We are looking for a passionate NPI Manufacturing Engineer to join our LSR Manufacturing Engineering team in Singapore.

At ResMed, our LSR Manufacturing Engineering team drives innovation, collaboration, and technical excellence to advance manufacturing processes, equipment, and facilities. We are committed to delivering world-class quality, efficiency, and cost-effectiveness for our globally recognized products. If you are passionate about cutting-edge technology, problem-solving, and making a meaningful impact, we’d love to hear from you!

Let’s Talk About the Role:

As an NPI Manufacturing Engineer, you will play a key role in developing and implementing manufacturing processes, equipment, and documentation to support new product introductions (NPI) and production demands. Working alongside an experienced manufacturing team, you will contribute to prototyping, process development, and operational excellence, directly influencing ResMed’s innovation journey.

Let’s Talk About Responsibilities:

Implement manufacturing processes, equipment, and facilities to meet current and future production needs.

Conduct process validation activities (IQ, OQ, PQ) and maintain detailed documentation within a regulated Quality System (ISO 13485, ISO 14971).

Solve complex engineering problems using data-driven decision-making and statistical analysis.

Collaborate with internal teams and external suppliers to evaluate and implement new technologies, automation, and digitization, aligning with smart manufacturing techology advancements.

Provide technical feedback and recommendations to design teams to ensure robust and manufacturable product designs.

Train production teams on new equipment, processes, and procedures, and provide technical support when needed.

Communicate technical concepts clearly across cross-functional teams through written, verbal, and graphical presentations.

Let’s Talk About You:
Required:

Bachelor’s degree in Engineering or a related discipline.

Experience in Medical Device manufacturing and process development.

Hands-on experience with process validation in a regulated environment (ISO 13485, ISO 14971).

Strong problem-solving skills and a quality-focused mindset.

Excellent communication and documentation skills.

Team player with a proactive, resourceful, and innovative attitude.

Preferred:

Experience in volume manufacturing, automation environments, and bringing new designs into production.

Hands-on experience troubleshooting and repairing jigs, fixtures, and equipment.

Experience with QMS audits.

Basic knowledge of smart manufacturing technologies and proficiency in data analytics (SQL, XML, Tableau, Power BI, or Cognos Analytics) to drive data-driven decision-making and process improvements."

Join Us!

Working with us is not just an opportunity to help millions of people live healthier, higher-quality lives. It’s an opportunity to shape an amazing future – for our patients, the planet, the company and your own career.   

So join us and together, let’s shape the future!   

#LI-APAC

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.