Lead Validation Specialist

Overview

Piper Companies is hiring a Lead Validation Specialist for a pharmaceutical and healthcare company that makes treatments for diabetes and chronic conditions located in Clayton, NC. The Lead Validation Specialist will assist with CQV activities in a sterile fill-finish facility. The Lead Validation Specialist will work onsite in Clayton, NC in a one-year contract role.

• Carry out equipment and system testing to confirm they are ready for operational use (IQ, OQ, PQ).
• Prepare and document validation activities, including test protocols and final reports.
• Make sure all systems operate in line with regulatory and quality standards.
• Troubleshoot issues that arise during validation and manage corrective actions as needed.
• Work closely with internal teams and vendors to support validation and startup efforts.
• Assist with key startup activities such as process validation, sterilization, and equipment commissioning.

• 7+ years of related experience
• Bachelor’s degree
• Experience qualifying various GMP systems
• Familiarity with FDA GMP guidelines, EU Annex 1, and standard validation practices

$145,000 - $165,000 at an hourly pay rate

Full Comprehensive Benefits:
Health, Vision, Dental, PTO, Paid Holiday and Sick Leave if Required by Law