Advance your career with Alsinova as a CMC Regulatory Writer, serving clients in Belgium’s biotech and pharmaceutical sectors. Focus on technical writing to support critical regulatory submissions. In this influential role, you will engage in writing technical documents for current and existing products, specifically focusing on CMC and facility aspects.

Your responsibilities include coordinating with various departments, ensuring the timely execution of the writing process, and addressing queries from regulatory authorities. A background with a minimum of three years in industry-related CMC writing is essential. Key Responsibilities:
Draft comprehensive CMC and facilities documentation
Manage the writing coordination with SMEs and departments




Respond to regulatory inquiries effectively
Verify compliance of department-provided data
Maintain project management using GRA tracking tools Requirements:
University-level education in Life Sciences or similar
Minimum of 3 years in CMC writing experiences
Experience in QA/production within the Biologics field
Familiarity with regulatory systems and procedures
Fluent in French and English; solid writing skills Utilize your skills in technical writing and regulatory compliance to support Alsinova and its clients.

📌 Cmc Regulatory Writer At Alsinova London
🏢 Alsinova
📍 London