Johnson & Johnson is committed to building a world where complex diseases are prevented, treated, and cured through healthcare innovation
Job Summary
Johnson & Johnson is committed to building a world where complex diseases are prevented, treated, and cured through healthcare innovation.
The role involves preparing and submitting regulatory dossiers, ensuring compliance, and collaborating with multiple departments including medical, marketing, and regulatory teams.
The position is exclusive for persons with disabilities (PCD) and based in São Paulo with a hybrid work model requiring three days per week in the office.
Matching Summary
Johnson & Johnson is committed to building a world where complex diseases are prevented, treated, and cured through healthcare innovation.
Skills & Requirements
Must-have
Regulatory dossier preparation and submission
Regulatory compliance and risk assessment
Cross-functional team collaboration
Regulatory intelligence and competitive analysis
Monitoring and implementing new legislation
Technical English proficiency
Hybrid work model
Nice-to-have
Problem solving skills
Interpersonal communication
Participation in product launch teams
Interaction with health authorities
Experience with MedTech and Innovative Medicine
Spanish language skills
Key Requirements
Degree in Pharmacy, Biology, Biochemistry, Microbiology, Chemistry or related fields
Professional experience in pharmaceutical regulatory affairs
Technical/intermediate English proficiency
Availability for hybrid work in São Paulo
Experience with regulatory submissions and agency interactions