5+

To have a strong technical background and experience in development of complex injectable and sterile dosage forms. Special consideration shall be given if exposed in onco injectable products

Intas is one of the leading multinational pharmaceutical formulation development, manufacturing and marketing companies in the world.

Aurobindo Pharma Limited is an Indian multinational pharmaceutical manufacturing company headquartered in HITEC City, Hyderabad, India.

Review of stability data. Review of analytical method validation data. Review of analytical method transfer.

Ph.D. or Master in Life Sciences, Biotechnology, Pharmacology, or related field. Strong understanding of the drug discovery pipeline and integrated biology workflows.

Looking for talented QC professionals with strong analytical skills and hands-on experience in pharmaceutical Quality Control operations. The ideal candidate should have a strong understanding of GLP, GMP, documentation, and regulatory compliance.

Hands-on experience in Blister, Strip, and Bulk Packaging (Primary & Secondary), Experience in QMS activities (handling of SOPs preparing, Training, Change Control/Deviations), Familiarity with Track & Trace and Serialization Systems.

Experience and having knowledge of raw material analysis, finished product analysis, qualification & calibration of laboratory instruments. SOP preparation, change control, deviation management and knowledge of LIMS. DMS and QMS, etc.

ITI, Diploma, B.Sc, B.Com, M.Sc, B.Tech, B.Pharm, M.Pharm with relevant experience. HPLC/ IP/ FP/ RM/Validation/Stability/GC/ Micro-biology at Hetero Pharma