We have the requirement of the following personnel to strengthen our teams(s):
(1) Team Lead (Q&V) - 4-5 years experience in qualification and validation of sterile dosage forms manufacturing facility, equipment, utilities and processes, including sterilization and manufacturing
(2) Team Members (Q&V) - Freshers to 2 years experience in qualification and validation of sterile dosage forms manufacturing facility, equipment, utilities and processes, including sterilization and manufacturing
(3) Team Lead (QA & GMP Compliance) - 4-5 years experience in the QA of sterile dosage forms, including preparation and review of qualification protocols/ reports, GMP reviews/ gap-analysis/ audits, various GMP document reviews.
(4) Team Members (QA & GMP Compliance) - Fresher-2 years experience in the QA of sterile dosage forms, including preparation and review of qualification protocols/ reports, GMP reviews/ gap-analysis/ audits, various GMP document reviews.
Interested candidates, please convey their intent on the following email address:
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