• cGMP Process Development (PD)…

    University of Southern California (Los Angeles, CA)
    …industry best practices, and advancements in cell therapy and cGMP manufacturing . + Prepares, calibrates, and maintains laboratory equipment for use. ... temporary and/or resource workers. Minimum Skills: Proficiency in operating and maintaining laboratory equipment used in cGMP manufacturing and quality… more
    University of Southern California (11/19/25)
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  • cGMP Vector Manufacturing Associate

    University of Southern California (Los Angeles, CA)
    …Science Minimum Experience: 3 years Minimum Skills: Proficiency in operating and maintaining laboratory equipment used in cGMP manufacturing and quality ... that make the university what it is. USC's Keck School of Medicine, current Good Manufacturing Practices ( cGMP ) facility is seeking a qualified cGMP Vector … more
    University of Southern California (12/23/25)
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  • cGMP Quality Control Associate

    University of Southern California (Los Angeles, CA)
    …years in cell therapy development Minimum Skills: Proficiency in operating and maintaining laboratory equipment used in cGMP manufacturing and quality ... that make the university what it is. USC's Keck School of Medicine, current Good Manufacturing Practices ( cGMP ) facility is seeking a qualified cGMP Quality… more
    University of Southern California (12/23/25)
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  • cGMP Facilities Assistant

    University of Southern California (Los Angeles, CA)
    …a Facilities Assistant to support essential operations within its current Good Manufacturing Practices ( cGMP ) facility. The successful candidate will be ... Additional responsibilities include the setup, installation, calibration, and validation of manufacturing and laboratory equipment. The Facilities Assistant will… more
    University of Southern California (12/20/25)
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  • Senior Scientist

    Eurofins US Network (Columbia, MO)
    …degree in chemistry, biochemistry, or biology and 5 years of experience working in a cGMP laboratory OR Master's degree and 3 years of experience working in a ... having an emerging global presence in Contract Development and Manufacturing Organizations. It also has a rapidly developing presence... cGMP laboratory OR PhD and minimum 1… more
    Eurofins US Network (01/03/26)
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  • Senior QA Auditor

    Cambrex High Point (Charles City, IA)
    …to Cambrex. Cambrex is a leading global contract development and manufacturing organization (CDMO) that provides drug substance development and manufacturing ... from North America and Europe, Cambrex offers a range of specialized drug substance technologies and capabilities, including continuous flow, controlled substances,… more
    Cambrex High Point (12/23/25)
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  • QA Validation Specialist

    Kelly Services (Irvine, CA)
    …**RESPONSIBILITIES:** + Assists in assuring facility, manufacturing , packaging, and Laboratory equipment are qualified to the required cGMP standards. + ... (Contract)** to join a leading pharmaceutical team supporting critical ** cGMP qualification and validation activities.** This **6-month contract** offers… more
    Kelly Services (01/01/26)
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  • MCS Associate Quality Control

    US Tech Solutions (Thousand Oaks, CA)
    …of Quality Control operations. The role requires adherence to current Good Manufacturing Practices ( cGMP ), safety guidelines, and regulatory requirements while ... in a timely manner + Operate, maintain, and troubleshoot laboratory instruments and specialized equipment as required.... and safety requirements. **Top must have skills:** + cGMP Compliance & Documentation + Laboratory Execution… more
    US Tech Solutions (12/24/25)
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  • Quality Control Manager

    Actalent (Largo, FL)
    …procedures for recording, monitoring, and maintaining quality results to ensure QC Laboratory performance adheres to cGMP standards and company procedures. The ... with manufacturing and quality assurance teams. Responsibilities + Develop laboratory staff to enhance performance. + Create and maintain systems for quality… more
    Actalent (12/31/25)
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  • Quality Control Analyst

    Glenmark Pharmaceuticals Inc., USA (Monroe, NC)
    …highly motivated member of the Quality Control (QC) Lab at the Monroe manufacturing facility, reporting to the QC Manager. Primary responsibilities for this position ... will be: perform QC analysis in compliance to cGMP in line with standards prescribed by USFDA. Maintain...JOB RESPONSIBILITIES: + Be cost effective and vigilant of laboratory reagents, glassware, etcetera to ensure department is within… more
    Glenmark Pharmaceuticals Inc., USA (01/01/26)
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  • Metrology Associate I

    Cook Medical (Pittsburgh, PA)
    …school diploma or equivalent with at least 2 years previous experience with laboratory equipment in a manufacturing facility. Minimum of 1-3 years' experience ... and oversee vendors throughout the facility and in the manufacturing suite* Assist in maintaining all equipment procedures and...but not limited to safety glasses, lab coat, gloves, specialized clothing including laboratory scrubs (pants and… more
    Cook Medical (11/20/25)
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  • Quality Control Associate

    Genentech (Oceanside, CA)
    …wear necessary personal protective equipment (PPE). + Work is performed in a cGMP -regulated manufacturing facility. + Work with analytical instruments that may ... products. Additional responsibilities include equipment management and maintenance, and laboratory duties. **The Opportunity** + Compliance and Quality System… more
    Genentech (12/24/25)
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  • R&D Operator

    Contract Pharmacal Corp (Hauppauge, NY)
    …new technologies, and being deeply involved in early-stage development within a cGMP environment. Job Type: Full-Time Location: Hauppauge, NY Works Hours: Monday - ... makes this role exciting: + Exposure to a variety of pharmaceutical manufacturing technologies + Opportunities to learn directly from experienced Scientists and… more
    Contract Pharmacal Corp (12/12/25)
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  • Biomedical Technician - Biomanufacturing Facility

    Cedars-Sinai (West Hollywood, CA)
    …facility located in West Hollywood, California. The CBC is comprised of a cGMP cell manufacturing facility, housing multiple cleanroom cell production suites, ... be used for human IND-enabling clinical trials. With combined expertise and a cGMP -compliant approach to manufacture cells at scale, the CBC will overcome many… more
    Cedars-Sinai (12/05/25)
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  • Aseptic Technician- 3rd Shift

    Actalent (Parsippany, NJ)
    …plus. + Experience with aseptic gowning and techniques. + Troubleshooting skills in laboratory and manufacturing processes. + Knowledge of sterilization and cell ... the 3rd shift to support the validation of new manufacturing areas, equipment, and processes. + This role involves...the efficiency of our operations while adhering to strict cGMP and Good Documentation Practices. Responsibilities + Assist with… more
    Actalent (01/03/26)
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  • **QC Raw Materials Scientist III*

    Actalent (St. Louis, MO)
    …+ Experience with compendial HPLC assays. + Knowledge of GMP regulations in a cGMP manufacturing environment. + Working knowledge of scientific principles for a ... + Perform all duties in compliance with Standard Operating Procedures, Good Manufacturing Practices, Good Laboratory Practices, and Safety guidelines. + Work… more
    Actalent (01/03/26)
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  • Senior Scientist: TASC

    Eurofins US Network (Columbia, MO)
    …GC, GCMS, and HPLC/UPLC, LCMS + Familiarity and/or experience in a laboratory setting is required in a cGMP -regulated environment. **Qualifications** + ... Eurofins is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in… more
    Eurofins US Network (12/30/25)
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  • Scientist II Pharmaceutical Analyst

    Cardinal Health (Mansfield, MA)
    …stability testing is desired. + Possess a thorough understanding of Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP) to ensure ... Services Center contributes to Cardinal Health_** Chemistry Services Center perform laboratory testing to characterize the chemistries of our medical device products… more
    Cardinal Health (12/17/25)
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  • Biologics Quality Assurance Auditor

    Actalent (Columbus, OH)
    …regulations, policies, procedures, and expectations of phase-appropriate current Good Manufacturing Practices ( cGMP ). Additionally, the QA Auditor participates ... support for the manufacture of phase 1/2a Investigational New Drug, Biologics manufacturing , and facility operations. This role works alongside the Quality Assurance… more
    Actalent (12/29/25)
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  • **Process Engineering (Charles City, IA) Talent…

    Cambrex High Point (Charles City, IA)
    …you'll be immersed in every stage of bringing new products from the laboratory to full-scale manufacturing , gaining hands-on experience with batch processes and ... to Cambrex. Cambrex is a leading global contract development and manufacturing organization (CDMO) that provides drug substance development and manufacturing more
    Cambrex High Point (12/18/25)
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