CIP CQV Engineer / Lead Validation Engineer

Job OverviewVerista unites a team of 500 skilled professionals dedicated to partnering with premier brands in the life sciences sector to address their unique business challenges. Our mission is to foster growth and innovation in the scientific community, assisting researchers, organizations, and businesses in tackling some of the most significant healthcare…

DescriptionVerista is a premier consulting firm comprised of over 500 dedicated experts collaborating with the most esteemed brands in the life sciences sector. We are committed to fostering growth and innovation within the scientific community, assisting researchers, organizations, and companies in tackling some of the most urgent healthcare challenges globally. Our innovative solutions and services empower informed decision-making, resulting from our substantial investment in our people and capabilities.Our growth is propelled by a team of world-class professionals who thrive in collaborative environments and share our mission to enhance the lives of our life sciences clients. We are passionate about making a positive impact every day.Company Culture Guidelines & Values:We empower and support our colleagues.We commit to client success at every turn.We have the courage to do the right thing.We promote an inclusive environment where colleagues feel respected, engaged, and challenged.We continuously acquire new skills and learn from our experiences to enhance our collective expertise.We are actively seeking a CQV Engineer with practical experience in supporting solution preparation systems within biopharmaceutical manufacturing environments. This role will primarily focus on solution preparation, buffer preparation, and media preparation unit operations, facilitating commissioning, qualification, and validation activities to ensure systems are designed, installed, tested, and qualified in accordance with cGMP and regulatory standards.The ideal candidate will possess extensive experience across the CQV lifecycle, including the authoring of validation documentation, assisting with equipment startup and commissioning activities, coordinating vendor testing, and ensuring systems are operationally ready. Familiarity with digital validation platforms such as Kneat is highly desirable.

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