Responsible for Review of periodic Validation /Qualification of APIs facility / QC /Micro Lab & water system, HVAC systems.
Responsible for Monitoring & Review of Process Validation, Cleaning Validation of equipment and processes
Shall be Involved in DQ / IQ / OQ /PQ & Re-Qualifications for APIs facility,QC / Micro Lab & Purified water systems.
Responsible for performing Validation of new products ,Preparation of Validation Master Plan and Policy Plan and its tracking and review
Responsible for preparation of Annual Product Quality Reports & quality trends
Responsible for the reviewing of APIs "Manufacturing Batch Production Records & Batch Cleaning Records".
Responsible for self inspections & to check the compliance of API manufacturing facility, Quality control /Microbiology Laboratory ,water system & Quality Control etc. with respect to cGMP & GLP requirement.
Change Control procedures Implication and Impact Assessment related to equipment ,engineering, system / facility.
Salary: Not Disclosed by Recruiter
Industry:Pharma / Biotech / Clinical Research
Functional Area:Production, Manufacturing, Maintenance
Role:Quality Assurance/Quality Control Executive
Employment Type:Permanent Job, Full Time
Desired Candidate Profile
UG:B.Pharma - Pharmacy
PG:M.Pharma - Pharmacy, MS/M.Sc(Science) - Any Specialization
Unichem Laboratories Ltd
Contact Company:Unichem Laboratories Ltd