At EBOS MedTech, we are here to improve lives by delivering life-changing solutions for patients that drive positive outcomes in their lives.
With a team of over 1,500 people operating in nine countries, we create opportunities to make a real difference for patients, healthcare professionals, and the people who make it all possible: our employees.
Our portfolio includes:
LifeHealthcare – medical device distribution in Australia and New Zealand
Australian Biotechnologies – allograft manufacturing
Cryomed Aesthetics – aesthetic technologies across ANZ
Transmedic – medical device distribution across SE Asia and Hong Kong
With scale, trusted brands, and specialist expertise across the region, we support healthcare providers with the products, partnerships, and service they rely on. We are driven by a passion for improving health and a shared commitment to making a positive impact.
This is a high-impact role for an experienced regulatory professional who wants to lead vigilance across a diverse ANZ medical device portfolio. This role can be based in Melbourne, Sydney or Brisbane. Reporting to the Head of Market Access, you will take ownership of post-market vigilance activities, work closely with senior stakeholders, manufacturers, and regulators, and help strengthen the systems, capability, and practices that support a high-performing function.
Key Responsibilities:
- Lead post-market vigilance across Australia and New Zealand.
- Provide expert guidance on sponsor obligations, field actions, and post-market compliance requirements.
- Strengthen vigilance processes, systems, training, and governance.
- Partner across Regulatory, Quality, Commercial, Supply Chain, Customer Service, and with manufacturers to resolve safety and compliance issues.
- Lead responses to TGA enquiries, post-market reviews, audits, and inspections.
- Monitor regulatory changes and translate them into practical actions for the business.
- Build capability across the team and embed a proactive, patient-focused approach.
Experience & Qualifications:
- Experience in post-market vigilance, post-market surveillance, or medical device regulatory compliance within a sponsor, distributor, manufacturer, or regulated healthcare environment.
- Strong knowledge of Australian and New Zealand medical device post-market requirements, including sponsor obligations and TGA vigilance reporting.
- Hands-on experience assessing complaints and adverse events, determining reportability, and managing regulatory submissions.
- Strong stakeholder management skills, with the ability to work effectively across teams and with external partner
- Sound judgement, strong attention to detail, and a practical, risk-based approach.
- Experience improving processes, delivering training, or building team capability will be highly regarded.
- Relevant tertiary qualifications in science, biomedical engineering, pharmacy, regulatory affairs, quality, or a related discipline.
At EBOS MedTech, you will join a business with scale, capability, and purpose. We offer the opportunity to work across a diverse portfolio, collaborate with experienced teams across ANZ and the wider region, and build your career in an environment that values practical leadership, strong relationships, and high standards.
As part of our team, you will enjoy a range of benefits, including:
- Educational assistance and access to learning resources
- Hybrid work options and flexible arrangements
- Generous parental leave and recharge days
- Volunteer leave and employee referral programs.
- Health insurance discounts
- Performance-based rewards for individual and company success
- Career development opportunities across nine countries
If you are an experienced post-market or regulatory professional looking for a role with breadth, visibility, and genuine influence, this is an opportunity to make your mark in a business that is committed to quality, safety, and better healthcare outcomes.
to join EBOS MedTech and help shape a trusted, high-performing post-market vigilance function across ANZ.
