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Cochlear

Director of Global Quality Systems

Posted An Hour Ago
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In-Office
Sydney, New South Wales
Senior level
In-Office
Sydney, New South Wales
Senior level
As Director of Global Quality Systems at Cochlear, you will oversee QMS processes, ensure compliance, drive CAPA effectiveness, and foster a quality culture across global manufacturing sites.
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Please submit your application as soon as possible, as we reserve the right to close this advertisement at any time.

Cochlear’s mission is to help people hear and be heard. As the global leader in implantable hearing solutions, Cochlear is dedicated to helping people with moderate to profound hearing loss experience a world full of sound. We aim to transform the way people understand and treat hearing loss and innovate to connect people with future technologies. Our employees tell us that the number one reason they enjoy working for Cochlear is the opportunity to make a difference to people’s lives. Learn and grow with us as we tackle the most complex challenges in helping more people to experience a lifetime of hearing.

We’re looking for a strategic leader to drive our Quality Management System (QMS) across global manufacturing sites, ensuring compliance, innovation, and a culture of quality that delivers life-changing hearing solutions to customers worldwide. 

As Director, Global Quality Systems, you’ll lead the definition, maintenance, and continuous improvement of QMS processes across Cochlear’s manufacturing sites. Reporting to the VP Global Quality Systems & Customer Quality Assurance, you’ll ensure compliance with global regulatory standards and deliver quality strategies that meet customer expectations. 

You’ll oversee key processes including documentation and change management, standards management, internal and external audits, QMS training, issue management, CAPA, and field actions. Working closely with regional quality leaders and senior business stakeholders, you’ll build a strong quality culture through training and awareness programs. Quality Systems Managers across CLTD, CBAS, and CVS will report to you, ensuring QMS certification and operational excellence. 

About the role:  

  • Lead Global QMS Strategy & Compliance 
    Define, maintain, and continuously improve QMS processes including documentation, change management, audits, training, issue management, CAPA, and field actions. 

  • Drive CAPA Program Effectiveness 
    Oversee investigations, ensure timely resolution, and embed learnings into system improvements. 

  • Champion Quality Culture 
    Lead training and awareness programs, mentor teams, and build capability across regions. 

  • Ensure Audit & Regulatory Readiness 
    Maintain compliance with ISO 13485, EU MDR, MDSAP, and FDA QMSR and other regulations as required; coordinate inspections and audits globally. 

  • Enable Continuous Improvement 
    Monitor quality objectives, prepare management reviews, and support enterprise-wide quality initiatives. 

  • Collaborate Globally 
    Work with senior leaders to align manufacturing processes with enterprise quality strategies. 

What You Bring 

  • Expertise in QMS for medical devices and global regulatory standards. 

  • Experience leading global quality teams, managing people managers, and driving cross-functional collaboration. 

  • Skills in project management, global process implementation, and data-driven decision-making. 

  • Leadership that inspires teams, fosters innovation, and builds a strong quality culture. 

  • Preferred: Background in medical device manufacturing and global product launches. 

 

Why Join Us? 

  • Make a global impact by shaping quality strategies that enable life-changing technology. 

  • Lead innovation and continuous improvement in a dynamic, purpose-driven environment. 

  • Collaborate with world-class teams and senior leaders across the globe. 

  • Thrive in a culture that values curiosity, learning, and excellence. 

If you feel that you have the skills and experience to be successful in this role and take on new challenges to build your career with Cochlear, please start your application by clicking the apply button below.

#CochlearCareers

How we recognise your contribution

At Cochlear we value and welcome the unique contributions, perspectives, experiences, and backgrounds of our employees and aim to build a culture that celebrates and leverages these differences, creating a sense of belonging and enabling our people to realise their full potential. Through our internal programs and employee benefits, we aim to create an environment where our people will feel value and supported. Whether your focus is on continuous learning, professional development or simply finding an environment which enables you to thrive whilst balancing family or personal life commitments, then we have several programs in place to support you.

For more information about Life at Cochlear, visit www.cochlearcareers.com

Top Skills

Eu Mdr
Fda Qmsr
Iso 13485
Mdsap
Quality Management Systems

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