QC Validation Engineer

Piper Companies is seeking a QC Validation Engineer to join a rapidly growing pharmaceutical manufacturing organization for an onsite contract position based in Clayton, NC. The QC Validation Engineer will play a key role in ensuring laboratory systems and instruments are properly qualified and maintained to meet regulatory expectations, while supporting cross-functional teams across quality and IT.

Responsibilities for the QC Validation Engineer include:

· Lead qualification efforts for laboratory instruments, including benchtop analytical equipment such as HPLC, GC, balances, pipettes, and TOC systems.

· Develop and execute validation protocols (IQ/OQ/PQ) for both standalone and computerized laboratory systems.

· Partner with IT and quality teams to support validation of computerized systems, including data integrity, system security, and backup processes.

· Troubleshoot validation issues and implement corrective actions in collaboration with internal stakeholders and vendors.

· Communicate validation strategies and outcomes clearly to both technical and non-technical team members across the organization.

Qualifications for the QC Validation Engineer include:

· 2–7 years of experience in validation within a regulated laboratory or pharmaceutical environment (2–5 years preferred).

· Hands-on experience with analytical lab equipment such as HPLC, GC, TOC, balances, and pipettes.

· Familiarity with computerized system validation concepts, including audit trails, data security, and system lifecycle documentation.

· Strong ability to collaborate across functions, including IT, QA, and laboratory personnel.

· Bachelor’s degree in Engineering, Life Sciences, or a related technical field.

Compensation for the QC Validation Engineer:

Salary Range: $135,000-$155,000/year (USD)

Comprehensive Benefits: Medical, Dental, Vision, sick leave if required by law, and 401K

This job opens for applications on 6/4/26. Applications for this job will be accepted for at least 30 days from the posting date.

Keywords: QC validation, equipment qualification, HPLC, gas chromatography, TOC, laboratory instruments, IQ OQ PQ, computerized system validation, CSV, data integrity, GMP, FDA regulations, validation protocols, analytical lab equipment, quality assurance, pharmaceutical manufacturing, IT collaboration, audit trails, calibration, troubleshooting, documentation, cross-functional collaboration, communication skills.

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