Drug Regulatory Affairs Jobs in Watertown, MA

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

from: linkedin.com - 29 days ago

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

from: linkedin.com - 9 days ago

Sobi - Waltham, Massachusetts

Program Leader Clinical Study Manager Medical Director Lead Medical Program Lead Drug Safety Manager and Physician Regulatory Affairs Manager Clinical Pharmacologist Marketing IT QA Patient Access External

from: resume-library.com - 6 days ago

Apnimed - Cambridge, MA, United States

launch First product launch with a company a plus Experience in a small company is a plus Experience and understanding with relevant regulatory and legal policies such as the Drug Supply Chain Security Act

from: linkedin.com - 7 days ago

Beacon Hill Staffing Group - Waltham, MA, United States

, Pharmacovigilance/Drug Safety, Medical Affairs, Supply Chain, Regulatory Affairs and Quality Assurance is a plus Experience with ValGenesis is a plus Practical experience with quality risk management and risk-based

from: linkedin.com - 17 days ago

AstraZeneca - Waltham, Massachusetts, USA

. Minimum Qualifications: Bachelor's degree in a science related field with at least 3 years of Regulatory strategy or related knowledge/experience. A solid knowledge of regulatory affairs within at least

from: Ivyexec.com - 10 days ago

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

from: linkedin.com - 9 days ago

Corbus Pharmaceuticals - Norwood, MA, United States

in Regulatory Affairs Experience in all types of regulatory submissions including but not limited to INDs, NDAs, MAA, Type A-D Meetings with FDA, Scientific Advice Consultations with the CHMP of EMA and MHRA, MAA

from: linkedin.com - 7 days ago

Editas Medicine - Cambridge, Massachusetts

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

from: resume-library.com (+1 source) - 8 days ago

Inozyme Pharma - Boston, MA, United States

of excellence, collaboration, and continuous learning. Qualifications: 1. Advanced degree (Ph.D., Pharm.D., or equivalent) in life sciences or a related field. 2. Minimum of 6 years of regulatory affairs

from: linkedin.com - 17 days ago