• Associate Director , Quality

    AbbVie (Worcester, MA)
    …validation & technical protocols & reports, lab investigations, manufacturing records & quality control data. + Establish & execute plans & commitments ... team including contributors in manufacturing, materials management, engineering, product development, Quality Systems, Product QA, Quality Control ,… more
    AbbVie (06/26/25)
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  • Associate Director , Clinical…

    Takeda Pharmaceuticals (Boston, MA)
    …true to the best of my knowledge. **Job Description** **About the role:** The Associate Director , Clinical and Safety Quality Compliance is responsible for ... involves defining and specifying activities, processes, and standards to meet quality requirements, auditing and monitoring processes, and ensuring compliance with… more
    Takeda Pharmaceuticals (07/25/25)
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  • Associate Director , Product…

    AbbVie (Waltham, MA)
    …capable of performing as leaders, team members and individuals. + Strong quality assurance / control , manufacturing, laboratory, technical support, regulatory, ... LinkedIn and Tik Tok (https://www.tiktok.com/@abbvie) . Job Description Responsible for quality of assigned products which may include small molecule pharmaceuticals… more
    AbbVie (07/11/25)
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  • Associate Director , Device Clinical…

    Takeda Pharmaceuticals (Lexington, MA)
    …is true to the best of my knowledge. **Job Description** **About the Role:** The Associate Director of Device Clinical Development (DCD) in the Drug Product and ... product training frameworks, and ensuring rigorous adherence to design control principles, while fostering collaboration across multidisciplinary teams to deliver… more
    Takeda Pharmaceuticals (06/06/25)
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  • Associate Director , Drug Substance…

    Sanofi Group (Cambridge, MA)
    **Job Title:** Associate Director , Drug Substance Commercial Development **Location** : Cambridge, MA **About the Job** Are you ready to shape the future of ... for the chemical process to deliver the drug substance quality target profile. The Chemical Process Development team will...join our growing Commercial Process Development team as an Associate Director . Under the direction of the… more
    Sanofi Group (06/27/25)
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  • Associate Director , Analytical…

    Takeda Pharmaceuticals (Lexington, MA)
    …to bring Better Health and a Brighter Future to people worldwide. As an Associate Director in Analytical Development, you will lead efforts to develop advanced ... technical assessments and risk analyses to inform program strategies. + Drive quality control and regulatory strategies for late-stage development, including… more
    Takeda Pharmaceuticals (07/02/25)
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  • Associate Director , GPS Knowledge…

    Bristol Myers Squibb (Devens, MA)
    …leveraged for downstream GPS use cases, such as effective AI deployment and high- quality self-service analytics. The Associate Director will be responsible ... advancing this vision. GPS is responsible for developing, manufacturing, and supplying quality clinical and commercial medicines to patients worldwide. This role is… more
    Bristol Myers Squibb (08/13/25)
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  • Associate Director , Correspondence…

    Evolent (Boston, MA)
    …for the mission. Stay for the culture. **What You'll Be Doing:** ** Associate Director , Correspondence Project and Program Management** This position serves ... high performing teams responsible for timely delivery of high-value and high- quality correspondence deliverables. + Responsible for the oversight of the… more
    Evolent (08/14/25)
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  • AI Governance Associate Director

    Wolters Kluwer (Waltham, MA)
    …requiring 8 days per month at an approved Wolters Kluwer location._** The **AI Governance Associate Director ** will serve as a key leader in the evolution and ... + Partner with internal teams (eg Legal, Security) to ensure governance control effectiveness and implement enhancements in response to audit findings. + Author… more
    Wolters Kluwer (06/20/25)
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  • Compliance Operations Lead, Associate

    Takeda Pharmaceuticals (Boston, MA)
    …and training solutions. + Act as Steward of the QMS within CPMQ (eg Quality Events, Serious Breach, Change Control , Risk Register, Regulatory Intelligence, Gap ... of my knowledge. **Job Description** **OBJECTIVES:** + Ensures Global and R&D Quality processes are embedded and effectively implemented across CPMQ + Partner with… more
    Takeda Pharmaceuticals (08/08/25)
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