• 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 (07/11/25)
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  • Lead Quality Systems Auditor

    Fresenius Medical Center (Waltham, MA)
    … and Compliance, Collaboration, No-Limits Mindset and Results Oriented. **PURPOSE AND SCOPE:** Lead Quality Systems Auditor will act as a Subject Matter Expert ... plans, conducts, and leads audits in accordance with the global QS audit program + Lead and...in the interpretation of FDA guidelines, Good Manufacturing Practices ( GMP ) and relevant quality standards for pharmaceuticals… more
    Fresenius Medical Center (06/28/25)
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  • Senior Specialist, Manufacturing Technical…

    Insight Global (Boston, MA)
    …Key Responsibilities: -Triage manufacturing issues in real-time on the manufacturing floor. - Lead and write investigations for quality events using root cause ... Job Description We are seeking a Senior Quality Records Specialist to join our Manufacturing Technical Operations (MTO) team in Boston. This role involves complete… more
    Insight Global (07/04/25)
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  • Compliance Head, US FDA

    Sanofi Group (Framingham, MA)
    …and high- quality responses and support the development and promotion of Global Quality Documentation. + Supports the preparation, execution and closure of ... purposes, and ensuring accurate reporting to Operations Management and Global Quality . . **Core member of critical.... . **Core member of critical governance** + Sanofi's GMP GDP Quality Council to facilitate sharing… more
    Sanofi Group (06/03/25)
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  • Site Quality Head

    Curia (Hopkinton, MA)
    …and drives Quality decisions at the site and also supports regional Director of Quality for global Quality initiatives + Provides hands on leadership and ... and packaging operations + Responsible for all aspects of GMP compliance. This includes quality oversight from...continuous improvement efforts + Ensure applicable requirements of Curia global Quality Systems are implemented and maintained… more
    Curia (05/20/25)
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  • Head, Analytical Controls (Sr. Director)

    Takeda Pharmaceuticals (Lexington, MA)
    …etc. in conjunction with senior staff and global line and function heads + Lead global CMC and Quality key initiatives and represent Pharm Sci to ... my knowledge. **Job Description** **How you will contribute:** + Lead and develop a global team of...Stability and Shelf life; c) Reference Standard Management; d) GMP Quality Systems + Contribute to product… more
    Takeda Pharmaceuticals (06/06/25)
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  • Lead Contracts Manager - Data Center…

    Meta (Boston, MA)
    **Summary:** Meta seeks highly engaged and experienced team players for lead roles to join our Design, Engineering & Construction (DEC) organization to direct ... join a high-powered team of industry leaders! **Required Skills:** Lead Contracts Manager - Data Center Design, Engineering &...team, peers, and outside business units to enhance the quality and efficiency of contracting processes 12. Ensure all… more
    Meta (06/25/25)
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  • Quality Assurance Specialist III,…

    Nitto Denko Corp. (Milford, MA)
    …+ BS/BA in science or equivalent work experience with 3-5 years' experience in either GMP Production or Quality Assurance. + Ability to provide expert advice and ... you will be responsible for interfacing with and providing quality input to client's manufacturing programs that are in...commercial readiness, and that are approved to manufacture in global regions. Key Responsibilities: + Act as QA project… more
    Nitto Denko Corp. (06/15/25)
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  • Head of Analytical Development and Quality

    Cambrex High Point (Waltham, MA)
    …Chemistry's state of the art complex-synthetics route development. Additionally, they will lead and advance the Quality Control function, collaborating with ... with the oversight of both analytical development activities and execution of Quality Control responsibilities. They will lead the analytical team, interface… more
    Cambrex High Point (06/08/25)
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  • Quality Control Senior Analyst I

    Takeda Pharmaceuticals (Lexington, MA)
    …to the best of my knowledge. **Job Description** **About the role:** As a Quality Control Senior Analyst, you will focus on the daily lab operations and execution ... derived from the compendia and non-compendial sources. You will maintain operational and GMP readiness of the QC area. Also, you will participate in more complex… more
    Takeda Pharmaceuticals (06/27/25)
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  • Director of Quality

    Symmons Industries (Braintree, MA)
    …all products meet or exceed company and industry standards, implement effective quality control systems, and lead initiatives to drive continuous improvement. ... quality metrics, ensuring continuous improvement in product quality and process performance. + Lead efforts...+ Knowledge of regulatory requirements and industry standards (ISO, GMP , etc.). + Ability to manage multiple priorities in… more
    Symmons Industries (07/11/25)
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  • Quality Control Analyst II

    Catalent Pharma Solutions (Chelsea, MA)
    ** Quality Control Analyst II** **Position Summary:** Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission ... and the latest technology platforms at more than 40 global sites, Catalent supplies billions of doses of life-enhancing...in North America. Catalent Pharma Solutions is hiring a Quality Control (QC) Analyst II who is responsible for… more
    Catalent Pharma Solutions (06/25/25)
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  • Quality Systems Sr Specialist

    Zimmer Biomet (Braintree, MA)
    …in pushing the boundaries of innovation and driving our mission forward. As a global medical technology leader for nearly 100 years, a patient's mobility is enhanced ... respected, empowered and recognised. **What You Can Expect** Maintain Site Quality programs to ensure compliance to domestic and international medical device… more
    Zimmer Biomet (07/08/25)
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  • QC Manager, Bioanalytical

    ThermoFisher Scientific (Plainville, MA)
    … testing. + Build a trained, competent team of QC analysts to support GMP testing. + Coordinate daily Quality Control activities for Molecular, Viral, Cell, ... (Mon-Fri) **Environmental Conditions** Adherence to all Good Manufacturing Practices ( GMP ) Safety Standards, Laboratory Setting, Office **Job Description** As part… more
    ThermoFisher Scientific (06/26/25)
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  • Director, Internal Audit

    Hologic (Marlborough, MA)
    …ISO 14971), MDSAP, and other global regulatory requirements. + Expertise in Quality Systems and GMP compliance in regulated industries such as medical ... a pivotal role in ensuring the effectiveness of our global Quality Systems. In this critical leadership...training. + Minimum of 10 years of experience in Quality Systems and GMP within medical devices,… more
    Hologic (06/17/25)
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  • IT Manager

    Medtronic (Billerica, MA)
    …(https://www3.benefitsolver.com/benefits/BenefitSolverView?page\_name=signon&co\_num=30601&co\_affid=medtronic) **About Medtronic** We lead global healthcare ... quality and compliance as needed. + Build and lead a high-performing, diverse IT team with clear goals...for Employers and the California Fair Chance Act. We lead global healthcare technology and boldly attack… more
    Medtronic (07/04/25)
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  • Enterprise Excellence Manager

    Teleflex (Chelmsford, MA)
    …: Up to 10% **Requisition ID** :12166 **About Teleflex Incorporated** As a global provider of medical technologies, Teleflex is driven by our purpose to improve ... the health and quality of people's lives. Through our vision to become...of healthcare. For more information, please visit **teleflex.com** . ** Global Operations -** Global Operations is a… more
    Teleflex (07/05/25)
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  • Proposal Manager - Gene Therapy Manufacturing Cdmo…

    Charles River Laboratories (Wilmington, MA)
    …with accuracy and meet client's expectations/timelines * Proactively Assist or lead proposal process improvement projects/initiatives * Coordinate all aspects of the ... sales proposal document production process to ensure the overall quality meets company and client standards * Research appropriate responses through supplied… more
    Charles River Laboratories (07/10/25)
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  • Auditing & Compliance Director - Software as…

    Wolters Kluwer (Waltham, MA)
    …month in the office (see approved locations on the posting). **OVERVIEW** You will be the global product quality lead in support of a broad portfolio of ... + Manage and guide system testing activities, including verification and validation. + Lead resolution of quality issues with on-market device software; drive… more
    Wolters Kluwer (06/11/25)
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  • Associate Director, Drug Product

    Rhythm Pharmaceuticals (Boston, MA)
    Company Overview Rhythm is a global , commercial-stage biopharmaceutical company committed to transforming the lives of patients and their families living with rare ... team in Boston, Massachusetts. The Associate Director will be the technical lead for Drug Product small molecule drug product development, manage outsourced… more
    Rhythm Pharmaceuticals (05/13/25)
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