• Global Head, Life Cycle Management Atsc Msat

    J&J Family of Companies (Raritan, NJ)
    validation requirements + Knowledge of data analytics/statistics and process automation + Ability to lead and influence multidisciplinary, cross-functional teams ... validation requirements + Knowledge of data analytics/statistics and process automation + Ability to lead and influence multidisciplinary, cross-functional teams… more
    J&J Family of Companies (09/11/25)
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  • Sr Associate Manufacturing - Line Lead (12hr Shift…

    Amgen (New Albany, OH)
    …Participate in the development, implementation, and issue resolution associated with process equipment Commissioning, Qualification and Validation . + Collaborate ... qualifications. **Basic Qualifications:** High school/GED + 4 years biotech or pharmaceutical manufacturing, process development or quality experience Or… more
    Amgen (09/07/25)
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  • Staff Engineer, Modeling

    Takeda Pharmaceuticals (Boston, MA)
    By clicking the "Apply" button, I understand that my employment application process with Takeda will commence and that the information I provide in my application ... to the best of my knowledge. **Job Description** **OBJECTIVE:** Synthetic Molecule Process Development (SMPD) is responsible for the development of robust and… more
    Takeda Pharmaceuticals (08/30/25)
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  • Quality Assurance Engineer

    Danaher Corporation (Muskegon, MI)
    …equipment Installation Qualification (IQ), Operation Qualification (OQ), Performance Qualification (PQ), process validation (PV), cleaning validation (CV) ... Assist and approve deviation investigations, corrective and preventative actions (CAPAs), process improvements related to equipment qualification and validation more
    Danaher Corporation (09/05/25)
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  • Design Quality Engineer

    Bio-Techne (Wallingford, CT)
    …and experimental design. + Technical excellence specific to equipment automation and process validation . + Must have strong communication skills, both verbal ... **Position Summary:** The Design Quality Engineer supports the qualification and validation of new products and product modifications, new equipment builds and… more
    Bio-Techne (08/28/25)
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  • Scientist I, Analytical R&D

    ThermoFisher Scientific (Florence, SC)
    …Conduct routine and non-routine chemical testing and method development/qualification for pharmaceutical raw materials, in- process samples, and active ... on raw materials, samples, stability, production intermediates, and active pharmaceutical ingredients, including method development and qualification activities. Support… more
    ThermoFisher Scientific (08/21/25)
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  • Scientist / Sr. Scientist, Analytical Development

    Cambrex High Point (Waltham, MA)
    …compendial testing. Qualifications/Skills + Proven experience in method development, validation , troubleshooting, and transfer for pharmaceutical synthetic ... entrepreneurial scientists dedicated to providing high-quality analytical support for synthetic process development projects. We are looking for a candidate who has… more
    Cambrex High Point (08/14/25)
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  • Principal Analytical Method Development Chemist

    Curia (Albuquerque, NM)
    …and existing pharmaceutical products within a CGMP environment. The Principal Process Chemist leads the introduction and scale-up of new products, ensures robust ... organization (CDMO) with over 30 years of experience partnering with pharmaceutical and biotech companies to provide life-saving treatments to patients. At… more
    Curia (08/12/25)
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  • Aseptic Process Technician/Operator (GMP)

    Mentor Technical Group (Monroe, NC)
    …MTG has the knowledge and experience to ensure compliance with pharmaceutical , biotechnology, and medical device safety and efficacy guidelines. With offices ... used in sterile drug product manufacturing. + Perform environmental monitoring and in- process checks to ensure compliance with aseptic conditions. + Prepare, stage,… more
    Mentor Technical Group (09/10/25)
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  • Senior QA Technical Reviewer

    Catalent Pharma Solutions (St. Petersburg, FL)
    …IQ/OQ/PQ documents regarding equipment, utilities, and computer systems; c) all product process validation and cleaning validation documents; d) all ... + Reviews and approves technical documents, such as: Technical Protocols and Reports, Process + Validation Protocols and Reports, Cleaning Validation more
    Catalent Pharma Solutions (09/03/25)
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