Manufacturing Associate Visa Sponsorship Jobs in California
Manufacturing associate visa sponsorship jobs in California are concentrated in the San Francisco Bay Area, Los Angeles, and San Diego, where companies like Applied Materials, Lam Research, and Thermo Fisher Scientific regularly hire for production and process roles. California's semiconductor, biotech, and medical device sectors drive consistent demand for international manufacturing talent.
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Get Access To All JobsINTRODUCTION
Stanford Laboratory for Cell and Gene Medicine (LCGM) is seeking a Clinical Manufacturing Quality Control Analyst 2 (Quality Control Specialist) to design, develop, evaluate and implement quality control testing, assays and procedures for clinical materials manufacturing consistent with principles of current Good Manufacturing Practice (cGMP) and aligned with the phase of the clinical investigation for treating patients with incurable diseases.
LCGM is a GMP multi-product biologics manufacturing facility that provides regulatory, quality systems, process development and manufacturing support to the School of Medicine, Lucile Packard Children’s Hospital (LPCH) and Stanford Health Care (SHC) in developing innovative cell and gene-based therapies for the treatment of disease and the promotion of health in pediatric and adult patients in Phase I/II clinical trials.
LCGM is a growing, dynamic team who are dedicated to supporting translational medicine and contributing to Stanford Medicine’s mission. We invite you to join our team!
DUTIES INCLUDE:
- Perform increasingly complex chemical, biochemical, biological and/or microbiological testing, assays and procedures related to quality control (QC), which constitute the quality, safety and efficacy of all analytical methods for clinical materials manufactured at Laboratory for Cell and Gene Medicine (LCGM).
- Perform tests related to assays; collect, interpret, analyze and report data related to test results including investigation of out-of-specification and/or non-conforming test results.
- Document QC related test methods, Standard Operating Procedures (SOPs), and instructions to ensure consistency with cGMP and documentation practices.
- Manage supplies related to clinical materials manufacturing. Create selection criteria, justification and qualification of raw materials. Responsible for examining and documenting materials used in clinical materials manufacturing, consistent with defined, relevant quality standards and cGMP.
- Perform complex analysis, monitor and trouble-shoot pertinent equipment (e.g., flow cytometers, hematologic analyzers).
- Investigate out-of-specification and/or non-conforming test results. Initiate, investigate as appropriate, and prepare deviation reports for SOPs and test methods with input from supervisor in order to implement prevention or corrective actions.
CORE DUTIES:
- Perform increasingly complex chemical, biochemical, biological and/or microbiological testing, assays and procedures related to quality control (QC), which constitute the quality, safety and efficacy of all analytical methods for clinical materials manufactured at Laboratory for Cell and Gene Medicine (LCGM).
- Perform tests related to assays; collect, interpret, analyze and report data related to test results including investigation of out-of-specification and/or non-conforming test results.
- Document QC related test methods, Standard Operating Procedures (SOPs), and instructions to ensure consistency with cGMP and documentation practices.
- Manage supplies related to clinical materials manufacturing. Create selection criteria, justification and qualification of raw materials. Responsible for examining and documenting materials used in clinical materials manufacturing, consistent with defined, relevant quality standards and cGMP.
- Perform complex analysis, monitor and trouble-shoot pertinent equipment (e.g., flow cytometers, hematologic analyzers).
- Investigate out-of-specification and/or non-conforming test results. Initiate, investigate as appropriate, and prepare deviation reports for SOPs and test methods with input from supervisor in order to implement prevention or corrective actions.
MINIMUM EDUCATION AND EXPERIENCE
Bachelor's degree in related scientific field and two years of related experience, or Master’s degree, or an equivalent combination of education and relevant work experience.
KNOWLEDGE, SKILLS AND ABILITIES:
- Applicable or related experience in clinical laboratory, hematology, blood banking, immunology or QC laboratory preferably in cGMP environment.
- Strong technical skills and experience with testing QC methods and concepts.
- Good understanding of cGMP or International Organization for Standardization (ISO) requirements, quality systems.
- Strong team-oriented, interpersonal skills and collaborative work style.
- Ability to manage and coordinate all tasks assigned and effectively complete all expected deliverables in a timely manner and proactively communicate changes in pre-established goals and deadlines.
- Excellent organizational skills and attention to detail.
- Excellent verbal and written communication skills.
INTRODUCTION
Stanford Laboratory for Cell and Gene Medicine (LCGM) is seeking a Clinical Manufacturing Quality Control Analyst 2 (Quality Control Specialist) to design, develop, evaluate and implement quality control testing, assays and procedures for clinical materials manufacturing consistent with principles of current Good Manufacturing Practice (cGMP) and aligned with the phase of the clinical investigation for treating patients with incurable diseases.
LCGM is a GMP multi-product biologics manufacturing facility that provides regulatory, quality systems, process development and manufacturing support to the School of Medicine, Lucile Packard Children’s Hospital (LPCH) and Stanford Health Care (SHC) in developing innovative cell and gene-based therapies for the treatment of disease and the promotion of health in pediatric and adult patients in Phase I/II clinical trials.
LCGM is a growing, dynamic team who are dedicated to supporting translational medicine and contributing to Stanford Medicine’s mission. We invite you to join our team!
DUTIES INCLUDE:
- Perform increasingly complex chemical, biochemical, biological and/or microbiological testing, assays and procedures related to quality control (QC), which constitute the quality, safety and efficacy of all analytical methods for clinical materials manufactured at Laboratory for Cell and Gene Medicine (LCGM).
- Perform tests related to assays; collect, interpret, analyze and report data related to test results including investigation of out-of-specification and/or non-conforming test results.
- Document QC related test methods, Standard Operating Procedures (SOPs), and instructions to ensure consistency with cGMP and documentation practices.
- Manage supplies related to clinical materials manufacturing. Create selection criteria, justification and qualification of raw materials. Responsible for examining and documenting materials used in clinical materials manufacturing, consistent with defined, relevant quality standards and cGMP.
- Perform complex analysis, monitor and trouble-shoot pertinent equipment (e.g., flow cytometers, hematologic analyzers).
- Investigate out-of-specification and/or non-conforming test results. Initiate, investigate as appropriate, and prepare deviation reports for SOPs and test methods with input from supervisor in order to implement prevention or corrective actions.
CORE DUTIES:
- Perform increasingly complex chemical, biochemical, biological and/or microbiological testing, assays and procedures related to quality control (QC), which constitute the quality, safety and efficacy of all analytical methods for clinical materials manufactured at Laboratory for Cell and Gene Medicine (LCGM).
- Perform tests related to assays; collect, interpret, analyze and report data related to test results including investigation of out-of-specification and/or non-conforming test results.
- Document QC related test methods, Standard Operating Procedures (SOPs), and instructions to ensure consistency with cGMP and documentation practices.
- Manage supplies related to clinical materials manufacturing. Create selection criteria, justification and qualification of raw materials. Responsible for examining and documenting materials used in clinical materials manufacturing, consistent with defined, relevant quality standards and cGMP.
- Perform complex analysis, monitor and trouble-shoot pertinent equipment (e.g., flow cytometers, hematologic analyzers).
- Investigate out-of-specification and/or non-conforming test results. Initiate, investigate as appropriate, and prepare deviation reports for SOPs and test methods with input from supervisor in order to implement prevention or corrective actions.
MINIMUM EDUCATION AND EXPERIENCE
Bachelor's degree in related scientific field and two years of related experience, or Master’s degree, or an equivalent combination of education and relevant work experience.
KNOWLEDGE, SKILLS AND ABILITIES:
- Applicable or related experience in clinical laboratory, hematology, blood banking, immunology or QC laboratory preferably in cGMP environment.
- Strong technical skills and experience with testing QC methods and concepts.
- Good understanding of cGMP or International Organization for Standardization (ISO) requirements, quality systems.
- Strong team-oriented, interpersonal skills and collaborative work style.
- Ability to manage and coordinate all tasks assigned and effectively complete all expected deliverables in a timely manner and proactively communicate changes in pre-established goals and deadlines.
- Excellent organizational skills and attention to detail.
- Excellent verbal and written communication skills.
Manufacturing Associate Job Roles in California
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Search Manufacturing Associate Jobs in CaliforniaManufacturing Associate Jobs in California: Frequently Asked Questions
Which companies sponsor visas for manufacturing associates in California?
California's largest sponsors of manufacturing associate roles include semiconductor equipment makers like Applied Materials, Lam Research, and KLA Corporation in the Bay Area, life sciences manufacturers like Thermo Fisher Scientific and Abbott in San Diego, and aerospace suppliers in the Los Angeles region. These companies have established immigration programs and a documented history of filing H-1B visa and other work visa petitions for manufacturing and production roles.
Which visa types are most common for manufacturing associate roles in California?
The H-1B visa is the most common pathway for manufacturing associates in California, provided the role qualifies as a specialty occupation requiring at least a bachelor's degree in a relevant field such as materials science, chemical engineering, or industrial engineering. Some roles in life sciences or semiconductor manufacturing may also support EB-2 or EB-3 immigrant visa petitions for candidates already on a nonimmigrant status pursuing permanent residence.
How to find manufacturing associate visa sponsorship jobs in California?
Migrate Mate is built specifically for international job seekers and filters manufacturing associate roles in California by visa sponsorship availability, so you're not sorting through listings from employers who don't sponsor. The platform surfaces positions at California employers with active sponsorship histories, particularly in the Bay Area, Los Angeles, and San Diego, where semiconductor, biotech, and medical device manufacturers concentrate their production hiring.
Which cities in California have the most manufacturing associate sponsorship jobs?
The San Francisco Bay Area, particularly Santa Clara, San Jose, and Fremont, leads for semiconductor and cleanroom manufacturing roles. San Diego is a strong market for medical device and biotech manufacturing, home to companies like Becton Dickinson and Hologic. Los Angeles and its surrounding cities support aerospace and defense manufacturing. These three metros account for the majority of California's sponsored manufacturing associate openings.
Are there state-specific considerations for manufacturing associates seeking visa sponsorship in California?
California's Department of Industrial Relations enforces wage orders that interact with federal prevailing wage requirements, meaning employers filing Labor Condition Applications for manufacturing associates must meet whichever standard is higher. California's concentration of semiconductor fabrication and GMP-regulated life sciences facilities also means many roles require cleanroom experience or specific certifications, which can strengthen a visa petition by demonstrating the specialized nature of the position.
What is the prevailing wage for sponsored manufacturing associate 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.