Responsible for managing QMS activities including deviations, change control, CAPA, and OOS/OOT, ensuring timely closure and compliance with GMP and data integrity standards.
CIRO Pharma Private Limited plant at Biotech Park Phase III is aimed at manufacturing of Anti-Cancer Drugs for regulatory markets like the U.S.A, U.K, Europe, Canada, and South America.
Fresher with ITI, Any Diploma/D.Pharm, B.Pharm, M.Pharm, B.Sc-Chemistry, M.Sc-Organic/Analytical Chemistry/ Biochemistry, B.Tech-Biotech, BE/B.Tech Chemical invited for internship
Sciences or Pharmacy Graduates B.Sc./M.Sc./B. Pharm./M. Pharm. with 1 to 5 years Experiences in any of QA function Validation / IPQA / QMS / Compliance / DQA / Lab QA of a formulation - Sterile / non Sterile dosage forms. Aculife Healthcare