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Responsibilities
- Conduct engineering studies and provide engineering solutions for technical related issues.
- Coordinate and support technical maintenance team in setting up production equipment. Ensure equipment are well maintained and operate at optimum condition with minimum breakdown.
- Carry out process improvement activities (LEAN-OEE), cost saving activities and quality-productivity improvement activities.
- Coordinate and support validation engineer in carry out validation activities for new production equipment.
- Coordinate activities of suppliers from conceptual discussion and specification through design and reviews to develop, qualify and implement manufacturing processes.
- Maintain products/process (legacy and new) and update documentations.
- Resolve quality issues related to new and existing products.
- Perform technical support (active participation) and problem solving, i.e. technical evaluation of design changes and product complaints.
- Bachelor's Degree in Engineering or engineering diploma/certificate with minimum of 7 years working experience.
- Have strong technical and problem-solving skills to ensure optimal project execution and implementation.
- Knowledgeable on effective and efficient product manufacturing processes.
- Hands on experience in equipment troubleshooting.
- Experience and interest in programming (PLC) would be added advantage.
- Have strong communication skills, proficient in written and spoken English.
- Able to work independently, be structured and systematic. Able to work in a cross-cultural team.
- Understand documentation work is part of work nature.
- Must have a sense of urgency and commitment to project schedules.
- See it as a challenge to work in a dynamic international environment.
- It will be an advantage to have relevant experience from the Medical Device industry including FDA requirements, Design Control, Process Validation and ISO 13485.
