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Regulatory affairs Jobs in Grand Prairie, TX
- Promoted
Senior Manager Regulatory Affairs CMC
VirtualVocationsArlington, Texas, United States- Promoted
- New!
ANALYST II, FACULTY AFFAIRS
Texas Tech University Health Sciences CenterTX, United States- Promoted
Director, AbilityOne Regulatory Compliance - Hybrid
SourceAmericaArlington, TX, United States- Promoted
- New!
NURSING ASSOCIATE DEAN, ACADEMIC AFFAIRS - HOUSTON
Adtalem Global Education IncTX, United StatesNorth American Regulatory Expert
Celanese CorporationIrving, United StatesDirector of Chemical, Environmental and Biological Regulatory Affairs
AgilentTX, US- Promoted
Regulatory Compliance Analyst
Lockheed Martin CorporationGrand Prairie, TX, United StatesManager, Regulatory Compliance - Gas
Liberty UtilitiesHayhurst, TX, US,- Promoted
- New!
FACULTY AFFAIRS MANAGER
University of Texas at AustinTX, United States- Promoted
Legal / Regulatory Counsel Sr.
United Global TechnologiesAustin, Texas Metropolitan Area, United States- Promoted
BA - Risk & Regulatory Reporting
Newt GlobalIrving, TX, United StatesRegulatory Affairs and Compliance Specialist
Suvida Healthcare LLCDallas, Texas, United States, 75208Regulatory & Environmental Advisor
PetroplanTexasRegulatory Affairs Intern
Veolia Water Technologies & SolutionsArlington, TX, USDirector, Regulatory Affairs – Texas / ERCOT
Invenergy LLCTX, USRegulatory Risk Officer-Hybrid
00002 Citibank, N.A.Irving Texas United StatesMedical Director (Medical Affairs)
CVS HealthTexas, Work At Home, US- Promoted
Regulatory Project Manager
JCW GroupDallas County, TX, United StatesRegulatory and Quality Manager
AmerisourceBergen Services CorporationGrand Prairie, TXSenior Manager Regulatory Affairs CMC
VirtualVocationsArlington, Texas, United States- Full-time
A company is looking for a Senior Manager / Associate Director in Regulatory Affairs CMC.Key ResponsibilitiesContribute regulatory CMC expertise to product development and registration for small molecule investigational productsOversee the preparation and review of CMC documents for regulatory submissions, ensuring compliance and timely deliveryCollaborate with cross-functional teams and external vendors to support regulatory milestones and strategiesRequired Qualifications, Training, and EducationBS / BA degree in a scientific or health sciences discipline5+ years of experience in CMC Regulatory AffairsExperience in rare disease is a plusFamiliarity with Veeva RIM or similar document management systemsProven ability to manage timelines and processes for CMC submissions