Regulatory affairs jobs in Waltham, 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..

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..

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..

This position will also provide support of the regulatory function through document management.. Works with Regulatory Affairs, Quality Assurance, Quality Control, Manufacturing, Research 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..

This individual will lead Regulatory Strategy, Regulatory Operations, and Regulatory CMC. Success in.. Develop and grow the Regulatory Affairs department in keeping with the needs of the company. coach 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..

Job Description The Associate Director of Regulatory Affairs will be responsible for the development and.. The Associate Director Regulatory Affairs will be responsible for oversight of the operational execution..

This position will also assist the Regulatory CMC team with special projects as assigned. Responsible.. Responsible for implementing regulatory strategies, including filing of all appropriate regulatory..

Requirements. Bachelor's degree in life sciences, pharmacy, or a related field with a minimum of 7 10 years of experience in oncology regulatory affairs within the biopharmaceutical industry..

Position Summary Lead the global Regulatory Affairs (RA) team and provide organizational guidance and.. Delivering strategic and tactical regulatory support to the business and project teams is a crucial..

Job Description Job Description Job Description We have multiple openings for Life Science Quality Assurance Analysts, Regulatory Affairs Specialist, and Quality Control Analysts. All of these..

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..

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 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..