Job Description

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Agilent inspires and supports discoveries that advance the quality of life. We provide life science, diagnostic and applied market laboratories worldwide with instruments, services, consumables, applications and expertise. Agilent enables customers to gain the answers and insights they seek -- so they can do what they do best: improve the world around us. Information about Agilent is available at you an individual with knowledge in IVD or Medical Devices, looking for a new challenge in your career? A job where your actions will have an impact on improving quality of life. Then we are looking for you

Come and join a highly collaborative environment where you will be part of our Global Regulatory Affairs team with the opportunity to be exposed to innovative IVD products across different regulatory classifications including hardware, software, and immunochemistry technologies.

We are searching for an experienced Regulatory Affairs Specialist to play a key role in coordinating and tracking international submissions mainly in the EMEA (non-EU) for new products along with renewals and changes to existing registrations.

Your main task will be:

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- Create, manage, and ensure closure of daily Regulatory blocks
- Become an expert with the GTS tool handling Regulatory release of IVD products
- Create, train, and implement tools for accurate tracking of product changes
- Collaborate with Global Regulatory Affairs ensuring regulatory assessments of changes is sought, obtained, and documented
- Oversight of Channel Partner business licenses and renewals
- Oversight of IVD registrations and renewals
- Collaborate with Global Regulatory Affairs ensuring timely registration of IVD products and their renewals

Qualifications

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- A university degree in a relevant field such as Life-Science/Engineer/Law etc.
- Significant regul

Sr. International Regulatory Affairs Specialist

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