Job Search

Validation Engineer

Clayton, North Carolina

Piper Companies Logo

Job Id:
169441

Job Category:

Job Location:
Clayton, North Carolina

Security Clearance:
No Clearance

Business Unit:
Piper Companies

Division:
Piper Clinical Solutions

Position Owner:
Jacqueline Norsworthy

Piper Companies is seeking a Validation Engineer to support a leading pharmaceutical manufacturing organization in a highly regulated environment. The Validation Engineer will play a critical role in ensuring GMP compliance through hands-on equipment qualification, validation activities, and cross-functional collaboration within sterile manufacturing operations.


Responsibilities of the Validation Engineer:

• Execute commissioning, qualification, and validation (CQV) activities for GMP equipment, utilities, and automated systems.

• Author, review, and execute IQ/OQ/PQ protocols and validation summary reports.

• Support validation efforts across systems including material handling, automated inspection, and sterilization equipment.

• Perform validation activities for washers, autoclaves, SIP/CIP systems, and aseptic processing equipment.

• Assist in validation of formulation, mixing, filling lines, isolators, RABS, and lyophilization systems.

• Troubleshoot validation issues and support deviation investigations and corrective actions.

• Collaborate with engineering, quality, and manufacturing teams to ensure compliance with regulatory requirements.

• Ensure adherence to FDA GMP regulations, EU GMP Annex 1, and industry validation standards.

• Maintain clear, thorough, and audit-ready documentation for all validation activities.


Qualifications of the Validation Engineer:

• Bachelor’s degree in Engineering, Life Sciences, or related technical discipline.

• 3+ years of CQV/Validation experience within pharmaceutical, biotechnology, or sterile manufacturing environments.

• Hands-on experience qualifying GMP equipment, utilities, and automated systems.

• Direct experience with one or more systems including material handling, automated inspection, sterilization equipment, or aseptic processing lines.

• Strong working knowledge of FDA GMP regulations, EU GMP Annex 1, and validation best practices.

• Proven experience authoring and executing IQ/OQ/PQ protocols and reports.

• Strong technical writing, troubleshooting, and cross-functional communication skills.


Compensation for the Validation Engineer includes:

• Salary range: $130,000 – $150,000 depending on experience

• Comprehensive benefits package including medical, dental, vision, 401(k), and PTO

• Onsite work environment (5 days per week in Clayton, NC)


This job opens for applications on 07/10/2026. Applications for this job will be accepted for at least 30 days from the posting date.


#LI-JN1

#LI-ONSITE

Apply For This Position


Personal Information

Required
Required
Required
Required
Required
Required
Required

Additional Details

Required
Required
Required

Voluntary Self-identification Form

Required
Required
Required

Veteran Status *

Discharge Date:

Resume Upload

Please note only files with .pdf, .docx, or .doc file extensions are accepted.

Currently selected file:

Don't have a resume?