First Name*

Last Name*

Email*

Phone Number*

Country*

Are you an employer or a jobseeker?*

Message

First Name*

Last Name*

Email*

Phone Number*

Country*

Are you an employer or a jobseeker?*

Message

First Name*

Last Name*

Email*

Phone Number*

Country*

Are you an employer or a jobseeker?*

Message

First Name*

Last Name*

Email*

Phone Number*

Country*

Are you an employer or a jobseeker?*

Message

Job type: Permanent

Discipline: Supply Chain

Location: Belgium

Support regulatory excellence and product quality through robust vendor audit and compliance practices.

̽��ϼ� is seeking a Vendor Quality Auditor to perform audit activities focused on external quality and compliance requirements. The role involves conducting audits to assess alignment with applicable regulatory and quality standards and supports the delivery of safe, compliant medical devices.

Responsibilities:

Perform audits of external manufacturing and quality processes to assess alignment with applicable standards and regulations.
Review production processes to identify opportunities for improvement.
Track and follow up on corrective and preventive actions arising from audit and assessment activities.
Potential quality or regulatory risks identified during audit activities are escalated in accordance with established processes.
Work with relevant internal stakeholders to investigate and resolve quality issues identified through audit and assessment activities.
Quality performance metrics are compiled and reported in line with defined reporting requirements.
Accurate and up-to-date audit documentation is maintained in accordance with quality and regulatory requirements.
Audit planning activities support the development and maintenance of a risk-based audit schedule.
Advanced technical expertise in processes, materials control, and manufacturing is applied to support quality improvement activities.

Key Skills and Requirements:

Recognised accreditation or certification in quality auditing is required.
Bachelor's degree in Biomedical, Electronics, Chemical, Mechanical, Materials Engineering, or a related field.
Experience in regulated industries such as medical devices or pharmaceuticals.
Demonstrated knowledge of applicable medical device quality regulations and the use of statistical quality tools
Effective written and verbal communication skills suitable for engagement across diverse stakeholder groups.
Familiarity with validation activities and documentation, as well as quality risk management
Ability to analyze data and translate findings into actionable proposals.
High proficiency in Microsoft Office and other relevant tools.
Valid driver's license and ability to travel as needed.
Language proficiency in English; additional language skills may be required depending on the location.

If you are having difficulty in applying or if you have any questions, please contact Nathan Berkley at n.berkley@proclinical.com.

Apply Now:

If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists please request a call back at the top of this page.

̽��ϼ� is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. ̽��ϼ� is acting as an Employment Agency in relation to this vacancy.

By submitting this application, you confirm that you've read and understood our privacy policy, which informs you how we process and safeguard your data - /privacy-policy