OnsiteMid Levelhealthtech# Associate - MSAT (C&Q)PfizerPendurthi, Andhra Pradesh, IndiaPosted 23 May 2026Pfizer is hiring a Validation Engineer to manage quality and validation processes within a sterile dosage facility. The role involves preparing, executing, and reviewing IQ/OQ/PQ protocols, performing data analysis for deviations, and ensuring compliance with FDA and cGMP standards. Candidates will collaborate with cross-functional teams to oversee equipment qualification and support plant technology transfers. This position requires 2-3 years of relevant experience in a regulated pharmaceutical environment.Matched by TALApply to this role now. Install TAL for a 24/7 AI agent that keeps finding roles personalised for you.Experience2-3 years## What you will work onPfizer is hiring a Validation Engineer to manage quality and validation processes within a sterile dosage facility. The role involves preparing, executing, and reviewing IQ/OQ/PQ protocols, performing data analysis for deviations, and ensuring compliance with FDA and cGMP standards. Candidates will collaborate with cross-functional teams to oversee equipment qualification and support plant technology transfers. This position requires 2-3 years of relevant experience in a regulated pharmaceutical environment.Quality 80/1005/5 clarityTier 1 companyRole is at a Tier-1 global pharmaceutical company with well-defined validation responsibilities.Very clear scope involving specific validation protocols, regulatory guidelines, and technical documentation requirements.- Bachelor's degree or equivalent experience- Proficiency in Microsoft Excel for data evaluation- 2-3 years experience in Quality Assurance and Validation- Knowledge of sterile manufacturing equipment validation## Tools and skillsms officeexcelcgmpfda regulationsvalidation principlessterile manufacturing equipmentiq/oq/pq protocolsNice to have: technical writing, laboratory process validation, equipment qualification, calibration, ai tools, chatgpt, microsoft copilot.