Quality Control Technician Visa Sponsorship Jobs in New Jersey
Quality control technician visa sponsorship jobs in New Jersey are concentrated in the state's pharmaceutical, chemical, and medical device sectors, with major employers like Johnson & Johnson, Merck, and Becton Dickinson operating facilities across central and northern New Jersey. Cities including Parsippany, Bridgewater, and Teaneck are active hiring hubs for sponsored QC roles.
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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
Performs functions associated with cGMP manufacturing operations within the drug product manufacturing and packaging facility, including performing visual inspection of both finished and in-process materials, verifying manufacturing data in the batch record system, and conducting testing on in-process materials. Uses sophisticated programs (such as POMS and SAP) to evaluate operating data, which can be used to determine acceptable quality limits and product release requirements.
Responsibilities
- Responsible to enter test results in manufacturing systems such SAP, POMS, and LIMS.
- Interprets experimental data for conformance with product and material specifications.
- Perform in-process laboratory tests such as Karl Fischer and Torque removal testing, as written per procedure.
- Responsible for correct documentation and compliance with GDP requirements of the tasks performed.
- Performs visual inspection of finished and in-process materials, classifies defects, and determines test disposition.
- Performs test methods as written to support product/material release.
- Reviews and verifies manufacturing operating settings.
- Makes suggestions for improvement based upon scientific and good manufacturing practices understanding.
- Understands and maintains a safe work environment for themselves and others in accordance with procedural requirements.
- Accepts responsibility for acquiring knowledge and experience to support continual personal development.
- Budget time effectively to carry out assigned tasks and takes initiative to be involved in team activities and decision making.
- Works with others to maintain a positive atmosphere to accomplish business objectives and is an active participant in the work structure and fosters positive working relationships with all levels of the organization.
Qualifications
- High School Diploma required.
- Technical Degree preferred.
- 1 to 2 years of experience conducting quality inspections in a pharmaceutical setting is required.
- 1-2 years of experience working in a laboratory setting is preferred.
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
Performs functions associated with cGMP manufacturing operations within the drug product manufacturing and packaging facility, including performing visual inspection of both finished and in-process materials, verifying manufacturing data in the batch record system, and conducting testing on in-process materials. Uses sophisticated programs (such as POMS and SAP) to evaluate operating data, which can be used to determine acceptable quality limits and product release requirements.
Responsibilities
- Responsible to enter test results in manufacturing systems such SAP, POMS, and LIMS.
- Interprets experimental data for conformance with product and material specifications.
- Perform in-process laboratory tests such as Karl Fischer and Torque removal testing, as written per procedure.
- Responsible for correct documentation and compliance with GDP requirements of the tasks performed.
- Performs visual inspection of finished and in-process materials, classifies defects, and determines test disposition.
- Performs test methods as written to support product/material release.
- Reviews and verifies manufacturing operating settings.
- Makes suggestions for improvement based upon scientific and good manufacturing practices understanding.
- Understands and maintains a safe work environment for themselves and others in accordance with procedural requirements.
- Accepts responsibility for acquiring knowledge and experience to support continual personal development.
- Budget time effectively to carry out assigned tasks and takes initiative to be involved in team activities and decision making.
- Works with others to maintain a positive atmosphere to accomplish business objectives and is an active participant in the work structure and fosters positive working relationships with all levels of the organization.
Qualifications
- High School Diploma required.
- Technical Degree preferred.
- 1 to 2 years of experience conducting quality inspections in a pharmaceutical setting is required.
- 1-2 years of experience working in a laboratory setting is preferred.
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 Control Technician Job Roles in New Jersey
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Search Quality Control Technician Jobs in New JerseyQuality Control Technician Jobs in New Jersey: Frequently Asked Questions
Which companies sponsor visas for quality control technicians in New Jersey?
New Jersey's life sciences and manufacturing base drives most QC technician sponsorship activity. Companies with established sponsorship histories include Johnson & Johnson, Merck, Becton Dickinson, Lonza, and Catalent, all of which operate large facilities in central and northern New Jersey. Staffing firms supporting pharmaceutical manufacturing, such as those placing contractors at FDA-regulated sites, have also filed sponsorships for QC technician roles in the state.
Which visa types are most common for quality control technician roles in New Jersey?
The H-1B visa is the most common visa category for quality control technicians in New Jersey, particularly for roles requiring a bachelor's degree in chemistry, biology, or a related science. Some employers also use the TN visa for Canadian and Mexican nationals in qualifying scientific QC roles. EB-3 green card sponsorship appears in pharmaceutical manufacturing, where employers with longer-term workforce needs sometimes support permanent residency for experienced technicians.
How to find quality control technician visa sponsorship jobs in New Jersey?
Migrate Mate filters job listings specifically for visa sponsorship, making it straightforward to search quality control technician openings in New Jersey without sorting through employers who don't sponsor. New Jersey's pharmaceutical corridor, running through Somerset, Morris, and Middlesex counties, generates consistent QC technician demand. Searching Migrate Mate by role and state surfaces active listings from life sciences employers with documented sponsorship histories in the region.
Which cities in New Jersey have the most quality control technician sponsorship jobs?
Bridgewater and Parsippany are the most active cities for sponsored QC technician roles, given the density of pharmaceutical headquarters and manufacturing sites in Somerset and Morris counties. Teaneck and Woodcliff Lake in Bergen County also see consistent hiring from biotech and medical device companies. Raritan, home to a major Johnson & Johnson campus, and Kenilworth, where Merck maintains significant operations, round out the top locations for QC sponsorship activity.
Are there any New Jersey-specific considerations for quality control technician visa sponsorship?
New Jersey's concentration of FDA-regulated facilities means many QC technician roles require working knowledge of cGMP (current Good Manufacturing Practices), which employers factor into sponsorship decisions alongside degree requirements. The state's university pipeline, including Rutgers University's pharmacy and biomedical programs, produces candidates familiar with regulated environments. Prevailing wage determinations for New Jersey QC technician positions reflect the high cost of living in the region, which affects the wage level an employer must certify on a Labor Condition Application.
What is the prevailing wage for sponsored quality control technician jobs in New Jersey?
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.