Opportunity Description
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...
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