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QA Lab associate IPL CAR-T

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  • Job title QA Lab associate IPL CAR-T
  • Function Quality
  • Sub function Quality Assurance
  • Category Experienced Analyst, Quality Assurance (P5)
  • Location Gent / Belgium
  • Date posted
  • Requisition number 2406227231W
  • Work pattern Fully Remote

Summary

About Innovative Medicine Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow. Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way. Learn more at https://www.jnj.com/innovative-medicine

Description

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:

BE022 GENT

Job Description:

We are searching for the best talent for QA Lab associate IPL CAR-T to be in Gent, Belgium.

This is an amazing chance to contribute to cutting-edge cellular therapy and make a positive impact on patients' lives!

As a QA Lab Associate for CAR-T, you will play a vital role in ensuring the highest quality standards for our CAR-T cellular therapy products. You will be integral to maintaining compliance with our internal policies and the highest global standards, contributing to a culture of quality and excellence.

You will be responsible for:

  • Investigate and Improve: Oversee laboratory investigations by timely reviewing and analyzing quality data to identify trends that enhance our performance.

  • Collaborative Spirit: Work together with your team on drafting, approving, and implementing standard operating procedures. Conduct regular spot-checks to ensure compliance with regulations and global policies.

  • Proactive Problem Solver: Thoroughly investigate non-conformances and ensure timely approvals and execution of corrective and preventive actions to minimize future challenges.

  • Commitment to Safety and Quality: Uphold safety standards and cGMP requirements while providing critical support for investigations, generating technical conclusions aligned with quality risk management.

  • Data Insight: Recognize and communicate patterns in quality data to management, offering guidance on complex quality issues and participating in innovative scientific initiatives.

  • Drive Continuous Improvement: Tackle quality challenges with a proactive attitude, developing effective solutions, and fostering continuous improvement across laboratory functions.

  • Support Laboratory Growth: Provide compliance oversight for laboratory expansion projects, including the qualification of analytical instruments, ensuring excellence in all laboratory operations.

Qualifications & Requirements:

  • A Master’s Degree in Engineering, Science, or an equivalent technical discipline is required.

  • At least 2 years of experience in Quality Assurance, demonstrating your expertise in the field.

  • A strong understanding of cGMP regulations and FDA/EU guidance is essential.

  • Experience with biotechnology methods such as flow cytometry, cell counting, and viability

If you’re ready to take on this exciting challenge and help us drive quality in the innovative field of CAR-T therapy, we would love to hear from you! Join us in making a difference — together we can elevate laboratory excellence and improve lives.#RPOAMS

QA Lab associate IPL CAR-T

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