Primary Responsibilities: Exposure for documentation of tablets, capsules, Liquid/Cream dosage form. Preparation and review of Process Validation Protocols and report. Preparation and review of Cleaning Validation Protocols and report. preparation and Review of Change Control / Deviation /CAPA. Actively Participate in Investigation of OOS / Batch Failure and Documentation for investigation. Handling of QMS related documents for its effective implementation. Enhancing Quality related trainings across the Organization. Making sure that manufacturing or production processes meet international and national standards. Maintaining controls and documentation procedures. Investigate and Documentation customer complaints regarding product performance, specifications, and reliability. Perform internal audits of the analytical laboratories and Quality Assurance systems as well as in-phase audits of GLP studies. Preparation / Review of APQR. Participating in self-inspections and regulatory inspections and Response Preparation Risk identification and Assessment. Handling of Equipment / Instrument - Qualification Document preparation. Writing/reviewing of Standard Operating Procedures (SOPs) as per regulatory requirement.Desired Skills, Qualifications & Experience: B.Pharm, M.Pharm. 2-4 years of experience.Job Types: Full-time, Regular / PermanentSalary: ?10,000.00 - ?15,000.00 per monthJadwal:
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