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Job Location | Vadodara |
Education | Not Mentioned |
Salary | Not Disclosed |
Industry | Recruitment Services |
Functional Area | Sales / BD |
EmploymentType | Full-time |
Roles and ResponsibilitiesBasic knowledge of FDA 21 CFR, Orange guide & EUGMP guide.Develop QMS documentations -Quality Manual, SOPs, Risk Management etc.Ensure products are manufactured, tested and released for distribution as per cGMP,Process validation,Training.Desired Candidate ProfileInitial set up of new formulation facility.10+ Years in pharmaceutical formulation manufacturing site.& site catering to US/EU market is must.Should have faced GMP inspections of reputed agencies.Perks and Benefits,
Keyskills :
21 cfrroot cause analysiscontinuous improvement culturesetcateringqmsmanualrisk managementprocess validationgmpcfrvalidationcontinuous improvement facilitationformulationcgmpmanagementriskdistributionkaizenfda