- 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
- Bausch + Lomb (St. Paul, MN)
- …change management. + Regional and/or Local - Responsible for pharmaceutical, consumer and medical device regulations in Regional and Local markets. The team ... with commercial leaders to define strategy and execute registrations, provides regulatory intelligence and ensures regulatory compliance. + Provide support… more
- Stryker (Minneapolis, MN)
- …Degree in nursing or clinical required + Minimum of three (3) years; in medical device clinical capacity or cath lab. + Proven understanding of cardiovascular ... The Field Clinical Specialist works using independent judgement, partners with local...device development + Document procedural case observations for regulatory requirements and ongoing continuous improvement + Other duties… 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
- Medtronic (MN)
- …experience in a clinical lab setting, clinical training, field sales/support in medical device , healthcare industry or equivalent experience -OR- + Associate's ... responsible for training and educating our sales and clinical specialist teams in the field of cardiac ablation to...a clinical lab setting, clinical training, field sales/support in medical device , healthcare industry or equivalent experience… more
- Abbott (Maple Grove, MN)
- …for diversity, working mothers, female executives, and scientists. For years, Abbott's medical device businesses have offered technologies that are faster, more ... people in more than 160 countries. Senior Clinical Project Specialist - Structural Heart Job Description Working at Abbott...help people with chronic pain or movement disorders, our medical device technologies are designed to help… 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
- Actalent (Minneapolis, MN)
- … handling. + Understanding of FDA/ISO certified environment. + Knowledge of medical device terminology. + Proficiency in surveillance and documentation review. ... Title: Post Market Surveillance SpecialistJob Description As a Post Market Surveillance Specialist , you will play a crucial role in maintaining complete complaint… 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
- Abbott (Minnetonka, MN)
- …Opportunity** This position works out of our Minnetonka, MN location in the CRM medical device division. We are seeking an experienced, high caliber Material and ... spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues… more