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About the Role · Our organization seeks a diligent Regulatory Affairs Specialist to spearhead regulatory affairs activities for medical devices. Key responsibilities include ensuring compliance with European regulations, specifically EU MDR – Regulation (EU) 2017/745. · The idea ...

Job Title: Regulatory Compliance Specialist · Job Description:We are seeking an experienced Regulatory Affairs expert to lead activities for medical devices ensuring compliance with European regulations (EU MDR - Regulation (EU) 2017/745). · The successful candidate will provide ...

Job Overview · This role leads Regulatory Affairs activities for medical devices ensuring compliance with European regulations. · Responsibilities include acting as an expert in medical device classification, focusing on Class IIa and IIb to ensure correct application of classifi ...

Regulatory Affairs Professional · This key role entails leading regulatory affairs activities for medical devices in compliance with European regulations such as the EU Medical Devices Regulation (2017/745). The primary responsibilities of this position include ensuring correct c ...

Regulatory Affairs Expertise: · To lead regulatory affairs operations for medical devices, ensuring compliance with European regulations as mandated by the EU MDR – Regulation (EU) 2017/745. · The role demands in-depth knowledge of medical device classification, focusing primaril ...

Compliance Expertise for Medical Devices · This role involves spearheading regulatory compliance activities for medical devices, ensuring seamless alignment with European regulations (EU MDR). You will serve as an expert in medical device classification, coordinating preparation, ...

Regulatory Affairs Specialist Role · We are seeking a highly skilled Regulatory Affairs Specialist to lead our medical device regulatory activities and ensure compliance with EU MDR regulations. · Develop and implement effective strategies for Class IIa and IIb medical device cla ...

Job Description: · About this position: · Lead regulatory affairs activities for medical devices to ensure compliance with European regulations. · Function as a specialist in medical device classification, ensuring accurate application of classification rules. · A strong backgrou ...

Regulatory Affairs Specialist · An exciting opportunity to grow your career within a rapidly expanding organization. · Lead Regulatory Affairs activities for medical devices ensuring compliance with European regulations (EU MDR). · Act as an expert in medical device classificatio ...

Regulatory Affairs Specialist · As a Regulatory Affairs Specialist, you will lead activities for medical devices ensuring compliance with European regulations. Your expertise in classification and regulatory affairs will be key to our success. · Missions · Lead Regulatory Affairs ...