Validation Veeva Consultant
Job ID: 08767
Location: Wilmington, DE [Hybrid]
Employment Type: Contract
Validation Consultant – Veeva
Duration: 6–12 Month Contract
About the Role
Our client is seeking a Validation Consultant to support the implementation and validation of a Veeva platform within a regulated environment. This role will focus on validation planning, data migration testing, compliance documentation, and ensuring alignment with GxP and 21 CFR Part 11 requirements.
Key Responsibilities
- Develop and execute validation strategies for the Veeva implementation.
- Create Validation Plans, risk assessments, and traceability matrices.
- Ensure system validation activities meet GxP and 21 CFR Part 11 compliance requirements.
- Review and validate data mapping and migration activities from legacy systems into Veeva.
- Execute migration testing cycles and support issue resolution activities.
- Author, review, and execute validation test scripts and related documentation.
- Ensure inspection readiness and completeness of validation documentation.
- Collaborate with business, quality, and technical teams throughout the validation lifecycle.
- Support audit and compliance activities related to system validation efforts.
Required Qualifications
- Experience supporting validation activities within regulated life sciences or pharmaceutical environments.
- Hands-on experience with Veeva platform validation.
- Strong understanding of GxP and 21 CFR Part 11 requirements.
- Experience developing Validation Plans, risk assessments, and traceability matrices.
- Experience validating data migration and data mapping activities.
- Experience authoring and executing validation test scripts.
- Strong documentation and compliance management skills.
- Ability to work cross-functionally with technical and business stakeholders.
Preferred Qualifications
- Experience supporting Argus to Veeva migration initiatives.
- Familiarity with CSV (Computer System Validation) methodologies.
- Experience supporting audit readiness and regulatory inspections.
- Experience within pharmaceutical, biotech, or clinical environments.