As a key EUDAMED Data Specialist, you will work closely with the project lead to support a data collection and validation project to implement the regulatory requirements of the EU Medical Devices Regulation regarding the European Database for Medical Devices (EUDAMED).

What you will do:

• Establish processes for timely and accurate data collection from internal sources that meet project requirements.

• Develop and implement validation schemes to ensure data accuracy and completeness, resolving discrepancies as needed.

• Create visual reports and presentations to effectively communicate data insights to stakeholders.

• Work with departments such as Labeling, Regulatory, Clinical, and R&D; facilitate meetings to promptly resolve data-related issues.

• Apply understanding of EU Medical Devices Regulation requirements in daily tasks.

What you will need:

Required:

• B.Sc. or Master’s degree in Data Science, Life Sciences, Regulatory Affairs, Engineering, or a related field.

• 0-2 years of experience in data management, including internships or relevant work experience, with participation in data collection and validation projects.

• Attention to detail for data accuracy, strong organizational and problem-solving skills, and proficiency in MS Office,

• Excellent communication skills in English, both written and verbal.

Preferred:

• Interest in regulatory topics, even if no direct experience in regulatory affairs.

• Additional language proficiency is a plus.

The position is initially limited 31.12.2025. Due to the large number of different positions and areas of responsibility, Stryker often offers the options of being taken on in a permanent position. 

Diversity is important to us. We welcome applications from people regardless of their ethnic, national or social origin, gender, disability, age or sexual identity.