Regulatory Affairs Manager II Post Market - Bedford, Massachusetts, United States

The purpose of the internship is to provide meaningful professional hands-on experience to students with leadership potential and proven academic performance. · ...

The purpose of the internship is to provide meaningful professional hands-on experience to students with leadership potential and proven academic performance. · To perform entry level work of a routine nature requiring application of standard techniques, procedures and criteria i ...

We are a worldwide leader in specialized diagnostics in the areas of Hemostasis, Acute Care Diagnostics, Transfusion, Autoimmunity and Transplant.The purpose of the internship is to provide meaningful professional hands-on experience to students with leadership potential and prov ...

Perform failure analysis on explanted biomedical implant product. Provide technical expertise to the Product Analysis Laboratory. · ...

Perform failure analysis on explanted biomedical implant product. · Perform failure analysis on explanted long-term biomedical implant product. · Work requires the application of theoretical principals, evaluation, ingenuity, and creative/analytical techniques to identify route c ...

The purpose of the internship is to provide meaningful professional hands-on experience to students with leadership potential and proven academic performance. Werfen hires students majoring in Engineering and Life Sciences fields into this internship program based on business nee ...

The Regulatory Affairs Manager II leads the company's post-market regulatory program to ensure global compliance for commercialized IL-labeled medical devices. · ...

The Regulatory Affairs Manager II leads the company's post-market regulatory program to ensure global compliance for commercialized IL-labeled medical devices and manages a team of regulatory professionals in this endeavor. · ...

The purpose of the internship is to provide meaningful professional hands-on experience to students with leadership potential and proven academic performance. · We expect the intern to gain an in-depth knowledge of the product and its associated processes, particularly the proces ...

The Regulatory Affairs Manager II leads the company's post-market regulatory program to ensure global compliance for commercialized IL-labeled medical devices and manages a team of regulatory professionals in this endeavor. · ...

The Regulatory Affairs Manager II leads the company's post‑market regulatory program to ensure global compliance for commercialized IL-labeled medical devices and manages a team of regulatory professionals in this endeavor. · ...

The Post Market Engineering Team Lead plays an integral part of Insulet's Quality Department as a hands-on technical leader conducting post market investigations of FDA approved medical devices. · ...

The Post Market Engineering Team Lead plays an integral part of Insulet's Quality Department as a hands-on technical leader conducting post market investigations of FDA approved medical devices. · Responsibilities · Provide work leadership/mentorship to team members... · ...

Maintain Post Market Surveillance documentation in accordance with procedures and Regulatory requirements to stand on its own in the event of an audit. Complete and submit documentation for reportable events to Competent Authorities within required timelines. · ...

We are searching for the best talent for Post Market Clinical Review SpecialistCollaborate with post market complaint operations · & regulatory review teams to ensure coding guidelines are adhered to. · ...

The Clinical Review Specialist will serve as clinical expert for the complaint intake review process providing clinical rationale linking patient clinical presentation procedural events and product interaction. · * Minimum of 5 years cardiology experience* Demonstrate effective c ...

Join us in pioneering breakthroughs in healthcare. For everyone. Everywhere. Sustainably. · ...

We are seeking a Post Market Quality Engineer III to manage end-to-end post-market surveillance activities for assigned products. · Owns and manages complex complaints. · Executes technical investigations using logs. · Fulfills global vigilance reporting requirements. · ...

We are searching for the best talent for Post Market Clinical Review Specialist. The Clinical Review Specialist will serve as clinical expert for the complaint intake review process. · Collaborate with the post market complaint operations and regulatory review teams to ensure cod ...

The Clinical Review Specialist will serve as clinical expert for the complaint intake review process. They will provide clinical rationale linking patient clinical presentation, procedural events, and product interaction. · Minimum of 5 years cardiology experience · Demonstrate e ...