 
        
        Job description
QAQC Project Controls – Mechanical Bias
Purpose of the Role
Every day we help our major global clients deliver ambitious and highly technical projects, worldwide. Our team is dynamic, innovative, and client-focused, supported by an inclusive and fun company culture. Our clients value our proactive approach, depth of expertise, integrity and the quality we deliver. As a result, our people get to enjoy working on some of the most exciting projects in the world.
The QA/QC Project Controls Specialist is responsible for ensuring the integrity, accuracy, and consistency of project controls data while maintaining compliance with quality standards across the lifecycle of data centre construction projects. This role bridges
project controls
,
cost and schedule management
, and
quality assurance
to ensure deliverables meet performance, reliability, and documentation standards expected in high-specification data centre environments.
Key Deliverables
The following duties fall within the purview of this role:
 * Develop, implement, and maintain QA/QC procedures in alignment with company and client standards.
 * Conduct regular audits on cost, schedule, and change control documentation to verify compliance and accuracy.
 * Manage non-conformance reports (NCRs), corrective actions, and root cause analysis.
 * Ensure subcontractor quality documentation aligns with project QA/QC requirements.
 * Review and verify data integrity within project control systems (Primavera P6, Power BI, Excel, etc.).
 * Interface with construction management, engineering, commissioning, and client representatives to ensure quality objectives are met.
 * Lead QA/QC progress meetings and maintain transparency on quality metrics.
 * Support lessons-learned sessions and contribute to continuous improvement initiatives across data centre projects.
Experience & Education
 * Must have a mechanical degree or equivalent
 * Minimum of 5+ years of document control experience
 * Knowledge of quality systems and regulatory requirements (21 CRF Part 11/210/211 – ideal but not essential)
 * Demonstrated knowledge/subject matter expertise in GMP, SOPs and quality systems
 * Works on multiple assignments in collaboration with various department system/project owners
 * Advanced Skills with MS Office applications Word, Excel, Access, Adobe Acrobat
 * Experience transitioning manual to electronic systems experience highly preferred
Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job. Duties, responsibilities, & activities may change at any time with or without notice. Daily interactions will be overseen in the UK by the Managing Director UK/EMEA. An employment contract will be implemented, providing the professional service processes related to pay, health/medical benefits, personal time, approved bank holidays, pension, & any additional benefits for our full-time employees in the UK, Europe, Middle East, Operations.