Cochlear is the global market leader in implant hearing solutions. Cochlear’s mission is to help people hear and be heard. Around the world, more people chose a Cochlear-branded hearing implant system than any other. A Cochlear Implant is an electronic device that is surgically implanted under the skin near the ear that restores hearing to those who suffer from severe hearing loss. It’s an incredible piece of engineering and the only product in the world that restores a sense through technology. Imagine using your experience to help people around the world to hear again. We can offer a unique opportunity to join Cochlear, an iconic Australian company, leading the world in implantable hearing solutions. Our mission is to help more people to hear.
The Opportunity
As Cochlear continues to grow, an exciting opportunity has become available for an experienced Senior Post Market Quality Specialist to join the global Post Market Surveillance team.
Reporting to the Global Post Market Surveillance Insights Manager who is located in Sydney, you will be a member of a global effort to ensure that Cochlear maintains our position as the global leader in hearing medical technology, and help hundreds of thousands of recipients across the world hear and be heard.
This role will be working closely with stakeholders across Europe, Americas and APAC, as a result, we are considering applications from both Goteborg and Sydney.

Your responsibilities include:

• Generating and maintaining of Post Market Surveillance Reports in line with global Medical Device regulatory requirements
• Developing critical post market documents to support medical device registration
• Collaborating with teams in Quality, Clinical, and Regulatory to ensure documentation and reporting meet global standards
• Analysing medical device quality data and producing dashboards that reveal critical post market insights
• Interrogating post market data, identify errors and proactively correct errors in data, systems and processes
• Monitoring product quality and contribute to Post Market Review meetings with data, insights and trends
• Partnering with diverse teams to further develop Cochlear’s Post Market Quality capabilities, and contribute to continuous improvement across the entire quality network

About You. As we grow our operations, we are looking for people who share our passion for delivering quality hearing solutions to our customers. To add value to Cochlear in this role, you’ll be able to demonstrate the following skills and experience:

• Bachelor in Science, Engineering or other related fields
• Experience with European Medical Device Regulation requirements
• Strong Excel skills
• Experience with Data Visualization platforms such as Tableau
• Experience with Business Intelligence software such as OBIEE (Oracle Business Intelligence Suite)
• A passion for data, analytics and a genuine curiosity for understanding data and trends
• A high level of detail orientation, a love of statistics and an interest in the Medical Device industry
• Background in Data Analytics & Business Intelligence is highly regarded

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 life full of hearing. We aim to give people the best lifelong hearing experience and access to innovative future technologies. We collaborate with the industry’s best clinical, research and support networks. That’s why more people choose Cochlear than any other hearing implant company. Learn and grow with us as we tackle the most complex challenges in helping more people to hear and experience life’s opportunities.
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
We want Cochlear to be a place where our people truly enjoy coming to work. 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
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. We offer flexible working arrangements, and we understand flexibility is not the same for everyone. We’re open to a conversation about what flexibility means for you.

Your responsibilities include:

• Generating and maintaining of Post Market Surveillance Reports in line with global Medical Device regulatory requirements
• Developing critical post market documents to support medical device registration
• Collaborating with teams in Quality, Clinical, and Regulatory to ensure documentation and reporting meet global standards
• Analysing medical device quality data and producing dashboards that reveal critical post market insights
• Interrogating post market data, identify errors and proactively correct errors in data, systems and processes
• Monitoring product quality and contribute to Post Market Review meetings with data, insights and trends
• Partnering with diverse teams to further develop Cochlear’s Post Market Quality capabilities, and contribute to continuous improvement across the entire quality networ

About You. As we grow our operations, we are looking for people who share our passion for delivering quality hearing solutions to our customers. To add value to Cochlear in this role, you’ll be able to demonstrate the following skills and experience:

• Bachelor in Science, Engineering or other related fields
• Experience with European Medical Device Regulation requirements
• Strong Excel skills
• Experience with Data Visualization platforms such as Tableau
• Experience with Business Intelligence software such as OBIEE (Oracle Business Intelligence Suite)
• A passion for data, analytics and a genuine curiosity for understanding data and trends
• A high level of detail orientation, a love of statistics and an interest in the Medical Device industry
• Background in Data Analytics & Business Intelligence is highly regarde