Medical Device Regulatory Compliance Specialist - Santa Cruz do Sul - beBeeRegulatoryAffairs

Título do emprego: Regulatory Affairs Specialist

Descrição

Job Title:
Regulatory Affairs Professional

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**Job Description:** We are seeking an experienced Regulatory Affairs professional to lead regulatory activities for medical devices. In this role, you will ensure compliance with European regulations and collaborate with internal teams to provide expert support on regulatory matters throughout the device lifecycle.

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**Key Responsibilities:*

• Lead regulatory affairs activities for medical devices ensuring compliance with EU MDR
• Act as an expert in medical device classification focusing on Class IIa and IIb
• Coordinate preparation review and maintenance of technical documentation EU MDR Annexes II and III

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