Project Manager, Sterility Assurance

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Company: Katalyst HealthCares and Life Sciences

Location: Round Lake, IL 60073

Description:

Job Summary:
This position will support the Sterility Assurance R&D organization by coordinating activities related to separation and R&D footprint activities. Including, but not limited to, setting up project management tools, leading meetings, and tracking work activities, as described in the Description of Role section.
Responsibilities:
  • Project management key activities related to the setup of the Sterility Assurance team for success as part of a new company.
  • Coordinate the plans, meetings, updates and closure of activities related to both separation and site relocations for footprint activities.
  • Develop tools that enable Sterility Assurance to work through separation and support the new company after separation. Examples include a tool to facilitate resource and testing support needed by other teams within the company.
  • Coordinate project to facilitate learning sessions and a community of practice within the company.
  • Provide regular updates to Sterility Assurance management.
  • Coordinate Sterility Assurance planning and execution of activities for separation and R&D footprint changes, including but not limited to knowledge transfer and setup of contract testing lab services. And report this information out to management and the Sterility Assurance team.
  • Coordinate activities with other functions outside of Sterility Assurance.
  • Developing online tools for other functions to request Sterility Assurance 1) resources for support of projects and 2) sample sterilization processing.
  • Coordinate activities in support of the Sterility Assurance in depth "Residency" Training.
Requirements:
  • Experience in project management.
  • Experience in software tools, such as SharePoint and Power BI.
  • Ability to effectively coordinate in cross-functional teams with limited guidance.
  • Strong organizational skills.
  • Strong communication skills.
  • Desirable Skills.
  • Knowledge of GDP/GMP/GLP practices.
  • Pharmaceutical or Medical Device knowledge is desirable.
  • Degree in management, engineering, or science related field.
  • B.S. with greater than 4 years of related experience.

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