• Sr Principal Product Security Engineer

    Medtronic (Boston, MA)
    …(https://www3.benefitsolver.com/benefits/BenefitSolverView?page\_name=signon&co\_num=30601&co\_affid=medtronic) **About Medtronic** We lead global healthcare ... security strategy that aligns with industry best practices and regulatory requirements + **Product Security** - Lead ...for Employers and the California Fair Chance Act. We lead global healthcare technology and boldly attack… more
    Medtronic (11/13/25)
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  • Sr. Principal Electrical Engineer (Affera)

    Medtronic (Newton, MA)
    …(https://www3.benefitsolver.com/benefits/BenefitSolverView?page\_name=signon&co\_num=30601&co\_affid=medtronic) **About Medtronic** We lead global healthcare ... County Fair Chance Ordinance for Employers and the California Fair Chance Act. We lead global healthcare technology and boldly attack the most challenging health… more
    Medtronic (11/08/25)
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  • Senior Director, Program Management, Neuroscience

    Bristol Myers Squibb (Cambridge, MA)
    …standing experience in all phases of research and drug development, including global regulatory submissions (IND/CTA through NDA/BLA/MAA/JNDA/ NDA China) and ... priority development asset(s). They operate as a strategic partner to the Global Program Lead (GPL), to shape and deliver the Target Product Profile (TPP) and… more
    Bristol Myers Squibb (11/01/25)
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  • Senior Staff Engineer, Modeling

    Takeda Pharmaceuticals (Boston, MA)
    …within the function and potentially cross-functionally. + Identify topics for initiatives and lead local/ global initiatives on behalf of senior staff. + Author ... a strong background in chemical reaction engineering and will tackle and lead challenging problems in chemical reactions by leveraging expertise in reaction… more
    Takeda Pharmaceuticals (08/29/25)
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  • Q&RA Coordinator - Project Manager I

    ThermoFisher Scientific (Waltham, MA)
    …Assist and lead in maintaining updates to company information on regulatory databases and generate reports as necessary eg FURLS, ISO certificate repository etc. ... realize their full potential as part of a fast-growing, global organization that values passion and unique contributions. Our...in Waltham, MA within the dynamic Corporate Quality & Regulatory Affairs team. You will be part of a… more
    ThermoFisher Scientific (10/29/25)
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  • Project Manager / Senior Project Manager, Patient…

    Norstella (Boston, MA)
    …on clinical trials, drug treatments, medical devices and what's new in the regulatory and commercial landscape. Relying on us to deliver vital advantage when making ... medical technology, biotechnology and healthcare service providers, including the top 10 global pharma and CROs. From drug and device discovery and development to… more
    Norstella (11/06/25)
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  • Healthcare Ethics and Compliance Operations…

    Oracle (Boston, MA)
    …compliance teams as well as our internal business groups to help address regulatory compliance issues that are essential to Oracle customers of all sizes globally ... leaders and external specialists on sophisticated, industry leading legal and regulatory compliance matters. **Preferred Qualifications:** + BA/BS degree and minimum… more
    Oracle (11/25/25)
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  • Head of Solid Tumor Clinical Development

    Astellas Pharma (Cambridge, MA)
    …required competencies to achieve functional and enterprise objectives. -Play a strategic lead role, in collaboration with Research, Regulatory Affairs and Early ... and with senior leadership of Clinical Operations, Quantitative Sciences, Regulatory and Pharmacovigilance/Medical Safety in the development and maintenance of… more
    Astellas Pharma (10/31/25)
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  • Director of Quality

    Catalent Pharma Solutions (Chelsea, MA)
    Director of Quality Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to develop, manufacture, and ... and the latest technology platforms at more than 40 global sites, Catalent supplies billions of doses of life-enhancing...and monitor Quality standards and requirements that meet Catalent, Regulatory and Customer requirements; + To ensure that the… more
    Catalent Pharma Solutions (11/11/25)
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  • Senior Manager, Benchtop IT Systems - Devens Cell…

    Bristol Myers Squibb (Devens, MA)
    …Manager collaborates cross-functionally with laboratory, manufacturing, quality, automation, and global IT teams to deliver solutions that enable scientific ... innovation and operational efficiency. **Key Responsibilities:** + Lead and manage the end-to-end lifecycle of benchtop and laboratory IT systems (LIMS, CDS, SDMS,… more
    Bristol Myers Squibb (11/21/25)
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