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Senior QMS Process Engineer
Senior QMS Process EngineerGForce Life Sciences • Westminster, CO, US
Senior QMS Process Engineer

Senior QMS Process Engineer

GForce Life Sciences • Westminster, CO, US
18 days ago
Job type
  • Temporary
  • Quick Apply
Job description

Senior QMS Process Engineer Overview :

  • We are seeking two (2)  Senior QMS Process Engineers  to support a project focused on upgrading Codebeamer and implementing system enhancements to align with organizational and regulatory needs.
  • These contract professionals will play a key role in authoring, revising, and optimizing Quality Management System (QMS) procedures to ensure compliance with global regulations while reflecting system and process improvements.
  • We are looking for a senior level engineer who can effectively interpret process changes and translate them into clear, compliant procedural requirements.

Key Responsibilities :

  • Draft, update, and optimize QMS procedures to align with Codebeamer upgrades, organizational standards, and regulatory requirements.
  • Collaborate with cross-functional Quality and R&D teams to ensure procedures accurately reflect best practices and compliance expectations.
  • Translate technical and regulatory requirements into clear, practical documentation for end users.
  • Support change management processes, ensuring procedural updates are properly controlled and communicated.
  • Ensure documentation is compliant with ISO 13485, 21 CFR Part 820, EU MDR, and internal quality system standards.
  • Partner with stakeholders to validate that documentation aligns with both product development processes and regulatory needs.
  • Required Qualifications :

  • Proven experience in the medical device industry, with strong knowledge of QMS documentation and procedures.
  • Hands-on experience authoring and revising procedures compliant with ISO 13485, 21 CFR Part 820, and EU MDR.
  • Familiarity with Codebeamer or similar ALM systems (e.g., Polarion, Jama, etc.).
  • Strong understanding of regulatory and product development processes across Quality Assurance and R&D.
  • Excellent technical writing, documentation, and organizational skills.
  • Ability to work independently, manage multiple priorities, and deliver within tight project timelines.
  • Preferred Qualifications :

  • Prior experience supporting system upgrades or documentation alignment projects.
  • Background in technical writing within regulated environments.
  • Strong collaboration and communication skills, with the ability to partner across functions.
  • Contract Details :

  • 3-month contract, 40 hrs / week Remote PR : 72-86 / hr Powered by JazzHR
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