Regulatory Affairs Manager

Job Title: Regulatory Affairs Manager Job Type: Full-time, permanent Location: North Hampshire, UK (hybrid - 3 days on-site) Cpl Life Sciences is partnering with a growing biopharmaceutical business to hire a Regulatory Affairs Manager into their global team. This is an excellent opportunity for someone looking to step away from large pharma into a more agile, high-impact environment, where you’ll gain broader exposure, real ownership, and visibility across the business. Why make the move? • Take ownership of global regulatory strategy and submissions • Work across international markets (EU, Middle East, Asia, Australia) • Gain exposure beyond siloed big pharma roles • Be part of a growing, dynamic company where your impact is visible Job Responsibilities: • Leading end-to-end regulatory activities across the product lifecycle • Managing international submissions (MAAs, variations, CTAs, lifecycle) • Acting as the regulatory lead across cross-functional teams • Engaging directly with health authorities and global partners • Contributing to CTD authoring and regulatory strategy Requirement: • 5+ years in EU Regulatory Affairs (medicinal products) • Strong MRP/DCP experience (essential) • Proven submission and strategy delivery experience • Confident working cross-functionally and with regulators • A proactive mindset suited to a fast-paced, growing business An excellent opportunity for the right person to take the next step within their regulatory career and gain exposure within an exciting environment. This is a hybrid role, requiring 3x a week on site in Hampshire, UK. Please also note this role does not offer job sponsorship. You MUST hold the full right to work in the UK with no restrictions. Please contact