At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com

Job Function:

Quality

Job Sub Function:

Quality Assurance

Job Category:

Professional

All Job Posting Locations:

Beerse, Antwerp, Belgium

Job Description:

Within Johnson & Johnson Innovative Medicine we are recruiting a quality associate for Investigational Medicinal Products (IMP) as member of our Clinical Supply Quality (CSQ) team based in Belgium.

In the Research & Development area we develop treatments that improve the health and lifestyles of people worldwide. R&D development areas encompass novel targets in neurologic disorders, gastroenterology, oncology, infectious disease, diabetes, hematology, metabolic disorders, immunologic disorders, pulmonary hypertension and reproductive medicine.

Our department CSQ is responsible for the release and certification of Investigational Medicinal Products used in worldwide clinical trials.

As CSQ associate, you will support the clinical release and quality oversight process of IMPs so that patient safety and compliance with applicable regulations are warranted.

The Janssen portfolio is continuously evolving, growing and therefore the CSQ - IMP RCC sub-team is looking for a QA Associate to strengthen the team in execution of the Regulatory Compliance Check and in supporting the implementation of our QA digital roadmap.

Are you interested in joining a team that is positively impacting patients' lives by ensuring high quality in our innovative products?

Are you data and document savvy? Do you have continuous improvement mindset? Do you have an affinity with systems? Do you easily connect & is a good team spirit important to you? This position is waiting for you!

Apply today for this exciting opportunity!

As a QA Associate you will:

Act as the Quality Point of Contact for Regulatory Compliance activities related to the release of Investigational Medical Products used in global clinical trials, this for supplies coming from internal as well as external manufacturers.
Work as One team with Quality and Clinical Supply Chain partners to ensure timely release and certification of clinical trial material in support of a reliable supply chain.
Ensure Quality and Compliance operational targets are met.
Ensure that quality records (e.g., deviation, CAPA, Change Control) are timely and accurately investigated and closed such that the internal and external customer expectations are met.
Continuously challenge the status quo and support the development and implementation of innovative initiatives that deliver sustainable improvement in organizational, quality and compliance performance.
Develops QA System User requirements together with the business partners and IT. Responsible for validating the QA User requirements. This includes timely creation and/or review of test scripts and execution of test scripts according to the agreed upon project planning.
Ensures GMP related documents are kept up to date by performing impact assessment of new requirements.
Acts as QA SME and provides first line support in collaboration with DPDS business partners and IT.

Job Qualifications

University degree or equivalent by experience with at least 2 years experience in the pharmaceutical industry.
In-depth knowledge in cGMP (domestic & international), J&J policies, standards and procedures.
Proven ability to work independently while staying connected with stakeholders.
Understands the business implications regarding quality positions and decisions. Understands the bigger picture.
Ability to quickly assimilate new technologies and system affinity.
Ability to translate QA operational requirements into system requirements
Demonstrated ability to work across organizational boundaries through influencing and partnering. Communication and presentation skills across all levels are important.
Able to think outside the box and come up with innovative and creative solutions to problems. Open-minded for new ideas and willing to pivot when necessary.
Able to adjust plans and priorities when circumstances change, to prioritize tasks and manage time effectively, and to show resilience in difficult situations.

Please apply by Wednesday 19th of November 2025.

Required Skills:

Preferred Skills:

Business Alignment, Business Behavior, Coaching, Compliance Management, Continuous Improvement, Data Analysis, Detail-Oriented, Goal Attainment, Human-Centered Design, Internal Controls, Issue Escalation, Problem Solving, Process Oriented, Quality Control (QC), Quality Management Systems (QMS), Quality Standards

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QA associate