• Clinical Documentation Global Head

    Sanofi Group (Cambridge, MA)
    …of sanofi revenues by expediting submission timelines and facilitating reviews by regulatory agencies of sanofi key assets. + He/she: Creates and executes a ... to dossier management. Maintain an environment of compliance aligned with regulatory requirements and best-in-class industry standards. + Provide strong leadership… more
    Sanofi Group (07/02/25)
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  • Director, Pharmaceutical Sciences Program…

    Takeda Pharmaceuticals (Boston, MA)
    …+ BS + 18 years of experience; MS + 16 years of experience; PhD + 10 years of experience **Technical Skills/Competencies:** + Ability to propose and influence ... engineering, analytical/organic/physical chemistry, process engineering, pharmaceutics, quality assurance and/or regulatory affairs. Advanced understanding in DMPK, Pharmacology and Toxicology.… more
    Takeda Pharmaceuticals (06/27/25)
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  • The Head of EGDS Innovation and Center…

    Sanofi Group (Cambridge, MA)
    …patient safety/pharmocovigilance, patient focused drug development, portfolio management, global regulatory and digital partners to foster innovation and ensure best ... maintain strategic partnerships with leading academic institutions, industry consortia, and regulatory bodies. + Stay abreast of emerging trends, methodologies, and… more
    Sanofi Group (06/05/25)
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  • Vice President, Cardiovascular Discovery

    Pfizer (Cambridge, MA)
    …work is conducted with highest quality and in accordance with relevant regulatory , QC, and compliance guidelines + Provide supervision and career development ... of other colleagues to achieve meaningful outcomes and create business impact. + MD/ PhD with a minimum of 15-20 yrs research experience leading a research laboratory… more
    Pfizer (08/20/25)
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  • Head of Digital Portfolio and Change Management…

    Takeda Pharmaceuticals (Boston, MA)
    …industry networks and partners + Actively engage with industry leaders, regulatory bodies, and technology providers to anticipate emerging trends, shape corporate ... Stay ahead of industry trends by engaging with external partners, regulatory bodies, and technology providers. **Educational Requirements and Experience:** + … more
    Takeda Pharmaceuticals (08/20/25)
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  • Systems Engineer

    Kelly Services (Haverhill, MA)
    …etc.) to ensure adherence and alignment to product requirements (technical, regulatory , cost etc.) per Edwards Vacuum's product development process. Communicate ... for reduction-to-practice in new products. Stay current on technical & regulatory advances in mixed refrigerants, helium refrigeration, general cryogenics and… more
    Kelly Services (08/20/25)
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  • Sr. Director, Access Strategy, Rheumatology

    Sanofi Group (Cambridge, MA)
    …payers. + Lead efforts to anticipate and adapt to changes in the regulatory and reimbursement landscape, ensuring compliance and sustained market access. + Identify ... teams, including Market Access Shared Services, Brand Strategy, Medical Affairs, Regulatory , Patient Support Services, distribution and Finance, to integrate access… more
    Sanofi Group (08/19/25)
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  • Nuclear Engineer 3

    Pacific Northwest National Laboratory (Boston, MA)
    …radioactive waste, and long-term performance of waste forms. Supports nuclear regulatory work, risk-informed nuclear regulatory analysis, and probabilistic risk ... relevant experience -OR- + MS/MA and 3+ years of relevant experience -OR- + PhD with 1+ year of relevant experience Preferred Qualifications: + Degree in Nuclear… more
    Pacific Northwest National Laboratory (08/19/25)
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  • Process Chemist

    Actalent (Cambridge, MA)
    …detailed, timely, and compliant electronic laboratory notebook in accordance with regulatory and internal standards. + Ensure proper maintenance of laboratory ... equipment and uphold strict adherence to safety protocols and regulatory guidelines. + Other duties as assigned. Additional Skills...in chemistry with 3+ years in pharmaceutical research or PHD with 0-3 years of experience + Strong experience… more
    Actalent (08/19/25)
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  • Senior Director, Clinical Research,…

    Merck (Boston, MA)
    …development strategy, study design, initiation, execution, monitoring, analysis, regulatory reporting, and publication. **Specifically, the Senior Director May ... closely with a cross-functional group of experts in commercialization, regulatory affairs, statistics, and manufacturing to manage clinical development projects;… more
    Merck (08/14/25)
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