QA

Infusion bags processing activities, In-process checks and Line Clearance activities, Handling of shift activities and manpower. Preparation of QRM, Incident and Investigation, OOL and OOS investigation, CC and CAPA, Protocols and CAPA closure reports.

Good exposure require in IPQA - OSD and Sterile, Qualification OSD and Sterile. Intas is one of the leading multinational pharmaceutical formulation development, manufacturing and marketing companies in the world.

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.

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.

Candidate should be well versed with the regulatory guidelines. Candidate should have shop floor experience of In-process control involving Non sterile and sterile operations.

Must know process validation cleaning validation verification and hold time studies. Candidate should also have exposure to EU, MHRA, and USFDA regulatory audits.

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.