GMP Process Architect - Cleanroom

For Senior Cleanroom / GMP Process Architect - Life Sciences & Advanced Manufacturing Services WHAT MAKES YOU A FIT:
The Technical Part:

• Bachelor’s degree in Architecture, Engineering, or related discipline and eight(8) years of experience in cleanroom, GMP, or high‑tech manufacturing facility design.
• Extensive experience in pharmaceutical, biotech, gene therapy, or advanced manufacturing facilities.
• Shift: Administrative and according to business needs.
• Experience in:
  • Strong knowledge of:
    • ISO 14644 cleanroom standards
    • cGMP facility design principles
    • HVAC zoning and pressurization strategies
    • Contamination control and material/personnel flow
  • Experience working on large‑scale, capital projects expansions, and renovations.
  • Proven ability to lead multidisciplinary teams and interface with clients and regulators.

• Our Next Piece is someone who treats everyone they meet like family, especially our resources, clients, and team members. In other words, being a customer service pro is one of your (many) talents. Being the Piece means you're full of bright ideas and eager to innovate, always bringing top‑quality results to the table. Are you ready to take on this new challenge?

Lead conceptual, preliminary, and detailed design of clean rooms and controlled environments (ISO 3–8) for sterile and non‑sterile manufacturing.

Develop cleanroom zoning strategies, airflow models, pressure cascades, and HVAC concepts to meet contamination control requirements.

Define personnel and material flows, gowning concepts, airlocks, and segregation strategies.

Specify cleanroom finishes, filtration systems, cleaning strategies, and utilities distribution aligned with process requirements.

Coordinate cleanroom layouts with process equipment, tool installations, skids, and utility interfaces.

Support semiconductor wafer fabrication, biotechnology, cell & gene therapy, and high‑containment processing environments.

• Ensure facility designs support scalability, flexibility, and future expansion.
• Ensure alignment with cGMP, ISO 14644, FDA, EMA, ISPE, PDA, and GLP requirements.
• Participate in GMP reviews, risk assessments, and regulatory readiness activities.
• Support development of Basis of Design (BOD), User Requirements (URS), and technical documentation.
• Serve as technical lead or subject matter expert (SME) for cleanroom and process architecture.
• Collaborate with MEP engineers, validation teams, construction managers, and vendors.
• Support design‑build and IPD delivery models, including construction administration and field coordination.