Quality Assurance Manager - Construction

Posted 6 days ago

fort pointHenrico (VA)

SENIORITY

Manager

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About the role

NOTE: No 3rd Party companies.....CONSTRUCTION QUALITY ASSURANCE MANAGER -EPC - PHARMACEUTICAL/LIFE SCIENCES/BIOTECHWe are seeking an experienced Construction Quality Manager for leading EPC to oversee construction quality performance for a major, $500M+ greenfield pharmaceutical manufacturing project. In this leadership role, you will manage EPCM contractors, suppliers, and CQV partners to deliver a world-class facility from design through startup.
Key Responsibilities: Quality Governance: Develop the Project Quality Management Plan (QMP), establish KPIs, and lead project quality reviews and risk assessments. Construction & Supplier Oversight: Manage owner-side quality surveillance across all disciplines (civil, mechanical, electrical, automation). Oversee supplier quality programs for critical GMP infrastructure and process equipment. Design & Engineering Quality: Review design quality processes, manage engineering deviations, and ensure design updates align with project standards. CQV & GMP Compliance: Coordinate with Commissioning, Qualification, and Validation (CQV) teams. Ensure all documentation supports FDA, EMA, and MHRA regulatory inspections. Audit & Team Leadership: Execute project audit programs, manage CAPAs, and foster a "right-first-time" quality culture across multidisciplinary contractor teams.
Required Qualifications
Education: Bachelor’s degree in Engineering, Construction Management, Life Sciences, or a related technical field.
Experience: 15+ years of capital project quality management experience.10+ years within pharmaceutical, biotech, or GMP-regulated industries. Proven track record on mega-projects exceeding $500M TIC.Complete project lifecycle experience (Design, Construction, CQV, Handover).
Skills: Deep knowledge of GMP requirements and pharmaceutical facility delivery.
Preferred Qualifications
Certifications: ASQ CMQ/OE, CQE, PE, or PMP.Project Expertise: Experience with cleanrooms, sterile processing, biologics, or cell and gene therapy facilities. Previous experience as an Owner’s Representative or managing EPCM oversight.

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