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Job description
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.
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Worksite address
san diego, CA, 92189, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.