Manufacturing Engineer

Description:

The Operations team partners closely with ResMed’s five business leaders to understand their needs then providing a variety of products and services to help them meet those needs including Customer and Technical Services, Global Quality Assurance and Regulatory Affairs, Supply Chain, manufacturing, logistics and distribution. Focused on enabling new product introduction and operating excellence, our team strives to improve time to market for new products and services, improve efficiencies in our cross-functional processes, and improve our supply chain through digitization and automation to increase value add to our customers.

• 12-month Fixed Term Contract

• Located at Bella Vista

We have an opportunity for a Manufacturing Engineer to join our team in a role that offers the challenge of a complex product, a fast paced engineering environment, and exposure to a broad range of manufacturing.

Let’s talk about Responsibilities

As a Manufacturing Engineer, you will apply advance skills and knowledge of manufacturing engineering discipline to develop and implement manufacturing processes, equipment, facilities and documents, in order to meet the current and future production volume, quality, OHS and cost requirements. Key deliverables include: introduce new products, equipment and processes into production in compliance with ResMed quality management system requirements. Implement continuous improvement initiatives to achieve best in class operational measures of quality & efficiency. To do this, you will have the following opportunity to -

• Implement manufacturing processes, equipment, facilities and documentation to meet production volumes and delivery requirements

• Promote a safe working environment as well as implementing & closing out actions for the continual improvement of work place safety

• Represent Manufacturing whilst working closely with Product Development to ensure robust, manufacturable products.

• Introduce & maintain production procedures, provide training on new equipment, processes & procedures.

• Assists in the development, execution, and testing of new and existing products

• Complete process validation activities & documentation.

• Identify & implement quality and efficiency measures including GMP, Six-Sigma LEAN improvement actions.

Let’s talk about Qualifications and Experience

• Tertiary qualifications in engineering such as Manufacturing, Mechatronics, Mechanical, Biomedical or any related discipline or equivalent experience consummate with the role

• Minimum of 2 years in Medical Device or Electronics or high-volume manufacturing and GMP

• Knowledge of manufacturing processes & equipment for high and low volume manufacturing environments, particularly in assembly and automation

• Excellent communication and documentation skills, including technical reports

• Experience with process validation within a regulated Quality System environment

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!