QC

Ensure compliance of online documentation and line clearance activities. Review and approve executed BMRs/BPRs, logbooks, and related records.

Responsible for ensuring the quality of incoming material in process & finished products to ensure compliance with regulatory & standard specifications.

Analysis of RM / IP / FP samples, Operation and troubleshooting of instruments such as HPLC, UV, KF, IR, and Dissolution Apparatus.

Titan, an integrated Pharmaceutical Group which is backed by the holistic approach towards catering multifarious integrated services, which aims to meet the concept-to-commercialization needs of our customers while providing quality pharma and API products that serve for life saving medications.

Responsible for performing the chemical and instrumentation analysis for In-process, raw materials, packing materials, intermediates and finished products to meet the dispatch timeline as per the monthly schedule received from PPIC.

Strong knowledge of GMP regulations including WHO, EU GMP, PICS, TGA, MHRA, USFDA & other global regulatory guidlines. Expertise in handling CAPA, CCF, deviations, market complaints, product recalls if any.

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

OSD-coating, Compression, Packing, Granulation, Ointment-External Preparation (General & Sterile Manufacturing). Injectable (Aseptic, SIP, CIP, Batch Manufaturing, Bulk Manufacturing, Dry Powder), Oral Liquid

M.Pharm, B.Pharm, M.Sc, B.Sc Openings, OSD (Granulation, Compression, Coating, Capsule), Injectable (Dry Powder Injectable)