We are looking for a REGULATORY AFFAIRS SPECIALIST to join our INTERNATIONAL TEAM.
You will play a key part in managing regulatory requirements to support product development, registration, and lifecycle management across multiple markets. Your knowledge will ensure compliance with local and international regulations, helping to successfully launch and maintain innovative products globally.
**Key Responsibilities**:
Ensururing consistency, completeness, accuracy and adherence to regulations and applicable guidelines and to the client’s need for all regulatory submissions.
Providing assistance during the procedures for the preparation of response documents.
Giving assistance during the procedure for preparation of the response document.
Giving support to the Client in the critical evaluation of the appropriate regulatory strategy.
**Essential requirements**:
Master’s degree in Pharmaceutical Chemistry and Technology, Pharmacy or similar.




At least 3-5 years of experience.
Excellent knowledge of English (written and spoken), essential for frequent contacts with international companies.
**Strong project management approach**: a structured, proactive approach to supporting project activities, with the ability to coordinate tasks, manage priorities, and communicate clearly with stakeholders throughout different phases of the work.
**Soft Skills**:
Strong communication and teamwork abilities
Attention to detail and solid organizational skills
Effective time management and problem‑solving
Adaptability and openness to continuous learning
**Contract details**:
**Type**: Permanent
**Location**: Pisa or Milan
Hybrid work **Benefits**:
€10 meal voucher per working day
Competitive corporate welfare plan
Birthday leave

📌 Regulatory Affairs Specialist (Pisa)
🏢 Regulatory Pharma Net
📍 Pisa