Regulatory affairs specialist jobs in Weymouth, MA

We are seeking an experienced Senior Regulatory Affairs Specialist with a strong background in In Vitro.. Skills Required. In Vitro Diagnostic Regulatory Experience. Expertise navigating regulations specific to..

Position Overview. The role involves leading strategic and operational aspects of Regulatory Affairs and.. Education. BS MS required. PhD or MD preferred. Experience. 15. years in Regulatory Affairs and Quality..

Monitor and evaluate the US regulatory affairs environment to maintain awareness of current and future.. Alternatively for further details or to talk directly to a life sciences recruitment specialist directly..

Hobson Prior is seeking a dedicated Global and US Regulatory Lead to join a dedicated team.. Monitor and evaluate the US regulatory affairs environment to maintain awareness of current and future..

Disc Medicine is seeking a Director, Regulatory Affairs CMC to serve as the Regulatory CMC lead for Disc.. RESPONSIBILITIES. Define and lead the execution of the global regulatory CMC strategy from early..

Bachelor's degree in a relevant life sciences field with at least 8 years of experience in the biopharmaceutical industry, particularly with biologics and regulatory affairs. Experience with..

Executive Director, Regulatory Affairs, Labeling Locations. United States. Massachusetts. Springfield.. Leads a team of labeling operations and compliance specialists. Oversee the development and management..

Are you a seasoned regulatory CMC leader looking for a new challenge? We are seeking a dynamic professional to lead a Global Regulatory Affairs CMC team in a top tier biopharmaceutical company..

Head of Regulatory Affairs. Immunology Oncology Job. 2035146 Job Description. Head of Regulatory Affairs.. This role is for a knowledgeable and experienced Regulatory Affairs professional to lead the development..

Provide overall company leadership and direction for worldwide Tecomet Quality Assurance and Regulatory Affairs Systems, encompassing both improvements and sustaining activities. Objectives..

Senior Manager of Regulatory Affairs and Quality Assurance. (Medical Device). Hybrid in MA Our client is.. As Senior Manager of RAQA you will be hands on with regulatory submissions both domestically and..

They have asked us to assist them in their search for a Director, Regulatory Affairs. Major tasks and.. Supports global regulatory strategy and execution on development programs, including maintaining strong..

Associate Director. Director, Regulatory Operations & Affairs at Treeline Biosciences (View all jobs.. This hands on position will be responsible for overseeing and managing all global regulatory activities..

As a Director, Regulatory Affairs, you will use your expertise to lead and mentor a team of high.. provide invaluable strategic, technical, and regulatory advice to help clients with their various..

Reporting to the CEO the SVP VP Global Regulatory Affairs drives the articulation and implementation of.. S)he is a strategic partner to the CEO on designing, articulating, and shaping global regulatory..

Job Description Regulatory & Scientific Affairs Manager. This position may be based in Decatur, IL.. Harvard, IL. or Fort Collins, COYour ResponsibilitiesReporting to the Global Head Regulatory Affairs..

Ensure that BH Material Subcontractor is compliant with all federal and state agency regulatory.. Fully understands and keeps abreast of changing program regulatory, compliance, accreditation, state..

This strategic leadership position is responsible for managing the Medical Affairs acthities to ensure.. Cross Functional Collaboration. Serve as a key liaison between clinical development, regulatory affairs..

Role Summary The Associate Director, Public Affairs will serve as a critical Policy & Advocacy team.. Serve as approved media specialist related to healthcare policy and various issues on behalf of Servier..