Manufacturing Engineer - Motors

ResMed is a global leader in the design, manufacture, and distribution of innovative products for the diagnosis, treatment, and management of respiratory disorders. The company has experienced sustained and significant growth since its inception. One of the principal contributors to this growth is innovation reflected in a commitment to producing world-class product lines. The global competitive environment is becoming more difficult which is resulting in a greater emphasis on innovation and a cost-effective approach to achieving market leadership through technological advances.

• Implement manufacturing processes, equipment, facilities, and documents to meet current and the future production volume and delivery requirements.
• To understand and supports the production line by resolving technical issues as required.
• Promote a safe working environment by following OH&S guidelines as well as implementing & closing out actions for the continual improvement of workplace safety.
• Represent Motor BU for respective PFT on new design project XFT, provide constructive technical feedback and recommendations to ensure robust, manufacturable product. Engage external suppliers as appropriate. Understand project risk, develop contingencies, track milestones and deliver project outcomes on time.
• Introduce & maintain production procedures.
• Provide training to operators on new equipment, processes & procedures as required.
• Complete process validation activities & documentation.
• Identify & implement GMP, Six-Sigma LEAN improvement actions.
• Assess and implement new processes, equipment, and technologies for longer-term manufacturing requirements.
• Acquire data and interpret through statistical analysis; partner with internal cross-functional teams to review data and provide recommendations on business process improvement opportunities.

• Mechanical aptitude with Tertiary qualifications in engineering or related discipline, with min 3 years of relevant working experience in high volume manufacturing environment.
• Experience in medical manufacturing will be preferred
• Familiar with ISO9001, ISO13485, FDA Quality System Regulations for medical devices (21 CFR part 820), and the Medical Device Directive (93/42/EEC) will be preferred
• Experience with process validation within a highly regulated Quality System environment, which include Continuous Improvement, Lean and Six Sigma
• Hands-on experience in basic troubleshooting / repairing of jigs, fixtures and equipment will be preferred
• Experience in Data Analytics, which include technical understanding of XML, data models and database design. Able to write SQL queries, and experience with some of the various analytics tools such as Tableau, Cognos Analytics or Power BI.