QA Officer Medical Devices (Temporary)
Join a leading international food company in Zoetermeer as a Quality specialist for an impactful 6-month contract. You'll define and implement the Quality Management System, conduct audits, and ensure compliance with NMD requirements for innovative medical devices. Collaborate with NMD experts to guarantee safe and efficient product development, manufacturing, and delivery.
This quality assurance role involves working with Class 2 medical devices, primarily nutrition pumps used for tube feeding. The product line also includes the associated sterile plastic containers and tubing sets.
If you're a passionate and driven Quality professional ready to make a difference, apply now to shape the future of medical device quality assurance.
Company profile
Join a leading international food company in Zoetermeer as a Quality specialist for an impactful 6-month contract. You'll define and implement the Quality Management System, conduct audits, and ensure compliance with NMD requirements for innovative medical devices. Collaborate with NMD experts to guarantee safe and efficient product development, manufacturing, and delivery.
This quality assurance role involves working with Class 2 medical devices, primarily nutrition pumps used for tube feeding. The product line also includes the associated sterile plastic containers and tubing sets.
If you're a passionate and driven Quality professional ready to make a difference, apply now to shape the future of medical device quality assurance.
Job profile
As a QA Officer for Medical Devices, you will play a crucial role in ensuring the quality and compliance of our products. Your tasks are diverse and include:- Supplier Management: You are responsible for qualifying, evaluating, and monitoring our suppliers to ensure they meet the set quality requirements.
- Conducting Audits: You will plan and conduct internal and external audits to assess and improve the effectiveness of our quality management system.
- Monitoring KPIs: You will track and analyze Quality Key Performance Indicators (KPIs) and report on them, with the goal of stimulating continuous improvement.
- Support Production V&V: You will support the production department with verification and validation activities for processes and products, in accordance with applicable regulations.
Requirements
We are looking for a proactive and meticulous professional who meets the following requirements:
- At least 3 years of demonstrable work experience within the medical device industry;
- In-depth knowledge of and experience with ISO 13485;
- Thorough knowledge of the EU Medical Device Regulation (MDR);
- Strong communication skills, both verbal and written;
- An independent and results-oriented work attitude;
- Excellent command of the English language.
Offer
You will receive a temporary contract for 6 months through our agency.
The salary indication for this role is a maximum of €5000 - gross per month based on a full-time work week. Salary is based on education and experience.
- 30 vacation days (based on a full-time annual contract);
- Travel expenses.
What will happen when you apply? Within four working days, we will let you know whether you are qualified for the position. If you do we will schedule an interview (digital or live). In this interview, we will inform you about the vacancy, the company, and the procedure. If we both agree this is a fitting opportunity we will introduce you to our client and continue to guide you through the whole application process. The Independent Recruiters Group has a large team of specialized recruitment consultants. Every recruiter has a strong focus regarding his/her field of expertise. This makes them the ideal sparring partner for both you, as the candidate, and the client.
