Australia Job Openings
IDE Group
Quality Associate
FULL TIME
August 20, 2024
Making a difference is what matters to us, and our values of being resourceful, curious, thinking positively, putting others first, embracing complexity and taking ownership to drive successful outcomes.
Our engagement surveys over the last 3 years have revealed that our people love working with us for:
- The people - intelligent people, collaborating together in smart ways to bring products to life
- Our purpose - every day we work at IDE is an opportunity to build better futures
- Variety of projects available
- This role is based in person at our Head Office in Sydney, Australia
- This role is based in person at our Head Office in Sydney, Australia
- This role is based in person at our Head Office in Sydney, Australia
- This role is full-time
- Leading the Quality function as Quality Lead on product development cross-functional teams.
- Supporting strategy development and planning of projects.
- Proactively supporting the scaling of processes to meet the needs of various projects.
- Identifying and implementing training needs.
- Providing review and approval of project deliverables.
- Monitoring compliance of project activities with QMS requirements.
- Sharing knowledge across the business.
- Supporting maintenance and improvement of the QMS in accordance with ISO 13485, 21CFR820 and ISO 9001.
- Carry out internal audits and spot checks.
- Continuous improvement of the quality framework to meet the needs of the business.
- Actively collect, analyse and communicate data on the QMS.
- Manage the control of QMS documentation and records.
- Create and update QMS documentation including SOPs.
- Train product development employees in IDE’s processes and quality management principles.
- Support in management of key QMS processes including equipment calibration, supplier qualification, and CAPA.
- Completion of allocated tasks to the specified level of quality and within agreed timeframes and budgets.
- A degree in Mechanical, Mechatronics or Biomedical Engineering, Industrial Design or similar applicable technical discipline.
- Minimum 2 years’ experience working in medical device development projects in a functional leadership role.
- Experience working in an ISO 13485-compliant QMS.
- Understanding of key Medical Device standards including ISO 14971 and IEC 62366.
- Experience in undertaking manufacturing planning, quality control and process validation in medical device manufacturing environments.
- Strong Microsoft Office skills, particularly Word and Excel.
- Exceptional mentoring program to ensure your career progresses where you want to go
- Employee Assistance Program
- Cross-Functional Team
- Social Activities
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