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SalaryYour new company
A leading pharmaceutical and medical device company is looking to bring a regulatory partner into the business on a 12-month contract to support the team on UK&I submissions. An exciting company with a great company culture.
Your new role
You will be responsible for developing and executing the UK regulatory submission strategy for innovative drug-device combination products from CTA's, MAA's, Variations. You will be responsible for interacting with the MHRA and EMEA regularly.
What you'll need to succeed
You must have drug-device combination experience and at least 8+ years of experience within regulatory in both pharma and medical devices. You must have a strong understanding of the EU and UK health authorities, and have experience working from CTA through to Post-Maintenance.
What you'll get in return
This is an initial 12-month contract and will be looking for someone to travel to the site 2 days per week. It is outside IR35, so you can go through your own company for this position.
What you need to do now
If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.
If this job isn't quite right for you, but you are looking for a new position, please contact Julia Bowden for a confidential discussion about your career.
