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CQV/Validation Engineer (GMP)

  • ... Posted on: Apr 10, 2026
  • ... Panda International
  • ... Ghent Metropolitan Area, New York
  • ... Salary: Not Available
  • ... Full-time

CQV/Validation Engineer (GMP)   

Job Title :

CQV/Validation Engineer (GMP)

Job Type :

Full-time

Job Location :

Ghent Metropolitan Area New York United States

Remote :

No

Jobcon Logo Job Description :

Asset Engineer – CAR-T (Belgium)Location: Ghent area, BelgiumWe are supporting a leading cell therapy manufacturer in hiring an Asset Engineer to strengthen their CAR‑T engineering team. In this role you will provide technical expertise for lab and process equipment used in the CAR‑T manufacturing process and support commissioning and qualification (C&Q) activities within cGMP clinical and commercial cell therapy facilities.The roleAs Asset Engineer you are a key contributor to reliable operations and asset lifecycle management. You work closely with project teams, vendors and site stakeholders to ensure equipment is introduced, qualified and maintained in line with global and local standards.ResponsibilitiesManage multiple equipment-related business requests and small projects via the change control quality system.Support and execute operational commissioning and qualification (C&Q) activities in line with global processes.Act as Asset Subject Matter Expert (SME) for CAR‑T equipment.Contribute to the creation and review of technical requirements and asset standards.Provide guidance on compliance and data integrity requirements.Identify and address gaps between global and local compliance processes and drive consistent technical practices across CAR‑T sites.Develop and maintain strong strategic relationships with key vendors.Drive continuous technical improvements across the asset base.Coordinate with internal departments and external suppliers to resolve technical issues and drive solutions.Support technical investigations during C&Q activities and day‑to‑day operations.Lead evaluation, business case development and implementation of new asset technologies.Your profileMaster’s degree in Science, Engineering, Bioengineering or a similar technical discipline.3+ years of experience in a pharmaceutical manufacturing and/or engineering environment.Proven experience with commissioning & qualification (C&Q) of equipment.Solid understanding of data integrity requirements (e.g. 21 CFR Part 11).Strong stakeholder management and communication skills.Proactive, structured and comfortable managing multiple initiatives in a GMP setting

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Jobcon Logo Position Details

Posted:

Apr 10, 2026

Reference Number:

25975_4390352148

Employment:

Full-time

Salary:

Not Available

City:

Ghent Metropolitan Area

Job Origin:

APPCAST_CPC

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Asset Engineer – CAR-T (Belgium)Location: Ghent area, BelgiumWe are supporting a leading cell therapy manufacturer in hiring an Asset Engineer to strengthen their CAR‑T engineering team. In this role you will provide technical expertise for lab and process equipment used in the CAR‑T manufacturing process and support commissioning and qualification (C&Q) activities within cGMP clinical and commercial cell therapy facilities.The roleAs Asset Engineer you are a key contributor to reliable operations and asset lifecycle management. You work closely with project teams, vendors and site stakeholders to ensure equipment is introduced, qualified and maintained in line with global and local standards.ResponsibilitiesManage multiple equipment-related business requests and small projects via the change control quality system.Support and execute operational commissioning and qualification (C&Q) activities in line with global processes.Act as Asset Subject Matter Expert (SME) for CAR‑T equipment.Contribute to the creation and review of technical requirements and asset standards.Provide guidance on compliance and data integrity requirements.Identify and address gaps between global and local compliance processes and drive consistent technical practices across CAR‑T sites.Develop and maintain strong strategic relationships with key vendors.Drive continuous technical improvements across the asset base.Coordinate with internal departments and external suppliers to resolve technical issues and drive solutions.Support technical investigations during C&Q activities and day‑to‑day operations.Lead evaluation, business case development and implementation of new asset technologies.Your profileMaster’s degree in Science, Engineering, Bioengineering or a similar technical discipline.3+ years of experience in a pharmaceutical manufacturing and/or engineering environment.Proven experience with commissioning & qualification (C&Q) of equipment.Solid understanding of data integrity requirements (e.g. 21 CFR Part 11).Strong stakeholder management and communication skills.Proactive, structured and comfortable managing multiple initiatives in a GMP setting

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