6490 - Senior CSV 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:

- Support development of UAT scope, test scenarios, and test scripts based on approved requirements and business processes

- Coordinate and support UAT execution, tester scheduling, evidence collection, defect tracking, retesting, traceability, and closure

- Draft and update SOPs, work instructions, job aids, templates, commissioning documents, and global procedure revisions

- Format documents according to client standards and Good Documentation Practices

- Route documents through the client’s electronic document management system and support review and approval workflows

- Support digitization of document and template libraries, including formatting, metadata, traceability fields, and document tracking

- Develop and format training materials, quick-reference content, and user communications

- Support change-control activities, adoption materials, and implementation action tracking

- Maintain deployment-readiness trackers covering user access, training completion, readiness checklists, cutover inputs, and open actions

- Support go-live and hypercare activities, including issue logging, routing, follow-up, and resolution tracking

- Assist with translation-package preparation and review coordination for Portuguese, Japanese, and Spanish content

- Coordinate with global C&Q representatives, subject matter experts, Quality, IT, site teams, and external vendors

- Provide clear progress, issue, risk, and action updates

Requirements:

- Bachelors Degree in industry-related discipline

- 5+ years of experience supporting regulated life sciences systems, validation, quality, engineering, or digital transformation projects

- Hands-on experience with UAT, test-script development, regulated documentation, or system deployment activities

- Working knowledge of GxP, CSV, CSA, validation, or regulated system implementation practices

- Experience authoring or revising SOPs, work instructions, test scripts, job aids, templates, or other controlled documentation

- Familiarity with requirements traceability, test evidence, defect management, document workflows, or deployment-readiness tracking

- Strong writing, organization, communication, and stakeholder-coordination skills

- Ability to manage multiple priorities and work independently within a global, cross-functional team

- Experience with digital C&Q, validation, quality, engineering, or manufacturing platforms preferred

- Experience with Kneat or a comparable digital validation solution preferred

- Experience with HP ALM/Quality Center, Jira, or another test-management platform preferred

- Experience with BMSDocs, Documentum, Veeva Vault, or another electronic document management system preferred

- Experience supporting enterprise or multi-site deployments preferred

- Familiarity with ch