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Qms Consultant Jobs (NOW HIRING)

Ketryx

QA/RA Consultant

Boston, MA · On-site +1

$130K - $150K/yr

You'll have the autonomy and expertise to drive repeatable QMS deployment processes while helping ... Provide expert consulting on ISO 13485, MDSAP, GxP, and other quality systems standards. * Scale ...

Ketryx

QA/RA Consultant

Boston, MA · On-site

$130K - $150K/yr

You'll have the autonomy and expertise to drive repeatable QMS deployment processes while helping ... Provide expert consulting on ISO 13485, MDSAP, GxP, and other quality systems standards. * Scale ...

Slipstream IT

PA

About the Role The Quality Systems Consultant is Slipstream's primary point of contact for one or more Veeva Vault managed-services accounts (QualityDocs, Training, and/or QMS). You'll own the day-to ...

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How much do qms consultant jobs pay per hour?

As of Sep 2, 2026, the average hourly pay for qms consultant in the United States is $40.04, according to ZipRecruiter salary data. Most workers in this role earn between $25.00 and $55.53 per hour, depending on experience, location, and employer.

What is a QMS consultant?

A QMS (Quality Management System) Consultant helps organizations develop, implement, and improve their quality management systems to comply with industry standards such as ISO 9001. They assess current processes, identify areas for improvement, and provide guidance to ensure regulatory compliance and operational efficiency. Their role includes documentation, training, audits, and continuous improvement strategies to enhance product or service quality.

What are the typical daily responsibilities of a QMS consultant?

As a QMS Consultant, your daily responsibilities may include reviewing and improving organizational processes, conducting internal audits, advising on compliance with relevant standards like ISO 9001, and developing quality documentation. You may also lead training sessions, facilitate corrective and preventive action initiatives, and collaborate closely with different department heads to implement effective quality solutions. Additionally, you'll be tasked with identifying areas for continuous improvement and ensuring best practices are communicated across the organization. This role offers a mix of hands-on problem-solving and strategic planning, making it both dynamic and impactful.

What are the key skills and qualifications needed to thrive as a QMS consultant?

To thrive as a QMS Consultant, you need a deep understanding of quality management systems (such as ISO 9001), process improvement methodologies, and strong analytical abilities, typically supported by a relevant degree and QMS certifications. Familiarity with tools like corrective and preventive action (CAPA) software, internal audit systems, and document control platforms is often required. Excellent communication, project management, and problem-solving skills help consultants effectively engage with diverse teams and clients. These skills and qualities ensure the successful development, implementation, and continual improvement of quality management systems for organizations.

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Qms Consultant jobs near you
Infographic showing various Qms Consultant job openings in the United States as of August 2026, with employment types broken down into 90% Full Time, 6% Part Time, and 4% Contract. Highlights an 85% Physical, 4% Hybrid, and 11% Remote job distribution, with an average salary of $83,289 per year, or $40 per hour.

QA/RA Consultant

Ketryx

Boston, MA • On-site, Remote

$130K - $150K/yr

Full-time

Re-posted 25 days ago

Job description

Job Title: QA/RA Consultant
Employment Status: Full-time
Office Hours: Monday - Friday; hybrid schedule
Location: Boston, Massachusetts
Compensation: $130,000 - $150,000, plus equity options. (Compensation dependent on experience level)

As a Ketryx QA/RA Consultant, you will lead quality management system implementations and regulatory compliance strategies for cutting-edge medical device clients as we scale our AI-powered compliance platform. This is a rare opportunity to shape the future of regulatory affairs. You'll have the autonomy and expertise to drive repeatable QMS deployment processes while helping shape the future of regulatory affairs through innovative technology and enabling the success of the world's most innovative companies. We offer the opportunity to work with high-growth clients, establishing best-in-class quality systems from the ground up using our revolutionary AI platform.

Our ideal candidate will have demonstrated success in quality systems management with 5-8 years of experience in the medical device industry. Someone who is strategic yet hands-on, passionate about regulatory excellence, and eager to leverage cutting-edge AI technology will thrive in this position. In this role, you'll have the opportunity to directly impact our mission to improve 100 million patient lives by 2030 by ensuring the highest quality standards for life-saving medical devices.

This position will be based in our Boston, Massachusetts office with a hybrid schedule (Monday, Tuesday, Thursday, Friday in office, Wednesday WFH option). 

About You:

You're a proven QMS expert who's successfully navigated complex medical device regulatory landscapes and is ready to scale your impact through innovative technology. You've built or significantly improved quality systems at medical device companies, consulting firms, or high-growth startups, and you're excited to combine your regulatory expertise with AI-powered tools to create something category-defining.

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.
Required Skills:
  • 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 start up.

Keywords: ISO 13485, MDSAP, Quality Management System (QMS), Management representative, Medical device quality, QMS setup, Regulatory consulting, Quality systems manager, Computer software validation, Cybersecurity, Usability, Startup experience, Series A/B, Boston/Massachusetts, Consulting firms, Quality assurance, Medical device industry

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