IPCA Labs

Ipca Laboratories Limited Invites experienced, dynamic, and self motivated candidates for Production Department

B.SC, B.Pharm, D. Pharma, with relevant experience in handling instrument i.e HPLC- Dissolution, GC, IR.UV, QC QMS, Material testing

Responsible for monitoring and ensuring quality of products and comply with cGMP standards. Monitoring of critical process parameters, line clearance before batch initiation, verification of RM and equipment. In process sampling for quality check like pH, moisture content, and reaction monitoring.

To Review Qualification Protocol and Reports of Equipment, Instrument, System.To Review Qualification Protocol and Reports of Computer System Validation CSV. Ensuring safe handling of Raw Materials and Packing Materials. Dispensing activity of RM and PM material.

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.

Minimum 1-3 years of relevant experience in operation and supervision of Compression, Granulation & Coating m/c i.e Fette, Glatt,Ganson,Imprinting etc.

B.Pharm/M.Pharm/D.Pharma; Having relevant experience to operate and maintenance of Compression Granulation, Coating m/c. Documentation QMS for Manufacturing Dept. experience in operation and supervision of CAM/ IMA/Blister/ CVC/ Cartonator/ Documentation QMS for Packing Dept.

Knowledge of Production Planning, Co-ordination with Corporate Planning Team for smooth function, Scheduling of Manufacturing, Follow-ups with Inter-Departments for production activity.

Ipca is a fully integrated, rapidly growing Indian pharmaceutical company with a strong thrust on export. Ipca API and Formulation produced at world class manufacturing facilities are approved by leading drug regulatory authorised including the USFDA.