Support lifecycle upgrades, VCR implementation, regulatory compliance initiatives and product robustness improvements that enhance manufacturing reliability, compliance and supply continuity
Ensure project schedules reflect GMP, validation, quality, regulatory and manufacturing constraints, with active management of non-compliance, rework and supply interruption risks
Integrate production windows, shutdowns, campaign plans, PPQ batches, cleaning validation, stability, sampling and quality release dependencies into executable project schedules
Assist project teams in developing execution strategies that balance compliance expectations, operational readiness, safety, cost, resource availability and manufacturing commitments
Develop, maintain and govern integrated Level 3 and Level 4 schedules covering engineering design, procurement, construction, commissioning, qualification, validation, regulatory, quality and operational readiness activities
Support Project Managers and Project Engineers in planning, monitoring and controlling schedule milestones, critical paths, interfaces, float, constraints and key deliverables
Establish, maintain and control schedule baselines through formal change control, impact assessment and governance processes
Qualifications
What makes you remarkable?
At Wood, we are committed to equal opportunities and welcome all talented individuals to consider joining our team. So even if you don't match every statement below but feel you have some of the experience, knowledge or skills needed for this role, we encourage you to apply. It will take all of us working together to deliver solutions to the world’s most critical challenges.
Tertiary qualification in engineering, science, project management, construction management, planning/scheduling or a related technical discipline
Formal training or certification in project controls, Primavera P6, Oracle Primavera Cloud, AACE, PMI-SP or equivalent is preferred
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Minimum 3–5 years' experience developing and maintaining integrated project schedules within pharmaceutical, biotechnology or other GxP-regulated industries
Demonstrated experience supporting LCM, validation, qualification, capital or compliance projects in a manufacturing environment
Advanced Primavera P6 and Oracle Primavera Cloud (OPC) scheduling and project controls capability
Strong understanding of pharma/biotech GMP environments, including qualification, validation lifecycle management, change control, data integrity, deviation/CAPA interfaces and regulatory compliance requirements
Knowledge of pharmaceutical Lifecycle Management (LCM), Validation Change Requests (VCR), Process Performance Qualification (PPQ) and technology transfer activities
Experience integrating commissioning, qualification and validation activities into project schedules
If you’re an experienced Project Planner, and ready for an exciting role, then we are keen to hear from you today.
Apply now and take the next step in your career with this exciting opportunity!