Job Title: Submission Specialist – Belgium (Zaventem)
We are seeking a Submission Specialist to join a dynamic regulatory submissions team at a leading global medical device company. This is a full-time, office-based role at their Zaventem, Belgium site. The position is for 12 months, with the potential for renewal and future permanent opportunities.
About the Company:
Our client is a global healthcare leader, developing innovative medical devices and solutions that improve patient outcomes worldwide. Their Zaventem site serves as a key European hub, supporting a range of clinical and regulatory operations.
Key Responsibilities:
• Prepare, review, and manage regulatory submissions, addressing requests from authorities and responding to inquiries.
• Ensure compliance with regulatory requirements across multiple EMEA countries, with knowledge of Southern Africa, Israel, or Eastern Europe considered a plus.
• Maintain clear and professional communication with authorities via phone and email.
• Collaborate with internal teams to support ongoing regulatory and clinical projects.
Experience & Skills Required:
• 2-3 years of experience in EMEA regulatory submissions preferred; additional experience is welcome.
• Experience in Pharma or Medical Device environments is highly valued.
• Strong communication skills and confidence managing calls with regulatory authorities.
• Ability to work effectively in a fast-paced, office-based environment.
This is an excellent opportunity for a detail-oriented professional looking to strengthen their regulatory submissions expertise within a global medical device organization.