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Salary
$15k – $32k per year (Estimated)
Location
In office (Johor Bahru)
Seniority
Middle · 3+ years exp
Employment
Full-Time
Overview
Company
Impact
Profile match
ResMed is a medical device company founded in Sydney in 1989 by a physician who had helped develop the first practical treatment for obstructive sleep apnoea and could not persuade anyone else to commercialise it. It makes the masks, flow generators and ventilators used to treat sleep apnoea and chronic respiratory disease, and it has built a large software business in the cloud platforms that manage those devices and the out-of-hospital care around them. Now headquartered in San Diego and listed in New York and Sydney, it shares the sleep apnoea market largely with Philips and benefited substantially from its competitor's device recall.

The Manufacturing Engineer is responsible for leading NPI manufacturing engineering activities, including process development, equipment readiness, routing, documentation, validation, and continuous improvement to meet volume, quality, safety (OHS), cost, yield, and line efficiency targets.

This role ensures product manufacturability by partnering with Product Development, Quality, Production, and Supply Chain teams to translate new product designs into stable, compliant, and production-ready manufacturing processes before handover.

Let’s talk about Responsibilities

  • Develop, implement, and optimize manufacturing processes, equipment, tooling, routing, work instructions, and documentation to meet NPI and production targets
  • Collaborate with Product Development teams to provide DFM/DFA input and ensure product designs are robust, manufacturable, serviceable, and scalable for production
  • Lead and support New Product Introduction (NPI) activities, including prototype builds, process trials, testing, risk assessment, verification, validation, and production handover
  • Troubleshoot and resolve manufacturing, process, equipment, and technical issues to improve yield, reduce downtime, and support stable production ramp-up
  • Establish and maintain production procedures, work instructions, SOPs, process flows, routings, cycle time standards, and controlled manufacturing documentation
  • Provide training and technical coaching to production teams on new equipment, processes, procedures, quality requirements, and safe ways of working
  • Drive continuous improvement initiatives using Lean, Six Sigma, GMP, data analysis, and structured problem-solving to improve cost, yield, quality, and efficiency
  • Ensure compliance with Quality, GMP, regulatory, and Occupational Health & Safety (OHS) standards throughout NPI development, validation, and production transfer
  • Initiate, execute, and document process validation activities, including protocol preparation, trial execution, data review, report completion, and evidence retention
  • Build strong cross-functional relationships with Production, Quality, Product Development, Supply Chain, and Engineering teams to remove risks and close NPI actions
  • Participate in or lead projects to improve manufacturing performance, COGS, yield, line efficiency, routing accuracy, cycle time, and technology readiness milestones
  • Use data-driven methods to identify trends, verify assumptions, evaluate options, and recommend effective technical actions.
  • Develop and maintain CAD models and engineering drawings to support process development, tooling, fixtures, validation, and manufacturing handover.

Let’s talk about Qualifications and Experience

Preferred:

  • Bachelor's Degree in Engineering (Mechanical, Manufacturing, Industrial, Mechatronics, or related field)
  • Minimum 3 years of relevant experience in manufacturing engineering, NPI engineering, process engineering, or a similar technical environment
  • Strong understanding of manufacturing processes, process validation, production systems, routings, cycle time studies, tooling, fixtures, and equipment readiness
  • Proven experience in troubleshooting and resolving technical, process, equipment, and manufacturability issues using structured problem-solving methods
  • Familiarity with GMP, quality systems, regulatory expectations, OHS requirements, and documentation control in a manufacturing environment
  • Ability to apply company policies, engineering standards, risk-based thinking, and data-driven decision making to solve a variety of technical challenges
  • Experience in medical device, healthcare, or other regulated manufacturing environments
  • Certification or hands-on experience with Lean Manufacturing, Six Sigma, process capability, validation, or operational excellence methodologies
  • Strong exposure to New Product Introduction (NPI), design transfer, prototype builds, process scale-up, and product lifecycle support.

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.

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