• GMP Compliance Expert

    Merck (Rahway, NJ)
    **Job Description** The Director of GMP Compliance will be a part of the Compliance Support and Remediation team within our company's Global Quality ... SMEs. **Job Function:** + serve as a subject matter expert for good manufacturing practices ( GMP ) for...authority/board of health as an inspector, investigator, product reviewer, compliance officer, or other GMP /regulatory role +… more
    Merck (11/01/24)
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  • Associate Director, Cleanroom Operations

    Bristol Myers Squibb (Summit, NJ)
    …Senior Managers, Managers, Team Leads and Material Handlers that interface with GMP cleaning and EM sampling partners responsible for all processes associated with ... GMP cleaning & EM Sampling within CAR T clinical...(future 12hr/7d Operation). This position assures individual and group compliance with all FDA, DEA, DOT, ISBT, CTPAT, OSHA,… more
    Bristol Myers Squibb (10/23/24)
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  • Senior Manager, Business Operations Lead

    Bristol Myers Squibb (Summit, NJ)
    …Sample Storage in Cryotanks), Patient Materials Mgmt (APH receipt and DP Packout), GMP Cleaning and EM Sampling within CAR T clinical and commercial operations in ... all tasks of MSS organization ranging for EM Sampling, GMP Cleaning, APH receipt, DP Packout, sample retrieval, sample...(future 12hr/7d Operation). The position assures individual and group compliance with all FDA, DEA, DOT, ISBT, CTPAT, OSHA,… more
    Bristol Myers Squibb (10/18/24)
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  • Environmental Health and Safety Manager

    Promotion In Motion (Somerset, NJ)
    …+ Manages annual EHS budget and prepares forecasts expenditures. + Follow PIM Brands GMP rules. + Report food safety and quality issues to Plant management and SQFP ... + Monitor associates for adherence to GMP 's. + Provide associates with the tools, programs, policies...minimize safety and occupational health hazards. + Support SQF/NSF compliance through active participation in internal audits and factory… more
    Promotion In Motion (11/02/24)
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  • Sr. Manager, Value Stream CAR-T Manufacturing in

    Bristol Myers Squibb (Summit, NJ)
    …Cell Therapy manufacturing processes, maintaining a culture of safety, compliance , innovation, and Continuous Improvement within the Manufacturing Operations ... adhere to the BMS values of Inclusion, Accountability, Innovation, Urgency and Passion ** GMP ** + Is accountable to ensure their Manufacturing Managers and their WCT… more
    Bristol Myers Squibb (11/03/24)
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  • Process Engineer - General Templates

    Insight Global (Rahway, NJ)
    …support consistent documentation and process standardization across the organization. Ensure compliance with GMP , FDA, and other regulatory standards throughout ... We are seeking a highly skilled and motivated Process Engineer / Subject Matter Expert (SME) with 2+ years of Drug Substance / Drug Product experience in… more
    Insight Global (10/04/24)
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  • Director, Small Molecule Analytical Research…

    Merck (Rahway, NJ)
    …+ Defining and implementing operational control strategies to ensure efficient GMP processes while maintaining high-level of compliance and scientific ... our small molecule portfolio. In this role, you will work with the GMP Analytical and Raw Materials teams on strategies associated with Operational Excellence. The… more
    Merck (10/12/24)
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  • Senior Specialist, Quality Assurance Label Control

    Bristol Myers Squibb (Summit, NJ)
    …guidelines. **Knowledge & Skills:** + Must have advanced knowledge and experience with GMP , Quality, and compliance . + Able to write and review technical ... + Responsible for ensuring accurate printed information on labels in compliance with health authority requirements. + Coordinates with production teams to… more
    Bristol Myers Squibb (10/22/24)
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  • Associate Director, Clinical Supply Project…

    Merck (Rahway, NJ)
    …chain metrics and/or participate in critical non-pipeline activities as a subject matter expert in a particular area of expertise. + Mentors new team members and ... in project / portfolio management. + Knowledge of Good Manufacturing Practices ( GMP ) and Good Clinical Practices (GCP) is highly desirable. **Preferred Experience… more
    Merck (10/12/24)
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  • Scientist

    ManpowerGroup (Franklin Twp, NJ)
    …analytical testing, adhering to standard operating procedures (SOPs), and ensuring compliance with regulatory guidelines such as cGMP and ICH regulations. The ... Fischer, following standard operating procedures (SOPs) and good manufacturing practices ( GMP ). + Review and interpret analytical data, investigate any deviations or… more
    ManpowerGroup (10/04/24)
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  • Associate Director, Cryo Operations

    Bristol Myers Squibb (Summit, NJ)
    …and multiple shifts (future 12hr/7d Operation). The position assures individual and group compliance with all FDA, DEA, DOT, ISBT, CTPAT, OSHA, VAWD, cGMPs and ... procedures, and corporate policies while maintaining a culture of safety, compliance , innovation, and Continuous Improvement. **Shifts Available:** Monday - Friday,… more
    Bristol Myers Squibb (10/29/24)
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  • Senior Manager, Cryo Operations, Inventory…

    Bristol Myers Squibb (Summit, NJ)
    …and multiple shifts (future 12hr/7d Operation). The position assures individual and group compliance with all FDA, DEA, DOT, ISBT, CTPAT, OSHA, VAWD, cGMPs and ... procedures, and corporate policies while maintaining a culture of safety, compliance , innovation, and Continuous Improvement. **Shifts Available:** Monday - Friday,… more
    Bristol Myers Squibb (11/03/24)
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  • Manager, Value Stream Cryo Operations

    Bristol Myers Squibb (Summit, NJ)
    …the ALCOA+ principles. + Perform Cell Therapy production steps to maintain hands-on expert knowledge of each Unit Operation, role model good execution and behaviors ... and CAPAs as required to restore area performance and ensure optimal compliance levels. Identify strategic and operational issues both internally and externally,… more
    Bristol Myers Squibb (10/31/24)
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  • Senior Specialist, Clinical Supplies Project…

    Merck (Rahway, NJ)
    …clinical supply planning group (eg, process improvement initiatives, subject matter expert roles, cross functional projects, etc.) + Demonstrates high capability to ... in project / portfolio management. + Knowledge of Good Manufacturing Practices ( GMP ) and Good Clinical Practices (GCP) is highly desirable. **Preferred Experience… more
    Merck (10/31/24)
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  • QC Analytical Associate III

    System One (Mahwah, NJ)
    …the internal QC change control system + Applies expertise of compliance requirements and therefore maintains an inspection-ready state laboratory + Participates ... as subject matter expert during audits/inspections + Works with internal departments and...immunology experience in a CGMP/GTP environment a must + GMP , Cell count, flow cytometry , documentation, flexibility, CBC,… more
    System One (10/30/24)
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