Quality Project Manager, Cell and Genetic Therapies (Contract)Apply Now
Location: Boston, Massachusetts 02210
Employment Type: Contract
Job Description
Contract Length: 6 months; hybrid position
Job Summary: The Quality Project Manager will be responsible for supporting cross-functional project teams executing Quality strategies within multiple programs.
Responsibilities:
Requirements:
Job Summary: The Quality Project Manager will be responsible for supporting cross-functional project teams executing Quality strategies within multiple programs.
Responsibilities:
- Work closely with area leads to develop and maintain integrated dashboards/ project plans.
- Identify/communicate interdependencies as well as critical path activities for the project(s).
- Track and monitor key milestones and decision points and work with team members to meet commitments and drive delivery of objectives.
- Be the central source of information for the project(s)
- Effectively communicate with team members, and key stakeholders on the status, objectives, risks, and mitigation plans associated with projects.
Requirements:
- Bachelor’s degree in engineering, life sciences or related field. Advanced degree (MS, or MBA) and/or PMP Certification preferred.?
- A minimum of 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.?
- A minimum of 3 years of experience in project management of pharmaceutical or medical devices.
- Experience interacting with Senior Management
- Working knowledge of cGMPs, and drug/device development lifecycle.
- 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.).
Contact
Eric Carmody
Life Science Recruiting Manager
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