Drug Regulatory Affairs Jobs in Foster City, CA

Meet - Redwood City, CA, United States

Senior Director, Regulatory Affairs (Generalist) Hybrid Role - 3 Days in Menlo Park, CA Meet is partnering with a late stage pediatric rare disease startup looking for a high-level Regulatory Affairs

from: linkedin.com - 11 days ago

Maze Therapeutics - South San Francisco, CA, United States

and budgets for clinical activities with overall company timelines and goals, in close coordination with project management, CMC, nonclinical development, regulatory affairs, and other stakeholders. Skills

from: linkedin.com - 11 days ago

AbbVie - South San Francisco, California

communication on Regulatory/FDA issues including Public Affairs, Clinical Development, Legal, & others such as Commercial. Interpret FDA/European Medicines Agency (EMA) regulations, guidelines, policy statements

from: resume-library.com - 7 days ago

Meet - Redwood City, CA, United States

the development of innovative drug products. This role requires a strong understanding of global regulations and extensive experience in regulatory affairs within the biotechnology or pharmaceutical industries

from: linkedin.com - 21 days ago

Bayside Solutions - Fremont, 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 - 16 days ago

Abbott Laboratories - Alameda, California

, engineering, or medical fields. Certification is a plus (such as RAC from the Regulatory Affairs Professionals Society.) 2-3 years of experience in regulatory preferred but may consider quality assurance

from: resume-library.com - 6 days ago

Astrix - South San Francisco, CA, United States

, Regulatory Affairs, and Manufacturing. Leading the developability assessment of new candidates, preclinical formulation, preformulation, and discovery pharmaceutics studies including API form selection

from: linkedin.com - 24 days ago

Jazz Pharmaceuticals - Palo Alto, California

subject matter expertise to key internal functions (regulatory, Quality, Clinical, CMC and formulations, Product Quality, Drug safety, Medical affairs) and their external contractors or collaborators

from: resume-library.com - 20 days ago

Ascendis Pharma - Palo Alto, California

with drug-device combination products preferred, but not required · Experience in filing regulatory dossiers including CTAs, IMPDs, INDs required; experience with BLAs/NDAs/MAAs is a plus · Ability to travel

from: resume-library.com (+1 source) - 22 days ago

Ascendis Pharma - Palo Alto, California

viewpoints and perspectives to all aspects of the business, from drug development to marketing. The Manager, Regulatory Affairs will be responsible for supporting and developing global regulatory strategies

from: resume-library.com (+1 source) - 24 days ago