Senior Validaiton Engineer

Role: CQV Engineer supporting commissioning, qualification, and validation activities for GMP-regulated facilities, utilities, equipment, and automation systems in the biopharma sector. Responsibilities include reviewing design and qualification documentation, executing IQ/OQ/PQ protocols, verifying installation and system functionality, coordinating testing with cross-functional teams, managing discrepancies, and supporting system handover and regulatory audits. Qualifications: Bachelor's in Engineering, Life Sciences, or related field; 7–11 years of experience in pharmaceutical or biotech validation, with deep knowledge of GMP, FDA requirements, and validation principles. High-Value: focus on process equipment, utilities, automation, and manufacturing systems within regulated environments; experience with protocols, engineering review, deviation management, and regulatory compliance. WorkSetup: not specified, but involves field testing, documentation, and cross-team collaboration.