Manager QARA CEE, Baltics, Balkans (Warsaw)

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 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 GroupJob Sub Function: Regulatory AffairsJob Category:ProfessionalAll Job Posting Locations:Prague, Czechia, Warsaw, Masovian, PolandJob Description:Johnson & 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, including consultation with works councils and other employee representative bodies, as may be required, 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.​DePuy Synthes is recruiting for a(n) Manager, QARA CEE, Baltics, Balkans, located in Warsaw, Poland or Prague, Czechia Job Overview The Manager, QARA CEE, Baltics, Balkans, provides operational leadership for quality assurance and regulatory affairs across Central & Eastern Europe, the Baltics, and the Balkans. This role is responsible for ensuring regulatory compliance, effective quality management system execution, and sustained market access for DePuy Synthes’ Orthopedics portfolio across multiple, diverse European markets. The role plays a critical part in managing quality and regulatory risk, supporting product lifecycle activities, and enabling compliant business continuity and growth in a highly regulated environment. The Manager partners closely with local market teams and global QARA stakeholders to ensure patient safety and compliance excellence. Key Responsibilities Lead and manage Quality Assurance and Regulatory Affairs activities to support product registrations, renewals, variations, and lifecycle management across CEE, Baltic, and Balkan markets. Ensure compliance with country‑specific regulatory requirements, EU MDR obligations, internal policies, and DePuy Synthes quality management system standards. Serve as the primary QARA point of contact for assigned CEE, Baltics, and Balkans markets. Coordinate regulatory submissions, technical documentation, renewals, and responses to health authority inquiries. Partner with cross‑functional teams including Quality, Supply Chain, Commercial, Legal, and Global QARA to support product availability, launches, and supply continuity. Monitor regulatory, quality, and enforcement changes across assigned markets and assess potential impacts to products, portfolios, and operations. Support and participate in regulatory inspections, quality audits, and compliance assessments as required. Contribute to continuous improvement initiatives to enhance QARA efficiency, compliance consistency, and inspection readiness across the region. Ensuring proactive engagement and shaping of regional policy initiatives that are critical to business strategy, continuity, and growth. Qualifications Education Required: Bachelor’s degree in Regulatory Affairs, Life Sciences, Engineering, or a related discipline. Preferred: Advanced degree or professional certification in Regulatory Affairs, Quality, or a related field. Experience and Skills Required: 6–8 years of progressive experience in Quality Assurance and/or Regulatory Affairs within the medical device, healthcare, or other regulated industries. Strong working knowledge of regulatory requirements across CEE, Baltic, and Balkan markets, including EU MDR. Experience managing product registrations and lifecycle activities across multiple countries. Ability to interpret regulatory and quality requirements and apply them to business and product decisions. Ability to manage multiple priorities in a complex, fast‑paced, and matrixed environment. Preferred: Experience supporting or multi‑country QARA portfolios. Experience working in a multinational or matrixed organization. Exposure to regulatory inspections, quality audits, or health authority interactions. Familiarity with EU MDR implementation, post‑market surveillance, and vigilance requirements. Demonstrated experience contributing to regulatory or quality process improvement initiatives. Regulatory Affairs or Quality certification (e.g., RAC or equivalent). Strong stakeholder management, communication, and collaboration skills. Other Language: English required; additional regional languages preferred. Travel: Moderate regional travel across CEE, Baltics, and Balkans. Certifications: RAC or equivalent preferred but not required. For more information on how we support the whole health of our employees throughout their wellness, career and life journey, please visit . Required Skills: Preferred Skills:Analytical Reasoning, Business Writing, Coaching, Compliance Risk, Fact-Based Decision Making, Industry Analysis, Legal Support, Process Improvements, Product Licensing, Public Policies, Regulatory Affairs Management, Regulatory Compliance, Regulatory Development, Regulatory Environment, Risk Assessments, Strategic Thinking, Technical CredibilityThe anticipated base pay range for this position is:zł231,000.00 - zł399,050.00Benefits: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.SummaryLocation: Warsaw, Masovian, Poland; Prague, CzechiaType: Full time