Regulatory Affairs - Centennial

The Regulatory Affairs Specialist assists the RA team to compile and submit necessary information for domestic and international registration of products marketed by CONMED. · ...

The Senior Regulatory Affairs Specialist plays a critical role in ensuring regulatory compliance and supporting cross-functional teams in the preparation submission and tracking of regulatory documentation. · This is an onsite role based in DENVER, US.Assist in executing product ...

Change people's lives and love what you do Cochlear is the most recognized brand in hearing health care. · Senior Regulatory Affairs Specialist · Position Spotlight: · What you'll need: Minimum 5+ years of regulatory experience and a strong background in FDA submission writing · ...

The Senior Regulatory Affairs Specialist contributes to achieving Cochlear's business outcomes by providing regulatory support and guidance to help bring innovative products to customers. · The role will work closely with colleagues based at the legal manufacturers and colleagues ...

Healing lives through bone repair – this mission is what inspires us every day. · Medical, vision, and dental insurance · ...

Cerapedics is a global commercial-stage ortho-biologics company transforming standard of care for bone repair healing bones faster at higher rates without compromising safety so patients can live their healthiest life. · Develop author assemble publish and submit IDE Annual Repor ...

Overview · We are seeking an experienced Director of Regulatory Affairs to lead global regulatory strategy, governance, and compliance for a diverse portfolio of medical devices. This role focuses on defining long‑term regulatory direction, ensuring organizational readiness for e ...

Overview · We are seeking an experienced · Director of Regulatory Affairs · to lead global regulatory strategy, governance, and compliance for a diverse portfolio of medical devices. This role focuses on defining long‑term regulatory direction, ensuring organizational readiness f ...

We are committed to creating an environment where every team member feels inspired, invested, cared for valued and have a strong sense of belonging.Zimmer Biomet is hiring a Sr Regulatory Affairs Specialist in Englewood Colorado to support Paragon 28 product lifecycle management ...

· ABOUT US · Cerapedics is a global, commercial-stage ortho-biologics company that aspires to transform the standard of care for bone repair, healing bones faster and at higher rates, without compromising safety, so that patients can live their healthiest life. Bone grafts, inc ...

: · ABOUT US · Cerapedics is a global, commercial-stage ortho-biologics company that aspires to transform the standard of care for bone repair, healing bones faster and at higher rates, without compromising safety, so that patients can live their healthiest life. Bone grafts, in ...

· ABOUT US   · Cerapedics is a global, commercial-stage ortho-biologics company that aspires to transform the standard of care for bone repair, healing bones faster and at higher rates, without compromising safety, so that patients can live their healthiest life. Bone grafts, in ...

We anticipate the application window for this opening will close on - 31 Jan 2026At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. · You'll lead with purpose, breaking down barriers to innovat ...

HepQuant is seeking a dedicated and motivated individual to be responsible for development, implementation, and execution of strategies for regulatory approvals to introduce new and modified products to market. · ...

This role is part of the Legal Team and supports the organization's regulatory change management process by monitoring federal and state regulatory developments, assessing potential impacts, and assisting in the development of strategies to ensure compliance. · Support the intake ...

Healing lives through bone repair – this mission inspires us every day. If that is inspiring to you as well, consider joining us as a Regulatory Affairs Manager. · ...

We are seeking a Regulatory Affairs Manager to assist with managing and executing the activities of Regulatory Affairs. As a Regulatory Affairs Manager working on the Regulatory Affairs team, you will be empowered through meaningful work and career development to coordinate close ...

As the Director of Regulatory Affairs, you are a critical leader and the ultimate regulatory authority within the Acute Care & Monitoring (ACM) operating unit for the product portfolio within your scope. · ...

Judi Health is an enterprise health technology company providing a comprehensive suite of solutions for employers and health plans,Solutions for self-insured employers, · Full-service pharmacy benefit management (PBM) · We're rebuilding trust in healthcare in the U.S. by deployin ...

We anticipate the application window for this opening will close on - 31 Jan 2026. At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. · You'll lead with purpose, breaking down barriers to innov ...