CQV Engineer - Validation Engineer

Verista is seeking a CQV Engineer - Validation Engineer to join their team. This role involves authoring, editing, and executing technical commissioning, qualification and validation documentation for standard equipment/systems/software, and processes. The ideal candidate will have a Bachelor's Degree or equivalent, experience in leading CQV activities specific to Process Equipment, and strong problem-solving and critical thinking skills. The position offers competitive pay, benefits, and growth opportunities in a fast-paced, people-focused culture.

Key responsibilities include:

• Running test scripts and documenting results
• Maintaining clear, detailed records of qualification and validation
• Completing user interface testing, software verification, and alarm testing on automated systems
• Developing, reviewing, and executing testing documentation
• Making recommendations for design or process modification based on test results

Requirements:

• Must be willing to work onsite in Columbus, OH
• Bachelor's Degree or equivalent
• Experience in GMP regulated environment
• Proficiency in Microsoft Office tools
• Strong communication and teamwork skills
• Attention to detail and organizational skills

Verista offers a comprehensive benefits package, including competitive pay, medical/dental/vision insurance, 401(k) with employer matching, paid time off, and various other perks. The company values empowering colleagues, client success, doing the right thing, and fostering an inclusive environment.

Join Verista to be part of a team dedicated to solving pressing healthcare challenges and making an impact in the life sciences industry.