6490 - Senior C&Q Engineer / Senior Validation Engineer

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 Senior Validation Engineer Responsibilities: Lead and support Commissioning & Qualification (C&Q/CQV) activities for GMP facilities, utilities, equipment, and manufacturing systems throughout the project lifecycle. Develop, review, and execute C&Q deliverables including URS, risk assessments, DQ, FAT/SAT, commissioning test plans, IQ/OQ/PQ protocols, traceability matrices, and qualification summary reports. Coordinate C&Q execution activities, including protocol scheduling, field execution, test evidence collection, punch-list management, discrepancy/deviation resolution, retesting, and final documentation closeout. Support development and implementation of risk-based qualification strategies in accordance with GMP requirements, ASTM E2500, GEP, and applicable site/client procedures. Author, review, and update C&Q procedures, protocols, work instructions, commissioning documents, test scripts, templates, and qualification reports in accordance with Good Documentation Practices. Manage C&Q documentation through electronic document management and digital qualification platforms, ensuring proper formatting, metadata, traceability, approvals, and document lifecycle control. Support digital C&Q execution and documentation, including configuration and use of Kneat or similar C&Q/validation platforms, electronic protocols, test evidence, workflows, and qualification records. Coordinate with Engineering, Automation, Quality, Operations, Maintenance, Facilities, IT, Subject Matter Experts, site teams, and external vendors to ensure C&Q activities are aligned with project schedules and operational requirements. Maintain C&Q project trackers covering protocol status, execution progress, open actions, punch-list items, deviations, documentation readiness, system turnover, and qualification closeout. Support facility and equipment turnover, commissioning completion, qualification readiness, and operational handoff to site teams. Provide clear status updates on C&Q progress, schedule, risks, issues, dependencies, and outstanding actions to project and site leadership. Support inspection and audit readiness by ensuring C&Q documentation is complete, traceable, technically justified, and compliant with applicable GMP requirements. Support multiple concurrent C&Q projects and priorities while maintaining quality, schedule, and documentation requirements across a global, cross-functional organization. Requirements: Bachelor’s degree in Engineering, Life Sciences, or another industry-related technical discipline. 5+ years of experience in C&Q/CQV, commissioning, qualification, validation, engineering, or technical project execution within regulated pharmaceutical, biotech, or life sciences environments. Demonstrated hands-on experience with commissioning and qualification of GMP facilities, utilities, equipment, manufacturing systems, or laboratory systems. Strong working knowledge of C&Q methodologies and deliverables, including URS, DQ, FAT/SAT, commissioning, IQ/OQ/PQ, traceability, risk assessments, deviations, and qualification summary reports. Working knowledge of GMP, GEP, ASTM E2500, risk-based qualification, and Good Documentation Practices. Kneat Power User Level 1 (or higher) certification highly preferred , with hands-on experience using Kneat or similar digital C&Q/validation platforms. Experience authoring, reviewing, and executing C&Q protocols, test scripts, commissioning documents, qualification reports, SOPs, work instructions, and other controlled documentation. Experience coordinating field execution with Engineering, Quality, Operations, Automation, Maintenance, vendors, and other cross-functional stakeholders. Familiarity with punch-list management, discrepancy/deviation resolution, change control, turnover, system handoff, and C&Q closeout activities. Strong understanding of requirements traceability, test evidence, documentation workflows, and qualification lifecycle management. Experience with HP ALM/Quality Center, Jira, or other project/test-management platforms preferred. Experience with BMS, Documentum, Veeva Vault, or other electronic document management systems preferred. Experience supporting large-scale pharmaceutical/biotech capital projects, facility expansions, equipment installations, or multi-site C&Q programs preferred. Strong written and verbal communication, organizational, problem-solving, and stakeholder-management skills. Ability to manage multiple priorities and work independently within a global, cross-functional project environment This role is remote; limited travel to client sites may be requested with advance notice . For US geography, the salary range for this position is shown below. The actual salary is dependent upon a variety of job-related factors such as pro