Randstad, as the EMEA Johnson & Johnson talent acquisition partner, is responsible for finding and contracting talent for the contingent roles at Johnson & Johnson. If you are selected for a role you will be engaged or employed by one of the Randstad recruitment companies in EMEA and will not be an employee of Johnson & Johnson.

Johnson & Johnson

Quality Assurance

Posted Feb 27, 2026
Job ID: JJJP00025203
Location
Beerse
Hours/week
40 hrs/week
Timeline
10 months
Payrate range
Unknown

Quality Assurance - Qualified Person (QP) -  Investigational Medicinal Products  - IMP

Location: Beerse, Belgium 

Duration of the contract: Until 31st December 2026 

Hours per week: 40 hours (hybrid working 3 days onsite, 2 days home office)


Essential: Qualified Person (QP) -  Investigational Medicinal Products  - IMP - Fluent English & Dutch, we have 2 roles one recently qualified and one more experienced


Imagine your next project ensuring the integrity of life-changing medicines before they ever reach a patient in a clinical trial. As a Quality Assurance professional, you are the final safeguard in a complex global supply chain, blending deep pharmaceutical expertise with unwavering quality standards.

In this role, you will act as a QP delegate, taking responsibility for the certification and release of investigational medicinal products (IMPs) used in worldwide clinical trials. You will provide quality oversight across multiple supply chains, ensuring that every tablet, vial, and package meets the rigorous standards our patients deserve.

roles and responsibilities 


You will support the operational quality performance and act as an expert resource in maintaining compliance levels across the Clinical Supply Chain.

This will involve:

  • Serving as Quality Point of Contact for the IMP release and certification process.

  • Review of batch documentation and analytical results.

  • Ensuring compliance with GMP and GDP requirements, the clinical trial regulation, and other relevant legislation.

  • Performing documented QA approval of GMP documentation and participating in quality review meetings.

  • Managing quality issues, deviations, and complaints, ensuring timely and proper investigations.

  • Supporting the preparation, execution, and follow-up of inspections and audits.

  • Leading and cooperating on process improvements within the QA Release Organization.



how to succeed


You are a detail-oriented quality professional who thrives on the complexity of pharmaceutical development and global regulations.

You will also bring:

  • A degree as a Certified Industrial Pharmacist.

  • At least 5 years of cross-functional experience in the pharmaceutical industry.

  • In-depth knowledge of pharmaceutical legislation (Eudralex, ICH, Ph.Eur., USP) and Clinical Trial regulations.

  • Fluency in Dutch and English (written and spoken).

  • Strong analytical thinking and decision-making skills.

  • Proficiency in systems such as SAP, Trackwise, and eLIMS.

  • A proactive mindset toward Safety, Health, and Environment (SHE) responsibilities.



benefits 

This role offers a very competitive hourly rate. This contract will run until 31st December 2026.

you are welcome here 

Johnson & Johnson is working to create an inclusive environment where diverse backgrounds, perspectives, and experiences are valued and each and every one of our people feels that they belong and can reach their potential. No matter who they are.

about Johnson & Johnson Innovative Medicine


 Patients inform and inspire our science-based innovations, which continue to change and save lives. Applying rigorous science and compassion, we confidently address some of the most complex diseases of our time and unlock the potential medicines of tomorrow. Our diverse portfolio spans multiple therapeutic areas — Oncology, Immunology, Neuroscience, Cardiovascular, Pulmonary Hypertension, and Retina. We are continuously working to develop treatments, aspiring to find cures, pioneering the path from lab to life, and championing patients every step of the way.

application process


 We are looking to process the first round of applications within the next 2 working days. We do not accept applications via email.

Diversity, Equity & Inclusion


 For more than 130 years, diversity, equity & inclusion (DEI) have been part of our cultural fabric at Johnson & Johnson and woven into how we do business every day. Our commitment to respect the dignity and diversity of all is embedded in our Credo.

We know that the success of our business depends on having the best talent in a workforce that reflects the diverse markets we serve around the world and an inclusive culture that values different perspectives and life experiences. That is why we are working to create an inclusive environment where diverse backgrounds, perspectives and experiences are valued and each one of our people feels that they belong and can reach their potential. No matter who they are. Diversity, Equity & Inclusion at Johnson & Johnson means “You Belong”.





Similar jobs

+ Search all jobs