Supplier Engineering (SE) works across Resmed and our suppliers to continuously improve performance, implement process controls and develop quality assurance plans. We ensure our supply chain network consistently delivers high-quality components that meet Resmed’s specifications, volume demands, and delivery timeline.
Let’s talk about Responsibilities
- Partner with Supply Chain Engineering, Product Development, Planning and GSA to ensure reliable, high-quality components supply is available for manufacturing.
- Build and maintain collaborative relationships with internal stakeholders and external suppliers to meet quality, availability & value requirements.
- Act as the technical link between Resmed and our electronics suppliers, clearly communicating product specifications and assessing supplier capabilities.
- Provide hands-on technical support and guidance to our suppliers, particularly in areas such as manufacturing of PCBAs, Power Supplies, and other electronic components.
- Validate Supplier Production Processes as part of New Product Introduction (NPI), Engineering Change Note (CN) and Supplier Change Requests (SRFC).
- Investigate and resolve supplier quality issues, driving root cause analysis, managing corrective actions (CAPA), and continuous improvement.
- Lead or contribute to cross-functional initiatives to improve product quality and supplier capability.
- Where required, participate in supplier audits and performance evaluations to ensure compliance with quality and regulatory standards.
- Where appropriate, provide mentorship to junior engineers and support departmental knowledge sharing.
Let’s talk about Qualifications and Experience
Required:
- Bachelor’s degree in Electronics Engineering or a closely related field
- 2+ years of functional engineering experience within a manufacturing environment as a Manufacturing, Process, Quality or Industrial Engineer.
- Excellent analytical and technical skills with strong attention to detail.
- Highly motivated and able to manage multiple projects at once.
- Willingness to travel within and outside of country of residency for short business-purpose trips
- undefinedExcellent interpersonal and communication skills (both verbal and written) for effective communication with all levels of organization. Demonstrated ability to work well with cross-functional departments and stakeholders in a proactive and constructive manner.
Preferred:
- Experience in PCBA (PCB Assembly) and power supply manufacturing processes.
- Knowledge of applying GD&T and geometrical drawing convention
- Experience in operating within highly regulated industry – preferably medical devices.
- Knowledge in requirements of relevant international standards such as ISO standards, IEC standards, FDA requirements etc
- Proficiency in use of relevant Quality Tools such as Six Sigma, Lean, APQP, or Kepner-Tregoe methodologies.
- Proficiency in use of relevant Statistical tools such as SPC, Gage R&R, Minitab or JMP.
- Project management skills and experience in leading cross-functional improvement initiatives.
- Skills in effective Supplier engagement & negotiation.
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Joining us is more than saying “yes” to making the world a healthier place. It’s discovering a career that’s challenging, supportive and inspiring. Where a culture driven by excellence helps you not only meet your goals, but also create new ones. We focus on creating a diverse and inclusive culture, encouraging individual expression in the workplace and thrive on the innovative ideas this generates. If this sounds like the workplace for you, apply now! We commit to respond to every applicant.
Skills Required
- Bachelor's degree in Electronics Engineering or a closely related field
- 2+ years of functional engineering experience in a manufacturing environment as a Manufacturing, Process, Quality, or Industrial Engineer
- Excellent analytical and technical skills with strong attention to detail
- Ability to manage multiple projects simultaneously
- Willingness to travel domestically and internationally for short business trips
- Excellent verbal and written communication skills
- Ability to work effectively with cross-functional departments and stakeholders
- Experience with PCBA and power supply manufacturing processes
- Knowledge of GD&T and geometrical drawing conventions
- Experience in a highly regulated industry, preferably medical devices
- Knowledge of relevant ISO, IEC, and FDA requirements
- Proficiency with Six Sigma, Lean, APQP, or Kepner-Tregoe methodologies
- Proficiency with SPC, Gage R&R, Minitab, or JMP
- Project management experience leading cross-functional improvement initiatives
- Supplier engagement and negotiation skills
ResMed Compensation & Benefits Highlights
The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about ResMed and has not been reviewed or approved by ResMed.
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Strong & Reliable Incentives — Bonuses are considered a meaningful component of total compensation and are paid regularly. Annual payouts and performance incentives are frequently highlighted alongside base pay.
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Healthcare Strength — Health coverage is described as comprehensive, including medical, dental, and vision plans that are viewed favorably. Wellbeing resources and flexibility around care reinforce the overall strength of the offering.
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Equity Value & Accessibility — An employee stock purchase plan is broadly available and regarded as a valuable ownership benefit. Equity elements are positioned as accessible parts of total rewards across many roles.
ResMed Insights
What We Do
ResMed provides medical equipment for treating, diagnosing, and managing sleep-disordered breathing and other respiratory disorders.








