
This senior CQV Engineer role supports cGMP clinical and commercial cell therapy manufacturing operations in Raritan, New Jersey. The position involves executing commissioning, qualification, and validation activities for facility equipment and processes while managing complex projects and cross-functional collaborations. Key responsibilities include authoring and executing CQV protocols, leading technical investigations and CAPA plans, and representing the team during regulatory and internal audits. The role appeals to professionals seeking to contribute to personalized medicine production within a compliant environment, offering opportunities to mentor junior staff and drive process excellence. Candidates must possess extensive experience in aseptic manufacturing and a deep understanding of FDA regulations and Good Tissue Practices.




















