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Director, Facilities & Equipment Quality Strategy – Technical Oversight Support
Gilead Sciences. Provide global Quality leadership for GMP facilities, utilities, and equipment across the company network .
Posted 9/22/2026full-timeSanta Monica • California • United StatesLead💰 $191,250 - $247,500 per yearWebsite
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates extensive expertise in Quality leadership for GMP facilities, utilities, and equipment, ensuring compliance with cGMPs and regulatory requirements while driving continuous improvement and risk-based oversight.
Highest-signal resume keywords
Quality Oversight For GMP FacilitiesRisk-Based OversightCommissioning, Qualification, And Validation ExperienceCell And Gene Therapy Manufacturing KnowledgeCQE Or CQA Certification
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Quality AssuranceFacilities ManagementEngineering PrinciplesReliability EngineeringRegulatory ComplianceContinuous ImprovementControl StrategiesData AnalysisCorrective And Preventive ActionsProcess Design Approval
Soft Skills
LeadershipCollaborationMentoringCommunicationProblem-Solving
Certifications & Qualifications
CQECQA
Industry Keywords
CGMPRegulated EnvironmentPharmaceutical ManufacturingQuality StandardsGovernance ForumsNetwork-Wide HarmonizationStakeholder EngagementFacilities Lifecycle ManagementQuality ControlRisk Management
About the role
Key responsibilities & impact- Provide global Quality leadership for GMP facilities, utilities, and equipment across the company network
- Define and maintain enterprise policies, standards, and strategies with Facilities and Engineering
- Provide independent Quality review and approval across facilities, utilities, and equipment lifecycles
- Ensure compliance with cGMPs, company policies, and regulatory requirements through risk-based oversight, escalation, and approval
- Lead network-wide harmonization and continuous improvement
- Establish, maintain, evaluate, and improve control strategies
- Serve as global Quality subject matter expert in governance forums
- Provide Quality oversight and approval for new process design and facility start-up
- Oversee significant investigations, corrective and preventive actions, and network-wide lessons learned
- Provide Quality oversight and approval for regulatory submissions and inspections
- Apply GMP requirements, standards, and best practices for facilities, utilities, and equipment
- Analyze performance and reliability data to prioritize risks and guide decisions
- Represent Quality in regulatory interactions
- Partner with Global Quality, Facilities, Engineering, Manufacturing, suppliers, and other stakeholders
- Build network capability through knowledge programs, communities of practice, and mentoring
- Provide leadership and guidance supporting quality, compliance, accountability, and continuous improvement
Requirements
What you’ll need- PhD with 8+ years of relevant experience in facilities management, engineering, quality assurance, or a related field within a regulated environment OR Master’s degree with 10+ years of relevant experience OR Bachelor’s degree with 12+ years of relevant experience OR Associate’s degree with 14+ years of relevant experience OR High School Degree with 16+ years of relevant experience
- Demonstrated knowledge and application of scientific, engineering, and Quality principles across the lifecycle of facilities, utilities, and equipment in a regulated manufacturing environment
- Experience providing Quality oversight for commissioning, qualification, and validation of facilities, utilities, and equipment
- Experience leading global, cross-functional teams, programs, or initiatives involving facilities, utilities, and equipment quality
- Experience applying reliability engineering and risk-based principles to pharmaceutical or similar manufacturing assets
- Experience with cell and gene therapy manufacturing and associated facilities, utilities, and equipment requirements
- In-depth knowledge of regulations and industry expectations applicable to cell and gene therapy facilities, utilities, and equipment
- Relevant professional certification, such as CQE or CQA
Benefits
Comp & perks- Discretionary annual bonus
- Discretionary stock-based long-term incentives
- Paid time off
- Company-sponsored medical insurance
- Company-sponsored dental insurance
- Company-sponsored vision insurance
- Company-sponsored life insurance