• CMC Product Quality

    Regeneron Pharmaceuticals (Troy, NY)
    The CMC Product Quality Regulatory Communications team is hiring! This team is responsible for being the primary Quality representative for product ... This role supports the development, coordination, and ownership of the quality and compliance elements of global regulatory communication/reporting regulations,… more
    Regeneron Pharmaceuticals (04/28/24)
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  • Director, CMC Product Development

    AbbVie (North Chicago, IL)
    …project plan to deliver high quality with respect to science, technology, compliance and cost effectiveness. + Leads CMC development teams for assigned ... teams and all CMC activities with respect to science, technology, quality , regulatory/ compliance requirements, budget and resources. *Multiple product more
    AbbVie (05/10/24)
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  • Director, GRA CMC Pharmaceuticals,…

    Takeda Pharmaceuticals (Boston, MA)
    …pharmaceutical Regulatory CMC experience including experience as an RA CMC product lead, or equivalent industry experience, with international experience ... first time. Maintain up-to-date knowledge and expertise of relevant CMC and quality guidelines and regulations and...proactively and utilize science and risk based approach to product development and LCM activities. + Contribute to creating… more
    Takeda Pharmaceuticals (03/13/24)
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  • Director, Regulatory Affairs CMC

    Taiho Oncology (Pleasanton, CA)
    …related areas. + In conjunction with Quality Assurance, manages regulatory compliance for sponsor activities for CMC , drug supply, documentation, Good ... Director, Regulatory Affairs CMC Pleasanton, CA, USA Req #355 Tuesday, March...truly global experience that helps cancer patients to improve quality of life . The size of our company… more
    Taiho Oncology (03/26/24)
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  • Director, Regulatory CMC

    Editas Medicine (Cambridge, MA)
    …or functional teams to provide regulatory guidance and support for CMC development and ensure compliance with applicable EMA/FDA/ICH/WHO/Global regulations ... future. Position Summary This role will lead and support the CMC strategies and submission including clinical trials applications, marketing applications, agency… more
    Editas Medicine (04/25/24)
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  • Vice President, GRA CMC , Biologics…

    Takeda Pharmaceuticals (Boston, MA)
    …role will collaborate with multiple stakeholders in R&D, GRA, GMS, Global Quality , and Commercial to develop innovative strategies for the management of development ... + Collaborate with stakeholders in R&D, GRA, GMS, Global Quality , and Commercial to develop innovative strategies for the...and bring current products to industry standards. + Represent CMC and GRA on key governance committees and play… more
    Takeda Pharmaceuticals (03/19/24)
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  • Sr. Director - CMC Development

    Lilly (Philadelphia, PA)
    …+ Collaborate with global partners and external vendors to ensure timely and quality delivery of CMC activities. + Drive continuous improvement initiatives to ... This position has overall responsibility for Avid's global investigational medicinal product (IMP) manufacturing, IMP and commercial product precursor and… more
    Lilly (05/03/24)
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  • Process Development Senior Principal Scientist…

    Amgen (Cambridge, MA)
    …for a career you can be proud of. Process Development Senior Principal Scientist - CMC Team Lead **Live** **What you will do** Let's do this. Let's change the world. ... + Serve as the Attribute Sciences team lead on a cross-functional product development team for a biologic in late-stage development with accountability of… more
    Amgen (03/15/24)
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  • Senior Associate Scientist, Cell Culture Process…

    Gilead Sciences, Inc. (Foster City, CA)
    …technology development and platform process evolution projects for increased productivity, high quality product , and speed to clinic. + Contribute to design ... Description** **Senior Associate Scientist, Cell Culture Process Development - Pre-Pivotal Biologics CMC Development - Foster City, CA** At Gilead, we're creating a… more
    Gilead Sciences, Inc. (03/02/24)
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  • Senior Director, GRA Pharmaceuticals

    Takeda Pharmaceuticals (Boston, MA)
    …and right first time. + Maintain up-to-date knowledge and expertise of relevant CMC and quality guidelines and regulations and establishes mechanisms to ... GRA Pharmaceuticals- Small Molecule where you will establish collaboration with Global CMC teams and leadership through networks and enable CMC regulatory… more
    Takeda Pharmaceuticals (03/13/24)
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  • Senior Scientist/Associate Director RACMC

    Daiichi Sankyo Inc. (Basking Ridge, NJ)
    …to regulatory process optimizations on relevant topics. **Responsibilities** - Supports CMC regulatory compliance activities for portfolio biologics to meet ... Reports, Biological Product Deviation Reports, and Drug Listings. Ensures that CMC documentation is complete, well organized, scientifically sound, of a high … more
    Daiichi Sankyo Inc. (04/12/24)
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  • mRNA Process Development - Scientific Data…

    Sanofi Group (Waltham, MA)
    …and Data Quality indicators to bolster data integrity and usability​​. Compliance with Data Standards: Lead the implementation and monitoring of best practices ... mRNA vaccine capabilities and research platform with R&D, digital, and CMC teams. Watch our Jobinar's replay ( _https://sanofi12.jobinar.com/_ ) to discover… more
    Sanofi Group (05/02/24)
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  • Senior Director - Analytical Regulatory Science

    Gilead Sciences, Inc. (Foster City, CA)
    …in the management of filing content and changes. + Evaluates and communicates risks for CMC control strategies and quality compliance to CMC RA ... teams. + Promotes continual improvement for analytical control strategies, quality compliance /business processes, and regulatory filing content taking… more
    Gilead Sciences, Inc. (04/19/24)
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  • Associate Director, GMP Quality Control

    Sumitomo Pharma (Columbus, OH)
    …development by making recommendations for manufacturing controls, sampling and testing to ensure product quality and compliance with GMPs from development ... individual for the position of Associate Director of GMP Quality Control, who oversees GMP compliance of...Specification Review Committees for GMP Drug Substance and Drug Product programs. + Review and approve Quality more
    Sumitomo Pharma (04/19/24)
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  • Lead for Global Regulatory Affairs, Plasma

    CSL Behring (King Of Prussia, PA)
    …**Global regulatory experience including knowledge of application submission processes and product life cycle management activities** **( CMC ) knowledge of the ... You will report to the VP, Head of GRA CMC . You will provide strategic leadership and oversight in...requirements. You will lead and direct strategy for regulatory compliance for all CSL Plasma Inc Operations to include:… more
    CSL Behring (04/14/24)
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  • Director, Early Phase Analytical Development

    AbbVie (North Chicago, IL)
    …inside and outside of Biologics CMC Development and R&D. + Assures compliance with AbbVie safety, quality and regulatory policies and government regulations. ... and formulation development. Biologics ARD partners with all functions across Biologics CMC to deliver high- quality drug products for patients. The Director,… more
    AbbVie (03/18/24)
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  • Senior Manager, Quality Assurance

    Gilead Sciences, Inc. (Foster City, CA)
    …for clinical and commercial products and programs. **Job Functions:** + Serve as QPTL ( Quality Product Team Lead) or QA Operational Lead (OL) for assigned ... Generate and or contribute to relevant metrics and annual product quality reports. + Review and approve...archives as needed **Essential Project Management Activities:** + Represents quality assurance in CMC Teams and/or PDM… more
    Gilead Sciences, Inc. (05/11/24)
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  • Product Solutions Manager III

    LA Care Health Plan (Los Angeles, CA)
    …process improvement plans, monitoring programs and enhancements to promote efficiency, quality , and compliance . Partner with functional areas to involve ... Mission: LA Care's mission is to provide access to quality health care for Los Angeles County's vulnerable and...Specifics: Medicare: Required: Experience and knowledge in Cal MediConnect ( CMC ) / D-SNP policy and product lines… more
    LA Care Health Plan (05/15/24)
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  • Senior Manager, Global Regulatory Strategy, US…

    AbbVie (Madison, NJ)
    …with regulations, company policies, procedures, and guidance in alignment with regulatory product strategy and the Quality Dossier Program (QDP). Qualifications ... to meet relevant US and Canada regulatory requirements. . Responsible for product (s) with multiple driver indications within a Therapeutic Area and support the… more
    AbbVie (03/26/24)
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  • Global Industrial Product Leader RSV…

    Sanofi Group (Swiftwater, PA)
    …Industrial Product group ( quality product leader, supply chain product leader, analytical product leader, CMC product leader, project ... **Global Industrial Product Leader RSV** **(Respiratory Syncytial Virus)** **ABOUT THE...to maintain a sustainable and reliable supply of cost-competitive quality vaccines for our customers around the world. **MAIN… more
    Sanofi Group (03/23/24)
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