Senior Validation Consultant

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The ideal candidate will have:

1. 10+ years of experience in Computer System Validation (CSV), with a focus on patient safety and regulatory compliance.
2. Experience driving critical projects in Patient Safety, Commercial, and Medical Affairs, ensuring audit readiness and continuous improvement.
3. Extensive CSV expertise in life sciences, especially in patient safety.
4. Proficiency in Argus Safety, Veeva, and regulatory standards (GxP, GDPR, FDA).
5. Strong documentation, compliance, and stakeholder collaboration skills.

Seniority level

• Mid-Senior level

Employment type

• Contract

Job function

• Quality Assurance

Industries

• Pharmaceutical Manufacturing

This job is active and open for applications.

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