Manufacturing Project Lead (Mask NPI)

About the role

ResMed is looking for a Manufacturing Project Lead (Mask NPI) based in Singapore. You will represent Manufacturing Engineering in cross-functional product development teams and lead manufacturing readiness for new mask products, coordinating process engineering activities across the product development lifecycle so that new products, equipment and processes enter production safely, efficiently and on schedule.

Key responsibilities

• Lead the Manufacturing cross-functional team to deliver manufacturing readiness for new product introductions.
• Develop and manage project plans covering milestones, dependencies, risks, mitigation actions and key commitments.
• Represent Manufacturing Engineering in Product Development project teams and share manufacturing insights with key decisions.
• Drive Design for Manufacturability and Design for Assembly with Product Development.
• Identify and implement manufacturing processes, equipment and technologies supporting quality, cost, delivery, safety and scalability.
• Coordinate subject matter experts and NPI stakeholders across process development, technology readiness, validation and manufacturing readiness.
• Communicate progress, risks and readiness through project reviews, quality governance forums and phase transitions.
• Align Product Development, Manufacturing and Supply Chain Leadership on priorities, strategies, risks and decisions.
• Solve technical, manufacturing and project challenges through structured problem-solving and collaboration.
• Support validation, pilot builds, production ramp-up and continuous improvement.

Required profile

• Degree in Mechanical Engineering, Mechatronics Engineering, Manufacturing Engineering or an equivalent discipline.
• Background in New Product Development or New Product Introduction in a high-volume production environment.
• Knowledge of the full product development lifecycle, including projects with significant technical or business impact.
• Proven ability to lead cross-functional projects and manage schedules, milestones, risks and dependencies.
• Sound understanding of manufacturing process development, validation and risk management methodologies.
• Ability to represent manufacturing process development, validation and risk management during quality and regulatory audits.
• Understanding of safe, efficient, robust and high-quality medical device manufacturing processes.
• Able to manage several projects or workstreams while balancing technical detail with business priorities.

Nice to have

• Medical device manufacturing and product commercialization exposure.
• Familiarity with Lean Manufacturing, Six Sigma or continuous improvement principles.
• Involvement in manufacturing readiness and production ramp-up activities.