Medical Device Regulation (MDR) Specialist

Position
Medical Device Regulation (MDR) Specialist

Responsibilities
• Manage the preparation of quality management system and MDR documents.
• Collaborate with other team members to contribute to clinical evaluation, MDR challenges, and educational material.
• Identify MDR challenges and actively contribute to their resolution.

Required Qualifications
• Bachelor’s degree or equivalent in clinical, technical or natural science.
• Fluency in English.

Desired Skills
• Experience in quality management systems and/or the medical device industry.
• Understanding on the fundamentals of MDR and Medical Device Clinical Evaluation.
• Strong organizational and structuring abilities.
• Proficient in scientific and medical writing.
• Understanding of AI fundamentals or experience in AI systems.
• Demonstrated problem-solving and analytical skills.

Salary
Depending on the applicant’s degree, skills, and previous experience (2600.00-4040.00€/month).

Application
If you are interested in this position, please submit a brief motivation letter (100-150 words) and CV (max 2 pages) detailing your relevant experience and skills. We look forward to hearing from you by the 31st of August 2023.

Questions
Oscar Brück
oscar.bruck@helsinki.fi

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