Drug Regulatory Affairs Jobs in Palo Alto, CA
Jazz Pharmaceuticals - Palo Alto, California
to clinical site(s) Contribute to CTSM budget and forecasting; track invoices to contracts Provide to Regulatory Affairs any applicable information or sections of IND/IMPD/CTA/etc. submissions Knowledge
Register your RESUMEfrom: resume-library.com - 13 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
Register your RESUMEfrom: resume-library.com (+1 source) - 23 days ago
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
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
Register your RESUMEfrom: resume-library.com (+1 source) - 26 days ago
Sonoma Biotherapeutics - South San Francisco, CA, United States
of potential partnering and lifecycle options. The Sr Medical Director shares medical expertise with his/her counterparts in other functional areas (e.g. regulatory affairs, research, drug safety, clinical
from: linkedin.com - 8 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 - 8 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
Register your RESUMEfrom: resume-library.com - 6 days ago
Integrated Resources, Inc ( IRI ) - Newark, CA, United States
, and will be interacting with cross-functional groups such as Quality Control, Manufacturing and Regulatory Affairs. ESSENTIAL DUTIES: • Perform a wide variety of quality assurance activities to ensure compliance
from: linkedin.com - 16 days ago
Harvey Nash - Newark, CA, United States
, such as batch record and quality control data review, line clearances, AQL inspection, and will be interacting with cross-functional groups such as Quality Control, Manufacturing and Regulatory Affairs. ESSENTIAL
from: linkedin.com - 16 days ago
Pfizer - San Francisco, California
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 - 18 days ago
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