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Quality Operations Manager Jobs in California (NOW HIRING)

Nurix

Senior Manager, Quality Operations

Brisbane, CA · On-site

Senior Manager, Quality Operations Nurix Therapeutics is a clinical-stage biopharmaceutical company focused on the discovery, development, and commercialization of targeted protein degradation ...

Nurix

Senior Manager, Quality Operations

Brisbane, CA · On-site

Senior Manager, Quality Operations Nurix Therapeutics is a clinical-stage biopharmaceutical company focused on the discovery, development, and commercialization of targeted protein degradation ...

Sobi

Quality Operation Manager (GMP)

San Diego, CA · On-site

The Quality Operations Manager will ensure compliance with applicable GxP requirements (GLP, GCP, GMP), applicable FDA and global regulatory expectations, and industry best practices. The position ...

Sobi

Quality Operation Manager (GMP)

San Diego, CA · On-site

The Quality Operations Manager will ensure compliance with applicable GxP requirements (GLP, GCP, GMP), applicable FDA and global regulatory expectations, and industry best practices. The position ...

FM Industries

Director, Quality Operations

Fremont, CA · On-site

$162K - $211K/yr

Confer with quality and operations management to develop plans to achieve goals * Assign work to direct reports, appraise performance, reward and discipline employees, address complaints and resolve ...

Moderna Therapeutics

$109K - $174K/yr

ModernaTX, Inc. seeks a Manager, Internal Quality Operations for its Norwood, Massachusetts location. Here's What You'll Do: * On behalf of a global biotechnology company, oversee Quality Assurance ...

FM Industries

Director, Quality Operations

Livermore, CA · On-site

$162K - $211K/yr

Confer with quality and operations management to develop plans to achieve goals * Assign work to direct reports, appraise performance, reward and discipline employees, address complaints and resolve ...

Danaher

Quality Operations Engineer

Lodi, CA · On-site

$70K - $85K/yr

This position reports to the Manager, Manufacturing Quality and is part of the Cepheid Quality Operations Team located in Lodi, California. This is an ON-SITE role supporting twenty-fourx7 ...

Danaher

Quality Operations Engineer

Lodi, CA · On-site

$70K - $85K/yr

This position reports to the Manager, Manufacturing Quality and is part of the Cepheid Quality Operations Team located in Lodi, California. This is an ON-SITE role supporting twenty-fourx7 ...

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Quality Operations Manager information

See California salary details

$38K

$89.9K

$136.7K

How much do quality operations manager jobs pay per year?

As of Jun 16, 2026, the average yearly pay for quality operations manager 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 quality in 3 words?

For a Quality Operations Manager, quality can be summarized as accuracy, consistency, and compliance. These core principles ensure products and processes meet standards, customer expectations, and regulatory requirements, often supported by tools like quality management systems (QMS) and certifications such as ISO. Focusing on these aspects helps maintain operational excellence and continuous improvement.

What does a Quality Operations Manager do?

A Quality Operations Manager is responsible for overseeing and ensuring that an organization's products or services consistently meet established quality standards. They develop and implement quality control processes, manage compliance with industry regulations, and lead teams to identify and resolve quality issues. Additionally, they work closely with production, engineering, and supply chain departments to improve efficiency and maintain high standards. Their role is critical in minimizing defects, reducing costs, and ensuring customer satisfaction.

What's a better word for quality?

For a Quality Operations Manager, a better word for quality could be 'excellence,' 'standard,' or 'performance,' depending on the context. These terms emphasize the level of achievement, consistency, and adherence to specifications that are central to quality management roles. Using precise language helps communicate expectations and improvements effectively within quality-focused environments.

What is the meaning of quality in a person?

In the context of a Quality Operations Manager, quality in a person refers to attributes such as integrity, attention to detail, reliability, and a commitment to continuous improvement. These qualities ensure consistent performance, adherence to standards, and effective problem-solving within quality management systems. Developing these traits supports maintaining high standards and fostering a culture of quality in the workplace.

How does a Quality Operations Manager typically collaborate with other departments to maintain product standards?

A Quality Operations Manager works closely with departments such as production, supply chain, and R&D to ensure that product quality standards are consistently met. They often participate in cross-functional meetings to address quality concerns, analyze root causes of issues, and implement corrective actions. Effective communication and teamwork are essential, as the manager needs to align quality objectives with overall business goals and foster a culture of continuous improvement across teams.

What is the best definition of quality?

For a Quality Operations Manager, quality refers to the degree to which products or services meet specified standards and customer expectations. It involves implementing processes, inspections, and continuous improvement to ensure consistency, reliability, and compliance with industry regulations.

What are the key skills and qualifications needed to thrive as a Quality Operations Manager, and why are they important?

To thrive as a Quality Operations Manager, you need expertise in quality management systems, process improvement, and a background in engineering or a related field, often supported by a bachelor’s degree. Familiarity with ISO standards, Six Sigma or Lean methodologies, and quality management software is typically required. Strong leadership, problem-solving abilities, and effective communication skills help drive quality initiatives and foster a culture of continuous improvement. These competencies are crucial to ensuring product consistency, regulatory compliance, and operational excellence.
What are the most commonly searched types of Quality Operations jobs in California? The most popular types of Quality Operations jobs in California are:
What are popular job titles related to Quality Operations Manager jobs in California? For Quality Operations Manager jobs in California, the most frequently searched job titles are:
What job categories do people searching Quality Operations Manager jobs in California look for? The top searched job categories for Quality Operations Manager jobs in California are:
What cities in California are hiring for Quality Operations Manager jobs? Cities in California with the most Quality Operations Manager job openings:
Quality Operations Manager jobs near you
Infographic showing various Quality Operations Manager job openings in California as of June 2026, with employment types broken down into 90% Full Time, 9% Part Time, and 1% Contract. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution, with an average salary of $89,855 per year, or $43.2 per hour.

Senior Quality Operations Manager

Retro

Redwood City, CA • On-site

Full-time

Medical, Dental, Vision, Retirement

Posted 27 days ago

Job description

Retro develops therapies for diseases driven by the biology of aging. We focus on cellular reprogramming and autophagy to rejuvenate cell and tissue function with the ultimate aim of adding 10 years to healthy human lifespan.
We are building a mission-driven, collaborative team operating with speed, transparency, and adaptability.
We are hiring anew member of the team who will own day-to-day Quality Operations across Retro's programs. In this role, you will own core QA operational processes, ensure the Quality Management System functions effectively as activity increases, and support compliant, phase-appropriate execution across clinical manufacturing and quality operations. You will work closely with internal teams and external partners to ensure quality processes are consistently applied and that clinical materials are reviewed, released, and managed in alignment with regulatory expectations. You will report to the Head of Quality and Analytical Development (Q&AD).
About you:
You are a practical, hands-on quality leader with deep experience in GMP Quality Assurance operations who enjoys making complex work run smoothly. You know how to build, run, and continuously improve the systems that keep quality execution on track-from document control and training to deviations, change controls, CAPAs, and batch review-while helping teams move quickly. You are just as comfortable in the details as you are stepping back to spot gaps, tighten processes, and keep work moving forward. You communicate clearly, work well across internal teams and external partners, and bring rigor, follow-through, and a low-ego, high-reliability approach to getting things done. You are motivated by the opportunity to help build quality operations that scale with Retro and support the development of therapies that extend healthy lifespan!
In this role, you will:
  • Own and execute day-to-day QA operations across programs, supporting compliant clinical manufacturing and quality system activities.
  • Own the maintenance, administration, and continuous improvement of the Quality Management System (QMS), including document control, training and qualification, deviation, change control, and CAPA workflows.
  • Support batch record review, particularly for internally manufactured products, and help ensure manufacturing documentation is complete, accurate, and inspection-ready.
  • Perform or coordinate QA disposition and release of drug product for clinical use in alignment with internal procedures and regulatory expectations.
  • Coordinate supplier, vendor, and CDMO qualification activities, including documentation, follow-up, and issue escalation.
  • Oversee training programs, including training compliance, operator qualification, and aseptic technique qualification.
  • Plan, coordinate, and support internal audits, including audit readiness, execution, and closure of follow-up actions.
  • Support regulatory inspections and partner audits, including preparation, on-site support, and response development.
  • Drive consistent application of quality processes and standards across programs, modalities, and operational teams.
  • Partner cross-functionally with Manufacturing, MSAT, Process Development, Quality Control, and Analytical Development to proactively identify quality risks and implement timely mitigation strategies.
  • Lead and contribute to continuous improvement initiatives that enhance compliance, operational efficiency, and scalability of QA systems.

You will excel in this role if you have:
  • 6+ years of progressive experience in Quality Assurance within a GMP-regulated biopharmaceutical environment, supporting clinical-stage development.
  • Hands-on experience supporting clinical manufacturing operations, including batch record review, deviation management, investigations, CAPAs, and change control.
  • Experience supporting qualification, oversight, and performance monitoring of suppliers, CDMOs, or CROs.
  • Experience performing QA disposition and/or release of clinical drug product.
  • Working knowledge of GMP regulations (e.g., FDA, EU, PIC/S) and phase-appropriate quality systems for clinical-stage products.
  • Strong cross-functional collaboration skills.
  • Demonstrate strong judgment in applying risk-based decision-making in a fast-paced, early clinical environment.
  • Communicate clearly and effectively across technical, operational, and quality stakeholders.
  • Demonstrate strong attention to detail, documentation quality, and inspection readiness.
  • A Bachelor's degree in a scientific or technical discipline (e.g., Biology, Chemistry, Engineering) or equivalent combination of education and experience.

It's a bonus if you have:
  • Experience supporting GCP environments, including an understanding of clinical trial quality requirements and data integrity principles.
  • Experience with aseptic manufacturing operations, including environmental monitoring, operator qualification, and contamination control strategies.
  • Prior involvement in regulatory inspections, partner audits, or customer audits, including preparation and response activities.
  • Experience with advanced therapy modalities (e.g., cell therapy, gene therapy, or other complex biologics).
  • Experience in early-stage or rapidly scaling organizations, with exposure to building or evolving quality systems.

$175,000 - $190,000 a year
At Retro, we don't use titles. New hires join as a "Member of X Team." Depending on experience, this role may align externally to the Manager or Senior Manager level in the broader biotech market.
Total compensation includes competitive base salary, generous equity, and benefits including:
  • Medical, dental, and vision insurance for you and your family
  • 401(k) plan with 4% matching
  • Flexible time off and 10 company holidays per year
  • Paid parental leave
  • Annual learning & development stipend
  • Daily Retro-sponsored lunch and snacks

We take pride in cultivating an environment that fosters collaboration, open communication, and authenticity. We believe that great results are best delivered by a highly creative team working in concert. We are an equal opportunity employer; we do not discriminate based on race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status. We are diverse in background and singular in mission.
We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.
We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.

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