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Quality Operations Manager Jobs in Newark, CA (NOW HIRING)

Retro

Senior Quality Operations Manager

Redwood City, CA · On-site

$175K - $190K/yr

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 ...

SOLID Surface Care, Inc.

Operations Manager

Hayward, CA · On-site

$120K/yr

Ensure jobs are completed safely, efficiently, on time, and to company quality standards. * Monitor labor utilization, project performance, and operational KPIs. * Manage fleet, equipment, inventory ...

CDimension

Operations Manager

San Jose, CA · On-site

Familiarity with quality, safety, and compliance standards relevant to manufacturing or R&D operations. * Bachelor's degree in Operations Management, Engineering, Business, or a related field ...

EoS Fitness

Operations Manager

Fremont, CA · On-site

Our Operations Manager, reporting to the District Operations Manager, is responsible for overseeing ... Ensuring high-quality customer service by addressing member concerns or complaints, managing ...

CVS Health

Operations Manager

San Jose, CA

$23.45 - $37.45/hr

... and quality in everything we do. Join us and be part of something bigger - helping to simplify ... Position Summary The Operations Manager is a member of the Store Management team, and as such ...

Trimble

Operations Manager

Sunnyvale, CA · On-site

Champion a culture of excellence by overseeing the Quality Management System to ensure strict adherence to AS9100, ISO 9001, and FAA standards. * Mentor and develop a high-performing operations team ...

Trimble, Inc.

Operations Manager

Sunnyvale, CA · On-site

Champion a culture of excellence by overseeing the Quality Management System to ensure strict adherence to AS9100, ISO 9001, and FAA standards. * Mentor and develop a high-performing operations team ...

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Quality Operations Manager information

See Newark, CA salary details

$43.3K

$102.4K

$155.8K

How much do quality operations manager jobs pay per year?

As of Sep 3, 2026, the average yearly pay for quality operations manager in Newark, CA is $102,402.00, according to ZipRecruiter salary data. Most workers in this role earn between $79,300.00 and $123,700.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a quality operations manager?

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.

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 role of a quality operations manager?

A quality operations manager oversees the implementation and maintenance of quality systems within an organization, ensuring products and services meet safety, quality, and regulatory standards. They analyze processes, lead continuous improvement initiatives, and often use tools like Six Sigma or ISO standards to enhance efficiency and compliance.

What are popular job titles related to Quality Operations Manager jobs in Newark, CA?

For Quality Operations Manager jobs in Newark, CA, the most frequently searched job titles are:

What job categories do people searching Quality Operations Manager jobs in Newark, CA look for?

The top searched job categories for Quality Operations Manager jobs in Newark, CA are:

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Cities near Newark, CA with the most Quality Operations Manager job openings:

Quality Operations Manager jobs near you
Infographic showing various Quality Operations Manager job openings in Newark, CA as of August 2026, with employment types broken down into 96% Full Time, 2% Part Time, and 2% Temporary. Highlights an 89% In-person, 3% Hybrid, and 8% Remote job distribution, with an average salary of $102,402 per year, or $49.2 per hour.

Senior Quality Operations Manager

Retro

Redwood City, CA

Full-time

Medical, Dental, Vision, Retirement

Re-posted 16 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 a new 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 bring:

  • Demonstrated success supporting Quality Assurance operations for clinical-stage small molecule products within a GMP-regulated environment (6+ years preferred)

  • Hands-on experience supporting clinical manufacturing operations, including batch record review, product disposition and release, investigations, deviations, CAPAs, and change control.

  • Experience building, implementing, or continuously improving phase-appropriate Quality Management Systems that enable compliant, scalable operations.

  • Experience partnering closely with internal scientific, technical, and operational teams to solve quality challenges in a collaborative, risk-based manner.

  • Experience qualifying and overseeing CDMOs, suppliers, and other external manufacturing partners.

  • Strong working knowledge of FDA and international GMP regulations, with the ability to apply them pragmatically in a fast-paced, clinical-stage environment.

  • Sound judgment and attention to detail, with the ability to balance compliance, scientific rigor, and operational efficiency.

  • A Bachelor's degree in a scientific or technical discipline (e.g., Biology, Chemistry, Engineering), or an 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

  • Longevity 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 and identifying potential inconsistencies or verification signals in application materials based on available information. 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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