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Quality Project Manager, Cell and Genetic Therapies (Contract)Apply Now

Location: Boston, Massachusetts 02210
Employment Type: Contract

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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.

  • 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. 

  • 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.).   


Eric Carmody
Life Science Recruiting Manager

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