Especialista Assuntos Regulatórios - Medical Devices
Philips(3 months ago)
About this role
A Regulatory Affairs Specialist (Medical Devices) at Philips supports regulatory strategy implementation and submission activities for smaller-scale projects, contributing to regulatory alignment and process improvements across product lifecycles. The role is part of a global regulatory team and operates in a hybrid working model.
Required Skills
- Regulatory Submissions
- Regulatory Compliance
- Labeling Review
- Documentation Control
- UDI/GTIN
- Stakeholder Management
- Change Control
- Regulatory Tools
- English Proficiency
Qualifications
- Degree in Biomedical Engineering
- Degree in Health Sciences
- Degree in Pharmacy
- Degree in Business Administration
- Degree in Law
- RAPS RAC (preferred)
About Philips
philips.comLearn more about Philips and how we help improve people’s lives through meaningful innovation in the areas of Healthcare, Consumer Lifestyle and Lighting.
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