Moulding Engineer

ResMed Inc; Singapore; Vor Ort; SGD 120.000 - 160.000; Vollzeit

Zusammenfassung

ResMed Inc is seeking a senior Moulding Engineer to lead LSR moulding processes and drive continuous improvement in high-volume medical device manufacturing. You will optimize cycle times, scrap reduction and OEE while mentoring engineers and coordinating trials with PLM, QA and manufacturing teams.

Ideal candidates bring 5–10+ years in injection moulding, strong problem-solving skills and knowledge of GD&T, ISO 13485 and GMP requirements.

Qualifikationen

• BS degree and relevant engineering background in moulding.
• Hands-on experience with LSR moulding and high-volume production.
• Experience in defect analysis, scrap reduction and process validation.
• Knowledge of GMP/ISO medical device requirements is a plus.
• Strong data-driven problem solving and capability to lead projects.

Aufgaben

• Implement, maintain & improve LSR moulding processes, equipment, facilities and documentation.
• Lead & manage multiple projects and collaborate with cross-functional teams.
• Develop robust moulding processes and support trials/qualifications.
• Reduce cycle time, scrap and manufacturing costs; improve OEE.
• Investigate moulding defects and customer complaints; coach juniors.
• Read drawings, GD&T and participate in design reviews; ensure CQI.
• Work in fast-paced environment with data-driven decisions.

Kenntnisse

LSR moulding

Process optimization

Defects troubleshooting

Scrap reduction

OEE improvement

Leadership

Cross-functional

Data-driven

Problem solving

Ausbildung

Bachelor's Degree in Mechanical Engineering

Manufacturing Engineering

Polymer Engineering

Chemical Engineering

Tools

GD&T ASME Y14.5-2018

ISO 13485

Jobbeschreibung

The primary role of Mounding Engineering function is to apply advance skills and knowledge of mounding engineering in process, equipment, facilities and documents, in order to meet the current and future production volume, quality, OH&S and cost requirements. Key deliverables include conducting process validation, scrap reduction and cost saving initiatives.Let’s talk about ResponsibilitiesTo implement, maintain & improve Liquid Silicone Rubber (LSR) Moulding Manufacturing processes, equipment, facilities and documentation to meet moulding production volumes and at all times follow OH&S guidelines.Possess Global mindset and ability to work with other geographical sitesLead & manage multiple Projects, Influence and Collaborate with other teamsLead, mentor or train junior engineers and techniciansDevelop robust moulding processes.Support mould trials and qualification.Reduce cycle time, Reduce Moulding Scrap and Manufacturing cost.Improve Overall Equipment Effectiveness (OEE).Investigate moulding defects and customer complaints.Work closely with Production, Planning, Quality, SQE, PD, PLE, GSA and Marketing teamsAble to work independently without guidance in fast-paced and high-pressure environmentDecision making based on data-driven and risk analysisStrong analytical and troubleshooting skillsLeadership and mentoring capabilityEffective communication with cross-functional teamsContinuous improvement mindset (Lean Manufacturing)Let’s talk about Qualifications and ExperienceEducation:Bachelor's Degree in:Mechanical EngineeringManufacturing EngineeringPolymer EngineeringChemical EngineeringExperience:5 to 10+ years of injection moulding experience.Strong hands-on experience in:LSR mouldingMulti-cavity mould processingMedical, automotive, or consumer product manufacturingHigh-volume automated manufacturing environmentsTechnical Skills:LSR material handlingLSR moulding machine and dosing unit operationLSR Process optimization, Defects troubleshooting and Scrap reductionMold Qualification and AccepanceTool Design ReviewProblem-Solving skills (such as DMAIC, Cause & Effect, 5 Whys)Automation and Robotic integrationAble to read and interpret Mechanical DrawingAble to read and interpret GD&T ASME Y14.5-2018Quality and Regulatory Knowledge:Statistical Process Control (Cpk, SPC)Hypothesis Test and Design of ExperiencePFMEA and Control PlansDQ/IQ/OQ/PQ process validationISO 13485 (medical devices)Safety standards (ISO, OSHA)GMP requirements (for medical manufacturing)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.