- Temporary
- Full Time
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Why join Stryker?
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Job description
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.