Engineering Technician (Contract Based - Cikarang)

Engineering Technician (Contract Based - Cikarang)

Do you have 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 the science and puts patients first Then AstraZeneca might be the one for you.

About AstraZeneca

AstraZeneca is a global, science-led, patient-focused biopharmaceutical company that focuses on the discovery, development, and commercialization of prescription medicines for some of the world's most serious diseases. But we are more than one of the world's leading pharmaceutical companies.

This is an exciting time to join our team as we continue to strengthen our manufacturing operations and deliver high-quality medicines to patients. At Indonesia Operations, Cikarang, you will have the opportunity to contribute directly to production excellence, operational compliance, and continuous improvement in a highly regulated environment.

What you'll do

We are currently looking for a Engineering Technician on contract basis (6 months) to join our Manufacturing team in Cikarang – Indonesia Operations.

Reporting to the Engineering Supervisor on dotted line and Manufacturing Director on solid line, you will be responsible for execute and maintain maintenance schedule for production equipment and AHU's and calibration schedule for all equipment as plan. You will implements good documentation practice for engineering related task of its respective area. You will responsible for strict compliance of all engineering production area with cGMP-rules Global Quality Policya and responsible for implementation of SHE and Depnaker's UKK (Industrial Hygiene and Safety) requirements in the work area, as well as implements Lean Principle 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
• Good communication skills

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

Why AstraZeneca

At AstraZeneca, we are dedicated to being a great place to work, where you are empowered to push the boundaries of science and unleash your entrepreneurial spirit. There is no better place to make a difference to medicine, patients, and society.

You will be part of a collaborative and inclusive environment that values ethical conduct, compliance, continuous improvement, and people development. We are committed to lifelong learning and giving our employees the opportunity to grow while contributing to the delivery of high-quality medicines for patients.

So, what's next

If you are ready to bring your expertise in engineering maintenance, equipment reliability, GMP compliance, and continuous improvement to AstraZeneca to AstraZeneca, we would love to hear from you.

If you're curious to know more, please reach out to [Confidential Information]

Where can I find out more

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