03 Aug
|
Cadila Pharmaceuticals
|
India
03 Aug
Cadila Pharmaceuticals
India
Description
Lead implementation, administration, and continuous enhancement of the LIMS platform. Configure and maintain users, workflows, specifications, templates, master data, and security roles. Ensure system availability, integrity, backup, and disaster recovery. Coordinate LIMS upgrades, patches, and change management activities. Lead validation activities including URS, FS, DS, IQ, OQ, PQ, and Validation Reports. Ensure LIMS remains in a validated state throughout its lifecycle. Manage periodic reviews, risk assessments, and revalidation activities. Ensure compliance with cGMP, GLP, 21 CFR Part 11, EU Annex 11, and ALCOA+ principles. Monitor audit trails and electronic records. Investigate data integrity events and implement CAPA. Support internal, customer, and regulatory audits.
📌 Manager (India)
🏢 Cadila Pharmaceuticals
📍 India