QA Engineer – Almere, Netherlands

We are seeking a QA Engineer join our medical device client in the Almere office. In this role, you will manage quality assurance activities, ensuring compliance with all relevant regulations. You will oversee regulatory assessments, collaborate with suppliers, and support product registrations and international regulatory submissions.

Key Responsibilities:

• Manage quality assurance and regulatory documentation to support product safety and compliance.
• Conduct regulatory assessments of product changes.
• Develop and maintain summaries for regulatory compliance.
• Coordinate the maintenance of product dossiers and technical files.
• Present and defend documentation during audits and inspections.
• Collaborate with the R&D team on risk assessments, complaint handling, and CAPA management.

Skills & Qualifications:

• Bachelor’s Degree or equivalent experience in medical device or pharmaceutical industries.
• Strong knowledge of medical device regulations and quality assurance practices.
• Technical writing proficiency.
• Excellent communication and presentation skills.
• Fluency in English (written and spoken).
• Proficient in Microsoft Office (Word and Excel).

What We Offer:

• Competitive salary
• 13th month
• 25 vacation day + 8% holiday pay
• Travel allowance
• Retirement plan
• Office perks

This is a fantastic opportunity to be part of a growing company with a bright future. If you meet the requirements and are ready for a new challenge, we’d love to hear from you.

Apply now or get in touch for further info!