Associate QA-CSC

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:
BE009 Turnhoutseweg 30

Job Description:

QA associate_ PQM QA-CSC

Job Description

Within Johnson  & Johnson Innovative Medicine we are recruiting a quality associate for Investigational Medicinal Products (IMP) as member of our QA Clinical Supply Chain (QA CSC) 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 QA CSC is responsible for the release and certification of Investigational Medicinal Products used in worldwide clinical trials.

As QA CSC 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 QA CSC - 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.
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