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Quality Manager Jobs in Santa Rosa, CA (NOW HIRING)

Talent Pool - Quality and Testing Engineer

Novato, CA · On-site

$84K - $109K/yr

Ensuring customer-focused quality management, achieving high effectiveness in terms of customer ... satisfaction and efficiency in cost management, including processes and tools to ensure flawless ...

Quality Engineer

Santa Rosa, CA

$78K - $101K/yr

The Quality Engineer will serve as a key contributor to Quality Management System effectiveness, laboratory quality oversight, audit readiness, validation activities, process improvement, and ...

Quality Engineer

Santa Rosa, CA · On-site

$78K - $101K/yr

The Quality Engineer will serve as a key contributor to Quality Management System effectiveness, laboratory quality oversight, audit readiness, validation activities, process improvement, and ...

Quality Engineer

Santa Rosa, CA · On-site

$78K - $101K/yr

The Quality Engineer will serve as a key contributor to Quality Management System effectiveness, laboratory quality oversight, audit readiness, validation activities, process improvement, and ...

Implement and manage Quality Control Program per contract specifications and project QC Plan. Requirements : * Work closely with the Project Superintendent and Project Manager coordinating quality ...

Implement and manage Quality Control Program per contract specifications and project QC Plan. Requirements : * Work closely with the Project Superintendent and Project Manager coordinating quality ...

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Quality Control Manager

Rohnert Park, CA · On-site

$75K - $100K/yr

Quality Control (QC) Manager in a metal manufacturing company is responsible for ensuring that raw materials, processes, and finished metal products meet required quality standards, specifications ...

Quality Control Inspector

Santa Rosa, CA · On-site

$24 - $26.75/hr

Follow Quality Management System (QMS) procedures while maintaining compliance with regulatory requirements. * Work safely and effectively within a cleanroom manufacturing environment. Required ...

Quality Technician II

Petaluma, CA

$20.75 - $28/hr

Aerospace quality management system experience (AS9100DD) and/or internal audit experience is preferred * Solid ability to accurately record and manage data, records, files and other documents to ...

Quality Technician II

Petaluma, CA · On-site

$20.75 - $28/hr

Aerospace quality management system experience (AS9100DD) and/or internal audit experience is preferred * Solid ability to accurately record and manage data, records, files and other documents to ...

Quality Technician II

Petaluma, CA

$20.50 - $27.75/hr

... QEs, managers, engineers or interested parties, processing of parts after completion, and ... Develops and maintains process instructions for quality-related activities. Performs semi-routine ...

Perform environmental monitoring and manage ERP (QAD) and MES transactions while effectively ... Experience: * 1-5 years of Quality Control experience, preferably in the medical device industry.

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Showing results 1-20

Quality Manager information

See Santa Rosa, CA salary details

$42.1K

$99.5K

$151.4K

How much do quality manager jobs pay per year?

As of Jul 27, 2026, the average yearly pay for quality manager in Santa Rosa, CA is $99,544.00, according to ZipRecruiter salary data. Most workers in this role earn between $77,100.00 and $120,300.00 per year, depending on experience, location, and employer.

What Does a Quality Manager Do?

As a quality manager, your job is to oversee Quality Assurance (QA) and Quality Control (QC) for each product or service assigned to you. Your duties include guaranteeing products and services meet the standards of your organization, keeping management aware of any problems with production, and ensuring that the manufacturing process goes as smoothly as possible. This job has different aspects depending on where a product or service is in the development cycle. Products that are still being designed need QA to make creation as smooth as possible, while released products require QC to ensure the expected level of quality is maintained.

How much do quality managers get paid?

Quality managers typically earn a median annual salary of around $70,000 to $110,000, depending on experience, industry, and location. They often hold certifications like Six Sigma or ISO auditor training and oversee quality assurance processes within organizations.

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

To thrive as a Quality Manager, you need expertise in quality control processes, data analysis, and regulatory compliance, typically supported by a relevant degree and experience in quality management systems. Familiarity with ISO standards, Six Sigma, and software tools like Minitab or SAP is highly valued, along with certifications such as CQE or Six Sigma Green/Black Belt. Strong leadership, problem-solving abilities, and excellent communication are crucial soft skills for driving continuous improvement and facilitating cross-departmental collaboration. These skills ensure product and process excellence, regulatory adherence, and organizational efficiency.

What is the difference between Quality Manager vs Quality Supervisor?

AspectQuality Manager

Required CredentialsTypically requires a bachelor's degree in quality assurance, engineering, or related field; certifications like ASQ CQE or Six Sigma are common.
Work EnvironmentOversees multiple teams or departments, strategic planning, and process improvement initiatives.
Employer & Industry UsageUsed across manufacturing, healthcare, and service industries to lead quality programs.
Common Search & ComparisonOften compared with Quality Supervisor due to overlapping responsibilities and career progression.

The main difference between a Quality Manager and a Quality Supervisor lies in their scope and responsibilities. A Quality Manager focuses on strategic quality initiatives, process improvements, and managing teams at a higher level, often requiring advanced certifications. In contrast, a Quality Supervisor typically oversees daily operations, supervises staff directly, and implements quality procedures. Both roles are essential in maintaining quality standards, but the manager role involves broader planning and leadership functions.

What is the salary of a QA manager?

The salary of a Quality Assurance (QA) Manager typically ranges from $70,000 to $120,000 annually, depending on experience, industry, and location. Senior QA managers with specialized skills or certifications can earn higher salaries, and the role often involves overseeing testing teams and quality processes.

What is the role of a quality manager?

A quality manager oversees an organization’s quality assurance and control processes to ensure products or services meet specified standards and customer expectations. They develop quality policies, conduct audits, analyze data, and implement improvements, often using tools like Six Sigma or ISO standards. Strong leadership, attention to detail, and certification such as CQE or CQE are common requirements for this role.

What are some common challenges Quality Managers face when implementing new quality standards across teams?

Quality Managers often encounter resistance to change when introducing new quality standards, as team members may be accustomed to established processes. Ensuring consistent understanding and adoption across departments requires clear communication, comprehensive training, and ongoing support. Additionally, balancing the need for compliance with production deadlines can be challenging, so Quality Managers must collaborate closely with operations, engineering, and leadership teams to align goals and foster a culture of continuous improvement.

Is it hard to be a quality manager?

Being a quality manager involves overseeing quality assurance processes, implementing standards like ISO, and managing teams, which can require strong attention to detail, problem-solving skills, and certifications such as Six Sigma. The role can be demanding due to the responsibility for product or service quality and compliance, but it also offers opportunities for professional growth and leadership.
What are the most commonly searched types of Quality jobs in Santa Rosa, CA? The most popular types of Quality jobs in Santa Rosa, CA are:
What job categories do people searching Quality Manager jobs in Santa Rosa, CA look for? The top searched job categories for Quality Manager jobs in Santa Rosa, CA are:
What cities near Santa Rosa, CA are hiring for Quality Manager jobs? Cities near Santa Rosa, CA with the most Quality Manager job openings:
Infographic showing various Quality Manager job openings in Santa Rosa, CA as of July 2026, with employment types broken down into 81% Full Time, 17% Part Time, 1% Temporary, and 1% Contract. Highlights an 86% Physical, 1% Hybrid, and 13% Remote job distribution, with an average salary of $99,544 per year, or $47.9 per hour.
Sr. Technical Manager, Supplier Quality Management BPO

Sr. Technical Manager, Supplier Quality Management BPO

BIOMARIN PHARMACEUTICAL

Novato, CA • On-site

Full-time

Posted 14 days ago


BioMarin Pharmaceutical rating

7.8

Company rating: 7.8 out of 10

Based on 8 frontline employees who took The Breakroom Quiz

51st of 86 rated pharmaceutical


Job description

Who We Are
BioMarin is a leading rare disease biotechnology company focused on genetically defined conditions.
Guided by our purpose to develop medicines that make a profound impact on people's lives, our global teams have delivered a portfolio of therapies since our founding in 1997. Our revolutionary treatments for conditions like achondroplasia (the most common form of dwarfism), PKU (phenylketonuria), CLN2, a form of Batten disease, and a number of forms of MPS (mucopolysaccharidosis) offer new possibilities for patients and families who previously had few, if any, available options. More recently, with the close of the Amicus acquisition, our portfolio has expanded to include therapies for Fabry disease and Pompe disease, expanding our ability to reach more people living with rare genetic conditions.
Our success comes from our unwavering commitment to excellence, our deep understanding of patient needs, our scientific expertise, and our world-class manufacturing capabilities. At the heart of BioMarin is a dedicated team of the brightest minds in the industry working together to deliver innovative therapies to patients and families around the world.
About Technical Operations
BioMarin's Technical Operations group is responsible for creating our drugs for use in clinical trials and for scaling production of those drugs for the commercial market. These engineers, technicians, scientists and support staff build and maintain BioMarin's cutting-edge manufacturing processes and sites, provide quality assurance and quality control to ensure we meet regulatory standards, and procure the needed goods and services to support manufacturing and coordinating the worldwide movement of our drugs to patients.

SUMMARY DESCRIPTION

The Sr. Manager, QA, Supplier Quality Management BPO is an operational leadership role responsible for the execution, day-to-day management, and continuous improvement of core Supplier Quality Management (SQM) processes supporting BioMarin's external supply network for GMP/GDP materials. This role serves as the Business Process Owner (BPO) for the SQM quality process and is accountable for ensuring the processes are consistently applied, effectively monitored, and continuously enhanced across the global supplier base.

The Sr. Manager owns and executes the GMP/GDP material audit program, tracks and maintains key performance metrics for the Supplier Quality department and drives measurable continuous improvement initiatives. Additionally, this role leads the digitalization and AI enablement agenda for the department - translating strategic direction from the Director into practical implementation of automation, analytics, and AI-enabled tools that improve efficiency, oversight, compliance and decision-making.

The Sr. Manager also provides hands-on support to the execution of Supplier Quality Category Manager activities, partnering closely with category managers, Procurement, and Technical Operations to ensure supplier qualification, quality agreements, changes, deviations, and performance activities are executed on time and to standard.

This position requires strong GxP execution expertise, disciplined process management, and the ability to operate effectively in a matrixed, cross-functional environment with a focus on delivery, compliance, and operational excellence.

RESPONSIBILITIES

GMP/GDP Material Audit Program Management

  • Manage the end-to-end execution of the GMP/GDP material supplier audit program (outsourced), including annual audit planning, scheduling, execution oversight, follow-up, CAPA tracking, and effectiveness verification.
  • Ensure audits are completed on schedule in alignment with the approved audit plan.
  • Coordinate internal and third-party auditors, ensuring consistent audit standards, timely reporting, and closure of audit observations.
  • Ensure supplier audit outcomes, identified risks, and corrective actions are appropriately documented, trended, and integrated into Supplier Lifecycle Management and Quality Management Review processes.
  • Support and represent Supplier Quality during regulatory inspections and external audits involving suppliers, providing audit program data and evidence of effectiveness.

Business Process Owner (BPO) - Supplier Quality Management Processes

  • Serve as the Business Process Owner for the Supplier Quality Management quality processes, including supplier qualification and lifecycle management, quality agreements, supplier changes, supplier deviations/CAPA, and supplier auditing.
  • Proactively monitor and maintain the health of these processes and their subprocesses, ensuring consistency of application across the global supplier base.
  • Maintain and update associated procedures, work instructions, templates, and training materials to sustain compliance with current and evolving global health authority requirements.
  • Drive process standardization, harmonization, and simplification across sites and functions.
  • Partner with Quality Systems, Compliance, and IT to ensure supporting systems and workflows enable efficient and compliant process execution.

Performance Metrics & Continuous Improvement

  • Define, track, and maintain the key performance indicators (KPIs) and metrics for the Supplier Quality department, including supplier performance, process health, audit program execution, and issue resolution timeliness.
  • Establish and manage reporting cadences and dashboards to enable trending, signal detection, and timely management review.
  • Identify improvement opportunities from metric trends and lead cross-functional continuous improvement initiatives to address them.
  • Drive a culture of data-driven decision-making and operational excellence within the Supplier Quality team.
  • Support management review processes with accurate, actionable performance data.

Digitalization & AI Implementation

  • Lead the execution of the department's digitalization and AI implementation roadmap, in alignment with the broader Quality Digital Strategy defined by the Director.
  • Identify, evaluate, and implement automation, advanced analytics, and AI-enabled solutions to improve supplier performance monitoring, risk identification, trend analysis, audit effectiveness, and process efficiency.
  • Partner with IT, Quality Systems, and business stakeholders to deliver sustainable, scalable digital solutions, including requirements definition, system configuration, and change management.
  • Drive effective use of Supplier Quality data by integrating information from eQMS, ERP, and external systems to generate actionable insights.
  • Champion adoption of digital and AI tools within the Supplier Quality team through training, communication, and hands-on support.

Supplier Quality Category Manager Execution Support

  • Support the execution of Supplier Quality Category Manager activities across assigned material categories, ensuring timely completion of supplier qualification, onboarding, and lifecycle management tasks.
  • Assist in the development and maintenance of Quality Technical Agreements with global suppliers to define quality expectations and responsibilities.
  • Support risk-based approaches to identify, assess, and mitigate supplier-related risks, ensuring continuity of supply and material quality.
  • Provide execution support for supplier performance management (scorecards), supplier investigations, CAPAs, and change assessments as needed.
  • Collaborate with category managers, Procurement, Manufacturing, and site QA to resolve supplier quality issues and drive supplier performance improvement.

Cross-Functional Collaboration

  • Partner with Global Procurement, Manufacturing, Technical Development, site QA, and other stakeholders to ensure supplier quality requirements are executed effectively across the supplier lifecycle.
  • Represent Supplier Quality in cross-functional process forums, working groups, and improvement projects.
  • Promote knowledge sharing and consistent application of best practices across sites and functions.

People & Team Contribution

  • Provide day-to-day guidance, coaching, and technical mentorship to Supplier Quality team members supporting the audit program, BPO activities, metrics, and digital initiatives.
  • Support onboarding, training, and capability development within the Supplier Quality team.
  • Foster a culture of quality, accountability, collaboration, and continuous improvement.

EDUCATION

  • Bachelor's degree in Life Sciences, Engineering, or a related discipline required.
  • Advanced degree (MS, PhD, MBA) desirable but not required.
  • Six Sigma, Lean, or auditor certification (e.g., ASQ CQA) desirable.

EXPERIENCE

  • Minimum of 10 years of experience in Quality Assurance, Supplier Quality, Manufacturing, or related roles within a highly regulated industry (biotechnology, pharmaceutical, medical device, or combination products).
  • Solid working knowledge of global quality and regulatory requirements (e.g., GMP, GDP, ISO standards, 21 CFR).
  • Demonstrated experience executing and managing supplier audit programs for GMP/GDP materials.
  • Prior experience as a Business Process Owner or equivalent process ownership role within a QMS environment strongly preferred.
  • Proven track record of defining and managing KPIs and delivering measurable continuous improvement outcomes.
  • Hands-on experience implementing digital, automation, analytics, or AI-enabled solutions in a Quality or regulated environment strongly preferred.
  • Experience working in a matrixed, global environment and driving results through influence as well as direct execution.
  • Excellent communication, collaboration, and stakeholder management skills, including the ability to present data and defend approaches to senior management and inspectors.
  • Strong organizational skills with the ability to manage multiple priorities and deliver on time.


Note: This description is not intended to be all-inclusive, or a limitation of the duties of the position. It is intended to describe the general nature of the job that may include other duties as assumed or assigned.
Equal Opportunity Employer/Veterans/Disabled
An Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability.
Ireland Safety Responsibility Support the organisation's commitment to environmental protection, injury prevention, and continual improvement of EHS management systems. Actively contribute to a safe and environmentally responsible workplace by identifying hazards, reporting incidents and participating in EHS initiatives and training.
Ireland Safety Responsibility
Support the organisation's commitment to environmental protection, injury prevention, and continual improvement of EHS management systems. Actively contribute to a safe and environmentally responsible workplace by identifying hazards, reporting incidents and participating in EHS initiatives and training.

Employment Type: Fulltime-Regular

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