Convatec has announced a major milestone in our R&D journey and commitment to our vision of pioneering trusted medical solutions to improve the lives we touch. We have unveiled plans to relocate the majority of our UK-based research and development (R&D) activities from Deeside to Manchester from 2027, alongside a significant expansion of our facilities in Boston. The new, planned Manchester facility has the potential to be a major R&D hub in our global network which will initially function as the company’s global testing laboratories, with cutting-edge analytical R&D capabilities including quality control and materials, regulatory functions, and health innovation, positioning Convatec at the forefront of medical technology development. Our new state-of-the-art facilities will also strengthen our collaboration with Manchester’s vibrant life sciences ecosystem, which includes leading universities, hospitals, and research institutions. About the role: The primary responsibilities of the position are to ensure regulatory compliance of a defined group of Convatec products, drive regulatory processes and activities (such as regulatory strategy, product registration, change control, review of marketing materials, etc) and continue to develop strong working relationships with internal and external customers. The person will be responsible for the management of global and regional regulatory projects, including, but not limited to, the regulatory aspects of new product development, product life cycle and changes to existing products. Key Responsibilities: • Advise on strategies and registration requirements for product development and marketed products • Write and submit regulatory dossiers (e.g., US FDA submissions, EU CE marking and UKCA Technical Documentation), and interface with authorities during the review process • Lead regulatory assessment and actions for changes to product and QMS processes • Ensure Regulatory compliance to maintain market approvals • Foster thorough knowledge of regulatory principles and compliance with regulatory policies throughout the organization through training and mentorship • Regulatory support to enquiries from customers and authorities • Provide guidance to business partners and junior regulatory staff regarding regulatory requirements including indications of risk and approximate timing for approval for planning purposes. Supports both new product development and currently marketed product portfolio • Review, interpret and communicate FDA/EU/international regulations and guidance documents to ensure complete and scientifically sound product submissions • Support base business activities, such as Annual Reports, Supplements, Labeling reviews, UDI • Identify and support or lead process improvement projects to streamline current activities and increase department efficiencies, including the update, enhancement, creation of new internal policies and procedures, and maintenance of existing procedures • Supports regulatory compliance to QSR, ISO, MDSAP, CE and other worldwide regulatory requirements as appropriate through customer complaints, internal and external audits, and training systems • Regulatory review and approval of documents supporting the QMS and product registrations • Participates as an active member of Industry, Regulatory or Scientific Committees, as appropriate • This position serves as a delegate for the line manager stated on this job description Authority: Regulatory approval of required documentation to support product development, registration and lifecycle management. Skills & Experience: • Preferred 1-2 years relevant experience, preferably in a regulatory affairs role in the life science industry • Understanding of the regulatory framework for medical devices. • Understanding of the Quality System Regulations ISO 13485:2016 including preparation and • implementation of standard operating procedures • Experience with Class I, II, and III sterile medical devices. • Preferred experience dealing directly with Notified Bodies, Competent Authorities, and/or the US FDA • Experience with US/EU submissions preferred. • Good time management and problem-solving skills. • Strong interpersonal and collaborative skills. • Ability to execute both reactively and proactively and in a timely manner. • Ability to conduct thorough research of regulatory requirements and related issues to identify potential solutions and available options. • Experience supporting change control and new product development projects • Strong analytical skills with good judgment-making capabilities. • Demonstrated organizational skills. • Strong oral and written communication skills. • Proficiency with Microsoft Office (Excel, Word, PowerPoint), Adobe Acrobat, and Internet-based regulatory resources, Trackwise, Documentum etc. Qualifications/Education: • A minimum of a bachelor’s degree in Science, Engineering, Medical Technology, or Nurse required. • An advanced degree and/or Regulatory Affairs Certification (RAC) is preferred.