Design Verification Lead

QCS Staffing; Texas; On-site; USD 110,000 - 150,000; Full time

Job summary

QCS Staffing Ltd is recruiting a Design Verification Lead for a US Texas life sciences project on an initial 12-month contract. The role focuses on leading design verification activities for GMP manufacturing packages and acting as primary liaison across engineering, operations, quality, and project teams.

You will ensure designs meet GMP and regulatory expectations, review process, equipment, and facility designs, and coordinate reviews throughout the project lifecycle.

Qualifications

• Extensive experience within pharmaceutical GMP environments.
• Experience supporting GMP facility or manufacturing process design.
• Strong understanding of cGMP requirements.
• Experience leading engineering packages during major capital projects.

Responsibilities

• 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.

Skills

GMP knowledge

Process design understanding

Stakeholder coordination

Design verification leadership

Job description

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.