Software Quality Engineer Visa Sponsorship Jobs in California
California is one of the most active states for software quality engineer visa sponsorship, driven by major tech employers across Silicon Valley, San Francisco, San Jose, and Los Angeles. Companies like Apple, Google, Salesforce, and Meta regularly hire for QA engineering roles and have established H-1B visa sponsorship programs to recruit international talent.
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Get Access To All JobsMAIN JOB RESPONSIBILITIES / COMPETENCIES
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Coordinate quality engineering activities supporting the Software as a Medical Device (SaMD), Quality System software, and Manufacturing software platforms to achieve business objectives.
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Provide technical expertise through the software lifecycle, with a focus on SaMD, in the following areas: design control, risk analyses, verification/validation strategy, maintenance and change management.
-
Develop strategy as part of cross-functional teams to support the compliant and effective release of SaMD and other software applications.
-
Provide guidance and leadership on development / review of design control and validation policies and procedures, and resolutions to quality engineering issues. Act as an effective leader or team member in supporting quality disciplines, decisions, and practices.
-
Provide technical expertise to the risk documentation process.
-
Provide guidance and leadership on investigations involving software nonconformances, product or component failures, or customer complaints by leading or participating in the investigation process, technical troubleshooting, FMEA, hazard, or other risk analysis, determining root cause and recommending CAPA.
-
Participate in the preparation of nonconformance investigations and responses, and completion of corrective action plans as needed.
-
Provide guidance and leadership on design processes and site engineering functions to identify critical parameters and improve process quality.
-
Participate on Design Control New Product development teams; advise the team on design control requirements; develop, review and approve design control deliverables related to quality engineering and validations.
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Other duties as assigned.
REQUIREMENTS
EDUCATION & TRAINING
- Bachelor’s degree, preferably in Engineering or sciences.
- Advanced degree preferred.
- Certified Quality Engineer (CQE) or equivalent preferred.
Experience
- Five years’ experience in validation and/or design control in the medical device software industry, including the practical application of FDA Quality System Regulation and ISO 13485; or equivalent combination of education/experience.
- Experience in medical device software change management required.
- Experience in vision care or intraocular lens industry preferred.
- General knowledge of medical device software requirements (IEC 62304, IEC 82304) required.
- Knowledge of international/ISO standards on ophthalmology preferred.
- Applicant must be knowledgeable about regulatory/compliance/validation issues, be self-motivated, intelligent and reliable.
SKILLS
- Experience in writing technical documents, especially compliance and/or validation/quality assurance documents and protocols required.
- Proficiency in written and spoken English required.
- Excellent project management, organization, writing, communication and presentation skills required.
- Ability to communicate in a wide variety of communication styles and to influence and build consensus across cross-functional groups.
- Must have strong written and oral communication skills.
COMPENSATION
- Pay range: $115K - $150K - Final compensation/salary will depend on experience.
STAAR Surgical is an Equal Employment Opportunity/Affirmative Action employer and all qualified applicants will receive consideration without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran or disability status, or any other characteristic protected by law.
LOCATION
Monrovia, CA, US
Job Code 2213
# of Openings 1
MAIN JOB RESPONSIBILITIES / COMPETENCIES
-
Coordinate quality engineering activities supporting the Software as a Medical Device (SaMD), Quality System software, and Manufacturing software platforms to achieve business objectives.
-
Provide technical expertise through the software lifecycle, with a focus on SaMD, in the following areas: design control, risk analyses, verification/validation strategy, maintenance and change management.
-
Develop strategy as part of cross-functional teams to support the compliant and effective release of SaMD and other software applications.
-
Provide guidance and leadership on development / review of design control and validation policies and procedures, and resolutions to quality engineering issues. Act as an effective leader or team member in supporting quality disciplines, decisions, and practices.
-
Provide technical expertise to the risk documentation process.
-
Provide guidance and leadership on investigations involving software nonconformances, product or component failures, or customer complaints by leading or participating in the investigation process, technical troubleshooting, FMEA, hazard, or other risk analysis, determining root cause and recommending CAPA.
-
Participate in the preparation of nonconformance investigations and responses, and completion of corrective action plans as needed.
-
Provide guidance and leadership on design processes and site engineering functions to identify critical parameters and improve process quality.
-
Participate on Design Control New Product development teams; advise the team on design control requirements; develop, review and approve design control deliverables related to quality engineering and validations.
-
Other duties as assigned.
REQUIREMENTS
EDUCATION & TRAINING
- Bachelor’s degree, preferably in Engineering or sciences.
- Advanced degree preferred.
- Certified Quality Engineer (CQE) or equivalent preferred.
Experience
- Five years’ experience in validation and/or design control in the medical device software industry, including the practical application of FDA Quality System Regulation and ISO 13485; or equivalent combination of education/experience.
- Experience in medical device software change management required.
- Experience in vision care or intraocular lens industry preferred.
- General knowledge of medical device software requirements (IEC 62304, IEC 82304) required.
- Knowledge of international/ISO standards on ophthalmology preferred.
- Applicant must be knowledgeable about regulatory/compliance/validation issues, be self-motivated, intelligent and reliable.
SKILLS
- Experience in writing technical documents, especially compliance and/or validation/quality assurance documents and protocols required.
- Proficiency in written and spoken English required.
- Excellent project management, organization, writing, communication and presentation skills required.
- Ability to communicate in a wide variety of communication styles and to influence and build consensus across cross-functional groups.
- Must have strong written and oral communication skills.
COMPENSATION
- Pay range: $115K - $150K - Final compensation/salary will depend on experience.
STAAR Surgical is an Equal Employment Opportunity/Affirmative Action employer and all qualified applicants will receive consideration without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran or disability status, or any other characteristic protected by law.
LOCATION
Monrovia, CA, US
Job Code 2213
# of Openings 1
Software Quality Engineer Job Roles in California
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Search Software Quality Engineer Jobs in CaliforniaSoftware Quality Engineer Jobs in California: Frequently Asked Questions
Which companies sponsor visas for software quality engineers in California?
California's largest tech employers are consistent H-1B sponsors for software quality engineer roles. Apple, Google, Meta, Salesforce, Adobe, and Nvidia have all filed LCAs for QA-related positions in recent OFLC disclosure data. Mid-size companies and enterprise software firms in Silicon Valley and Los Angeles also sponsor regularly, particularly those with dedicated QA or release engineering teams.
Which visa types are most common for software quality engineer roles in California?
The H-1B is by far the most common visa for software quality engineers in California, as the role typically qualifies as a specialty occupation requiring a bachelor's degree in computer science, software engineering, or a related field. Candidates already holding L-1B status from multinational transfers or OPT from a California university are also common pathways into full sponsorship with a California-based employer.
Which cities in California have the most software quality engineer sponsorship jobs?
San Jose, San Francisco, and the broader Silicon Valley corridor account for the highest concentration of software quality engineer sponsorship roles in California. Cupertino, Sunnyvale, and Mountain View see consistent hiring from hardware and platform companies. Los Angeles has grown significantly, particularly in media-tech, gaming, and aerospace software, with San Diego adding roles in biotech software and defense contracting.
How to find software quality engineer visa sponsorship jobs in California?
Migrate Mate is built specifically for international candidates looking for visa sponsorship jobs, including software quality engineer roles in California. You can filter by state and role to see employers actively sponsoring in California's tech hubs. Migrate Mate focuses on verified sponsorship opportunities, which saves time compared to applying broadly and discovering late in the process that a company won't sponsor.
Are there any California-specific considerations for software quality engineers seeking visa sponsorship?
California's prevailing wage requirements are among the highest in the country for software quality engineers, given the cost of living in the Bay Area and Los Angeles. Employers must certify on the Labor Condition Application that they will pay at or above the prevailing wage for the work location, so roles based in San Francisco or San Jose reflect that market. University programs at UC Berkeley, UCLA, and Stanford also feed a strong pipeline of OPT candidates into California QA roles, which many employers are already familiar sponsoring.
What is the prevailing wage for sponsored software quality engineer jobs in California?
U.S. employers sponsoring a visa must pay at least the prevailing wage, which is what workers in the same role, area, and experience level typically earn. The Department of Labor sets this rate to make sure companies aren't hiring foreign workers simply because they'd accept lower pay than a U.S. worker. It varies by job title, location, and experience. You can look up current prevailing wage rates for any occupation and location using the OFLC Wage Search page.