Gujarat

Personnel monitoring. Trend analysis and reporting. Sample handling. EM monitoring in aseptic process area including Grade A,B,C and D

The Manager, Regulatory Affairs – CMC is responsible for developing and implementing regulatory strategies related to Chemistry, Manufacturing, and Controls (CMC) for pharmaceutical or biologic products.

Qualification of equipment & Documentation, IPQA, QMS-Ohange Control CAPA, Deviation, Process Validation, Cleaning Validation, APQR, Audit Compliance.

M.Pharm / MSc Medicinal Plants with specialization in the concerned subject. Candidature by scholar who completed his/her regular Ph.D. tenure on campus will not be considered.

Hands on experience of chromatography technique, Protein Purification, Centrifuge and Filtration.

Method development, Method Validation and routine analysis in Orals and Non-orals Formulations.

M.Sc / M.Pharma; Audit facilitating and compliance report preparation. Ensuring Compliance in Production, Warehouse, Engineering facility and QC lab. Daily Plant Round for compliance monitoring.

Responsible for preparation & review of the master documents of sterile manufacturing department and warehouse department for Parenteral facility.

M.Sc / M.Tech. in any branch of Biology or M.Sc. in Natural or Agricultural Sciences from a recognized university, with at least two years of research experience in academia or industry.