15 Aug
|
Marksans Pharma
|
India
15 Aug
Marksans Pharma
India
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.
📌 Quality Control Officer Csv South Goa (India)
🏢 Marksans Pharma
📍 India