Supervising in-process quality control and managing bulk approvals and finished goods (FG) release. Hands-on experience in instrumental and analytical testing of raw materials (RMs).
Identifying quality-related issues and implementing effective solutions to mitigate them.
Maintaining comprehensive records of quality tests, inspections, and other related activities Leading continuous quality improvement initiatives to enhance overall performance.
Maintaining comprehensive records of quality tests, inspections, and other related activities.
Supervise Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), and plant housekeeping on a daily basis while ensuring proper record maintenance.
Required Skills
Must be excellent in written and spoken English; net savvy and adept at computer skills.
Logical thinking.
Organizing.
Good in communication.
Required Qualification:- B.Pharm/M.Pharm/B.Sc/M.Sc - ChemistrySalary :- Upto 4.00 LPAIf you are interested for this opening please send updated resume on same mail with following details.Total No. of Years Experience :-Current CTC :-Expected CTC :-Notice Period :-