IT & Software

Senior QA & Validation Specialist (GMP | Veeva QMS)

Jobtailor

San Diego · Canada · United States

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-Ljbffr

Reference: WJ-5385_3299599

Apply now

Continue on the employer's official application - the same link they use for every candidate.

More jobs

This role is listed on GigBlows for discovery and search. Hiring decisions and applications are handled by the employer or their chosen application system.