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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Location: San Diego, CA
Job Type: Full Time
Work Arrangement: On-Site
With extensive experience in developing biologics and bioconjugates, we offer a seamless service delivered by fully integrated teams, from early discovery to commercial manufacturing.
Forward-thinking and committed, we find the best solution and use the right technologies to design, develop and manufacture your products to ensure we get vital medicines to patients quickly and safely.
We are dedicated to quality excellence. We are driven to get better treatments to market, efficiently and responsibly by reducing timelines and delivering the highest quality products and services.
We are Abzena. More than a CDMO, we are a responsible and dedicated partner that takes care of your products from concept to patient.
ROLE AND RESPONSIBILITIES
The Manufacturing Associate I will primarily be responsible for performing all aspects of biologics production in a single use facility, including cell vial thaw and inoculum train expansion inside a Bio-Safety Cabinet, operation of wave and stirred-tank bioreactors up to 2000 L, clarification and sterile filtration, and master cell bank fills. In addition, this role will include operation of chromatography skids in conjunction with multi-use and single-use columns, processing intermediates by depth filtration, ultrafiltration and diafiltration, and performing bulk drug substance fills.
Responsibilities
- Operate under cGMP manufacturing conditions
- Ensure compliance to training on all activities prior to GMP execution
- Adhere to appropriate gowning procedures required for working in Class 10,000 and Class 100,000 cleanrooms
- Perform operations in a bio-safety cabinet using aseptic technique and maintain asepsis of all closed container sterile processes
- Setup, operate and maintain bioprocessing equipment including single-use bioreactors up to 2000 L, large scale filtration skids, and automated filling machines and analytical instruments for cell culture such as Nova Bioprofile and Vi-Cell systems
- Perform production activities including thawing of cell stocks, inoculum train expansions, cell culture maintenance in bioreactors, depth and sterile filtration, and master cell bank and bulk drug substance fills
- Setup, operate and maintain bioprocessing equipment including AKTA ready column chromatography skids, FlexAct automation skids, large scale filtration skids, and analytical instruments such as SoloVPE
- Perform production activities including depth filtration, purification by affinity, ion exchange, and hydrophobic interaction chromatography, viral inactivation and filtration, tangential flow filtration, sterile filtration, and bulk drug substance fills
- Troubleshoot process related issues as they arise
- Inventory manufacturing lab supplies and ensure items are properly stocked
- Participate in batch readiness activities such as general planning and coordination, material requests and transfer, and material and equipment staging
- Maintain cleanroom standards for cleanliness and order
- Conduct activities in support of production schedules as directed by senior staff
- Work effectively and efficiently in a team environment
- Communicate effectively with clients, supervisors, colleagues, and staff, and provide status of floor operation to leads on a regular basis
- Support multiple projects simultaneously
- Cross-train on various tasks including formulation of media and buffers, and operations to support overall success of the Biologics group
- Review GMP records for completeness, accuracy, and compliance on a daily basis in conformance with regulatory requirements
- Review manufacturing SOPs, master batch records, specifications, and other applicable cGMP documentation
- Adhere to quality standards set by regulations and Abzena policies, procedures, and mission
- Operate to the highest ethical and moral standards
- Perform additional duties as assigned
BASIC QUALIFICATIONS
- 1 – 2 years cell culture experience in a GMP pharmaceutical/biotech environment role with a technical degree or equivalent combined years of both
- Demonstrate knowledge and understanding of cGMPs and how they apply to responsibilities
- A proven ability to confidently compute basic arithmetic operations
COMPENSATION
- Salary Range: $45,000 - $60,000 a year
FLSA: Non-Exempt
Abzena is an equal opportunity employer that is committed to diversity and inclusion in the workplace. We prohibit discrimination and harassment of any kind based on race, color, sex, religion, sexual orientation, national origin, disability, genetic information, pregnancy, or any other protected characteristic as outlined by federal, state, or local laws.
This policy applies to all employment practices within our organization, including hiring, recruiting, promotion, termination, layoff, recall, leave of absence, compensation, benefits, and training.
We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.

Location: San Diego, CA
Job Type: Full Time
Work Arrangement: On-Site
With extensive experience in developing biologics and bioconjugates, we offer a seamless service delivered by fully integrated teams, from early discovery to commercial manufacturing.
Forward-thinking and committed, we find the best solution and use the right technologies to design, develop and manufacture your products to ensure we get vital medicines to patients quickly and safely.
We are dedicated to quality excellence. We are driven to get better treatments to market, efficiently and responsibly by reducing timelines and delivering the highest quality products and services.
We are Abzena. More than a CDMO, we are a responsible and dedicated partner that takes care of your products from concept to patient.
ROLE AND RESPONSIBILITIES
The Manufacturing Associate I will primarily be responsible for performing all aspects of biologics production in a single use facility, including cell vial thaw and inoculum train expansion inside a Bio-Safety Cabinet, operation of wave and stirred-tank bioreactors up to 2000 L, clarification and sterile filtration, and master cell bank fills. In addition, this role will include operation of chromatography skids in conjunction with multi-use and single-use columns, processing intermediates by depth filtration, ultrafiltration and diafiltration, and performing bulk drug substance fills.
Responsibilities
- Operate under cGMP manufacturing conditions
- Ensure compliance to training on all activities prior to GMP execution
- Adhere to appropriate gowning procedures required for working in Class 10,000 and Class 100,000 cleanrooms
- Perform operations in a bio-safety cabinet using aseptic technique and maintain asepsis of all closed container sterile processes
- Setup, operate and maintain bioprocessing equipment including single-use bioreactors up to 2000 L, large scale filtration skids, and automated filling machines and analytical instruments for cell culture such as Nova Bioprofile and Vi-Cell systems
- Perform production activities including thawing of cell stocks, inoculum train expansions, cell culture maintenance in bioreactors, depth and sterile filtration, and master cell bank and bulk drug substance fills
- Setup, operate and maintain bioprocessing equipment including AKTA ready column chromatography skids, FlexAct automation skids, large scale filtration skids, and analytical instruments such as SoloVPE
- Perform production activities including depth filtration, purification by affinity, ion exchange, and hydrophobic interaction chromatography, viral inactivation and filtration, tangential flow filtration, sterile filtration, and bulk drug substance fills
- Troubleshoot process related issues as they arise
- Inventory manufacturing lab supplies and ensure items are properly stocked
- Participate in batch readiness activities such as general planning and coordination, material requests and transfer, and material and equipment staging
- Maintain cleanroom standards for cleanliness and order
- Conduct activities in support of production schedules as directed by senior staff
- Work effectively and efficiently in a team environment
- Communicate effectively with clients, supervisors, colleagues, and staff, and provide status of floor operation to leads on a regular basis
- Support multiple projects simultaneously
- Cross-train on various tasks including formulation of media and buffers, and operations to support overall success of the Biologics group
- Review GMP records for completeness, accuracy, and compliance on a daily basis in conformance with regulatory requirements
- Review manufacturing SOPs, master batch records, specifications, and other applicable cGMP documentation
- Adhere to quality standards set by regulations and Abzena policies, procedures, and mission
- Operate to the highest ethical and moral standards
- Perform additional duties as assigned
BASIC QUALIFICATIONS
- 1 – 2 years cell culture experience in a GMP pharmaceutical/biotech environment role with a technical degree or equivalent combined years of both
- Demonstrate knowledge and understanding of cGMPs and how they apply to responsibilities
- A proven ability to confidently compute basic arithmetic operations
COMPENSATION
- Salary Range: $45,000 - $60,000 a year
FLSA: Non-Exempt
Abzena is an equal opportunity employer that is committed to diversity and inclusion in the workplace. We prohibit discrimination and harassment of any kind based on race, color, sex, religion, sexual orientation, national origin, disability, genetic information, pregnancy, or any other protected characteristic as outlined by federal, state, or local laws.
This policy applies to all employment practices within our organization, including hiring, recruiting, promotion, termination, layoff, recall, leave of absence, compensation, benefits, and training.
We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.
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 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.
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