Validation Engineer (ONSITE)

Piper Companies is hiring a Validation Engineer for a pharmaceutical manufacturing company located in Clayton, NC. The Validation Engineer will focus on executing validation protocols for critical equipment and processes ensuring compliance with regulatory standards and company procedures. The Validation Engineer will need to sit on site 5 days per week in Clayton, NC and is a long term open ended contract opportunity.

Responsibilities for the Validation Engineer:

• Execute validation protocols for aseptic manufacturing processes and equipment.
• Support validation activities for filling isolator equipment and Optima filling lines.
• Document and maintain validation records in compliance with GMP standards.
• Collaborate with cross-functional teams to ensure timely completion of validation deliverables.
• Utilize TIMS (or similar systems) for protocol execution and documentation.
• Ensure adherence to regulatory requirements and company quality standards throughout validation activities.

Requirements for the Validation Engineer:

• 2–5 years of validation experience in aseptic pharmaceutical manufacturing.
• Hands-on experience with filling isolator equipment; experience with Optima filling lines preferred.
• Familiarity with TIMS or similar validation management systems (e.g., Kneat).
• Strong understanding of GMP and regulatory compliance requirements.

Compensation for the Validation Engineer:

• $90,000-$120,000 depending on experience
• Full Comprehensive Benefits: Health, Vision, Dental, PTO, Paid Holiday and Sick Leave if Required by Law

Keywords: Validation Engineer, aseptic pharmaceutical manufacturing, aseptic processing, filling isolator equipment, Optima filling lines, validation protocols, GMP compliance, TIMS, Kneat, protocol execution, documentation, Novo Nordisk, Fill Finish Expansion, onsite work, pharmaceutical validation, equipment validation, process validation, regulatory compliance, quality assurance, validation management systems, sterile manufacturing, injectable drug manufacturing, contract assignment, long-term project, validation experience

#LI-AG1

#ONSITE

This job opens for applications on 11/26/2025. Applications for this job will be accepted for at least 30 days from the posting date.