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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
Like this job?
BetaYour Career Agent finds similar jobs for you every day.
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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