Default company background
beBeeMedicalDevice

Vagas na beBeeMedicalDevice em Brasil

26 vagas na beBeeMedicalDevice em Brasil

  • beBeeMedicalDevice Santana de Parnaíba

    Regulatory Affairs Specialist Role Overview · This position involves managing regulatory affairs for medical devices, ensuring compliance with European regulations (EU MDR – Regulation (EU) 2017/745). The role requires strong expertise in Class IIa and IIb medical devices. · Key ...

  • beBeeMedicaldevice Juazeiro do Norte

    Regulatory Affairs Specialist · Location: Brazil (Remote opportunity) · We are seeking a skilled Regulatory Affairs Specialist to lead regulatory activities for medical devices, ensuring compliance with European regulations. The ideal candidate will have a strong expertise in Cla ...

  • beBeeMedicalDevice Dourados, MS

    Regulatory Compliance Expert · This is an excellent opportunity for a highly skilled Regulatory Compliance Expert to lead regulatory activities for medical devices in Brazil. The role involves ensuring compliance with European regulations, Class IIa and IIb medical device classif ...

  • beBeeMedicalDevice Ponta Grossa, PR

    Regulatory Compliance Expert · We are seeking a seasoned Regulatory Compliance Expert to drive our medical device regulatory initiatives forward. · The ideal candidate will possess 6+ years of experience in Regulatory Affairs for medical devices and demonstrate expertise in Class ...

  • beBeeMEDICALDEVICE Vila Velha

    Job Overview · We are seeking a seasoned Regulatory Affairs Specialist to join our team. The ideal candidate will have extensive experience in Regulatory Affairs for medical devices, with a proven track record of ensuring compliance with European regulations (EU MDR). · Responsib ...

  • beBeeMedicalDevice Guaíba

    Regulatory Affairs Specialist · In an ever-evolving regulatory landscape, our company seeks a seasoned Regulatory Affairs Specialist to lead the way in ensuring compliance and driving strategic partnerships. · A leader who can position themselves as a technical and functional ref ...

  • beBeeMedicalDevice Ipojuca

    Regulatory Affairs Professional · We are seeking a seasoned Regulatory Affairs Specialist to join our team in Brazil. · ...

  • beBeeMedicalDevice Valinhos, SP

    Regulatory Affairs Specialist Job Overview · This is a senior role that involves leading regulatory affairs activities for medical devices. The specialist will be responsible for ensuring compliance with European regulations. · ...

  • beBeeMedicalDevice Uberlândia, MG

    Regulatory Affairs Professional · Location: Brazil (Remote opportunity) · Are you a strategic partner to our clients in Regulatory Affairs, acting as a technical and functional reference? · We are looking for an experienced individual with 6+ years of experience in Regulatory Af ...

  • beBeeMedicalDevice São José dos Pinhais

    Regulatory Affairs Specialist · In this role, you will be responsible for leading Regulatory Affairs activities for medical devices ensuring compliance with European regulations (EU MDR – Regulation (EU) 2017/745). · ...

  • beBeeMedicalDevice Itapema

    Regulatory Affairs Expert · This is a key role in our organization, responsible for ensuring compliance with European regulations. The successful candidate will have significant experience in Regulatory Affairs for medical devices and be able to lead regulatory activities. · Lead ...

  • beBeeMedicalDevice Eldorado do Sul

    Regulatory Affairs Professional · We are seeking a highly skilled Regulatory Affairs Specialist to join our team. As a Regulatory Affairs Specialist, you will be responsible for ensuring the compliance of medical devices with European regulations (EU MDR – Regulation (EU) 2017/74 ...

  • beBeeMedicalDevice Campinas, SP

    Regulatory Affairs Specialist Job Description · A dynamic and rapidly expanding organization seeks a skilled Regulatory Affairs Specialist · The selected candidate will be responsible for leading regulatory affairs activities for medical devices, ensuring compliance with European ...

  • beBeeMedicalDevice Jundiaí, SP

    Regulatory Affairs Specialist · This role is ideal for experienced professionals in Regulatory Affairs for medical devices. · Promote Regulatory Affairs excellence across medical device operations, adhering to EU MDR guidelines. · Demonstrate expertise in Class IIa and IIb medica ...

  • beBeeMedicalDevice São Luís

    Job Title: Regulatory Affairs Specialist · Description: · We are seeking a highly skilled professional to lead regulatory affairs activities for medical devices, ensuring compliance with European regulations (EU MDR). The ideal candidate will have expertise in medical device clas ...

  • beBeeMedicalDevice Montenegro

    Regulatory Affairs Specialist · In a rapidly expanding international environment, we are seeking an experienced Regulatory Affairs Specialist to lead our medical devices activities. This dynamic and highly regulated role requires strong expertise in Class IIa and IIb medical devi ...

  • beBeeMedicalDevice Jaraguá do Sul

    Regulatory Affairs Expert · Overview: · In this pivotal role, you will lead Regulatory Affairs activities for medical devices ensuring compliance with European regulations. You will act as an expert in medical device classification, focusing on Class IIa and IIb ensuring correct ...

  • beBeeMedicalDevice Brasilia

    Regulatory Affairs Specialist Job Description · We are seeking a skilled Regulatory Affairs Specialist to join our team. In this role, you will be responsible for leading regulatory affairs activities for medical devices and ensuring compliance with European regulations. · Key Re ...

  • beBeeMedicalDevice Rio Branco

    Regulatory Affairs Professional · Lead regulatory affairs activities for medical devices, ensuring compliance with European regulations. Act as an expert in medical device classification and coordinate the preparation of technical documentation. · Your Profile: · 6+ years of expe ...

  • beBeeMedicalDevice Francisco Beltrão, PR

    Regulatory Compliance Expertise · This role involves leading regulatory affairs activities for medical devices in compliance with European regulations. · The successful candidate will act as an expert in medical device classification, focusing on Class IIa and IIb. Key responsibi ...