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Senior Expert Regulatory Affairs (m/f/x)
Németország
- Teljes munkaidő
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1-3 év tapasztalat • Angol felsőfok
Főbb feladatok- Develop and implement global regulatory pathways for product authorizations
- Oversee preparation and submission of regulatory documents to authorities
December 02. -
- Teljes munkaidő
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1-3 év tapasztalat • Angol középfok
Főbb feladatokPOSITION DESCRIPTION We are seeking an experienced and motivated professional to join our software quality assurance team. In this key role, you will help ensure compliance with IVDR, FDA 21 CFR Part 820, and cybersecurity requirements for medical device software. - Partner with development teams...
December 02. -
- Teljes munkaidő
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1-3 év tapasztalat • Német középfok
Főbb feladatok- Lead and inspire a global team of about 30 scientists and technical experts, fostering innovation, collaboration, and excellence.
- Spearhead the formulation and manufacturing process development for small molecule animal health products, from enabling formulations to tech transfer.
November 19. -
- Teljes munkaidő
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1-3 év tapasztalat • Angol középfok
Főbb feladatok- You are responsible for quality related topics like change control, deviations and/or complaints related to DS products at CMOs
- Define together with the CMO effective CAPAs and track the timely implementation
November 10. -
- Teljes munkaidő
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1-3 év tapasztalat • Angol felsőfok • Német felsőfok
Főbb feladatokServe as the medical device subject matter expert to both internal and external customers for product development, risk assessment, training, implementation, literature reviews, complaints, safety signals, field action, voice of the customer, and voice of the business....
November 06. -
- Teljes munkaidő
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1-3 év tapasztalat • Angol felsőfok • Német felsőfok
Főbb feladatok- Collect data and prepare progress reports, KPIs, and metrics for regional and global reporting, including monthly reports, management reviews, and quarterly quality reports.
- Support ad hoc global quality reporting by gathering data and providing contextual insights to regional QA Senior Management.
November 12.
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