Masters Degree in Food Technology, Chemistry, Pharmaceutical Chemistry, Forensic Pharmacy, M.Pharm or equivalent from a recognized University. Should have adequate knowledge of English, Hindi, and Computer Proficiency.
To be responsible for Receipt, verification, storage and issuance of laboratory chemicals and glassware. To be responsible for Preparations of volumetric solutions, test solutions, limit test solutions and indicator solutions.
Candidate acquainted of Quality Management System Document like Change control, Deviation and their Investigations, CAPA and Audit Management. This role will focus on ensuring the highest standards of quality throughout the manufacturing process, specifically for active pharmaceutical ingredients
Monitoring for Documents compilation activities for New product filing , Re-Registration, renewals from plant dossier filing , sample requirements etc. Participation in Action plan discussion for queries from different Regulatory agencies and monitoring for submission of data/documents from plant.
To ensure compliance of computerized systems, PLC, SCADA-controlled equipment, and automation systems with regulatory requirements 21 CFR Part 11, EU Annex 11, GAMP 5, etc. by executing validation activities as per approved procedures and maintaining validated states throughout the system lifecycle.
B.Pharm, M.Pharm ; Granulation, Compression, Coating, FBE, Capsule Hard Gelatin and Soft Gelatin, Blister Packing Primary and secondary for Cytotoxic, Sex Hormones