About us: Network Partners is looking for “best in class”’ RA Specialists to join our team. We are a spirited, high-growth company focused on the success of our clients and our colleagues. We put a new spin on consulting and staffing that allows you to work at a company dedicated to the discipline of Regulatory Affairs while simultaneously working for some of the world’s largest and well known medical device and pharmaceutical companies. It’s the best of both worlds!

About this role:  Our medical device client needs a RA Project Lead to support a transformation project focused on implementing electronic Instructions for Use for selected products.   In this role, your RA experience will be required in order to understand the impact of IFU, packaging and labeling changes to product registrations.  Your value will be evident as you plan the completion of global regulatory submittals and manage the regulatory project team.  This work can be performed remotely.

This role requires at least 5 years of Regulatory Affairs experience as well as Project Management experience.  To be successful you should have an understanding of medical device IFU requirements as well as Quality Management system experience.  It would be beneficial if you have experience with Class III products as well experience implementing eIFU in a company with global distribution.

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