Ensure operational excellence by managing instrumentation and automation systems, driving compliance, and supporting continuous improvement across Biocon’s biopharma manufacturing facilities.

Key Responsibilities

• Coordinate all activities related to document control, including technical documents, drawings, and commercial correspondence.
• Input and maintain document data in registers, ensuring accuracy and up‑to‑date information.
• Generate, review, and maintain procedures, protocols, and reports related to QMS and EHS management systems.
• Ensure latest approved documents/protocols for instrumentation and automation are in place and accessible.
• Review, register, and safeguard documents under secure custody with easy traceability.
• Gain familiarity with manufacturing processes and related equipment to support engineering operations.
• Communicate with external vendors for site services, repairs, and techn...