Design Verification Lead – US, Texas – Initial 12-Month Contract – Life Sciences 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.
What you’ll deliver:
- Lead design verification activities for assigned GMP manufacturing packages.
- Act as the primary point of contact for designated process or manufacturing workstreams.
- 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.
What you’ll need:
- 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.
Don’t miss your chance to be part of something extraordinary, apply now and let’s talk!