Posted:2 days ago| Platform:
On-site
Full Time
Education Qualification : B. pharm, M.pharm, Msc. Experience : 3-4 years. Job Description: Reviewing of all documents such as batch records, final release or rejection of every batch products for distribution and sale. Planning and managing all activities of quality assurance to assure quality of all products manufactured by company. Handling the change control systems. Conductance of out of specification investigations. Carrying out investigation of deviations making sure that all critical deviations are investigated and resolved. Conductance of vendor evaluation. Assisting and approval of rejection of out of specifications, out of trend, change control and related areas. To follow reporting system to the executive to head on daily/weekly/monthly basis as per standard procedure. Issuance, archival, and management of quality documents. Observation of overall activity performance during production. Routine GMP auditing of manufacturing process, control, and related areas. Job Type: Full-time Benefits: Leave encashment Provident Fund Schedule: Day shift Education: Bachelor's (Preferred) Experience: Quality assurance: 3 years (Preferred) Work Location: In person
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