Home
Jobs
Barrington James
Quality Assurance Consultant

Quality Assurance Consultant

On site

Brussels, Belgium

Freelance

13-03-2026

Share this job:

Score my CV

Job Specifications

Role Overview:

As a GMP QA Consultant, you will play a critical role in maintaining the integrity, quality, and compliance of clinical trials. You will conduct audits and monitor processes to ensure adherence to GMP and local regulatory requirements.

Key Responsibilities:

Conduct internal and external audits of clinical trials to ensure compliance with GMP and applicable regulatory requirements.
Review clinical trial documentation, including protocols, CRFs, informed consent forms, and regulatory submissions.
Identify, document, and track deviations, non-compliance, and quality issues, and recommend corrective actions.
Collaborate with clinical operations, regulatory, and medical teams to ensure high-quality trial conduct.
Participate in vendor and site audits as required.
Maintain QA documentation and prepare reports for management and regulatory inspections.

How to apply:

If you are interested in this opportunity, please send your CV and a short cover letter highlighting your relevant experience. Applications will be handled in confidence and reviewed on a rolling basis.

About the Company

The global Life Sciences industry is dominant in today's world. Drug development processes are progressing faster than ever before. The need for vaccines, treatments and medical devices continues to grow at an exponential rate to ensure treatment for disease reaches those it needs to. That means for Barrington James, we grow at the same speed. With 14 global offices specialising in niche areas of the Life Science industry, we are ready to support our growing group of clients in sourcing the most, senior, specialist and rare... Know more