Offer summary

Qualifications:

University degree in Life Science, Engineering, or Law., Significant experience with IVD or medical device regulations., Ability to interpret regulatory standards and requirements., Excellent communication skills in English..

Key responsibilities:

Coordinate and track international regulatory submissions in the EMEA region.

Manage regulatory blocks and ensure their timely closure.

Collaborate with global teams to assess and document regulatory changes.

Oversee registration renewals and licenses for IVD products.

Job description

Job Description

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 www.agilent.com.

Are 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:

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

A university degree in a relevant field such as Life-Science/Engineer/Law etc.
Significant regulatory experience with a solid understanding of IVD/medical device regulations and registration requirements.
Ability to interpret regulations and standards in relation to specific products.
Excellent interpersonal and communication skills in English

In order to succeed the successful candidate will have proven capability in analytical and critical thinking, collaborating across global teams, strong organization skills, ability to run multiple ongoing responsibilities, and driving tasks through to completion.

We offer:

An independent job in collaboration with good colleagues, in a growth-orientated organization
A true commitment to work/life balance
An opportunity to learn and grow in the field of Regulatory Affairs
Agilent Result Bonus, Stock Purchase Plan, Life Insurance, Pension, Healthcare, Employee Assistance Program, Holiday, Company activities.

Additional Details

This job has a full time weekly schedule. It includes the option to work remotely.

Agilent Technologies Inc. is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other protected categories under all applicable laws.