IPCA Labs

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.

Responsible for guiding and coaching employees, monitoring their productivity, and overseeing regular equipment safety and maintenance. Responsible for performing batch execution in Sterile Injectable lines manufacturing and packaging.

Ipca is a fully integrated, rapidly growing Indian pharmaceutical company with a strong thrust on export.

Candidate should have Exposure of Fette, Sejong, Legacy, Korsch, Cadmach or any other machine having Automatic Weight Control , Compaction Force Control, Handling of QMS Work

Can handle instrument i.e HPLC- Dissolution 3C, IR,UV, QC QMS, Material testing xposure on EM, water testing, MLT testing of FP and RM/Stability samples , Analysis and review of Micro samples, reports.