Quality Associate

23 hours ago

Sydney, New South Wales, Australia IDE Group Full time $90,000 - $120,000 per year

The Company

IDE Group is dedicated to creating meaningful MedTech ventures. Guided by our values, principles, and processes, we've partnered with clients on more than
500 projects
across the medical technology landscape—including respiratory care, drug delivery, connected devices, and point-of-care diagnostics.

What matters most to us is making a difference. We live our values every day:
Be Resourceful, Be Curious, Think Positive, Put Others First, Embrace Complexity, and Take Ownership.

Our people love working at IDE because of:

  • The People
    – intelligent, collaborative colleagues who bring products to life
  • The Purpose
    – every day is an opportunity to build better futures
  • The Work
    – diverse projects and stimulating intellectual challenges

The Role

In your role as a
Quality Associate
, you will use your knowledge and skills to understand, believe and support IDE in carrying out its "Why". You will do this by:

  • Carrying out the objective of the Quality Functional Group at IDE by continuously improving IDE's Quality Management System.
  • Ensuring that quality is championed throughout the organisation and work is executed with a high degree of technical excellence for IDE and its Clients, satisfying project stakeholders in support of producing commercially successful results.
  • Working with the business units and other IDE functional groups and stakeholders to maintain IDE's ISO 13485 Certification and the development and performance of IDE's technical and quality management capabilities.

Qualifications & Experience

  • A degree in one or more of the following: Industrial Design, Mechanical Engineering, Mechatronic Engineering, Biomedical Engineering, or similar applicable technical discipline.
  • 2+ years of experience in or exposure to Medical Device Development process and Quality Management Systems such as ISO 13485, ISO 9001 or similar.
  • Experience in or exposure to electro-mechanical systems, medical devices, consumer products, or technical products (high and low volume products).
  • Experience working in multi‐disciplinary project-based R&D environments with technical personnel collaborating on design problems within a multi‐disciplinary R&D environment.
  • Experience in project management, reviewing outputs from technical personnel of various disciplines in a cross-disciplinary team.
  • Experience in undertaking internal and supplier audits.
  • Experience in undertaking risk management and risk analysis activities, including tools such as Hazards Analysis and FMEA.
  • Experience in undertaking auditing and quality control activities in medical device manufacturing environments.
  • Strong Microsoft Office skills, particularly Word and Excel.

The Benefits

  • Career progression opportunities and a strong mentoring program
  • A collaborative, purpose-driven culture with smart, passionate colleagues
  • Access to our Employee Assistance Program and wellbeing initiatives
  • Exposure to diverse MedTech projects that make a real-world impact

If you're ready to apply your quality expertise to meaningful MedTech projects that improve lives, we'd love to hear from you. Apply today to join IDE Group and help us build better futures.

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