• Merck & Co. (Rahway, NJ)
    …matter expertise - Knowledge of order management, supply chain operations and document control . #MSJR #eligibleforERP GCSCareer25 #VETJOBS #GCSCareer - Current ... High School Diploma with 10+ years equivalent industry experience in Pharmaceutical Clinical Supply (packaging, labeling, logistics and clinical supply inventory… more
    HireLifeScience (05/29/25)
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  • Document Control Specialist

    Catalent Pharma Solutions (Chelsea, MA)
    ** Document Control Specialist - Quality Assurance** **Position Summary:** Catalent, Inc. is a leading global contract development and manufacturing ... North America. Catalent Pharma Solutions is hiring a QA Document Control Specialist who is...of relevant work experience in the regulated Biotechnology or Pharmaceutical industries or relevant comparable background highly preferred; +… more
    Catalent Pharma Solutions (05/21/25)
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  • Document Control Specialist

    Actalent (Parsippany Troy Hills, NJ)
    Job Title: Document Control Specialist Job Description We are seeking a meticulous and highly organized Document Control Specialist to join our ... a strong understanding of workflow execution. + In-depth knowledge of GxP-compliant document control practices, including document lifecycle management and… more
    Actalent (05/31/25)
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  • Document Control Specialist

    Actalent (Parsippany Troy Hills, NJ)
    Job Title: Document Control Specialist Job Description Join our team as a Document Control Specialist where you will play a crucial role in ... managing and overseeing the document control processes within our organization. Your...knowledge, preferably with GxP Documents. + Clinical, research, or pharmaceutical experience is advantageous. + Technical writing experience within… more
    Actalent (05/29/25)
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  • Document Control Specialist

    Astrix Technology (Indianapolis, IN)
    ** Document Control Specialist ** Quality Assurance Indianapolis, IN, US Pay Rate Low: 26.42 | Pay Rate High: 31.25 + Added - 28/05/2025 Apply for Job _Our ... client is seeking a Document Control Specialist to join...eQMS experience required (will be primarily pulling documents) + Pharmaceutical experience preferred **_We strongly encourage candidates who have… more
    Astrix Technology (05/29/25)
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  • Quality Assurance Specialist

    Glenmark Pharmaceuticals Inc., USA (Monroe, NC)
    …and losses in the process and build improved efficiency + Under guidance of the Senior QA Specialist Document Control , the QA Specialist - Document ... Quality Assurance Specialist , Document Control Department: QA Manufacturing Location: Monroe, NC START YOUR APPLICATION… more
    Glenmark Pharmaceuticals Inc., USA (03/11/25)
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  • Document Control Specialist

    Spectrum Plastics Master (Tucson, AZ)
    JOB PURPOSE: The Document Control Technician is responsible for maintaining and improving the company's document control system to ensure organized, ... labels, forms, and quality records. . Lead the conversion of the current paper-based document control system to an electronic QMS platform; support activities up… more
    Spectrum Plastics Master (05/04/25)
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  • Document Control Specialist

    Teledyne (Montgomeryville, PA)
    …research, deepwater oil and gas exploration and production, medical imaging and pharmaceutical research.​ We are looking for individuals who thrive on making an ... Description** **Job Summary:** Develop, support, and maintain documentation and configuration control . Support the quality assurance group and its ISO 9001/AS9100… more
    Teledyne (04/22/25)
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  • Quality Documentation Specialist

    Astrix Technology (Indianapolis, IN)
    …help you continue to succeed and grow in the life sciences industry!_ _Our Quality Control Document Specialist position is a great opportunity to work with ... **Quality Documentation Specialist - Pharmaceutical ** Quality Assurance Indianapolis,...months! + Great benefit package offered upon conversion! **Quality Control Document Specialist ** **Daily Tasks**… more
    Astrix Technology (05/07/25)
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  • Analytical Quality Assurance Specialist

    Glenmark Pharmaceuticals Inc., USA (Monroe, NC)
    …research-based pharmaceutical company. POSITION SUMMARY: The Analytical Quality Assurance (AQA) Specialist will work with the Quality Control team to work ... Analytical Quality Assurance Specialist Department: Analytical QA Location: Monroe, NC START YOUR APPLICATION… more
    Glenmark Pharmaceuticals Inc., USA (03/18/25)
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  • Pharmaceutical QA Senior Specialist

    Eurofins (Sanford, NC)
    …of Quality method validation/ QC equipment qualification, QC protocol, reports, QC process control document , new and existing procedures, and Quality Control ... quality, technical or engineering experience within biotech of the pharmaceutical industry + Experience in a Quality Control...assurance role, preferably in Quality Assurance for a Quality Control role in the document such as:… more
    Eurofins (05/15/25)
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  • Quality Control Specialist

    BGB Group (New York, NY)
    Quality Control Specialist at BGB Group (View all jobs) (http://www.bgbgroup.com/careers.html) New York, NY BGB Group QC Specialist , Studio Our Agency BGB ... that offers a wide range of services, including traditional pharmaceutical advertising, promotional medical education, payer marketing, and consulting services.… more
    BGB Group (05/03/25)
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  • Control Specialist

    West Pharmaceutical Services (St. Petersburg, FL)
    Control Specialist Requisition ID: 69807 Date: May 28, 2025 Location: St Petersburg, Florida, US Department: Maintenance Description: This is a Monday - Friday ... wide variety of duties with machinery maintenance, especially in electrical and control system wiring and troubleshooting. Program, repair and perform PMs on… more
    West Pharmaceutical Services (05/29/25)
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  • QMS Specialist - 2nd Shift

    Eurofins (Louisville, KY)
    …and maintain high standards for product quality and safety. Key Responsibilities: 1. Document Control Management: + Oversee the lifecycle of all QMS ... revision, approval, and archiving on electronic QMS. + Manage and maintain document control processes, ensuring compliance with applicable standards such as… more
    Eurofins (05/13/25)
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  • Regulatory Affairs CMC Specialist

    Chiesi (Boston, MA)
    About us Based in Parma, Italy, Chiesi is an international research-focused pharmaceuticals and healthcare group with 90 years' experience, operating in 30 countries ... self-care). We are proud to be the largest global pharmaceutical group to be awarded B Corp Certification, a...looking for Purpose Currently seeking for a Regulatory Affairs Specialist to support preparation of CMC related submissions and… more
    Chiesi (05/17/25)
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  • Specialist I, Form/Fill

    Novo Nordisk (Bloomington, IN)
    …6 weeks paid family medical leave + Free access to Novo Nordisk-marketed pharmaceutical products + Tuition Assistance + Life & Disability Insurance + Employee ... matters. Primary - Drug Product Primary Manufacturing produces sterile pharmaceuticals . The department includes equipment preparation, product formulation, material… more
    Novo Nordisk (05/17/25)
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  • QA Specialist I - Quality Systems

    Charles River Laboratories (Rockville, MD)
    …a career that you can feel passionate about. **Job Summary** The QA Specialist I - Quality Systems is responsible for supporting Quality Systems, including ... investigation/deviation management, CAPA tracking, Effectiveness Verification, and change control . This position will facilitate the compiling, trending (as… more
    Charles River Laboratories (05/22/25)
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  • QA Specialist II - Quality Systems…

    Charles River Laboratories (Rockville, MD)
    …a career that you can feel passionate about. **Job Summary** The QA Specialist II Quality Systems and Compliance is responsible for supporting Quality Systems, ... including investigation/deviation management, CAPA tracking, Effectiveness Verification, and change control . This position will facilitate the compiling, trending (as… more
    Charles River Laboratories (05/11/25)
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  • Quality Assurance Specialist

    Eurofins (North Brunswick Township, NJ)
    …network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organization ... biological substances and products. Job Summary: Under minimal supervision, the Quality Assurance Specialist III will ensure systems and processes are in a state of… more
    Eurofins (05/08/25)
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  • QA Specialist II - Shift is 12pm - 10:30pm,…

    Charles River Laboratories (Rockville, MD)
    …you can feel passionate about. **Job Summary** The Quality Assurance Specialist II is responsible for supporting Quality Systems, including investigation/deviation ... management, CAPA tracking, Effectiveness Verification, change control , internal and external audits. This position will facilitate...certified quality audit is a plus * Experience in pharmaceutical or bio- pharmaceutical field * Education or… more
    Charles River Laboratories (04/11/25)
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