• Merck & Co. (Rahway, NJ)
    …(KPI), Leading International Teams, Management Process, Manufacturing Scale-Up, Medical Device Regulations, Medical Devices, Packaging Engineering, ... fields Required Skills and Experience: Subject matter expertise in packaging and/or medical device and combination product components as well as development… more
    HireLifeScience (10/16/25)
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  • Tris Pharma (St. Louis, MO)
    …in a pharmaceutical, biotechnology, business to business (B2B), capital equipment, medical device and/or related industry REQUIRED.(SR)/Healthcare Sales Rep - ... medicines addressing unmet patient needs. We have over 150 US and International patents - including applications - and several marketed branded and generic… more
    HireLifeScience (10/28/25)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …includes clinical or basic research in a pharmaceutical company, a Medical device /Diagnostic company, Academic Research Organization (ARO), hospital/ medical ... pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and… more
    HireLifeScience (11/07/25)
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  • ValSource, Inc. (Durham, NC)
    …Commissioning, Qualification and Validation (CQV) experience in Pharmaceutical, Biotech, Medical Device or related GMP manufacturing environment preferred. ... environments. Knowledge of Industry guidelines (ISPE, PDA), US and international regulations (FDA, ICH, ISO, EU) for validation of...ValSource will include: Paid Time Off (PTO) and Holidays Medical / Dental / Vision Insurance - premiums 100%… more
    HireLifeScience (10/27/25)
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  • Unknown (Madison, WI)
    …and Supplies Medical Specialties Oncology Radiotherapy Specialties oncology medical device tumor cancer radiosurgery radiation therapy robotic radiosurgery ... healthcare fraud and abuse compliance, preferably with NASDAQ experience. Experience in the medical device industry or a highly regulated life sciences sector is… more
    job goal (12/05/25)
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  • Unknown (Dallas, TX)
    …Industry-leading provider of medical devices & transformative healthcare innovations Industry Medical Device Type Public Company About the Role The Company ... Global Sourcing to spearhead its procurement and supply chain activities on an international scale. The successful candidate will be tasked with the development and… more
    job goal (12/05/25)
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  • Unknown (Concord, NH)
    …the Company Respected provider of high-quality medical technology & services Industry Medical Device Type Privately Held About the Role The Company is ... role in leading and managing all facets of its medical technology business unit. The successful candidate will be...Building and maintaining strong relationships with customers, suppliers, and international teams is also a key aspect of the… more
    job goal (12/05/25)
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  • Unknown (Fort Worth, TX)
    …learning dental software artificial intelligence dental radiology pathology detection medical device software clinical performance software diagnostic technology ... partnership management, and will play a key role in international expansion efforts. To excel in this position, candidates...in dental care. While experience in the dental or medical field is helpful, it is not a mandatory… more
    job goal (12/05/25)
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  • Medical Device Program Manager

    US Tech Solutions (San Bruno, CA)
    …knowledge of Quality Concepts (eg, Statistical Analysis, NC/CAPA, Audits) and US and International Medical Device Regulations & Regulatory Agencies (eg, FDA, ... + Managing cross-functional or cross-team projects to bring regulated medical device products to market. + Ensuring product specifications are defined… more
    US Tech Solutions (10/17/25)
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  • Future Opportunities - Join Our Talent Pipeline…

    AbbVie (Irvine, CA)
    …with FDA's Quality System Regulation (QSR), ISO13485, the Canadian Medical Device Regulations, and all other international regulatory requirements with which ... that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a...our talent pipeline and considered for future opportunities. The Device Engineer will work collaboratively with a team to… more
    AbbVie (09/17/25)
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  • Post Market Surveillance Manager- Shockwave…

    J&J Family of Companies (Santa Clara, CA)
    …industry practices, techniques, and standards in compliance with applicable domestic and international Medical Device Post Market Surveillance regulations. ... Medical portfolio aims to establish a new standard of care for medical device treatment of atherosclerotic cardiovascular disease through its differentiated… more
    J&J Family of Companies (10/31/25)
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  • Medical Safety Officer (MSO)- Heart…

    J&J Family of Companies (Danvers, MA)
    medical device /pharma industry, and clinical research. + Knowledge of local/ international medical device regulations and advanced statistical methods. ... be located in Danvers, MA. The MSO role is to provide medical safety stewardship for Medical Device (MD) products. Although a medically independent voice is… more
    J&J Family of Companies (11/14/25)
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  • Senior Regulatory Affairs Specialist…

    Abbott (Plymouth, MN)
    …+ Maintains ongoing surveillance and analysis of all pertinent domestic and international medical device regulations to ensure submission requirements ... US device regulations and/or experience with EU and other international medical device regulations and submissions. + Experience with risk management,… more
    Abbott (09/27/25)
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  • Regulatory Coordinator - Days - 8:00am to 5:00pm

    LSI Solutions (Victor, NY)
    …lines, helping to gather regulatory intelligence regarding updates to US and international medical device regulations, and supporting Rest-of-World (ROW) ... requested by distributors, with direction. + Communicates with distributors for ROW medical device registration, with direction. + Maintains the ROW Regulatory… more
    LSI Solutions (11/28/25)
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  • Head of Medical Device & SaMD…

    Takeda Pharmaceuticals (Lexington, MA)
    …design, implementation, and continuous improvement of operations and quality systems for medical device and digital health technologies, ensuring compliance with ... combination products, in vitro diagnostics (IVDs), and Software as a Medical Device (SaMD) across all business units, geographies, and therapeutic modalities… more
    Takeda Pharmaceuticals (10/10/25)
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  • Quality Engineer

    Globus Medical, Inc. (Audubon, PA)
    …with all company policies and procedures and maintaining compliance with US FDA and international medical device regulations and ISO 13485 quality system ... preferred) + 3-5 years' experience in quality assurance; experience in the medical device industry preferred + GMP and ISO experience + Strong proficiency in… more
    Globus Medical, Inc. (12/06/25)
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  • Sr. Manager Document Control and Training

    Integra LifeSciences (Princeton, NJ)
    International requirements as defined in FDA Regulations, ISO Standards, European Medical Device Directives, and other International Regulations. This ... policies, US Food and Drug Administration regulations, ISO 13485, the Canadian Medical Device Regulations (CMDR), the EU Medical Device Regulation,… more
    Integra LifeSciences (10/03/25)
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  • Regulatory Affairs Specialist II

    Abbott (Pleasanton, CA)
    …necessary detail. + Maintains ongoing surveillance and analysis of all pertinent international medical device regulations to ensure submission requirements ... also have access to: + Career development with an international company where you can grow the career you...working mothers, female executives, and scientists. For years, Abbott's medical device businesses have offered technologies that… more
    Abbott (10/09/25)
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  • Senior Manufacturing Engineer

    Abbott (St. Paul, MN)
    …and work experience. + Minimum 5 years manufacturing engineering experience. Medical device experience required. International manufacturing experience ... also have access to: + Career development with an international company where you can grow the career you...Development to ensure Design for Manufacturability in the electromechanical medical device space. + Analyze and solve… more
    Abbott (11/15/25)
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  • Biocompatibility & Toxicology Senior Scientist

    DEKA Research & Development (Manchester, NH)
    …and conducting biocompatibility and toxicological evaluations + Expertise in US and international medical device biocompatibility requirements including ISO ... Biocompatibility & Toxicology Senior Scientist to join our team focused on medical device and combination product development. The individual in this role will… more
    DEKA Research & Development (10/17/25)
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