4-5

Person should know QMS, IPQA, validation, Qualification, Cleaning Validation, Risk Assessment, CSV, regulatory requirements, Market Complain, Vendor Qualification, OOS, OOT, Product Recall, Investigation, Regulatory requirement, audit & response.

M.Sc, M.Pharma, B.Pharma. Working in QC analyzing, Stability. In process. FP. RM sample. Handling instruments like HPLC. GC. FTIR. UV, DR. SSA. etc. versatile In handling SAP. documentation like preparing STPs and review of analytical hard copies and electronic data.

Granulation, Coating, Compression, Bottle Packing Machine Exposure, RMG, FBE, FETTE, Autocoaters /Bottle Packing line with track and trace system. To supervise and monitor day to day activities of processing and holding of drug product as per define and approved procedures for stability batches and commercial batches.

Experience in API Production, Bulk Drug, API Production To be responsible for Batch start up activity, monitoring, calibration of balance and other instruction given by the Superior, Should have exposure in reactors, centrifuges, and a clean room equipped with sound knowledge in cGMP and SOPs.

The individual has experience in handling various analytical techniques such as such as HPLC, GC, CE-SDS, SEC, ELISA, qPCR, DSC, Bioassay, Karl Fischer, UV, LC-MS, Dissolution, Disintegration, X-ray diffraction, etc.

Cliantha Research, a full-service Clinical Research Organization, is a leading provider of Clinical research services, based in Ahmedabad, India.

Face-to-Face meetings with all pharmaceutical companies: technical leaders, Purchase, QA decision makers. Develop and implement strategies to acquire new clients and achieve sales targets.

Sciences or Pharmacy Graduates with 3 to 8 years Experiences in parenteral vial , ampoules, bottles of glass or Plastic through, BFS technology. Candidate worked in production compliances, remediation, and having experiences of managing quality system document

Experience in testing of finished products, LST and stability samples. Preferably worked in FDA Approved organizations. Hands on knowledge of cGMP, GLP, 21 CFR and any other regulatory requirements.