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Deviation and CAPA Support. Assist in documentation and tracking of deviations, change controls, and CAPAs. Participate in root cause analysis and follow-up actions.

M.Pharm Pharmacology. Literature search and designing of Bioavailability BA and Bioequivalence BE studies of oral and non-oral products - injectable, derma, ophthalmic etc. towards different regulatory submission.

Handling of Change Controls, CAPA's, Unplanned Deviations, Planned Deviation, Investigations and Audit Management in Trackwise software

Sun is building the future of healthcare. We invite passionate professionals to join India's No. 1 pharmaceutical company and help deliver medicines that change lives worldwide.

Build and maintain long-term, trust-based relationships with healthcare professionals. Understand customer needs and offer effective solutions.

Seasoned experience in handling of various EU procedure like DCP, MRP, National. National phase handling for EU procedures.

Raw material & finished product analysis. HPLC / GC / UV/ IR / Dissolution testing. Stability & validation samples analysis, OOS / OOT handling & documentation

IPQA, Vendor Qualification, Technology Transfer, QMS, Validation, Qualification, Documentation Quality Risk Assessment

To develop promotional content and manage label updates in alignment with brand and regulatory requirements and ensure delivery of high-quality, compliant, and impactful content across multiple channels.