Lead Validation Expert CQV Projects

Position: Lead Validation Expert for CQV Projects
Atkins Ralis seeks a Lead Validation Expert as a Senior CQV Specialist to drive validation efforts in the pharmaceutical sector. Ensure product quality by adhering to stringent cGMP regulations and validate project success.

In this influential role, you'll manage validation processes while providing technical leadership to enhance compliance. Collaboration with the CQV team will be essential in developing, reviewing documentation, and executing testing protocols to meet industry standards effectively.

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

Drive quality assurance and project excellence as a Senior CQV Specialist with Atkins Ralis.
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