Vagas na beBeeRegulatoryAffairs em Brasil

Job Opportunity · Main Responsibilities: · • Manage regulatory submissions and site start-up activities across various regions to ensure timely completion. · • Collaborate with international teams to maintain compliance with clinical trial regulations, including Swiss and global ...

Job Title: · We are seeking a skilled professional to lead regulatory affairs activities for medical devices within the European Union framework. · This role involves oversight of regulatory compliance and classification in accordance with EU regulations, · Actioning as an expert ...

Job Overview: · We are seeking a dedicated and detail-oriented professional to oversee the submission process for clinical trials across Brazil, Argentina, and Chile. · The successful candidate will be responsible for ensuring compliance with Swiss and international regulations, ...

We're seeking a seasoned professional to lead our regulatory affairs efforts. As a Regulatory Affairs Specialist, you'll be responsible for ensuring compliance with EU MDR regulation and driving improvements across multiple areas. · Your Key Responsibilities: · Lead Regulatory Af ...

Job Title: Regulatory Affairs Specialist · We are seeking a highly skilled and experienced Regulatory Affairs Specialist to join our team in Brazil, Chile, and Argentina. · This is an exciting opportunity for someone to work on freelance basis with solid experience in Ethics Comm ...

Job Summary · We are seeking an experienced Regulatory Affairs Specialist to join our team. This role is responsible for ensuring compliance with regulatory requirements for medical devices. · Main responsibilities: · <ul style= ...

Job Description: · We are seeking an experienced Regulatory Affairs Specialist to join our team. As a key member of the organization, you will be responsible for ensuring compliance with European regulations (EU MDR) and providing expert support in CE Marking processes. · Mission ...

Job Overview: · The Regulatory Affairs Specialist is responsible for ensuring quality, consistency, and timeline adherence across local submissions in Brazil, Argentina, and Chile. · Oversight of regulatory submissions includes site start-up activities. · This role ensures compli ...

Regulatory Affairs Professional · A challenging role has opened up in a rapidly expanding international organization. We are seeking an experienced Regulatory Affairs Specialist to lead our team's activities related to medical devices. · Ensure compliance with European regulation ...

Job Title: Regulatory Affairs Specialist · Upsilon Global seeks a freelance Regulatory Affairs Specialist to oversee local submissions across Brazil, Argentina and Chile ensuring quality consistency and timeline adherence. · Benefits: · highly competitive salary package that incl ...

Job Description · We are seeking a skilled Regulatory Affairs Specialist to oversee centralized oversight and execution of local submission management. · This individual will play a critical role in ensuring regulatory compliance and provide strategic support for the development ...

Our ideal candidate will play a pivotal role in ensuring regulatory compliance for medical devices. The position requires strong expertise in EU MDR and Class IIa/IIb medical devices, with experience working with Notified Bodies and health authorities. · The successful profession ...

Job Description · We are seeking an expert in regulatory affairs to lead our medical device team. The ideal candidate will have a strong understanding of European regulations and experience working with Notified Bodies. · The successful candidate will be responsible for ensuring ...

Job Description · We are seeking a highly skilled Regulatory Affairs Specialist to join our team. This is an excellent opportunity for an experienced professional looking to advance their career in regulatory affairs. · The successful candidate will be responsible for providing c ...

Job Title: Regulatory Affairs Specialist · We are seeking a highly skilled and experienced Regulatory Affairs Specialist to join our team. In this role, you will be responsible for ensuring compliance with European regulations (EU MDR) for medical devices. · Key Responsibilities: ...

Job Overview: · We are seeking a skilled Regulatory Affairs Specialist to lead our medical device compliance efforts. · Responsibilities · Mission Objectives: · Drive regulatory affairs activities for medical devices, ensuring adherence to EU MDR regulation (EU) 2017/745 and rel ...

Regulatory Affairs Specialist · About this Position: · <ul style= ...

Regulatory Affairs Specialist Opportunity · About the Role · We are seeking a highly skilled Regulatory Affairs Specialist to provide centralized oversight and execution of local submissions across Brazil, Argentina, and Chile. · Manage regulatory submissions and site start-up ac ...

Job Title: · Regulatory Affairs Professional · **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 te ...

As a Regulatory Affairs Specialist, you will be responsible for leading regulatory activities related to medical devices ensuring compliance with EU MDR regulations. · Mission Objectives: · Audit and maintain technical documentation in accordance with Annexes II & III of the EU M ...