Job description
This role will offer you:
- An opportunity to join a world leader within Cell Therapy and be influential in the direction of the company.
You will be responsible for:
- Lead matrixed teams internally and with CDMOs to support GMP production, including production of plasmid DNA, viral vector, and cell drug product (as required).
- Identify opportunities for continuous improvement and innovation initiativeto enhance manufacturing efficiency, productivity, and quality.
- Develop and lead cross-functional virtual site teams (VSTs) that include representatives from MSAT, Quality, QC, and Supply Chain and are accountable for product supply from CDMOs
- Proactively identify potential manufacturing risks and challenges and develop contingency plans to address issues that may arise during production.
- Plan, track, and manage manufacturing timelines, deliverables, and budgets for multiple projects simultaneously.
You will bring the following:
- BSc, MSc or PhD in a Scientific or Engineering discipline along with significant industry experience managing external partners.
- Strong knowledge of Cell and Gene Therapy manufacturing processes preferred, biopharma experience essential.
- Familiarity with regulatory standards and quality systems in the biopharmaceutical industry.
- Strong project management, organization, collaboration, and conflict resolution skills and experience.