Analyze and normalize multiple streams of data to gauge the health of the risk management system
Work with Subject Matter Experts (SMEs) to create a framework for Risk-based dashboards to be used for real-time decision-making and management reporting
Provide detailed input to stakeholders on how to implement risk controls as well as create and implement controls
Identify inefficiencies in Medline’s global quality management system
Take action to address identified inefficiencies
Develop timelines for all projects and ensure that deadlines and goals are being met
Frequently update management and team on progress
Proactively work with members of the division or project team to identify issues that might delay the project; make recommendations to improve timelines for project completion

Requirements

Bachelor of Science Degree in Biology, Chemistry, Engineering or Statistics-based degree
At least 2 years of QA/QE experience in a cGMP Device or environment
Complete device life cycle experience related to design, production, use of a device, and ISO 14971
Experience with Data visualization tools/business intelligence tools such as Tableau, Power BI, or Qlik
Experience leading multiple, complex projects
Strong ability to manage multiple priorities
Self-starter attitude
Good oral and writing skills
Ability to work independently and as a team in an efficient manner

Benefits

Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

data analysisrisk managementrisk controlsquality managementproject managementdata visualizationbusiness intelligencecGMPISO 14971device life cycle

communicationteamworkproblem-solvingtime managementself-starterorganizational skillsleadershipadaptabilityproactive approachattention to detail