About this role
The team is seeking a Manager for IT Quality Assurance and Computerized System Validation (CSV) to lead their validation efforts in the drug safety sector. This role requires a strong understanding of GxP-compliant applications and a commitment to ensuring best practices in CSV are consistently applied.
Key Responsibilities:
- Provide validation expertise on GxP-compliant applications in the drug safety space.
- Serve as a Subject Matter Expert (SME) in CSV practices.
- Review and approve key CSV deliverables, including Requirement Specifications, Validation Plans, Test Plans, Traceability Matrices, Test Summary Reports, Qualification Scripts, and Validation Summary Reports.
- Lead validation and User Acceptance Testing (UAT) activities for client product implementation projects.
- Collaborate with cross-functional teams to ensure compliance and quality standards are met.
Required Skills & Qualifications:
- Bachelor's degree in Computer Science, Information Technology, or a related field.
- 5-8 years of experience in IT Quality Assurance and Computerized System Validation.
- Strong knowledge of GxP regulations and industry best practices.
- Experience with validation documentation and deliverables.
- Excellent communication and leadership skills.
- Ability to work effectively in a team-oriented environment.
What we offer:
- Opportunity to work with a dynamic team in a growing organization.
- Professional development and career advancement opportunities.
- A collaborative work environment that values innovation and quality.
Applications are read by our talent team, usually within two working days.
If you look like a fit we will call you, and you will hear from us either way.