Job brief We are looking to hire a skilled PLC / SCADA / CSV Validation Engineer who should have excellent knowledge of machine mechanics, a logical approach, and the ability to work with minimal supervision.
Responsibilities : Development of PLC / CSV validation Documents / Protocols like Validation Plan (VP) Requirement specification documents like (URS / FRS / DQ), Risk Assessment (RA), IQ, OQ, PQ and Validation Report (VR).
Validation practices with good knowledge on 21 CFR Part 11, GAMP 5 Guidelines, EU Annex 11 and GxP (GMP,GDP, GCP, GLP) Standards.
Testing automated systems for efficiency, safety, and reliability. Execution of systems as per approved protocol. Troubleshooting system errors.
Documenting processes. Requirements : BE / Diploma Instrumentation / Electrical / Electronic Engineering. 1 to 4 years of experience in Pharmaceutical industry.
Detailed knowledge of PLC automation software applications. Ability to work with minimal supervision. Ability to travel when required. Location : Verna, Goa.