Associate Director, RA UK & Ireland in Leeds

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.

As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.

DePuy Synthes is recruiting for a(n) Associate Director, RA UK & Ireland, located in Leeds, United Kingdom or Cork, Ireland. Johnson & Johnson announced plans to separate our Orthopedics business to establish a standalone orthopedics company, operating as DePuy Synthes. The process of the planned separation is anticipated to be completed within 18 to 24 months, subject to legal requirements, including consultation with works councils and other employee representative bodies, regulatory approvals and other customary conditions and approvals. Should you accept this position, it is anticipated that, following conclusion of the transaction, you would be an employee of DePuy Synthes and your employment would be governed by DePuy Synthes employment processes, programs, policies, and benefit plans.

The Associate Director, RA UK & Ireland provides senior regulatory leadership for the United Kingdom market, ensuring compliance with UK and applicable EU regulatory requirements while enabling timely market access and lifecycle management of DePuy Synthes products. This role has a significant impact on business continuity and growth by shaping local regulatory strategy, managing regulatory risk, and partnering closely with Commercial, Quality, Supply Chain, and Global Regulatory teams within a highly regulated environment.

• Lead and oversee regulatory affairs activities for the UK local market in alignment with global and regional regulatory strategies.
• Ensure compliance with UK regulatory requirements, applicable EU MDR provisions, internal policies, and quality system standards.
• Provide strategic regulatory guidance to support product registrations, variations, renewals, and lifecycle management activities.
• Serve as the senior regulatory affairs point of contact and escalation lead for the UK local operating company.
• Partner with Commercial, Quality, Supply Chain, and Global Regulatory teams to support compliant product distribution and business initiatives.
• Monitor regulatory changes and assess potential impacts to products, portfolios, and business operations in the UK.
• Lead for UKCA marking strategy for DePuy Synthes.
• Support internal audits, external audits, and health authority inspections related to regulatory activities.
• Lead, coach, and develop regulatory team members, fostering strong regulatory capability and compliance culture.
• Ensuring proactive engagement and shaping of regional policy initiatives that are critical to business strategy, continuity, and growth.

• Education: Bachelor’s degree in Regulatory Affairs, Life Sciences, Engineering, or a related discipline (required). Advanced degree in a scientific or regulatory field (preferred).
• Experience and Skills: Typically 8–10 years of progressive experience in Regulatory Affairs within medical devices, healthcare, or another regulated industry. Strong working knowledge of UK regulatory requirements and regulatory operating models. Demonstrated experience leading regulatory strategy and execution at the country level. Experience supporting audits, inspections, and health authority interactions. Ability to manage regulatory risk and complex stakeholder environments effectively. Experience with UKCA regulations.
• Preferred: Experience working in a multinational or matrixed organization. Familiarity with International regulatory operating models. Experience supporting orthopedic or medical device product portfolios. Exposure to regulatory strategy development and regulatory transformation initiatives. Regulatory Affairs Certification (RAC) or equivalent. Strong communication, leadership, and decision‑making skills.

Other: Language: English. Travel: Limited; occasional domestic or regional travel. Certifications: Regulatory certifications preferred but not required.

Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status or other characteristics protected by federal, state or local law.