Make your mark for patients
We are looking for a Regulatory CMC Scientist to join us in our Global Regulatory team, based in any of our Brussels (Belgium), Slough (UK) or Raleigh/Atlanta (US) offices.
About the role
Define the strategy, planning and preparation (writing and review) of CMC submission documentation for regulatory submissions (new marketing applications, variations) from a global/regional perspective to achieve timely approvals to meet business needs.
Who you'll work with
You will work within the Regulatory CMC team and partner with other technical and regulatory functions across the business.
What you'll do
Responsible for regional and global CMC submissions in line with agreed global regulatory strategy, and within agreed timelines.
Contribute and ensure adequate provision of regulatory CMC input to all Health Authority (HA) interactions on CMC matters in all regions
Ensures effective communication of CMC regulatory strategy, risks, and overall plan to GRA Teams, Technical, Development and Commercial Teams
Highlights anticipated and ongoing critical issues arising through the product life cycle in a timely manner to senior management to enable communication to key stakeholders
Lead or contribute to ongoing process improvement and department initiatives within the CMC Regulatory Affairs function, including process improvements, SOP review and development, and evaluation/implementation of digital strategies and tools.
Interested? For this position you'll need the following education, experience and skills:
Bachelor's degree, Master's preferred in a relevant life science or business-related discipline
Demonstrated ability to leverage digital tools, structured data, and regulatory information systems to enhance CMC and Device regulatory strategy, submission quality, lifecycle management, and decision-making across global markets
Significant relevant experience in the pharmaceutical industry preferably in Regulatory Affairs CMC with focus on biological entities
Proven track record of successful authoring and contribution to delivering CMC sections of marketing authorisations for new biological entities
Knowledge of GMP requirements, standard systems (e.g. change management systems and tools)
Effective interpersonal, presentation and communication skills with established internal and external stakeholders
Proven leadership, problem-solving ability, flexibility, influence, and effective teamwork skills.
Are you ready to 'go beyond' to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!
At UCB, we've embraced a hybrid-first approach to work, bringing teams together in local hubs to foster collaborative curiosity. Unless expressly stated in the description or precluded by the nature of the position, roles are hybrid with 40% of your time spent in the office.
