Cell Therapy Validation Engineer — GMP/CSV Expert
Listed on 2026-10-06
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Engineering
Quality Engineering, Pharma Engineer, Regulatory Compliance Specialist -
Quality Assurance - QA/QC
Quality Engineering, Regulatory Compliance Specialist
Made Scientific, a US-based cell therapy CDMO, is seeking a Validation Engineer to manage and advance Equipment and Facility Validation programs, ensuring compliance with cGMP and regulatory standards. The role supports GMP operations and maintains validated state for equipment, systems, and facilities.
The candidate will lead IQ/OQ/PQ execution, perform CSV activities per FDA and GAMP 5 guidelines, and collaborate with Manufacturing, Quality Assurance, and Engineering to drive risk assessments,
Consider building your career as a Cell Therapy Validation Engineer — GMP/CSV Expert at Made Scientific.
Please review the full job details above before applying.
If your experience matches this role, we encourage you to apply.
All applications are reviewed carefully by our team.
The position is based in Princeton, NJ, United States.
This opportunity is part of our work in Engineering.
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