Travere Therapeutics seeks a Quality Assurance/Validation professional to monitor and advance technical documentation within cGMP frameworks. You will engage with cross-functional teams and leverage Veeva QMS for protocols and reports, ensuring compliance across manufacturing and analytical activities.
The role requires 5+ years in GMP QA, strong technical writing skills, and the ability to travel up to 10% domestically and internationally. Onsite work in San Diego is expected.
#J-18808-LjbffrSenior QA & Validation Specialist (GMP | Veeva QMS) in san diego at Unknown Company
This position is listed as full time and onsite.