CQV Engineer Consultant

Piper Companies is seeking a CQV Engineer Consultant for an advanced biologics CDMO located in Holly Springs, North Carolina (NC) . The ideal CQV Engineer Consultant will have experience working in validation and / or process engineering, filling line experience, and be a self-motivated individual with the ability to own projects. This is an on-site position in Holly Springs, NC.

Responsibilities of the  CQV Engineer Consultant :

• Execute IQ / OQ / PQ validation protocols for parenteral filling and automated inspection equipment.
• Collaborate with cross-functional teams on new line installations, process improvements, and equipment commissioning.
• Take technical ownership of key validation projects, driving timelines and deliverables.
• Optimize performance of automated inspection systems through hands-on troubleshooting and continuous improvement.
• Contribute to the development and refinement of validation strategies as part of the Performance Qualification (PQ) team.
• Support documentation efforts using Kneat or similar platforms; training available for motivated learners.

Qualifications for the  CQV Engineer Consultant :

Compensation for the CQV Engineer Consultant :

This job opens for applications on 10 / 20 / 2025. Applications for this job will be accepted for at least 30 days from the posting date.

Keywords :  CQV Engineer, Validation Engineer, Sterile Manufacturing, Aseptic Filling, Aseptic Processing, Equipment Qualification, IQ / OQ / PQ Protocols, Automated Inspection Systems, Hands-on Troubleshooting, Performance Qualification (PQ), Cross-functional Collaboration, Equipment Commissioning, Continuous Improvement, Kneat Validation Software, GMP Compliance, Pharmaceutical Engineering, Technical Ownership, Self-starter, Cleanroom Environment

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