Take the lead in shaping safe, compliant, and innovative medical technologies that transform patient care.
Proclinical is seeking a Medical Device Engineer Lead to support regulatory and engineering functions within the neurology and pharmaceutical sectors. This role focuses on ensuring compliance, quality, and innovation in medical device development. The position is remote, offering flexibility, and is available for an immediate start with a two-year contract duration.
This is a remote role based in Belgium.
Responsibilities:
- Lead the design, development, and lifecycle management of medical devices.
- Ensure compliance with relevant regulatory standards and guidelines.
- Collaborate with cross-functional teams to drive project milestones and deliverables.
- Conduct risk assessments and implement mitigation strategies.
- Oversee documentation processes to maintain accuracy and adherence to quality standards.
- Provide technical expertise and guidance to internal and external stakeholders.
- Monitor industry trends and integrate best practices into device development.
Key Skills and Requirements:
- Strong knowledge of medical device regulations and standards.
- Proven experience in medical device engineering and lifecycle management.
- Excellent problem-solving and analytical skills.
- Ability to work collaboratively in a multidisciplinary environment.
- Strong communication skills to effectively convey technical information.
- Proficiency in relevant engineering tools and software.
If you are having difficulty in applying or if you have any questions, please contact Elise Stewart at e.stewart@proclinical.com.
Apply Now:
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Proclinical is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Proclinical is acting as an Employment Agency in relation to this vacancy.
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