Your new company You will be joining a leading organisation within the pharmaceutical sector, supporting the development and manufacture of complex drug products. The business is recognised for its innovative approach, strong client partnerships, and commitment to sustainability, working closely with global regulatory bodies. Your new role As a Regulatory Manager, you will take on a highly visible, client-facing position and be responsible for leading regulatory strategy. You will provide expert guidance on regulatory pathways, supporting customers in achieving approvals across regions such as the EU and US. Your role will involve leading regulatory aspects of development projects, reviewing and approving key documentation (including DMFs, technical files, and CTD submissions), and acting as a primary point of contact for regulatory agencies such as the MHRA, EMA, and FDA. As second in command, you will also play a key leadership role, managing a small team with scope to grow, contributing to regulatory intelligence across the business, and representing the regulatory function in senior-level internal and external meetings. What you'll need to succeed To be successful in this role, you will ideally have: Around 10 years of regulatory experience within pharmaceuticals or medical devices Strong experience in successful filings in EU and/or US markets Proven ability to lead regulatory projects and manage multiple priorities...