Piper Companies
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
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
5–10 years of experience in validation, process engineering, or CQV within sterile manufacturing environments.
Proven ability to independently author and execute validation protocols.
Extensive hands‑on experience with aseptic filling lines.
Skilled in equipment troubleshooting and execution—comfortable working directly with machinery.
Self‑motivated “doer” with a proactive mindset and strong ownership of tasks.
Familiarity with automated inspection systems is a plus.
Compensation
Salary Range : $60-$70/hour dependent on experience
Comprehensive Benefits : Sick leave if required by law, medical, dental, vision, 401K
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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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
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
5–10 years of experience in validation, process engineering, or CQV within sterile manufacturing environments.
Proven ability to independently author and execute validation protocols.
Extensive hands‑on experience with aseptic filling lines.
Skilled in equipment troubleshooting and execution—comfortable working directly with machinery.
Self‑motivated “doer” with a proactive mindset and strong ownership of tasks.
Familiarity with automated inspection systems is a plus.
Compensation
Salary Range : $60-$70/hour dependent on experience
Comprehensive Benefits : Sick leave if required by law, medical, dental, vision, 401K
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
#J-18808-Ljbffr