• Lead SaMD Technical Program Manager

    Wolters Kluwer (Chicago, IL)
    …a pivotal role in driving the development and delivery of Software as a Medical Device (SaMD) products. This position is responsible for enabling engineering ... The Principal SaMD TPM acts as a bridge between engineering, product, regulatory affairs , clinical, and quality assurance teams, facilitating strategic… more
    Wolters Kluwer (12/04/25)
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  • Project Manager III

    Actalent (Irvine, CA)
    …to lead Quality Assurance (QA) activities for a strategic M&A initiative in the medical device industry. This role demands a strong leader capable of navigating ... complex situations and collaborating effectively with cross-functional teams, including Regulatory Affairs (RA) and Clinical Affairs (CA). Responsibilities +… more
    Actalent (01/06/26)
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  • Clinical Monitoring Manager

    Cook Medical (West Lafayette, IN)
    …or 2 years of experience as Monitoring Manager; * Sound knowledge of GCP and global medical device regulations, with experience working on medical device ... correctly understood and applied; + Through close collaboration with Clinical Affairs global leadership, help ensure global alignment regarding monitoring processes… more
    Cook Medical (12/17/25)
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  • Medical Science Liason

    Astrix Technology (Boston, MA)
    …Work closely with internal teams such as Clinical Development, Regulatory Affairs , and Commercial to provide medical insights that inform strategic ... medical affairs role within the pharmaceutical, biotechnology, or medical device industry. + Scientific Expertise: Deep understanding of therapeutic… more
    Astrix Technology (10/12/25)
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  • Site Compliance Manager

    AbbVie (Waco, TX)
    …departments such as the Device Analysis Lab, Quality Assurance, Regulatory Affairs , Clinical Studies, Customer Care, Operations, and Marketing departments ... 21 CFR 803, 21 CFR 4, CMDR SOR/98-282, ISO 13485:2016, European Union Medical Device Regulation and applicable international vigilance regulations. + Conduct,… more
    AbbVie (12/10/25)
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  • Medical Safety Manager - Complaints…

    Philips (San Diego, CA)
    … Medical /Clinical Affairs or Medical Safety/ Medical Affairs Risk Management in Meical Device industry. Prior hands-on bedside/clinical experience ... ** Medical Safety Manager, Complaints Handling** The Medical...assessments on complaints related to harm to assist in regulatory reportability determination and serves as the primary clinical… more
    Philips (01/07/26)
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  • Manager, QA External Manufacturing

    Olympus Corporation of the Americas (Center Valley, PA)
    … products to ensure products meet current Good Manufacturing Practices, applicable medical device regulatory requirements, and for supporting business ... Duties** + Supports supplier quality activities for sourced finished Medical Device products and leads these supplier...Notes: || United States (US) || Pennsylvania (US-PA) || Center Valley || Quality & Regulatory Affairs … more
    Olympus Corporation of the Americas (10/31/25)
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  • Medical Director Pharmacovigilance, Rare…

    Takeda Pharmaceuticals (Boston, MA)
    …and communicate safety issues with other functional areas such as Clinical Development, Regulatory Affairs , Quality Assurance, Medical Affairs , ... for the following job opportunity: **JOB LOCATION:** Cambridge, MA **POSITION** : Medical Director Pharmacovigilance, Rare Disease & PDT **POSITION DESCRIPTION** :… more
    Takeda Pharmaceuticals (12/27/25)
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  • Medical Science Liaison

    BD (Becton, Dickinson and Company) (San Antonio, TX)
    …surgery-specific medical device experience) + Strong expertise in medical affairs , KOL engagement, and the clinical/ regulatory landscape specific ... on medical strategy and key objectives with cross-functional partners, including medical , clinical, commercial, regulatory , R&D, and market access teams. +… more
    BD (Becton, Dickinson and Company) (12/20/25)
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  • Biostatistician

    Olympus Corporation of the Americas (Center Valley, PA)
    …+ Interpret statistical results; collaborate with cross-functional teams (clinical operations, regulatory affairs , medical writing, data management) to ... Data Management and Systems collaborating closely with MCA - Medical Affairs and Clinical Affairs ...is required. + Minimum of 6 years previous in pharmaceutical/ medical device industries or health care services… more
    Olympus Corporation of the Americas (12/05/25)
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