We are looking for a Global Regulatory Affairs CMC Lead to join our Global Regulatory Affairs team, based in any of our Brussels (Belgium), Slough (UK) or Atlanta/Raleigh (US) offices.
About The Role
You will lead regulatory strategies, planning and preparation of global or regional specific CMC submissions for assigned projects/products across the full product lifecycle, from early development to post approval. Working closely with cross functional teams, you will shape high quality regulatory documentation, engage with health authorities, and support timely approvals that meet patient and business needs. This role plays a key part in ensuring regulatory excellence and continuous improvement across global markets.
Who You’ll Work With
You will be working in a team that brings together regulatory, manufacturing, quality, and supply experts from around the world. The team collaborates closely with other functions in global regulatory affairs, and development, technical and supply teams, creating strong partnerships to support innovative therapies. You will also engage with global stakeholders and external authorities, contributing your expertise across cross‑functional projects.
What You’ll Do
* Define and deliver regulatory strategies for global or regional specific CMC submissions for assigned projects/products across development and post approval stages.
* Lead complex regulatory submissions, ensuring consistency, quality, and alignment with agreed global strategies.
* Author and review regulatory CMC documentation within agreed timelines.
* Represent regulatory CMC expertise in cross functional project teams and authority interactions, as needed.
* Anticipate risks across the product lifecycle and communicate solutions clearly to key stakeholders.
* Support process improvement initiatives and mentor colleagues within the regulatory team.
Qualifications
* A degree in a scientific or technical discipline; advanced or regulatory qualifications are an advantage.
* Extensive experience in pharmaceutical industry and in regulatory roles, including global submissions and working with health authorities supporting regulatory discussions.
* Excellence and proven track record of successful regulatory strategic authoring and contribution to delivering regulatory CMC documentation of new marketing authorisations, clinical trial applications and post‑approval submissions.
* Experience working with health authorities and supporting regulatory discussions and responses.
* Demonstrated ability to leverage digital tools, structured data, and regulatory information systems to enhance regulatory strategy, submission quality, lifecycle management, and decision‑making across global markets.
* Ability to participate or lead and embed digital and process innovation initiatives within the team, driving harmonisation, efficiency, and regulatory excellence across cross‑functional and global teams.
UCB is an equal opportunity employer. All employment decisions will be made without regard to any characteristic protected by applicable laws.
Should you require any adjustments to our process to assist you in demonstrating your strengths and capabilities contact us on EMEA-Reasonable_Accommodation@ucb.com. Please note should your enquiry not relate to adjustments; we will not be able to support you through this channel.
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