Medical Affairs Specialist — Scientific Writing & Strategy

Kenvue; Lisboa; Hybride; EUR 55 000 - 85 000; Plein temps

Avantages offerts par ce poste

Health insurance

Life insurance

Pension Plan

Résumé du poste

Kenvue is seeking a Medical Affairs Specialist to join the Southern Europe Cluster (Portugal & Selected Markets). You will provide medical reviews, support scientific substantiation, and collaborate with cross-functional teams to ensure regulatory and scientific accuracy.

The role involves developing trainings, supporting launches, and maintaining medical information resources while adhering to regulatory requirements and company policies.

Qualifications

• Bachelor’s degree in Health Sciences, Pharmacy, Life Sciences, Medicine, or a related field.
• 2–3 years of experience in Medical Affairs within pharma/biotech/OTC industry.
• Strong scientific knowledge and the ability to communicate clinical and medical information to healthcare professionals.

Responsabilités

• Provide medical review and approval of promotional and non-promotional materials in line with applicable codes and regulations.
• Lead medical writing activities, including CCDS updates and clinical overviews.
• Provide scientific and medical expertise to internal stakeholders with accuracy and compliance.
• Support development of product claims and evidence-generation plans.
• Collaborate with cross-functional teams across marketing, regulatory, and pharmacovigilance.
• Respond to medical information requests in a timely, balanced manner.
• Develop and deliver scientific trainings for internal and external stakeholders.
• Support new product launches and lifecycle initiatives.

Connaissances

Scientific knowledge

Communication skills

Cross-functional collaboration

Independent work

Formation

Bachelor’s degree in Health Sciences/Pharmacy/Life Sciences/Medicine

Description du poste

Kenvue is seeking a Medical Affairs Specialist to join the Southern Europe Cluster (Portugal & Selected Markets). You will provide medical reviews, support scientific substantiation, and collaborate with cross-functional teams to ensure regulatory and scientific accuracy.

The role involves developing trainings, supporting launches, and maintaining medical information resources while adhering to regulatory requirements and company policies.