Your Next Great Opportunity: Making a Global Impact in Regenerative Medicine
At Maverick Bio, we are not just building a business, we are saving and improving lives. Our innovative biomaterials drive advances in regenerative medicine and medical devices worldwide.
As our Quality Manager, you will play a key role in ensuring the highest quality standards across our operations, safeguarding our compliance with international regulations, and driving continuous improvement. If you are a meticulous professional who thrives in a structured, high-precision environment, this is your chance to lead quality excellence in a global industry.
Why Join Maverick Bio?
Real Impact, Unexpected Place
We may not be a household name, but our products touch lives across the globe. From life-saving procedures to cutting-edge medical research, your expertise will help ensure Maverick Bio continues making a difference.
Real People, Real Work
Join a down-to-earth team that values collaboration, innovation, and action. You’ll have the freedom to drive quality improvements, maintain regulatory excellence, and see your impact firsthand.
Real Growth
This is your opportunity to lead high-stakes quality initiatives, work with global partners, and challenge the status quo to push boundaries in medical manufacturing.
What You Will Do
• Lead quality assurance and compliance efforts, ensuring adherence to ISO 13485 and other industry standards.
• Oversee regulatory audits and certification processes, maintaining compliance with global medical device regulations.
• Implement and enhance quality management systems (QMS) to drive efficiency and consistency.
• Provide strategic leadership in risk management, CAPA processes, and supplier quality control.
• Work closely with cross-functional teams to embed a culture of quality across the organisation.
What We Are Looking For
• Proven experience in quality management within a regulated industry (medical devices, pharmaceuticals, biotechnology, or manufacturing).
• Strong knowledge of ISO 13485, GMP, and regulatory requirements for medical products.
• Detail-oriented, precise, and process-driven, with a strong ability to uphold quality standards.
• Analytical and problem-solving skills, with experience leading quality investigations and improvements.
• Effective communication skills, with the ability to lead audits, engage with regulatory bodies, and influence stakeholders.
• Leadership experience, with the ability to mentor and develop a team while maintaining high performance.
Who You Are
• Diligent and quality-focused, with a deep understanding of rules and regulations.
• Precise and conscientious, ensuring accuracy and compliance in all aspects of your work.
• A strategic thinker, comfortable making authoritative decisions within structured frameworks.
• Able to train and coach others, fostering a quality-first mindset across teams.
• Quick to connect and communicate, providing clarity and expertise in fast-paced situations.
Ready to Take the Lead?
Join a company that embraces innovation, fosters growth, and makes a real difference globally.
Click Apply Now to submit your resume and cover letter.
Have questions? Contact our friendly People and Culture Team on 02 6885 1200 for a confidential conversation.
Equal Opportunity at Maverick Bio
We celebrate diversity and welcome applicants from all backgrounds. Maverick Bio is an Equal Opportunity Employer and encourages applications from individuals of all abilities, genders, races, religions, and orientations.
