6367 - CQV Documentation Specialist / Project Engineer

Job Description

Description Verista’s 500 experts team up with the world’s most recognizable brands in the life science industry to solve their business needs. The nature of our business is to empower growth and innovation within the scientific community and to help researchers, organizations, and companies solve some of the world’s most pressing healthcare challenges. Verista provides innovative solutions and services that empower informed decision-making and are the result of our significant investment in our people and our capabilities. Our ability to grow is driven by world-class people who thrive in a team environment and share our mission to enable life sciences clients to improve lives. Our talented and dedicated professionals are committed to making an 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 encourage an inclusive environment where our colleagues feel respected, engaged, and challenged. We constantly acquire new skills and learn from our experiences to enhance our collective expertise Job Overview: We are seeking a CQV Documentation Specialist / Project Engineer to support high-volume CQV documentation, QSR generation, package assembly, traceability, and closeout for a GMP equipment qualification project. This role is critical to ensuring documentation deliverables remain aligned with the project schedule and inspection-ready expectations. Project Engineer Responsibilities: Support generation, formatting, routing, tracking, and closeout of CQV deliverables Support URS revisions, readiness checklist packages, IOQ/PQ packages, and QSRs Maintain deliverable trackers, package status, review comments, and closeout logs Supp