Downstream CQV Engineer – Biologics GMP Validation; Onsite
Listed on 2026-10-06
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Engineering
Pharma Engineer, Quality Engineering, Regulatory Compliance Specialist -
Quality Assurance - QA/QC
Quality Engineering, Regulatory Compliance Specialist
Piper Companies seeks a Downstream CQV Engineer to join a biologics manufacturing organization in Holly Springs, NC, onsite for a long-term contract. You will support commissioning, qualification, and validation across downstream processing systems to ensure readiness for production in a greenfield facility.
Candidates should have 5+ years in CQV/validation within GMP, hands-on field verification, and the ability to interpret P&IDs and perform system walkdowns.
This role, Downstream CQV Engineer – Biologics GMP Validation (Onsite) at Piper Companies, could be your next career step.
We have an opening for a Downstream CQV Engineer – Biologics GMP Validation (Onsite) in Holly Springs, NC, United States within Engineering.
This role, Downstream CQV Engineer – Biologics GMP Validation (Onsite) at Piper Companies, could be your next opportunity.
Are you ready to take on the Downstream CQV Engineer – Biologics GMP Validation (Onsite) role at Piper Companies?
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