PROJECT MANAGER III
On-siteLargo, Florida, United States
Job Summary
Lead multiple complex, high-risk, and strategic customer projects simultaneously from initiation through commercial execution, directing teams across R&D, manufacturing, and supply chain. Develop comprehensive project strategies that align customer expectations with organizational capabilities while managing scope, schedule, quality, budget, and risk. Serve as the primary strategic liaison for key accounts, building trusted partnerships and leading executive-level governance meetings. Manage a portfolio of projects exceeding $5M in value, prioritizing initiatives and monitoring financial performance to ensure milestone collection and profitability. Anticipate challenges, implement mitigation strategies, and remove barriers affecting execution. Represent the company during customer audits and regulatory interactions as needed.
Required Qualifications
- Bachelor's degree in Business, Engineering, Life Sciences, Pharmaceutical Sciences, Chemistry, or related discipline
- Minimum 10+ years of progressive project management experience
- Minimum 5 years managing complex technical projects within pharmaceutical, OTC, medical device, cosmetic, or CDMO manufacturing environments
- Demonstrated experience leading cross-functional teams
- Experience managing multiple concurrent projects exceeding $5M in combined portfolio value
- 5+ years of Clinical Pharmaceutical/RX Project Management Experience
Desired Qualifications
- Project Management Professional (PMP) certification
- Lean Six Sigma Green Belt or higher
- Experience within FDA-regulated manufacturing environments
- Knowledge of cGMP regulations
- Experience with Stage-Gate product development processes
- Experience with technology transfer and commercialization projects
- Experience implementing PMO standards and governance
- PMP Certification
- Lean Six Sigma certification
- Advanced project management or leadership training
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