Quick overview
Job description
Qualification Lead Role:
· Primary focus is to ensure that the qualification of the OT system, quality management for IT and OT systems, ensuring that the required validation / qualification deliverables are implemented according to the Customer Quality Manual and the relevant regulatory requirements
· According to the Customer procedures, author, review and/or approve various validation / qualification deliverables
· Review / approve validation / qualification deliverables as provided by the supplier of the relevant system(s), ensure that such deliverables are compliant to the Customer requirements
· Lead the project test resources in relation to the validation / qualifications related activities of the project
· Act as the project’s quality representative in relation to testing activities, engaging with local site QA and/or QA eCPL
· Report on the status of the various quality-related activities for key stakeholders
· Engagement with the suppliers to advise the suppliers on the suitable completion of supplier provisioned validation / qualification deliverables.
Required Validation Activities
- Qualify IT/OT systems per Customer Quality Manual.
- Author, execute and review URS, FS, IQ, OQ and test protocols in Kneat.
- Perform test execution, troubleshooting and defect resolution.
- Review supplier deliverables and verify compliance.
- Coordinate with QA, PCM, ITOT teams and suppliers.
- Participate in FAT, SAT, commissioning and startup activities.
Desired Experience Profile
The candidate profiles proposed for this RFP emphasize:
- Strong CSV/CQV experience.
- GMP-regulated pharmaceutical manufacturing background.
- GAMP 5, EU GMP Annex 11, 21 CFR Part 11 knowledge.
- Experience with PLC, SCADA, DCS, MES, Historian, and IT/OT systems.
- Hands-on IQ/OQ/PQ execution and FAT/SAT support.
- Experience using Kneat, ValGenesis, Veeva Vault, TrackWise, ServiceNow or similar validation platforms.
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