Job Title

Advance your career as a CQV Engineer focused on pharmaceutical and biotech manufacturing. This role emphasizes hands-on execution in the commissioning, qualification, and validation processes. In this position, you will actively participate in the preparation and execution of validation tasks while collaborating with cross-functional teams to ensure compliance. Your strong background in GMP-regulated environments and utilities will help drive project success and uphold quality standards. Key Responsibilities: Execute commissioning and validation protocols Conduct functional and performance testing Collaborate on installation verification and resolutions Document deviations and manage investigations Maintain compliance with industry standards and best practices Requirements: 5+ years of CQV experience in regulated facilities Bachelors in Engineering or Life Sciences Knowledge of utilities and process equipment Proficient in reading technical documentation Strong organization and communication skills Use your CQV skills to enhance quality and efficiency in modern pharmaceutical operations. #J-18808-Ljbffr