At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com Job Function: Regulatory Affairs Group Job Sub Function: Regulatory Product Submissions and Registration Job Category: People Leader All Job Posting Locations: ES001 Johnson / Surgical / Madrid, FR018 Issy les Moulineaux_Stalingrad, GB025 ACT London, UK, IT004 Pratica di Mare Pomezia, Norderstedt, Schleswig-Holstein, Germany Job Description: Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments. Your unique talents will help patients on their journey to wellness. Learn more at https://www.jnj.com/medtech As the EMEA Content Compliance Manager, you will lead the Regulatory approval process for advertising, promotional materials, and claims across Johnson & Johnson MedTech EMEA. This role is pivotal in ensuring regulatory and scientific content compliance within a highly regulated MedTech environment. You will manage a team of Regulatory reviewers across MedTech and EMEA countries, ensuring consistency, quality, and compliance in all content submissions. You will collaborate with cross-functional teams and external stakeholders to uphold quality standards, drive operational excellence, and ensure alignment with internal procedures and external regulations. Key Responsibilities · Lead audits of the copy approval process and ensure adherence to EU and country regulations and laws. · Serve as a key contact for regulatory and compliance-related inquiries. · Maintain and optimize procedures and ensure alignment with internal and external standards. · Oversee the lifecycle of approved materials, including auditing marketing platforms and managing expired assets. · Consolidate and disseminate copy review results and provide counsel on the process. · Own KPIs for monthly copy review data and initiate re-trainings as needed. · Lead and develop a team of Regulatory reviewers across MedTech and EMEA countries. · Ensure consistent interpretation and application of regulatory standards across markets. · Foster a high-performance culture focused on compliance, collaboration, and continuous improvement. · Partner with Regulatory, Medical, Legal, Healthcare Compliance, Data Privacy, Communications, Marketing, Quality and other teams. · Host business meetings and support external audits. · Collaborate with the IT team to identify and implement system, AI and IA improvements. · Propose and implement process enhancements for continuous improvement. · Deliver training for new copy review participants and maintain training materials. · Ensure training plans are updated in line with corporate and franchise procedures. · Independent resources and budget management. Qualifications · Bachelor’s degree or higher · Strong and comprehensive experience in regulatory roles within a regulated industry, preferably in MedTech · Strong knowledge of regulatory compliance and quality assurance · Proven ability to manage teams and lead cross-functional projects · Excellent communication, organizational, and change management skills · Experience with compliance audits and procedure development · Proficiency in MS Office, Adobe Acrobat, and digital platforms Preferred Skills · Strategic thinking and business data analysis · Project management and multitasking capabilities · Ability to work in international, multicultural environments · Quick learner with a flexible working approach · Strong customer orientation and sense of urgency Join Us If you're passionate about regulatory excellence and content compliance in the MedTech space, and thrive in a collaborative, fast-paced environment, we invite you to apply and make a meaningful impact on patient outcomes.