Medical Device Engineer

Drive innovation and compliance in cutting-edge medical devices shaping the future of neurology and pharma.

Proclinical is seeking a Medical Device Engineer to support regulatory and engineering activities within the neurology and pharmaceutical sectors. This role focuses on ensuring compliance, driving innovation, and contributing to the development of medical devices. The position is remote and offers a two-year contract with an immediate start.

Responsibilities:

• Collaborate with cross-functional teams to ensure medical device compliance with regulatory standards.
• Support the design, development, and lifecycle management of medical devices.
• Conduct risk assessments and implement mitigation strategies.
• Prepare and review technical documentation for regulatory submissions.
• Provide technical expertise in troubleshooting and resolving device-related issues.
• Ensure adherence to quality management systems and industry best practices.
• Monitor and interpret changes in regulatory requirements and implement necessary updates.

Key Skills and Requirements:

• Strong understanding of medical device regulations and standards.
• Experience in device design, development, and lifecycle management.
• Proficiency in preparing technical documentation for regulatory purposes.
• Ability to conduct risk assessments and implement corrective actions.
• Familiarity with quality management systems and compliance processes.
• Excellent problem-solving and communication skills.
• Ability to work effectively in a remote, collaborative environment.
  

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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