Drug Regulatory Affairs Jobs in Massachusetts
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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
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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
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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
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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
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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
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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
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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
Register your RESUMEfrom: resume-library.com - 11 days ago
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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
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