M.Pharm, B.Pharm, M.Sc ; Exposure to method validation, method transfer on various QC instruments LCMS, HPLC, GC, Dissolution, Malvern 3000 etc. Familiarity with protocol, report preparation.
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.
This non-supervisory role in the Reference Standard Laboratory involves performing necessary project tests and maintaining a GLP-compliant environment. The incumbent leverages their technical expertise and pharmaceutical analysis knowledge to conduct collaborative testing and ensure efficient and effective laboratory operations.
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
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