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 Cutting-edge 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 jnj.ComAs 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.Job Function: Regulatory Affairs GroupJob Sub Function: Regulatory AffairsJob Category: People LeaderAll Job Posting Locations: Palm Beach Gardens, Florida; Raynham, Massachusetts; Toronto, Ontario; West Chester, PennsylvaniaJohnson & Johnson announced plans to separate our Orthopaedics business to establish a standalone orthopaedics 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, 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. In that case, details of any planned changes would be provided to you by DePuy Synthes at an appropriate time and subject to any necessary consultation processes.Job OverviewThe Associate Director, RA Canada provides regulatory leadership for the Canadian market,



ensuring compliance with local regulatory requirements while enabling timely and sustainable market access for DePuy Synthes products. This role plays a critical leadership position within the Regulatory organization, partnering with commercial, quality, and global regulatory teams to shape regulatory strategy, manage risk, and support business growth in a highly regulated environment.Key ResponsibilitiesLead and oversee regulatory affairs strategy and execution for the Canada local market in alignment with global regulatory objectives.Ensure compliance with Health Canada requirements, internal policies, and quality system standards.Provide strategic regulatory guidance to support product registrations, renewals, variations, and lifecycle management.Serve as the senior regulatory point of contact and escalation lead for Canada Local Market Support.Partner with cross‑functional stakeholders including Commercial, Quality, Supply Chain, Legal, and Global Regulatory Affairs.Monitor regulatory changes in Canada and assess potential impacts to products, portfolios, and operations.Support regulatory inspections, audits, and health authority interactions as required.Lead, coach, and develop regulatory talent, fostering strong compliance, accountability, and performance.Ensure proactive engagement and shape regional policy initiatives that are critical to business strategy, continuity, and growth.QualificationsEducationBachelor’s degree in Regulatory Affairs, Life Sciences, Engineering,



or a related discipline (required).Advanced degree or professional certification in Regulatory Affairs (preferred).Experience and SkillsRequired:Typically 8–10 years of progressive experience in Regulatory Affairs within the medical device or other regulated industries.Strong knowledge of Canadian regulatory requirements and Health Canada processes.Demonstrated experience leading regulatory strategy and execution at the country level.Proven ability to manage regulatory risk and complex stakeholder environments.Strong leadership, communication, and decision‑making skills.Ability to operate effectively in a global, matrixed organization.Preferred:Experience supporting US or global regulatory operating models.Experience working in multinational medical device or healthcare organizations.Exposure to regulatory inspections, audits, and authority negotiations.Demonstrated success driving regulatory transformation or process improvement initiatives.Regulatory Affairs Certification (RAC) or equivalent.OtherLanguage: English required; French proficiency preferred.Travel: Moderate national travel; occasional international travel. If based in a US location, 50% travel could be expected.Certifications: RAC or equivalent preferred but not required.Johnson & Johnson is an Equal Chance 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. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act.Johnson & Johnson is committed to providing an interview process that is inclusive of our applicants’ needs. If you are an individual with a disability and would like to request an accommodation, external applicants please contact us via https://www.Jnj.Com/contact-us/careers, internal employees contact AskGS to be directed to your accommodation resource.The anticipated base pay range for this position is $124,000.00 - $212,750.00.Extra benefits information is available at https://www.Careers.Jnj.Com/employee-benefits.#J-18808-Ljbffr

📌 Associate Director, Ra Canada - $124,000 - $212,750 A Year (Winnipeg)
🏢 Johnson & Johnson
📍 Winnipeg