NPI Manufacturing Engineer
Resmed
Date: 3 days ago
City: Johor Bahru
Contract type: Full time

The NPI (New Product Introduction) Manufacturing Engineer plays a key role in supporting the successful industrialization and launch of new headgear products within ResMed Malaysia’s manufacturing operations. The role ensures new designs are manufacturable, processes are robust, equipment and documentation are ready, and products are introduced on time, within budget, and in compliance with quality, regulatory, and EHS requirements.
Key Responsibilities
Education & Experience
Key Responsibilities
- NPI Project Support
- Collaborate with global R&D, program managers, and manufacturing teams to transition new headgear designs from concept to mass production.
- Participate in design reviews to provide manufacturability and process feasibility analysis feedback (DFM/DFA).
- Support Gate reviews and ensure deliverables are completed per NPI roadmap.
- Process & Equipment Development
- Develop, qualify, and validate new manufacturing processes for sewing, lamination, bonding/gluing, cutting, and assembly of headgear.
- Work with Equipment & Technology Development team to specify, source, and validate new production equipment/tooling.
- Conduct process capability studies (Cp, Cpk) and ensure process robustness.
- Validation & Documentation
- Prepare and execute process validation protocols (IQ/OQ/PQ) in compliance with medical device regulations.
- Generate and release manufacturing documentation including Work Instructions (WI), Control Plans, and PFMEA.
- Support ECO implementation and BOM/routing setup in ERP system.
- Quality & Compliance
- Ensure processes and documentation comply with ISO 13485, FDA, MDSAP and internal QMS requirements.
- Collaborate with Quality Engineering on CTQ (Critical to Quality) identification, risk analysis, and control strategy.
- Support supplier qualification and PPAP for critical materials (fabrics, foams, elastics).
- Pilot Builds & Launch
- Support engineering builds, V&V, ECS, and pilot runs, ensuring build readiness, data collection, and issue resolution.
- Drive yield improvement, FPY (First Pass Yield), and cycle time achievement before ramp-up.
- Support training of operators and technicians during new line setup.
- Continuous Improvement & Handover
- Identify opportunities for cost reduction (VAVE), process simplification, and automation.
- Ensure smooth handover of stabilized processes to Sustaining Engineering/Operations.
- Document lessons learned for future product launches.
Education & Experience
- Bachelor’s Degree in Mechanical, Manufacturing, Industrial, Bio medical or related Engineering discipline.
- 2–5 years of experience in New Product Introduction, process development, or manufacturing engineering (preferably in medical device, textile, or consumer product industries).
- Knowledge of sewing, lamination, bonding/gluing, and textile-based assembly processes.
- Experience in process validation (IQ/OQ/PQ), statistical analysis, and capability studies.
- Familiar with PFMEA, control plan, SPC, DOE, and Lean Six Sigma tools.
- Proficiency in CAD (SolidWorks, AutoCAD) and MS Office/Project is an advantage.
- ERP/MRP systems knowledge (SAP, Oracle, or equivalent) is desirable.
- Strong problem-solving, project management and analytical skills.
- Effective communication and cross-functional teamwork in a global environment.
- Ability to work under tight timelines with a high level of accountability.
- On-time completion of NPI deliverables at each gate.
- Process capability and FPY achievement before ramp-up.
- Compliance to validation and QMS requirements (no audit findings).
- Successful handover of stable processes to Sustaining team.
- Contribution to cost, quality, and efficiency improvements.
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