• Cipla (Hauppauge, NY)
    …generated during batch process and accountability in the batch record . Review of engineering records (temperature and humidity data, calibration ... batch manufacturing and packaging, as per manufacturing & batch packaging record instructions. Collection of in-process...and follow company policies, safety requirements, cGMP and SOP's. Review of online batch records ,… more
    HireLifeScience (11/07/25)
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  • Cipla (Fall River, MA)
    …but are not limited to the following : Works with Manufacturing/Packaging to deliver timely batch record review across all shifts. Reviews and approval of ... master batch records . Develops appropriate disposition metrics, works...and SOP's. Knowledge of GDP. Creation and maintenance of batch record and cGMP documentation templates. Closure… more
    HireLifeScience (10/30/25)
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  • Legend Biotech USA, Inc. (Raritan, NJ)
    …support manufacturing to ensure sterility of the product/process is not compromised.Support batch review & material release in SAP for In-house reagents.Support ... myeloma.Legend Biotech is seeking a QA Shop Floor Specialist II /III as part of the Quality Operations team based...use on the manufacturing floor.Utilize multiple electronic quality systems, batch records and SAP.Work in a team… more
    HireLifeScience (11/04/25)
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  • Legend Biotech USA, Inc. (Raritan, NJ)
    …preferred.Experience authoring and executing documentation including but not limited to: Batch Records , SOPs, Work Instructions, CQV protocols.Experience with ... an immunotherapy in the treatment of multiple myeloma.Legend Biotech is seeking CQV Specialist II as part of the Technical Operations team based in Raritan, NJ. Role… more
    HireLifeScience (10/29/25)
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  • Quality Assurance Specialist II

    Nitto Denko Corp. (Milford, MA)
    …this opportunity : In this position you will support day-to-day QA Operations activities such as batch record review , release of raw materials, review of ... + Responsible for reviewing, approving, scanning, and binding quality records / batch records , and raw materials...Provide sound decision-making and guidance on all aspects of batch record review and raw… more
    Nitto Denko Corp. (11/11/25)
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  • QA Release Supervisor II /III

    Grifols Shared Services North America, Inc (Clayton, NC)
    …quality in meetings. Specific duties will depend on the assignment and may include review of manufacturing or testing records , preparation or review of ... and services in more than 110 countries and regions. **First Shift** **Supervisor II , QA:** The Supervisor II , Quality Assurance is responsible for supervising… more
    Grifols Shared Services North America, Inc (11/11/25)
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  • QA Specialist II - Operations

    PCI Pharma Services (Madison, WI)
    …to internal procedures and external standards. Primary responsibilities for this role includes Batch Record Review , Lot Disposition, and Quality System ... compliance with cGMPs, site SOPs, and regulatory requirements. Prioritize record review in support of business needs...status and communicate release needs throughout the organization + Review and approve master batch records more
    PCI Pharma Services (11/22/25)
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  • Quality Inspector II (Monday-Friday Third…

    Bausch + Lomb (Tampa, FL)
    …Assurance. **Key Activities/Responsibilities/Job Functions:** + Follows standard operation procedures and review to batch records to ensure compliance ... of the Job:** The assurance of quality product and batch records from the manufacturing departments. Evaluates...applicable visual inspections, testing intervals and/or methods, as per batch record instructions and current SOP. +… more
    Bausch + Lomb (11/12/25)
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  • Quality Program Manager II

    Curia (Albuquerque, NM)
    …primary quality assurance contact for CURIA-Albuquerque clients + Responsible for ensuring batch records have been thoroughly reviewed before product disposition ... improvement initiatives + Will provide quality training related to batch review , sitewide + Read/interpret SOPs to...pressure to meet customer and business deadlines associated with batch record lot release Other Qualifications +… more
    Curia (11/06/25)
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  • Quality Assurance Inspector II

    Amneal Pharmaceuticals (Branchburg, NJ)
    …and PM records , Pest control records and contractor related functions) + Review of online batch records in terms of completeness of signatures, ... + Conduct in process testing per manufacturing and packaging batch record instructions. + Prepare controlled /...product environmental operating conditions. + Plus the following: + Review of engineering records (temperature and humidity… more
    Amneal Pharmaceuticals (10/10/25)
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  • Document Control Administrator II

    Actalent (St. Louis, MO)
    …supporting our mission to deliver extraordinary solutions. Responsibilities + Scan and archive batch records and other cGMP documents. + Organize, pack, ship, ... and receive batch records . + Perform sample and product...precision. + Perform document-related tasks such as printing, periodic review , reconciliation, issuance, archiving, scanning, record retention,… more
    Actalent (12/04/25)
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  • QA Inspector II

    BD (Becton, Dickinson and Company) (San Diego, CA)
    …proper label description, material number, batch number and storage temperature. + Review packaging batch records to ensure the correct Technical Data ... + Review and verify the completion of batch records and release products to Finished...in pulling and maintaining QA retains. + Oversee company record archival system. This may include scanning records more
    BD (Becton, Dickinson and Company) (12/04/25)
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  • Quality Assurance Specialist II

    Sumitomo Pharma (Morrisville, NC)
    …product manufacturing and aseptic techniques. + Relevant experience and knowledge of manufacturing, batch record review , and/or analytical analyses for the ... experienced individual for the position of **Quality Assurance Specialist II ** reporting to the Senior Manager Quality Assurance of...providing QA review /approval of the completed Manufacturing batch records in a timely manner and… more
    Sumitomo Pharma (11/15/25)
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  • Quality Assurance Specialist II

    Actalent (Parsippany Troy Hills, NJ)
    …with cGMPs and GLPs. + Conduct and document major and minor deviation investigations. + Review Executed Batch Records for Biologics DS and DP. + Participate ... document deviation investigations related to GxP operations and perform reviews of Executed Batch Records for Biologics Drug Substance (DS) and Drug Product… more
    Actalent (12/04/25)
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  • Material Services Coordinator I, II ,…

    Tucson Electric Power (Tucson, AZ)
    …to verify completeness and accuracy of source documents. + Ability to compile, review for accuracy, and file applicable compliance records that impact the ... **Material Services Coordinator I, II , or III** Company **Tucson Electric Power** Location...Manage department group mailboxes. Creates and maintains Inventory Item records in an enterprise resource management application like Oracle.… more
    Tucson Electric Power (12/02/25)
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  • Associate II , Quality Assurance

    Catalent Pharma Solutions (Kansas City, MO)
    …specifications + Component Release Packets + Reclass Approvals + Proficient in JD Edwards (IMS) + Pre- Batch Record Review + Post- Batch Record ... **Associate II , Quality Assurance** **Position Summary** Catalent, Inc. is...join Catalent:** + Defined career path and annual performance review and feedback process + Diverse, inclusive culture +… more
    Catalent Pharma Solutions (11/22/25)
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  • Automation Engineer II

    Catalent Pharma Solutions (Chelsea, MA)
    **Automation Engineer II ** **Position Summary:** Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to ... for DPI in North America. Catalent Pharma Solutions is hiring an Automation Engineer II . The Automation Engineer II is expected to assist senior engineering… more
    Catalent Pharma Solutions (10/16/25)
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  • Production Operator II - Part-Time…

    CVS Health (Glasgow, KY)
    …+ Performs final production check of completed documents for completeness and accuracy. + Review of completed batch records for compliance with cGMPs ( ... of materials and products as directed by procedures and/or batch record requirements. + Responsible for labeling,...either reconciliation or production activities. + Maintenance of logs, batch records , and all applicable documentation in… more
    CVS Health (11/19/25)
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  • Quality Analyst II

    Teva Pharmaceuticals (Salt Lake City, UT)
    …as LIMS, TrackWise, EAM * Responsible for serving as QA backup as final review /release of production batch records . * Responsible for completing training ... Quality Analyst II Date: Nov 14, 2025 Location: Salt Lake...Good Manufacturing Practices (cGMP's), Standard Operating Procedures (SOP's) and Batch Record instructions. * Responsible for performing… more
    Teva Pharmaceuticals (11/15/25)
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  • Senior Production Operator (SPO) II , 12…

    Pfizer (Mcpherson, KS)
    …all safety requirements (eg PPE, LOTO, etc.) and process step requirements (eg SOP, Batch Records ). + Communicate and inform management of all safety issues, ... to read, interpret, and perform job duties described in operating procedure, product batch records , and other equipment related documentation (eg vendor manuals,… more
    Pfizer (11/27/25)
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