Regulatory affairs associate jobs in Boston, MA

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..

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

Manages the planning, preparation, and submission of regulatory dossiers in support of project goals.. Serves as the Regional Regulatory Lead (RRL) for assigned drug development programs. Leads cross..

Syndax Pharmaceuticals is looking for an Associate Director, Regulatory Affairs Learn more about the.. The Role. Syndax has an exciting new opportunity for an Associate Director, Regulatory Affairs..

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..

We're looking for an Associate Director of Regulatory Affairs , working in the Pharmaceuticals and.. Provides strategic regulatory leadership to project teams in early and late stage clinical development..

Associate Director, Regulatory Affairs CMC Dyne Therapeutics is a clinical stage muscle disease company.. www.dyne tx.com , and follow us on X, LinkedIn, and Facebook. Role Summary. The Associate Director..

We are seeking an Associate Director Director of Regulatory Affairs to join the company. This candidate.. This role will lead US submission work. Your role. You will provide regulatory expertise for product..

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..

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..

Important for this role are a working knowledge and appreciation of research and development strategies and processes, laboratory operations, lab regulatory requirements, budgeting, and resource..

Position Summary The Associate Director of Global Regulatory Affairs Chemistry, Manufacturing, and.. Define and lead the development of high quality regulatory submissions. Manage, track, and assure..

You will play a pivotal role in shaping and executing regulatory strategies for medical device software.. Requirements. Bachelor's degree or higher in Science, Engineering, Regulatory Affairs, or a related..

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..

Working towards a mission to make the world a healthier place. Due to an exciting growth trajectory, they are looking for a Senior Director Regulatory Affairs to join the leadership team at this..

Title. Executive Director Regulatory Affairs Location. Waltham, MA Position Overview. Our Medical Device.. This position demands a hands on Regulatory Executive who possesses strong business acumen, outstanding..

This role is considered Hybrid. Responsibilities. The Associate Director, Regulatory Affairs CMC is.. The Associate Director is a key member of multidisciplinary teams responsible for preparation of high..

As the Clinical Regulatory Affairs Specialist, you will play a critical role in managing essential.. You will ensure the success of clinical trials by overseeing the submission of regulatory packages..

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..

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..