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How would you like the opportunity to work with in one of the largest biopharmaceutical projects in the world? If yes, then this is the assignment for you!
Our client is currently seeking the skills of a Project Manager to join their team. Our client develops and delivers life changing medicines to millions of people globally and as part of their growth. With their Drug Substance (DS) manufacturing network growing rapidly, they are committed to growing their portfolio of commercial biologics products supplied worldwide – and this is your opportunity to be involved!
What You'll Do
- Support project managers in planning and delivering defined work scopes on time and within budget.
- Coordinate daily activities with project team members to ensure timely completion.
- Act as package or area lead within projects.
- Prepare regular reports and presentations for stakeholders.
- Track actions and mitigation activities in the project risk management plan.
- Organize and lead effective work sessions (e.g., PDR meetings).
- Ensure compliance with project management processes (CPDP), engineering standards, and safety regulations.
- Assist in resource planning and cost optimization.
- Contribute to sourcing strategy, vendor negotiations, and integration of multiple suppliers.
- Coordinate permitting of planned assets and manage supplier performance.
- Participate in Mechanical Completion walkdowns and close punch items.
- Support commissioning, qualification, and system start-up activities.
- Manage lifecycle documentation, including as-built drawings and O&M packages.
- Oversee FAT and SAT events, documentation, and deviation closure.
- Experience as a Project Manager, ideally within pharmaceutical environments.
- Proven background in GMP compliance and clean room projects.
- Strong stakeholder and vendor management skills.
- Ability to work on-site as required.
Ready to apply?
Join QCS Staffing and take your career to the next level!
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