Onsite Validation Engineer; CQV GMP Facilities
Listed on 2026-10-12
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Quality Assurance - QA/QC
Quality Engineering -
Engineering
Pharma Engineer, Quality Engineering
Piper Companies seeks a Validation Engineer for a leading pharmaceutical manufacturer in Clayton, NC. The role requires full onsite work in Clayton and targets a seasoned professional with CQV experience across GMP environments, facility systems, and QC laboratories.
Responsibilities include leading CQV activities, developing IQ/OQ/PQ docs, and ensuring compliance with FDA/EU GMP standards. A 2-year contract with potential extensions is offered.
Are you ready to take on the Onsite Validation Engineer (CQV) – GMP Facilities role at Piper Companies?
This role is for the Onsite Validation Engineer (CQV) – GMP Facilities role at Piper Companies.
We are seeking a motivated Onsite Validation Engineer (CQV) – GMP Facilities to join Piper Companies in Clayton, NC, United States.
Consider building your career as a Onsite Validation Engineer (CQV) – GMP Facilities at Piper Companies.
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