• Utilities Engineer

    CSL Behring (Kankakee, IL)
    …Specifications (URS), Risk Assessments, Safety Assessments and participates in validation activities including review of IQ/OQ protocols, executions and summary ... technical support to operations, maintenance, manufacturing, automation, quality assurance, validation , reliability engineering and project engineering. + Support the… more
    CSL Behring (06/24/25)
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  • Senior Associate Scientist, Disc Bioanalytical

    Charles River Laboratories (Mattawan, MI)
    …pharmacokinetic/pharmacodynamic studies. Staff participate in the development and validation of quantitative LC/MS/MS methodology, sample analysis, and ... operational area + Independently lead the lab staff in the completion of method validation studies + Provide support to staff members as required by operational area… more
    Charles River Laboratories (06/19/25)
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  • Principal Supplier Quality Auditor

    Hologic (Newark, DE)
    …CFR 820, ISO 13485). + In-depth knowledge of medical device and/or pharmaceutical regulations, including risk management processes (eg, pFMEAs) and validation ... (CBA), or IRCA Lead Auditor Registration is a must. + Familiarity with validation protocols, root cause analysis, GR&R, PPAP, and global regulations (FDA, Canada,… more
    Hologic (06/18/25)
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  • QA Associate

    Kelly Services (West Chester, OH)
    …QA activities such as batch release, change control, process validation , deviation investigations, SOPs, supplier management, distribution center management, and ... (Deviations, Product Complaints) + Support Aseptic Manufacturing operations + Validation Plans, Protocols, and Reports + Standard Operating Procedures +… more
    Kelly Services (06/18/25)
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  • Director, Cell Therapy Competitive Intelligence

    Bristol Myers Squibb (Madison, NJ)
    …forensics capability (asymmetric intelligence) via extrapolation, triangulation and internal expert validation . + Executes all projects within budget assigned, in a ... degree preferred. + A minimum of 10 years of experience within the pharmaceutical /biotech industry, including at least 5 years of experience in competitive, market… more
    Bristol Myers Squibb (09/16/25)
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  • QC Microbiologist

    Actalent (La Verne, CA)
    …and safety of raw materials, in-process and final products, as well as validation -related and critical utility samples. This role is ideal for individuals who are ... techniques and working in a cleanroom environment. + Experience with pharmaceutical and microbiological testing, including bioburden and endotoxin testing. +… more
    Actalent (09/16/25)
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  • Scientific Application Specialist

    Bristol Myers Squibb (New Brunswick, NJ)
    …have knowledge of software development lifecycle (SDLC) and of computer systems validation (CSV) + Experience working in large and/or complex IT programs, preferably ... within the pharmaceutical development and quality control domains. + Must have...and quality control domains. + Must have experience in pharmaceutical industry and an understanding of the drug development… more
    Bristol Myers Squibb (09/15/25)
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  • Environmental Monitoring and Sampling Technician

    Mentor Technical Group (PR)
    …MTG has the knowledge and experience to ensure compliance with pharmaceutical , biotechnology, and medical device safety and efficacy guidelines. With offices ... coordination with other departments, the guidance and resources to support validation projects, troubleshooting, lots of production, and process optimization. +… more
    Mentor Technical Group (09/14/25)
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  • Quality Operations Drug Product: Associate

    Pfizer (Groton, CT)
    …This role will offer the opportunity to collaborate with partner lines across Pharmaceutical Sciences Small Molecule (PSSM), as well as with other groups within PSSM ... Groton CT drug product manufacturing, including quality touchpoints in cleaning validation , master batch records, working batch records, review of executed batch… more
    Pfizer (09/14/25)
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  • Quality Control Specialist

    Mentor Technical Group (Juncos, PR)
    …MTG has the knowledge and experience to ensure compliance with pharmaceutical , biotechnology, and medical device safety and efficacy guidelines. With offices ... Responsibilities: * Laboratory experience in a GMP environment within the Pharmaceutical and/or Biotech industry * Fully bilingual communications skills (English and… more
    Mentor Technical Group (09/14/25)
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