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Quality Manager for Medical Software Development
3 weeks ago
You must have at least 1 year of experience within quality assurance and/or regulatory affairs. You should also have strong knowledge of quality management systems and regulatory requirements within MDR and ISO 13485.
Qualifications:
- A master's degree in healthcare, medical or life science is preferred
- A positive can-do attitude with a thorough and structured mindset
- Excellent communication skills in English and experience with working within or leading cross-functional projects
Additional Requirements:
- Knowledge of software as a medical device is desired
- Experience with working in a changing and dynamic environment with tight deadlines