Senior PMO / Transition Project Manager – Pharmaceutical Manufacturing SitePara ser considerado para una entrevista, por favor, asegúrese de que su solicitud se ajusta plenamente a las especificaciones del puesto que se encuentran a continuación.Location:Valles OrientalIndustry:Pharmaceutical ManufacturingContract Type:Project-based consultingProject Duration:~6 monthsStart:ImmediateRole OverviewWe are seeking an experiencedSenior PMO / Project Managerto support acritical pharmaceutical manufacturing site transition to new management. This large and complex transformation project requires strongproject governance, operational coordination, and regulatory compliance oversight.The PMO will be responsible for establishing arobust project management framework, ensuring alignment across all functional workstreams, and delivering the project within the remaining timeline while maintainingGMP compliance and operational continuity.This role requires strong experience inpharmaceutical manufacturing environments, cross-functional leadership, and the ability to operate in ahigh-visibility, high-urgency project environment.Key ResponsibilitiesProject Governance & PlanningEstablish and implement theoverall project governance structureacross all relevant functions including Quality, Regulatory, Supply Chain, HSE, Manufacturing, IT, and HR.Develop and maintain acomprehensive project roadmap, including milestones, deliverables, timelines, and critical path.Define and manageproject workstreams, ensuring clear ownership and accountability.Lead regularproject governance meetings and steering committee updates.Project Management & ExecutionCoordinate project execution across multiple workstreams to ensuretimely and compliant delivery.Monitor project progress against definedKPIs, milestones, and deliverables.Provideclear and structured project reportingto stakeholders and leadership.Escalate risks, delays, or resource constraints in a proactive and structured manner.Risk Management & ComplianceIdentify and manageproject risks, particularly those related to:GMP complianceRegulatory requirementsData integrityOperational continuityLegal and quality standardsDevelop and monitorrisk mitigation and contingency plans.Ensure project documentation and processes remainaudit-ready at all times.Documentation & ReportingEstablish and maintainstructured project documentation, including:Project plansRisk registersIssue logsGovernance documentationProgress reportsProvideaccurate and objective reportingto the project team and executive stakeholders.Operational Transition CoordinationSupport coordination of activities related to:Business Continuity Planning (BCP)Asset transferWorkforce transitionKnowledge transfer and documentationEnsure alignment between operational teams during the transition.Plant Entanglement & Separation ManagementLead theidentification and assessment of operational entanglementswithin the plant.Coordinate the development and follow-up ofremediation plans and service agreementsrequired for operational separation or transition.Workstream CoordinationEnsure structuredlaunch and coordination of project workstreams.Facilitate collaboration between internal teams and external partners.Providead-hoc project supportwhen required (e.g., internal audit feedback loops, compliance processes).Required Experience8–15+ years of experience inProject Management / PMO roles.Strong experience managingcomplex transformation projects in pharmaceutical manufacturing environments.Proven experience implementingproject governance frameworks and structured PMO processes. xcskxlj Strong understanding ofGMP and pharmaceutical regulatory environments.Experience coordinatingcross-functional teamsacross Quality, Regulatory, Manufacturing, Supply Chain, and HSE.Key CompetenciesStrongproject planning and execution skillsExcellentstakeholder management and communicationAbility to operate inhigh-pressure environments with tight timelinesStrongrisk management and problem-solving capabilitiesStructured, detail-oriented, andhighly organizedPreferred QualificationsExperience withmanufacturing site transitions, carve-outs, or ownership transfersExperience inpharma operational transformation programsPMP, Prince2, or similarproject management certification