GMP Process Architect - Cleanroom

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.

The Personality Part:

• 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?

As a Piece of Fits, You Will:

• Lead conceptual, preliminary, and detailed design of cleanrooms 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.

Who We Are:

We are a service provider company that is different from the rest. We pride ourselves in how we treat the most important piece of our company's puzzle: you! We integrate Engineering, Construction, Maintenance, Utilities, and Specialized Technical services across the Island (and in the US as well!). Our company is flexible, family-oriented, and focused on the well-being of our resources while providing our pharmaceutical, medical device, and manufacturing industry clients with top-notch quality talent. We're FITS!

Are you the Next Piece?