Regulatory affairs jobs in Revere, MA

RA CMC member on Regulatory, Pharmaceutical Development, and Production project teams throughout.. As part of the Global Regulatory Affairs CMC team, you will report to the Senior Director Global..

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..

The Manager, Regulatory Affairs is responsible for supporting the regulatory function and its.. The incumbent functions as the regulatory representative on cross functional teams as well as prepares..

Director, Regulatory Affairs. Permanent. Boston, MA Proclinical is seeking a Director, Regulatory.. In this role, you will have the opportunity to define and implement innovative regulatory strategies to..

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..

Responsibilities. Providing regulatory guidance to cross functional partners, developing global.. Represent Regulatory Affairs on assigned project teams through all phases of product development and..

Role. Regulatory Affairs Associate Want to apply Read all the information about this position below.. Location. Remote Duration. 7 Months Main Responsibilities Provide regulatory input to product lifecycle..

The role. Serves as a strategic regulatory leader for assigned drug development programs and uses.. Manages the planning, preparation, and submission of complex regulatory dossiers in support of project..

Prepares and coordinates the preparation of documentation packages for regulatory CMC submissions.. Responsible for maintenance of regulatory affairs product files to support compliance. Review SOPs and..

Description We're looking for a Manager of Regulatory Affairs , working in Biotechnology Medical Devices.. Works with Regulatory Affairs management to define regulatory strategy and to compile and submit, in a..

They are seeking a Regulatory Affairs Manager (Contractor) who can provide day to day execution for.. Reporting into the Senior Director of Regulatory and Clinical Operations, you will be responsible for..

Posted Date. Aug 28 2024 Job Purpose Ensure the development of appropriate regional regulatory.. Bachelor's degree Experience in Regulatory Affairs within a pharmaceutical organization Experience..

The Senior Director of Regulatory Affairs will play a key role in advancing innovative SASS programs.. Key Job Duties include, but are not limited to. Lead the development and execution of regulatory..

Reporting to the Senior Director of Regulatory Affairs CMC, you will work closely with cross functional.. As the Regulatory CMC lead for these programs, you will have the opportunity to devise and implement..

Job Title. Global Vice President of Regulatory Affairs Please ensure you read the below overview and.. United States (Flexible Remote) Reports to. Chief Medical Officer (CMO) Department. Regulatory Affairs..

Job Title. Global Vice President of Regulatory Affairs Location. United States (Flexible Remote) Reports.. Chief Medical Officer (CMO) Department. Regulatory Affairs Position Type. Full Time, Executive Level..

Senior Director Regulatory Affairs. Confidential Title. Senior Director Regulatory Affairs Structure.. Due to an accelerated growth trajectory, the client is looking for a Senior Director Regulatory Affairs..

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..

The candidate will be responsible for leading the Regulatory Affairs function and will oversee and.. This role involves extensive interaction with regulatory agencies, especially with the FDA, seeking..

Overview. The Associate Director, Regulatory Affairs reports to the Senior Director, Regulatory Affairs.. Key responsibilities. Implement the overall clinical and nonclinical global regulatory strategy across..