Production

M.Pharm / B.Pharm / M. tech / B. tech / B.E. / B.sc / Diploma / ITI; Tablet, Capsule - Granulation, Compression, Coating, Inspection, Capsule Filling and Wurster coater. HPLC, GC, IR, UV, Dissolution and other QC Equipment, QC Method Validation and Transfer.

Bachelor of Pharmacy; Exposure in Pellets, Hard Gelatin Capsules, Soft Gelatin Capsules & Packing in OSD Formulation Manufacturing. Exposure in Pellets, Hard Gelatin Capsules, Soft Gelatin Capsules, Tablet & Packing

Execute the production planning in Liquid manufacturing block and ensure the production plan achievement as per plan. Responsible to ensure the entry and exit, gowning and personnel hygiene procedures are followed in liquid manufacturing block.

B.Sc / M.Sc / B.Pharma / M.Pharma; Review HPLC methods, chromatograms, and system suitability. Ensure HPLC sequences comply with methods. Prepare and review IQ, OQ, and PQ for new instruments. Conduct pre-investigations for OOS, OOC, OOT, and lab incidents. To perform line clearance, FG Sample withdrawal, Online GMP Monitoring, To Support of Product and Process Validation

Diploma/D. Pharmacy/B. Pharmacy; Operating Granulation, Compression, Coating, Capsule Filling, Blister & Bottle Packing Equipment. Supervising Granulation & Packing Lines. Experience in Autoclave, Filling, Vial Washing, Packing Areas

Manage granulation, compression, coating, pelletization and capsule filling area. Manage bulk bottle, blister packing. Track and Trace, serialization and documentation. Handle machines like CVC, Servo, Countec, CAM, BQS, HONGA & UHLMANN.

Pharmacy PhD / M.Pharm / B.Pharm with experience, in Pharmaceutical Production with FDA / DCA approval.  Responsible for planning, coordination and control of manufacturing process to ensure that the products are produced efficiently, and the correct amount is produced at the right cost and level of quality. Communication, Decision Making ability, Leadership Quality, Analytical Skill, Adaptability, Problems Solving & etc.

Supervision of Micro Section Microbiological Analysis of Raw Material, Finished Product, Water Samples, Stability ad Hold Time study Samples. Review and Verification of Micro documents, Preparation of Protocols and SOP, QMS, Environment Monitoring Media Preparation, GPT Test, Microbial, Limit Test of Finished Product and Raw Material, Water Testing etc. - Calibration and Validation of Microbiological Instruments.

HPLC, GC, Dissolution apparatus and UV Visible Spectrometer. Should also have knowledge of weight analysis, stability studies, for Injectable dosage forms.Also require candidate with experience of Bio Assay QMS and analytical data Review. B.Pharm / M.Pharm. Supervising and Controlling Production areas like Isolator, Aseptic Filling, Vial Washing, Autoclave, Lyophilizer and Visual Inspection. Should have knowledge of QMS activities.