• Senior Manager, Market Quality - MDR

    Olympus Corporation of the Americas (Westborough, MA)
    …Compliance Manager at 1-888-Olympus (###). Posting Notes: || United States (US) || Massachusetts (US-MA) || Westborough || Quality & Regulatory Affairs (QA/RA) ... by staying **True to Life.** **Job Description** The Manager, Senior Global MDR Submission is responsible for... Submission is responsible for managing Market Quality- COE MDR team for the regulatory assessment and… more
    Olympus Corporation of the Americas (03/26/24)
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  • Sr . Regulatory Affairs

    Philips (San Diego, CA)
    …Implements internal or external quality system audits. + Reporting to the Director of Regulatory Affairs , the Senior RA Specialist will collaborate with ... Recommends strategies for earliest possible approvals of clinical trials applications. + Regulatory Affairs representative for the CT/AMI Systems and assists… more
    Philips (04/09/24)
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  • Senior Regulatory Affairs

    Actalent (Cuyahoga Falls, OH)
    …in accordance with cGMPs, QSRs, MDRs and the Quality Management System. Skills: Regulatory affairs , Regulatory , Medical device, Fda, Regulatory ... documents, Regulatory compliance, Iso 13485, Gmp, eu mdr , 21cfr 820, Labelling, Quality assurance, Compliance Additional Skills...is preferred. - 3-5 years of progressive experience in regulatory affairs required - Prior knowledge of… more
    Actalent (04/13/24)
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  • Solta Senior Manager, Regulatory

    Bausch Health (Bothell, WA)
    …proven and effective aesthetic care options to consumers and physicians alike. Reporting to the Sr Dir, Global Regulatory Affairs , the Sr Manager, ... globally distributed products. This role is not a regional regulatory but global regulatory position which under...Medical Device license applications (Class II or above), EU MDR technical file dossier (Class II or above). *… more
    Bausch Health (03/26/24)
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  • Senior Regulatory Affairs

    Kelly Services (Cuyahoga Falls, OH)
    Kelly Science & Clinical is seeking a ** Senior Regulatory Affairs Specialist near Cuyahoga Falls, OH.** **Direct Hire** **Shift:** Monday - Friday 8am-5pm ... technology field + 5+ years of progressive experience in regulatory affairs required + Appropriate combination of...be acceptable + Prior knowledge of 21CFR 820, ISO13485, MDR QMS requirements required + Experience with medical device… more
    Kelly Services (04/13/24)
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  • Senior Regulatory Affairs

    ConvaTec (Lexington, MA)
    …about Convatec, please visit http://www.convatecgroup.com **Job Summary:** In this role as a Senior Regulatory Affairs Specialist at Convatec, you will be ... division's global regulatory strategies and processes. The Senior Regulatory Affairs Specialist will...820 and EU Medical Devices Directive 93/42/EEC / EU MDR 2017/745: + 510(k) submissions, 3-5 minimum + Preparation… more
    ConvaTec (04/16/24)
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  • Principal Regulatory Affairs

    Medtronic (Santa Rosa, CA)
    …Rosa, CA or Mounds View, MN. Careers that Change Lives Reporting to the Senior Manager, the Principal Regulatory Affairs Specialist will support Research ... Principal Regulatory Affairs Specialist - Structural Heart...PMAs, IDE and PMA Supplements/Reports, Shonin applications, and EU MDR Technical Documentation in addition to Change Management assessments.… more
    Medtronic (04/06/24)
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  • Solta Manager, Regulatory Affairs

    Bausch Health (Bothell, WA)
    …in a science related field. + Should have over 7 years of experience as Sr . Regulatory Affairs Specialist. + Should have experience of independently ... care options to consumers and physicians alike. The Manager, Regulatory Affairs provides direct support to Solta...Medical Device license applications (Class II or above), EU MDR technical file dossier (Class II or above). +… more
    Bausch Health (01/27/24)
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  • Regulatory Affairs Specialist

    Healgen Scientific Limited (Houston, TX)
    Regulatory Affairs Specialist Regulatory ...21 CFR Part 820), ISO 13485, and other global regulatory requirements (such as MDR in the EU). ... flow cytometry. About the role The purpose of a Regulatory Affairs Specialist is to ensure compliance...execution. Complete other projects and responsibilities as assigned. The Senior Level RA Specialist will perform the above duties… more
    Healgen Scientific Limited (04/08/24)
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  • Associate Director Regulatory

    Abbott (St. Paul, MN)
    …software, vessel closure devices and peripheral stents. **The Opportunity** This **Associate Director Regulatory Affairs ** will work on-site at our St. Paul, MN ... As a manager, the function of an Associate Director Regulatory Affairs is to combine knowledge of...internal stakeholders. + Consults with and provides advice to senior management of the Company on strategies and plans… more
    Abbott (03/20/24)
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  • Associate Director, Regulatory

    AbbVie (North Chicago, IL)
    …Facebook, Instagram, YouTube and LinkedIn. Job Description The Associate Director, Regulatory Affairs , Strategic Global Labeling - Combination Products and ... with Global industry trends and best practices in combination product and device regulatory affairs , review and comment on changing regulation and guidance. +… more
    AbbVie (03/18/24)
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  • Sr . Product Stewardship Engineer

    Abbott (Westford, MA)
    …in engineering, safety management quality, environmental science, scientific discipline or regulatory affairs + Technical experience in chemical, mechanical or ... their health and get on with their lives. **WHAT YOU'LL DO** The Senior Product Stewardship Engineer will support the Vascular Division. This position will lead… more
    Abbott (04/05/24)
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  • Sr . Quality Compliance Engineer

    Terumo Medical Corporation (Elkton, MD)
    Sr . Quality Compliance Engineer Date: Apr 16, 2024 Req ID: 3191 Location: Elkton, MD, US Company: Terumo Medical Corporation Department: Quality Systems & Compliance ... **Job Summary** The Senior Quality Compliance Engineer will work with the ...+ Coordinate input from various stakeholders, such as Medical Affairs and PMS, required to draft Health Hazards Evaluations… more
    Terumo Medical Corporation (04/17/24)
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  • Development Sr Engineer I

    Zimmer Biomet (Warsaw, IN)
    …of the product development process in compliance with Zimmer Biomet procedures and global regulatory requirements + Supports Regulatory Affairs team with the ... documentation, preparation of materials for and conducting pre-submission question regulatory meetings + Supports clinical affairs in...in new product development + FDA QSR and EU MDR medical device regulatory requirements, and industry/… more
    Zimmer Biomet (04/14/24)
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  • Senior Regulatory Compliance…

    Stryker (Mahwah, NJ)
    …Here are 10 reasons to join our Regulatory Affairs /Quality Assurance team: https://www.strykercareersblog.com/post/10-reasons-to-join-strykers- regulatory ... More information is available at www.stryker.com We are currently seeking a ** Senior Specialist, Regulatory Compliance** to join our Joint Replacement Division… more
    Stryker (04/10/24)
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  • Senior Staff Specialist, Regulatory

    Stryker (Mahwah, NJ)
    …Here are 10 reasons to join our Regulatory Affairs /Quality Assurance team: https://www.strykercareersblog.com/post/10-reasons-to-join-strykers- regulatory ... our award-winning organization by visiting stryker.com We are currently seeking a ** Senior Staff Specialist, Regulatory Compliance** to join our **Joint… more
    Stryker (04/05/24)
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  • Senior Director, Medical Safety

    GRAIL (Menlo Park, CA)
    …oversees ongoing safety risk-benefit assessments and provide support to Quality and Regulatory Affairs organizations + Partner closely and effectively with ... (NASDAQ:ILMN). For more information, please visit www.grail.com . The Sr . Director, Medical Safety will lead the development and...+ Connect with respective colleagues in the Clinical, Medical Affairs , Global Regulatory Affairs , and… more
    GRAIL (03/02/24)
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  • Senior Project Manager, Clinical Evaluation

    Abbott (Maple Grove, MN)
    …device regulations and guidelines, and product and therapeutic area knowledge to support Regulatory Affairs medical device submissions in the EU for CE Marking ... and exchange of documents between stakeholders (eg, internal personnel such as Regulatory Affairs , R&D Engineering, Clinical Engineering, A&P and Marketing,… more
    Abbott (02/21/24)
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  • Senior Associate, RA Device/Combination…

    AbbVie (Irvine, CA)
    …Follow @abbvie on Twitter, Facebook, Instagram, YouTube and LinkedIn. Job Description Regulatory Affairs - Device/Combination products supports regulatory ... process. Experience with eCTD tools and EDMS applications. + Background in regulatory affairs , manufacturing, marketing, or quality assurance sufficient to… more
    AbbVie (03/19/24)
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  • Global Director Quality Compliance: External…

    Olympus Corporation of the Americas (Westborough, MA)
    …by applicable federal, state or local law. Posting Notes: || United States (US) || Massachusetts (US-MA) || Westborough || Quality & Regulatory Affairs (QA/RA) ... staying **True to Life.** **Job Description** Leads and directs regulatory compliance communications to ensure compliance of the Global...areas of compliance risk and present these risks to senior leadership at Olympus in a clear and concise… more
    Olympus Corporation of the Americas (02/27/24)
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