3-4

Executed end-to-end project management for new product development from project initiation through to filing of the dossier, liaising with cross functional teams to respond to deficiencies and receipt of approval from the regulatory agency.

Experience in routine Analysis, Analytical Method Development as well as Characterization for different products of Orals, Injectables, Peptides, other dosage form and Active Pharmaceutical Ingredients

Established in 2016, ANNORA Pharma is committed to provide medicines with highest quality, safety and efficacy that meets the needs of the customers with applicable statutory and regulatory requirements.

Coordinate for timely vendor payments. Ensure compliance with procurement policies and procedures. Assist in contract negotiations and maintain vendor relationships.

M. Pharm with 10 years of experience in handling ADME assays and HPLC and LCMS, MS Or Fresh Ph.D. in similar disciplines

To perform line clearance activity before starting of different operations like dispensing, manufacturing, filling, inspection, sealing, labeling & packing.

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.