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Regulatory Affairs Specialist
2 months ago
We are seeking a highly skilled Medical Devices Regulatory Affairs Associate to join our team in Australia. As a key member of our Medical Devices Consulting team, you will play a critical role in ensuring the regulatory compliance of our clients' products.
Your primary objective will be to maximize client commercial success by ensuring appropriate licensing and regulatory compliance of client's products. You will have the opportunity to work on various medical devices technologies, supporting a wide range of quality and regulatory activities.
To be successful in this role, you must have formal qualifications in science or engineering, with 3 to 5 years' experience working in medical devices regulatory affairs either in industry or a consulting setting. You should have hands-on experience in the preparation of regulatory and technical submissions, preferably with the TGA, and a strong track record of success.
We offer a dynamic work environment, flexible working options, and opportunities for professional growth and development. If you are a motivated and results-driven individual with a passion for regulatory affairs, we encourage you to apply for this exciting opportunity.
", "requirements": "- Formal qualifications in science or engineering
- 3 to 5 years' experience working in medical devices regulatory affairs
- Hands-on experience in the preparation of regulatory and technical submissions
- Strong track record of success
- Dynamic work environment
- Flexible working options
- Opportunities for professional growth and development