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How much do quality risk management jobs pay per year?

As of Jun 23, 2026, the average yearly pay for quality risk management in the United States is $91,047.00, according to ZipRecruiter salary data. Most workers in this role earn between $70,500.00 and $110,000.00 per year, depending on experience, location, and employer.

What is a Quality Risk Management job?

A Quality Risk Management (QRM) job involves identifying, assessing, and mitigating risks that could impact product quality, compliance, or business operations. Professionals in this role apply risk management principles to processes in industries like pharmaceuticals, manufacturing, and healthcare. They work to ensure that risk control strategies align with regulatory requirements and industry standards. Responsibilities often include conducting risk assessments, implementing mitigation plans, and maintaining compliance with frameworks such as ICH Q9. Their goal is to enhance product quality, patient safety, and business continuity.

What is the role of quality risk management?

In quality risk management, professionals identify, assess, and prioritize potential risks to product quality and patient safety. They develop strategies to mitigate or control these risks, ensuring compliance with regulatory standards and maintaining product integrity throughout the development and manufacturing processes.

What are the key skills and qualifications needed to thrive in the Quality Risk Management position, and why are they important?

To excel in Quality Risk Management, you need a strong understanding of risk assessment methodologies, quality management systems, and regulatory standards, often backed by a degree in science, engineering, or a related field. Familiarity with tools such as ISO 9001, FMEA, CAPA systems, and compliance management software is commonly required, and certifications like Six Sigma or ASQ can be advantageous. Excellent analytical thinking, attention to detail, and persuasive communication help professionals effectively identify risks and collaborate across departments. These skills are essential to design robust quality processes, mitigate operational risks, and ensure consistent compliance and product safety.

How much does a risk manager get paid?

Risk managers in quality risk management typically earn a median annual salary between $80,000 and $120,000, depending on experience, industry, and location. Certifications such as Certified Risk Management Professional (CRMP) can enhance earning potential, and the role often requires strong analytical skills and knowledge of regulatory standards.

What are typical challenges faced in a Quality Risk Management role?

One common challenge in Quality Risk Management is balancing rigorous regulatory compliance requirements with operational efficiency in fast-paced environments. Professionals must often manage competing priorities, respond quickly to emerging risks, and coordinate with cross-functional teams to implement effective mitigations. You may also encounter the need to continuously stay updated on changing industry standards and regulations. Overcoming these challenges requires proactive problem-solving, strong organizational skills, and the ability to communicate complex risk scenarios clearly to both technical and non-technical stakeholders.

What is the role of a quality risk manager?

A quality risk manager is responsible for identifying, assessing, and mitigating risks that could impact product quality and compliance within an organization. They develop risk management strategies, implement quality systems, and ensure adherence to industry standards, often using tools like FMEA and risk assessments. Certification such as RAC or ISO 31000 knowledge is common in this role.

Is risk management high paying?

Risk management roles, including those in quality risk management, often offer competitive salaries that increase with experience, certifications, and industry. Professionals with specialized skills such as risk assessment, compliance, and data analysis tend to earn higher wages, especially in regulated industries like pharmaceuticals and manufacturing.
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What cities are hiring for Quality Risk Management jobs? Cities with the most Quality Risk Management job openings:
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Quality Risk Management jobs near you
Infographic showing various Quality Risk Management job openings in the United States as of June 2026, with employment types broken down into 95% Full Time, 2% Part Time, and 3% Contract. Highlights an 94% Physical, 1% Hybrid, and 5% Remote job distribution, with an average salary of $91,047 per year, or $43.8 per hour.

QA Specialist IV-Quality Risk Management

Lonza

Portsmouth, NH

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 28 days ago

Lonza rating

8.2

Company rating: 8.2 out of 10

Based on 41 frontline employees who took The Breakroom Quiz

26th of 71 rated pharmaceutical

Job description

QA Specialist IV - Quality Risk Management

Location: This position is based in our Portsmouth, NH office. The typical work schedule is Monday through Friday, 8:00 AM-5:00 PM EST.

What you will get:

Below you will find a comprehensive summary of the benefits package we offer:

  • Performance-related bonus.

  • Medical, dental and vision insurance.

  • 401(k) matching plan.

  • Life insurance, as well as short-term and long-term disability insurance.

  • Employee assistance programs.

  • Paid time off (PTO).

Compensation for this role will be determined by the candidate's qualifications, skills, experience, and relevant knowledge.

What you will do:

The QA Specialist IV - Quality Risk Management (QRM) plays a critical role in ensuring compliance with cGMP regulations by advancing and maintaining an effective, site-wide risk management program. This individual serves as a subject matter expert in QRM principles and tools, partnering cross-functionally to embed risk-based decision-making into quality systems and operational processes. The role is responsible for facilitating risk assessments, providing technical guidance, and driving continuous improvement initiatives to enhance product quality, patient safety, and regulatory compliance. This position operates with a high degree of independence while aligning with broader organizational and global quality objectives.

  • Ensure compliance with cGMP regulations by supporting and advancing the site's Quality Risk Management (QRM) program as a key component of the overall Quality System

  • Serve as a subject matter expert (SME) on QRM principles, providing technical guidance, training, and hands-on support across departments

  • Partner with cross-functional teams to plan, facilitate, and execute risk assessments, including tool selection, risk evaluation, and mitigation strategies

  • Collaborate with departments to understand project needs and design effective, inspection-ready risk management solutions

  • Lead and facilitate risk assessment activities (e.g., FMEA, HACCP, What-if, process mapping), ensuring outcomes are scientifically sound and compliant

  • Support integration of QRM principles into day-to-day operations and decision-making across the site

  • Review and approve QRM documentation to ensure alignment with internal procedures and regulatory expectations

  • Drive continuous improvement of the QRM program through lessons learned, trend analysis, and process enhancements

  • Develop, maintain, and deliver QRM training materials to support site-wide knowledge and adoption

  • Identify and implement advanced risk management tools and methodologies to enhance program effectiveness

  • Support global and site-level initiatives requiring QRM expertise

  • Ensure adherence to Data Integrity principles in all activities in accordance with company policies and regulatory expectations

  • Act as a representative for the QRM program during internal audits, customer audits, and regulatory inspections

  • Operate with minimal day-to-day supervision while aligning work to broader organizational goals

What we are looking for:

  • Bachelor's degree in Life Sciences, Engineering, or a related field (advanced degree preferred)

  • 5-8+ years of experience in a GMP-regulated environment within Quality Assurance, Quality Systems, or related function

  • Strong working knowledge of cGMP regulations (FDA, EMA, ICH) and application of Quality Risk Management principles (ICH Q9)

  • Proven experience leading and facilitating risk assessments using tools such as FMEA, HACCP, Fishbone, What-if analysis, and process mapping

  • Demonstrated ability to design and implement practical, compliant, and inspection-ready risk management solutions

  • Experience developing and delivering technical training to diverse audiences

  • Strong analytical and problem-solving skills, with the ability to assess risk impact and drive effective mitigation strategies

  • Excellent communication and interpersonal skills, with the ability to influence and collaborate across all levels of the organization

  • Ability to manage multiple priorities and lead projects independently in a fast-paced environment

  • Familiarity with data integrity principles and regulatory expectations

  • Experience supporting audits and inspections, with the ability to clearly defend QRM approaches and decisions

  • Certification in Quality (e.g., ASQ CQE/CQA) or formal risk management training is a plus

About Lonza

At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone's ideas, big or small, have the potential to improve millions of lives, and that's the kind of work we want you to be part of.

Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we offer equal employment opportunities to all qualified applicants regardless of race, religion, color, national origin, sex, sexual orientation, gender identity, age, disability, veteran status, or any other characteristic protected by law. If you're ready to help turn our customers' breakthrough ideas into viable therapies, we look forward to welcoming you on board.

Ready to shape the future of life sciences? Apply now.

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