Santosha Pattanaik

Production Executive @Aurobindo Pharma Ltd

Hyderabad, IN

Handling and operation of steam sterilizer, dry heat tunnel sterilizer, and vial washing machine. Managing compounding solution preparation using reactors, pressure vessels and filtration skids. Execution and integrity testing of filters used in production. Execution and handling of particle counter in production area. Supervision of CIP & SIP operations and line clearance verification. Preparation and review of SOPs, BPRs, Validation Protocols ensuring compliance with regulatory standards. Ensured strict data integrity compliance across all production documentation, maintaining ALCOA+ principles in BMRs, BPRs, logbooks, and electronic systems. Handling QMS activities: Change Control, Deviations and CAPA. Execution of Validations – Hands-on experience in Equipment Validation, process validation, cleaning validation, SIP validation, equipment qualification and aseptic process simulations. Ensuring timely calibration, validation, and preventive maintenance of equipment. Conducting on-the-job training and department training activities. Managing ERP activities: batch release, inputs, outputs, and records. Coordinating procurement of raw materials, packing materials, filters, and other production essentials. Supported regulatory inspections and audits (USFDA, MHRA, WHO, ANVISA). Trained production staff on Good Documentation Practices (GDP) and data integrity requirements to minimize errors and deviations. Well-versed in cGMP, USFDA, EMA, MHRA, WHO guidelines for sterile injectable/sterile API facilities. Handling of Cephalosporin products: Ceftriaxone, Cefotaxime, Cefuroxime, Cephalothin, Cefoperazone, Cefepime & Ceftazidime for Injection.

Council of Higher Secondary Education, Odisha

Intermediate (Science)

Berhampur University

B.Sc. in Chemistry

Board of Secondary Education, Odisha

High School Diploma

Vinayaka Missions University

Master of Chemistry