Production

Exposure of Equipment and Utility Qualifications. Good Knowledge of Process Validation, Cleaning Validation. Management of QM5. Exposure of Stability and Artwork Management Analytical QA Handling of OOS, Risk Assessment, Self Inspection, APQR

Candidate should have experience with the GEA Granulation line, compression processes in the oncology sector, and coating with Glatt and ACG equipment. Experience in handling regulatory audits is a must. Proficiency in English communication is required.

Strong knowledge of GMP, GDP, and regulatory compliance for pharmaceutical warehousing. Exposure of various instruments/ software like empower 3, LIMS and other software.

Candidate should be well versed with operation and maintenance of ointment manufacturing plant and handling PLC, SCADA. Handling of tube filling activity and packing activity of ointment, creams, lotions.

Exposure to OSD Manufacturing operations like Granulation, Compression, Pellet coaling, Capsule filling, Primary Packing & Secondary Packing. Expertise in e-BPR and e-log will he added advantage. Experience of HPLC, UV spectrophotometer and Dissolution Tester operation. Experience of Analytical Method Validation/Transfer. Experience of GC, ICPMS and/or LCMS operation.

Depyrogenation tunnel, Filling Machine, vial washing Machine, Autoclave operation, Aseptic practices etc. Shift handling, QMS, External vial washing, Sealing Machine, Filling machine, Aseptic practices

Established in 1991, Lactose India Limited is a young and innovative company specializing in the manufacturing of Excipients Lactose, Colour Coatings, Lactulose, Solid Dosage Forms, Liquid Dosage Forms, at Vadodara, Gujarat.

M.Pharm, B.Pharm, M.Sc, B.Sc, ITI, Diploma. 2-6 years of experience in operating of Granulation, Compression, Packing.

M.Pharm/ B.Pharm/ M.Sc/ B.Sc; experience in production including operation and supervision of autoclave operation TS and component, Filter integrity, aseptic & control area operation, vial washing and filling machine operation. Injectable /parenteral/sterile manufacturing experience is a must. experience in bulk manufacturing/aseptic filling, control/aseptic area operation, vessel operation including CIP/ SIP process handling, machine operation Steam Sterilizer, Vial Washing, and GMP documentation.