Quality Lead
Enregistrez cette offre et organisez votre recherche
Créez un compte gratuit pour enregistrer des offres d'emploi, créer des alertes et revenir à cette liste depuis votre tableau de bord.
PM Group are seeking an experienced Quality Lead (Turnover) to oversee all site quality matters, with primary focus on Turnover activities for a major pharmaceutical construction project in Ghent, Belgium. This critical role requires a seasoned professional to establish and maintain the highest quality standards throughout the construction and commissioning phases of a state-of-the-art pharmaceutical manufacturing facility.
Responsibilities
The successful candidate will be responsible for implementing comprehensive quality management systems, ensuring GMP compliance, and managing all quality-related activities from construction through to facility handover and validation.
Managing Project Completions for multiple systemsApproval of Vendor Turnover Packages (VTOPs)Approval of Trade Turnover Packages (TTOPs)Coordination of Trade WalkdownsPunchlist Management and closeoutManaging Engineering Document ControlTransfer of VTOPs & TTOPs to OperationsReceipt, review and acceptance of As Built DrawingsManagement of Non GMP Change ControlsAuditing of the following groups to ISO and project standards:Construction Management TeamConstruction ContractorsSuppliers and VendorsMetrics tracking and reporting in relation to Completions, Turnover and QualityProvide expertise and guidance in relation to construction QA for all construction activities onsiteEstablish a ‘Right First Time’ culture onsite.Ensure all construction activities comply with Good Manufacturing Practice requirements and regulatory standardsDirect daily quality activities across all construction disciplines and contractorsOversee quality documentation, IQ/OQ protocols, and validation master plansCoordinate internal and external quality audits, regulatory inspections, and client assessmentsLead investigation and resolution of quality issues and deviationsMonitor subcontractor quality performance and compliance with project specificationsDeliver quality training programs for project teams and contractorsQualifications
Degree in Engineering, Science, Quality Management, or related disciplineMinimum 8+ years in quality management roles on major construction / engineering projectsProven experience in pharma facility construction quality managementDeep understanding of GMP, and Belgian/EU pharmaceutical regulationsExtensive experience with ISO 9001, quality management systems, and validation processesFluent English essential; Dutch/French advantageousQualified internal auditor with experience managing regulatory inspectionsProfessional quality qualification advantageous Experience with cleanroom construction and controlled environment validation advantageousUnderstanding of pharmaceutical engineering standards
D&I
Inclusion and Diversity are core to our culture and values. Wherever we work, we commit to a culture of mutual respect and belonging by building a truly inclusive workplace rich in diverse people, talents and ideas. Valuing the contributions of all our people and respecting individual differences will sustain our growth into the future.
PM Group is committed to ensuring our hiring process is fair and accessible to all and will provide candidates with disabilities with reasonable accommodations required to participate in the recruitment process. If you require any assistance in this regard, please let us know.
For more company information visit our company website > Meet Our Team - careers | PM Group
#LI-EB1
The successful candidate will be responsible for implementing comprehensive quality management systems, ensuring GMP compliance, and managing all quality-related activities from construction through to facility handover and validation.
Managing Project Completions for multiple systemsApproval of Vendor Turnover Packages (VTOPs)Approval of Trade Turnover Packages (TTOPs)Coordination of Trade WalkdownsPunchlist Management and closeoutManaging Engineering Document ControlTransfer of VTOPs & TTOPs to OperationsReceipt, review and acceptance of As Built DrawingsManagement of Non GMP Change ControlsAuditing of the following groups to ISO and project standards:Construction Management TeamConstruction ContractorsSuppliers and VendorsMetrics tracking and reporting in relation to Completions, Turnover and QualityProvide expertise and guidance in relation to construction QA for all construction activities onsiteEstablish a ‘Right First Time’ culture onsite.Ensure all construction activities comply with Good Manufacturing Practice