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Director Quality Jobs in San Ramon, CA (NOW HIRING)

Astra Space, Inc.

Director, Quality

Alameda, CA · On-site

$211K - $250K/yr

The Opportunity As the Founding Director of Quality and Mission Assurance, you will be the ultimate owner of reliability and risk management for all our space hardware programs. You will build and ...

FM Industries

Director, Quality Operations

Fremont, CA · On-site

$162K - $211K/yr

The Director of Quality Operations is responsible for the planning, leadership and operational execution of the organization's quality departments at the site level as well as customer and supplier ...

FM Industries

Director, Quality Operations

Livermore, CA · On-site

$162K - $211K/yr

The Director of Quality Operations is responsible for the planning, leadership and operational execution of the organization's quality departments at the site level as well as customer and supplier ...

Renesas Electronics

Dir, Quality Assurance

San Jose, CA · On-site

Company Description Renesas is hiring a Director of Product Assurance to lead quality for its rapidly growing Module business within the Performance Core Power group. This is a high-impact leadership ...

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Director Quality information

See San Ramon, CA salary details

$34.6K

$140.4K

$238.6K

How much do director quality jobs pay per year?

As of Aug 7, 2026, the average yearly pay for director quality in San Ramon, CA is $140,361.00, according to ZipRecruiter salary data. Most workers in this role earn between $101,700.00 and $168,700.00 per year, depending on experience, location, and employer.

What does a director of quality do?

A Director of Quality oversees the quality assurance and quality control processes within an organization to ensure that products or services meet established standards and regulatory requirements. They develop and implement quality management systems, lead teams responsible for inspections and audits, and work closely with other departments to promote continuous improvement. The Director of Quality also analyzes quality data, manages compliance with industry regulations, and often interacts with customers or external auditors to address quality concerns.

What are the key skills and qualifications needed to thrive as a director of quality, and why are they important?

To succeed as a Director of Quality, you need extensive knowledge in quality management systems, regulatory compliance, and process improvement, often supported by a bachelor's or master's degree in a relevant field. Familiarity with tools such as Six Sigma, ISO standards, and quality auditing software, along with certifications like CQE or Six Sigma Black Belt, is typical. Exceptional leadership, analytical thinking, and effective communication are critical soft skills for driving quality initiatives and leading cross-functional teams. These competencies ensure organizational standards are upheld, continuous improvement is achieved, and regulatory risks are minimized.

What is the difference between Director Quality vs Quality Manager?

AspectDirector QualityQuality Manager
CredentialsBachelor's or Master’s in Quality Management, Engineering, or related field; certifications like ASQ CQE or CQABachelor's in Quality, Engineering, or related; certifications like ASQ CQE or CQA often preferred
Work EnvironmentStrategic leadership in quality initiatives, overseeing multiple departments or sitesOperational focus, managing daily quality processes and teams
Employer & Industry UsageUsed in manufacturing, healthcare, aerospace, and industries with complex quality systemsCommon in manufacturing, production, and service industries

The main difference between a Director Quality and a Quality Manager lies in their scope and strategic focus. The Director Quality typically oversees the entire quality program at a higher level, setting policies and long-term goals, while the Quality Manager handles daily operations and implements quality procedures. Both roles require similar credentials and certifications, but their responsibilities and strategic influence differ significantly.

How does a director of quality typically collaborate with cross-functional teams to drive continuous improvement initiatives?

A Director of Quality plays a key role in partnering with departments such as manufacturing, engineering, supply chain, and regulatory affairs to identify and resolve process inefficiencies and ensure compliance with quality standards. They often lead cross-functional meetings, facilitate root cause analyses, and champion a culture of continuous improvement by implementing best practices and quality tools like Six Sigma or Lean methodologies. Effective communication and the ability to influence stakeholders at all levels are essential, as the Director of Quality ensures that all departments are aligned with organizational quality goals and regulatory requirements.
What are the most commonly searched types of Quality jobs in San Ramon, CA? The most popular types of Quality jobs in San Ramon, CA are:
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What job categories do people searching Director Quality jobs in San Ramon, CA look for? The top searched job categories for Director Quality jobs in San Ramon, CA are:
What cities near San Ramon, CA are hiring for Director Quality jobs? Cities near San Ramon, CA with the most Director Quality job openings:
Director Quality jobs near you
Infographic showing various Director Quality job openings in San Ramon, CA as of August 2026, with employment types broken down into 1% As Needed, 76% Full Time, 19% Part Time, 3% Contract, and 1% Nights. Highlights an 90% Physical, 1% Hybrid, and 9% Remote job distribution, with an average salary of $140,361 per year, or $67.5 per hour.

Director, Quality

Denali Therapeutics

South San Francisco, CA • On-site

$192K - $249K/yr

Full-time

Medical, Retirement

Re-posted 4 days ago

Job description

Neurodegenerative diseases are one of the largest medical challenges of our time. Denali Therapeutics is a biotechnology company dedicated to developing breakthrough therapies for neurodegenerative diseases through our deep commitment to degeneration biology and principles of translational medicine. Denali is founded on the collaboration of leading scientists, industry experts, and investors who share the vision that scientific discovery energetically applied to translational medicine is the key to delivering effective therapies to patients.

We invite you to consider an opportunity with Denali to help achieve our goal of delivering meaningful therapeutics to patients.

This position will provide quality oversight of Denali's external manufacturing and laboratory network (CMO/CLOs) and support internal/external CMC development activities. This position will also contribute to establishing the internal quality framework including developing quality documentation and will represent Quality cross functionally within Denali for given project activities.

Key Accountabilities/Core Job Responsibilities:

  • Oversee GMP and GLP quality operations at CMOs, including quality documentation reviews and approvals, from Manufacturing and Quality Control, such as batch records, change controls and specifications, disposition of Denali products and audits as needed.

  • Oversee product quality aspects of the supply chain and distribution networks from GLP tox batches to Commercial release.

  • Establish and support quality systems and operations, including document control, deviation reporting and temperature excursions.

  • Support CMC development including review and approval of specifications, stability studies, method validation, QC test methods, process validation and material distribution activities.

  • Support CMC commercial operations including establishing infrastructure, SOPs and execution for Product Launch activities.

  • Support efforts to implement and utilize the QMS through the internal electronic document management system and associated eQMS modules.

  • Write and approve SOPs and Policies related to compliance and quality.

  • Represent Quality on cross functional working groups and projects as required, ensuring the provision of program execution consistent with all regulatory guidance.

  • Serve as a back-up to the other technical quality team members to support the CMC and Supplier teams and leadership as required.

  • Lead direct report(s) through annual goal setting, growth planning, adherence to company policies, maintain training compliance and provide ongoing feedback on growth, development and areas of improvement.

Qualifications/Skills:

  • BS in a scientific discipline; MS preferred; professional certification in quality, compliance and/or regulatory is a plus

  • 10 + years of GMP experience in the Pharmaceutical industry.

  • 8+ years of management experience

  • Experience with CMOs, and CMC development. Large molecule or commercialization experience is a plus.

  • Current and strong working knowledge of 21 CFR 210-211, Part 11, 610 & 820 cGMP/GLPs; EU cGMP/GLPs; and ICH quality and development guidelines.

  • Familiarity with eQMS systems.

  • Able to travel domestically and internationally.

Salary Range: $192,000.00 to $249,000.00 .Compensation for the role will depend on a number of factors, including a candidate's qualifications, skills, competencies, and experience. Denali offers a competitive total rewards package, which includes a 401k, healthcare coverage, ESPP and a broad range of other benefits. Learn more at https://www.denalitherapeutics.com/careers

This compensation and benefits information is based on Denali's good faith estimate as of the date of publication and may be modified in the future.

Denali is committed to its core company value of unity by creating a diverse and inclusive environment. We are proud to be an equal opportunity employer and do not discriminate against any employee or applicant for employment because of race, color, sex, age, national origin, religion, sexual orientation, gender identity and/or expression, status as a veteran, basis of disability, or any other federal, state, or local protected class.

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