• Senior Director , Global Regulatory Affairs…

    Lilly (Indianapolis, IN)
    …are defined based on approved submissions for products and communicated to Manufacturing and Quality Assurance . + Accountable to approve use of CMC content to ... to make life better for people around the world. **Purpose:** The Senior Director of Global Regulatory Affairs - CMC (GRA-CMC) leads and manages the scientific… more
    Lilly (03/26/25)
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  • Sr. Director , Medical Affairs QA

    Daiichi Sankyo Inc. (Basking Ridge, NJ)
    …areas centered around rare diseases and immune disorders. **JOB SUMMARY** The Senior Director , Head Medical affairs Quality Assurance in Global RD/PV ... is dedicated to the creation and supply of innovative pharmaceutical therapies to improve standards of care and address...QA is accountable to drive the implementation of a quality strategy and quality plan closely aligned… more
    Daiichi Sankyo Inc. (04/26/25)
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  • Associate Director , Internal Audit

    BeOne Medicines (San Mateo, CA)
    …+ Support Group Operations Lead to develop, implement, and maintain the Quality Assurance and Improvement Program (QAIP), conducting internal and external ... **General Description:** The Associate Director , Internal Audit, plays a vital role in...audit reports and impactful presentations to executive leadership. Prepare high- quality reports that enhance transparency and accountability, aligning with… more
    BeOne Medicines (05/20/25)
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  • Development Transformation Lead, Director

    Amgen (Washington, DC)
    …+ 10+ years of experience in clinical development, clinical operations, or clinical quality assurance within pharmaceutical , biotech, or CRO environments. + ... the lives of patients while transforming your career. **Development Transformation Lead, Director ** **What you will do** Let's do this. Let's change the world.… more
    Amgen (05/09/25)
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  • Technical Director (Metals) - Eurofins…

    Eurofins (Tacoma, WA)
    …regarding analytical techniques and capabilities. + Investigates issues raised by clients, quality assurance , sales, and other departments to find root cause ... Northwest in Tacoma, WA is seeking a new Technical Director . The Technical Director serves as a...of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in discovery pharmacology,… more
    Eurofins (05/16/25)
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  • Director , Advanced Therapies…

    J&J Family of Companies (Malvern, PA)
    …knowledge to excel in their roles. + Collaborate cross-functionally with R&D, quality assurance , regulatory affairs, and manufacturing teams to integrate ... https://www.jnj.com/innovative-medicine We are searching for the best talent for a ** Director , Advanced Therapies Characterization** to be in Malvern, PA. Purpose:… more
    J&J Family of Companies (04/23/25)
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  • Medical Director Pharmacovigilance, Rare…

    Takeda Pharmaceuticals (Boston, MA)
    …with other functional areas such as Clinical Development, Regulatory Affairs, Quality Assurance , Medical Affairs, Marketing, Manufacturing, and Legal; ensure ... following job opportunity: **JOB LOCATION:** Cambridge, MA **POSITION** : Medical Director Pharmacovigilance, Rare Disease & PDT **POSITION DESCRIPTION** : Takeda… more
    Takeda Pharmaceuticals (04/05/25)
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  • Director of Engineering

    Prose (Brooklyn, NY)
    Quality & Regulatory Compliance + Collaborate with R&D, Innovation, NPI, Tech, Quality Assurance and Operations to ensure products meet regulatory, safety, ... Job Summary: We are seeking a strategic and hands-on Director of Engineering to lead our engineering, industrialization, packing engineering and process improvement… more
    Prose (05/19/25)
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  • Program Director - Global Facilities…

    Lilly (Indianapolis, IN)
    …defined as delivering asset capability or capacity with safety, cost, schedule, and quality assurance . + Interface/Communication: Ability to lead from a regional ... issue resolution, anticipate scope changes, and implement project work safely with quality , speed, and value. + Compliance: Lead with a disciplined, structured… more
    Lilly (05/16/25)
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  • Senior Director , Regulatory Affairs CMC

    BeOne Medicines (San Mateo, CA)
    …In-depth knowledge of ICH requirements, global regulatory CMC requirements; Knowledge/experience in Quality Assurance and GMP regulation is a plus. * Experience ... authoring and managing CTD CMC sections to ensure on-time and high- quality submissions for investigational, marketing, and post-approval applications. * Lead or/and… more
    BeOne Medicines (05/10/25)
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