5+

B.Pharm / M. Sc; Handling the Lab instruments of HPLC, Dissolution, D. T., Apparatus, Weighting Balance, Friability, Hardness Tester, FTIR, UV-Spectrophotometer. Analysis of Raw Material, In-process, Finish Products, Stability Tastings, Process Validation, Participate in Lab incident/OOS/OOT/Analytical Deviation.

Candidate should have strong understanding of OSD manufacturing processes and knowledge of cGMP and relevant regulatory requirements. Monitoring critical process parameters during manufacturing. Candidate should have sound knowledge of QMS - Incidents, Change control, Deviations etc. Should be able to handle the team of 8-10 persons

Planning and performance of Validation, Verification of analytical methods as per the relevant procedures, protocols. Experience in Handling of GC, HPLC, IC, UV instruments with Lab solutions, Empower, Chromelon, Magic net software and experience on LIMS.

Compression, Coating, Capsule Filling, FBP. QC Microbiology, IP/FP, Stability, GLP,RM. QA IPQA, AQA, APQR.

Qualified to degree level in biosciences or an equivalent healthcare or pharmaceutical industry background, with proven competency in patient safety pharmacovigilance/clinical development.

PhD, MS, BS in relevant functions in the Pharmaceutical, Biotechnology Industry, or equivalent. Subject matter expertise in regulatory affairs and related activities.

Familiarity with high-performance organizational tools and a strong understanding of digital manufacturing processes, computer system validation requirements, and quality management within biologics production and quality.

Glenmark Pharmaceuticals Limited is a research‐led, global pharmaceutical company, having a presence across branded, generics, and OTC segments; with a focus in the therapy areas of Respiratory, Dermatology and Oncology.

Experience in production planning, change control, line clearance, deviation handling, autoclave operation TS and component, aseptic & controlarea operation, documentation, both SVP and LVP manufacturing etc.