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Working student for support Product Regulatory Affairs Concentrates(m/w/x)
Updating global and country-specific medical device registration dossiers. Structured working style and attention to detail required. Connect across teams and countries.
Requirements
- Enrolled student in Life Sciences, Regulatory Affairs, Biomedical Engineering, Pharmacy, or related field
- Strong attention to detail
- Structured working style
- Interest in international regulatory requirements
- Interest in medical device compliance
- Good analytical skills
- Confidence in handling data
- Fluent in English
- Additional languages are a plus
Tasks
- Contribute to global and country-specific registration dossiers
- Update registration dossiers for medical devices
- Support registration activities with internal tools
- Prepare regulatory documentation and declarations
- Assist in regulatory impact assessments
- Update technical documentation for MDR compliance
- Review labeling for European and international regulations
- Coordinate international certification processes
- Execute certification and legalization processes
- Analyze and evaluate registration data
- Use internal tools for statistical analysis
Education
- Currently in higher education
Languages
- English – Fluent
- other – Basic
Benefits
Other Benefits
- Care for patients
- Care for colleagues
- Advancing kidney care with innovation
Social Impact
- Care for communities
Informal Culture
- Connect across teams
- Connect across countries
Purpose-Driven Work
- Commitment to doing the right thing
- Growing with purpose
- Advancing kidney care with integrity
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Working student for support Product Regulatory Affairs Concentrates(m/w/x)
Updating global and country-specific medical device registration dossiers. Structured working style and attention to detail required. Connect across teams and countries.
Requirements
- Enrolled student in Life Sciences, Regulatory Affairs, Biomedical Engineering, Pharmacy, or related field
- Strong attention to detail
- Structured working style
- Interest in international regulatory requirements
- Interest in medical device compliance
- Good analytical skills
- Confidence in handling data
- Fluent in English
- Additional languages are a plus
Tasks
- Contribute to global and country-specific registration dossiers
- Update registration dossiers for medical devices
- Support registration activities with internal tools
- Prepare regulatory documentation and declarations
- Assist in regulatory impact assessments
- Update technical documentation for MDR compliance
- Review labeling for European and international regulations
- Coordinate international certification processes
- Execute certification and legalization processes
- Analyze and evaluate registration data
- Use internal tools for statistical analysis
Education
- Currently in higher education
Languages
- English – Fluent
- other – Basic
Benefits
Other Benefits
- Care for patients
- Care for colleagues
- Advancing kidney care with innovation
Social Impact
- Care for communities
Informal Culture
- Connect across teams
- Connect across countries
Purpose-Driven Work
- Commitment to doing the right thing
- Growing with purpose
- Advancing kidney care with integrity
About the Company
Fresenius Medical Care
Industry
Healthcare
Description
Das Unternehmen ist der weltweit führende Anbieter von Produkten und Dienstleistungen für Menschen mit Nierenerkrankungen.
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