• Manufacturing Technician

    Catalent Pharma Solutions (Chelsea, MA)
    …GEA Niro SD1, SD4 and SD7, the latter being the largest Good Manufacturing Practices ( CGMP ) unit of its kind for DPI in North America. Catalent Pharma Solutions in ... individual operates in accordance with environmental, health, safety, and cGMP guidelines. The Manufacturing Technician executes production activities under direct… more
    Catalent Pharma Solutions (10/09/25)
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  • Manufacturing Technician II (2nd Shift)

    Nitto Denko Corp. (Milford, MA)
    …implementation of assigned production operations working within defined production schedules in a cGMP environment.This is a 2nd shift position and comes with a 15% ... systems (process skids). + Two plus years of experience in cGMP manufacturing environment. Performance/other experience can be considered pending manager discretion.… more
    Nitto Denko Corp. (10/05/25)
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  • Manufacturing Associate

    Catalent Pharma Solutions (Chelsea, MA)
    …GEA Niro SD1, SD4 and SD7, the latter being the largest Good Manufacturing Practices ( CGMP ) unit of its kind for DPI in North America. Catalent Pharma Solutions in ... This individual operates in accordance with environmental, health, safety, and cGMP guidelines. This individual is responsible for the hands-on execution of… more
    Catalent Pharma Solutions (10/01/25)
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  • Plant Engineer

    Sanofi Group (Framingham, MA)
    …This organization is responsible for providing Engineering support for all cGMP process and utility systems at Framingham Biologics, maintaining these systems ... an industrial manufacturing environment + Direct experience with regulated environments (ie cGMP , OSHA, EPA) + Experience utilizing Quality Systems (CCR, ECM) +… more
    Sanofi Group (09/27/25)
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  • Sr. Staff Engineer

    Takeda Pharmaceuticals (Boston, MA)
    …and control strategies. + Lead the technology transfer from development to cGMP manufacturing sites, ensuring process robustness and compliance. + Partner with ... continuous processes a plus + Sound knowledge of current Good Manufacturing Practices ( cGMP ) preferred + Experience working in a pilot plant preferred + Previous… more
    Takeda Pharmaceuticals (09/25/25)
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  • Head of Scientific Excellence

    Sanofi Group (Framingham, MA)
    …industry, specifically in R&D and/or MSAT (industrial development) with manufacturing cGMP considerations, and global CMC projects. + 5+ years of experience ... (mammalian and/or microbial) and/or product analytics. + Good understanding of cGMP requirements and facility operations. + High experience in exposure to… more
    Sanofi Group (09/23/25)
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  • Quality Control Analyst II, Raw Material (2nd…

    Nitto Denko Corp. (Milford, MA)
    …raw materials, in-process materials and finished products in accordance with cGMP guidelines. The appropriately trained individual may provide training and guidance ... samples in a timely manner in support of project plans in accordance with cGMP guidelines. + Review data for compliance against specifications and GMP regulations. +… more
    Nitto Denko Corp. (09/21/25)
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  • Team Leader, Distribution

    ThermoFisher Scientific (Tewksbury, MA)
    …the team follows all safety requirements and Current Good Manufacturing Practices ( cGMP ) requirements + Ensure that personnel issues or operational conditions are ... of work experience leading a team + Preferred: Experience in a cGMP environment **Knowledge, Skills, Abilities:** + Ability to mentor, train, empower, influence,… more
    ThermoFisher Scientific (09/18/25)
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  • Scientist - GMP, Chemistry

    ThermoFisher Scientific (Boston, MA)
    …persons are responsible to ensure activities occur in an efficient and cGMP compliant manner while fostering the customer's vision and values. Additional key ... knowledge of general chemistry + Strong knowledge of US and EU cGMP regulations/guidance and some experience with regulatory agency inspections. + Strong knowledge… more
    ThermoFisher Scientific (09/18/25)
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  • Manufacturing Technician (Machine Operator)

    Bio-Techne (Devens, MA)
    …perform assembly/packing and complete all documentation accurately and according to cGMP /ISO standards. Provide written documentation of required data throughout the ... pounds and stand for long periods of time. + Experience working in a cGMP /ISO facility a plus. **Minimum Physical Requirements:** + Remain seated in a normal… more
    Bio-Techne (09/12/25)
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