Elevate your career as a Lead CQV Specialist with Atkins Ralis, driving validation leadership in the pharmaceutical industry. This role entails ensuring compliance with international cGMP regulations for high-quality outcomes.
In your senior role, you will manage the development and review of all critical documentation. Collaborating with team members, you will facilitate testing and data analysis, while troubleshooting any issues that arise. Your expertise will directly support the CQV department in achieving their overarching goals.
Key Responsibilities:
• Oversee the creation of qualification and validation documentation
• Execute testing protocols to ensure compliance
• Conduct analysis on complex test data
• Troubleshoot diverse issues and recommend optimizations
• Provide leadership support to meet departmental objectives
Requirements:
• Bachelor’s degree in Engineering or Science
• At least 8 years of experience in validation
• Specialized knowle...