REGULATORY MEDICAL AFFAIRS PROJECT jobs in UNITED STATES, United Kingdom #2

Job Summary: This manager will serve as liaison between DDG brand holder and HQ regulatory team on the DDG medical...: Communicate with brand holder and HQ regulatory team to write, analyze, and edit technical documents for medical devices...

of One Regulatory Voice for the region on project issues Represent the international markets on the GRST and serve as a core member... between Global and Local, the IRLs lead International Regulatory Teams, educate and communicate Project specific information (follow...

of Regulatory Affairs in project team meetings · Related activities include leading project team meetings, liaising...Description Regulatory Affairs Projects Manager Corporate Statement Nephron Pharmaceuticals Corporation...

Regulatory Affairs for Biologics is responsible for leading a matrix team of professionals, who work with a specific product in... Gilead’s global portfolio of biological products in CMC Regulatory Affairs. This position will provide leadership...

Regulatory Affairs Project Manager Position Summary Catalent Pharma Solutions is hiring a Regulatory Affairs... Project Manager. The Regulatory Affairs Manager is responsible for ensuring that the company aligns with all of the...

Are you a Regulatory Affairs professional seeking a Project Manager opportunity with an innovative and growing Medical... Management and Regulatory Affairs – WE WANT TO MEET YOU! Ventura Solutions is a trusted medical device and pharmaceutical...

Requisition ID: 60142 Title: Sr. Project-Program Manager, Regulatory Affairs Division: Arthrex, Inc. (US01) Location... in orthopedics. Arthrex is actively searching for a Sr. Project Manager, Program Manager - Regulatory Affairs who...

. Position Description As an Associate Specialist in Post-market Regulatory Affairs, plays a crucial role in ensuring... that our medical devices continue to meet regulatory requirements and maintain their safety and effectiveness after they have been...

: Quality Assurance & Regulatory Affairs Manager Location: Charlotte, NC (Onsite Position) Some relocation assistance may... be available Position Summary: Reporting to the Director of Quality Assurance & Regulatory Affairs, The Quality Assurance and Regulatory...

Medical and play a crucial role in revolutionizing medical devices. As a Specialist in Premarket Regulatory Affairs... and understanding of regulatory requirements between project teams and Applied Medical’s global regulatory resources. Performance...

PURPOSE AND SCOPE: Assists in the support of the daily operational activities within Regulatory Operations for the... preparation of regulatory submissions required to market new or existing licensed pharmaceuticals and device products in the...

, exemptions, and changes of protocol) and advise investigators and research coordinators regarding potential ethical, regulatory... committee, subcommittee, or special project groups. This may include research and writing, coordinating meeting schedules...

pipeline and considered for future opportunities. The Director Regulatory Affairs Global Regulatory Lead, Global Regulatory... serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives...

with applicable regulations and policies. Advise project teams on subjects such as premarket regulatory requirements, export... or standards. Prepare responses to customer requests for information, such as product data, written regulatory affairs statements...

We are looking for a Regulatory Affairs Specialist for Food Packaging to join our team in Omaha, Nebraska! As the... Regulatory Affairs Specialist for Food Packaging, reporting to the Sr Regulatory Affairs Specialist, you will identify and manage...

Requirement: 5 years of experience in IVD Regulatory Affairs or Medical Device Regulatory Affairs as a Regulatory Affairs... in IVD Regulatory Affairs or Medical Device Regulatory Affairs as a Regulatory Affairs Specialist, or a related...

more than 35 countries worldwide, with headquarters in Foster City, California. Head of CMC Regulatory Affairs – Small... Molecules KEY RESPONSIBILITIES The Head of CMC Regulatory Affairs – Small Molecules is responsible for Gilead’s global...