About the job
Are you passionate about quality and continuous improvement? Do you thrive in a dynamic environment where your expertise directly contributes to the safety and performance of life-changing products? Then we are looking for you!
As a QA Officer, you will play a key role in maintaining and strengthening our Quality Management System while supporting daily operational quality activities. You will act as a trusted quality partner across the organization, helping ensure compliance, driving improvements, and promoting a strong quality culture throughout the business.
What will you do?
As QA Officer, you will be responsible for a broad range of operational quality activities, including: Coordinating and leading operational quality meetings, including topics such as CAPA, product holds, and quality planning.
Investigating and following up on non-conformities, complaints, and other quality-related events.
Collaborating closely with internal departments and external manufacturing partners to resolve quality issues.
Supporting and participating in both internal and external audits.
Executing product release activities in accordance with established procedures.
Monitoring bioburden and pyrogen testing activities.
Managing and archiving quality documentation, including batch records and quality files.
Serving as the subject matter expert for quality-related processes within the ERP system.
Writing, reviewing, and maintaining quality procedures, work instructions, and other QMS documentation.
Acting as a quality ambassador by promoting awareness, compliance, and continuous improvement across the organization.
What do you bring?
To be successful in this role, you have: A relevant technical education at MBO/MBO+ level.
At least 2 years of experience in a quality-related position within the medical device, pharmaceutical, or food industry.
Strong analytical skills and a structured way of working.
A proactive mindset and excellent communication skills.
The ability to balance pragmatism, flexibility, and resilience in a fast-paced environment.
Knowledge of ISO 13485 and Medical Device Regulations (preferred).
Good command of both Dutch and English, spoken and written.
Experience with Microsoft Office applications, including Word, Excel, Outlook, and PowerPoint.
What we offer?
A challenging and varied position within a growing and innovative organization.
The opportunity to make a real impact on quality and compliance.
A collaborative international working environment.
Professional development opportunities and room for personal growth.
The chance to work alongside passionate colleagues dedicated to excellence and patient safety.
Do you want to refer someone for this job?
https://tsc-life.app.personio.com/recruiting/applications/refer
Ready to make an impact?
Are you ready to help us maintain the highest quality standards and contribute to a culture of continuous improvement? We'd love to hear from you.
The vacancy is open until 31 July 2026 . Following the closing date, we will begin the selection process and carefully review all applications.
Apply today and become our next QA Officer.
Acquisition in response to this vacancy is not appreciated.