Field- CQV Engineer in Pharmaceutical Manufacturing

Position: Field-Based CQV Engineer in Pharmaceutical Manufacturing
Advance your career as a CQV Engineer focused on pharmaceutical and biotech manufacturing. This role emphasizes hands-on execution in the commissioning, qualification, and validation processes.

In this position, you will actively participate in the preparation and execution of validation tasks while collaborating with cross-functional teams to ensure compliance. Your strong background in GMP-regulated environments and utilities will help drive project success and uphold quality standards.

Key Responsibilities:

• Execute commissioning and validation protocols

• Conduct functional and performance testing

• Collaborate on installation verification and resolutions

• Document deviations and manage investigations

• Maintain compliance with industry standards and best practices

Requirements:

• 5+ years of CQV experience in regulated facilities

• Bachelor’s in Engineering or Life Sciences

• Knowledge of utilities and process equipment

• Proficient in reading technical documentation

• Strong organization and communication skills

Use your CQV skills to enhance quality and efficiency in modern pharmaceutical operations.
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