Vagas na beBeeMedicalDeviceExpert em Brasil

Regulatory Affairs Position Overview · A technical professional acts as a strategic partner to clients. · Our ideal candidate will have expertise in Class IIa and IIb medical devices, European regulations (MDR), and Notified Bodies interaction. · Key Responsibilities: · Collabora ...

Regulatory Affairs Specialist · Join us in shaping the future of medical devices. · This role requires a strategic partner to support our clients through regulatory complexities, ensuring compliance with EU MDR (EU) 2017/745. · ■ Job Description · Act as an expert in Class IIa an ...

Regulatory Affairs Specialist · Description: · This is a dynamic role that requires the management of regulatory affairs for medical devices, ensuring compliance with European regulations (EU MDR – Regulation (EU) 2017/745). · <p REQUIRED SKILLS AND QUALIFICATIONS:</p<ul style= ...

Regulatory Affairs Expert · We are seeking a highly skilled Regulatory Affairs expert to lead our medical device team. The successful candidate will be responsible for ensuring compliance with European regulations, including the EU MDR. · The ideal candidate will have a strong ba ...

Regulatory Affairs Professional · The role involves leading Regulatory Affairs activities for medical devices, ensuring compliance with European regulations (EU MDR). · Key Responsibilities: · Lead Regulatory Affairs activities for medical devices, ensuring compliance with EU MDR ...

Regulatory Affairs Specialist · We are seeking a highly skilled Regulatory Affairs Specialist to lead regulatory affairs activities for medical devices. · The ideal candidate will have 6+ years of experience in Regulatory Affairs for medical devices, strong expertise in Class IIa ...

Regulatory Affairs Specialist · We are seeking a highly skilled Regulatory Affairs professional to lead our medical device regulatory activities in Europe. The ideal candidate will have expertise in Class IIa and IIb devices, European regulations (EU MDR), and strong analytical s ...

Job Overview: · A Regulator with expertise in medical devices is required to lead regulatory activities ensuring compliance with European regulations. The role involves providing strategic support to clients across multiple industries, analyzing and managing regulatory changes, a ...

Regulatory Affairs Professional Role Overview · Job Description:As a Regulatory Affairs Specialist, you will be responsible for ensuring compliance with European regulations and acting as an expert in medical device classification. · You will lead regulatory affairs activities fo ...

Regulatory Affairs Specialist · Location: Brazil, remote opportunity. · <ul class= ...