QM Associate – Product Registrations (part-time 20h/week)
Munich, BY, Germany Hybrid
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About the role
Our key to success is our creative, talented and hard-working team, which consists of around 2000 dedicated and inspiring individuals in 25 locations worldwide. To succeed in reaching our targets, we are seeking committed colleagues who can stand behind our core values curious, authentic and useful. As a QM Associate – Product Registrations you will be part of the international Regulatory Affairs team overseeing and managing medical device approvals around the world. Your goal is the worldwide registration of the Brainlab medical devices in correspondence with regulatory authorities (e.g. Health Canada, Australian TGA) in order to make our technology available to hospitals and patients around the world.
What you'll bring
- Interest in quality management and regulatory affairs
- Knowledge of international regulations for medical devices is an advantage
- Ability to manage multiple projects
- Very strong attention to detail
- Proficient in the use of MS Office
- Excellent communication skills in English
- Other languages are an advantage
- Degree in engineering or life sciences preferred, but other degrees may be considered