Production

B.Pharm, M.Pharm, M.Sc, B.E. with 2 to 10 Years of relevant experience of IPQA, Qualification, QMS, Sterility Assurance, QA IT related activities in Injectable Manufacturing Plant.

Skilled in handling equipment such as reactors, centrifuges CF, vacuum tray dryers VTD, agitated nutsche filters , etc. Strong expertise in unit operations. Well-versed in production activities including raw material verification, batch charging, batch monitoring, and GMP documentation.

Must be from Parenteral background & exposure to Aseptic vial, Bottle filling process is desirable. To be aware and responsible for achieving quality objective and fulfilling the requirements of applicable quality procedures. Sound technical knowledge of Aseptic area & Controlled area related activities.

As per the batch manufacturing procedures and packing protocols, samples such as in-process samples, finished product samples, stability samples, control samples, cleaning samples, and other samples should be collected and submitted

 IPQA Mfg. & Packing, Shop floor activities, Review of equipment audit trails, BMR, BPR review, line clearance. Process Validation, equipment, Utility qualification.

0-2 years Knowledge of GMP, FFS, Semi solid manufacturing process, BMR -BPR preparation, knowledge of ALCOA, Audit readiness, EHS adherence in manufacturing

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

Compounding, aseptic operations and aseptic behaviors equipment trouble shooting and solution oriented. Ensuring online documentation, CFT co-ordination, etc.

Candidate having experience of Bio-similar product manufacturing. Large scale bioreactor, Continuous centrifuge Trouble shooting, risk assessment, root cause analysis.