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Quality Assurance III

Job in North Chicago, Lake County, Illinois, 60086, USA
Listing for: The Fountain Group
Full Time position
Listed on 2026-02-03
Job specializations:
  • Healthcare
    Data Scientist
Salary/Wage Range or Industry Benchmark: 60000 - 80000 USD Yearly USD 60000.00 80000.00 YEAR
Job Description & How to Apply Below

Overview

Bill: $65.67
Pay: $46-$43
Spread:
Duration: 10 months

Job Description

This individual will work in the Global Quality System & Strategic Transformation organization supporting global projects and initiatives related to Quality Risk Management. Activities include all aspects of project management such as leading global projects, creation of deliverables, working with stakeholders and driving technical enhancements. The individual will directly work with the Global Quality Risk Management team and be responsible for assessing regulations, developing governance, executing risk documents, and maintaining records.

This role involves active collaboration with a cross-functional team in manufacturing sites, manufacturing, scientists, supply chain, quality, and other global functions. This global function includes monitoring, tracking, and supporting various efforts and initiatives in the Quality System.

Responsibilities
  • Lead meetings to facilitate and/or support the QRM projects.
  • Actively collaborate with a cross-functional team to complete project milestones per established timeline.
  • Assist the functional areas on completing the milestones, as needed.
  • QA review of the governance or risk document content in compliance with established governing documents.
  • Oversee, monitor and track key deliverables associated with project implementation and metrics.
Qualifications
  • Bachelor's degree in Chemistry, Pharmacy, Biology, Microbiology, Engineering, or other technical/scientific area.
  • Minimum of 5 years of experience in Quality Assurance and/or Quality System oversight. Quality Risk Management, Compliance, and supply chain experience required.
  • Project Management experience required.
  • Highly motivated and confident facilitating meetings with people from different levels including executives and scientific/technical experts.
  • Experience interpreting regulatory documents such as ICH, US/EU and other key GMP regulations to develop risk management governance (e.g., impurities risk assessment, shortage prevention planning).
  • Experience working with changes to process or document control and familiar with Track Wise and Veeva.
  • Skills:

    result-oriented, strong oral and written communication, excellent interpersonal skills, self-starter, attention to detail, time management in a fast-paced environment, teamwork, and problem solving. Experience with metrics, visualizations for executives, concise messaging, and data analytics. Experience with automation and developing IT solutions.
  • Computer system skills including: advanced or intermediate skills with Microsoft Office (Word, Visio, PowerPoint, Excel, Power

    BI, Teams, SharePoint, etc.), Track Wise, and Veeva.

Bussiness Unit:
Operations-Quality Assurance (OPQA)

Cost Allocation:
1008|CC|QA Systems PR (634243)

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