Roles and Responsibilities

- Develop and execute equipment qualification protocols (IQ, OQ, PQ) according to regulatory requirements.

- Conduct risk assessments and implement corrective actions (CAPA) as necessary.

- Collaborate with cross-functional teams to ensure compliance with QRM principles and 21 CFR Part 11 regulations.

- Perform validation activities for recent equipment installations, including verification of software and hardware functionality.

- Ensure timely completion of all equipment qualification tasks within budgeted timeframes.

Desired Candidate Profile

- 4-8 years of experience in Equipment Qualification/Validation role in Pharmaceutical industry.

- Bachelor's degree in B.Pharma or M.Pharma from a recognized institution.

- Strong understanding of GMP guidelines, QRM principles, and 21 CFR Part 11 regulations.

- Proficiency in developing IQ/OQ/PQ protocols, conducting risk assessments, implementing CAPAs.

📌 Equipment qualification Engineer (Telangana)
🏢 Aurobindo Pharma
📍 Telangana