Your new company

Are you ready to join a pioneering team in the biotechnology industry? We are a global leader dedicated to transforming genetic discoveries into life-changing medicines. Our innovative approach targets the root causes of genetic conditions, offering hope and improved health outcomes to patients worldwide. This is a great opportunity to join a loyal and high-growth team that have all been in business for a minimum of 8 years.

Your new role

You will be going in as a Senior Regulatory Affairs Associate. This position focusses on providing regulatory affairs support to both ongoing development programs and approved product lifecycle activities. You will Support the EU Lead in regard to planning. Assist with the development of the EU submissions for e.g. PRIME and Orphan Drug Designation, ATMP classification. This is a great opportunity to grow as an individual but also as a regulatory professional.

What you'll need to succeed

EU, Early stage and clinical experience, EMA submissions. You will have a minimum of 1–2 years of regulatory affairs experience.

What you'll get in return

You will get a good work-life balance, the opportunity to grow and develop under fantastic leadership. Alongside a competitive market salary.

What you need to do now

George.costard1@hays.com

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 us for a confidential discussion about your career.