Your Responsibilities:
* Implementation, training, maintenance, and improvement of the quality management system according to GxP principles and applicable regulations
* Management of suppliers, subcontracted activities, and customers
* Ensuring company authorizations and licenses are in place and valid
* Decision and documentation of the final disposition of medicinal products requiring OP release, including sample management
* Support for new business development projects focusing on quality and regulatory aspects
* Acting as a Qualified Person (QP) for medicinal products according to DIRECTIVE 2001/83/EC and Belgian Royal Decrees
* Responsible for Good Distribution Practices (GDP) in Belgium and delegated tasks for GDP activities in the Netherlands
* Liaison with RIP for information/publicity and medical samples according to Belgian Royal Decrees
* Ensuring compliance with regulations on "medical samples" according to Belgian Royal Decre
Requirements:
* Industrial Pharmacist
* Registered Qualified Person for medicinal products
* Experience in internal & external audits
* Experience with food supplements
* Deep knowledge of regulatory procedures and RA dossiers