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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 We are seeking a CQV Engineer to support change control and deviation management activities .  This role will play a critical part in maintaining compliance, supporting quality systems, and ensuring manufacturing changes are properly assessed, documented, and executed in a regulated cGMP environment. The ideal candidate will have hands-on experience in change management, deviation investigations, and CQV lifecycle support within pharmaceutical or medical device manufacturing. Validation Engineer / CQV Engineer Responsibilities: Change Control Management Author, review, and manage change controls impacting systems, equipment, and processes Perform impact assessments, including evaluation of product quality, validated state, and regulatory impact Collaborate with cross-functional teams (Engineering, Quality, Validation, Manufacturing) to ensure timely and compliant change implementation Support execution of change control deliverables, including updates to validation documentation (IQ/OQ/PQ, protocols, reports) Deviation Management Lead and support deviation investigations, including root cause analysis and corrective/preventive actions (CAPAs) Ensure deviations are thoroughly documented, investigated, and closed within required timelines Partner with Quality teams to ensure compliance with internal procedures and regulatory expectations CQV & Compliance Support Device Assembly Packaging Maintain alignment with cGMP and Good Documentation Practices (GDP) Support validation impact assessments and execution activities related to changes Review and approve validation and technical documentation as required Participate in audits and inspections, providing SME support for change control and deviation processes Cross-Functional Collaboration Interface with Manufacturing, Quality Assurance, Automation, and Engineering teams  Support continuous improvement initiatives related to quality systems and CQV processes Communicate project status, risks, and issues to stakeholders Requirements: Bachelor’s degree in Engineering, Life Sciences, or related field 1-3 years of experience in CQV, Validation, or Quality Engineering in a regulated industry Strong experience with: Change control systems Deviation investigations and root cause analysis cGMP and GDP environments Familiarity with device assembly/packaging operations is highly preferred Experience supporting validation lifecycle activities (IQ/OQ/PQ) is a plus Strong technical writing and documentation skills Excellent communication and cross-functional collaboration abilities Onsite job requirement in Indianapolis, IN For US geography, the salary range for this position is shown below. The actual salary is depend