6187 - Sr. Validation Engineer / CQV Engineer - Change Management Focus

Company: Verista, Inc.
Location: Indianapolis
Posted on: February 15, 2026

Job Description:

Job Description 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 Verista is seeking a detail-oriented Validation / CQV Engineer with strong experience in change management and documentation control within regulated pharmaceutical manufacturing environments. This role supports commissioning, qualification, validation, and lifecycle change activities to ensure systems, equipment, and processes meet GMP, regulatory, and client requirements . The ideal candidate brings hands-on experience managing validation documentation, coordinating cross-functional stakeholders, and leading change control activities to support compliant and efficient project execution. Sr. Validation Engineer / CQV Engineer Responsibilities: Validation & CQV Execution Support commissioning, qualification, and validation (CQV) activities for laboratory and manufacturing systems within GMP environments Prepare, review, and route validation deliverables including protocols, reports, assessments, and supporting documentation Ensure validation documentation is accurate, complete, traceable, and compliant with regulatory and client standards Apply Good Documentation Practices (GDP) in authoring, reviewing, and maintaining validation records Change Management & Change Control Lead and support change control processes associated with validated systems, equipment, and procedures Coordinate the end-to-end change lifecycle, ensuring impacts are properly assessed, documented, and approved Act as a liaison between Quality, Engineering, Manufacturing, and client stakeholders to communicate changes effectively Ensure changes are seamlessly integrated into validation strategies, procedures, and controlled documentation Documentation & Data Integrity Manage large volumes of validation documentation, including qualification packages, assessments, and remediation records Utilize electronic document management systems (EDMS) and SharePoint to organize, track, and retrieve documentation Support data integrity assessments and remediation efforts as required Perform final document reviews prior to approval to ensure alignment with internal and client expectations Cross-Functional Collaboration Collaborate with Quality Assurance, Engineering, Manufacturing, and client teams to gather technical input and execute validation strategies Provide guidance and support to team members in locating documentation and navigating validation and change processes Support project timelines by proactively tracking deliverables, approvals, and dependencies Requirements: Bachelor's degree in Engineering, Life Sciences, or a related technical discipline 2-4 years of experience supporting validation and CQV activities in pharmaceutical or regulated manufacturing environments Demonstrated experience with change management and change control processes Strong working knowledge of GDP, GMP, and regulatory expectations Proficiency with EDMS platforms and Microsoft SharePoint Excellent organizational, communication, and problem-solving skills Ability to work effectively within cross-functional teams Onsite work requirement in Indianapolis, IN 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 professional background, training, work experience, location, business needs, market demand, and competitive market practice. Therefore, in some circumstances, the actual salary could fall outside of this expected range. This salary range is subject to change and may be modified in the future. *Verista is an equal opportunity employer. National (US) Range $59,951—$102,623 USD Benefits Why Choose Verista? High growth potential and fast-paced organization with a people-focused culture Competitive pay plus performance-based incentive programs Company-paid Life, Short-Term, and Long-Term Disability Insurance. Medical, Dental & Vision insurances FSA, DCARE, Commuter Benefits Supplemental Life, Hospital, Critical Illness and Legal Insurance Health Savings Account 401(k) Retirement Plan (Employer Matching benefit) Paid Time Off (Rollover Option) and Holidays As Needed Sick Time Tuition Reimbursement Team Social Activities (We have fun!) Employee Recognition Employee Referral Program Paid Parental Leave and Bereavement Verista collects and processes personal data in accordance with applicable data protection laws. If you are a California Job Applicant, see the privacy notice for further details. For more information about our company, please visit us at Verista.com

Keywords: Verista, Inc., Greenwood , 6187 - Sr. Validation Engineer / CQV Engineer - Change Management Focus, Engineering , Indianapolis, Indiana