Quality Assurance Associate – Clinical Supply Quality

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Job Function:
Quality

Job Sub Function:
Quality Assurance

Job Category:
Professional

All Job Posting Locations:
Beerse, Antwerp, Belgium

Job Description:
We are searching for the best talent for a Quality Assurance Associate - Clinical Supply Quality (CSQ).

Purpose

We are looking for a Quality Assurance Associate to join the Clinical Supply Quality (CSQ) Post-Certification team.

In this role, you will help ensure the quality, safety, and compliance of investigational medicines used in clinical trials around the world.

Working across Quality, Supply Chain, Clinical Development, and Manufacturing, you will contribute to the delivery of compliant investigational products and support the development of innovative therapies for patients.

Are you interested in building expertise in quality investigations, clinical supply quality, and complaint management while working across global teams and clinical development programs?

The Clinical Supply Quality Post-Certification team provides global quality oversight for clinical supply logistics and owns the clinical complaint handling process for investigational products used in Johnson & Johnson clinical studies.

You will be responsible for

In this role, you will support the management and investigation of Clinical Product Quality Complaints and logistics-related quality issues.

Working with cross-functional partners, you will help ensure quality concerns are investigated effectively, risks are appropriately assessed, and actions are implemented in a timely manner.

You will contribute to complaint investigations, quality review activities, and continuous improvement initiatives while helping maintain compliance and supporting the safe supply of investigational medicines used in clinical trials.

Key responsibilities include:


* Investigating clinical product quality complaints and logistics-related quality issues


* Coordinating cross-functional investigations to identify root causes and define appropriate actions


* Assessing the potential impact of events on product quality, patient safety, and clinical trial continuity


* Supporting implementation and follow-up of correcti...