Drug Regulatory Affairs Jobs in Massachusetts

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 - 10 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 - 10 days ago

Pfizer - Cambridge, Massachusetts

potential of our existing and future commercially available medicines. + The role will partner closely with Pfizer Oncology stakeholder groups (including Research, Early and Late Development, Regulatory

from: HealtheCareers.com - 10 days ago

Mantell Associates - Boston, MA, United States

sciences or a related field Minimum of 6 years of regulatory affairs experience in the biopharmaceutical industry, with a focus on rare diseases/oncology and orphan drug development Proven track record

from: linkedin.com - 11 days ago

MapLight Therapeutics, Inc. - Burlington, MA, United States

, in vivo physiology, and spatial transcriptomics to identify novel drug targets and develop effective therapies to address psychiatric symptoms. What You’ll Do: Reporting to the VP, Regulatory Affairs

from: linkedin.com - 13 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 - 3 days ago

MapLight Therapeutics, Inc. - Burlington, MA, United States

Collaborate with CMC, Program & Portfolio Management, Clinical, and Regulatory Affairs to develop program-specific strategies for appropriate data generation in support of development candidate nomination, IND

from: linkedin.com - 16 days ago

Cellarity - Somerville, MA, United States

development, medical affairs, new product planning, regulatory affairs, and corporate communications. Represent drug substance holistically internally and externally as needed. Activities include due diligence

from: linkedin.com - 19 days ago

Editas Medicine - Cambridge, Massachusetts

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

from: resume-library.com - 11 days ago

ONO PHARMA USA - Cambridge, MA, United States

and management experience in the PV, Regulatory Affairs department of an established United States-based pharmaceutical company, having worked directly with the Food and Drug Administration (FDA) to successfully

from: linkedin.com - 20 days ago