Job Description

Chipton-Ross is seeking a Project Manager Scientific II for a contract opportunity in Round Lake, IL.

BASIC QUALIFICATIONS (REQUIRED SKILLS/EXPERIENCE):
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.
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

POSITION RESPONSIBILITIES:
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.
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

PREFERRED QUALIFICATIONS (DESIRED SKILLS/EXPERIENCE):
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.

REQUIRED EDUCATION:
Accredited B.S. degree.

WORK HOURS:
Full Time, First Shift

Job Tags

Full time, Contract work, Relocation,

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