Car-t Asset Engineer

Johnson & Johnson MedTech

Beerse, Antwerp, Belgium
Not specified (assumed hybrid based on general industry trends).
Technical management of lab and process equipment
Commissioning and qualification (c&q) activities
Compliance with gmp guidelines
Johnson & Johnson MedTech is seeking a Car-t Asset Engineer to provide technical expertise for lab and process equipment involved in CAR-T therapy, focusing on compliance and operational excellence within their manufacturing facilities in Belgium. The ideal candidate will possess a Master's degree in a technical discipline and have a minimum of three years of experience in pharmaceutical manufacturing or engineering environments

Job Summary

  • The Asset Engineer provides technical expertise for lab and process equipment used in the CAR-T process and supports Commissioning and Qualification activities within cGMP Clinical and Commercial Cell Therapy Manufacturing plants.
  • This position offers a meaningful role where your work has a direct impact on cancer patients’ lives and a supportive environment that values your growth, creativity, and contributions.
  • Johnson & Johnson provides a diverse and inclusive workplace where everyone can thrive and is an Affirmative Action and Equal Opportunity Employer.

Matching Summary

Match Score: 85

Johnson & Johnson MedTech is seeking a Car-t Asset Engineer to provide technical expertise for lab and process equipment involved in CAR-T therapy, focusing on compliance and operational excellence within their manufacturing facilities in Belgium. The ideal candidate will possess a Master's degree in a technical discipline and have a minimum of three years of experience in pharmaceutical manufacturing or engineering environments.

Skills & Requirements

Must-have

  • Technical management of lab and process equipment
  • Commissioning and qualification (C&Q) activities
  • Compliance with GMP guidelines
  • Asset lifecycle management projects
  • Collaboration with project teams and vendors

Nice-to-have

  • Hands-on, solution-oriented mindset
  • Experience with audits or inspections
  • Fluent in Dutch language
  • Strong analytical and communication skills
  • Collaborative and open approach

Key Requirements

  • Master’s Degree in Science, Engineering, or Bioengineering
  • Minimum 3 years pharmaceutical manufacturing experience
  • Experience in commissioning & qualification (C&Q) is a plus
  • Fluent in English
  • Knowledge of GMP guidelines

Work Rights

Not specified

Tailored Resume

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