CSV Engineer III

We are PCI Pharma Services and we are looking for a CSV Validation Engineer III to join our Quality and Compliance team. In this role, you'll take the lead in developing and executing validation strategies for GxP computer systems.

Requirements

• 5+ years of hands-on experience in a cGMP-regulated environment, with at least 3 years focused on automation and validation.
• Strong knowledge of validation for manufacturing equipment, utilities, clean media systems, and facilities.
• Experience with industry standards like GAMP and regulations including 21 CFR Part 11, 210, 211, 820, and ICH Q7A.
• A deep understanding of system risk assessments, gap analysis, and remediation plans.
• Excellent communication and documentation skills—able to write clear, audit-ready validation deliverables.
• Team-first mindset with the ability to work independently on multiple complex projects.
• Proficiency in Microsoft Office and database systems.

Benefits

• Competitive compensation
• Benefits