Senior CQV Specialist for Pharma Validation

Join Atkins Ralis as a Senior CQV Specialist focusing on pharma project validation. Oversee compliance with cGMP regulations to maintain high product quality in this critical role.
You will take charge of the validation processes, providing essential technical leadership to your team. This role not only emphasizes your ability to develop and review documentation but also entails coordinating tests and analyzing intricate data for regulatory compliance and process optimization.
Key Responsibilities:
• Develop and review validation documentation for diverse clients
• Coordinate and execute testing protocols against established requirements
• Analyze test data and manage equipment operations
• Troubleshoot validation and testing issues efficiently
• Provide senior support to the CQV team for project goals
Requirements:
• Bachelor's degree in Engineering or related field
• 8+ years of validation experience in regulated environments
• Expertise in equipment ...