Pharmaceutical Regulatory Affairs Jobs

Clarivate - , MA, United States

solutions. Qualifications and Experience: Master’s Degree in life sciences A minimum of 10 years’ experience in Pharmaceutical Regulatory Affairs/Regulatory Intelligence across major markets (Europe, North

from: linkedin.com - 14 days ago

Charles River Laboratories, Inc. - Wayne, PA, US

as a satisfactory substitute for the specific education and experience listed above. • Certification/Licensure: None. • Other: Knowledge of cGMP and/or regulatory affairs pertaining to the pharmaceutical

from: Charles River Laboratories, Inc. - 4 days ago

Astria Therapeutics, Inc. - Boston, MA, United States

inspection readiness Actively partner with Clinical Development, Clinical Operations, Regulatory Affairs, Nonclinical Development, Pharmaceutical Sciences, Discovery and Translational Sciences and other

from: linkedin.com - 11 days ago

Formulated Solutions - Largo, FL, United States

, an individual must be able to perform each essential duty satisfactorily. accommodations may be made to enable individuals with disabilities to perform the essential functions. years of Regulatory Affairs

from: linkedin.com - 13 days ago

Primary Talent Partners - Round Lake, Illinois

within a pharmaceutical company, CRO, or similar organization. Strong understanding of FDA regulations and regulatory affairs practices related to medicinal products. Primary Talent Partners is an Equal

from: resume-library.com - 3 days ago

EPM Scientific - Boston, MA, United States

degree (e.g., MS, PhD, JD) preferred. Minimum of 10 years of progressive leadership experience in regulatory affairs and quality assurance within the pharmaceutical or biotechnology industry, with a focus

from: linkedin.com - 14 days ago

i-Pharm Consulting - , CA, United States

to a wide range of Pharmaceutical, Medical Device, Biotechnology and Contract Research Organisations (CROs). i-Pharm has specific expertise in Clinical Research, Medical Affairs, Regulatory Affairs

from: linkedin.com - 13 days ago

Bristol Myers Squibb - Princeton, United States

degree (MD, PhD, PharmD, DNP) Minimum 5 years of experience in pharmaceutical industry; prior experience in oncology medical affairs is preferred Demonstrates thorough understanding of medical review

from: jobrxiv.org - 13 days ago

Bayside Solutions - , CA, United States

related field is preferred. 15+ years of pharmaceutical/biotech drug development experience with 5+ years of experience in global CMC regulatory affairs with working experience and content knowledge in CMC

from: linkedin.com - 14 days ago

Bayside Solutions - Santa Clara, CA, United States (+1 location)

related field is preferred. 15+ years of pharmaceutical/biotech drug development experience with 5+ years of experience in global CMC regulatory affairs with working experience and content knowledge in CMC

from: linkedin.com - 14 days ago