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Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in pharmaceutical facility design, ensuring compliance with Good Manufacturing Practice (GMP) requirements while optimizing operational flows and supporting facility expansion. Proven ability to coordinate multidisciplinary project teams on large-scale capital projects.
Highest-signal resume keywords
Pharmaceutical Facility DesignGood Manufacturing Practice (GMP)Cleanroom ZoningContamination ControlMultidisciplinary Project Coordination
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Facility LayoutManufacturing AdjacenciesMaterial Flow OptimizationOperational FunctionalityFacility ProgrammingOperational Readiness PlanningCQVValidation Requirements
Certifications & Qualifications
Professional RegistrationIndustry Certification
Industry Keywords
Pharmaceutical ManufacturingBiotechnologyVaccine ManufacturingFDAEMAISPECapital ProjectsDesign Standards
About the role
Key responsibilities & impact- Provide specialized expertise in pharmaceutical facility layout, manufacturing adjacencies, cleanroom zoning, material and personnel flow, contamination control strategies, and operational functionality
- Ensure facility designs meet current Good Manufacturing Practice (GMP) requirements
- Support efficient manufacturing operations, future expansion, and long-term maintainability
- Optimize material, personnel, and operational flows
- Support facility expansion, maintainability, and operational performance goals
- Coordinate facility planning activities across engineering and operational teams
Requirements
What you’ll need- Bachelor’s degree in Engineering, Architecture, or a related technical discipline
- Minimum 10 years of experience supporting GMP facility planning or design for pharmaceutical, biotechnology, or vaccine manufacturing facilities
- Experience with cleanroom zoning, manufacturing adjacencies, and contamination control
- Strong knowledge of pharmaceutical facility design principles and GMP requirements
- Experience working with multidisciplinary project teams on capital projects in excess of $500M TIC
- Prior experience within PMC or Owner’s Representative organizations for capital projects in excess of $1B TIC preferred
- Knowledge of FDA, EMA, ISPE, and industry design standards preferred
- Experience supporting facility programming and operational readiness planning preferred
- Familiarity with CQV and validation requirements preferred
- Professional registration or relevant industry certification preferred
Benefits
Comp & perks- 401K plan with company match
- Medical insurance
- Dental insurance
- Vision insurance
- Life insurance
- AD&D insurance
- Flexible spending account
- Disability benefits
- Paid time off
- Flexible work schedule
- Professional training and development
- Career advancement opportunities