QC

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

responsible for overseeing day-to-day operations, ensuring compliance with regulatory standards, and driving continuous improvement across all processes. Oversee daily QC and microbiology operations, ensuring CGMP and regulatory compliance.

M.Sc / B.Pharm / M.Pharm; Finished, AMV and Stability Section, knowledge of Instrument - HPLC, GC. Preferably know-how of Chromeleon Software

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.

B.Pharm, M.Sc, M. Pharm with 3-8 years of experience in IPQA and manufacturing, packing QMS related activities in oral solid dosage form tablets, capsules, soft gelatin capsules, pellet Dosage form manufacturing facilities.

Granulation, Compression, Coating, Liquid & Nasal, Machine Operators and Executives. Exposure in exhibit batch manufacturing, Product site transfers.

B.Sc, M.Sc Chemistry, B.Pharma, Minimum 60% in Highest Education is must for candidates having less than 5 yrs exp. Candidates who have given interview within last 06 months are not eligible for interview.

Candidates having hands-on experience in Analysis of Raw Material, Packaging Material, Finished Goods, Stability, Method Transfer and Laboratory Investigations. Should have sound knowledge of QMS like Deviations, Change Control, Vendor Management etc.

Stallion Laboratories incorporated in 1988 as an integrated private sector Pharmaceutical Formulation Manufacturer, has acquired an unmatched record of managing niche product in formulations with a WHO GMP approved production facility and GLP qualified stringent quality control.