
Device Development Lead
6 days ago
We are seeking a seasoned device engineer to take on key responsibilities in the medical devices industry.
- Develop and implement quality management systems that meet international standards such as ISO 13485 and MDD 93/42/EEC.
- Conduct risk assessments and manage risks associated with medical devices using EN ISO 14971.
- Collaborate with cross-functional teams to ensure compliance with regulatory requirements.
- Solid knowledge of non-active devices and sterilization processes is essential.
Requirements:
- Bachelor's degree in a relevant field such as engineering or life sciences.
- Strong understanding of medical device regulations and standards.
- Excellent communication and interpersonal skills.
About the Role:
This is a challenging opportunity for an experienced device engineer who can contribute to the development of high-quality medical devices.
Benefits:
The ideal candidate will have a strong focus on quality management and regulatory affairs, with a solid understanding of medical device regulations and standards.
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