Medical Affairs Supervisor

Description
Kenvue is proud to be 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, or protected veteran status and will not be discriminated against on the basis of disability.
Kenvue is currently recruiting for:
**Medical Affair Supervisor**
This position is based in Pomezia (hybrid working scheme).
**Who We Are**
At Kenvue, we realize the extraordinary power of everyday care. Built on over a century of heritage and rooted in science, we're the house of iconic brands - including NEUTROGENA®, AVEENO®, TYLENOL®, LISTERINE®, JOHNSON'S® and BAND-AID® that you already know and love. Science is our passion; care is our talent. Our global team is made up with 22,000 diverse and brilliant people, passionate about insights, innovation and committed to deliver the best products to our customers. With expertise and empathy, being a Kenvuer means to have the power to impact life of millions of people every day. We put people first, care fiercely, earn trust with science and solve with courage - and have brilliant opportunities waiting for you Join us in shaping our future-and yours.
**Qualifications**:
**What You Will Do**
The **Medical Affairs Supervisor **supports all departments inside the company who need a scientific/ technical support on portfolio products. In addition, the Medical Affairs Supervisor is appointed the role of "Responsible for Scientific Service", an institutional role notified to local competent authority (AIFA).
The Medical Affair Supervisor will be responsible for:
- Scientific Service notified to local competent authority (AIFA). Includes the following responsibilities as per national requirements: o Annual communication to AIFA o HCP advertising notification to AIFA
- Medical Affairs local lead, responsible for local Medical Affairs team
- Medical review and approval of promotional materials and activities in accordance with applicable Codes of Practice and regulations, Company policy and any other relevant regulations;
- Assist in development of claims for Consumer Health products;
- Partnership and collaboration with different internal departments as appropriate (e.g., Marketing, Regulatory, Pharmacovigilance, Brand Activation, Professional );
- Assist in defense of key claims upon challenge by competitor companies and challenge on competitor advertising as appropriate;
- Management of internal and external medical information enquiries;
- Development of content for product training and providing training to employees;
- Maintenance of local/cluster Medical Affairs systems (e.g., claims database);
- Medical writing (e.g., COs to support Regulatory changes);
- Maintenance of applicable local WIs/SOPs
**What We Are Looking For**
Required Qualifications
- Master's degree in Medicine or Pharmaceutical Sciences (i.e.: Pharmacy, CTF - Pharmaceutical Chemistry and Technology)
- Microsoft Office skills
- Excellent written and verbal communication skills and fluency in English language
- Strong analytical skills and technical proficiency
- Effective communication skills
- Knowledge related to: products, markets, drug regulations, internal procedures and regulations, internal procedures and regulations.
- Solid knowledge of pharmaceutical concepts
**What's In It For You**
- Competitive Benefit Package
- Learning & Development Opportunities
- Employee Resource Groups
Primary Location Europe/Middle East/Africa-Italy-Lazio-Pomezia (Santa Palomba)
Job Function Medical Affairs
Organization: Johnson & Johnson S.p.A.