QMS Systems Specialist

iMPact Business Group, Inc.

Cary, IL

JOB DETAILS
SKILLS
Change Control, Change Management, Coaching, Cross-Functional, Detail Oriented, Document Control, Document Management, Documentation, English Language, FDA (Food and Drug Administration), German Language, ISO (International Organization for Standardization), Maintain Compliance, Medical Equipment, Mentoring, Microsoft Excel, Microsoft Office, Microsoft PowerPoint, Microsoft SharePoint, Microsoft Word, Multitasking, Organizational Skills, Problem Solving Skills, Process Improvement, Product Support, Project/Program Coordination, Quality Control, Quality Management, Records Management, Regulations, Regulatory Requirements, Research & Development (R&D), Staff Motivation, System Integration (SI), Team Player, Technical Writing, Writing Skills
LOCATION
Cary, IL
POSTED
23 days ago

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)

About the Company

i

iMPact Business Group, Inc.

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!

COMPANY SIZE
100 to 499 employees
INDUSTRY
Staffing/Employment Agencies
FOUNDED
2004
WEBSITE
https://impactbusinessgroup.com