Associate Director RA Operations & Distributor Management, EMEA

Biopharma Careers; Warszawa; Híbrido; PLN 318.000 - 547.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Annual bonus

Vacation days

Parental leave

Descripción de la vacante

Johnson & Johnson in Warsaw, Poland is seeking an Associate Director of RA Operations & Distributor Management, EMEA, to drive regulatory execution and distributor activities across the region.

You will lead portfolio planning, align global and local regulatory strategies, and collaborate with cross-functional teams to support product launches, lifecycle management, and strategic priorities. Hybrid work and global impact offered.

Formación

• Master's degree in Science, Engineering, or a related field.
• Minimum 6 years of Regulatory Affairs experience within the medical device industry.
• Experience leading complex cross-functional programs in a matrix organization.

Responsabilidades

• Lead regulatory portfolio planning, prioritization, and execution across EMEA.
• Oversee distributor management activities and MDRIM leadership.
• Collaborate with Regulatory Affairs, Commercial, Quality, Supply Chain, and other partners.
• Identify risks and drive improvements in regulatory processes and tools.

Conocimientos

Regulatory Affairs

Cross-functional leadership

Stakeholder management

Strategic thinking

Risk management

Educación

Master's degree in Science or Engineering

Descripción del empleo

Johnson & JohnsonPosted October 21, 2026# Associate Director RA Operations & Distributor Management, EMEAWarsaw, Poland Full timeRegulatory Affairs Associate DirectorNotify me about similar jobsView Full Job & Apply at Johnson & JohnsonJohnson & Johnson is the source of truth for this posting and owns the application process. We surface normalized context and market comparison you won't find on the original listing.## About this opportunityAt 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 jnj.com .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.**Job Function:**Regulatory Affairs Group**Job Sub Function:**Regulatory Affairs**Job Category:**People Leader**All Job Posting Locations:**Warsaw, Masovian, Poland**Job Description:**DePuy Synthes is recruiting for an **Associate Director, RA Operations & Distributor Management, EMEA** located in Warsaw, Poland.PurposeWe are looking for an Associate Director, RA Operations & Distributor Management, EMEA to join DePuy Synthes.In this role, you will drive regulatory execution across EMEA by managing regulatory operations and distributor management activities. Working closely with Global, Regional, and Local Regulatory Affairs teams, as well as Commercial, Quality, Supply Chain, and other key partners, you will support product launches, lifecycle management activities, and strategic business priorities.Are you interested in leading regulatory operations across a diverse EMEA portfolio while helping ensure timely execution of regulatory activities that support patients and healthcare professionals across the region?You will be responsible forIn this role, you will provide leadership for regulatory portfolio planning, distributor market execution, and operational activities across EMEA. You will help ensure regulatory priorities are aligned across regions and functions while supporting efficient execution of product lifecycle activities and regulatory commitments.Key responsibilities include:Leading regulatory portfolio planning, prioritization, and execution across EMEAAligning global, regional, and local regulatory strategies to support business needsEnsuring effective execution of Regulatory Affairs activities across distributor marketsBuilding strong partnerships with Regulatory Affairs, Commercial, Quality, Supply Chain, and other cross-functional teamsDriving improvements in regulatory processes, tools, and ways of workingOverseeing the timely provision of regulatory documentation to local teams through leadership of central services activitiesLeading the MDRIM Management teamSupporting regulatory activities associated with commercial tender processesLeading, coaching, and developing contractors, trainees, and other assigned resourcesManaging priorities, resources, and budget activities within a matrix environmentIdentifying risks, resolving issues, and calling out significant challenges when requiredSupporting communication and coordination between regional, local, and global partners to ensure effective execution of regulatory activitiesQualifications / RequirementsWe are looking for someone who combines regulatory expertise, critical thinking, and the ability to operate effectively in a complex global environment.EducationMaster's degree or equivalent in Science, Engineering, or another relevant fieldExperienceMinimum of 6 years of Regulatory Affairs experience within the medical device industryExperience leading complex cross-functional programs and managing multiple prioritiesExperience working within a matrix organization and collaborating across functions and geographiesKnowledge & SkillsStrong understanding of medical device regulations and regulatory requirements across EMEAStrong strategic planning, analytical, and problem-solving skillsExcellent communication, presentation, and stakeholder management skillsDemonstrated ability to influence senior stakeholders within a matrix organizationAbility to work independently and make sound, timely decisionsAbility to identify and manage risks while maintaining focus on business prioritiesStrong collaboration and leadership capabilitiesDemonstrates an understanding of AI concepts and frameworks, including awareness of responsible and ethical AI practices, and uses effective prompting techniques to support efficiency and productivityWhat we offerWe offer a collaborative environment where learning, innovation, and professional development are encouraged.In this role, you will have the opportunity to work across global and regional Regulatory Affairs organizations, contribute to strategic portfolio decisions, and support innovative medical technologies that help improve patient outcomes.Our commitment to inclusionAt Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation is powered by bringing together people with different backgrounds, experiences, and perspectives.We are proud to be an equal opportunity employer and welcome applications from qualified candidates of all backgrounds.If you require a reasonable accommodation during the application, interview, or onboarding process, support is available. Please let us know how we can help.#LI-Hybrid#DePuySynthesCareers**Required Skills:****Preferred Skills:**Business Writing, Compliance Risk, Developing Others, Fact-Based Decision Making, Inclusive Leadership, Industry Analysis, Innovation, Leadership, Legal Support, Managing Managers, Operations Management, Policy Development, Product Licensing, Public Policies, Regulatory Affairs Management, Regulatory Compliance, Regulatory Development, Regulatory Environment, Strategic Thinking**The anticipated base pay range for this position is:**zł318 000,00 - zł547 400,00**Benefits:**In addition to base pay, we offer the following benefits\\*: an annual bonus with set target (% of pay) depending on pay grade / location, where the actual amount is based on the employees’ and companies’ performance of the previous calendar year, or sales commissions. Moreover, we offer vacation days, parental leave for a minimum of 12 weeks, bereavement leave, caregiver leave, volunteer leave, well-being reimbursement, programs for financial, physical and mental health. We also offer service anniversary and recognition awards, and subject to the terms of their respective plans, employees - and in some location’s eligible dependents - can participate in several insurance plans. For more information, visit Employee benefits | Supporting well-being & career growth | Johnson & Johnson Careers.\\*This is for informative purposes only. Amounts and actual benefits may vary by location and are subject to change.