What are the responsibilities and job description for the Project Manager Scientific II position at Integrated Resources, Inc?
Title: Project Manager, Sterility Assurance
Location: Round Lake, IL
Duration: 12 Months
Summary of Role:
" 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.
Description of Role:
" 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.
Responsibilities include:
" 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
Qualifications. The preferred candidate will have:
" 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
o Knowledge of GDP/GMP/GLP practices.
o Pharmaceutical or Medical Device knowledge is desirable.
" Degree in management, engineering, or science related field.
o B.S. with greater than 4 years of related experience.
Location: Round Lake, IL
Duration: 12 Months
Summary of Role:
" 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.
Description of Role:
" 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.
Responsibilities include:
" 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
Qualifications. The preferred candidate will have:
" 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
o Knowledge of GDP/GMP/GLP practices.
o Pharmaceutical or Medical Device knowledge is desirable.
" Degree in management, engineering, or science related field.
o B.S. with greater than 4 years of related experience.
