IPCA Labs

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. 

fresher B.Pharm / M.Pharm / M.Sc/B.SC; To perform IPQA, APQR, Market Complaints activities. Review of BMR, BPR, CAPA, QMS, OOS. Can handle instrument i.e HPLC- Dissolution.GC, IR.UV, QC QMS, Material testing. Candidates must be open to work in shift duties and having pharma experience in regulated plant like USFDA, MHRA should apply.

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

Minimum 1-6 years of relevant experience in operation and supervision of CAM, IMA, Blister, CVC, Cartonator, Documentation QMS for Packing Dept

Craft and maintain BPCRs and SOPs with precision, Lead documentation management using EDMS to uphold data integrity and compliance, Drive training and compliance efforts through our LMS, Ensure all production documentation aligns with regulatory standards and internal policies.

Production QMS Quality Management System Handling of QMS activities like Deviation, Incident, Investigation, CCP, Protocol Preparation, Risk Assessment etc.

Handling of QMS activities like Deviation, Incident, Investigation, CCP, Protocol Preparation, Risk Assessment etc.

Experience of QC analytical, LIMS software handling, Master preparation in LIMS, preferably ONE Lab and Labware. Candidates may also apply who has good hands on experience on Caliber, StartLIMS , Labvantage or other LIMS.