetting, surface plating, and swabbing.Familiarity with cleanroom operations and ISO standards related to environmental monitoring and microbiology.Ability to follow SOPs and quality control procedures in a regulated environment.Experience with cell culture, cell counts, and related microbiological assays.Competence in incubation, subculturing, plating, and gram staining.Ability to read, interpret, and document microbiological test results accurately.Bachelor’s degree in a related scientific field (such as Microbiology, Biology, or a similar discipline).Gowning certification or the ability to obtain gowning qualification for cleanroom work.Strong attention to detail and adherence to quality and compliance standards.

Additional Skills & Qualifications

Experience using MODA or similar databases for documenting environmental monitoring and microbiology data.Knowledge of bioburden testing and quality control practices in pharmaceutical or biotechnology settings.Familiarity with CAR-T, cell therapy, or related biotechnology manufacturing environments.Understanding of environmental monitoring program design and execution in GMP facilities.Experience working under SOPs and quality systems aligned with ISO and regulatory expectations.Ability to work independently and as part of a team in a fast-paced, growth-oriented environment.Strong organizational skills and the ability to manage multiple monitoring and testing tasks.Willingness to participate in extensive environmental monitoring training and ongoing skill development.

Work Environment

This role is based in a cleanroom aseptic environment within a GMP-regulated facility, focused on supporting advanced biotechnology and cell therapy operations. The QC Microbiology Analyst will work primarily on 2nd shift, with available schedules including Sunday to Wednesday from approximately 3:30 pm to 2:00 am and Wednesday to Saturday from approximately 3:30 pm to 2:00 am, depending on assignment. Initial training will take place on first shift, Monday through Friday from 8:00 am to 4:30 pm, for an estimated duration of 4–6 weeks. The position involves continuous work in controlled cleanroom areas, including gowning and maintaining strict aseptic and cleanliness standards. The environment requires consistent use of microbiology equipment, incubators, and monitoring devices, as well as regular use of databases such as MODA for documentation. Team members follow defined SOPs, quality procedures, and safety guidelines while working with microorganisms and performing environmental monitoring. The organization is expanding its operations, offering opportunities to grow within a fast-paced, innovative biotechnology setting focused on CAR-T and cell therapy.Job Type & Location

This is a Contract to Hire position based out of Allendale, NJ.

Pay and Benefits

The pay range for this position is $30.00 - $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 Allendale,NJ.

Application Deadline

This position is anticipated to close on Jun 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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Job DescriptionJob Description

Job Description

Job Function and Description

Identified responsibilities include:

•        Collect samples from manufacturing areas to evaluate environmental classification or critical utility integrity.

•        Conduct critical biological, chemical and physical analyses such as raw materials, initial, in-process and final products, and samples collected from environmental monitoring programs at the company manufacturing facilities, etc.

•        Use sophisticated laboratory instrumentation and computer systems to collect and record data (such as LIMS system). Perform assays requiring precise analytical skills and understanding of biology and chemistry principles.

•        Complete all testing, including special project/protocol testing in a timely and appropriate manner.

•        Initiate and obtain applicable approval for test requests.

•        May maintain inventory/supplies necessary to conduct routine testing.

•        Follow continuous improvement practices (QLP, 5S, LEAN, etc.)

•        Performs equipment maintenance and calibrations as required.

•        Maintain data integrity and ensure compliance with company SOPs and specifications, FDA, GLP, QSR and cGMP regulations. Perform release functions in LIMS or other computerized systems.

•        May perform other duties as assigned.

·         Education and Experience Requirements

•        Typically requires bachelor's degree in chemistry, biological science, or other related technical field. Some related work experience preferred.

 

Microbiology:

Environment monitoring, critical utility sampling, endotoxin testing, bioburden for raw materials and in process, process samples, microbial identification and final product sterility testing.

 

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Job DescriptionJob DescriptionJob Title: Microbiology Analyst
Job Description

We are seeking a Microbiology Analyst to support lab testing and quality initiatives within a regulated environment. This hands-on, lab-based role involves working with microbiological testing to ensure product quality and safety across life sciences industries.

ResponsibilitiesPerform routine microbiology testing following SOPs and regulatory guidelines, including cGMP, GLP, and ISO standards.Execute tests such as sterility, bioburden, endotoxin (LAL), environmental monitoring, growth promotion, microbial identification and counts, as well as water and utility testing.Prepare media, reagents, and samples for testing.Maintain accurate documentation and laboratory records.Support quality control activities, audits, and investigations.Ensure lab cleanliness, equipment maintenance, and adherence to safety compliance.Assist with data reporting, inventory management, and continuous improvement initiatives.Essential SkillsProficiency in microbiology testing, including LAL and environmental monitoring.Strong attention to detail and documentation skills.Ability to work effectively in a fast-paced laboratory setting.Additional Skills & QualificationsDegree in Biology, Microbiology, or a related field.At least 2 years of laboratory experience preferred, but entry-level candidates are welcome.Exposure to GMP/GLP or regulated lab environments is preferred.Work Environment

This is an on-site laboratory role requiring extended periods of standing and working with lab equipment. The position may involve occasional off-hours or weekend work.

Job Type & Location

This is a Contract to Hire position based out of Hercules, CA.

Pay and Benefits

The pay range for this position is $26.00 - $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 Hercules,CA.

Application Deadline

This position is anticipated to close on Jun 29, 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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Job DescriptionJob DescriptionJob Title: Microbiology Supervisor
Job Description

The Microbiology Supervisor leads QC Microbiology operations within a sterile pharmaceutical manufacturing environment, combining hands-on technical expertise with day-to-day team leadership. This role oversees routine microbiological testing, drives investigations and environmental monitoring strategy, and partners cross-functionally to support aseptic operations and overall quality initiatives in a fast-paced GMP setting.

ResponsibilitiesOversee the day-to-day operations of the QC Microbiology laboratory, ensuring testing timelines, quality standards, and regulatory expectations are consistently met.Lead, coach, and mentor a team of microbiologists, including responsibility for training, scheduling, and performance management.Review and approve microbiological data, including bioburden, sterility, and environmental monitoring results, to support product release decisions.Own and manage investigations related to deviations, out-of-specification results, and environmental monitoring excursions, ensuring thorough root cause analysis and appropriate follow-up.Perform data analysis and trending of microbiological and environmental monitoring data to identify risks and recommend improvements to contamination control strategies.Partner closely with Manufacturing, Quality Assurance, and other cross-functional teams to support aseptic operations and resolve quality issues in a timely manner.Support method validation, transfer, and optimization activities for microbiology assays to ensure robust and reliable testing methods.Drive the implementation of corrective and preventive actions (CAPAs) and lead continuous improvement initiatives within the microbiology laboratory.Ensure inspection readiness at all times and maintain strict compliance with GMP, FDA, and other applicable regulatory requirements.Contribute to the development, review, and refinement of microbiology-related procedures, protocols, and documentation to maintain a high standard of quality and consistency.Essential SkillsBachelor’s degree in Microbiology, Biology, or a closely related scientific field.4+ years of experience working in a GMP-regulated microbiology laboratory, preferably within the pharmaceutical industry.Prior experience leading or mentoring teams in a QC Microbiology environment.Strong knowledge of environmental monitoring programs in sterile or aseptic manufacturing settings.Proficiency with sterility testing and bioburden testing methodologies and their application to product release and contamination control.Solid understanding of aseptic technique and aseptic processing support within a regulated environment.Experience conducting and managing investigations, including deviations and CAPAs, in a GMP or FDA-regulated setting.Demonstrated ability to review complex microbiological data and make sound, quality-based decisions.Familiarity with FDA expectations and GMP requirements as they relate to microbiology and sterile manufacturing.Additional Skills & QualificationsExperience supporting sterile or aseptic pharmaceutical manufacturing operations.Proven ability to collaborate effectively with cross-functional teams such as Manufacturing and Quality Assurance.Strong analytical and problem-solving skills with the ability to interpret trends in environmental monitoring and microbiological data.Ability to manage multiple priorities in a fast-paced laboratory environment while maintaining attention to detail.Effective written and verbal communication skills for clear documentation, reporting, and team guidance.Continuous improvement mindset with a focus on enhancing laboratory processes, contamination control, and overall quality performance.Work Environment

The role operates within a controlled cleanroom environment that requires appropriate gowning and adherence to strict aseptic and contamination control procedures. Work is performed in a GMP- and FDA-regulated facility with established environmental monitoring and quality systems. The position involves routine work in QC microbiology laboratories and cleanroom areas, following defined procedures, documentation practices, and regulatory standards to ensure product quality and patient safety.

Job Type & Location

This is a Permanent position based out of Costa Mesa, CA.

Pay and Benefits

The pay range for this position is $80000.00 - $100000.00/yr.

pto/holiday 401k benefits health benefits dental vision medical

Workplace Type

This is a fully onsite position in Costa Mesa,CA.

Application Deadline

This position is anticipated to close on Jun 26, 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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Job DescriptionJob DescriptionJob Title: Microbiologist
Job Description

This role performs a wide range of microbiological assays and environmental monitoring activities to support clinical and commercial manufacturing. The microbiologist conducts qualitative, quantitative, and investigational testing on raw materials, in-process samples, finished products, components, and facility utilities in compliance with USP, FDA, cGMP, GLP, and internal standard operating procedures. The position involves interpreting results against specifications, documenting findings, supporting investigations and CAPA activities, and may include guiding and training junior staff members.

ResponsibilitiesPerform microbiological assays on facility water systems, in-process and finished products, filling components, raw materials, and environmental monitoring samples.Execute microbial bioburden testing of water systems, in-process and finished products, containers, components, and environmental samples.Perform endotoxin testing via Kinetic Turbidimetric Assay and Gel Clot methods on water systems, in-process and finished products, containers, components, and raw materials.Conduct container closure integrity testing of finished products using dye ingress methods.Perform particulate matter testing of finished products using the HIAC Liquid Particle Counting System.Conduct 14-day sterility testing utilizing a Walker Barrier System isolator.Carry out routine environmental monitoring in classified manufacturing areas according to approved plans in coordination with laboratory personnel.Perform viable air sampling using SAS 100 and SAS Super 180 instruments.Perform non-viable particulate sampling using Met One equipment.Conduct viable surface sampling through plating and swabbing techniques.Perform personnel monitoring as part of the gowning qualification program.Execute utilities sampling, including purified water, water for injection (WFI), gases, and clean steam, in accordance with approved procedures.Collect and test microbial bioburden and endotoxin samples from facility water systems and clean steam.Collect and submit conductivity and Total Organic Carbon (TOC) samples to the chemistry laboratory.Coordinate sampling activities with manufacturing to avoid disruption of operations while maintaining aseptic technique and contamination control.Ensure accurate sample identification, labeling, traceability, and timely transfer of samples to the quality control laboratory.Complete sampling documentation in full compliance with GMP, GDP, and data integrity (ALCOA+) requirements.Enter and manage environmental monitoring and laboratory assay data within a digital Laboratory Information Management System (LIMS).Trend out-of-specification (OOS) sample results and conduct routine trend analysis of microbiological data.Identify trends or atypical results and promptly escalate them to leadership for further investigation.Conduct minor and major investigations, including OOS investigations, as necessary.Assist with the execution of Corrective and Preventive Action (CAPA) projects related to microbiological and environmental monitoring findings.Operate general laboratory equipment, including autoclaves and glassware washers, in accordance with procedures.Perform enumeration and verification of sample plates and canisters.Handle laboratory waste disposal in accordance with safety and environmental procedures.Document sample collection and testing activities clearly and accurately.Perform peer review of sampling and testing results to ensure data accuracy and compliance.File paperwork and maintain organized laboratory records and documentation.Conduct investigations, special projects, or other non-routine sampling and testing as required.Train junior analysts in new and existing procedures, techniques, and applicable regulations as directed by supervision.Mentor analysts by providing technical guidance, helping resolve technical problems, and reviewing documents.Take initiative to seek out additional assignments and contribute proactively to laboratory operations.Work safely in accordance with regulations, standards, and procedures to eliminate unreasonable risk to health and the environment.Notify management of unsafe conditions or practices, unlawful activities, or activities that present unreasonable health or environmental risk.Report all safety and environmental incidents to management immediately.Perform other related duties as assigned by management.Essential SkillsBachelor’s degree in Microbiology, Biology, or a similar life science discipline preferred.Minimum of 5+ years of laboratory experience, preferably in the pharmaceutical industry.Proven ability to perform environmental monitoring of cleanrooms and facility water systems.Hands-on experience with kinetic LAL and gel-clot LAL endotoxin testing methods.Experience performing filtration testing and particulate matter testing using appropriate instrumentation such as HIAC liquid particle counters.Experience conducting 14-day sterility testing using isolator systems such as the Walker Barrier System.Proficiency in operating laboratory equipment including autoclaves and glassware washers.Strong knowledge and application of aseptic techniques and appropriate cleanroom behaviors.Working knowledge of cGMPs, GLPs, USP, FDA, and other relevant regulatory requirements.Ability to follow and apply standard operating procedures and approved testing methods.Ability to use computer systems for data analysis and documentation, including LIMS.Proficiency with Microsoft Excel, PowerPoint, and Access.Experience with investigation writing, including OOS and deviation investigations.Ability to train personnel on various procedures and communicate effectively with team members and cross-functional groups.Good interpersonal skills and strong verbal and written communication abilities.Demonstrated self-motivation, energy, enthusiasm, and a team-oriented approach.Knowledge of laboratory safety and material safety practices.Additional Skills & QualificationsExperience performing routine environmental monitoring in classified manufacturing areas, including surface, air, and personnel monitoring.Familiarity with environmental monitoring equipment such as SAS 100, SAS Super 180, and Met One instruments.Experience with utilities sampling for purified water, WFI, gases, and clean steam.Understanding of contamination control principles and cleanroom gowning requirements.Ability to ensure sample traceability, accurate labeling, and timely delivery to the QC laboratory.Working knowledge of data integrity principles, including ALCOA+.Ability to identify atypical results and potential contamination risks and to escalate appropriately.Experience supporting CAPA activities related to microbiological and environmental monitoring issues.Ability to mentor and support junior analysts in resolving technical challenges and ensuring documentation quality.Work Environment

This position operates in a regulated pharmaceutical laboratory and classified manufacturing environment with a strong focus on cGMP, GLP, and safety standards. Work involves frequent activity in cleanrooms and controlled areas to perform environmental monitoring and utilities sampling, as well as time in the laboratory operating equipment such as autoclaves, glassware washers, isolators, particle counters, and environmental monitoring instruments (SAS 100, SAS Super 180, Met One). The role requires adherence to contamination control practices, aseptic technique, and cleanroom gowning requirements. Documentation is completed in both electronic systems, including LIMS and standard office software, and in controlled paper records, with strict attention to data integrity. The schedule includes shift-based work, with potential assignments from Tuesday to Saturday or Sunday to Thursday, typically on shifts such as 6:00 pm to 2:30 am or 10:00 am to 6:30 pm, depending on operational needs. The environment emphasizes safety, prompt reporting of incidents or unsafe conditions, and collaborative work with manufacturing and other support groups.

Job Type & Location

This is a Contract position based out of Raleigh, NC.

Pay and Benefits

The pay range for this position is $35.00 - $42.00/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 Raleigh,NC.

Application Deadline

This position is anticipated to close on Jun 24, 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 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 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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Job DescriptionJob DescriptionJob Title: Microbiologist
Job Description

This role performs a wide range of microbiological assays and environmental monitoring activities to support clinical and commercial manufacturing. The microbiologist conducts qualitative, quantitative, and investigational testing on raw materials, in-process samples, finished products, components, and facility utilities in compliance with USP, FDA, cGMP, GLP, and internal standard operating procedures. The position involves interpreting results against specifications, documenting findings, supporting investigations and CAPA activities, and may include guiding and training junior staff members.

ResponsibilitiesPerform microbiological assays on facility water systems, in-process and finished products, filling components, raw materials, and environmental monitoring samples.Execute microbial bioburden testing of water systems, in-process and finished products, containers, components, and environmental samples.Perform endotoxin testing via Kinetic Turbidimetric Assay and Gel Clot methods on water systems, in-process and finished products, containers, components, and raw materials.Conduct container closure integrity testing of finished products using dye ingress methods.Perform particulate matter testing of finished products using the HIAC Liquid Particle Counting System.Conduct 14-day sterility testing utilizing a Walker Barrier System isolator.Carry out routine environmental monitoring in classified manufacturing areas according to approved plans in coordination with laboratory personnel.Perform viable air sampling using SAS 100 and SAS Super 180 instruments.Perform non-viable particulate sampling using Met One equipment.Conduct viable surface sampling through plating and swabbing techniques.Perform personnel monitoring as part of the gowning qualification program.Execute utilities sampling, including purified water, water for injection (WFI), gases, and clean steam, in accordance with approved procedures.Collect and test microbial bioburden and endotoxin samples from facility water systems and clean steam.Collect and submit conductivity and Total Organic Carbon (TOC) samples to the chemistry laboratory.Coordinate sampling activities with manufacturing to avoid disruption of operations while maintaining aseptic technique and contamination control.Ensure accurate sample identification, labeling, traceability, and timely transfer of samples to the quality control laboratory.Complete sampling documentation in full compliance with GMP, GDP, and data integrity (ALCOA+) requirements.Enter and manage environmental monitoring and laboratory assay data within a digital Laboratory Information Management System (LIMS).Trend out-of-specification (OOS) sample results and conduct routine trend analysis of microbiological data.Identify trends or atypical results and promptly escalate them to leadership for further investigation.Conduct minor and major investigations, including OOS investigations, as necessary.Assist with the execution of Corrective and Preventive Action (CAPA) projects related to microbiological and environmental monitoring findings.Operate general laboratory equipment, including autoclaves and glassware washers, in accordance with procedures.Perform enumeration and verification of sample plates and canisters.Handle laboratory waste disposal in accordance with safety and environmental procedures.Document sample collection and testing activities clearly and accurately.Perform peer review of sampling and testing results to ensure data accuracy and compliance.File paperwork and maintain organized laboratory records and documentation.Conduct investigations, special projects, or other non-routine sampling and testing as required.Train junior analysts in new and existing procedures, techniques, and applicable regulations as directed by supervision.Mentor analysts by providing technical guidance, helping resolve technical problems, and reviewing documents.Take initiative to seek out additional assignments and contribute proactively to laboratory operations.Work safely in accordance with regulations, standards, and procedures to eliminate unreasonable risk to health and the environment.Notify management of unsafe conditions or practices, unlawful activities, or activities that present unreasonable health or environmental risk.Report all safety and environmental incidents to management immediately.Perform other related duties as assigned by management.Essential SkillsBachelor’s degree in Microbiology, Biology, or a similar life science discipline preferred.Minimum of 5+ years of laboratory experience, preferably in the pharmaceutical industry.Proven ability to perform environmental monitoring of cleanrooms and facility water systems.Hands-on experience with kinetic LAL and gel-clot LAL endotoxin testing methods.Experience performing filtration testing and particulate matter testing using appropriate instrumentation such as HIAC liquid particle counters.Experience conducting 14-day sterility testing using isolator systems such as the Walker Barrier System.Proficiency in operating laboratory equipment including autoclaves and glassware washers.Strong knowledge and application of aseptic techniques and appropriate cleanroom behaviors.Working knowledge of cGMPs, GLPs, USP, FDA, and other relevant regulatory requirements.Ability to follow and apply standard operating procedures and approved testing methods.Ability to use computer systems for data analysis and documentation, including LIMS.Proficiency with Microsoft Excel, PowerPoint, and Access.Experience with investigation writing, including OOS and deviation investigations.Ability to train personnel on various procedures and communicate effectively with team members and cross-functional groups.Good interpersonal skills and strong verbal and written communication abilities.Demonstrated self-motivation, energy, enthusiasm, and a team-oriented approach.Knowledge of laboratory safety and material safety practices.Additional Skills & QualificationsExperience performing routine environmental monitoring in classified manufacturing areas, including surface, air, and personnel monitoring.Familiarity with environmental monitoring equipment such as SAS 100, SAS Super 180, and Met One instruments.Experience with utilities sampling for purified water, WFI, gases, and clean steam.Understanding of contamination control principles and cleanroom gowning requirements.Ability to ensure sample traceability, accurate labeling, and timely delivery to the QC laboratory.Working knowledge of data integrity principles, including ALCOA+.Ability to identify atypical results and potential contamination risks and to escalate appropriately.Experience supporting CAPA activities related to microbiological and environmental monitoring issues.Ability to mentor and support junior analysts in resolving technical challenges and ensuring documentation quality.Work Environment

This position operates in a regulated pharmaceutical laboratory and classified manufacturing environment with a strong focus on cGMP, GLP, and safety standards. Work involves frequent activity in cleanrooms and controlled areas to perform environmental monitoring and utilities sampling, as well as time in the laboratory operating equipment such as autoclaves, glassware washers, isolators, particle counters, and environmental monitoring instruments (SAS 100, SAS Super 180, Met One). The role requires adherence to contamination control practices, aseptic technique, and cleanroom gowning requirements. Documentation is completed in both electronic systems, including LIMS and standard office software, and in controlled paper records, with strict attention to data integrity. The schedule includes shift-based work, with potential assignments from Tuesday to Saturday or Sunday to Thursday, typically on shifts such as 6:00 pm to 2:30 am or 10:00 am to 6:30 pm, depending on operational needs. The environment emphasizes safety, prompt reporting of incidents or unsafe conditions, and collaborative work with manufacturing and other support groups.

Job Type & Location

This is a Contract to Hire position based out of Raleigh, NC.

Pay and Benefits

The pay range for this position is $35.00 - $42.00/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 Raleigh,NC.

Application Deadline

This position is anticipated to close on Jun 24, 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 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 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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Job DescriptionJob Description

Microbiologist Supervisor

Job Description

The Microbiologist Supervisor leads a quality control microbiology laboratory, overseeing daily testing, release activities, and laboratory investigations in a GMP environment. This role manages a team of microbiologists, ensures compliance with SOPs and regulatory expectations, supports R&D activities, and drives continuous improvement across laboratory processes and systems.

Responsibilities

Provide day-to-day oversight of microbiology laboratory operations, ensuring accurate, timely testing and release of laboratory results.Supervise a team of approximately nine direct reports, supported by team leads, and allocate resources effectively to meet testing schedules and project timelines.Review, approve, and provide guidance on microbiological testing, including microbial limits testing, environmental monitoring, and microbiological assays.Initiate, lead, and complete laboratory investigations to closure, ensuring thorough root cause analysis and implementation of appropriate corrective and preventive actions.Conduct training for direct reports on microbiological techniques, aseptic practices, SOPs, and relevant quality and safety procedures.Participate in and support training activities required to maintain technical competency and compliance with current standards and regulations.Lead and participate in continuous improvement initiatives to optimize laboratory workflows, enhance data quality, and improve overall efficiency and compliance.Provide ongoing performance-based feedback to direct reports, including conducting annual performance reviews and supporting professional development.Manage laboratory equipment calibration and qualification programs, ensuring instruments are maintained in a qualified state and documentation is complete and accurate.Support R&D laboratory activities by providing microbiology expertise, testing support, and technical guidance as needed.Ensure all laboratory work follows GMP requirements, SOPs, and safety guidelines, maintaining a high standard of data integrity and documentation.Collaborate with cross-functional teams, including quality, operations, and R&D, to address microbiology-related issues and support product quality and process improvements.Ensure proper execution and documentation of environmental monitoring programs in accordance with established procedures and regulatory expectations.Promote a culture of quality, safety, and accountability within the laboratory team.

Essential Skills

Bachelor’s degree in a scientific discipline, ideally microbiology or biology.5+ years of experience working in a laboratory setting.2+ years of supervisory or leadership experience in a laboratory environment.

Work Environment

This role is based in a laboratory environment within a GMP-regulated facility, focusing on quality control microbiology activities. Standard working hours are approximately 8:00 a.m. to 5:00 p.m., with an expectation of around 45 hours per week to support operational needs. The position requires regular on-site presence in the lab, working with microbiological samples, sterilization processes, and environmental monitoring systems, while adhering to established safety and SOP requirements.

Job Type & Location

This is a Permanent position based out of Minneapolis, MN.

Pay and Benefits

The pay range for this position is $75000.00 - $90000.00/yr.

Medical, Dental, Vision, 401K, etc.

Workplace Type

This is a fully onsite position in Minneapolis,MN.

Application Deadline

This position is anticipated to close on Jun 23, 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 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 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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Job DescriptionJob Description

Microbiology Lab Manager
Nashville, TN | Full-Time | Day Shift | No Weekends

 

We are seeking an experienced Microbiology Manager to lead laboratory operations and ensure high-quality diagnostic testing that supports exceptional patient care. This role oversees daily microbiology lab functions, staff development, regulatory compliance, and quality improvement initiatives.

 

Key Responsibilities

Manage daily microbiology laboratory operations and staffEnsure compliance with CAP, CLIA, JCAHO, FDA, and CMS standardsLead staff hiring, training, scheduling, and performance managementMaintain quality control and laboratory accreditation readinessCollaborate with the medical director to improve lab performance and patient outcomes

 

Qualifications

Bachelor’s degree in Medical Technology, Biology, Chemistry, or related fieldNational Certification as Medical Technologist required3+ years Microbiology Technologist experienceExperience in a high-volume hospital or clinical lab

 

Compensation & Benefits

Salary up to $110K$15K Sign-On BonusUp to 10% Incentive BonusRelocation assistance (case-by-case)Company DescriptionLanceSoft is rated as one of the largest staffing firms in the US by SIA. Our mission is to establish global cross-culture human connections that further the careers of our employees and strengthen the businesses of our clients. We are driven to use the power of our global network to connect businesses with the right people, and people with the right businesses without bias. We provide Global Workforce Solutions with a human touch.Company DescriptionLanceSoft is rated as one of the largest staffing firms in the US by SIA. Our mission is to establish global cross-culture human connections that further the careers of our employees and strengthen the businesses of our clients. We are driven to use the power of our global network to connect businesses with the right people, and people with the right businesses without bias. We provide Global Workforce Solutions with a human touch. Read Less

Job DescriptionJob Description

High Performance Technologies, Inc. (HPTech) is an infrastructure-centered firm focusing on practice, research, policy, and technology transfer.  HPTech was established in 2003 with the primary purpose of serving the U.S. federal government at their facilities and project sites.  Our uniqueness lies in our ability to integrate physical sciences, social sciences, engineering, planning, and policy when developing and delivering infrastructure solutions.

​HPTech is currently pursuing an upcoming major federal contract, and we are identifying candidates who would be interested in working with us should we be awarded the contract.  At this stage, we are looking for a Concrete Research Technician who will be responsible for assisting concrete research engineers in the execution of research projects and maintaining cleanliness/order of the laboratory. Duties may include, but not limited to, making concrete formwork, mixing concrete, coring, preparing concrete specimens for testing purposes, maintaining general lab cleanliness, moving items with a forklift or crane, basic rigging, and installing instrumentation under the supervision of an concrete research engineer. The work will be performed in a state-of-the-art concrete laboratory at a government facility.

​Qualifications

At least a high school diploma required, an Associate degree in Civil Engineering Technology preferred.At least 4 years of experience as a construction materials  technician.Proficiency in performing various ASTM and AASHTO test procedures, including ASTM C39, ASTM C78, ASTM C150, ASTM C157, ASTM C469, ASTM C496, ASTM C512, ASTM C595, ASTM C1556, ASTM C1585, ASTM C1856, AASHTO TP119, and AASHTO PP84.Excellent verbal, and writing skills.Excellent team and collaborative skills.ACI Concrete Laboratory Testing Technician Level 2 certification.

This anticipated position, which is contingent upon the contract award to HPTech, would be based in McLean, Virginia.

Candidates must be legally authorized to work in the United States.

For timely consideration, apply by August 17, 2022.​

HPTech is an Equal Opportunity Employer

All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or veteran status.

Company DescriptionHigh Performance Technologies, Inc. (HPTech) is an infrastructure-centered firm focusing on practice, research, policy, and technology transfer. HPTech was established in 2003 with the primary purpose of serving the U.S. federal government at their facilities and project sites. Our uniqueness lies in our ability to integrate physical sciences, social sciences, engineering, planning, and policy when developing and delivering infrastructure solutions.Company DescriptionHigh Performance Technologies, Inc. (HPTech) is an infrastructure-centered firm focusing on practice, research, policy, and technology transfer. HPTech was established in 2003 with the primary purpose of serving the U.S. federal government at their facilities and project sites. Our uniqueness lies in our ability to integrate physical sciences, social sciences, engineering, planning, and policy when developing and delivering infrastructure solutions. Read Less

Job DescriptionJob Description

Polymer Resources is seeking a Color Lab Supervisor for a position based at our Farmington, CT facility.

At Polymer Resources, we compound Engineering Thermoplastic materials that are used in both Injection Molding and Profile Extrusion applications serving Medical, Automotive, Consumer, and Industrial markets. We specialize in producing Custom Colored products, and in providing materials with specific property profiles that meet the needs of our customers. We are a service company that provides specialty plastics; and as a result, we have on-time delivery rates greater than 99% with low returns and projected double-digit growth over the next three years.

Polymer Resources is a hands-on organization where everyone makes an impact. It is a great team atmosphere where people truly support each other.

Summary:

The Color Lab Supervisor is part of the production team at Polymer Resources and will report to the Lab Manager. In this role the incumbent will assist with organizing mixing operators for pending orders - as well as assist Quality Technicians on testing products and approving color for ongoing production jobs. Must be able to adjust and fix colors in a fast-paced environment. Candidate will be required to match colors with engineering resins and will be “hands on” with color match capabilities to match the customers supplied parts, chips and/or material.

In addition, this Candidate will be responsible for ensuring that the manufacturing plant is running safely and efficiently with on spec color and specifications while working closely with the Production Supervisors.

Requirements:

· Excellent eyesight (color) – test will be administered to understand ability to see colors.

· Able to use and understand a spectrophotometer to measure color.

· Ability to multi-task and perform a variety of duties.

· A team player willing to do what is needed to get the job done.

· Excellent communication skills – able to communicate well and give clear directions with production supervisors to keep the plant running safely and efficiently.

· Positive attitude and Creative

· Above average math Skills

· Excellent attendance and able to work overtime as needed.

· Strong desire to be part of a winning team.

 

Salary commensurate with qualifications and experience and an excellent benefit package that includes: Medical/Vision & Dental, 401 (k) Plan/Roth Plan, Flex 125 Plan (HCR, DCR, HSA), Life Insurance, Identity Theft as well as additional available coverages.

 

Company DescriptionSalary will be determined based on experience.Company DescriptionSalary will be determined based on experience. Read Less

Job DescriptionJob Description

PURPOSE

This role specializes in overseeing, mentoring, leadership, and advanced technical expertise in the operation, maintenance, and optimization of laboratory equipment and processes to support the organization in engineering experimentation and analysis.

ESSENTIAL DUTIES

• Interpret internal and external customer requirements to meet desired outputs while suggesting alternatives.

• Participate in technical product evaluations by assisting with equipment selection and data acquisition capabilities of the equipment.

• Communicate technical knowledge, specification, and business direction to an extended audience of internal and external customers.

• Document laboratory operation, maintenance, and protocols accurately and comprehensively.

• Monitor and manage inventory levels of laboratory supplies and equipment parts.

• Define, create, and provide training on laboratory procedures and equipment.

• Install, manage and maintain laboratory equipment, including calibration, troubleshooting, and coordinating repairs of complex equipment issues.

• Research and report equipment upgrade and advancements, including lifecycle and prioritization, for the organization to consider.

• Define, create, and implement laboratory procedures that comply with relevant standards, regulations, and safety protocols while staying informed of regulatory changes and updating procedures accordingly.

• Ensure laboratory operations comply with relevant standards, regulations, and safety protocols.

• Read, interpret, and create pneumatic and electrical schematics.

• Assist and mentor in building circuits for test set-ups and data acquisition.

• Troubleshoot pneumatic and electrical circuits.

• Create and input data utilizing corporate management system software that include drawings, equipment documentation, operations manuals, quotes, and procedure documentation.

• Perform guided and/or independent research on a variety of topics and provide summarized data results.

• Complete assigned tasks while providing suggestions for improving departmental processes.

• Hands on technical support for an extended audience (technical and non-technical) of internal and external customers.

• Participate on and/or lead teams to accomplish tasks, processes, and corporate directives.

• Travel mainly for the purpose of training, customer support, or trade shows. (Less than 10%)

• All other duties as assigned.

• Record daily activities.

PHYSICAL DEMANDS/WORK ENVIRONMENT

• Capacity to work indoors in an office, laboratory, and/or manufacturing environment.

• Ability to work in a stationary position for prolonged periods of time.

• Capability to lift objects or equipment weighing up to 51 pounds with or without reasonable accommodation.

• Physical aptitude to use basic hand tools in a laboratory and/or manufacturing environment.

• Ability to travel and/or attend meetings domestic and internationally outside of normal business hours.

MINIMUM REQUIREMENTS

• Associates degree in a technical discipline, or the equivalent in appropriate education and experience as determined by management utilizing internal SMC career development criteria.

• Novice understanding to apply project management principles, methodologies, and documentation.

• Competent understanding of common assembly processes.

• Competent in operating and maintaining laboratory equipment and instrumentation.

• Competent understanding of mechanical and electrical systems.

• Competent in conducting research using corporate resources.

• Competent at efficient use of time to effectively plan and execute multiple duties.

• Fluent to utilize basic inspection equipment in a laboratory environment. (Calipers, micrometers, flow meter, voltmeter, etc.)

• Fluent to utilize advanced inspection equipment in a laboratory environment. (microscopes, CMM, Contour/Roundness Measuring Instruments, etc.)

• Fluent ability to communicate utilizing corporate office software.

• Competent ability to take verbal and/or written direction on tasks, training, or departmental / company policies.

• Competent ability to communicate, in English, with internal and external customers tactfully and professionally

• 0+ years (preferred) relevant work experience.

Company DescriptionSMC Corporation of America is a part of a global organization that supports our customers in every industrialized country and is the U.S. subsidiary of SMC Corporation based in Japan. Since its establishment, SMC has been a leader in pneumatic technology, providing the various industries with technology and products to support automation based on the guiding principle of “contributing to automation labor savings in industry.” Over the past 50+ years, SMC's products have become established as a recognized international brand through sales, technical, supply and after sale services in world markets. Sales have grown to achieve a 30% global market share.

Subsidiaries and joint ventures have been setup in a total of 53 countries. Production facilities are located in 30 countries. In addition, a sales network extends throughout 83 countries, with local services in 500 locations. SMC offers technology accumulated through the years, engineers that bring it to life in new products, production capacity which can deliver a variety of products in a short time, and an extensive sales network in the U.S. and throughout the world.

With its goal of ever more advanced automation, and using its many achievements as a base, SMC is developing high-quality, highly reliable products to contribute to automation in industry, as well as in familiar areas of everyday life.Company DescriptionSMC Corporation of America is a part of a global organization that supports our customers in every industrialized country and is the U.S. subsidiary of SMC Corporation based in Japan. Since its establishment, SMC has been a leader in pneumatic technology, providing the various industries with technology and products to support automation based on the guiding principle of “contributing to automation labor savings in industry.” Over the past 50+ years, SMC's products have become established as a recognized international brand through sales, technical, supply and after sale services in world markets. Sales have grown to achieve a 30% global market share.\r\n\r\nSubsidiaries and joint ventures have been setup in a total of 53 countries. Production facilities are located in 30 countries. In addition, a sales network extends throughout 83 countries, with local services in 500 locations. SMC offers technology accumulated through the years, engineers that bring it to life in new products, production capacity which can deliver a variety of products in a short time, and an extensive sales network in the U.S. and throughout the world.\r\n\r\nWith its goal of ever more advanced automation, and using its many achievements as a base, SMC is developing high-quality, highly reliable products to contribute to automation in industry, as well as in familiar areas of everyday life. Read Less

Job DescriptionJob Description

If you are tired of a corporate setting and being treated like a number instead of a human with value, then consider working with us.

Total Aspect Design is a small engineering firm that provides engineering, consulting, and design to process/chemical plants. TAD is privately owned and family oriented. The employees at TAD wear multiple hats to complete their assignments. The candidate will need to be self-motivating and willing to search for the solution to the opportunities we are presented. The candidate will typically be on a 2-3 man team and working on multiple projects at once. The candidate will start off working in our office and also at the client’s site. Local travel will be necessary. Working from home will be optional when the candidate has proven to be self sufficient.

The candidate must:

· have a bachelor’s in engineering

· be able to work in the United States

The ideal candidate will be able to:

· specify and size pumps and understand pump curves

· calculate heat balances and size heat exchangers

· understand pressure drop and calculate pipe sizes

· understand P&ID drawings

· understand mechanical drawings

· understand physical and chemical properties of materials

· specify instruments for processes

· understand basic programming to be able to communicate with controls engineers

The ideal candidate will know how to use:

· AutoCAD and SolidWorks

· Office products

Company DescriptionTotal Aspect Design, LLC is an engineering company. We provide engineering, consulting, and design to process/chemical plants.Company DescriptionTotal Aspect Design, LLC is an engineering company. We provide engineering, consulting, and design to process/chemical plants. Read Less

Job DescriptionJob Description

Currently hiring for a senior level power generation technician. Must have 15 plus years of experience in the generator industry. Must have own tools and be proficient in troubleshooting all makes and models of generators. ATS experience is a plus.

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Job DescriptionJob DescriptionJob Type: Full Time
Expected Hours: 40
Shift Time: Day Shift, 5:00 AM -3:30 pm, Monday - Thursday

Our client is an industry leader in weatherproofing solutions that is looking to add a chemical operator to its team. The Chemical Operator will work alongside the production team and will be responsible for weighing and mixing chemical ingredients during the chemical process.

*Storing, retrieving, mixing, and monitoring chemicals used in the production process.
*Recording information, such as ingredients, weights, and temperature.
*Troubleshooting issues with production equipment and processes.

Must have a High school diploma or equivalent
Must be be Clean Shaven
Must have mechanical aptitude
Must have the ability to lift 50 lbs

#ZRLH

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Job DescriptionJob Description

Founded in 1986, St. Charles Community College (SCC) has a reputation as one of the best two-year colleges in the state of Missouri. SCC's service area includes a six-county region with a population exceeding 540,000. SCC's main campus, located in Cottleville, has won architectural awards for its innovative, contemporary design. The college's Dardenne Creek Campus features the Center for Healthy Living and the Field to Table Institute. Opening Fall 2025, the Innovation West Campus located in Wentzville features the Regional Workforce Innovation Center. With a focus on innovation, St. Charles Community College is a leader in delivering high quality education in a state-of-the-art learning environment. The success of SCC is rooted in the mission of serving the community by "focusing on academic excellence, student success, workforce advancement, and life-long learning within a global society."

SCC is seeking a full time Institutional Effectiveness Coordinator to assist with the department's administrative and operational activities by coordinating a wide range of processes and projects for the Department of Institutional Research and Effectiveness. This position serves as the primary point of contact for faculty, staff, students, and visitors. The Institutional Effectiveness Coordinator organizes, maintains, and disseminates departmental and institutional information for internal use and, as appropriate, public distribution.

ESSENTIAL DUTIES AND RESPONSIBILITIES

Serves as a collaborative team member supporting day-to-day departmental operations, including customer service, document preparation and distribution, mail processing, office supply ordering and inventory, equipment monitoring, calendar and travel management, and related administrative tasks.Organizes and maintains electronic filing systems, report archives, and tracking logs specific to operational and reporting functions.Assists with the preparation of tables, charts, graphs, dashboards, or other visual materials for reports and presentations.Provides administrative and technical support related to data entry, coding, document formatting, publication and dissemination.Assists with the coordination of assessment activities by compiling documentation, tracking reporting schedules, supporting survey administration, and maintaining assessment records related to academic and administrative outcomes.Serves as primary administrator for department websites; updates content and ensures accuracy and timelines.Creates, updates, distributes, and tracks surveys in support of institutional research, assessment, and operational needs. Conducts research and literature reviews on assigned topics and tracks state and federal reporting schedules and requirements.

REQUIRED SKILLS AND ABILITIES

Demonstrate knowledge of standard office procedures with the ability to provide effective administrative support to departments and leadership.Ability to organize and schedule appointments, coordinate travel, and prepare, modify and format correspondence, memoranda, reports, spreadsheets, and other documents.Ability to work under pressure in a fast-paced environment, particularly during peak reporting and academic periods Capable of managing multiple projects simultaneously, exercising independent judgement to plan, prioritize and execute workload.Demonstrates logical reasoning skills to analyze Situations and determine appropriate solutions.Contribute to the achievement of team and departmental goals and supports a work environment that promotes diversity, equity, inclusion, and belonging.May assist with cross-training staff and provide back-up support or supplemental services during periods of high demand.Interacts with others in a professional, welcoming, and service-oriented manner consistent with the mission and goals of the college. Self-motivated with strong organizational, communication, and problem-solving skills.Required to maintain departmental intranet and internet sites, social media platforms, and publications.

 

EDUCATION AND EXPERIENCE

Associates degree or higher plus two (2) years' experience in related field, OR High School diploma or equivalent with a minimum of four years related experience.Requires regular and predictable attendance.

Please include a cover letter that addresses the following:

Your interest in this position and St Charles Community CollegeA summary of your relevant experience and key qualificationsSpecific examples of accomplishments or skills that align with this role

**Will be subject to a criminal background check.

St Charles Community College is an Equal Opportunity Employer

Company DescriptionFounded in 1986, St. Charles Community College (SCC) has a reputation as one of the best two-year colleges in the state of Missouri. SCC's service area includes a six-county region with a population exceeding 540,000. SCC's main campus, located in Cottleville, has won architectural awards for its innovative, contemporary design. The college's Dardenne Creek Campus features the Center for Healthy Living and the Field to Table Institute. Opening Fall 2025, the Innovation West Campus located in Wentzville features the Regional Workforce Innovation Center. With a focus on innovation, St. Charles Community College is a leader in delivering high quality education in a state-of-the-art learning environment. The success of SCC is rooted in the mission of serving the community by "focusing on academic excellence, student success, workforce advancement, and life-long learning within a global society."Company DescriptionFounded in 1986, St. Charles Community College (SCC) has a reputation as one of the best two-year colleges in the state of Missouri. SCC's service area includes a six-county region with a population exceeding 540,000. SCC's main campus, located in Cottleville, has won architectural awards for its innovative, contemporary design. The college's Dardenne Creek Campus features the Center for Healthy Living and the Field to Table Institute. Opening Fall 2025, the Innovation West Campus located in Wentzville features the Regional Workforce Innovation Center. With a focus on innovation, St. Charles Community College is a leader in delivering high quality education in a state-of-the-art learning environment. The success of SCC is rooted in the mission of serving the community by "focusing on academic excellence, student success, workforce advancement, and life-long learning within a global society." Read Less

Job DescriptionJob Description

A-Line Staffing is now hiring a Scientist I, Analytical Chemistry Development in Vernon Hills, IL 60061. The Scientist I would be working for a Fortune 500 pharmaceutical company and has career growth potential. This would be full-time / 40+ hours per week.

Analytical Chemist  Compensation

The pay for this position is $35.79 per hourBenefits are available to full-time employees after 90 days of employmentA 401(k) with a company match is available to full-time employees with 1 year of service on our eligibility dates

 

Analytical Chemist Highlights

This position is a contract assignment with potential to hire on permanently based upon attendance, performance, and business needsMonday-Friday schedule; standard business hoursOnsite position located in Vernon Hills, ILOpportunity to work within a pharmaceutical analytical chemistry development environment

 

Analytical Chemist Responsibilities

Perform analytical chemistry testing and development activities in support of pharmaceutical productsUtilize wet chemistry and instrumental analytical techniques including pH, titration, UV-Vis, GC, and HPLCGenerate, review, and maintain scientific documentation in compliance with GMP requirementsAuthor technical reports and other scientific documentationTroubleshoot analytical issues and implement effective solutionsInterpret written, oral, diagrammatic, and schedule-based instructionsSupport laboratory investigations and method development activitiesMaintain compliance with FDA regulations, company policies, and laboratory proceduresManage multiple projects and priorities simultaneously while meeting deadlines

 

Analytical Chemist  Requirements

Bachelor's or Master's Degree in Chemistry, Pharmaceutics, or a related scientific field2-4 years of pharmaceutical analytical chemistry experienceExperience with wet chemistry and instrumental analytical techniques (pH, titration, UV-Vis, GC, HPLC)Experience working in an FDA-regulated environmentKnowledge of GMP documentation requirementsExcellent scientific writing and technical documentation skillsDemonstrated knowledge of scientific methods and laboratory techniquesAttendance is mandatory for the first 90 days

 

Analytical Chemist Preferred Qualifications

Master's Degree in Chemistry, Pharmaceutics, or related science disciplineExperience supporting analytical method development and validation activitiesStrong troubleshooting and problem-solving abilitiesAbility to multitask and prioritize work in a fast-paced laboratory environmentStrong communication and collaboration skills

 

If the position is a good fit, apply to this posting today with Silvana M. with A-Line for immediate consideration!

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Job DescriptionJob DescriptionQLM is looking for an advanced-level specialist to perform field operations duties. This full-time position involves technical work related to highway materials testing and geotechnical engineering. Responsibilities include assisting with geotechnical field operations involving conventional soil borings using standard penetration testing methods and performing subsurface investigations. The position includes field sampling and laboratory testing. Work is performed as part of a team, often outdoors in all weather conditions, to support subsurface drilling investigations, geophysical surveys, and other geotechnical field testing statewide. This role requires the use of Personal Protective Equipment and the ability to perform tasks that involve heavy lifting.
Work as part of a team to perform field and/or test pit full‑scale roadway modeling and foundation testing in accordance with applicable test methods. Learn and perform soils and earthwork testing that requires advanced skills or specialized training/qualification. Routinely use computers to collect and report results in the appropriate database.Perform material preparation and testing activities.Maintain field equipment to ensure it remains in proper working condition.Perform other duties as assigned.

Ability to work outdoors in Florida’s harsh environmental conditionsProficiency in computer applications including word processing, spreadsheets, and databasesAbility to troubleshoot equipment and perform basic mechanical tasksStrong problem‑solving skills, including the ability to troubleshoot unforeseen mechanical issuesAbility to travel occasionally on short notice, including working alternate schedulesEffective written and verbal communication skillsAbility to establish and maintain effective working relationshipsAbility to use hand tools, engineering tools, equipment, and instrumentsAbility to work effectively in a team environmentAbility to stand for long periods and lift 50 pounds repeatedly throughout a 10-hour workday
Quality Labor Management (QLM) provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, gender, transgender status or sexual orientation, gender identity, national origin, age, disability, genetic information, marital status, amnesty, or status as a covered veteran in accordance with applicable federal, state, and local laws. The Company complies with applicable Federal state and local laws governing nondiscrimination in employment in every location in which the company has facilities. Read Less

Job DescriptionJob Description

Title: Product Scientist

Location: Emeryville, CA - 94608-1004

Duration: 06+ Months (possible extension)

What You Will Bring:

A desire to drive your future and accelerate your career and the following experience and knowledge:

Food science, science, or engineering ideally in a fast-moving consumer goods market.Working on teams and independently with the guidance of a manager.Personal drive and organization; prioritizing and managing activities.Planning, and executing work plans with some supervision.Identifying problems proactively and creating and implementing solutions independently (problem solving).Applying fundamental technical understanding to interpret and analyze data to reach clear conclusions.Communicating effectively verbally and in writing, including technical writing.Putting the consumer at the heart of development activities.

Additional Job Description:

More About This Role:

What You Need To Know About This Position:

You will be working on Bar, the leading bar brand in the category.Great learning with experienced developers and best performing team.

You Will Experience Wide Ranges Of Projects Including:

Innovation: Near term innovation and renovation.Core maintenance: Resolve quality issues, BCP, Margin and support plant performance improvement, and other duties as assigned. Making benchtop samples to support development work; shipping and receiving samples and ingredients.

Job Specific Requirements:

BS in Food Science, Chemical Engineering or related field.1-3 years of experience in related field.Strong technical foundation and technical curiosity.Participate in cross functional teams to identify and resolve technical issues.Write process specifications that deliver consistent, high-quality products across numerous manufacturing facilities.Excellent written and oral communication.Company DescriptionFounded in 1998 and headquartered in Farmington Hills, MI, Kyyba has a global presence delivering high-quality resources and top-notch recruiting services, enabling businesses to effectively respond to organizational changes and technological advances.

At Kyyba, the overall well-being of our employees and their families is important to us. We are proud of our work culture which embodies our core values; incorporating value, passion, excellence, empowerment, and happiness, creates a vibrant and productive atmosphere. We empower our employees with the resources, incentives, and flexibility that they need to support a healthy, balanced, and fulfilling career by providing many valuable benefits and a balanced compensation structure combined with career development.

Kyyba is an Equal Opportunity Employer.

Kyyba does not discriminate on the basis of race, religion, color, sex, gender identity, sexual orientation, age, non-disqualifying physical or mental disability, national origin, veteran status or any other bCompany DescriptionFounded in 1998 and headquartered in Farmington Hills, MI, Kyyba has a global presence delivering high-quality resources and top-notch recruiting services, enabling businesses to effectively respond to organizational changes and technological advances.\r\n\r\nAt Kyyba, the overall well-being of our employees and their families is important to us. We are proud of our work culture which embodies our core values; incorporating value, passion, excellence, empowerment, and happiness, creates a vibrant and productive atmosphere. We empower our employees with the resources, incentives, and flexibility that they need to support a healthy, balanced, and fulfilling career by providing many valuable benefits and a balanced compensation structure combined with career development.\r\n\r\nKyyba is an Equal Opportunity Employer.\r\n\r\nKyyba does not discriminate on the basis of race, religion, color, sex, gender identity, sexual orientation, age, non-disqualifying physical or mental disability, national origin, veteran status or any other b Read Less