Warehouse Validation Engineer
Clayton, North Carolina
Job Id:
158264
Job Category:
Job Location:
Clayton, North Carolina
Security Clearance:
No Clearance
Business Unit:
Piper Companies
Division:
Piper Clinical Solutions
Position Owner:
Gray Young
Piper Companies is seeking a Warehouse Validation Engineer to support automation and material handling initiatives within a leading pharmaceutical organization. This role is ideal for professionals with expertise in validation, robotics, and automated systems in GMP-regulated environments.
Key Responsibilities of the Warehouse Validation Engineer:
- Develop, execute, and analyze Installation Verification (IV), Operational Verification (OV), and Performance Verification (PV) protocols.
- Author validation plans, master plans, and related documentation to ensure compliance with corporate and regulatory standards.
- Lead investigations for validation discrepancies and apply structured root cause analysis methodologies.
- Participate in FAT/SAT commissioning and oversee validation activities for automated systems.
- Manage change controls and maintain validated state for warehouse automation systems.
Qualifications of the Warehouse Validation Engineer:
- Bachelor’s degree in Engineering, Computer Science, or related field (advanced degree preferred).
- 7+ years of validation or quality experience in a pharmaceutical setting.
- 3–5 years of hands-on experience with robotics, automation, and SAP systems preferred.
- Strong knowledge of GMP, GAMP 5, 21 CFR Part 11, and FDA/ICH guidelines.
- Excellent documentation, problem-solving, and project management skills.
Compensation & Benefits of the Warehouse Validation Engineer:
- Salary range: $100,000 – $135,000, based on experience.
- Comprehensive benefits package including health, vision, dental, PTO, paid holidays, and sick leave (as required by law).
Keywords: Warehouse Validation Engineer, pharmaceutical automation, robotics, intralogistics, ASRS, AGVs, AMRs, SCADA, WCS, SAP, GMP, GAMP5, validation protocols, FAT, SAT, compliance, root cause analysis, change control, FDA regulations.
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