3-4

Identify serious adverse events and special scenarios. Indegene help biopharmaceutical, emerging biotech and medical device companies develop products, get them to the market, and grow their impact through the life cycle in a more effective, efficient, and modern way.

Having Injectable Experience of Analytical Method Validation for Assay, Related Substances Content by HPLC and Residual Solvents by CC, Preparation and Review of Method Validation and Method Equivalency and Method Transfer Protocols and Reports.

Supervise production lines, including Granulation, Compression, Coating, and Packing. Good verbal and written English communication skills

To perform Gap analysis of defined procedures in Batch Manufacturing Record / Batch Packing Record / Standard Operating Procedure / Protocol and initiation of corrective actions. 

Hands on Experience on, Stability Studies, Analytical Method Validation & Finished Goods.

Experience in review of HPLC, GC, LCMS calibration data & Analytical Data review &Review of Analytical Method Validations, Method Transfers, Protocols & Reports.

Able to perform Biochemical techniques, Chromatography techniques, Electrophoresis techniques, Immuno assay techniques, Cell culture techniques and Molecular techniques

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.

QMS Activities, Deviation, Change Control, Market Compliance, IPQA, Review of BMR & BPR, Lab QA, Exposure in OSD & Sterile