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GForce Life Sciences

GForce Life Sciences

via Jazzhr

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Senior QMS Process Engineer

Anywhere
contractor
Posted 9/29/2025
Direct Apply
Key Skills:
QMS documentation
ISO 13485
21 CFR Part 820
EU MDR
Codebeamer
Technical writing
Regulatory compliance
Change management

Compensation

Salary Range

$150K - 179K a year

Responsibilities

Author, revise, and optimize QMS procedures to ensure compliance with regulatory standards and system upgrades.

Requirements

Senior-level experience in medical device QMS documentation, regulatory standards compliance, and familiarity with ALM systems like Codebeamer.

Full 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

This job posting was last updated on 10/6/2025

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