2-3

Prepare and review Batch Manufacturing Records BMR and Batch Packaging Records BPR, Master Formula Records MFR.

Handling of batch manufacturing and filling activity with regulatory exposure in Sterile area.

Supervise production lines including Granulation, Compression, Coating, and Packing. Good verbal and written English communication skills.

Quality Control Analyst will play a critical role in ensuring the integrity and safety of our pharmaceutical products. Youll conduct analytical testing on raw materials, in-process samples, and finished goods, adhering to Standard Operating Procedures and current Good Manufacturing Practices

B.Sc./M.Sc./B.Pharm/M.Pharm Chemistry ; Analytical Method Validation RM/PM, SPEC/STP/Protocol & Report Preparation

B.Sc, B.Pharma & M.Sc with relevant experience, Compression, Granulation, Coating, Stability/ FP / HPLC/ CC

Blister & Bottle Packing, Liquid Manufacturing Filling, Sachet filling. Diploma, BSc, B.Pharm, M.Pharm

Experience in granulation, compression, capsule & coating oral liquid manufacturing areas of regulated markets. FDA approved personnel in tablet manufacturing would be preferred.

Line clearance during dispensing of raw material and packing material. QA Verification during dispensing of raw material and packing material.