Regulatory Submissions Manager Sandwich, Kent Salary: Up to £19.75 per hour DOE Hours: Monday to Friday, 37.5 hours per week Contract: 12 months Are you an experienced dossier manager looking for your next challenge? Our client, a leader in the pharmaceutical industry, is seeking a detail-oriented and highly organised professional to join their regulatory team. This is a fantastic opportunity to play a key role in ensuring the successful submission of regulatory dossiers to health authorities worldwide. Why join our client? Competitive hourly rate of up to £19.75 per hour (DOE) 12-month contract with a well-respected organisation Opportunity to work in a fast-paced, highly regulated environment Be part of a team that values precision, collaboration, and innovation The Role As a Regulatory Submissions Manager, you will be responsible for the operational management of dossier preparation and submission, ensuring compliance with global regulatory standards. You will oversee the dossier build, technical publishing, and submission processes, working within strict deadlines and liaising with multiple stakeholders across different regions. Key Responsibilities Manage the technical aspects of dossier preparation, including publishing and submission to health authorities. Oversee document receipt, translations, and compliance with submission milestones. Ensure regulatory requirements are met across multiple national and regional dossiers. Engage with submission managers, publishing leaders, and key stakeholders to optimise document reuse across different markets. Guide submission processes and contribute to process improvements. Lead the interpretation of regulatory guidelines and ensure adherence to industry standards. Monitor regulatory compliance submissions, including safety reports and promotional materials. About You To be successful in this role, you should have: A degree in Pharmacy, Life Sciences, Business, or Information Technology (or equivalent professional experience). Experience in regulatory dossier management, publishing, or regulatory operations within the pharmaceutical industry. Strong knowledge of regulatory requirements, submission standards, and dossier preparation. Advanced skills in Microsoft Office and technical publishing tools. Excellent organisational, communication, and problem-solving skills. The ability to work independently, manage multiple projects, and meet tight deadlines. Apply Now If you have the skills and experience required for this role, we would love to hear from you. Apply today to take the next step in your regulatory career Morgan Jones is committed to creating a diverse and inclusive environment and is proud to be an equal-opportunity employer. All qualified applicants will receive consideration for employment without regard to race, colour, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, or veteran status. About Morgan Jones: Morgan Jones Limited acts as an employment agency. By applying, you accept the Terms & Conditions as well as the Privacy, Cookie, and Data Retention Policy, which can be found on our website.Due to the high volume of applicants we receive, if you have not heard back from us within 72 hours, please assume that you have been unsuccessful on this occasion.To view other great opportunities, visit our website or follow Morgan Jones on Facebook, Instagram, Twitter, or LinkedIn.