Jobs · Quality Assurance · Massachusetts

QA/RA Consultant

Ketryx · Boston, MA · 2 wk ago
HybridQuality Assurance$130k–$150k/yrFull-time

About the role

A proven QMS expert with 5-8 years of experience in the medical device industry, leading quality management system implementations and regulatory compliance strategies for cutting-edge medical device clients. This role offers the opportunity to shape the future of regulatory affairs through innovative technology and enable the success of the world’s most innovative companies.

Responsibilities

  • Lead Quality Management System (QMS) setup and deployment for medical device clients.
  • Own and manage QMS templates and regulatory compliance frameworks.
  • Provide expert consulting on ISO 13485, MDSAP, GxP, and other quality systems standards.
  • Scale operations to support high-growth clients.
  • Develop repeatable QMS deployment processes leveraging AI platform capabilities and automatic compliance.
  • Shape the future of regulatory affairs through innovative product development.
  • Work independently on complex quality assurance projects requiring minimal oversight.
  • Ensure customer success across the entire customer engagement lifecycle.

Requirements

  • 4-8 years of experience in quality systems management, management representative or senior specialist role.
  • Familiar with eQMS implementation, validation and implementation.
  • Deep expertise in Quality Management System setup, sub-systems, and implementation.
  • Strong knowledge of ISO 13485 and Global QMS requirements.
  • Expertise in AI, Digital, and Cyber Compliance.
  • Deep understanding of medical device cybersecurity.
  • Experience as quality management representative in regulated environments.
  • Experience with regulatory and Notified Body submission requirements.
  • Background in medical device industry quality systems.
  • Ability to work independently and own complex regulatory projects.
  • Proven track record in consulting or client-facing roles.

Preferred Skills

  • Experience at large medical device companies (Stryker, Medtronic, Boston Scientific).
  • Background with consulting firms specializing in QMS setup.
  • Startup experience (Series A/B) with QMS implementation.
  • Specializations in cybersecurity, usability, or computer software validation.
  • Experience scaling quality operations in high-growth environments.
  • Knowledge of AI applications in regulatory affairs.
  • Submission experience.
  • Experience working in an early stage, product-based startup.

What We Offer

  • Competitive compensation
  • Generous stock options possible
  • Opportunity to learn and grow as part of a global team
  • Generous PTO for full-time

Ketryx is an equal opportunity employer.

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