Pharmaceutical Regulatory Affairs Jobs in Philadelphia, PA
Takeda Pharmaceutical - Philadelphia, United States (+1 location)
Affairs CMC team, you will report to the Executive Director and Head, CMC Regulatory Affairs – Pharmaceuticals. How you will contribute: Leads the Early Development Pharmaceuticals GRA CMC regulatory team
from: us.lifeworq.com - Yesterday
EPM Scientific - Philadelphia, PA, United States
We are looking for a Senior Director of Global Regulatory Affairs CMC to join a leading pharmaceutical organization in the Greater Philadelphia area. The Senior Director, Global Regulatory CMC
from: linkedin.com - 4 days ago
Spark Therapeutics - Philadelphia, PA, US
and/or clinical experience; global experience preferred; Prior pharmaceutical experience in neurology (Clinical Development or Medical Affairs), and prior experience in conducting clinical research preferred; gene
from: Spark Therapeutics - More than 30 days ago
CSL Behring - King of Prussia, Pennsylvania
regulatory activities within GRA NA for assigned products throughout development and after commercialization. Be a GRA NA representative for assigned projects to the Global Regulatory Affairs Strategy Team
Register your RESUMEfrom: resume-library.com - 3 days ago
CSL Behring - King of Prussia, Pennsylvania
for pharmaceuticals (e.g. project management, CMC, non-clinical, clinical, Regulatory Affairs). Competencies •The ability to work cross-functionally in a matrix environment is essential. •Excellent communication skills
Register your RESUMEfrom: resume-library.com - 8 days ago
Johnson and Johnson - Spring House, PA
portfolio, as required. * A minimum of a Bachelor's degree is required, preferably in Life Sciences, Business Management, Regulatory Affairs or a related discipline. Advanced degree preferred. * A minimum
from: Johnson and Johnson - 9 days ago
Johnson and Johnson - Spring House, PA
, Regulatory Affairs or a related discipline. Advanced degree preferred. * A minimum of 7 years of industry/business experience is required. * A minimum of 3 years of experience in a Pharmaceutical, MedTech
from: Johnson and Johnson - 9 days ago
Charles River Laboratories, Inc. - Malvern, PA, US
be accepted as a satisfactory substitute for the specific education and experience listed above. • Certification/Licensure: None • Other: Knowledge of cGMPs or regulatory affairs pertaining
from: Charles River Laboratories, Inc. - 20 days ago
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