Title:
Myofunctional Research Co – Helensvale QLD
Assist with the coordination of company Design and Development projects and quality support in accordance with the quality management system and applicable global regulatory requirements for medical devices.
Core objectives include:
Coordinating Design and Development projects from product realisation through to commercialization.
Maintaining documentation relating to Design and Development in-line with our Quality and Regulatory requirements.
Representing Design and Development for internal and external audits.
Assisting the Quality and Regulatory department with as required.
Maintaining QMS documentation, including update of SOPs, Work Instructions and other document control related activities.
UndertakingInternalAudits within organization and amongst business partners for supplier control.
Coordinate the CAPA process and Non-conformance Process.
Desired Knowledge and Experience
A background in the medical device industry.
Experience with project planning for Design and Development
Familiarity with ISO ***** and *****.
Ability to work under pressure.
Organisational and time management skills.
Excellent attention to detail.
Ability to work well as part of a team.
Please note that this job description serves to illustrate the general scope and responsibilities of the position and is not intended to be an exhaustive list of duties.
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