• Sr. Compliance Manager

    Abbott (Sylmar, CA)
    Regulatory Compliance/ Affairs experience in In Vitro Diagnostics and medical device manufacturing or other similarly regulated environment. + Knowledge ... the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices , nutritionals and branded generic medicines. Our 114,000… more
    Abbott (11/14/25)
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  • Director Pediatric Neurology Research - Pediatrics…

    Rush University Medical Center (Chicago, IL)
    **Job Description** Location: Chicago, Illinois Business Unit: Rush Medical Center Hospital: Rush University Medical Center Department: Pediatrics-Res Adm **Work ... Neurology Research will be responsible for the overall fiscal, regulatory , operational, administrative, and personnel management of the Pediatrics Neurology… more
    Rush University Medical Center (11/16/25)
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  • Clinical Development Portfolio Director-Patient…

    Philips (Cambridge, MA)
    …the right fit if:** + You have a minimum of 15+ years' combined experience in Medical Device Clinical Research and Medical Device development within FDA ... Japan and China. + You have a detailed understanding of Clinical & Medical Affairs , leveraging expertise to propose innovative ideas, providing meaningful input… more
    Philips (11/05/25)
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  • Assembly

    Adecco US, Inc. (Southington, CT)
    …*Must be familiar with and comfortable using computers. *Working knowledge of the medical device regulatory procedures, lean manufacturing, and manufacturing ... Assembler - Medical Device Assembler, Operations - Adecco...quantity and good manufacturing practices to satisfy customer and Regulatory Affairs requirements. Read and/or understand operating… more
    Adecco US, Inc. (10/28/25)
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  • Quality Manager

    Abbott (Pleasanton, CA)
    …+ Two (2) years of Quality Systems, Quality Assurance and/or Regulatory Compliance/ Affairs experience in medical device manufacturing or other similarly ... the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices , nutritionals and branded generic medicines. Our 114,000… more
    Abbott (11/14/25)
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  • Director, PMO - Clinical

    Stryker (Fremont, CA)
    …do:** **Technical Responsibilities:** + Works with Divisional Leadership, KOLs, Marketing, Clinical Affairs and Regulatory Affairs and regional organizations ... internal stakeholders. + Works with Divisional Leadership, Marketing, Clinical Affairs and Regulatory Affairs and...desired):** **Preferred Skills** **/ Tools:** + Deep experience in medical device clinical research + 10+ years… more
    Stryker (11/20/25)
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  • Scientific Technical Writer

    Roche (Indianapolis, IN)
    …Near Patient Care products. In close collaboration with our interfaces in Marketing, R&D, Regulatory Affairs and IT, we ensure that our customers receive the ... in planning completion deadlines and close collaboration with relevant internal interfaces, eg Regulatory Affairs and Marketing + take on the role of Subject… more
    Roche (11/23/25)
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  • Senior Manufacturing Quality Engineer

    Cook Medical (Bloomington, IN)
    …function teams including quality, engineering, production, clinical, and regulatory affairs .- Provide leadership in the understanding of medical device ... FDA 21 CFR 820, ISO 13485, and other applicable regulatory requirements. Must work and interact effectively and professionally...degree and 5-8 years of experience- Demonstrates knowledge of medical device regulation (ISO 13485, 21CFR) and… more
    Cook Medical (11/22/25)
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  • Associate Manager, Clinical Trial Reimbursement

    Abbott (Austin, TX)
    …the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices , nutritionals and branded generic medicines. Our 114,000 ... for diversity, working mothers, female executives, and scientists. **The Opportunity** Our medical devices help more than 10,000 people have healthier hearts,… more
    Abbott (10/25/25)
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  • Senior Clinical Data Manager

    Olympus Corporation of the Americas (Center Valley, PA)
    …of 6 years of experience. + Prior experience in a sponsor, CRO, or medical device company. In-depth knowledge and experience with FDA regulations and familiarity ... and GCDMP. + Strong expertise in implementing and maintaining systems for global medical device trials (Class II/III or combination products). + Excellent… more
    Olympus Corporation of the Americas (10/28/25)
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