Medical Device Safety Reviewer – Temporary

About the role

The Medical Device Safety Reviewer provides medical safety reviews of medical device complaints, ensuring appropriate medical interpretation and consistency in adverse event assessments. This role serves as a subject matter expert for assigned medical devices, collaborates with clinical and cross‑functional stakeholders, and supports the evaluation of medical device safety issues to help ensure patient safety and regulatory compliance.

Key responsibilities

• Provide medical safety review for individual complaints involving patient harm with the use of Vantive’s medical devices.
• Ensure appropriate medical interpretation and consistency are applied to medical device‑related adverse event assessments.
• Provide medical safety review for complaints with no patient harm that need an individual assessment.
• Work with clinical counterparts as needed.
• Act as an expert for assigned medical devices, maintaining current knowledge of the full product portfolio and safety profiles.
• Communicate and consult with stakeholders including R&D, Quality, and Regulatory teams.
• Support internal and external customers regarding evaluation of medical device safety issues.

Required profile

• Healthcare professional (RN) preferably with a Bachelor’s degree in nursing (US only) or equivalent.
• At least 5 years of medical professional experience (hospital, patient care, or equivalent).
• Preferable knowledge of the renal therapeutic area.
• Ability to work in a cross‑functional, multicultural team setting.
• Knowledge and understanding of national and international medical device regulations and regulatory guidelines.
• Knowledge of medical aspects of medical device safety and vigilance in pre‑ and post‑market settings.

What we offer

• Minimum annual base salary €40,800 (starting salary may be higher based on experience and qualifications).
• Competitive bonus and benefits package designed to support well‑being, professional growth, and life beyond work.