Senior CSV Validation Engineer - Remote

Verista; Harvard (MA); On-site; USD 110,000 - 150,000; Full time

Benefits offered by this job

Competitive pay

401(k) Retirement Plan (Employer Match

Paid Time Off

Health Insurance

Tuition Reimbursement

Job summary

Verista is seeking a Senior Validation Engineer to support UAT scope, create test scripts, and manage evidence collection and defect tracking. You will draft SOPs, ensure documentation follows client and regulatory standards, and coordinate with global QA and IT teams.

This remote role may require limited travel to client sites with advance notice. The ideal candidate has 5+ years in regulated life sciences validation, hands-on UAT experience, and familiarity with Kneat, HP ALM, Jira, and

Qualifications

• Bachelors Degree in industry-related discipline.
• 5+ years supporting regulated life sciences systems or similar projects.
• Hands-on with UAT, test scripts, and validated documents.
• Experience with GMP/CSV/validation practices and document control.

Responsibilities

• Support UAT scope and test script development based on requirements.
• Coordinate UAT execution, scheduling, evidence collection and defect tracking.
• Draft and update SOPs and templates to client standards.
• Format documents per Good Documentation Practices.
• Assist with translation-package preparation for multilingual content.
• Coordinate with global QA, IT, and site teams.

Skills

Regulatory experience

UAT / test-script development

Stakeholder coordination

Documentation quality

Communication skills

Education

Bachelor's Degree in discipline

Tools

Kneat

HP ALM/Quality Center

Jira

Veeva Vault

Documentum

Job description

Verista is seeking a Senior Validation Engineer to support UAT scope, create test scripts, and manage evidence collection and defect tracking. You will draft SOPs, ensure documentation follows client and regulatory standards, and coordinate with global QA and IT teams.

This remote role may require limited travel to client sites with advance notice. The ideal candidate has 5+ years in regulated life sciences validation, hands-on UAT experience, and familiarity with Kneat, HP ALM, Jira, and