• Laboratory Equipment IT Engineer, Regeneron Cell…

    Regeneron Pharmaceuticals (Cambridge, MA)
    …recovery of data as needed + Creating and maintaining configuration specifications for cGMP software for process control , monitoring and testing + Ensuring ... a typical day might include the following:** + Supporting all manufacturing and QC equipment within RCM's 30,000 SF Phase 1 clinical manufacturing facility +… more
    Regeneron Pharmaceuticals (07/26/25)
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  • Lab Tech II-Evening Shift

    US Tech Solutions (Waco, TX)
    …Technical Prefer three (3) to seven (7) years of experience in either ** Quality Control / Quality Assurance** functions within the **device, food, or ... with ethics, environmental health and safety, financial, human resources, cGMP procedures, general business policies, requirements and objectives. The incumbent… more
    US Tech Solutions (10/17/25)
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  • Technical Services Scientist

    Kelly Services (Greenville, SC)
    …with internal and regulatory requirements. + Collaborate with cross-functional teams including Quality Assurance, Validation, Quality Control , and Supply ... Support the compliant manufacturing of commercial pharmaceutical products under cGMP guidelines. + Develop, define, and optimize pharmaceutical manufacturing… more
    Kelly Services (09/30/25)
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  • Sr. Principal/Advisor - Sterility Assurance

    Lilly (Indianapolis, IN)
    …technical programs that govern implementation and execution of Sterility Assurance control strategies across the Lilly Parenteral Product Network (PPN). This ... well as external to Lilly, to ensure strategies are in-line with technical, quality and regulatory guidance and current expectations, as well as align with business… more
    Lilly (08/15/25)
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  • GMP Cleaning and Sanitization Group Leader

    Mentor Technical Group (Juncos, PR)
    …log books. + Performs related duties as assigned + Serve as back-up to Quality Control Environmental Sampling / Monitoring Activities (refer to Job Description). ... in accordance to the assigned client facilities standards and SOP and cGMP requirements. Responsibilities: + Ensure the assigned team keeps client site/facilities… more
    Mentor Technical Group (08/08/25)
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  • Global Head, BioAnalytics, CMC Development

    Sanofi Group (Framingham, MA)
    …lives and delivering compelling growth. Our Global Chemical Manufacturing and Control (CMC) Development function within Global R&D covers multiple modalities, ... and Project Management) and with other Sanofi functions (eg, Research, Quality Assurance, Regulatory Affairs, Manufacturing & Supply, Business Development). **Scope… more
    Sanofi Group (09/20/25)
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  • Pharmacy Technician - Sterile Compounding

    Akina Pharmacy (Sterling, VA)
    …components. Ability to identify and remove expired or damaged inventory. + Quality Control and Assurance: Commitment to ensuring compounded sterile preparations ... Exceptional attention to detail in documenting all compounding activities, including calculations, quality control checks, and compliance with USP guidelines and… more
    Akina Pharmacy (10/06/25)
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  • Scientist / Sr. Scientist, Analytical Development

    Cambrex High Point (Waltham, MA)
    …pharmaceutical synthetic molecules. Knowledge of regulatory guidelines and experience in quality control testing are preferred. Candidates must possess strong ... ICH guidelines, and regulatory expectations (FDA, EMA). + Experience in quality control testing, stability programs, outsourced testing management, and… more
    Cambrex High Point (08/14/25)
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  • Senior QA Validation Specialist - CSV Systems…

    Curia (Rensselaer, NY)
    …and provides technical assistance to Engineering Services, R&D, Production, Maintenance and QA/ QC in Validation and Quality Assurance-related issues. This role ... position does not have supervisory responsibilities. Essential job duties + Provide quality review and approval of validation activities associated with changes to… more
    Curia (09/19/25)
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  • Manufacturing Associate I

    Charles River Laboratories (Northridge, CA)
    …to making a positive impact on the world by providing the highest quality cellular material and services to biotech and pharmaceutical companies and research ... procedures, building monitoring systems and laboratory logbooks. Maintain proper control of operations by following SOP's, Manufacturing Procedures, GMP's, ISO… more
    Charles River Laboratories (09/17/25)
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