• Legend Biotech USA, Inc. (Raritan, NJ)
    …of an immunotherapy in the treatment of multiple myeloma.Legend Biotech is seeking an Associate MES Engineer as part of the Manufacturing Excellence team based ... in Raritan, NJ. Role OverviewThe Associate MES Engineer will be part of MSAT team...will be part of MSAT team reporting to the Manufacturing Execution Systems Lead and will be responsible for… more
    HireLifeScience (08/28/25)
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  • Merck & Co. (Rahway, NJ)
    …the Final Study ReportMaintain contact with all stakeholders (project leader, regulatory affairs, quality assurance etc.) and keeps them informed of the study ... DescriptionJOB DESCRIPTION SUMMARY Primary activities include but are not limited to: The Associate Principal Scientist is a DVM and/or PhD whose primary function is… more
    HireLifeScience (10/09/25)
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  • Legend Biotech USA, Inc. (Raritan, NJ)
    …with written Policies and procedures as required for batch releasePerform First Quality review for executed batch records dailyPerform other assigned duties as may ... as eLims samples data, MES calculations, EBR completeness, SAP data, and Quality IssuesDocument retrieval from local files and archives, as required for submissions… more
    HireLifeScience (10/03/25)
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  • QA Associate Manufacturing

    Actalent (Cranbury, NJ)
    … ManufacturingJob Description We are seeking a dedicated QA Associate Manufacturing professional to provide quality assurance support within our ... highest standards of quality and compliance. Responsibilities + Provide quality assurance support in manufacturing , packaging, and warehouse areas for… more
    Actalent (10/11/25)
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  • Manufacturing Associate III

    Catalent Pharma Solutions (Princeton, NJ)
    ** Manufacturing Associate III** **Position Summary:** Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose ... late-stage and commercial-scale autologous and allogeneic cell therapy production. The ** Manufacturing Associate III** is responsible for advising and supporting… more
    Catalent Pharma Solutions (09/17/25)
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  • Associate Director, External…

    Merck (Rahway, NJ)
    …Achieve compliance goals through a risk-based approach (Safety Regulations, Quality Assurance , Risk Management, Deviation Management, Product Release, ... External Manufacturing Operations, Drug Delivery Systems and Devices within our Manufacturing Division ( Associate Director). This role serves as a Virtual… more
    Merck (08/18/25)
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  • Manufacturing Associate

    Kerry (Clark, NJ)
    …Dry Operator Follow the use of Personal Protection Equipment and Good Manufacturing procedures to maintain good housekeeping and ensure compliance with all safety ... and environmental laws and regulations. Follow all manufacturing instructions on formula batch sheet using proper compounding techniques to ensure product quality more
    Kerry (09/16/25)
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  • Manufacturing Associate

    Kerry (Clark, NJ)
    …subject to eligibility requirements). Key responsibilities To compound batches which meet quality and consistency standards in a cost effective, safe and timely ... working knowledge of all raw materials before use, ie: mixing/heating to ensure quality and consistency in batches. 3. Utilize inventory lot rotation for all… more
    Kerry (09/16/25)
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  • Associate Director, Drug Product,…

    BeOne Medicines (Pennington, NJ)
    **General Description:** This role in the Manufacturing Science and Technology (MST) department supports BeOne's Drug Product Manufacturing site in New Jersey ... transfer, validation, continued process verification, investigations, change management and manufacturing startup. Reporting to the MST leadership, this role is… more
    BeOne Medicines (09/18/25)
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  • Manufacturing Operator - Warehouse, Weekend…

    Integra LifeSciences (Plainsboro, NJ)
    …pathways to advance patient outcomes and set new standards of care. The ** Manufacturing Operator/Warehouse Associate ** will verify and keep records of all ... records, and other procedures to comply with regulatory requirements, Good Manufacturing Practices (GMP), Quality Systems Regulations, Standard Operating… more
    Integra LifeSciences (09/13/25)
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  • Quality Assurance Manager

    Compass Group, North America (New York, NY)
    …Must have strong knowledge in Preventive Controls for Human Food. A strong background in manufacturing , quality assurance and strong understand of FSMA is a ... Manager** is responsible for development and maintenance of all QA programs, meeting USDA, FDA and customer requirements and...least 6 years of directly related experience required in Quality Assurance and Food Safety manufacturing more
    Compass Group, North America (10/01/25)
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  • Quality Assurance Technician

    Primo Brands (Jersey City, NJ)
    …such as preparation of media, reading and interpreting microbial growth. *Exposure to Quality Assurance or Production in a food or beverage processing facility. ... than 150,000 retail outlets. **If you are a current associate of Primo Brands, please apply via myADP or...but are not limited to the following:** *Accountable for Quality KPIs such as First Time Right, non-conforming product… more
    Primo Brands (08/30/25)
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  • Associate Principal Scientist, Regulatory…

    Organon & Co. (Jersey City, NJ)
    …manner. Strong listening skills. + Demonstrated sound understanding of related fields (eg, manufacturing , analytical, quality assurance ) and the ability to ... the Director or Executive Director in Organon Regulatory CMC, the Associate Principal Scientist is responsible for developing and implementing Regulatory Chemistry,… more
    Organon & Co. (10/09/25)
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  • RTH Assembly - Associate

    FreshRealm (Linden, NJ)
    … environment applying common processes, procedures, and equipment. + Knowledge of quality assurance practices. + Experience applying and enforcing routine Good ... Linden, NJ location. FreshRealm is looking for a Kitchen Associate that will receive produce & raw foods, assemble,...Meal kits to recipe specifications, ship kits following Good Manufacturing Practices, and meet health and safety standards. +… more
    FreshRealm (07/31/25)
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  • Receiving Associate

    FreshRealm (Linden, NJ)
    … environment applying common processes, procedures, and equipment. + Knowledge of quality assurance practices. + Experience applying and enforcing routine Good ... Receive foods, assemble Meal kits to recipe specifications, ship kits following Good Manufacturing Practices, and meet health and safety standards. + Works on a… more
    FreshRealm (08/13/25)
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  • Associate Principal Scientist, Clinical…

    Merck (Rahway, NJ)
    …Study Report + Maintain contact with all stakeholders (project leader, regulatory affairs, quality assurance etc.) and keeps them informed of the study progress. ... _Primary activities include but are not limited to:_ The Associate Principal Scientist is a DVM and/or PhD whose...and key opinion leaders in relevant fields. + Conduct quality control inspections of study protocol, study documentation files… more
    Merck (10/09/25)
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  • Production Associate

    Aerotek (Piscataway, NJ)
    **Job Title: Production Associate ** Job Description The production associate assists with production activities, adhering to GMPs and the company's HACCP plan ... for SQF compliance, sanitation, traceability requirements, and quality standards. This role includes responsibilities such as assembling or disassembling lines,… more
    Aerotek (10/01/25)
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  • Associate Director, MSAT, Downstream Drug…

    Otsuka America Pharmaceutical Inc. (Princeton, NJ)
    **Job Summary** **​** The Associate Director, MSAT - Downstream provides specialized technical leadership and oversight for all downstream manufacturing ... and risk assessment. + Provide expert technical oversight of downstream manufacturing operations at CDMOs, including review of batch records, deviation… more
    Otsuka America Pharmaceutical Inc. (07/18/25)
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  • Associate Director, Hypercell, Process…

    Bristol Myers Squibb (Summit, NJ)
    …process monitoring improvements + Collaborate with cross-functional teams including MS&T, QA , Regulatory, and Manufacturing to support tech transfer, validation, ... protocols/reports + Continued Process Validation (CPV) reports, Annual Product Quality Reports (APQRs), summarizing process performance and improvement opportunities.… more
    Bristol Myers Squibb (10/11/25)
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  • Associate Director, Submissions Content…

    Merck (Rahway, NJ)
    …review of process questions and issues related to submission content management, quality and standards compliance + Engage across functional areas to identify ... IT activities, change management and training + Partner with QA and Standards to ensure the content management solution...Develop and evaluate metrics as part of a data quality monitoring plan to determine where process improvements or… more
    Merck (10/04/25)
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