• Global Category Manager-Clinical Development…

    Takeda Pharmaceuticals (Cambridge, MA)
    …leading or supporting the procurement, sourcing, outsourcing, purchasing or buying of compliance or clinical supplier categories. You will be assigned to support ... Takeda's Research & Development "R&D" organization and lead or support compliance or clinical supplier categories, including but not limited to: Compliance more
    Takeda Pharmaceuticals (05/23/25)
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  • Site Quality Head

    Curia (Hopkinton, MA)
    …where our work has the power to save lives Curia is a global contract development and manufacturing organization (CDMO) with over 30 years of experience partnering ... with pharmaceutical and biotech companies to provide life-saving treatments to...is directly responsible for oversight of total quality and compliance operations at the assigned site. This role uses… more
    Curia (05/20/25)
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  • Sr Medical Director

    Adecco US, Inc. (Waltham, MA)
    Adecco Healthcare & Life Sciences is hiring a contract Sr. Medical Director for our Medical Supply and Instrumentation partner in Waltham, MA. The anticipated hourly ... development, business objectives, quality initiatives and management, process improvement, compliance , and innovation. Applies therapeutic area expertise and indication-specific… more
    Adecco US, Inc. (05/30/25)
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  • Rheumatology / Gastroenterology Senior Health…

    Pfizer (Boston, MA)
    …effectively across multiple virtual engagement platforms based on customer preferences/ compliance guidelines; able to integrate guidance from management and other ... Co-Pay Resources. + Present terms of sale of product or existing contract terms where appropriate and with approved language; proactively answer on-label questions;… more
    Pfizer (05/29/25)
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  • Document Control Specialist, Quality Assurance

    Catalent Pharma Solutions (Chelsea, MA)
    …Quality Assurance** **Position Summary:** Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to develop, ... is committed to a Patient First culture through excellence in quality and compliance , and to the safety of every patient, consumer, and Catalent employee.** **The… more
    Catalent Pharma Solutions (05/21/25)
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  • Global Category Manager - Clinical Development…

    Takeda Pharmaceuticals (Boston, MA)
    …leading the procurement, sourcing, outsourcing, purchasing or buying of Compliance Services categories, including but not limited to pharmacovigilance services.** ... to support Takeda's Research & Development "R&D" organization and lead Compliance Services categories, including but not limited to pharmacovigilance services.** You… more
    Takeda Pharmaceuticals (05/02/25)
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  • Sr. Director, Commercial Operations VVS and ATX

    ThermoFisher Scientific (Waltham, MA)
    …of new and existing business relationships including strategic client program management and contract compliance + Ensure that there are robust processes in ... forecast and supply chain demands for clients + Ensure engagement and compliance with all SalesForce.com and sales management activities + Provide input into… more
    ThermoFisher Scientific (04/11/25)
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  • Buyer/Planner

    Catalent Pharma Solutions (Chelsea, MA)
    …- GMP** **Position Summary:** Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to develop, ... is committed to a Patient First culture through excellence in quality and compliance , and to the safety of every patient, consumer, and Catalent employee.** **The… more
    Catalent Pharma Solutions (04/10/25)
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  • Research Technician I - In Vivo PK

    Charles River Laboratories (Worcester, MA)
    …well being. * Collect and record research data and biological specimens in compliance with applicable guidelines and regulations (GLPs, SOPS). * Read basic study ... new drugs to market. **About Charles River** Charles River is an early-stage contract research organization (CRO). We have built upon our foundation of laboratory… more
    Charles River Laboratories (05/31/25)
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  • Scientist - In Vivo Pharmacology; Early…

    Lilly (Boston, MA)
    …or related scientific field and 1+ years' experience working in pharmaceutical industry or contract research organization **Additional Skills/Preferences:** + ... alignment with Lilly procedure quality standards and Good Documentation Practices + Ensure compliance with all health and safety regulations + Weekend work may be… more
    Lilly (05/30/25)
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