• Director, Pneumococcal Franchises (PCV) - Vaccines…

    Merck (West Point, PA)
    …our company's Global and regulatory requirements and current Good Manufacturing Practices ( cGMP ). + Promote a safe, compliant, and inclusive culture within the ... organization and teams. **Minimum Education and Experience Requirement** + Bachelor of Science (BS) in Biological Sciences, Chemical Engineering, Biochemical Engineering, Bioengineering, or related field with twelve (12) years of required experience; **OR** +… more
    Merck (08/27/25)
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  • Specialist, Engineering, Maintenance & Utilities

    Merck (West Point, PA)
    …ASME, IEEE, NFPA, CFR 1910, NIST, and/or ANSI). **Preferred:** + Knowledge of cGMP for pharmaceutical and/or vaccine manufacturing + Lean Six Sigma Methodology + ... Root Cause Analysis + Failure Mode Effects Analysis + Knowledge in reliability engineering (including asset life cycle management) + Computerized Management Maintenance Systems: SAP/EAM/Maximo/etc. + CMRP certification Note: This description is not intended to… more
    Merck (08/27/25)
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  • Associate - Technical Operations - US Commercial

    Lilly (Philadelphia, PA)
    …technical area + Experience working with Radiopharmaceuticals + Knowledge of cGMP drug substance/drug product manufacturing and quality control + Impeccable ... organizational skills + Ability to work independently in a highly focused manner + Excellent interpersonal skills and ability to collaborate with internal and external parties + Superior written and verbal communication skills + Excellent computer skills (eg… more
    Lilly (08/27/25)
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  • Spclst, Quality Control

    Merck (West Point, PA)
    …in Quality control (QC) with working knowledge of current Good Manufacturing Practices ( cGMP ) or standardization of labs + Ability to work independently and within a ... cross-functional team. + Good technical, communication (oral and written), interpersonal, and teamwork skills. + Self-motivated with a positive attitude and proven performance record. VETJOBS \#Eligableforerp Current Employees apply HERE… more
    Merck (08/26/25)
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  • Document Specialist

    Globus Medical, Inc. (Audubon, PA)
    …controlling, and auditing documentation that is required for Quality and cGMP compliance. Essential Functions: + Issue Quality System documents and coordinate ... training process. + Issue device master record documents (manufacturing process specifications, inspection plans, routers, etc.) and other technical documents during development, release, and maintenance phases of product realization. + Process Document Change… more
    Globus Medical, Inc. (08/26/25)
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  • Manufacturing Technician

    BioFire Diagnostics, LLC. (Philadelphia, PA)
    …Manufacturing experience preferred. + Experience in a lab setting and work requiring cGMP is preferred but not required. Knowledge, Skills & Abilities: + Proficient ... in math, specifically unit conversions. + Good oral/written communication, pipetting/liquid handling of multiple volumes. + Maintain attention to detail for extended periods of time. + Execute repetitive tasks and maintain high level of consistency over time.… more
    BioFire Diagnostics, LLC. (08/26/25)
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  • Digital Quality Systems Manager

    ThermoFisher Scientific (Pittsburgh, PA)
    …to GSG business including 21CFR820, 21CFR803, ISO 9001, ISO 13485, IVDR, cGMP 's, FDA Guidelines, USP, and GxP. + Detailed knowledge of medical device ... manufacturing processes and experience with risk management regulations and standards, including FDA 21 CFR 820, MDSAP, IVDR, ISO 13485, and ISO 1497. + Detailed knowledge of software validation best practices; especially those in a regulated environment. +… more
    ThermoFisher Scientific (08/23/25)
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  • Manufacturing Co-Op

    BioFire Diagnostics, LLC. (Philadelphia, PA)
    …attention of the Supervisor for resolution + Comply with safety requirements, cGMP , SOP and manufacturing documentation + Prepare, fill, label and package solutions ... for production and distribution + Execution of critical and routine/non-routine production operations + Record data and update inventory into database + Clean production equipment or work areas + Assist management in verification and validation of… more
    BioFire Diagnostics, LLC. (08/23/25)
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  • Scientist - Container Closure Integrity…

    Merck (West Point, PA)
    …years of relevant work experience in current Good Manufacturing Practices ( cGMP ) laboratory environment. **Required** **Experience | Knowledge | Skills** + Relevant ... analytical execution, development, validation, and/or quality control (QC) as it pertains to Vaccines and/or Biologicals. + Knowledge in Container Closure Integrity Testing or compendial testing. + Ability to learn new techniques, troubleshooting assays,… more
    Merck (08/21/25)
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  • FFIP Project Manager

    Sanofi Group (Swiftwater, PA)
    …Bachelor's Degree is required + 2+ years of experience in a cGMP -compliant pharmaceutical/ biotech, medical device, food industry environment, or an equivalent ... regulated setting. + Requires 100% on-site presence during regular workdays, with occasional support during off-shift hours, either remotely or on-site. + Must have excellent written and verbal communication skills, as well as the ability to actively, and… more
    Sanofi Group (08/21/25)
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