Manufacturing Associate Visa Sponsorship Jobs in Illinois
Illinois is one of the Midwest's leading manufacturing states, with major employers like Caterpillar, Abbott Laboratories, and Deere & Company operating facilities across the Chicago metro, Peoria, and Rockford. Manufacturing associate roles here span medical devices, heavy equipment, and food processing, with a steady track record of H-1B visa and EB-3 visa sponsorship.
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Get Access To All JobsPosition Summary
The Drug Product Manufacturing Associate I / II / III, is a regular employee in a full-time non-exempt position at Kashiv BioSciences, LLC, in Chicago, IL. This employee will be responsible for the manufacturing of Biotechnology products for clinical and commercial human use. Employee employs aseptic techniques while working in controlled and classified environments, some of which require complete aseptic gowning. Must comply with Kashiv BioSciences policies, procedures (SOP), FDA current Good Manufacturing Practices (cGMP), and any other government requirement.
Essential Duties & Responsibilities
- To take Line Inspection/Line clearance of the Packaging area.
- To operate syringe labeling machine, label counting, blister packaging, check weigher, serialization, aggregation, and temper evident sealing Machines by following respective SOP.
- To visually inspect labeled syringes, blister packs, printed cartons, or shippers for any defects.
- Responsible for submission of samples.
- To participate in investigations if needed.
- To pack syringes with other necessary components manually in cartons.
- To check the weight of cartons to ensure no missing components.
- To packed good cartons into the shipper and do palletization.
- To submit documents and material requests to start packaging operations to the respective department.
- To verify all drug product syringes before starting of packaging activity.
- To electronically record all the process steps (If required).
- To complete logbooks, Batch Records, and other cGMP documentation accurately and in a timely manner.
- To remove and dispose soiled / expired, rejected syringes, materials from the area.
- To assure that the packaging rooms and surrounding areas are maintained within the required conditions for clean room manufacturing.
- To report all nonconformance or events that arise during the shift to the Supervisor.
- To comply with all safety, cGMP and Company policies, practices, and procedures.
- To perform other functions (Manufacturing, Visual inspection) as required or assigned.
- To comply with all company policies and standards.
Position Requirements and Qualifications
Education:
- Associate degree or higher college in Biology, Chemistry, Biotechnology, Pharmacy or related preferred
- Or an equivalent of 1 – 2 years (for associate 1 and 2) and 3 – 4 years (For associate 3) of industry experience required.
- Operation of packaging machines (Labeling, blister packing, serialization, aggregation etc.) is preferred.
Special Skills:
Language:
- Basic verbal and written communication skills in English with the ability to understand technical information, procedures, batch records, and other documents in English.
- Excellent interpersonal skills.
Reasoning Skills:
- The candidate should have the ability to operate complex systems and equipment in accordance with current GMPs, SOPs, and safety guidelines under minimum supervision.
- Basic skills for identifying problems and troubleshooting of the equipment and manufacturing processes.
- Ability to work independently, within SOP, prescribed guidelines, or as a team member and the demonstrated ability to follow detailed directions.
Computer and/or Technical Skills:
- Skills for working with Computer systems, such as: POMS, LIMS, SAP, NetSuite etc.
- Operation and understanding of word processing, spreadsheets, and data management
- Knowledge of GMP and safety requirements.
- Knowledge of biotechnology operations such as, Aseptic Filtration Systems, Aseptic Sampling, Filter Integrity Testing, stirrer plate, floor scale, peristaltic pump, Weigh Scales, etc.
Work Environment & Physical Demands:
General work environment and physical demands as required to successfully perform the essential functions of this job. Ability to work flexible hours as needed. Ability to work under pressure and meet deadlines. Some travel may be involved.
Supervisory Responsibility, if any: No
This position description is not a complete list of all responsibilities, duties or skill required for the job and is subject to review and change at any time, with or without notice, in accordance with the needs of the organization.
Position Summary
The Drug Product Manufacturing Associate I / II / III, is a regular employee in a full-time non-exempt position at Kashiv BioSciences, LLC, in Chicago, IL. This employee will be responsible for the manufacturing of Biotechnology products for clinical and commercial human use. Employee employs aseptic techniques while working in controlled and classified environments, some of which require complete aseptic gowning. Must comply with Kashiv BioSciences policies, procedures (SOP), FDA current Good Manufacturing Practices (cGMP), and any other government requirement.
Essential Duties & Responsibilities
- To take Line Inspection/Line clearance of the Packaging area.
- To operate syringe labeling machine, label counting, blister packaging, check weigher, serialization, aggregation, and temper evident sealing Machines by following respective SOP.
- To visually inspect labeled syringes, blister packs, printed cartons, or shippers for any defects.
- Responsible for submission of samples.
- To participate in investigations if needed.
- To pack syringes with other necessary components manually in cartons.
- To check the weight of cartons to ensure no missing components.
- To packed good cartons into the shipper and do palletization.
- To submit documents and material requests to start packaging operations to the respective department.
- To verify all drug product syringes before starting of packaging activity.
- To electronically record all the process steps (If required).
- To complete logbooks, Batch Records, and other cGMP documentation accurately and in a timely manner.
- To remove and dispose soiled / expired, rejected syringes, materials from the area.
- To assure that the packaging rooms and surrounding areas are maintained within the required conditions for clean room manufacturing.
- To report all nonconformance or events that arise during the shift to the Supervisor.
- To comply with all safety, cGMP and Company policies, practices, and procedures.
- To perform other functions (Manufacturing, Visual inspection) as required or assigned.
- To comply with all company policies and standards.
Position Requirements and Qualifications
Education:
- Associate degree or higher college in Biology, Chemistry, Biotechnology, Pharmacy or related preferred
- Or an equivalent of 1 – 2 years (for associate 1 and 2) and 3 – 4 years (For associate 3) of industry experience required.
- Operation of packaging machines (Labeling, blister packing, serialization, aggregation etc.) is preferred.
Special Skills:
Language:
- Basic verbal and written communication skills in English with the ability to understand technical information, procedures, batch records, and other documents in English.
- Excellent interpersonal skills.
Reasoning Skills:
- The candidate should have the ability to operate complex systems and equipment in accordance with current GMPs, SOPs, and safety guidelines under minimum supervision.
- Basic skills for identifying problems and troubleshooting of the equipment and manufacturing processes.
- Ability to work independently, within SOP, prescribed guidelines, or as a team member and the demonstrated ability to follow detailed directions.
Computer and/or Technical Skills:
- Skills for working with Computer systems, such as: POMS, LIMS, SAP, NetSuite etc.
- Operation and understanding of word processing, spreadsheets, and data management
- Knowledge of GMP and safety requirements.
- Knowledge of biotechnology operations such as, Aseptic Filtration Systems, Aseptic Sampling, Filter Integrity Testing, stirrer plate, floor scale, peristaltic pump, Weigh Scales, etc.
Work Environment & Physical Demands:
General work environment and physical demands as required to successfully perform the essential functions of this job. Ability to work flexible hours as needed. Ability to work under pressure and meet deadlines. Some travel may be involved.
Supervisory Responsibility, if any: No
This position description is not a complete list of all responsibilities, duties or skill required for the job and is subject to review and change at any time, with or without notice, in accordance with the needs of the organization.
Manufacturing Associate Job Roles in Illinois
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Search Manufacturing Associate Jobs in IllinoisManufacturing Associate Jobs in Illinois: Frequently Asked Questions
Which companies sponsor visas for manufacturing associates in Illinois?
Illinois manufacturers with documented sponsorship histories include Abbott Laboratories, Baxter International, Caterpillar, and Illinois Tool Works. These companies regularly file H-1B and PERM labor certifications for manufacturing and production roles. Sponsorship activity is most concentrated among large employers in the Chicago metro, Peoria, and the Quad Cities corridor, where manufacturing operations are substantial enough to support dedicated immigration programs.
Which visa types are most common for manufacturing associate roles in Illinois?
EB-3 immigrant visas are common for manufacturing associate positions because the category covers skilled and semi-skilled workers without requiring a bachelor's degree. H-1B visas are used when the role requires a specialized engineering or technical degree. Some employers also sponsor TN visas for Canadian and Mexican nationals in qualifying technical manufacturing roles. The appropriate category depends on the specific job duties and educational requirements the employer defines.
Which cities in Illinois have the most manufacturing associate sponsorship jobs?
The Chicago metropolitan area, including suburbs like Waukegan, Aurora, and Schaumburg, accounts for the largest share of manufacturing associate sponsorship activity in Illinois. Peoria is a significant hub due to Caterpillar's headquarters and supplier network. Rockford has a strong aerospace and precision machining base, and the Quad Cities region along the Iowa border supports heavy equipment and agricultural manufacturing employment.
How to find manufacturing associate visa sponsorship jobs in Illinois?
Migrate Mate aggregates visa sponsorship jobs specifically for international candidates, including manufacturing associate roles in Illinois. Filtering by state and role on Migrate Mate surfaces employers who have sponsored work visas in the past, which is a meaningful signal of willingness to do so again. This saves significant time compared to manually researching sponsorship histories for each employer across Illinois's many manufacturing corridors.
Are there any Illinois-specific considerations for manufacturing associate visa sponsorship?
Illinois participates in the federal prevailing wage system, so employers sponsoring manufacturing associates must pay wages meeting Department of Labor standards for the specific occupation and region. Chicago-area prevailing wages are generally higher than downstate rates, which affects the economics of sponsorship for smaller manufacturers. Illinois also has a strong community college and technical training pipeline, meaning some employers prefer local candidates, making early outreach to large industrial employers advisable for international applicants.
What is the prevailing wage for sponsored manufacturing associate jobs in Illinois?
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.