Validation Engineer: GMP, ISO 13485 & FDA Compliance
Listed on 2026-10-17
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Quality Assurance - QA/QC
Regulatory Compliance Specialist, Quality Engineering -
Engineering
Regulatory Compliance Specialist, Pharma Engineer, Quality Engineering, Biomedical Engineer
Boxx-Technologies, Inc. is seeking a Validation Engineer to lead development, execution, and documentation of validation protocols for GMP/ISO/FDA‑compliant processes. You will drive QA/QC improvements and ensure product safety across manufacturing operations.
You will conduct risk assessments, lead cross‑functional teams, and maintain meticulous validation documentation to support regulatory compliance and continuous improvement.
Are you ready to take on the Validation Engineer: GMP, ISO 13485 & FDA Compliance role at Boxx-Technologies,-Inc.?
We have an opening for a Validation Engineer: GMP, ISO 13485 & FDA Compliance in Austin, TX, United States within Engineering.
This role, Validation Engineer: GMP, ISO 13485 & FDA Compliance at Boxx-Technologies,-Inc., could be your next move.
We would love to welcome a new Validation Engineer: GMP, ISO 13485 & FDA Compliance to our team in Austin, TX, United States.
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