21 Drug Regulatory Affairs Jobs in Massachusetts - page 2
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Director, US Regulatory Affairs, Ad/Promo & Labeling Proclinical Staffing - Cambridge, MA, United States Regulatory Affairs representative, you will work with brand on competitively positioning assigned products appropriately while maintaining compliance with applicable FDA regulations, company policies 19 days ago
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Project Manager, CMC Regulatory Affairs GSK - Waltham, MA ) with managerial support Basic Qualifications: BS in a Life Sciences or related field. Two or more years of experience in Chemistry, Manufacturing and Controls (CMC) regulatory affairs or product development 11 days ago
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Senior Director, CMC HireMinds - Watertown, MA, United States development and manufacturing plans at external partners. Coordinate/author/review drug substance relevant sections of regulatory documents (IND, IMPD, NDA and MAA) Collaborate with the Project Management 22 days ago
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Regulatory Manager BostonGene - Waltham, MA, United States . Provide regulatory support for due diligence activities related to external diagnostic companies. Qualifications PhD and/or MS degree preferred within Regulatory Affairs, Life Sciences, or Engineering. 6 27 days ago
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Pharmaceutical Program Manager The Fountain Group LLC - Cambridge, Massachusetts , Clinical Research, Regulatory, CMC, Marketing or other drug development related function Description: As part of the GMSO Program Management team, you will report to the Strategy & Operations Lead 6 days ago
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VP, Early Clinical Development Astria Therapeutics, Inc. - Boston, MA, United States Development, Clinical Operations, Regulatory Affairs, Nonclinical Development, Pharmaceutical Sciences, Discovery and Translational Sciences and other functions in driving asset and company strategy to fruition 27 days ago
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VP, Regulatory Affairs & Quality Vigil Neuroscience - Watertown, MA, United States the lives of patients and their families. The Vice President, Regulatory Affairs & Quality is in charge of providing subject matter expertise on all matters related to FDA and global regulatory requirements 29 days ago
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Director, Regulatory CMC Editas Medicine - Cambridge, MA and advanced degree preferred with a minimum of 10 years’ experience in drug development/regulatory affairs and a minimum 8 years in CMC regulatory affairs. Experience with both US FDA and EMA with drugs More than 30 days ago
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Senior Director, Global Regulatory Strategy, Therapeutic Area Lead Biogen - Cambridge, Massachusetts, USA Required Skills: 15+ years of experience in drug development and regulatory affairs in the biotechnology or pharmaceutical industry. 5 years of leadership experience in a regulatory affairs management role More than 30 days ago
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Senior Manager, Regulatory Affairs Editas Medicine - Cambridge, MA and advanced degree preferred. Minimum of 7+ years’ experience in drug development and a minimum 4+ years in regulatory affairs. Prior BLA, sBLA, NDA, sNDA, or MAA experience is preferred. Prior IND, CTA More than 30 days ago
Top locations
- Cambridge, MA (12)
- Waltham, MA (6)
- Boston, MA (5)
- Watertown, MA (3)
- Burlington, MA (2)
- Somerville, MA (1)