Project Engineer - 12 Month Contract

This position is a Fixed-Term Contract (FTC) role with a duration of 12 months.Job PurposeThe Project Engineer is responsible for the planning, execution, and delivery of capital and technical projects that support manufacturing, packaging, utilities, and facility operations. This role ensures projects are delivered safely, on time, within budget, and in compliance with GMP, safety, and regulatory requirements. The Project Engineer partners cross‑functionally with Operations, Quality, Validation, EHS, Maintenance, and external contractors to support business growth, lifecycle management, and continuous improvement initiatives in a pharmaceutical manufacturing environment.Key ResponsibilitiesProject Management & ExecutionLead capital and expense projects from concept through commissioning and handover.Develop project scopes, schedules, cost estimates, URS and execution plans.Manage contractors, vendors, and internal resources to ensure safe and compliant execution.Track project progress, risks, and budgets; communicate status to stakeholders.GMP Compliance & Quality SystemsSupport Change Controls, Deviations, CAPAs, and Quality Records related to projects.Ensure project activities comply with GMP, safety, and regulatory standards.Support equipment qualification and validation activities (IQ/OQ/PQ).Ensure that on the day the new equipment starts running, the PM schedules, spare parts, and SOPs are already live in the CMMS (Maintenance System).Validate that all vendors meet compliance standards and are active in the approved vendor list.Capital Planning & Asset Lifecycle ManagementSupport capital planning, justification, and prioritization activities.Coordinate equipment upgrades, replacements, and obsolescence initiatives.Ensure effective turnover of projects to Operations and Maintenance.Cross-Functional CollaborationAct as a liaison between Engineering, Operations, Quality, Validation, EHS, and Maintenance.Support training, knowledge transfer, and documentation related to new systems and equipment.Continuous ImprovementIdentify opportunities to improve safety, reliability, efficiency, and cost.Support Lean, TPM, automation, and digital manufacturing initiatives.Promote standardization and engineering best practices across the site.Key Performance IndicatorsProject ExecutionProjects delivered on time and within budget (90%)Contractor safety performance and complianceEffective project turnover and documentation completionOperational PerformanceReduction in project‑related downtime and disruptionsSuccessful startup and performance of new equipmentQuality & ComplianceOn‑time closure of Change Controls, Deviations, and CAPAs (91%)Audit findings related to project execution (count/severity)Maintenance & ReliabilityPreventive maintenance readiness at project handover (100%)Reduction in repeat issues related to new installationsContinuous ImprovementNumber of improvement initiatives supportedCost savings or avoidance achieved ($)Our Ideal Candidate:Strong technical knowledge of manufacturing, packaging equipment, and utilities in a GMP‑regulated environment.Proven experience managing capital projects, equipment installations, and contractors.Solid understanding of GMP compliance, including change control, deviations, CAPAs, and equipment qualification (IQ/OQ/PQ).Experience supporting pharmaceutical manufacturing or packaging operations.Engineering degree or similar degreePMP - Project Management ProfessionalPgMP - Program Management ProfessionalLean Six Sigma Black BeltCMRP - Certified Maintenance & Reliability ProfessionalSkills and Experience:Effective cross‑functional collaboration with Operations, QA, Validation, EHS, and Maintenance.Strong organizational, communication, and problem‑solving skills.Ability to lead individual projects while co-ordinating with site stakeholdersAbility to co-host meetings with PMODemonstrated knowledge of GMPs and Pharma standardsManage vendors and ensure CAPEX are in line with company policies and standardsCooperating and communicating with the project manager and other project participants and collaborating with senior engineers to create more efficient project methods and to maintain the project's profitability.Experience in Pharmaceutical Production or support, with a exposure to Technical Transfer of Pharmaceutical products and production is desirable but not essential based on the production skills demonstrated with evidenceKnowledge and experience of pharmaceutical manufacturing processes, process development and validation,Exposure to automation, equipment installations, and validation activities.Experience supporting manufacturing and packaging operations.Working knowledge of HVAC, utilities, and facility systems.