Join a leading global pharmaceutical manufacturer dedicated to sustainability and societal well-being. Reporting directly to the Engineering Projects & Systems Lead, you will drive CAPEX and non-CAPEX projects from initiation through to final handover. This dynamic role offers full ownership of project life cycles, budgets, and cross-functional team leadership within a progressive, collaborative culture.
Key Responsibilities
- Project Management: End-to-end delivery of engineering projects, including feasibility studies, goal-setting, scheduling, and resource coordination.
- Financial Accountability: Full ownership of project cash flow and budget management.
- Leadership: Motivate and guide internal cross-functional teams and external vendors/service providers.
- Validation & Compliance: Lead the generation and execution of cGMP validation and lifecycle documentation (URS, FDS, FAT, SAT, IQ/OQ, Risk Assessments).
- Systems Support: Maintain MES-controlled documents, including System Configuration and Descriptions.
- Handover & Review: Ensure controlled business unit handovers and conduct post-project evaluations for continuous improvement.
What We Are Looking For
Essential:
- Proven project engineering/management or validation experience within a pharmaceutical manufacturing environment.
- Demonstrated track record of delivering equipment and engineering projects on time and within budget.
- Strong financial acumen relating to engineering project performance.
- Deep understanding of the project lifecycle from concept through to qualification.
- Exceptional communication, analytical problem-solving, and time-management skills, with the ability to thrive and prioritize in a fast-paced environment.
Preferred:
- Direct experience in drug manufacturing.
- Experience within a cGMP start-up environment.
