We are seeking a skilled professional with 2–5 years of experience in Quality Control (QC) Systems Validation within the pharmaceutical or life sciences industry. The role involves validating laboratory software and computerized systems to ensure compliance with regulatory and data integrity requirements. Responsibilities include preparation and execution of validation documents, risk assessments, test protocols, deviation handling, and system lifecycle support. Candidates should have knowledge of GxP regulations, 21 CFR Part 11, data integrity principles, and computerized system compliance. Experience with laboratory applications, documentation practices, and cross\-functional coordination is essential. Immediate to short\-notice joiners are preferred.
Pay: ₹400,000\.00 \- ₹500,000\.00 per year
Work Location: In person
QC Systems Validation Consultant
Instrumentation and control solutions · AP, IN