Contract Duration: 12 months (with potential extension)Working Model: OnsiteDiscipline: Engineering / Project DeliveryRole OverviewAn experienced Senior Project Engineer is required to support the delivery of capital and improvement projects within a GMP-regulated pharmaceutical manufacturing site. The role sits within a global engineering framework and is responsible for managing projects from concept through commissioning and qualification, ensuring delivery to scope, schedule, cost, quality, and EHS standards.This is a hands-on project delivery role, requiring strong cross-functional coordination and technical problem-solving capability in a live manufacturing environment.Project Delivery & LeadershipLead engineering projects end-to-end, ensuring delivery on time, within budget, and aligned to business objectivesScope new engineering projects and support capital approval processesCoordinate commissioning, qualification, and handover activitiesLead and participate in cross-functional project teamsManage interfaces with internal departments and external suppliersEngineering & Technical SupportTroubleshoot process and equipment issues impacting manufacturingReview existing systems (process, E&I, structural, safety, and documentation)Support constructability, maintainability, and operability assessmentsCoordinate P&IDs, technical documentation, and engineering deliverablesProject ControlsProject cost estimating, forecasting, tracking, and reportingProject scheduling, progress reporting, and risk managementResource planning and coordinationConduct retrospective project reviews and lessons learnedCompliance & QualityEnsure compliance with cGMP, EHS, and site engineering standardsSupport deviation investigations and corrective actionsEnsure documentation is completed in line with GDP requirementsSupport validation, MSAT, operations, facilities, and quality teamsStakeholder EngagementProvide regular updates to management and stakeholdersFacilitate effective communication across project teamsSupport training related to new or modified equipment/processesQualifications & ExperienceThird-level qualification in Engineering or ScienceMinimum 3 years’ experience in a pharmaceutical or regulated manufacturing environmentProven experience delivering engineering projects in a GMP settingExperience with Lean, Six Sigma, or structured problem-solving methodologiesExperience working within large, multinational engineering teamsStrong working knowledge of MS Word, Excel, and OutlookStrong teamwork and collaboration skillsCustomer- and results-focused mindsetHigh attention to detail and strong technical aptitudeEffective problem-solving and decision-making abilityAdaptable, proactive, and self-motivated
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