Regulatory Affairs Director
Vor 6 Tagen
Are you a skilled professional looking to make a meaningful impact in the medical device industry? Metric Bio, a pioneering company in skin cancer treatment, is seeking an experienced Quality and Regulatory Affairs Leader to drive their regulatory strategy in Munich, Germany.
About the RoleWe are seeking a highly motivated and accomplished individual with a strong background in quality management and regulatory affairs. As our Quality and Regulatory Affairs Leader, you will be responsible for developing and leading Quality System strategies to maintain and exceed regulatory compliance.
You will optimize and streamline quality and regulatory processes for efficient, global compliance. This role offers an exciting opportunity to shape the future of skin cancer treatment and contribute to the development of innovative, non-invasive solutions.
- Develop and lead Quality System strategies to ensure compliance with regulatory requirements such as ISO 13485 and 21 CFR 820.
- Orient and optimise quality and regulatory processes for streamlined, global compliance.
To be successful in this role, you will need:
- 4+ years of hands-on experience in quality management and regulatory affairs for medical devices.
- In-depth knowledge of medical device QMS (ISO 13485 / 21 CFR 820) and experience leading audits with notified bodies.
As a member of our team, you can expect:
- A competitive salary of €120,000 - €150,000 per annum, commensurate with your experience.
- The opportunity to work on cutting-edge projects that have a real impact on patient care.
- A collaborative and dynamic work environment that supports your growth and development.
Please note: Salary estimates may vary based on individual circumstances.
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