Gujarat

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. 

Handling in plant specific area in shift, Good skill to handle API production equipment at shop floor along with handling of manpower

Experience In Method Validation, Method Transfer, RM, OC, CLP, Investigation etc. Experience In Documentation, Qualification, Process validation

Planning, Receipt and storage of Packing & Raw materials. Exposure of regulatory audits / SAP. Filling area / Batch Manufacturing / QMS.

Responsible for coordination with various departments like Regulatory Affairs, Manufacturing, Warehouse, Quality Assurance, Quality Control, Engineering for execution of Scale-up and Exhibit batches. 

Emcure is fast-growing Indian pharmaceutical company engaged in developing, manufacturing, and marketing a broad range of pharmaceutical products globally.