Specialist QA
On-siteJuncos, Juncos, Puerto Rico
EXPIREDJuncos, Juncos, Puerto RicoOn-siteContractDoctorate Or Professional DegreeSmall
ContractDoctorate Or Professional DegreeSmall
Job Summary
Manage quality organization activities including deviations, validation reports, qualifications, and investigations within a highly regulated biopharmaceutical environment. Lead technical writing efforts while ensuring compliance with industry standards. Requires a Doctorate or Masters degree with at least two years of directly related experience, or a Bachelor's degree with four years, alongside bilingual Spanish and English proficiency. Full-time position with competitive compensation.
Required Qualifications
- Quality Professional
- experienced working in biopharmaceutical industry
- quality organization supporting deviations
- validation reports
- qualifications
- investigations
- at least 5 years of experienced in a highly regulated environment
- Doctorate or Masters + 2 years of directly related experience
- Bachelors + 4 years of directly related experience
- Associates + 8 years of directly related experience
- Bilingual (Spanish/English)
- Technical Writing
Hiring someone like this?
Get your role in front of qualified candidates on Sorce.