Quality Engineer Visa Sponsorship Jobs in Illinois
Illinois quality engineer roles are concentrated in Chicago's advanced manufacturing corridor and suburban tech hubs like Schaumburg, Lisle, and Downers Grove. Major employers including Abbott Laboratories, Caterpillar, Boeing, and Motorola Solutions have established track records of sponsoring work visas for quality engineering talent across medical devices, aerospace, and industrial manufacturing.
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About AbbVie
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on LinkedIn, Facebook, Instagram, X and YouTube.
Job Description
Genetic, Environmental, and Occupational Toxicology (GEO Tox) is a diverse team of scientists with the goals of supporting patient, environmental, and employee safety. The candidate will support risk assessments for occupational, environmental, manufacturing, and product regulatory filings. The position will support programs across AbbVie’s therapeutic areas and involve a broad range of modalities across all stages from early discovery throughout development to marketed products.
We are seeking an early career toxicologist to join our team in Development Sciences, Pre-clinical Safety.
Responsibilities:
- Critically evaluate literature and toxicology reports/summaries and utilize tools such as read-across and in silico data to generate toxicology risk assessments including extractables and leachables, health-based exposure limits (HBELs) including permitted daily exposure limits (PDEs) and occupational exposure limits (OELs).
- Support product quality toxicology risk assessments to support non-conformances and product complaints.
- Experience supporting medical devices and combination products under ISO 10993.
- Successful collaboration with multi-functional teams to align on safety and compound hazard classifications banding for implementation throughout the company.
- Support occupational health (hazard) categorizations and chemical registrations, including Globally Harmonized System of Classification and Labelling of Chemicals GHS/CLP, and Safety Data Sheets (SDS).
Qualifications
Requirements:
- Bachelor degree in toxicology, pharmacology, or related science with typically seven years of experience, or Master degree with 5 years of relevant experience
- Understand relevant scientific literature and apply theoretical framework to execute tasks/projects in a timely manner
- Minimum of 3 years experience in a pharmaceutical/biopharmaceutical, GMP/GLP, or other regulatory setting desired
- Exceptional collaboration, multi-tasking, and communication skills
- Excellent writing skills and attention to detail
- Ability to work in a fast-paced environment, comfortable with multitasking to meet project deadlines
Desired skills:
- Risk assessment authoring experience
- Toxicity data mining in relevant databases, internal, and external literature for use in compound risk assessments, classification, and labelling.
- Knowledge and/or experience with regulatory guidance, i.e., ISO, ICH, etc.
- Proficiency in Microsoft Office and other computer software systems
Additional Information
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:
- The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future.
- We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.
- This job is eligible to participate in our short-term incentive programs.
Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company’s sole and absolute discretion, consistent with applicable law.
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.
US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html
US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
https://www.abbvie.com/join-us/reasonable-accommodations.html
Company Description
About AbbVie
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on LinkedIn, Facebook, Instagram, X and YouTube.
Job Description
Genetic, Environmental, and Occupational Toxicology (GEO Tox) is a diverse team of scientists with the goals of supporting patient, environmental, and employee safety. The candidate will support risk assessments for occupational, environmental, manufacturing, and product regulatory filings. The position will support programs across AbbVie’s therapeutic areas and involve a broad range of modalities across all stages from early discovery throughout development to marketed products.
We are seeking an early career toxicologist to join our team in Development Sciences, Pre-clinical Safety.
Responsibilities:
- Critically evaluate literature and toxicology reports/summaries and utilize tools such as read-across and in silico data to generate toxicology risk assessments including extractables and leachables, health-based exposure limits (HBELs) including permitted daily exposure limits (PDEs) and occupational exposure limits (OELs).
- Support product quality toxicology risk assessments to support non-conformances and product complaints.
- Experience supporting medical devices and combination products under ISO 10993.
- Successful collaboration with multi-functional teams to align on safety and compound hazard classifications banding for implementation throughout the company.
- Support occupational health (hazard) categorizations and chemical registrations, including Globally Harmonized System of Classification and Labelling of Chemicals GHS/CLP, and Safety Data Sheets (SDS).
Qualifications
Requirements:
- Bachelor degree in toxicology, pharmacology, or related science with typically seven years of experience, or Master degree with 5 years of relevant experience
- Understand relevant scientific literature and apply theoretical framework to execute tasks/projects in a timely manner
- Minimum of 3 years experience in a pharmaceutical/biopharmaceutical, GMP/GLP, or other regulatory setting desired
- Exceptional collaboration, multi-tasking, and communication skills
- Excellent writing skills and attention to detail
- Ability to work in a fast-paced environment, comfortable with multitasking to meet project deadlines
Desired skills:
- Risk assessment authoring experience
- Toxicity data mining in relevant databases, internal, and external literature for use in compound risk assessments, classification, and labelling.
- Knowledge and/or experience with regulatory guidance, i.e., ISO, ICH, etc.
- Proficiency in Microsoft Office and other computer software systems
Additional Information
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:
- The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future.
- We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.
- This job is eligible to participate in our short-term incentive programs.
Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company’s sole and absolute discretion, consistent with applicable law.
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.
US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html
US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
https://www.abbvie.com/join-us/reasonable-accommodations.html
Quality Engineer Job Roles in Illinois
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Search Quality Engineer Jobs in IllinoisQuality Engineer Jobs in Illinois: Frequently Asked Questions
Which companies sponsor visas for quality engineers in Illinois?
Abbott Laboratories, Baxter International, Boeing, Caterpillar, Motorola Solutions, and Illinois Tool Works are among the Illinois employers with documented histories of sponsoring H-1B visa and other work visas for quality engineers. Medical device and pharmaceutical manufacturers in the Chicago metro area file a significant share of these petitions, reflecting the state's strength in regulated industries that require specialized quality assurance expertise.
Which visa types are most common for quality engineer roles in Illinois?
The H-1B is the most common visa category for quality engineers in Illinois, as the role typically requires a bachelor's degree in engineering or a related technical field, meeting the specialty occupation standard. Engineers from Australia may qualify for the E-3 visa. Canadians and Mexicans with qualifying credentials can explore the TN visa under the USMCA, which does not require a lottery and is processed at the port of entry.
Which cities in Illinois have the most quality engineer sponsorship jobs?
Chicago and its northwest suburbs account for the largest share of quality engineer sponsorship activity in Illinois. Schaumburg, Downers Grove, Lisle, and Waukegan host significant manufacturing and medical device operations. Peoria is notable for Caterpillar's engineering footprint, and the broader I-88 technology corridor between Oak Brook and Aurora has a concentration of employers in automotive, electronics, and industrial manufacturing that regularly hire quality engineers.
How to find quality engineer visa sponsorship jobs in Illinois?
Migrate Mate filters job listings specifically for roles where employers are open to visa sponsorship, making it straightforward to identify quality engineer positions in Illinois without manually screening hundreds of postings. You can narrow results by location, filtering for Chicago, Schaumburg, Peoria, or other Illinois cities, and focus on industries like medical devices, aerospace, and industrial manufacturing where sponsorship is most common for this role.
Are there any state-specific considerations for quality engineers seeking sponsorship in Illinois?
Illinois's concentration of FDA-regulated industries, particularly medical devices and pharmaceuticals in the Chicago suburbs, means quality engineers with backgrounds in ISO 13485, 21 CFR Part 820, or pharmaceutical GMP standards are in consistent demand. University pipelines from the University of Illinois Urbana-Champaign, Northwestern, and Illinois Institute of Technology supply engineering talent, and employers in these regulated sectors are generally experienced with the H-1B sponsorship process.
What is the prevailing wage for sponsored quality engineer 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.