Design Verification Lead

Be part of a next-generation pharmaceutical project that’s transforming how medicines are made. We’re supporting a major new-build facility in Texas, a multi-billion-dollar investment designed to push the boundaries of science and engineering. We’re looking for a Design Verification Lead to support this project and help deliver this world-class program.

• Lead design verification activities for assigned GMP manufacturing packages.
• Act as the primary point of contact for designated process or manufacturing work streams.
• Ensure designs comply with GMP requirements, regulatory expectations, and operational needs.
• Coordinate design reviews between engineering, operations, quality, process, and project stakeholders.
• Review and verify process, equipment, and facility designs throughout the project lifecycle.

• Extensive experience within pharmaceutical, biotechnology, API, or related GMP- regulated manufacturing environments.
• Demonstrated experience supporting GMP facility or manufacturing process design.
• Strong understanding of cGMP requirements and pharmaceutical manufacturing operations.
• Experience owning, coordinating, or leading engineering packages during major capital projects.
• Background in process engineering, project engineering, process design, manufacturing engineering, or related disciplines.