Regulated capacity needs proven professionals

For clients building in pharma and life sciences

The clients who call us are usually adding capacity: a new suite, a new line, a full greenfield facility, in pharmaceutical, biopharmaceutical or wider life-sciences manufacturing. What they need is the layer of people who translate design intent into a qualified, inspection-ready plant, and who have carried that accountability before under GMP. That includes the client-side teams feeding construction and managing the main contractors, not only the site delivery layer.

• Project controls, planning, cost management and reporting
• Estimating, cost control and cost engineering
• Commercial management: commercial leads, quantity surveyors and contracts management
• Programme and project management support
• Procurement and supply-chain management on the client side
• Commissioning, qualification and validation (CQV)
• Process, clean-utilities and facilities engineering management
• CSA, MEP and construction management for GMP environments
• Start-up specialists for new suites and lines

What we get asked for

The inspection-ready build Qualification specialists whose documentation packages have already stood in front of an inspector. Keyword matching cannot find that; sector knowledge can.

The capacity race A product approval turns a plan into a deadline. We find the engineering professionals who scale a site without breaking its quality culture.

The handover that sticks From construction complete to operations-owned: start-up specialists who close out the project and leave a plant the site team can actually run.

For candidates in this sector

If you lead CQV packages, run GMP construction, manage the commercial function or lead process engineering on capital projects anywhere in pharma or life sciences, we would like to know what you want next. Register your interest and someone from our team talks you through the live roles and projects we are working on.