Senior CQV Specialist at Atkins Ralis (Calgary)

Join Atkins Ralis as a Senior CQV Specialist and lead project validation efforts in the pharmaceutical industry. This role focuses on compliance with cGMP regulations and guarantees product quality. In this senior role, you will oversee validation processes and provide technical leadership.

You will develop and review documentation, coordinate testing, and analyze complex data to ensure regulatory compliance. Collaboration with the CQV team will be crucial in achieving department goals and optimizing processes and equipment.

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...