CQV Engineer - GMP Validation for Pharma Facilities

Stark Pharma Solutions Inc. is seeking a CQV Engineer to support commissioning, qualification and validation activities for pharmaceutical manufacturing facilities in Austin, TX. The role emphasizes IQ/OQ/PQ execution, validation documentation, and compliance with GMP, FDA, and industry standards. You will lead cross-functional collaborations with Engineering, Manufacturing, Quality Assurance and Regulatory teams, develop and review protocols, maintain traceability, and support audits to drive #J-18808-Ljbffr Stark Pharma Solutions Inc