iMPact Business Group, Inc. logo

QMS Systems Specialist

iMPact Business Group, Inc.

  • Cary, IL
  • 2 days ago
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    Skills

    • Change Controlunmatched
    • Change Managementunmatched
    • Coachingunmatched
    • Cross-Functionalunmatched
    • Detail Orientedunmatched
    • Document Controlunmatched
    • Document Managementunmatched
    • Documentationunmatched
    • English Languageunmatched
    • FDA (Food and Drug Administration)unmatched
    • German Languageunmatched
    • ISO (International Organization for Standardization)unmatched
    • Maintain Complianceunmatched
    • Medical Equipmentunmatched
    • Mentoringunmatched
    • Microsoft Excelunmatched
    • Microsoft Officeunmatched
    • Microsoft PowerPointunmatched
    • Microsoft SharePointunmatched
    • Microsoft Wordunmatched
    • Multitaskingunmatched
    • Organizational Skillsunmatched
    • Problem Solving Skillsunmatched
    • Process Improvementunmatched
    • Product Supportunmatched
    • Project/Program Coordinationunmatched
    • Quality Controlunmatched
    • Quality Managementunmatched
    • Records Managementunmatched
    • Regulationsunmatched
    • Regulatory Requirementsunmatched
    • Research & Development (R&D)unmatched
    • Staff Motivationunmatched
    • System Integration (SI)unmatched
    • Team Playerunmatched
    • Technical Writingunmatched
    • Writing Skillsunmatched

    Description

    Our client, a Global Medical Device Manufacturer, has an immediate opening for a QMS Systems Specialist for a 12 Month+ contract.   Our client offers results-driven people a place where they can make a difference - every day!  You will also have the opportunity to work with other like-minded, self-directed and detail oriented Top Talents in an extremely collaborative and professional environment. 

     

    We are seeking a highly motivated Staff Quality Systems Specialist (Contractor) to support QMS integration activities by leading and owning the Change Control process within a regulated medical device environment.


     In this role, you will ensure that all changes are appropriately documented, assessed for impact, and effectively implemented in alignment with quality and regulatory requirements. You will also mentor cross-functional stakeholders on proper change execution and support the integration of quality system processes across the organization.


     This position is ideal for a detail-oriented professional with strong technical writing skills and a deep understanding of how quality system processes interact (e.g., change control, document control, training, and records management).

     

    This role requires close collaboration with teams in Germany and flexibility to align with CET/CEST working hours.

     

    Position Description 

     

    • Own and manage the Change Control process to ensure compliance, consistency, and effectiveness
    • Review and approve change records for completeness, accuracy, and appropriate impact assessments
    • Ensure changes are implemented appropriately, including verification of downstream activities (e.g., documentation updates, training completion, record retention)
    • Drive process improvements and standardization to support integration efforts
    • Evaluate process gaps and define compliant, scalable solutions
    • Collaborate with cross-functional teams to align change activities with integration timelines and business needs
    • Mentor and guide change owners and stakeholders on proper change control processes
    • Provide coaching on impact assessment, documentation expectations, and process requirements
    • Promote consistent and high-quality execution of change activities across the organization
    • Develop and revise quality system documentation, including procedures, work instructions, and change records
    • Ensure documentation is clear, accurate, and compliant with internal and regulatory requirements
    • Partner with Quality, Regulatory, R&D, and Operations teams to ensure alignment on changes and integration efforts
    • Act as a quality representative in project discussions and integration activities
    • Communicate progress, risks, and recommendations to key stakeholders


    What you need

     

    • Bachelor's degree in engineering, science, or a related field
    • 5+ years of experience in a regulated environment (medical device preferred)
    • Proven experience with Change Control processes and quality system integration or harmonization
    • Experience supporting integration of products, systems, or acquired businesses is strongly preferred
       

    REQUIRED

     

    • Strong knowledge of Quality Management Systems (QMS) and applicable regulatory requirements (e.g., FDA, ISO 13485, EU MDR)
    • Deep understanding of interactions between Change Control, Document Control, Training, and Records processes
    • Excellent technical writing and documentation skills
    • Strong organizational, problem-solving, and project coordination abilities
    • Ability to influence, mentor, and drive consistent process execution across cross-functional teams
    • Ability to manage multiple priorities in a fast-paced, integration-focused environment
    • Strong attention to detail and commitment to quality and compliance
    • Collaborative mindset with a proactive, solution-oriented approach
    • Proficiency in Microsoft Office applications, including Word, Excel, PowerPoint, Teams, and SharePoint
    • Fluency in English (written and verbal)
    • Ability to work flexible hours to accommodate German time zones

     

    Preferred qualifications:

     

    • Experience supporting QMS integration in a global environment
    • German language proficiency (written and verbal)

    Numbers & Facts

    LocationCary, IL
    IndustryStaffing/Employment Agencies
    Company Size100 to 499 employees
    Year Founded2004
    Websitehttps://impactbusinessgroup.com

    About Company

    Working with iMPact

     

    Here at iMPact we have helped connect candidates to opportunities available in Information Technology, Accounting/Finance, Engineering, and Business Process/Administration. We have full-time, part-time and contract positions available in Michigan, Florida as well as nationwide.

     

    Our headquarters is located in Grand Rapids, MI and we also have an office in Tampa, FL. When you’re working with us, one of our experienced recruiters will connect you with matching opportunities and they will be there every step of the way to help you through the application, interviewing and onboarding process to ensure success.

     

    To connect with one of our recruiters, submit your application for one of our open positions, or visit our website www.impactbusinessgroup.com to submit your resume for general consideration. We look forward to hearing from you!

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