PpThe Medical Affairs Manager, Italy coordinates medical leadership within DePuy Synthes orthopaedic portfolio in Italy, collaborating with cross‑functional teams to advance patient care and clinical outcomes. /ph3Key Responsibilities /h3ulliServe as the primary medical and scientific expert for assigned orthopedic products and therapeutic areas in Italy. /liliDevelop and execute local medical affairs plans aligned with global and regional strategies. /liliProvide medical input into clinical studies, post‑market surveillance, and real‑world evidence activities. /liliSupport investigator‑initiated studies and collaborative research in compliance with company policies and local regulations. /liliDeliver high‑quality scientific exchange and education to healthcare professionals, including presentations and advisory boards. /liliPartner with Regulatory, Quality, Marketing, and Commercial teams to ensure accurate, compliant medical content and product communication. /liliReview and approve medical materials to ensure scientific accuracy and regulatory compliance. /liliMonitor medical trends, clinical literature, and competitive activity to inform strategy and decision‑making. /li /ulh3Qualifications /h3ullibEducation Required: /b Advanced degree in a scientific or healthcare discipline (e.g., MD, PharmD, PhD, MSc in Life Sciences or related field). /lilibPreferred: /b Medical degree (MD) or doctorate with specialization relevant to orthopedics or medical devices. /lilibExperience and Skills Required (6–8 years): /b /liulliExperience in Medical Affairs, Clinical Affairs, or a related scientific role within medical devices or pharmaceuticals. /liliDemonstrated knowledge of clinical research, evidence generation, and medical compliance standards. /liliExperience engaging with healthcare professionals and key opinion leaders in a scientific, non‑promotional manner. /liliStrong analytical, communication, and presentation skills. /liliAbility to work effectively in cross‑functional, matrixed environments. /liliSolid understanding of local (Italian) healthcare systems and regulatory requirements. /li /ullibPreferred (orthopedics, trauma, sports medicine, related surgical specialties): /b /liulliPrior involvement in clinical trial management or post‑market clinical follow‑up. /liliExperience supporting product launches or lifecycle management from a medical affairs perspective. /liliFamiliarity with European medical device regulations and clinical evaluation requirements. /liliLeadership experience mentoring junior medical or clinical colleagues. /li /ulliFluency in Italian and English (written and spoken) is required. /liliUp to ~30% domestic travel within Italy; limited international travel as needed. /liliRelevant clinical or research certifications are a plus. /liliValid driver’s licence required for field engagement. /li /ulpJohnson 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. /p /p #J-18808-Ljbffr