Siegfried seeks a trainee regulatory affairs professional to join its El Masnou site within a specialized pharmaceutical CDMO environment. The role involves supporting quality documentation reviews, regulatory assessments, and lifecycle management activities while developing expertise in CMC and regulatory compliance under experienced mentorship.

Responsibilities

- Review quality documentation linked to Technical Release modules for alignment with approved dossiers
- Support CDMO clients on product lifecycle activities, particularly CMC and quality matters
- Evaluate and update regulatory documentation to ensure compliance with current requirements
- Conduct regulatory assessments of historical dossiers to identify modernization opportunities
- Collaborate cross-functionally to optimize departmental processes and document workflows

Requirements

- Bachelor's or Master's degree in Pharmacy, Chemistry, Biology, Biotechnology, or related discipline
- Strong interest in regulatory affairs and pharmaceutical industry
- Fluent English proficiency, written and spoken
- Analytical capability and attention to detail
- Document management and organizational skills
- Proactive attitude with collaborative teamwork ability

📌 Trainee Regulatory Affairs (España)
🏢 Siegfried
📍 España