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Bedford, Bedford, United Kingdom Werfen Full timeJob SummaryThe Principal Regulatory Specialist is responsible for ensuring compliance with regulatory requirements for medical devices and in vitro diagnostics. This role involves developing and implementing regulatory strategies, preparing regulatory plans and submissions, and collaborating with cross-functional teams to ensure regulatory compliance.Key...
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Bedford, Bedford, United Kingdom Werfen Full timeJob SummaryThe Principal Regulatory Specialist is responsible for ensuring compliance with regulatory requirements for medical devices and in vitro diagnostics. This role involves developing and implementing regulatory strategies, preparing regulatory plans and submissions, and collaborating with cross-functional teams to ensure regulatory compliance.Key...
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Regulatory Affairs Specialist
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Bedford, Bedford, United Kingdom Lantheus Medical Imaging Inc Full timeRegulatory Affairs SpecialistLantheus Medical Imaging Inc is a leading company in the field of medical imaging, with a strong commitment to innovation and patient care. We are seeking an experienced Regulatory Affairs Specialist to join our team.Key Responsibilities:Develop and implement regulatory strategies for advertising and promotional materials,...
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Regulatory Affairs Specialist
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Bedford, Bedford, United Kingdom Lantheus Medical Imaging Inc Full timeRegulatory Affairs SpecialistLantheus Medical Imaging Inc is a leading company in the field of medical imaging. We are seeking an experienced Regulatory Affairs Specialist to join our team. The ideal candidate will have a strong background in regulatory affairs, with a focus on labeling and promotional communications. The successful candidate will be...
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Regulatory Affairs Specialist
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Bedford, Bedford, United Kingdom Werfen Full timeJob SummaryThe Principal Regulatory Specialist is a key member of the Werfen team, responsible for ensuring compliance with regulatory requirements for medical devices and in vitro diagnostics. This role requires a strong understanding of FDA, MDSAP, IVDR, MDR, and international regulations, as well as ISO and other international...
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Bedford, Bedford, United Kingdom Werfen Full timeJob SummaryThe Principal Regulatory Specialist is a key member of the Werfen team, responsible for ensuring compliance with regulatory requirements for medical devices and in vitro diagnostics. This role requires a strong understanding of FDA, MDSAP, IVDR, MDR, and international regulations, as well as ISO and other international...
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Regulatory Affairs Specialist
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Bedford, Bedford, United Kingdom Werfen Full timeJob SummaryThe Principal Regulatory Specialist is a key member of the Werfen team, responsible for ensuring compliance with regulatory requirements for medical devices and in vitro diagnostics. This role requires a strong understanding of FDA, MDSAP, IVDR, MDR, and international regulations, as well as ISO and other international...
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Regulatory Affairs Specialist
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Bedford, Bedford, United Kingdom Werfen Full timeJob Summary:Werfen is seeking a highly skilled Regulatory Affairs Specialist to join our team. As a key member of our regulatory team, you will be responsible for ensuring compliance with regulatory requirements for our medical devices in China and Japan.Key Responsibilities:Participate in design and risk management teams to provide guidance on regulatory...
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Regulatory Affairs Specialist
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Bedford, Bedford, United Kingdom Werfen Full timeOverviewWerfenWerfen is a global leader in the development, manufacturing, and distribution of specialized diagnostic instruments, reagents, and data management solutions. With a strong focus on innovation and quality, we provide healthcare professionals with valuable and complete solutions to improve hospital efficiency and enhance patient care. Our...
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Senior Regulatory Affairs Specialist
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Bedford, Bedford, United Kingdom Werfen Full timeJob Summary:We are seeking a highly skilled Regulatory Affairs Specialist to join our team at Werfen. As a key member of our regulatory team, you will be responsible for ensuring compliance with regulatory requirements for medical devices in China and Japan.Key Responsibilities:Participate in design and risk management teams to provide guidance on regulatory...
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Senior Regulatory Affairs Specialist
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Senior Regulatory Affairs Specialist
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Regulatory Compliance Specialist
2 months ago
Brayson Consulting Ltd is looking for a dedicated part-time Regulatory Compliance Specialist to support our client's new care service. This role is ideal for someone with a background as a Registered Manager who is interested in potential future advancement to a full-time managerial position.
The Regulatory Compliance Specialist will be tasked with:
- Ensuring adherence to all relevant CQC regulations and standards.
- Monitoring compliance practices within the organization.
- Providing guidance and support to staff on compliance-related matters.
We seek a candidate who is detail-oriented and possesses a strong understanding of compliance frameworks in the healthcare sector. This is an excellent opportunity to contribute to a growing organization while ensuring the highest standards of care are maintained.