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
Ciron has carved a niche for itself in the sphere of operations of manufacturing Ampoules, Vials, Eye / Ear / Nasal drops, Lyophilized products and Lyophilized bulk
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.
M.Pharm, M.Sc ; Manage the R&D projects with Internal stakeholders & partners from project Kick off to dossier filing. Job role and provide all the critical activities to be performed, prepare micro plan for very major milestone based on project plan and ensure timely.
M.Pharm / Ph.D ; Candidates having 3 to 8 years experience in Product development of Solid Orals, Onco OSD, Liquid Orals and Sterile formulations. Markets handled : Regulated / ROW / Domestic.