---

---

Location

Providence, RI | United States

---

Job description

Quality Project Manager


Must Have:

• Bachelor s degree in engineering, life sciences or related field. Advanced degree (MS, or MBA) and/or PMP Certification preferred.?
• 6+ years of experience in the biopharmaceutical or medical device industry.
• Previous experience in Quality/Manufacturing/Product Development or EU Medical Device Regulation (MDR) or CE Marking preferred.?
• 3+ years of experience in project management of pharmaceutical or medical devices.
• Working knowledge of cGMPs, and drug/device development lifecycle.
• Ability to work effectively in a cross-functional, matrixed environment, prioritizing and managing multiple tasks simultaneously, integrating cross-functional issues and balancing competing priorities effectively.
• Experience independently developing complex project timelines, define project scope, convey timeline visuals (Gantt Charts)
• Expertise in Microsoft suite (Project, PowerPoint, SharePoint, Word, Excel, Outlook, Teams, OneNote, Visio, PowerBI). Experience with other PM tools a plus (e.g., Think-Cell, OnePager, Office Timeline, etc.).

Report this job

• Dice Id: gardner
• Position Id: 10331

---

Job tags

---

---

Salary