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| Job Location | Navi Mumbai |
| Education | Not Mentioned |
| Salary | Not Disclosed |
| Industry | Pharma / Biotech |
| Functional Area | uality (QA-QC) |
| EmploymentType | Full-time |
Knowledge of GMP and QMS standardsKnowledge of regulatory affairs proceduresKnowledge of documentationTo Check the in process inspection of semi finished and finished productTo document all the reports.Maintain discipline in controlled areasTo analyze the non conforming product & make the action plan for the same.To audit the process parameters in Clean room & Controlled areasDocumentation as per ISO : 13485, WHO, GMP & CE MarkingHandling, maintaining the documents of market complaintsTo conduct and manage development of packaging materialTo manage the testing of raw material, packing material and finished goodsReview of documents and records
Keyskills :
qmsgmpisoqualityassurancequalitymaintenanceinnavimumbaiforqualityassuranceqainthanequalityauditinmumbaiforqaiso13485qainnavimumbaiqmsstandardqualitytesting