Regulatory cmc in Medford, MA

Consumer Compliance Senior Internal Audit Associate Boston, United States of America The primary function of the...

Job Description General Summary: The Director, Regulatory CMC (Chemistry Manufacturing Controls) is responsible for the development and implementation of post-approval global regulatory CMC strategies for a marketed cell and gene therapy...

Job Description General Summary: The Director, Regulatory CMC (Chemistry Manufacturing Controls) leads a cell therapy combination product program from development through commercialization through the execution of global regulatory CMC...

About the role: At Takeda, we are a forward-looking, world-class R&D organization that unlocks innovation and delivers transformative therapies to patients. By focusing R&D efforts on four therapeutic areas and other targeted...

Innova Solutions is immediately hiring for a Regulatory Affairs Manager III Position: Type: Full Time, Contract Duration: 06 Months (Possibility to...

About the role: At Takeda, we are a forward-looking, world-class R&D organization that unlocks innovation and delivers transformative therapies to patients. By focusing R&D efforts on four therapeutic areas and other targeted...

Pioneering trusted medical solutions to improve the lives we touch: Convatec is a global medical products and technologies company, focused on solutions for the management of chronic conditions, with leading positions in advanced wound care,...

GENERAL SUMMARY/ OVERVIEW STATEMENT: The IACUC Regulatory Compliance Specialist has the overall responsibility for ensuring regulatory compliance within the areas of the animal care and use program that fall under the responsibility of the...

Company Overview Since its inception over a decade ago,CRISPR Therapeuticshas transformed from a research-stage company advancing programs in the field of gene editing, to a company with a diverse portfolio of product candidates...

Site Name: Cambridge 300 Technology Square, GSK House, Stevenage, Upper Merion, USA - Maryland - Rockville, USA - North Carolina - Durham Posted Date: Apr 22 2024 Are you looking for a role where you will serve as a key strategic...

About the role: At Takeda, we are a forward-looking, world-class R&D organization that unlocks innovation and delivers transformative therapies to patients. By focusing R&D efforts on four therapeutic areas and...

Job Description Overview: Great Science. Deep Compassion. Real Impact. Alkermes is offering exciting opportunities through our commitment to work together to help improve the lives of people...

Pharvaris is a late-stage biotech company developing bradykinin B2 receptor antagonists for bradykinin-mediated diseases, with offices in Switzerland (Zug), the Netherlands (Leiden) and the USA (greater Boston area). We aim at bringing new, more...

Become a member of the BioNTech Family! Based in Cambridge, MA and Gaithersburg, MD. We are committed to improving the health of people worldwide with our fundamental research and our work in the area of development of immunotherapies...

We are currently seeking a Global Regulatory Affairs Lead (GRL) who will be the fully accountable decision maker for the development & execution of creative, thoughtful, and robust global regulatory strategies for their products in Sanofis...

Job Title: Quality and Regulatory Project Manager Gabriele & Company, recruiters for manufacturing and supply chain professionals, is assisting a globally renowned, small medical device company whose...

Mass General Brigham Health Plan is an exciting place to be within the healthcare industry. As a member of Mass General Brigham, we are on the forefront of transformation with one of the world's leading integrated healthcare systems. Together, we...

**Mgr Regulatory Affairs - req1193** **OVERVIEW** Responsible for pre-market and post-market activities as assigned by the Director, Regulatory Affairs to include new product planning and remedial actions on released...

Apply now and our proprietary system will quickly have you in front of a live recruiter. The Opportunity Description We're looking for a Manager of Regulatory Affairs, working in Biotechnology/Medical Devices...

Who We Are: Xenon Pharmaceuticals (NASDAQ:XENE) is a neuroscience-focused biopharmaceutical company committed to discovering, developing, and commercializing innovative therapeutics to improve the lives of people living with neurological and...

Overview: Be Seen and Heard at EyePoint Pharmaceuticals ...

Great that you're thinking about a career with BSI! About the role: BSI America Professional Services Inc. (BSI) is hiring a Health, Safety and Environmental Technician/Specialist to support the EHS department at a client site in the...

Manager/Senior Manager, CMC, Drug Product Manager/Senior Manager, CMC, Drug Product 2013639 Location:Boston, MA(Hybrid) Therapeutic Areas: Undisclosed Job Overview: Seeking a...

Recent Pharma/ CRO experience required Regulatory Operations Contractor Regulatory Affairs Location(Boston) Contract Term: Contract...

Regulatory Labeling Strategy 100 % Remote - must work EST hours Max PR: $165 an hour Provides regulatory expertise and guidance to Clinical, Pharmacovigilance,...

Responsibilities: Prepares regulatory strategies and maintains submissions for U.S. and International markets, including but not limited to 510(k)s and Technical Files, to ensure timely approval of devices and continued...

CMC Process Development Consultant 2023623 Location: Greater Boston, MA (Hybrid) Therapeutic Area: Oncology Job Overview: In this role, the main focus will be on managing CMC processes,...

Responsibilities: ...

Why Join Us? Be a hero for our rare disease patients At Ultragenyx, we fundamentally believe that taking real impactful action to care for the needs of patients and our people is always the right thing to do. To achieve...

Director of Policy & Regulatory Affairs | Eastern US, REMOTE |$165k - $175k base + bonus Are you a regulatory affairs and energy policy professional with experience in the RTOs (PJM), FERC and...