Associate Director, Manufacturing

Overview Position: Associate Director, Manufacturing Location: Tuas, Singapore Department: Global Manufacturing Operations, Supply Chain Position Overview As Associate Director, Manufacturing, you will lead all factory operations at ResMed’s Tuas site, driving safety, efficiency, and compliance while aligning with our global manufacturing strategy. This pivotal role is central to driving operational excellence, workforce capability, and strategic growth while delivering reliable output at the right cost and quality. You will champion transformation through automation, digitalization, and new product introductions, positioning Tuas as a cornerstone of ResMed’s global manufacturing network. Responsibilities Manufacturing Leadership Oversee multi-factory operations to ensure safety, regulatory compliance, and performance excellence. Execute site strategy that balances capacity, cost, quality, and resilience. Align cross-functional priorities, continuous improvement efforts, and new product launches. Ensure adherence to ResMed’s Quality Management System and all applicable local regulations. Production Excellence Deliver production targets on time, meeting stringent quality and cost standards. Maximise asset utilisation, optimise production planning, and deploy resources effectively. Provide technical leadership in issue resolution, CAPAs, and continuous improvement. Collaborate with Engineering and Global Operations on NPIs, process optimisation, and equipment upgrades. Maintain facilities and equipment to ensure operational readiness. Manage indirect costs through strategic sourcing and supplier partnerships. People & Culture Lead and develop factory managers, team leaders, and operators to foster a high-performance culture. Build robust succession plans and long-term workforce strategies. Promote engagement, learning, and development in line with ResMed’s values. Cultivate strong communication and alignment across all factory teams. Performance & Continuous Improvement Monitor and report site-wide KPIs including output, OEE, labour efficiency, cost, quality, and safety. Drive initiatives to close performance gaps and deliver sustainable results. Align operational execution with strategic business goals. Collaborate with stakeholders to ensure successful project outcomes. Champion GMP, Lean, Six Sigma, and future-ready manufacturing principles. Key Competencies Proven leadership in people development and team performance. Strong analytical and data-driven decision-making skills. Ability to balance global priorities with local execution. Exceptional communication and stakeholder management. Passion for innovation and continuous improvement. Qualifications & Experience Minimum Requirements Bachelor’s degree in Engineering or related discipline. Extensive experience in high-volume manufacturing environments. Demonstrated success in leading teams and developing talent. Strong background in production systems, GMP, and regulatory compliance. Proficiency in MS Office and business reporting tools. Formal training in project management, Six Sigma, DFSS, or related methodologies. Preferred Postgraduate qualification in business, manufacturing, or operations management. Experience in medical devices or other regulated industries. Certifications in Lean, Six Sigma, DFSS, or project management. Familiarity with Objective or equivalent document management systems. Joining us is more than saying “yes” to making the world a healthier place. It’s about a career that’s challenging, supportive and inspiring. We focus on creating a diverse and inclusive culture and encourage ideas that drive excellence. If this sounds like the workplace for you, apply now. We commit to respond to every applicant. #J-18808-Ljbffr