• Research Associate II

    System One (Oro Valley, AZ)
    Job Title: Research Associate II Location: Oro Valley, AZ Type: Contract, Potential for extension or conversion to permanent Overview Responsible for conducting ... research, development and manufacturing laboratory experimentation and other scientific activities to support...and professional societies. Follows company policies and procedures for GMP , GLP, Design Control and others as appropriate. Maintains… more
    System One (05/10/25)
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  • Supervisor, Manufacturing Fill Finish

    Catalent Pharma Solutions (Harmans, MD)
    …and routine tasks in the aseptic production of finished drug product biologics for Phase I/ II & commercial GMP manufacturing . The Supervisor is critical to ... minimum of 5+ years of experience in biopharmaceutical based GMP manufacturing operations, related technical field, or...this experience should be in fill/finish processing) **OR** + Associate 's degree or HS Diploma with 8+ years' experience… more
    Catalent Pharma Solutions (04/11/25)
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  • Support Services Associate II

    WuXi AppTec (Philadelphia, PA)
    **Overview** Responsible for the support activities and disinfection of GMP space, equipment and associated areas involved in the manufacture of Master and Working ... Gene Therapy products and final product fills according to current Good Manufacturing Practices (cGMPs). **Work Schedule: Wednesday - Saturday** **: 4:00pm -… more
    WuXi AppTec (05/21/25)
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  • Maintenance Mechanic II /III-Overnights

    Dart Container (Waxahachie, TX)
    …meet the company quality standards + Follow and commit to safety and GMP (Good Manufacturing Practices) + Install, diagnose, analyze, maintain, modify, repair ... Maintenance Mechanic II /III-Overnights Apply now " Date: May 16, 2025...quality standards + Follow and commit to safety and GMP (Good Manufacturing Practices) + Install, diagnose,… more
    Dart Container (05/16/25)
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  • Bulk Formulation Chemist II

    Grifols Shared Services North America, Inc (San Diego, CA)
    …School Diploma. + 2 to 4 years of related experience in a laboratory or commercial manufacturing setting with an Associate 's degree + 1 to 3 years of related ... San Diego, CA is seeking a Bulk Formulation Chemist II . The Bulk Formulation Chemist II will...processes. May be assigned to one or more functional Manufacturing areas. We are seeking individuals with varying levels… more
    Grifols Shared Services North America, Inc (05/14/25)
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  • QC Sample Receipt Analyst II (2pm-11pm)

    Fujifilm (College Station, TX)
    …Operating Procedures (SOPs) and other related Good Laboratory Practices. (GLP)/Good Manufacturing Practices ( GMP ). + Manage test samples, critical reagents ... **Position Overview** The Sample Management Analyst II , under general direction, will be responsible for...GED, AND at least two (2) years of relevant GMP Experience OR; + Associate 's degreepreferably in… more
    Fujifilm (05/09/25)
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  • Validation Specialist/ Validation Engineer I…

    Grifols Shared Services North America, Inc (Clayton, NC)
    …countries and regions. **Overview:** The Engineer I - Validation / Engineer II - Validation / Validation Specialist I position supports Fractionation, Purification, ... functional problem-solving involving Quality Operations, Regulatory Affairs, Engineering and Manufacturing . * Makes independent decisions within defined areas of… more
    Grifols Shared Services North America, Inc (04/16/25)
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  • Specialist II , Form/Fill (Weekend…

    Novo Nordisk (Bloomington, IN)
    …Substance: + Equivalent technical expertise of process and equipment with that of Senior Manufacturing Associate + Review and approve documents in EDMS + Revise ... + High School/GED required + 5 years pharmaceutical and/or manufacturing experience required + 5 years GMP ...and/or manufacturing experience required + 5 years GMP experience required + Technical Requirements: + Proficient in… more
    Novo Nordisk (05/10/25)
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  • QA Specialist II , Data Integrity

    Fujifilm (College Station, TX)
    …improve existing or introduce new ways of working. + Strong experience with GMP , manufacturing processes, quality and regulatory requirements. + Ensure smooth ... Integrity projects at FDBT. The Quality Assurance (QA) Specialist II for Data Integrity will be responsible for the...a 'Quality Culture' by coaching in the application of GMP Principles including the underlying rational of those principles.… more
    Fujifilm (04/10/25)
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  • Research Packaging Coord II

    University of Rochester (Rochester, NY)
    …**Responsibilities:** GENERAL SUMMARY Possess a moderate understanding of current Good Manufacturing Practices (cGMP) as defined in 21 CFR FDA regulations and ... needed basis. Expected to apply their moderate understanding of current Good Manufacturing Practices (cGMP) experiences along with strong critical thinking skills to… more
    University of Rochester (04/26/25)
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