B.Pharm

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.

Performing post-submission processing activities such as receiving acknowledgment from authority of submission receipt; capturing and the electronic receipt and metadata in RIM; communicating submission receipt to key stakeholders

M.Pharm, B.Pharm, M.Sc, B.Sc ; Must have experience in Granulation & Coating, Review BMR & BPR and follow QMS.

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, B.Pharm, M.Sc, B.Sc ; QMS, Manufacturing, Ampoule Washing, Visual Inspection, Autoclave, Lyo, Filling & Sealing, Terminal Sterilization.

Responsible for the quality of the multichannel digital content delivered to customers. Partner with all teams to understand and implement systemic controls wherever possible, across the software supply chain, from design till release. Explore and adopt quality improvement tools or methodologies.

Graduation or Post Graduation in Science - Preferably Pharmacy At least 5 years ideally experience in the Pharmaceutical or related industry, ideally with a mix of Manufacturing, QA operations, Distribution Warehouse management and Regulatory Affairs

M.Pharm, B.Pharm, M.Sc, B.Sc ; Labelling & Filling Operator | Lyophilized | Autoclave | Vial Sealing | Filling Activities | Compounding | PFS | ALUS | Ophthalmic | Cartridge | Growing Ophthalmic