Job Details

ID #44715735
State Massachusetts
City Boston
Job type Contract
Salary USD competitive competitive
Source Real Staffing
Showed 2022-08-09
Date 2022-08-09
Deadline 2022-10-08
Category Et cetera
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Contract - Quality Assurance Project Manager in Boston

Massachusetts, Boston, 02108 Boston USA

Vacancy expired!

Title: Contract - Quality Assurance Project Manager

Location: Boston (On-site)

Duration: 6+ Month contract

About the Company: A global Pharmaceutical Company

Benefits: Real Staffing offers medical, dental, vision, 401K, voluntary life insurance, short term/long term disability.

About the Role: The Senior Project Manager, Quality Projects will be responsible for managing multiple cross functional Google Cloud Platform and GMP submission and inspection readiness workstreams. This will include organizing teams, managing project schedules, developing project metrics, and developing material that will be presented in governance meetings. This role will collaborate with Sr. leadership within the Quality organization, as well as operational stakeholders in the GMP and Google Cloud Platform areas.

Your Main Responsibilities
  • Collaborate with Quality Leadership to develop and scope submission and inspection readiness workstreams. This will include identifying project team members for given workstreams
  • Create and manage workstream project schedules according to business needs.
  • Ensure deliverables are monitored to the agreed upon timelines, collaborating with workstream leads
  • Work with teams to resolve and find solutions to challenges as they come up. Will escalate project and scheduling challenges that are unable to be resolved to management
  • Collaborate with teams to develop metrics to measure progress and highlight any areas of focus
  • Set-up and facilitate routine meetings to drive the project and create awareness
  • Create meeting materials used for project status updates at governance meetings.

Requirements
  • Bachelor's degree in life sciences, computer science, economics or other discipline requiring quantitative skills preferred
  • 6 to 8 years of experience in biopharmaceutical/pharmaceutical or related industry with strong background in quality and continuous improvement
  • Experience with organizing cross functional teams and motivating them to achieve common goals
  • Preference for experience in managing regulatory submission projects
  • Preference for experience in cell and gene therapy

EOE Statement: Specialist Staffing Group is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status.

To find out more about Real please visit

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