1

Quality Assurance Associate Jobs in San Ramon, CA

Quality Assurance Engineer

Union City, CA ยท On-site

$136 - $156/hr

Job Summary The Quality Assurance (QA) Engineer is responsible for all activities involving quality assurance and compliance with applicable regulatory requirements. The position manages quality ...

New

Bachelors or Associate's degree AND * 3+ years of experience in a QA or related role. Qualifications Additional Information All your information will be kept confidential according to EEO guidelines.

Job Title QE Lead / QA Manager (Embedded QE) Location Sunnyvale, California We are seeking a QE Lead / QA Manager to lead an embedded quality engineering team. The role involves managing integration ...

Position : QA Lead Duration : 6 + months Location : San Ramon, CA We are looking for an experienced QA engineer (10+ years) Key skills are listed below. Must Have skills: o Minimum 3 years of ...

Bachelors or Associate's degree AND * 3+ years of experience in a QA or related role. Additional Information All your information will be kept confidential according to EEO guidelines.

As the Quality Assurance (QA) Lead, you will partner across multiple functions to drive quality excellence, ensure compliance with applicable quality system regulations and software standards, and ...

Partner with engineering and QA to translate release requirements into automated coverage and ... All our associates working with us are expected to embrace our RACE values: R - Results Matter, A ...

QA Lead

San Ramon, CA ยท On-site

Company Description IT Role: QA Lead Location: San Ramon, CA Duration: Fulltime BGV will be done for the selected candidates. Must have- QA lead Mainframe experience Cards experience Migration ...

As the Quality Assurance (QA) Lead, you will partner across multiple functions to drive quality excellence, ensure compliance with applicable quality system regulations and software standards, and ...

Application Development Project Management Quality Assurance Business/Systems Analysis Datawarehouse & Business Intelligence Infrastructure & Network Services Risk Management & Compliance Business ...

Quality Assurance Supervisor

Pittsburg, CA ยท On-site

$55K - $60K/yr

Supervise and coordinate daily quality assurance activities, including inspections, testing, and documentation to ensure compliance with food safety standards (FDA, USDA, HACCP, GMP, SQF, and company ...

Application Development Project Management Quality Assurance Business/Systems Analysis Datawarehouse & Business Intelligence Infrastructure & Network Services Risk Management & Compliance Business ...

Sanmina is seeking a Quality Assurance Engineer with 2+ years of experience in electronics manufacturing and high-volume production environments. In this role, you will develop, evaluate, and ...

QA Specialist

San Jose, CA ยท On-site

$67K - $77K/yr

Description Job Summary The QA Specialist implements company and regulatory quality standards company wide. Audits and reviews quality data according to established procedures that drive proactive ...

QA Specialist

San Jose, CA ยท On-site

$67K - $77K/yr

Job Type Full-time Description Job Summary The QA Specialist implements company and regulatory quality standards company wide. Audits and reviews quality data according to established procedures that ...

Showing results 41-60

Quality Assurance Associate information

See San Ramon, CA salary details

$14

$32

$69

How much do quality assurance associate jobs pay per hour?

As of Aug 20, 2026, the average hourly pay for quality assurance associate in San Ramon, CA is $32.73, according to ZipRecruiter salary data. Most workers in this role earn between $20.96 and $38.41 per hour, depending on experience, location, and employer.

What does a quality assurance associate do?

A Quality Assurance Associate is responsible for monitoring and evaluating the various processes involved in product development and production to ensure they meet established quality standards. Their duties typically include conducting inspections, documenting findings, assisting in process improvements, and ensuring compliance with regulatory requirements. They play a critical role in identifying defects, reducing errors, and maintaining the overall quality of products or services before they reach customers.

What skills and qualifications are needed to be a quality assurance associate?

To excel as a Quality Assurance Associate, you need a solid understanding of quality control principles, attention to detail, and often a degree in a related field like chemistry, biology, or engineering. Familiarity with industry-standard quality management systems (such as ISO 9001), statistical analysis software, and documentation tools is typically required. Strong problem-solving skills, effective communication, and the ability to work collaboratively are highly valued in this role. These skills ensure that products and processes consistently meet standards, reduce errors, and maintain compliance with regulatory requirements.

What are common challenges faced by quality assurance associates in ensuring consistent product quality?

Quality Assurance Associates often encounter challenges such as managing tight production deadlines while maintaining thorough testing standards, addressing unexpected defects, and adapting quickly to new regulatory or product requirements. Effective communication with production, development, and regulatory teams is crucial for resolving issues efficiently. Staying current with evolving quality standards and continuously improving testing processes are also important for success in this role.

What is the difference between Quality Assurance Associate vs Quality Control Inspector?

AspectQuality Assurance AssociateQuality Control Inspector
CertificationsOften requires certifications like ASQ CQIA or related quality assurance trainingMay require certifications such as ISO auditor or specific industry standards
Work EnvironmentInvolves process audits, documentation, and improving quality systemsFocuses on inspecting products or materials for defects
Employer & Industry UsageCommon in manufacturing, pharmaceuticals, and tech industriesPrimarily in manufacturing, food production, and assembly lines

While both roles focus on quality, the Quality Assurance Associate emphasizes developing and maintaining quality systems and processes, whereas the Quality Control Inspector concentrates on inspecting products for defects. Both roles are essential for ensuring product quality but differ in scope and responsibilities.

Is a Quality Assurance Associate an entry-level job?

A Quality Assurance Associate position is often considered entry-level, suitable for candidates with little to no prior experience in quality assurance or related fields. It typically requires basic knowledge of testing procedures, attention to detail, and may involve training on specific tools or software used in quality control processes.

What is the role of a quality assurance associate?

A quality assurance associate is responsible for monitoring and testing products or services to ensure they meet quality standards and specifications. They often develop testing procedures, document issues, and collaborate with teams to improve processes, using tools like checklists and quality management systems. Attention to detail and knowledge of industry regulations are essential for this role.

What are the most commonly searched types of Quality Assurance jobs in San Ramon, CA?

The most popular types of Quality Assurance jobs in San Ramon, CA are:

What job categories do people searching Quality Assurance Associate jobs in San Ramon, CA look for?

The top searched job categories for Quality Assurance Associate jobs in San Ramon, CA are:

What cities near San Ramon, CA are hiring for Quality Assurance Associate jobs?

Cities near San Ramon, CA with the most Quality Assurance Associate job openings:

Infographic showing various Quality Assurance Associate job openings in San Ramon, CA as of August 2026, with employment types broken down into 1% As Needed, 82% Full Time, 12% Part Time, 4% Contract, and 1% Nights. Highlights an 87% Physical, 2% Hybrid, and 11% Remote job distribution, with an average salary of $68,084 per year, or $32.7 per hour.

Quality Assurance Engineer

Mizuhosi

Union City, CA โ€ข On-site

$136 - $156/hr

Other

Medical, Dental, Vision, Life, Retirement

Posted 2 days ago

New


Job description

Location: Union City, CA, US, 94587

About Company

Mizuho OSI is the leader in the markets for specialty surgery and patient positioning. The companyโ€™s portfolio includes specialty surgical tables for procedure-specific approaches that improve patient outcomes in spine and orthopedic surgeries along with disposable and reusable surgical patient care products.

Job Summary

The Quality Assurance (QA) Engineer is responsible for all activities involving quality assurance and compliance with applicable regulatory requirements. The position manages quality assurance programs and processes to ensure the quality of product conforms to the established procedures and applicable regulatory requirements. The position utilizes technical expertise on the FDAโ€™s QMSR, ISO 13485, ISO 14971, EU MDR for Class I and Class II medical devices for capital equipment and their accessories.

The QA Engineer position supports Mizuho OSI in achieving established goals and objectives and follows the Corporate Vision, Mission & Values Statements, to maintain the services and quality levels set by Mizuho OSI.

Responsibilities
  • Provide QA Engineering input and guidance during manufacturing, production and design activities in support of new product introductions and modifications to existing products. The support includes but is not limited to the review and approval of validation documentation, test reports, and procedures according to change control requirements.
  • Conduct Internal Audits to ensure compliance with the established procedures and applicable regulatory requirements. Manage all aspects of the audit lifecycle: to include scheduling, planning, issuing agendas, executing, issuing reports, reviewing and approving reports, evaluating responses, requesting clarification, issuing CA/PA and closing out of audits.
  • Maintain and continuously improve the inspection readiness program to ensure the site is always prepared for regulatory and internal audits. Serve as a support during external audits (e.g., Notified Bodies, FDA, Corporate), including logistics, documentation, and auditee coaching.
  • Manage processing of Complaints and CAPAs. Act as SME for the assigned issues to contain, investigate, develop action plans, and drive to closure as required within prescribed timelines.
  • Monitor and ensure compliance with applicable regulatory standards applicable to Mizuho OSI (QMSR, ISO 13485, ISO 14971, EU MDR, REACH, RoHS, PFAS, etc.). Participate in the development and implementation of quality policies, procedures, and processes aligning with GMPs and applicable regulations. Work closely with multi-functional teams / system owners to lead and/or support continuous improvement initiatives related to QMS improvement. Develop quality data management tools, applicable compliance performance metrics (KPIs) and remediation plans for identified non-conformances.
  • In collaboration with RA, Marketing and Manufacturing teams, manage all aspects of labeling process for registered company products, ensuring accuracy, compliance, and consistency of labeling content throughout product lifecycle. Maintain internal procedures for labeling design, processing, and control to ensure compliance with applicable requirements by regularly reviewing and updating the procedures as necessary.
  • Review and develop documentation for acceptance, monitoring and validations for EO/Gamma/E-Beam sterilization and clean/controlled manufacturing environment.
  • Utilize standard statistical analysis techniques to determine product acceptance: evaluate process capabilities; and develop statistically sound tolerance limits based on product specifications, recommend sampling plans, inspection methods, etc.
  • Responsible for a professional work area to include cleanliness, organization, and overall QA department appearance.
  • To be willing to share knowledge and instruct other members of the department and the company, by passing along skills and information to assist them in their development.
  • To help create an ongoing effort through personal action and by contributing ideas to support both the department and Companyโ€™s ongoing improvement efforts.
  • To understand Mizuho OSIโ€™s business objectives and the relationship between the department and those objectives.
  • To understand, follow and support Mizuho OSIโ€™s internal Quality System policies, procedures and work instructions including but not limited to applicable external regulations (FDAโ€™s QMSR, ISO 13485, ISO 14971 and applicable International Standards).
Qualifications & Requirements
  • Bachelorโ€™s degree in science or related field; and 8-12 years of related experience in mechanical or electromechanical medical device manufacturing or Master's degree and 6+ years or PhD Degree and 3+ years.
  • Experience with mechanical and electro-mechanical medical device manufacturing.
  • Previous experience with managing quality systems: CAPA, Complaints processing, NCR, MRB, Deviations.
  • Thorough knowledge on ISO standards, FDAโ€™s QMSR, EU MDR and other regulations as applicable to Mizuho OSIโ€™s products.
  • Familiar with ISO/IEC/IEEE 12207 (Systems and software engineering โ€” Software life cycle processes) and IEC 62304 (life-cycle requirements for the development of medical software and software within medical devices).
  • Possess Equipment Qualification Experience (IQ/OQ/PQ). Provide assistance and/or perform inspection, and electrical safety testing. Ability to perform basic statistical analysis, calculating C&R, create and reconcile reports, demonstrate strong analytical skills, and attention to detail.
  • Knowledge of sterilization methods for medical devices. Thorough understanding of acceptance, monitoring and validations for EO/Gamma/E-Beam sterilization and clean/controlled manufacturing environment
  • ASQ Certification for CQE, CQA. Auditor certification for ISO 13485 is desirable.
  • Demonstrated knowledge of engineering applications, CAD and Solid Modeling software. General understanding of Geometric Dimensioning and Tolerance (GD&T) skills.
  • Familiarity with โ€œLeanโ€ manufacturing principles is preferred.
  • Ability to work independently and collaboratively with small and cross functional teams.
  • Excellent computer skills including operating Windows based personal computers, various office equipment and machines, and telephone system. Ability to efficiently and effectively use Microsoft products such as Outlook, Word, Excel, Project, Visio and PowerPoint to analyze data, produce trend charts and presentation.
  • Ability to clearly express oneself verbally in the English language (additional languages also preferred) using good grammar, vocabulary, eye contact, and friendly voice inflection with all employees. Ability to communicate effectively with employees and other business contacts in a courteous and professional manner.
  • Ability to clearly and effectively express oneself through written means, to properly use such technical factors as grammar, punctuation, vocabulary, and correct spelling. To be able to prepare business letters, memorandums, and reports. Excellent verbal and written communication skills, strong presentation, project and organizational skills.
  • Excellent customer focus with a high sense of urgency to create positive experiences, and if applicable, resolutions. Ability to provide excellent interpersonal and communication skills.
  • Ability to function calmly in a fast-paced environment managing multiple priorities simultaneously. To be able to positively manage situations of a dynamic nature; to be able to modify plans, actions, and decisions considering changing situations and circumstances while still meeting, or proposing modified, deadlines.
  • To respond sensitively to the needs and feelings of others regardless of position; to accept interpersonal differences, to maintain rapport, and to interact effectively with all levels of employees within the organization.
  • To be able to demonstrate an understanding, and the regular use of a time management process, which systematically structures oneโ€™s own work to provide for effective task performance and to plan and prioritize items to meet future demands.
  • Ability to establish and accomplish goals independently and to function as a positive and productive team member.
  • Neat and professional appearance and outgoing people-oriented personality which conveys pride in working for Mizuho OSI and which is demonstrated with a ready smile and a willingness to assist others.

Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions.

Salary range: $1 36 ,000- $1 56 ,000 DOE + annual potential bonus + comprehensive benefits package

EOE STATEMENT

Mizuho OSI is an Equal Opportunity Employer and makes business decisions based on job related criteria only. Company policy prohibits unlawful discrimination based on race, color, religious creed, gender, religion, marital status, registered domestic partner status, age, national origin or ancestry, physical or mental disability, medical condition including genetic characteristics, sexual orientation, sexual identity, or any other consideration made unlawful by federal, state or local laws.

Mizuho OSI conducts criminal conviction background checks and drug screening through a third-party screening vendor which includes searches of address history, criminalconvictions,court records,education verification, employment verification, and reference checks. In addition, depending on the nature of the position for which you are applying, a motor vehicle driving report, a credit report, and/or ID checks in other non-U.S. countries are also included.

Criminal conviction background checks will run after an applicant has received and accepted a conditional offer of employment. After a conditional offer is made and before any background check is performed, applicants will receive background check disclosure and consent forms under state and federal laws, such as the Fair Credit Reporting Act and the Investigative Consumer Reporting Agencies Act. Existence of a criminal record is not an automatic bar to employment. An assessment will be made about whether the conviction has a direct and adverse relationship to the job in question.No job offer will be withdrawn, and no adverse action will be taken against any employee, based on the results of a criminal conviction background check, without an individualized assessment of whether the applicantโ€™s conviction history has direct and adverse relationship with the specific duties of the job in question.

Top Reasons To Join The Mizuho OSI Team
  • Privately held company with a tradition of market leadership and best-in-class innovation
  • Fast-paced entrepreneurial culture focused on dramatically improving patient outcomes through personal empowerment
  • Emphasis on continuous improvement and celebration of our values of R.E.S.P.E.C.T. and the Mizuho OSI Way.
  • Create innovative solutions designed and manufactured at our HQ in Northern California
The Mizuho OSI Way

In 1978, we set out to change the way patients undergo surgery. As a Mizuho OSI customer, you can expect our commitment to the followingโ€ฆ

  • We commit to your satisfaction. If you are dissatisfied, we will strive to make it right.
  • We do things the right way. We commit to hire people with competence, generosity and a caring attitude.
  • We motivate our employees to use their individual strengths to provide creative solutions, changes, and innovations.
  • We anticipate your needs through customer experiences, thus nurturing our relationships.

Collectively, this creates an environment that enables and inspires healthcare professionals to improve the lives of patients.

Dare to go further. Care to do more.

BENEFITS
  • medical
  • dental
  • vision
  • life insurance
  • 401k with matching
  • educational assistance
  • and more.
FOR OUR SERVICE MEMBERS AND VETERANS

Mizuho OSI values the service Veterans and their family members have given to our country and we support the hiring of returning Service Members and military spouses. If you are a Veteran or wounded warrior and would like assistance with the employment process at Mizuho OSI, please contact HR at (510) 429-1500.

FOR PERSONS WITH DISABILITIES

If you are a person with a disability or a disabled Veteran and are applying for a job with Mizuho OSI, we would like to ensure your application process goes as smoothly as possible. If you need additional assistance, information or answers to your questions, feel free to contact HR at (510) 429-1500.

#J-18808-Ljbffr