Our client is a large multinational company leader in the pharma industry with over 10,000 employees worldwide. The company is renowned for innovative solutions that contribute to enhancing health and well-being globally.

As a Regulatory Affairs Manager - Pharma - Belgium, you will have the following responsibilities:

• Oversee and manage the regulatory affairs department.


• Develop regulatory strategies for product development and life cycle management.


• Prepare, submit and manage regulatory submissions.


• Ensure compliance (GMP, GDP, GCL) with local and international regulations.


• Manage product registrations and renewals.


• Coordinate with internal teams to ensure regulatory strategies are implemented effectively.


• Stay updated on changes in regulatory legislation and guidelines.


• Manage and respond to regulatory inquiries and inspections.


• Provide regulatory affairs training to staff as needed.

As a Regulatory Affairs Manager - Pharma - Belgium, you will have the following profile:

• A Master degree in Life Sciences, Pharma, Engineering or related field.


• Minimum 3-5 years of experiences in regulatory affairs within the Healthcare & Lifesciences industry.


• Knowledge of local and international regulatory requirements.


• Strong organizational and project management skills.


• Experiences in People Management or coaching of new joiners.


• Excellent communication and interpersonal skills.


• Fluent in English, Dutch & English.