About the job:
This is an exceptional opportunity for a forward-thinking, data-driven professional to join a premier, global biopharmaceutical leader at their state-of-the-art facility.
If you excel at bridging the gap between engineering, manufacturing, and quality teams, this role offers an incredible platform to control the full lifecycle of a project
This position requires 3 onsite requirements.
Key Responsibilities
Operational Readiness Execution: Support end-to-end readiness planning across critical validation and manufacturing milestones. Maintain a proactive 12-18 month outlook to ensure equipment, testing, and production activities are perfectly sequenced for a safe start-up.
Cross-Functional Alignment: Align readiness plans across Manufacturing, Quality, Engineering, and EHS into a single, cohesive workflow. Ensure team handoffs, constraints, and critical dependencies are transparent and actively managed.
Progress Tracking & Metrics: Establish structured tracking mechanisms to monitor project health. Validate updates from various departments, manage data-driven reporting cycles, and provide leadership with clear visibility into training status and action closures.
Risk Mitigation: Proactively identify project bottlenecks, schedule conflicts, and operational risks. Partner with key stakeholders to define robust mitigation plans and escalate critical issues to ensure safe and reliable operations.
Skills, Attributes & Experience:
Degree (Level 8 or Bachelor's) in a relevant Science or Engineering discipline.
Prior experience within a manufacturing or large-scale project environment in the pharma or biotech sector is required.
A solid understanding of project lifecycle phases, including commissioning, qualification, and operational readiness within a regulated environment.
Strong proficiency in MS Office, project management software, and a proven ability to build dashboards or data visualizations.
Great communication, and problem-solving skills with the ability to drive accountability across diverse teams.
