Vagas na beBeeMedical em Brasil

Job Title: Regulatory Affairs Specialist · Regulatory affairs plays a crucial role in ensuring compliance with EU medical device regulations. · You will lead activities related to medical devices, focusing on European regulation and guidelines. · You will be responsible for leadi ...

Key Objectives: · Oversee regulatory affairs for medical devices ensuring compliance with European directives, specifically EU MDR (Regulation 2017/745) · Serve as an expert in medical device classification focusing on Class IIa and IIb to guarantee correct application of classif ...

Regulatory Affairs Specialist Job Description · Assume a key role in ensuring regulatory compliance for medical devices, driving business growth through strategic partnerships with clients. · ...

About Our Team · We are a leading developer and manufacturer of medical imaging solutions. · Our dedication to innovation drives excellence in ultrasound and other diagnostic technologies. · ...

About Us: · We are a leading developer and manufacturer of medical imaging solutions, with a strong presence in over 100 countries. Our company is dedicated to innovation and excellence in ultrasound and other diagnostic technologies. · ...

Regulatory Affairs Professional · We are seeking an expert in medical device classification to lead regulatory affairs activities ensuring compliance with European regulations. · ...

About Us: · We are a leading developer and manufacturer of medical imaging solutions, with a strong presence in over 100 countries. We are dedicated to innovation and excellence in ultrasound technology. · ...

Job Title: · Regulatory Affairs Specialist · Description of the Position: · The ideal candidate will be responsible for leading Regulatory Affairs activities for medical devices, ensuring compliance with European regulations. This includes coordinating the preparation, review, an ...

Job Description · Regulatory Affairs Specialist · In this role, you will be responsible for managing the regulatory lifecycle of medical devices. · You will lead regulatory affairs activities to ensure compliance with European regulations and coordinate the preparation, review, a ...

Regulatory Affairs Expertise · The successful candidate will spearhead regulatory affairs operations for medical devices ensuring conformity with European regulations (EU MDR – Regulation (EU) 2017/745), including Class IIa and IIb classification rules. · Coordinate the preparati ...

Job Title: Regulatory Affairs Expert · Job Description: · Lead regulatory compliance initiatives for medical devices ensuring adherence to European Union regulations. · Expertise in medical device classification, focusing on Class IIa and IIb to ensure accurate application of rul ...

Regulatory Affairs Specialist Job Description · The primary role of a Regulatory Affairs Specialist is to lead and manage regulatory activities for medical devices. This includes staying up-to-date with the latest changes and developments in the field, particularly from EU agenci ...

Regulatory Affairs Professional · We are seeking a highly skilled Regulatory Affairs professional to lead our team in the medical devices industry. This role involves ensuring compliance with European regulations and providing expert support in CE Marking processes and conformity ...

Regulatory Affairs Expert · Job Description: · <div style= ...