Telangana

Having experience in handling of shift Activities, BMR compilations Good technical Knowledge on Process & Equipments and should have Regulatory Exposure

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

aseptic vial filling operations, machine setup & operation, line clearance, IPC activities, equipment cleaning, cGMP compliance, GDP documentation, and sterile manufacturing processes. 

Candidates must have a Master's degree (M.Sc./M.Tech./M.V.Sc./M.Pharm. or M.B.B.S or B. Tech. degree) in any branch of Life Sciences with a consistently good academic record. 

Masters Degree in Natural Sciences or Bachelors degree in Engineering or Technology or Medicine from a recognized University or equivalent

Masters Degree in Biochemistry, Biotechnology, Molecular Biology from a recognized University with NET/ GATE qualification. 

Handling QMS as per Regulatory requirements. Handling Deviations, CAPA, Change Controls, OOS investigations. Responsible to process internal quality audits.

Walk in interviews in Hyderabad for our API and CDMO Plants at Telangana and Andhra Pradesh

Oversee IPQA activities during injectable manufacturing & packaging Review and approve BMR/BPR ensuring cGMP compliance Handle deviations, CAPA, and audit readiness (QMS) Lead QA team activities and drive continuous improvement initiatives