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GN Group

Senior Quality Assurance Specialist

Posted 6 Days Ago
Be an Early Applicant
In-Office
Sydney, New South Wales
Mid level
In-Office
Sydney, New South Wales
Mid level
Lead day-to-day Quality and Regulatory requirements for the ANZ business, ensuring compliance with ISO13485 and local regulations, conducting audits, and training colleagues.
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At GN Hearing, we’re driven by a simple but powerful purpose: to make life sound better. As one of the world’s leading innovators in hearing solutions, we combine cutting-edge technology, quality, and care to transform lives every day.

We’re now looking for a Senior Quality Assurance Specialist to join our high-performing Operations team in Sydney. This role is pivotal in ensuring compliance with ISO13485, local regulations, and GN’s global quality management system across Australia and New Zealand.
 

What You’ll Do

As the Senior QA Specialist, you will:

  • Lead and manage day-to-day Quality and Regulatory requirements for the ANZ business.

  • Act as the local Subject Matter Expert for ISO13485 and quality processes, driving compliance across the organisation.

  • Conduct internal audits, coordinate Management Reviews, and lead CAPA board meetings.

  • Oversee custom product validation and spreadsheet validation activities.

  • Partner with global QA/RA teams on process improvements and issue resolution.

  • Manage ANZ vigilance reporting, complaints handling, and regulatory submissions.

  • Train colleagues on quality and regulatory requirements to uplift knowledge across the business.

  • Provide expert input into risk assessments, supplier qualification, and continuous improvement initiatives.

What You’ll Bring

We’re looking for a quality professional who is motivated, proactive, and passionate about improving systems and outcomes. You will have:

Essential

  • Minimum 4 years’ experience with ISO13485 in a medical device production environment.

  • Strong knowledge of Australian medical device regulations (TGA).

  • Hands-on experience in auditing, process validation, and risk assessment.

  • Excellent communication skills, with the ability to influence at all levels.

  • A science, biochemistry, or related degree.

Desirable

  • Experience with TGA Advertising Code compliance.

  • People management exposure.

  • Additional training in validation, biocompatibility, or risk assessment

  • Product Quality Engineering experience

Why Join Us?

  • Be part of a global organisation that genuinely improves lives.

  • Work with a passionate and collaborative ANZ QA/RA team, connected with global colleagues.

  • Enjoy a permanent, full-time role in our shiny new Sydney facility with a supportive and inclusive culture.

  • Access opportunities for professional growth, learning, and development.

Please note: We’ve got this recruitment process covered. Should we require external support, we will reach out to our preferred recruitment partners directly.

Top Skills

Auditing
Australian Medical Device Regulations
Iso13485
Process Validation
Risk Assessment

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