Hobson Prior is seeking a Regulatory Manager. This role involves managing product registrations, submitting regulatory documents, preparing regulatory files, and updating technical files to comply with the Medical Device Regulation (MDR). The role requires a good understanding of regulatory standards and the ability to handle complex regulatory situations.

Please note that to be considered for this role you must have the right to work in this location.

Responsibilities:

• Review and update technical files to ensure compliance with the Medical Device Regulation (MDR).
• Prepare comprehensive regulatory files for both new and existing products.
• Organize and submit regulatory files to various regulatory bodies in a timely and accurate manner.
• Manage the product registration and renewal processes in overseas markets.
• Stay updated with regulatory developments and inform relevant parties about their implications.
• Organise and maintain all regulatory documentation to keep it current and easily accessible.

Key Skills & Requirements:

• A degree in regulatory affairs, life sciences, or a related field.
• Experience in the regulatory affairs field within the medical device industry.
• Good understanding of the EU MDR and other relevant legal frameworks.
• Experience in submitting regulatory documents.

For more information, please contact Toby Shelton.

Apply now

If you are interested in learning more or applying to this exciting opportunity then please click 'Apply' and upload a copy of your CV. Alternatively for further details or to talk directly to a life sciences recruitment specialist directly please select 'Contact me' at the top of this page.

Hobson Prior is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Hobson Prior is acting as an Employment Agency in relation to this vacancy.

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