About this role
Specialist Care Therapeutic Area, Global Regulatory Affairs and Patient Safety - Temporary at Chiesi Farmaceutici S.p.A.. Location: Paris or Bois-Colombes. Role: leading filings, managing submissions, supporting authorities Requirements: Experience in European regulatory lifecycle management (MRP/DCP, centralized procedures), strong attention to detail, proactive problem solving, and fluent English; temporary maternity-cover role. Category: Research and Development (R&D) Seniority: Mid Level Commitment: Temporary Workplace: Hybrid Languages: English