Medical Devices H-1B1 Singapore Sponsorship Jobs in California
H-1B1 Singapore visa sponsorship jobs in California's medical devices sector are concentrated in the Bay Area, San Diego's Biocom corridor, and Los Angeles, with major employers including Stryker, Intuitive Surgical, Abbott, and Edwards Lifesciences actively filing Labor Condition Applications for Singaporean professionals in engineering, regulatory affairs, and clinical roles.
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Get Access To All JobsINTRODUCTION
Viant Medical is a global medical device design and manufacturing services provider that partners and innovates with customers to provide the highest quality, life enhancing medical devices. With nearly 6,000 associates across 24 locations worldwide, we offer a unique combination of small-company service and attention with big-company resources. Together, We’re in It for Life.
ROLE AND RESPONSIBILITIES
The Quality Engineer II is primarily responsible for problem identification, data collection and trend analysis, reporting, and initiation of corrective and/or preventative action for in process, product and equipment related quality issues. This includes responsibility for the quality aspects of qualification and/or validation of molds, products, processes and equipment.
What you'll do:
- Support and uphold the Viant Values: Customer Oriented, Integrity, Servant Leadership, Own It, Teamwork, and Be Agile.
- Adhere to company policies and procedures.
- Problem Resolution: identification, data collection and trend analysis, reporting, and initiation of corrective and/or preventative action
- Open, investigate, and close NCRs
- Open, investigative, and close complaints
- Continuous Quality Improvement: systems, documents, software and technical tools. Update procedures as required.
- Product line ownership, customer facing role
- Reporting of internal and external quality problems and trends.
- Execute Validations
- Coordinates activities between Engineering, Manufacturing and Quality, including qualification and validation.
- Monitoring and improvement of SPC systems, sampling plans and statistical methods.
- Cost of Quality reporting and analysis, as required.
- Training of personnel to improve technical skills, job knowledge and performance.
- Create control plans and PFMEAs.
- Back-up to QS Management Representative, as assigned.
- Plan, prepare, and execute Internal Audits, as assigned.
- Alternate Inspectors in Quality Assurance as needed.
- Coordinate with other departments as a member of problem-solving teams.
- Assist Inspectors in Quality Assurance as needed.
- Perform Quality Manager duties when required.
- Perform other duties as assigned by the Quality Manager.
- Represent Viant with customers, vendors, and outside auditors.
- Execute Document Control functions as deemed necessary.
BASIC QUALIFICATIONS
- 2-3+ years of experience in Medical Device industry or related field.
- High school diploma required, bachelor's degree in technical or related field preferred.
- Working in medical device or other FDA regulated industry.
- Comprehensive understanding of ISO 9001, ISO 13485, JPAL MHLW Ordinance 169, and or FDA QSR regulatory requirements.
- Computer literate with working knowledge of MS Word, Excel, and Access, desired candidate will have prior work history in MSA, SPC, Mini-tab, Infinity, sterilization, & clean room environment.
- Proficient with math, statistics, and reading comprehension. Proficient understanding of QMS. Excellent oral and written communication skills.
- Solid understanding of Quality System Regulations (Complaint, NCR, root cause, etc.) Functional Quality statistical knowledge (AQL, sampling, etc.)
- At least two (2) year experience in a supervision and/or management role preferred.
- Demonstrated experience to lead teams and projects and good organizational skills.
- Previous experience in plastic injections molding related environment.
- Knowledge and background in the Medical Device industry preferred.
BENEFITS
- Medical, dental, and vision benefits-effective on date of hire
- Generous paid time off benefits and 10 paid Holidays
- Company-paid life insurance
- 401k plan with company match
- Low-cost nutrition and mental health visits
- Up to $150-off your gym membership annually
- Discounted Pet Insurances for your furry friends
- Access to individualized financial planning meetings
- Employee Discount Program with savings on electronics, home goods, gym equipment, and more
- Discounted family caregiving support
We offer market competitive compensation. Potential salary range for this role is $90k-$105k. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law.
Viant provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, gender, sexual orientation, national origin, age, disability, marital status, amnesty, or status as a covered veteran in accordance with applicable federal, state, and local laws. Viant complies with applicable state and local laws governing nondiscrimination in employment in every location in which the company has facilities.
INTRODUCTION
Viant Medical is a global medical device design and manufacturing services provider that partners and innovates with customers to provide the highest quality, life enhancing medical devices. With nearly 6,000 associates across 24 locations worldwide, we offer a unique combination of small-company service and attention with big-company resources. Together, We’re in It for Life.
ROLE AND RESPONSIBILITIES
The Quality Engineer II is primarily responsible for problem identification, data collection and trend analysis, reporting, and initiation of corrective and/or preventative action for in process, product and equipment related quality issues. This includes responsibility for the quality aspects of qualification and/or validation of molds, products, processes and equipment.
What you'll do:
- Support and uphold the Viant Values: Customer Oriented, Integrity, Servant Leadership, Own It, Teamwork, and Be Agile.
- Adhere to company policies and procedures.
- Problem Resolution: identification, data collection and trend analysis, reporting, and initiation of corrective and/or preventative action
- Open, investigate, and close NCRs
- Open, investigative, and close complaints
- Continuous Quality Improvement: systems, documents, software and technical tools. Update procedures as required.
- Product line ownership, customer facing role
- Reporting of internal and external quality problems and trends.
- Execute Validations
- Coordinates activities between Engineering, Manufacturing and Quality, including qualification and validation.
- Monitoring and improvement of SPC systems, sampling plans and statistical methods.
- Cost of Quality reporting and analysis, as required.
- Training of personnel to improve technical skills, job knowledge and performance.
- Create control plans and PFMEAs.
- Back-up to QS Management Representative, as assigned.
- Plan, prepare, and execute Internal Audits, as assigned.
- Alternate Inspectors in Quality Assurance as needed.
- Coordinate with other departments as a member of problem-solving teams.
- Assist Inspectors in Quality Assurance as needed.
- Perform Quality Manager duties when required.
- Perform other duties as assigned by the Quality Manager.
- Represent Viant with customers, vendors, and outside auditors.
- Execute Document Control functions as deemed necessary.
BASIC QUALIFICATIONS
- 2-3+ years of experience in Medical Device industry or related field.
- High school diploma required, bachelor's degree in technical or related field preferred.
- Working in medical device or other FDA regulated industry.
- Comprehensive understanding of ISO 9001, ISO 13485, JPAL MHLW Ordinance 169, and or FDA QSR regulatory requirements.
- Computer literate with working knowledge of MS Word, Excel, and Access, desired candidate will have prior work history in MSA, SPC, Mini-tab, Infinity, sterilization, & clean room environment.
- Proficient with math, statistics, and reading comprehension. Proficient understanding of QMS. Excellent oral and written communication skills.
- Solid understanding of Quality System Regulations (Complaint, NCR, root cause, etc.) Functional Quality statistical knowledge (AQL, sampling, etc.)
- At least two (2) year experience in a supervision and/or management role preferred.
- Demonstrated experience to lead teams and projects and good organizational skills.
- Previous experience in plastic injections molding related environment.
- Knowledge and background in the Medical Device industry preferred.
BENEFITS
- Medical, dental, and vision benefits-effective on date of hire
- Generous paid time off benefits and 10 paid Holidays
- Company-paid life insurance
- 401k plan with company match
- Low-cost nutrition and mental health visits
- Up to $150-off your gym membership annually
- Discounted Pet Insurances for your furry friends
- Access to individualized financial planning meetings
- Employee Discount Program with savings on electronics, home goods, gym equipment, and more
- Discounted family caregiving support
We offer market competitive compensation. Potential salary range for this role is $90k-$105k. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law.
Viant provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, gender, sexual orientation, national origin, age, disability, marital status, amnesty, or status as a covered veteran in accordance with applicable federal, state, and local laws. Viant complies with applicable state and local laws governing nondiscrimination in employment in every location in which the company has facilities.
Medical Devices Job Roles in California
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Search Medical Devices Jobs in CaliforniaMedical Devices Jobs in California: Frequently Asked Questions
Which medical devices companies in California sponsor H-1B1 Singapore visas?
California-based medical devices companies with documented H-1B1 Singapore Labor Condition Application filings include Intuitive Surgical, Abbott, Stryker, Edwards Lifesciences, Boston Scientific, and Becton Dickinson. Smaller contract manufacturers and diagnostics firms in the San Diego and Bay Area corridors also file H-1B1 LCAs, particularly for biomedical engineering and quality systems roles. Filing history varies by year and business need, so verifying current LCA activity through OFLC records is advisable.
Which California cities have the most medical devices H-1B1 Singapore sponsorship jobs?
San Diego leads in medical devices H-1B1 visa Singapore sponsorship volume, anchored by the Biocom cluster around Sorrento Valley and Carlsbad. The Bay Area follows closely, with concentrations in Santa Clara, Sunnyvale, and Fremont serving device manufacturers and combination product companies. Los Angeles, Irvine, and the greater Orange County area also host significant medical devices operations, particularly in orthopedics, diagnostics, and interventional cardiology.
What types of medical devices roles typically qualify for H-1B1 Singapore sponsorship?
Roles that commonly qualify require at least a bachelor's degree in a directly related specialty field. In medical devices, this includes biomedical engineers, electrical and mechanical engineers, regulatory affairs specialists, clinical research associates, quality engineers, and software engineers developing device software. Roles classified under relevant Standard Occupational Classification codes with degree-level entry requirements generally meet the H-1B1 specialty occupation standard. O*NET occupational profiles can help confirm degree requirements for a specific title.
How do I find medical devices H-1B1 Singapore sponsorship jobs in California?
Migrate Mate is built specifically for this search: you can filter jobs by visa type, state, and industry to surface California medical devices roles where employers have verified H-1B1 Singapore LCA filing history. This removes the guesswork of approaching companies that have never sponsored the visa. Beyond Migrate Mate, reviewing OFLC LCA disclosure data by employer name and California worksite can help you identify active sponsors in device manufacturing, regulatory, and clinical functions.
Are there California-specific or industry-specific factors that affect H-1B1 Singapore sponsorship in medical devices?
California requires employers to post LCA notices at the worksite, which is standard but enforced strictly given the state's active labor enforcement environment. In medical devices, FDA-regulated roles often require specific degree fields and demonstrated technical expertise, which supports the specialty occupation determination but also means employers assess fit carefully before filing. Companies operating under FDA Quality System Regulation frameworks, common across California device manufacturers, tend to have established immigration programs familiar with H-1B1 processing for Singaporean nationals.
What is the prevailing wage for H-1B1 Singapore medical devices 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.