Job Title: Regulatory Affairs Officer Salary: £40,000 - £45,000 Location: Hertfordshire, UK Job Type: Permanent A growing Pharmaceutical manufacturer are looking to expand their Regulatory team with the addition of a Regulatory Affairs Specialist. They are looking for an individual that shard working and self- motivated to assist with all things regulatory. Key Responsibilities: Oversee all aspects of the lifecycle maintenance for registered Marketing Authorizations (MAs) Assist in the preparation, compilation, and publication of documentation for the Common Technical Document (CTD) dossier. Collaborate with in-house teams, third-party designers, and contract sites to develop and update packaging artwork. Create and maintain patient information leaflets and packaging components, managing artwork to ensure compliance with regulatory standards and company approval systems. Lead and/or assist in submitting licenses and authorizations for new products and modifications to existing products. Experience and Qualifications Required: Bachelors degree required, ideally in sciences, engineering, medical/scientific writing, or public health administration. At least 2 years of experience in Regulatory Affairs or a related field. Proven experience in preparing technical documentation for regulatory submissions. Ability to work independently and manage daily regulatory responsibilities for a product portfolio. How to apply: Apply to e.smailesx4lifesciences to learn more about the role or connect with me on LinkedIn to hear about regular job updates available with X4 Life Sciences.