• Aequor (East Syracuse, NY)
    …is preferred.Working knowledge and experience in the biopharmaceutical development process, GMP , PAT, CMC and regulatory guidance, ICH guidelines, and compendial ... coordinating timely transfer of test methods with and to Quality Control laboratories is desired. Specific Knowledge, Skills, Abilities, etc.Strong written, verbal,… more
    HireLifeScience (07/31/25)
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  • Merck & Co. (Rahway, NJ)
    …matter expertise- - Knowledge of order management, supply chain operations and document control - #MSJR #eligibleforERP GCSCareer25 #VETJOBS #GCSCareer Current ... GMP ), Interactive Voice Response (IVR), Interpersonal Relationships, Inventory Control System, Inventory Management, Key Performance Indicators (KPI), Management… more
    HireLifeScience (07/24/25)
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  • Merck & Co. (Rahway, NJ)
    …matter expertise -Knowledge of order management, supply chain operations and document control . -#MSJR #eligibleforERP GCSCareer25 #VETJOBS #GCSCareer Current ... Analysis, Detail-Oriented, Financial Risk Management (FRM), Good Manufacturing Practices ( GMP ), Interpersonal Relationships, Inventory Control System, Inventory… more
    HireLifeScience (07/24/25)
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  • Eisai, Inc (Exton, PA)
    …into the production suites.The Associate Director writes, reviews, and/or approves GMP documents, including validation protocols and reports, and SOPs, along with ... Development groups as well as with Facilities, Quality Assurance, Quality Control , Regulatory, and CMC Program Management departments.The Associate Director of… more
    HireLifeScience (05/29/25)
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  • GMP Document Control

    ManpowerGroup (Rockville, MD)
    Our client, a leader in the pharmaceutical industry, is seeking a Pharma Document Control Associate to join their team. The ideal candidate will have strong ... will align successfully in the organization. **Job Title:** Pharma Document Control Associate **Location:** Rockville, MD **Pay...per respective SOP. + Archive and maintain GLP and GMP documents with an accurate inventory, both on and… more
    ManpowerGroup (06/03/25)
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  • QA Document Management Associate

    Lilly (Lebanon, IN)
    …within a GMP -regulated environment. **Additional Preferences:** + Strong knowledge of GMP regulations and document control processes. + Experience with ... ( GMP ) library, document inventory, ensuring true copy accuracy, and overseeing document control within our electronic document system. This role also… more
    Lilly (06/27/25)
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  • Manager, QA Document Control

    Catalent Pharma Solutions (Harmans, MD)
    …are met and leading continuous improvement initiatives. The Document Control function supports both the GMP and development operations. Catalent, ... support Phase I/II/III/commercial operations. + Manages document control processes and systems for GMP activities...document control processes and systems for GMP activities in compliance with internal procedures and policies,… more
    Catalent Pharma Solutions (07/23/25)
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  • Quality Assurance Specialist, Document

    Glenmark Pharmaceuticals Inc., USA (Monroe, NC)
    Quality Assurance Specialist, Document Control Department: QA Manufacturing Location: Monroe, NC START YOUR APPLICATION ... POSITION SUMMARY : Under the direction of the QA Document Control Supervisor, the QA Specialist -...study Experience : + 0-2 years of Pharmaceutical and FDA/ GMP industry experience is preferred. + Previous Quality experience… more
    Glenmark Pharmaceuticals Inc., USA (06/10/25)
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  • QA Document Control Coordinator (1st…

    Herbalife (Lake Forest, CA)
    QA Document Control Coordinator (1st Shift) Category: Quality Position Type: Regular Full-Time External ID: 17057 Location: Lake Forest, CA, United States Date ... LinkedIn share to linkedin Apply Now **Overview** **THE ROLE:** The First Shift Quality Document Control Coordinator will work onsite at our state of art… more
    Herbalife (06/27/25)
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  • Sr. Manager Document Control

    Integra LifeSciences (Princeton, NJ)
    …to advance patient outcomes and set new standards of care. The Sr. Manager, Document Control and Training is responsible for leading the Corporate Document ... position is also responsible for assessing, developing and maintaining the Corporate Document Control and Training Administration Programs in compliance with US… more
    Integra LifeSciences (07/08/25)
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  • Document Control Technician

    Actalent (Columbus, OH)
    …Diploma or GED. + Must have some kind of prior experience with document control . + Experience working with GMP or FDA regulations is strongly preferred, but ... continuous improvement initiatives in manufacturing processes. Responsibilities + Perform essential Document Control functions in a timely manner to support… more
    Actalent (07/23/25)
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  • Document Control Specialist

    Insight Global (Durham, NC)
    …of experience in a GMP -regulated environment -Strong understanding of GDP and document control processes -Experience with GLIMS or similar data entry systems ... Job Description The Document Control Specialist is responsible for...are carried out in compliance with Good Manufacturing Practices ( GMP ) and safety regulations. Key Responsibilities: -Print and review… more
    Insight Global (07/18/25)
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  • Document Control Clerk

    Actalent (Random Lake, WI)
    Job Title: Document Control Specialist Job Description We are seeking a dedicated Document Control Specialist to manage and create Pallet Tag IDs for all ... NetSuite. Essential Skills + Experience in quality assurance and quality control . + Familiarity with GMP , FDA, and USDA regulations. + Knowledge of food safety… more
    Actalent (07/24/25)
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  • Quantity Surveyor

    AECOM (Abilene, TX)
    …but are not limited to GMP buyout review process, cost related document control , invoice process, change order process, contingency usage, limitations, and ... provided in UNIFORMAT II and CSI format. + Undertake GMP finalization exercise following the completion of GC bid...to the actual work carried out identifying any final GMP savings. + Work with GC and construction management… more
    AECOM (06/04/25)
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  • Quality Control Technician

    Promotion In Motion (Somerset, NJ)
    …+ Conduct GMP inspections to ensure compliance. + Monitor, verify and document Critical Control Points (CCP) for Food Safety. + Recommend improvements to ... Quality Control Technician Job Details Job Location Somerset -...to Plant management and SQFP + Follow PIM Brands GMP rules + Monitor fellow employees for adherence to… more
    Promotion In Motion (07/17/25)
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  • Lead Document Coordinator (3rd Shift)

    Regeneron Pharmaceuticals (Rensselaer, NY)
    We are hiring a Lead Document Coordinator to assist our Document Control team! As a Lead Document Coordinator, you will provide support to the process of ... controlling and maintaining documentation to ensure effective and efficient application of GMP . Documentation within this process includes, but is not limited to,… more
    Regeneron Pharmaceuticals (05/28/25)
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  • Quality Control Associate

    FreshRealm (Lancaster, TX)
    …to support the production/warehouse team and the entire facility up to and including GMP enforcement, allergen control , food defense and line checks. + Work with ... in Lancaster, TX. FreshRealm is looking for a Quality Control Associate that will perform quality checks and tasks...QC associates on standard operating procedures (food safety, GMP , allergens, CCPs, food defense, PPE / hygiene policies)… more
    FreshRealm (06/02/25)
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  • Senior Quality Control Analyst I (GC)

    Cambridge Isotope Laboratories, Inc. (Andover, MA)
    Cambridge Isotope Laboratories, Inc. (CIL) is searching for a Senior Quality Control Analyst I based onsite in our Andover, MA facility. CIL is the global leading ... Group and has had consistent growth for over 40 years. The Senior Quality Control Analyst I is responsible for providing direction, guidance and training to QC… more
    Cambridge Isotope Laboratories, Inc. (07/18/25)
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  • Quality Control Analyst II (LC/MS)

    Cambridge Isotope Laboratories, Inc. (Andover, MA)
    Cambridge Isotope Laboratories, Inc. (CIL) is searching for a Quality Control Analyst II, based onsite in our Andover, MA facility. CIL is the global leading company ... had consistent growth for over 40 years. The Quality Control (QC) Analyst II is responsible for conducting routine...is responsible for conducting routine and non-routine analysis of GMP and ISO materials under general supervision and in… more
    Cambridge Isotope Laboratories, Inc. (07/18/25)
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  • Specialist, Label Control

    Bristol Myers Squibb (Summit, NJ)
    …place than here at BMS with our Cell Therapy team. The Specialist, Label Control at the Summit, NJ Cell Therapy manufacturing facility is responsible for supporting ... site Label Control activities at Summit in accordance with BMS policies,...& Skills:** + Must have knowledge and experience with GMP , Quality, and compliance. + Able to write and… more
    Bristol Myers Squibb (07/29/25)
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