• Production Helper - 1st shift (7am - 3:30 pm)

    Heritage Pharma Labs Inc.d/b/a Avet Pharmaceuticals Inc. (East Brunswick, NJ)
    …granulation/blending, or soft gel function following the instructions in the manufacturing batch record . + Assist the Manufacturing Operator in equipment ... according to machine requirements or SOP. + Appropriately document activities in batch records , forms, and other GMP documents. + Offer suggestions to superiors… more
    Heritage Pharma Labs Inc.d/b/a Avet Pharmaceuticals Inc. (11/21/25)
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  • Production Operator II - Soft Gel Encapsulation…

    Heritage Pharma Labs Inc.d/b/a Avet Pharmaceuticals Inc. (East Brunswick, NJ)
    …such as coating, compression, encapsulation, granulation/blending and soft gel function per Manufacturing batch record . + In addition, must be able to : + ... and identifying problems such as bottlenecks. + Clearly document activities in batch records , forms and other GMP documents. + Offer suggestions to superiors and… more
    Heritage Pharma Labs Inc.d/b/a Avet Pharmaceuticals Inc. (11/14/25)
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  • Senior Technician, Filling Operations (Onsite)

    Merck (Rahway, NJ)
    …system. Knowledge of PAS-X is preferable. + GMP: Follow established inspection batch records , protocols and quality standards to ensure compliance with ... Manufacturing Practices (GMP), Laboratory Techniques, Manufacturing Quality Control, Master Batch Records , Material Selection, Pharmaceutical Process Development,… more
    Merck (12/13/25)
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  • Quality Assurance Specialist III

    Actalent (Parsippany Troy Hills, NJ)
    …GLPs. + Conduct and document major and minor deviation investigations. + Review Executed Batch Records for Biologics DS and DP. + Participate in cross-functional ... industry is preferred. + Experience in QA review of Executed Batch Records . + Technical writing skills for deviations and investigations. Work Environment… more
    Actalent (12/19/25)
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  • Quality Laboratory Manager

    System One (Freehold, NJ)
    …retention samples. . Ensure downtime and quality-related notes are properly documented in batch records . Training & Production Support: . Instruct and train ... complaints, providing necessary information. . Ensure timely review of production batch records by quality personnel. . Systematically place items on hold and… more
    System One (12/18/25)
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  • Specialist, Lead Manufacturing Associate, Cell…

    Bristol Myers Squibb (Summit, NJ)
    …**Responsibilities:** + Execute operations described in Standard Operating Procedures (SOPs) and batch records + Executes transactions and process in all ... in their work + Complete documentation required by governing controlled documents and batch records . Ensure that all documentation produced by their team is… more
    Bristol Myers Squibb (12/09/25)
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  • Packaging Operator

    Teva Pharmaceuticals (Edison, NJ)
    …clearance activities. * Complete required documentation, including room and equipment logbooks, batch records , and verification checks. * Stage and transfer ... products as needed. * Verify packaging components and bulk product against batch records and protocols. * Stack finished goods cases on pallets, shrink-wrap… more
    Teva Pharmaceuticals (12/16/25)
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  • Media Prep Technician

    Astrix Technology (New Brunswick, NJ)
    …Responsibilities include operating large-scale equipment (500L-2000L), maintaining accurate and complete batch records , and ensuring strict adherence to quality ... ranging from 500L to 2000L. + Maintain detailed and accurate batch records in compliance with GMP requirements. + Perform routine cleaning, maintenance,… more
    Astrix Technology (12/12/25)
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  • Engineer, Process

    dsm-firmenich (Belvidere, NJ)
    …quality investigations related to deviations and failures. May review and sign batch records and reports non-conformances. Adjust and calculate formulations for ... batch records as needed. + Other duties assigned by Belvidere leadership. **We Bring:** + Unique career paths across health, nutrition and beauty - explore what… more
    dsm-firmenich (11/05/25)
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  • Quality Control Analyst II / III - Biologics

    System One (Piscataway, NJ)
    …and revise SOPs, QC methods, technical reports, and investigation summaries + Support batch release, batch record reviews, and regulatory dossier preparation ... + Lead and/or support laboratory investigations, deviations, OOS results, and CAPAs + Participate in Quality Events and regulatory inspections (eg, PAI) + Collaborate with cross-functional teams to ensure laboratory readiness and continuous improvement… more
    System One (11/18/25)
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