Descrizione dell'offerta di lavoro
For an innovative international biotechnology company, we are currently looking for an highly experienced Senior Director Regulatory Affairs (F/M/X) to lead the regulatory strategy and operations in Italy and support the preparation of a highly promising oncology launch.
Key Responsibilities
Lead all regulatory activities for Italy in alignment with national and EU requirements
Drive scientific consultations, pre?submission meetings, and interactions with Italian authorities
Oversee labeling, packaging, promotional material review, and HCP communication
Monitor Italian regulatory developments and communicate implications to global teams
Represent Regulatory Affairs internally and externally; contribute to industry associations
Lead and optimize regulatory processes, SOPs, audits, inspections, and compliance




Manage quality defects, recalls, and regulatory licenses
Provide leadership, resource planning, and strategic direction for the Italian RA organization
Required Qualifications
Master's or PhD in a scientific or medical discipline
10+ years of regulatory leadership xlwpduy experience in pharma/biotech
Strong knowledge of Italian and EU regulatory frameworks
Oncology experience preferred
Excellent communication skills in Italian and English
Proven ability to analyze scientific information and engage effectively with authorities
Ability to thrive in a dynamic, fast?paced environment; willingness to travel up to 30%
#J-*****-Ljbffr

📌 Senior Director Regulatory Affairs (Lecce)
🏢 subrosa Health & Capital group
📍 Lecce