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Quality Risk Management Jobs in California (NOW HIRING)

AbbVie

Senior Quality Engineer, Risk Management

Irvine, CA · On-site

$95K - $128K/yr

The Senior Quality Engineer, Risk Management has various objective/functions related to Third Party Manufacturing (TPM) plants and PQA functions. During routine operations, the Senior PQA Analyst is ...

AbbVie

Senior Quality Engineer, Risk Management

Irvine, CA

$95K - $128K/yr

The Senior Quality Engineer, Risk Management has various objective/functions related to Third Party Manufacturing (TPM) plants and PQA functions. During routine operations, the Senior PQA Analyst is ...

AbbVie

Senior Quality Engineer, Risk Management

Irvine, CA · On-site

$95K - $128K/yr

The Senior Quality Engineer, Risk Management has various objective/functions related to Third Party Manufacturing (TPM) plants and PQA functions. During routine operations, the Senior PQA Analyst is ...

AbbVie

Senior Quality Engineer, Risk Management

Irvine, CA

$95K - $128K/yr

The Senior Quality Engineer, Risk Management has various objective/functions related to Third Party Manufacturing (TPM) plants and PQA functions. During routine operations, the Senior PQA Analyst is ...

AbbVie

Senior Quality Engineer, Risk Management

Irvine, CA · On-site

$95K - $128K/yr

The Senior Quality Engineer, Risk Management has various objective/functions related to Third Party Manufacturing (TPM) plants and PQA functions. During routine operations, the Senior PQA Analyst is ...

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All JobsQuality Risk Management JobsQuality Risk Management Jobs in California

Quality Risk Management information

See California salary details

$38K

$89.9K

$136.7K

How much do quality risk management jobs pay per year?

As of Jun 9, 2026, the average yearly pay for quality risk management in California is $89,855.00, according to ZipRecruiter salary data. Most workers in this role earn between $69,600.00 and $108,600.00 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 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.

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 does a quality risk manager do?

A quality risk manager identifies, assesses, and mitigates risks that could impact product quality and compliance within an organization. They develop risk management plans, analyze data, and ensure adherence to industry standards such as ISO or GMP, often using tools like FMEA. Their role supports maintaining product safety, efficacy, and regulatory compliance.
What are popular job titles related to Quality Risk Management jobs in California? For Quality Risk Management jobs in California, the most frequently searched job titles are:
What job categories do people searching Quality Risk Management jobs in California look for? The top searched job categories for Quality Risk Management jobs in California are:
Quality Risk Management jobs near you
Infographic showing various Quality Risk Management job openings in California as of May 2026, with employment types broken down into 67% Full Time, and 33% Part Time. Highlights an 100% In-person job distribution, with an average salary of $89,855 per year, or $43.2 per hour.
Senior Specialist Quality Engineer

Senior Specialist Quality Engineer

AstraZeneca

Los Angeles, CA • On-site

$100K - $151K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 12 days ago

AstraZeneca rating

8.6

Company rating: 8.6 out of 10

Based on 43 frontline employees who took The Breakroom Quiz

16th of 71 rated pharmaceutical

Job description

As the Sr. Specialist Quality Engineering (QE) you will be responsible for the oversight of the Quality Risk Management, CQV, CSV programs for the Cell Therapy operation of the Tarzana facility. This includes Quality Review and Approval for including Quality Risk Assessments, Technical Reports, Validation Planning, Change Controls, Validation Protocols, Reports, as well as leading the technical quality arm of the Quality department.
You will ensure that operations are compliant with the cGMP standards established by AstraZeneca and relevant regulatory agencies.
Responsibilities
  • You will provide leadership, direction and mentoring to ensure that the QE organization is successful in meeting the quality and manufacturing objectives in support of site goals.
  • Represent the QE department and/or the Quality Organization on assigned site governance and operational teams internally, and as an empowered functional representative externally to ensure deliverables are aligned with site business objectives.
  • Provide support to the Quality Site Lead, Compliance and Site Support, for operational and long-term growth, and demonstrate excellent communication skills through internal and external channels.
  • Own the sites Quality Risk Management program, including generation and maintenance of the sites Risk Registry
  • Quality oversight of the Commissioning, Qualification, and Validation Program by providing strategic planning, leadership and guidance to the validation teams as needed.
  • Quality oversight of the Computerized System Validation Program by providing strategic planning, leadership and guidance to the CSV and IT teams as needed.
  • Quality oversight and support of Data Integrity Compliance program.
  • Technical Quality support to cross functional teams responsible for Tech Transfers, Change Controls, Deviations related CAPAs

Minimum Qualifications:
  • B.S. degree in Science, Engineering, Pharmacy, or related technical field with a minimum of 6 years of applicable experience
  • M.S. degree in Science, Engineering, Pharmacy, or related technical field with a minimum of 3 years of applicable experience
  • Minimum of 1 years of Cell Therapy/Biologics Quality Control experience
  • Minimum of 1 years of management/supervisory/project management experience preferred
  • Experience with product launches, health authority inspections, and global commercial product distribution requirements preferred
  • Proven ability to work in a fast-paced environment across multiple technical functions.
  • Demonstrated ability to make decisions under pressure that balance patient safety, compliance, and supply.
  • Ability to influence senior stakeholders, both internally and externally

Preferred Qualifications:
  • Advanced degree in Science, Engineering, Biochemistry, Pharmacy or related technical field
  • Demonstrated track record in leadership of change management in a positive and non-disruptive manner to the company's values.
  • Experience with Cell Therapy regulatory inspections
  • Experience engaging with global regulatory bodies.
  • Proven track record of attracting and developing talent.
  • Extensive working knowledge of international Cell Therapy GxP regulatory frameworks, regulations, and guidance

The annual base pay for this position ranges from $100,880.80 - $151,321.20. Our positions offer eligibility for various incentives-an opportunity to receive short-term incentive bonuses, equity-based awards for salaried roles and commissions for sales roles. Benefits offered include qualified retirement programs, paid time off (i.e., vacation, holiday, and leaves), as well as health, dental, and vision coverage in accordance with the terms of the applicable plans.
Date Posted
28-May-2026
Closing Date
18-Jun-2026
Our mission is to build an inclusive environment where equal employment opportunities are available to all applicants and employees. In furtherance of that mission, we welcome and consider applications from all qualified candidates, regardless of their protected characteristics. If you have a disability or special need that requires accommodation, please complete the corresponding section in the application form.

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