Regulatory Data Specialist (m/f/d) fixed-term employment until 31.12.2025
Date de publication :
22 octobre 2024Taux d'activité :
100%Type de contrat :
Durée indéterminée- Lieu de travail :Selzach
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:
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Establish processes for timely and accurate data collection from internal sources that meet project requirements.
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Develop and implement validation schemes to ensure data accuracy and completeness, resolving discrepancies as needed.
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Create visual reports and presentations to effectively communicate data insights to stakeholders.
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Work with departments such as Labeling, Regulatory, Clinical, and R&D; facilitate meetings to promptly resolve data-related issues.
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Apply understanding of EU Medical Devices Regulation requirements in daily tasks.
What you will need:
Required:
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B.Sc. or Master’s degree in Data Science, Life Sciences, Regulatory Affairs, Engineering, or a related field.
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0-2 years of experience in data management, including internships or relevant work experience, with participation in data collection and validation projects.
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Attention to detail for data accuracy, strong organizational and problem-solving skills, and proficiency in MS Office,
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Excellent communication skills in English, both written and verbal.
Preferred:
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Interest in regulatory topics, even if no direct experience in regulatory affairs.
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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.
Contact
Stryker GmbH