M
Marksans Pharma
Quality Control - Officer (CSV)
2 months ago
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Important information
Contract type:
Permanent
Work mode:
Onsite
Published on:
10 August 2026
What they need
- Prepare and review validation documents, including (VP), (URS), (FS), (RA)
(IQ), (OQ), (PQ), (VSR)
- Perform periodic review and revalidation of computerized systems.
- Conduct risk assessments and determine validation scope.
- Review audit trails and ensure electronic records comply with data integrity requirements.
- Support regulatory inspections and customer audits.
- Manage change control, deviations, CAPA, and incident investigations related to computerized systems.
- Prepare SOPs and provide CSV training to laboratory personnel.
- Participate in software upgrades, migrations, and implementation projects.
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