Our client is an innovative medical device company. The company develops and manufactures a breakthrough solution that improves patient care.
The company commercializes its devices in European hospitals and targets a global business development.
To ensure the growth of our client, we are looking for a QA Manager (M/F).
Responsibilities
As a QA Manager, you will ensure the compliance and efficiency of quality processes in line with ISO 13485 standards. Based in Liège, Belgium, with occasional EU travel, you will implement and maintain quality management systems and work closely with other departments to meet quality requirements.
Your main responsibilities are:
- Maintain and monitor Quality objectives.
- Ensure compliance with ISO 13485:2016 and other applicable QMS standards.
- Act as the management representative for quality matters (ISO 13485:2016).
- Promote Quality Systems, Objectives, and Policies.
- Manage internal and external audits, including supplier audits.
- Host third-party audits (notified body, competent authority and customer).
- Oversee the complaint and feedback process.
- Collaborate with operations to establish quality agreements with suppliers.
- Identify and implement process improvements.
- Analyze risks and trends in complaints, deviations, and audits to define corrective and preventive actions.
Profile
- You hold a Bachelor’s or Master’s degree in a relevant technical field.
- You have at least 5 years of experience in a highly regulated sector, knowledge of ISO 13485:2016 is an asset.
- You understand the regulatory environment for medical devices.
- You bring strong communication, organizational, and problem-solving skills.
- You are able to plan, organize, and execute tasks effectively in your field.
- You are practical, self-disciplined, and work well independently.
- You demonstrate team spirit, adaptability, and a customer-oriented mindset.
- You have a strong attention to detail and are committed to regulatory compliance.
- You communicate fluently in English (both written and spoken), with French or other languages considered a plus.
- You are open to travel up to 20% and have a valid driver’s license.
Offer
- A challenging and diversified position within a high-potential fast-growing innovative medical device company.
- The opportunity to participate in the development of the company.
- To work in a human size, dynamic, respectful, and professional environment.
- International exposure, with learning and development opportunities.
- An attractive compensation package in line with the position responsibilities and your experience.
Your application and related information will remain strictly confidential.