Senior CSV Engineer – Remote UAT & Documentation
Verista
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Benefits offered by this job
Job summary
Verista is seeking a skilled UAT and validation specialist to support regulated life sciences projects. You will assist with test-script development, evidence collection, and go-live activities, while coordinating with global CQ/QA teams.
The role emphasizes documentation control, SOP creation, and translation coordination in a remote work setup with occasional travel to client sites.
Qualifications
- Bachelors Degree in industry-related discipline.
- 5+ years in regulated life sciences systems, validation, quality, or digital transformation.
- Kneat Power User Level 1 or higher certification highly preferred.
- Hands-on UAT, test-script development, regulated documentation, or system deployment experience.
- Knowledge of GxP, CSV, and validated system practices.
- Experience authoring or revising SOPs, test scripts, templates, or controlled docs.
- Familiarity with requirements traceability, test evidence, and deployment readiness tracking.
- Strong writing, organizational, and stakeholder coordination skills.
- Ability to work independently within a global team.
- Experience with digital C&Q, validation, quality, or manufacturing platforms.
Responsibilities
- Support UAT activities, test-script development, and evidence collection.
- Coordinate Go-Live and hypercare activities with issue logging and resolution.
- Prepare and revise SOPs, templates, and training materials.
- Support translation packages and multilingual document updates.
- Coordinate with global CQ, QA, IT, and site teams.
Skills
Education
Tools
Job description
Verista is seeking a skilled UAT and validation specialist to support regulated life sciences projects. You will assist with test-script development, evidence collection, and go-live activities, while coordinating with global CQ/QA teams.
The role emphasizes documentation control, SOP creation, and translation coordination in a remote work setup with occasional travel to client sites.
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