Engineering Technician

Engineering Technician (Contract Based - Cikarang)

Do you possess expertise in pharmaceutical engineering and a passion for quality, GMP, and SHE compliance? Would you like to apply your expertise to help deliver life‑changing medicines in an organisation that follows science and puts patients first? Then AstraZeneca might be the one for you.

We are currently looking for an Engineering Technician on a 6‑month contract basis to join our Manufacturing team in Cikarang – Indonesia Operations.

Reporting to the Engineering Supervisor on the dotted line and the Manufacturing Director on the solid line, you will be responsible for executing and maintaining the maintenance schedule for production equipment and AHUs, as well as the calibration schedule for all equipment as planned. You will implement good documentation practice for engineering‑related tasks of its respective area. You will be responsible for strict compliance of all engineering production areas with cGMP‑rules Global Quality Policy and for implementation of SHE and Depnaker’s UKK (Industrial Hygiene and Safety) requirements in the work area, as well as for implementing Lean Principles in Cikarang Site.

In this role you will:

• Execute maintenance activities:
  Perform preventive maintenance activities in SAP according to schedule, execute work orders and assigned CAPAs, and help ensure all maintenance work is completed in a timely manner.
• Maintain equipment reliability:
  Support the maintenance of production equipment and AHUs to meet operational requirements with minimal interruption and help maintain spare part availability in the area.
• Support calibration and compliance:
  Carry out calibration‑related activities as planned and help maintain zero deviations caused by preventive maintenance and calibration work.
• Assist investigations and audits:
  Support investigations by initiating deviations, participating in problem‑solving activities, and completing assigned CAPAs on time, while also supporting self‑inspections and internal/external audits.
• Coordinate with vendors and documentation:
  Accompany and monitor vendor activities, prepare like‑for‑like change documentation when required, and ensure engineering documentation is updated and properly managed.
• Drive continuous improvement:
  Perform Gemba as planned and support Lean, TPM, maintenance, SHE, and quality maturity initiatives across the site.
• Support systems and administration:
  Use PM SAP for daily maintenance activities and support document archiving, storage, destruction, PR/PO processing, and vendor registration activities.
• Contribute to people development and compliance:
  Participate proactively in IDP, training needs analysis, and skill matrix development, while completing required training and acting in line with the Code of Conduct and company policies.

Essential for the role:

• Diploma / Vocational High School graduate in Engineering
• At least 3–5 years of practical experience as an engineering technician in a pharmaceutical company
• Familiarity with GMP and SHE standards
• Familiarity with engineering tools, technical drawings, and machinery used in pharmaceutical manufacturing
• Familiarity with workshop tools and equipment
• Familiarity with PLC and electrical systems
• Ability to read and speak in English
• Ability to use a computer and printer for document‑related work
• Familiarity with Microsoft Office and Teams

Desirable for the role:

• Experience supporting deviation investigations, problem‑solving activities, and CAPA execution
• Exposure to internal audits, external audits, and self‑inspections
• Experience using SAP PM or similar maintenance management systems
• Understanding of spare parts management and vendor coordination
• Knowledge of Lean Manufacturing, TPM, and Gemba
• Experience working cross‑functionally with Production, SHE & Facility Management, TT and Packaging Development, Warehouse, Quality Control, Quality Assurance, and Supply Chain