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Qa Ra Consultant Jobs (NOW HIRING)

Ketryx

QA/RA Consultant

Boston, MA · On-site +1

$130K - $150K/yr

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 ...

Ketryx

QA/RA Consultant

Boston, MA · On-site

$130K - $150K/yr

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 ...

Transformcap

QA/RA Consultant

Boston, MA · On-site

$125 - $150/hr

Job Title: QA/RA Lead Employment Status: Full-time Office Hours: Monday - Friday; hybrid schedule ... Provide expert consulting on ISO 13485, MDSAP, GxP, and other quality systems standards * Scale ...

QT Imaging, Inc.

Senior QA/RA Specialist

Novato, CA · On-site

$125 - $150/hr

Serve as the primary QA/RA representative on cross-functional project teams, ensuring quality and regulatory requirements are incorporated throughout the product lifecycle. * Lead document control ...

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How much do qa ra consultant jobs pay per hour?

As of Sep 8, 2026, the average hourly pay for qa ra consultant in the United States is $52.71, according to ZipRecruiter salary data. Most workers in this role earn between $44.95 and $59.62 per hour, depending on experience, location, and employer.

What is a QA RA consultant?

QA RA Consultants are professionals who specialize in Quality Assurance (QA) and Regulatory Affairs (RA) within industries such as pharmaceuticals, medical devices, and biotechnology. They help organizations ensure that their products comply with regulatory requirements and quality standards set by government agencies like the FDA or EMA. QA RA Consultants provide expert advice on regulatory submissions, quality management systems, audits, and compliance strategies, helping companies bring products to market efficiently and safely. Their role is crucial for maintaining product safety, efficacy, and ongoing compliance throughout the product lifecycle.

What are some typical challenges a QA RA consultant faces when working with multiple clients in regulated industries?

QA/RA Consultants often juggle various projects for clients in highly regulated sectors, such as pharmaceuticals or medical devices. A common challenge is adapting quickly to each client's unique processes and regulatory requirements while ensuring compliance with evolving industry standards. Effective time management and communication are crucial, as consultants must balance competing priorities and frequently coordinate with cross-functional teams. Staying current with regulatory changes and proactively identifying compliance gaps can make a significant difference in delivering value to clients.

What are the key skills and qualifications needed to thrive as a QA RA consultant, and why are they important?

To thrive as a QA/RA Consultant, you need expertise in quality assurance, regulatory affairs, and industry standards, often supported by a degree in life sciences or engineering and relevant certifications (such as RAC or CQE). Familiarity with regulatory databases, document management systems, and tools like ISO 13485, FDA regulations, and EU MDR is typically required. Strong analytical thinking, attention to detail, and excellent communication skills set outstanding consultants apart. These competencies are vital to ensure product compliance, successful regulatory submissions, and effective collaboration with clients and regulatory bodies.

What is the difference between Qa Ra Consultant vs Qa Analyst?

AspectQa Ra ConsultantQa Analyst
CertificationsISTQB, CSTE, CSQAISTQB, CSTE, CSQA
Work EnvironmentConsulting firms, client sites, project-basedIn-house teams, software development companies
Industry UsageUsed across various industries for quality assurance consultingPrimarily in software development and IT

The Qa Ra Consultant and Qa Analyst roles share similar certifications and work environments, but the Qa Ra Consultant typically works in consulting settings, providing strategic quality assurance advice to multiple clients. In contrast, the Qa Analyst usually operates within a single organization, focusing on testing and quality control of software products.

What cities are hiring for Qa Ra Consultant jobs?

Cities with the most Qa Ra Consultant job openings:

What states have the most Qa Ra Consultant jobs?

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Infographic showing various Qa Ra Consultant job openings in the United States as of June 2026, with employment types broken down into 1% Locum Tenens, 1% As Needed, 95% Full Time, 2% Part Time, and 1% Temporary. Highlights an 89% Physical, 3% Hybrid, and 8% Remote job distribution, with an average salary of $109,635 per year, or $52.7 per hour.

QA/RA Consultant

Ketryx

Boston, MA • On-site, Remote

$130K - $150K/yr

Full-time

Re-posted yesterday

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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