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
• Bachelor’s in Engineering or Life Sciences
• Knowledge of utilities and process equipment
• Proficient in reading...