Senior CQV Specialist at Atkins Ralis

Elevate your career with Atkins Ralis as a Senior CQV Specialist, focusing on project validation in the pharmaceutical industry. Lead compliance with cGMP regulations to ensure product quality and integrity.

In this senior role, you'll oversee critical validation processes and deliver technical leadership. Your expertise will be central to developing and reviewing comprehensive validation documentation, coordinating essential testing, and analyzing complex data to achieve regulatory compliance in a highly regulated environment.

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 qualification and process validation

• Solid knowledge of cGMP regulations

• Excellent verbal and written communication skills

Utilize your validation skills with Atkins Ralis to enhance project success and quality assurance.
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