Senior Program Manager
$109,500–$208,500 year
HybridCampoverde, Lazio, Italian Republic
Job Summary
Lead matrixed cross-functional teams of scientists and engineers to manage large global projects for Oncology biologics programs, covering process development, manufacturing, quality assurance, and quality control across multiple sites. Implement site transfers, new indications, and lifecycle projects on time and within budget while proactively driving technical issues to closure by collaborating with R&D, Quality, and Supply Chain. Manage concurrent projects with minimal supervision, develop risk mitigation plans, and define budget requirements to report monthly actuals and schedules. After product launch, oversee capacity strategy, assurance of supply programs, and cost reduction initiatives across the network. Requires 10+ years in pharmaceutical manufacturing and plant experience.
Required Qualifications
- Bachelor's Degree in Engineering, science, or closely related discipline, or equivalent technical experience plus demonstrated competence
- 10+ years of combined experience in positions related to process development, project management, engineering/process support and manufacturing
- Must have strong knowledge of GMP Manufacturing, Supply Chain, Validation, Engineering, CMC technical development and pharmaceutical regulations
- Must have demonstrated organizational and planning skills, excellent verbal and written communication skills
- Must have demonstrated strong project management skills with successful delivery of projects
- Must be able to effectively facilitate the resolution of complex scientific, technical, analytical and business issues across functional lines
- Plant experience a must
Desired Qualifications
- PMP certification a plus
- Proficiency in multiple languages a plus
Hiring someone like this?
Get your role in front of qualified candidates on Sorce.