OverviewAs Regulatory Affairs Expert, you ensure ZEISS Sun Lens products meet EU and global requirements, coordinating with regional teams.
You will act as the primary contact for EU regulators and manage product approvals, recalls, and safety actions.
The role involves maintaining regulatory records, advising other departments, and training staff on regulatory topics.
You will monitor regulatory changes and align global compliance across markets, enabling safe, compliant product delivery.
Retribuzione / BenefitsCompetitive salary based on skills and experience
Premio – Production, attendance and participation
Home working (3 days on site and 2 days smart working)
ResponsabilitàEnsure regulatory compliance for lens products in EU and other regions, focusing on PPE and MDR
Coordinate with global regulatory teams to harmonize requirements across markets
Act as main contact for EU regulators; manage approvals, incident reports, recalls, and safety actions




Maintain regulatory databases and document control; track approvals
Support Supply Chain, Procurement, and Customer Service with regulatory queries (import issues, chemical safety)
Review marketing and communications materials for regulatory compliance
Provide training on regulatory topics and coordinate global training efforts
Monitor regulatory changes and inform global team of updates
Requisiti fondamentaliScience degree (preferably in chemistry or materials science)
2+ years of regulatory affairs experience (PPE or medical devices)
Strong knowledge of EU and international regulations
Fluent in Italian and English
Good communication, teamwork, and organizational skills
Proficient with Microsoft Office
Willing to travel
communication
teamwork
organization
Regulatory knowledge (PPE and medical devices)
EU and international regulations
Microsoft Office

📌 Regulatory Affairs Expert (Varese)
🏢 Carl Zeiss
📍 Varese