Investigation Coördinator

☞ Johnson & Johnson

看过: 101

更新日: 12-11-2025

位置: Beerse Antwerp

类别: 质量保证/质量控制

行业: Hospitals Health Care

工作类型: Full-time

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工作内容

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

We are searching for the best talent for Investigation coordinator to be in Beerse, Belgium.

We are excited to invite talented individuals to join us as we seek an Investigation Coordinator to be based in Beerse, Belgium.

CAR-T represents a groundbreaking advancement in the treatment of blood cancers, leveraging the power of the patient’s own immune system. Through the genetic modification of T-cells, we can help eliminate cancer cells, offering renewed hope to patients with limited treatment options. We are dedicated to growing our CAR-T treatment capabilities across Europe, including our established site in Beerse and our new production facility in Ghent. We are eager to welcome strong candidates who are enthusiastic about contributing to this innovative and hopeful journey. As part of the Innovative Medicine Supply Chain Group, which is a proud member of the Johnson & Johnson family of companies, we are currently recruiting a QC CAR-T Investigation Coordinator for our CAR-T hub in Europe.

You Will Be Responsible For

  • Support daily operations within Quality Control (QC) and collaborate closely with supervisors, analysts, production teams, the warehouse, and Quality Assurance (QA).
  • Lead complex investigations and compile comprehensive final investigation reports based on detailed root cause analyses.
  • Define and implement corrective actions while supervising their efficiency, ensuring timely execution and closure. If a QC investigation spans multiple departments, you will guide a multidisciplinary team and serve as the QC representative in those investigations.
  • Initiate and support improvement projects aimed at improving safety, quality, efficiency, and customer satisfaction within the team.
  • Develop and conduct training and awareness sessions within QC.
  • Provide support during health authority inspections by preparing substantive materials.
  • Supervise and streamline quality levels across various laboratories.

Qualifications And Requirements

  • A minimum of a Master’s degree in a field related to biochemistry or biotechnology.
  • Knowledge of current Good Manufacturing Practices (cGMP) regulations and FDA/EU guidance.
  • Strong organizational skills, along with a capacity for independent and flexible working, are required.
  • Excellent written and verbal communication skills are necessary.
  • Professional experience in a GMP-regulated environment, particularly in quality control, is advantageous.
  • Proficiency in Microsoft Office programs is required.
  • A solid understanding of laboratory processes and systems is preferred.

We invite you to become a part of our mission as we work together to transform the landscape of CAR-T treatments and improve patient outcomes.#RPOAMS
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最后期限: 27-12-2025

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