Specialist QA with experience in Pharmaceutical GMP manufacturing.
Functions:
- Product MPs.
- Environmental Characterization reports.
- Sanitary utility systems.
- Represent QA on NPI team.
- Investigations.
- Site audits.
- Risk Assessments.
- Automation activities.
- Facilities and environmental programs.
- Work Orders.
- CAPA
- Change controls.
- Lot disposition and authorize lots for shipment.
Requirements
- Doctorate or Master degree and 3 years of directly related experience or Bachelor degree and 5 years of directly related experience or Associates degree and 10 years of directly related
- Bilingual (Spanish/English)(Written/Spoken)
- Technical writing
- Computer literacy
Doctorate or Master degree and 3 years of directly related experience or Bachelor degree and 5 years of directly related experience or Associates degree and 10 years of directly related Bilingual (Spanish/English)(Written/Spoken) Technical writing Computer literacy