Drug Regulatory Affairs Jobs in Norwood, MA
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 - 9 days ago
GQR - Waltham, MA, United States
in computer system validation. Experience with computer systems supporting R&D functions such as Clinical, Pharmacovigilance/Drug Safety, Medical Affairs, Supply Chain, Regulatory Affairs, and Quality Assurance
from: linkedin.com - 8 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 - 8 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 - 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 - 8 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
Register your RESUMEfrom: resume-library.com - 9 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 - 9 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 - 11 days ago
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
from: Pharmadiversityjobboard.com - 9 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 - 18 days ago
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