Regulatory Operations Specialist - Medicines in Kingston upon Hull

b Overview /b p As Regulatory Operations Specialist, you will manage regulatory dossiers and lifecycle activities across medicinal regulations to support timely, compliant submissions. You will work with cross-functional teams to ensure audit-ready documentation and robust regulatory processes. You will navigate a fast-paced FMCG regulatory landscape, maintaining dossier accuracy post-launch and ensuring supply continuity. This role offers impact across global markets, shaping compliant products in Reckitt’s health portfolio. /p b Pay / Benefits /b ul li Parental benefits /li li Employee Assistance Program /li li Life insurance for all employees globally /li li Global share plans /li li Short-term incentives /li li Pay-for-performance philosophy /li /ul b Responsibilities /b ul li Support regulatory requirements across multiple markets to maintain dossier maintenance and post-launch compliance /li li Deliver high-quality submissions within agreed timelines and coordinate with partner functions /li li Provide GMP documentation support for Reckitt medicinal manufacturing sites globally /li li Maintain compliant use of systems and ensure audit readiness across activities /li /ul b Key requirements /b ul li Experience in regulatory affairs and dossier creation for global registrations /li li Knowledge of regional and global regulatory environments and their impact on dossiers /li li Experience preparing and submitting medicinal product dossiers and supporting documentation /li li Ability to manage multiple projects independently and within a team /li li Bachelor of Science in a relevant scientific discipline (e.g., Chemistry, Biology, Microbiology, Pharmacy) /li li Strong written and verbal communication to convey regulatory information clearly /li /ul ul li Collaborative /li li Results-driven /li li Strong communication /li li Regulatory dossier preparation /li li Global registrations and regulatory submissions /li li GMP documentation /li /ul