Become a Regulatory Affairs Consultant with Alsinova in Belgium, where you'll support pharmaceutical clients in navigating regulations and ensuring compliance for their products. This pivotal role involves both big pharma and small biotech projects.

Your mission will include overseeing product registration and guiding clients through complex regulatory landscapes. You will provide expertise in submitting regulatory documents and collaborating with cross-functional teams to support product launches.

Your analytical skills and technical writing abilities will be essential in addressing health board inquiries and regulatory variations.

Key Responsibilities:
Facilitate transparent communication of regulatory requirements
Author CTD, BLA, and NDA submissions




Collaborate with internal teams for high-quality submissions
Respond to regulatory inquiries promptly
Assess regulatory impacts of post-approval changes

Requirements:
Master’s degree in Life Sciences
Experience in pharmaceutical regulatory affairs
Strong understanding of drug regulations
Fluent in English and French or Dutch
Excellent negotiation and communication skills

Advance your career in a supportive workplace dedicated to qualified growth and meaningful impact in the pharmaceutical field.
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📌 Regulatory Affairs Consultant For Pharma London
🏢 Alsinova
📍 London