Onsite Senior Validation Engineer – GMP Biotech Automation
Listed on 2026-10-13
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Engineering
Quality Engineering, Pharma Engineer -
Quality Assurance - QA/QC
Quality Engineering
Piper Companies is seeking a Senior Validation Engineer to join a rapidly growing biotechnology manufacturing organization on an onsite contract in Clayton, NC. The Senior Validation Engineer will lead validation activities for automated manufacturing systems, equipment, and processes in a regulated GMP environment.
Responsibilities include developing, executing, analyzing, and reporting IV, OV, and PV protocols; managing change controls; authoring validation plans and quality records; and
For the Onsite Senior Validation Engineer – GMP Biotech Automation position at Piper Companies, we are reviewing applications now.
The following position is for a Onsite Senior Validation Engineer – GMP Biotech Automation with Piper Companies.
Our team is growing, and we are hiring a Onsite Senior Validation Engineer – GMP Biotech Automation in Clayton, NC, United States.
This position is for the Onsite Senior Validation Engineer – GMP Biotech Automation role at Piper Companies.
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