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Quality System Manager Jobs in California (NOW HIRING)

The opportunity As the leader of our Quality Management System at Archer, you will play a pivotal role in shaping the quality framework for our first certified aircraft, Midnight. Operating at the ...

Objective: Assist in implementing the SMI Quality system at designated SMI facility Assist in ... Process control Assists in project management as requested by project manager. Ensure maintenance ...

This role provides leadership and oversight for key quality system functions, including but not limited to Health Hazard Evaluations (HHE), and nonconformance management. This position will support ...

This role provides leadership and oversight for key quality system functions, including but not limited to Health Hazard Evaluations (HHE), and nonconformance management. This position will support ...

Quality Manager Engineering - Fremont, California The Quality Manager is a key leader within Pivotal Systems' quality organization, reporting to the Director of Quality, and plays a central role in ...

Quality Manager Engineering - Fremont, California The Quality Manager is a key leader within Pivotal Systems' quality organization, reporting to the Director of Quality, and plays a central role in ...

The Quality Systems & QC Manager is responsible for leading and continuously improving Kern Steel ... Ensure quality system processes, procedures, inspection practices, and documentation requirements ...

Perform other tasks as may be directed by the Conformity Assessment Group Presidents or Sr. VP, Quality System. Basic Hiring Criteria: * Bachelor's degree in Engineering, Quality Management, or a ...

Showing results 41-60

Quality System Manager information

See California salary details

$53.3K

$97.3K

$152K

How much do quality system manager jobs pay per year?

As of Aug 18, 2026, the average yearly pay for quality system manager in California is $97,322.00, according to ZipRecruiter salary data. Most workers in this role earn between $74,500.00 and $120,900.00 per year, depending on experience, location, and employer.

What does a quality system manager do?

A Quality System Manager oversees the development, implementation, and maintenance of an organization's quality management systems. They ensure that all processes and products meet established quality standards and comply with relevant regulations. Their responsibilities include auditing processes, managing documentation, training staff on quality procedures, and driving continual improvement initiatives. By monitoring performance and addressing non-conformities, they help organizations deliver consistent, high-quality products or services.

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

To thrive as a Quality System Manager, you need a solid background in quality management principles, regulatory compliance, and process improvement, typically with a degree in engineering, life sciences, or a related field. Familiarity with ISO standards (e.g., ISO 9001), quality management software, and relevant certifications like Six Sigma or ASQ certifications is important. Strong leadership, problem-solving, and communication skills help drive cross-functional initiatives and foster a culture of continuous improvement. These skills ensure effective implementation of quality systems, compliance with industry standards, and sustained operational excellence.

What are some common challenges faced by a quality system manager when implementing new quality standards across an organization?

Quality System Managers often encounter challenges such as resistance to change from staff, aligning new standards with existing processes, and ensuring consistent understanding across departments. Building strong communication channels and providing thorough training are essential to facilitate adoption. Additionally, maintaining regulatory compliance while tailoring the system to the organization's unique needs requires careful planning and collaboration with cross-functional teams.

What is the difference between Quality System Manager vs Quality Assurance Manager?

AspectQuality System ManagerQuality Assurance Manager
CertificationsISO 9001 Lead Auditor, CQEASQ CQE, Six Sigma Green/Black Belt
Work EnvironmentOversees quality management systems across departmentsFocuses on product quality and testing processes
Industry UsageCommon in manufacturing, aerospace, automotivePrevalent in manufacturing, healthcare, software
Primary FocusMaintaining and improving quality management systemsEnsuring product quality through testing and inspection

The Quality System Manager primarily manages the overall quality management system, ensuring compliance with standards like ISO 9001. The Quality Assurance Manager concentrates on product quality, testing, and inspection processes. Both roles require similar certifications and are vital in manufacturing and related industries, but their focus areas differ—system oversight versus product quality assurance.

What are the most commonly searched types of Quality System jobs in California?

The most popular types of Quality System jobs in California are:

What cities in California are hiring for Quality System Manager jobs?

Cities in California with the most Quality System Manager job openings:

Infographic showing various Quality System Manager job openings in California as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $97,322 per year, or $46.8 per hour.

Quality System Specialist (Veeva eQMS Specialist)

Viking Therapeutics, Inc.

San Diego, CA

$95K - $115K/yr

Full-time

Re-posted 2 days ago


Job description

Description

 We are seeking an experienced Veeva eQMS Specialist with deep expertise in Veeva Basics, ideally someone who has led or played a key role in full implementations across QualityDocs, QMS, Training, and other Vault Quality modules. This role will partner closely with Quality and cross-functional teams to translate business needs into scalable system design, ensuring that our Veeva ecosystem supports compliant, efficient, and future-ready quality operations. The ideal candidate is detail-oriented, organized, and passionate about driving quality excellence in a fast-paced environment.


Essentials Duties and Responsibilities

The main responsibilities of this role include:

Lead or support different implementation phases of Veeva Basics modules and processes including Quality Docs, Quality Events, Supplier Quality, supporting SOPs and training 

Configure and optimize workflows, document types, metadata, training assignments, quality processes, and user roles

Conduct detailed process mapping of current-state and future-state eQMS processes (e.g., Document Management, Change Control, Deviations, CAPA, Complaints, Training)

Facilitate workshops with cross-functional stakeholders for training on new processes within Veeva

Lead or support historical CMC documents migration in Veeva

Identify opportunities for process improvements and automation within Veeva

Maintain updates to Veeva releases, including impact assessments and SOP revisions

Develop user training materials and deliver hands-on training for business end users

Provide ongoing support, troubleshoot issues, and manage enhancement requests

Serve as a subject matter expert (SME) for Veeva Basics within the Quality organization 

Maintain and manage controlled records, including batch/test records, logs, reports, and quality management documentation

Assist in preparing materials for internal audits and ensuring documentation readiness for regulatory inspections

Collaborate with senior team members to improve and implement quality management systems and training programs

Assist in preparing reports and documentation related to deviations, corrective actions, and change controls

Support Quality Management System (QMS) activities including investigations, complaints, CAPAs, inspections, quality metrics, and continuous improvement initiatives.

Perform additional tasks as assigned

Requirements

Education and Experience Requirements

Bachelor's Degree in a related field and/or 3-5 years related experience in a regulated industry

Minimum of three (3) years of relevant QA experience in a GMP-regulated environment.

Hands-on experience with full Veeva Vault or Veeva Basics implementations, ideally within the Vault Quality Suite (QualityDocs, QMS, Training)

Veeva Vault Administrator or Vault Quality certification (a plus)


Knowledge and Skills Requirements

Strong working knowledge of GxP, 21 CFR Part 11, Annex 11, and core quality system processes

Experience working with global teams and regulated environments

Experience in managing enhancements post-implementation and supporting continuous improvement

Strong written and verbal communications skills

Attention to detail and ability to manage multiple priorities

VIKING THERAPEUTICS

Viking Therapeutics, Inc., is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status. Viking Therapeutics also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA.


Notice to Agency and Search Firm Representatives

Viking Therapeutics, Inc. is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Viking employee by a third-party agency and/or search firm without a valid written & signed search agreement, and assignment of specific position, will become the sole property of Viking Therapeutics, Inc. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral.


Salary Description

$95,000.00 - $115,000.00 annual salary