jobs in Biocon Biologics

Kerja Sepenuh Masa, Instrumentation - Automation Engineer di Biocon Biologics Johor - Maukerja

Instrumentation - Automation Engineer

Biocon Biologics

Kongsi
Simpan

Lokasi Kerja

  • Gelang Patah Johor Malaysia

Penerangan Kerja

Tanggungjawab

Job Summary

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 technical support.
  • Provide daily reporting of activities and escalate issues to superiors.
  • Support commissioning and validation activities (FAT, SAT, DQ, IQ, OQ, PQ).
  • Attend, record, and conduct trainings as per training matrix/schedule.
  • Participate in projects related to process optimization, facility upgrades, and cost/energy management programs.
  • Propose objectives and targets for work areas and ensure compliance with timelines.
  • Ensure smooth execution of internal and external audits related to QMS and EHS, and close findings within stipulated timelines.
  • Provide routine improvement proposals on equipment, processes, and quality systems.


Requirements

  • Bachelor’s degree in Engineering (Instrumentation, Automation, Electrical, or related discipline).
  • 3–5 years of experience in instrumentation and automation within pharmaceutical, biopharma, or regulated manufacturing industries.
  • Strong knowledge of QMS, EHS, and compliance frameworks.
  • Hands‑on experience with commissioning, validation, and troubleshooting of automation systems.
  • Familiarity with manufacturing processes, equipment, and vendor management.
  • Excellent documentation skills with attention to detail and compliance with ALCOA principles.
  • Strong analytical, problem‑solving, and communication skills.
  • Ability to work collaboratively in cross‑functional teams and manage multiple priorities.

Peringatan Penting

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