Senior Program Manager for IVDR Compliance

2 weeks ago


Glostrup, Glostrup Kommune, Denmark Agilent Technologies Full time

We are seeking a seasoned project management professional to join our team as a Senior Program Manager for IVDR compliance.

About the Role

As a Senior Program Manager, you will be responsible for leading project teams to successfully transition Agilent's existing IVD pathology portfolio to compliance with the European Regulation on IVDR.

The ideal candidate will have a relevant Master's background related to Life Science or Engineering and experience in coordinating project teams and delivering results in a highly regulated industry.

You will develop project plans, budgets, and resource plans in collaboration with stakeholders, lead geographically diverse cross-functional project teams, and manage relationships and inter-dependencies with other projects.

A strong understanding of working with design control documentation for in vitro diagnostic or medical devices is essential, as well as excellent English verbal/written communications skills.

This is a fantastic opportunity to work with a dynamic team, contribute to the lifecycle management of state-of-the-art diagnostic assays benefiting cancer patients worldwide, and enjoy a competitive compensation and benefits package.



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