• Global Quality Lead

    Sanofi Group (Framingham, MA)
    **Job Title:** Global Quality Lead , GMP , GDP Audit and Inspection - Pipeline Launch **Location:** Framingham, MA or Morristown, NJ **About the Job** We ... in Sanofi. + **Scope:** Manufacturing & Supply, Research & Development, Countries, Digital, Global Quality organizations in Sanofi. And third parties outside of… more
    Sanofi Group (05/03/25)
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  • Director, Quality Assurance GMP

    Nitto Denko Corp. (Milford, MA)
    About this opportunity : The Director, Quality Assurance GMP Operations is responsible for quality oversight of the manufacturing process and operations. ... internal and external stakeholders to drive compliance and continuous improvement of GMP operations. Key Responsibilities + Provide quality expertise, oversight… more
    Nitto Denko Corp. (04/16/25)
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  • Validation Lead , Quality Assurance

    Astellas Pharma (Westborough, MA)
    **Validation Lead , Quality Assurance** Do you want to be part of an inclusive team that works to develop innovative therapies for patients? Every day, we are ... is headquartered in Massachusetts. Astellas is announcing a **Validation Lead , Quality Assurance** opportunity at their **Astellas...policies and procedures and industry best practices. The Validation Lead will ensure that all critical GMP more
    Astellas Pharma (03/25/25)
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  • Director Global Supplier Quality

    Danaher Corporation (Putnam, CT)
    …System (https://www.danaher.com/how-we-work/danaher-business-system) which makes everything possible. Director Global Supplier Quality Job Description Summary ... ideas into impact - innovating at the speed of life. As a global leader in high-tech filtration, separation, and purification, Pall Corporation thrives on helping… more
    Danaher Corporation (05/13/25)
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  • Investigations and CAPA Lead

    Astellas Pharma (Westborough, MA)
    …and present monthly metrics on the status of nonconformances and CAPAs to quality management and relevant AIRM and global stakeholders. + Risk Management: ... **Investigations and CAPA Lead ** Do you want to be part of...Sciences, Engineering, or Chemistry with 7+ years of related Quality Assurance experience within GMP -regulated industry, or… more
    Astellas Pharma (04/03/25)
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  • Manager, Quality Assurance

    Astellas Pharma (Westborough, MA)
    …into quality initiatives, and support the qualification and ongoing GMP readiness of AIRM's clinical manufacturing programs. The position involves close ... + GMP Operations Oversight: Provide day-to-day QA leadership for GMP operations, including Manufacturing, Quality Control, Facilities, and Materials… more
    Astellas Pharma (04/19/25)
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  • Senior Director, Devens Digital Plant and Site IT…

    Bristol Myers Squibb (Devens, MA)
    …BioPharma Operating Units, the Sr. Director, BI&T, Devens Digital Plant and Site BI&T Lead will be directly accountable to the US Biologics Leader and Devens Campus ... a standing member of the Devens Campus leadership team. **Key Responsibilities:** + Lead a matrixed organization composed of both site direct reports and groups of… more
    Bristol Myers Squibb (04/20/25)
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  • Quality Assurance Specialist III

    Nitto Denko Corp. (Milford, MA)
    …that the QA project team is well trained in phase appropriate GMPs, global GMP API regulations, directives and have familiarity with Avecia's manufacturing ... : In this role you will be responsible for interfacing with and provide quality input to client's manufacturing programs that are in early stages of development or… more
    Nitto Denko Corp. (04/23/25)
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  • Quality Continuous Improvement Specialist

    Sanofi Group (Framingham, MA)
    **Job Title:** Quality Continuous Improvement Specialist **Location** : Framingham, MA **About the Job** We deliver 4.3 billion healthcare solutions to people every ... diseases and bring hope to patients and their families. Quality Assurance (QA) is responsible for quality ...solutions, transformation and change management. We are an innovative global healthcare company with one purpose: to chase the… more
    Sanofi Group (05/10/25)
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  • Quality and Regulatory Support Manager

    Danaher Corporation (Marlborough, MA)
    …for Cytiva is responsible for supporting the Business and Customers in a global environment by providing quality documents and regulatory support in ongoing ... do: + Support the Business and Customers in a global environment by providing quality documents and...field + Five or more years of experience in GMP , quality , product management or a related… more
    Danaher Corporation (04/01/25)
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  • Associate Director, EMES Operational Excellence…

    Bristol Myers Squibb (Devens, MA)
    …Cell Culture Biologics Manufacturing facility plays a central role in the Global Product Development and Supply (GPS) network as the company's first European ... will produce multiple therapies for the company's growing biologics portfolio. Global Biologics Laboratory (GBL) responsible for the release testing of Biologics… more
    Bristol Myers Squibb (05/15/25)
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  • Sr Principal Engineer, Cell Therapy Technical…

    Bristol Myers Squibb (Devens, MA)
    …development through commercialization. This includes facility fit assessments, development of GMP documentation (eg, batch records, forms), training, quality ... external manufacturing partners + Process engineering and standardization to support global manufacturing scale-up and robustness We are seeking a **Senior Principal… more
    Bristol Myers Squibb (05/10/25)
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  • Senior Engineer - Automation Systems, Cell Therapy

    Bristol Myers Squibb (Devens, MA)
    …cross-functional teams. + Experience with QMS systems (Veeva, or similar) and GMP Quality Processes (Deviation Management, Change Controls, etc.) required. + ... . **Position Summary:** This position serves as a sub-team lead or senior individual contributor on the Process Automation...for multiple systems to support the operation of all GMP and non- GMP control systems and other… more
    Bristol Myers Squibb (05/06/25)
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  • Scientist, Analytical Development

    Sanofi Group (Framingham, MA)
    …progression of multiple therapeutic candidates into the clinic. We are an innovative global healthcare company with one purpose: to chase the miracles of science to ... possible. Ready to get started? **Main Responsibilities** + Participate in and/or lead the development, qualification, and transfer of analytical methods in support… more
    Sanofi Group (05/01/25)
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  • Manager, Senior Engineer I, Raw Materials

    Bristol Myers Squibb (Devens, MA)
    …in their personal lives. Read more: careers.bms.com/working-with-us . BMS is a global biopharmaceutical company leading the way in medical innovation to help ... 1 to join the raw materials team within the Cell Therapy GMSAT ( Global Manufacturing Science and Technology) department. The Raw Materials team is responsible for… more
    Bristol Myers Squibb (05/14/25)
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  • Director, Manufacturing Analytics

    Bristol Myers Squibb (Devens, MA)
    …their personal lives. Read more: careers.bms.com/working-with-us . **Position Summary** Lead the Manufacturing Analytics team for Cell Therapy Technical Operations ... teams to leverage and re-use analytics effectively across the enterprise. + Lead network governance forums to provide prioritization and monitoring of deployment of… more
    Bristol Myers Squibb (05/14/25)
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  • Principal Systems Engineer

    Olympus Corporation of the Americas (Westborough, MA)
    …. **Job Description** The Principal R&D Systems Engineer will lead or support Systems Engineering aspects on new product development ... collection of user needs/feedback on product requirements and concepts + Lead the requirements development and management process, incorporating risk management… more
    Olympus Corporation of the Americas (03/29/25)
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  • (Night Shift) Manager, Manufacturing, Cell Therapy

    Bristol Myers Squibb (Devens, MA)
    …and provide Operations project information and activities status to Planning, Manufacturing, Quality Assurance / Operations, Global Supply and other associated ... and operational issues to prevent deviations and maintain a compliant environment. Lead and manage the development of corrective and preventative actions, deviation… more
    Bristol Myers Squibb (05/14/25)
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