Overview
Quality Assurance Manager Jobs in Raamsdonksveer, North Brabant, Netherlands at SYNERGIE Advanced Patient Support
Title: Quality Assurance Manager
Company: SYNERGIE Advanced Patient Support
Location: Raamsdonksveer, North Brabant, Netherlands
Vacancy: QA Manager (Part-time: 24–28 hours per week)
Location: Raamsdonksveer, The Netherlands
Acquisition by recruitment and selection agencies in response to this vacancy is not appreciated.
About SYNERGIE Advanced Patient Support
SYNERGIE Advanced Patient Support develops and delivers innovative solutions within the healthcare sector. Quality, safety, and compliance are central to everything we do. To strengthen our team, we are looking for an independent and detail-oriented QA Manager who will further professionalize and maintain our quality processes.
The Position
As QA Manager, you will be responsible for maintaining, improving, and monitoring the company’s Quality Management System (QMS). You will work closely with multiple departments and ensure that processes comply with applicable laws, regulations, and international quality standards.
What will you do
- Manage and optimize the Quality Management System (QMS)
- Ensure compliance with ISO 13485:2016 and relevant regulations
- Prepare, coordinate, and follow up on internal and external audits
- Create, manage, and update quality documentation and procedures
- Identify, analyze, and follow up on deviations, CAPAs, and risk analyses
- Perform incoming goods quality inspections
- Process and follow up on supplier non-conformities (NCs)
- Conduct sampling inspections and product testing protocols
- Advise management and colleagues on quality-related matters
- Support continuous improvement initiatives throughout the organization
- Work independently within a small and collaborative team
What do you bring
- Bachelor-level working and thinking ability
- Educational background in Quality Management, Mechanical Engineering, Biomedical Sciences, or similar
- Proven experience with and knowledge of ISO 13485:2016
- Experience in a regulated environment, preferably medical devices or healthcare
- Knowledge of risk management and document control processes
- Experience with EU MDR is considered an advantage
- Strong analytical skills and attention to detail
- Independent and structured working style
- Good communication skills in English (spoken and written)
- Experience with audits and quality improvement projects is a plus
What we offer
- Part-time position (24–28 hours per week) with flexible scheduling
- Working in a small, professional, and committed team
- High level of independence and responsibility
- Room for initiative and process improvement
- Competitive salary and appropriate secondary benefits
- A dynamic organization with international growth ambitions
Interested?
Are you the quality-driven professional who can combine structure, compliance, and continuous improvement? We would be pleased to get to know you.
