Location
Providence, RI | United States
Job description
- Ability to work effectively in a cross-functional, matrixed environment, managing multiple tasks and priorities simultaneously.
- Bachelor s degree in engineering, life sciences, or related field required; advanced degree or PMP certification preferred.
- Minimum 6 years of experience in biopharmaceutical or medical device industry, with at least 3 years in project management.
- Strong organizational skills, ability to thrive in a fast-paced environment, and comfortable managing high-visibility projects.
- Proficiency in Microsoft suite (Project, PowerPoint, SharePoint, Word, Excel, Outlook, Teams, OneNote, Visio, PowerBI) required.
- Previous experience in Quality/Manufacturing/Product Development or EU Medical Device Regulation (MDR) or CE Marking preferred.
- Experience interacting with Senior Management and connecting enterprise strategy to project objectives.
- Expertise in developing complex project timelines and defining project scope.
- Capability to convey project timelines visually using tools like Gantt Charts.
- Strong written and verbal communication skills, with a sense of urgency and accountability.
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- Dice Id: 91099677
- Position Id: 8195315
Job tags
Salary
