• 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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  • Associate Director - Drug Product…

    Novo Nordisk (Boulder, CO)
    About the Department The Boulder Site is home to the specialized technical operations/CMC team for oligonucleotides and RNAi therapeutics. The CMC team works ... and is one of the world's leading centers for oligonucleotide innovation and manufacturing . Together, we are driving change. Are you ready to make a difference?… more
    Novo Nordisk (01/06/26)
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  • Chemical Process Technician ( Manufacturing

    Cambrex High Point (Waltham, MA)
    …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 (12/13/25)
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  • Quality Control Data Review Supervisor

    Cambrex High Point (Charles City, IA)
    …for analytical data review activities within a cGMP Quality Control laboratory supporting API and intermediate manufacturing . This role is responsible for ... and effective CAPA implementation within TrackWise. + Maintain and manage cGMP -compliant laboratory documentation systems, including instrument logbooks, … more
    Cambrex High Point (01/08/26)
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  • Bioassay Scientist - Sr. 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. The Group also has a rapidly developing... cGMP laboratory OR PhD and minimum 1… more
    Eurofins US Network (01/08/26)
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  • Quality Control Chemist I

    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 (01/08/26)
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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 Chemistry Analyst II

    Actalent (Rockville, MD)
    …Osmolality, CE, size exclusion chromatography, and GDP. + Understanding of Good Manufacturing Practices ( cGMP ). + Strong scientific knowledge and hands-on lab ... method and instrument issues successfully. + Independently contribute to Laboratory Investigations, OOS/OOT results, Deviations, CAPA, and Change Control record… more
    Actalent (01/10/26)
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  • Quality Control Analyst

    Actalent (Vernon Hills, IL)
    …Procedures (SOPs) for equipment and instrumentation in compliance with current Good Manufacturing Practices ( cGMP ). Your analytical skills will be key in ... analyzing, interpreting, and reporting experimental results while maintaining detailed laboratory notebooks and electronic records. Responsibilities + Conduct routine… more
    Actalent (01/09/26)
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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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  • QC Chemist

    Actalent (Cranbury, NJ)
    …apparatus, UV-Vis spectrometer, FT-IR) is highly preferred. + Current Good Manufacturing Practices ( cGMP ), FDA, and other regulatory requirements knowledge. ... in a laboratory setting with exposure to chemicals, reagents, and specialized equipment. The team consists of approximately 10 people. This position may require… more
    Actalent (01/10/26)
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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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