Principal CQV Engineer / Lead Validation Engineer

Position OverviewVerista’s dedicated team of over 500 professionals collaborates with some of the most prominent brands in the life sciences sector, addressing their business challenges. We are committed to fostering growth and innovation within the scientific community, assisting researchers, organizations, and companies in tackling critical healthcare issu…

Job OverviewVerista is home to a team of 500 experts collaborating with some of the most esteemed names in the life sciences sector to address critical business challenges. We are dedicated to fostering growth and innovation in the scientific community, assisting researchers, organizations, and companies in tackling pressing healthcare issues. Our innovative solutions and services empower informed decision-making, stemming from our considerable investment in our workforce and capabilities.Our growth is propelled by exceptional individuals who thrive in collaborative environments and share our mission of enabling life sciences clients to enhance lives. Our skilled and committed professionals strive to make a meaningful impact every day.Company Culture Guidelines & Values:We empower and support our colleagues.We are dedicated to client success in every endeavor.We uphold the courage to do what is right.We cultivate an inclusive environment where our colleagues feel respected, engaged, and challenged.We continually develop new skills and learn from our experiences to enhance our collective expertise.We are currently looking for a CQV Engineer with hands-on expertise in downstream bioprocessing systems to lead commissioning, qualification, and validation activities within a biopharmaceutical manufacturing setting. This role will emphasize downstream unit operations and purification equipment, ensuring that systems are designed, installed, tested, and qualified in compliance with cGMP and regulatory standards.The ideal candidate will demonstrate extensive experience throughout the CQV lifecycle, including the ability to author validation documentation, facilitate commissioning activities, coordinate vendor testing, and ensure systems are primed for operational readiness. Familiarity with digital validation platforms such as Kneat is highly advantageous.

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