Senior Construction Quality Manager - GMP & CQV (Pharma)

KBR, Inc.; Richmond (VA); Vor Ort; USD 180.000 - 240.000; Vollzeit

Zusammenfassung

KBR, Inc. seeks an experienced Construction Quality Manager to oversee quality performance on a major pharmaceutical manufacturing project in the United States.

The role will supervise EPCM contractors, construction teams, suppliers, and inspectors to ensure GMP, codes, and project specs are met through design, CQV, startup, and handover. Responsibilities include establishing the Project Quality Management Plan, governance, audits, supplier QA programs, and readiness for FDA/EMA inspections.

Qualifikationen

• Bachelor's degree in Engineering, Construction Management, Quality Management, Life Sciences, or related technical discipline.
• 15+ years of quality management experience on major capital projects.
• 10+ years in pharmaceutical/Life Sciences GMP environments.
• Experience leading quality programs on projects >$500M TIC.
• Experience across design, construction, CQV, startup, and handover phases.
• Extensive GMP knowledge and pharmaceutical facility delivery processes.
• Proven ability to lead multidisciplinary quality organizations and contractor teams.

Aufgaben

• Develop and implement the Project Quality Management Plan (QMP).
• Lead project quality reviews, audits, management assessments, and compliance evaluations.
• Oversee design quality review processes and contractor quality programs.
• Manage owner-side QA/QC across civil, structural, architectural, mechanical, electrical, instrumentation, automation, utilities, and process installation activities.
• Coordinate CQV readiness with Commissioning, Qualification, Validation, and Compliance teams.
• Lead quality investigations of nonconforming work and maintain quality dashboards.

Kenntnisse

Quality leadership

GMP knowledge

QA/QC oversight

Audit programs

Regulatory readiness

Ausbildung

Bachelor's degree in Engineering/Quality

Jobbeschreibung

KBR, Inc. seeks an experienced Construction Quality Manager to oversee quality performance on a major pharmaceutical manufacturing project in the United States.

The role will supervise EPCM contractors, construction teams, suppliers, and inspectors to ensure GMP, codes, and project specs are met through design, CQV, startup, and handover. Responsibilities include establishing the Project Quality Management Plan, governance, audits, supplier QA programs, and readiness for FDA/EMA inspections.