- Actalent (St. Paul, MN)
- …on sustaining engineering. The team is responsible for managing changes to medical devices after commercialization, ensuring that any changes in raw materials do ... standards. Responsibilities + Manage and sustain engineering changes for commercialized medical devices. + Ensure product integrity amidst changes in raw materials.… more
- Fujifilm (St. Paul, MN)
- …activities. + Keep abreast of new legislation and enforcement matters relevant to the medical device industry as well as industry and compliance best practices. ... Degree. + 2 to 3 years of corporate compliance experience in the medical device and/or pharmaceutical industry and working knowledge of healthcare related… more
- Abbott (Plymouth, MN)
- …of international regulatory affiliates. + Compile, prepare, review and submit medical device submissions to regulatory agencies + Interfaces directly ... scientific affairs function. **Preferred** **Qualifications** + 4+ years of related regulatory submission experience from medical device , pharmaceutical,… more
- Abbott (Plymouth, MN)
- …changes for compliance with applicable regulations. + Compile, prepare, review and submit medical device submissions to regulatory agencies + Supports all ... ongoing surveillance and analysis of all pertinent domestic and international medical device regulations to ensure submission requirements world-wide are… more
- Abbott (St. Paul, MN)
- …in a broader enterprise/cross-division business unit model. + Experience working in the Medical Device industry. + Regulatory Affairs Professionals Society ... to various international affiliates. + Maintains pertinent domestic and international medical device regulations to ensure submission requirements world-wide are… more
- Medtronic (Minneapolis, MN)
- …profile._ + Bachelor's degree in a technical discipline + Minimum 7 Years of medical device regulatory experience with Bachelor's degree + Or minimum ... or familiarity with software regulations and requirements. The **Principal Regulatory Affairs Specialist ** develops strategies for worldwide...5 Years of medical device regulatory experience with… more
- Abbott (Plymouth, MN)
- …necessary detail. + Maintains ongoing surveillance and analysis of all pertinent medical device regulations to ensure submission requirements worldwide are ... their lives. **The Opportunity** We are seeking a **Principal Regulatory Affairs Specialist ** to join Abbott's Electrophysiology...device regulations, or with EU and other international medical device regulations and submissions. + Must… more
- Abbott (St. Paul, MN)
- …to various international affiliates. * Maintains pertinent domestic and international medical device regulations to ensure submission requirements world-wide are ... heart disease. The Opportunity - We are seeking a Regulatory Operations Specialist I for our St....of education and work experience + Some experience with medical device industry preferred. + Experience working… more
- Medtronic (Mounds View, MN)
- …2+ years of experience in regulatory affairs **Nice to Have** + 4+ years of medical device regulatory affairs experience + Local to CO and willing to ... Day in the Life** We are seeking a Senior Regulatory Affairs Specialist to join our team...Quality Management Systems (QMS) + Technical Writing + International medical device regulatory submission/approval experience,… more
- Abbott (St. Paul, MN)
- …for the treatment of structural heart disease. The Opportunity We are recruiting for a Regulatory Affairs Specialist I to join our team on-site in St. Paul, MN. ... of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000...As an individual contributor, the function of a Regulatory Affairs Specialist I is to provide… more
- Medtronic (Fridley, MN)
- …travel to enhance collaboration and ensure successful completion of projects. The Senior Medical Safety Specialist is responsible for providing medical ... multiple functions including Research and Development, Risk Management, Quality/Post-Market Vigilance, Regulatory , and Clinical. You will apply your medical … more
- Medtronic (Minneapolis, MN)
- …M&T Structural Heart Business is one of the fastest growing businesses in the medical device industry and expanding rapidly to serve patients globally. The ... In this exciting role as a Principal Field Clinical Specialist , you will provide day-to-day field clinical study support,...Serves as a technical resource to support a specific medical product or solution. + All other duties as… more
- Edwards Lifesciences (Minneapolis, MN)
- …difference to patients around the world. As a part of the Field Clinical Specialist team, you will be a critical part of delivering our patient focused innovations, ... inspiring journey. In this role, the identified Field Clinical Specialist will support field clinical cases for a new... will support clinical cases for a pre-commercial phase device - travel will include coverage of local region… more
- Abbott (St. Paul, MN)
- …Stewardship + Experience in restricted substance management (eg, REACH, RoHS) + Medical device manufacturing experience preferred + Must possess critical ... spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues… more
- Fujifilm (St. Paul, MN)
- …+ Comply with all applicable US Food and Drug Administration (US FDA) medical device regulatory requirements, applicable ISO 13485 standard requirements ... in Architecture and Project Management. + At least 5 years of medical device planning experience is required. + Educational Requirements: + Bachelor's degree in… more
- Medtronic (Mounds View, MN)
- … Specialist ** , you will be responsible for supporting the development of medical device labeling for the Structural Heart and Aortic, Peripheral Vascular ... + Ensures that labeling, art, film, and plate proofs meet all medical , legal, and regulatory requirements. + Monitors changes in labeling regulations in the US… more
- Fujifilm (St. Paul, MN)
- …+ Comply with all applicable US Food and Drug Administration (US FDA) medical device regulatory requirements, applicable ISO 13485 standard requirements ... **Position Overview** The Sales Specialist , Diagnostic Oncology, in the Invitro Diagnostics Division,...with Key Accounts and Opinion Leaders within the Liver/Hepatology Medical Oncology community. Manage specific assigned geographic areas and… more
- Medtronic (Minneapolis, MN)
- …relations, medical affairs, compliance, or contract management in the medical device , pharmaceutical, or healthcare industry. **T** **o be considered ... a more connected, compassionate world. **A Day in the Life** The **Physician Relations Specialist ** will serve as a key liaison between the company and its physician… more
- Fujifilm (St. Paul, MN)
- …+ Comply with all applicable US Food and Drug Administration (US FDA) medical device regulatory requirements, applicable ISO 13485 standard requirements ... **Position Overview** The Credit & Collections Specialist is a highly independent role with limited...against COVID-19, absent being granted an accommodation due to medical or sincerely held religious belief or other legally… more
- Fujifilm (St. Paul, MN)
- …+ Comply with all applicable US Food and Drug Administration (US FDA) medical device regulatory requirements, applicable ISO 13485 standard requirements ... + $49,500 variable comp opportunity + Company Car + Medical , Dental, Vision + Life Insurance + 401k +...against COVID-19, absent being granted an accommodation due to medical or sincerely held religious belief or other legally… more