QA Engineer Visa Sponsorship Jobs in Massachusetts
Massachusetts QA engineers are in demand across the state's biotech corridors in Cambridge and Waltham, financial tech firms in Boston, and defense contractors on the Route 128 belt. Companies like Wayfair, Biogen, and Raytheon Technologies have active sponsorship histories. The state's dense university network feeds strong international candidate pipelines into QA roles.
Find QA Engineer JobsOverview
Showing 5 of 102+ QA Engineer Jobs in Massachusetts with Visa Sponsorship
See all 102+ QA Engineer Jobs in Massachusetts with Visa Sponsorship
Sign up for free to unlock all listings, filter by visa type, and get alerts for new QA Engineer Jobs in Massachusetts with Visa Sponsorship.
Get Access To All JobsCompany 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
This QA Specialist is responsible for reviewing and release of semi-finished, and finished drug product. It also involves ensuring adherence to Standard Operation Procedures and current Good Manufacturing Practices. Quarantine and monitor product on hold and preparing required batch disposition documentation for international sites as required.
- Performing the Quality Assurance review and release of semi-finished product, validation, media, and final products.
- Review batch records to support product release schedule, ensuring regulatory compliance, customer satisfaction and delivery of products.
- Quarantine and monitor product in “on hold” status prior to disposition.
- Prepare required batch disposition documentation and provide to international markets as required to ensure current Good Manufacturing Practices compliance.
- Identify and resolve all batch record discrepancies to prevent a regulatory impact.
- Assist department supervisors in maintaining dispositioned batch records to provide an efficient and secure storage and retrieval process.
- Perform all Final Product and disposition. Following global and SOPs for release in SAP. Exercise independent judgement in every batch based on evidence provided. i.e. CAPAs and their effectiveness.
- Performing the Quality Assurance check of all batch related documents for manufacturing, production, validation, and quality assurance departments. Responsible for the final sign-off of the product being released to the market.
- Ability to exercise independent judgement and critical thinking.
Qualifications
Bachelor’s Degree in the Sciences or technical field or equivalent experience.
5 years of experience in a quality role or experience handling and reviewing documentation records.
Intermediate Microsoft Word and Microsoft Excel skills. SAP experience preferred.
3 years of experience in a GMP Environment.
Prefer experience in an aseptic manufacturing environment.
Working knowledge of Quality Assurance systems, cGMP’s, ISO 13485, CMDRs, and EMEA regulations preferred.
Competency utilizing Electronic Systems ie. Maximo and Trackwise for Quality checks.
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
This QA Specialist is responsible for reviewing and release of semi-finished, and finished drug product. It also involves ensuring adherence to Standard Operation Procedures and current Good Manufacturing Practices. Quarantine and monitor product on hold and preparing required batch disposition documentation for international sites as required.
- Performing the Quality Assurance review and release of semi-finished product, validation, media, and final products.
- Review batch records to support product release schedule, ensuring regulatory compliance, customer satisfaction and delivery of products.
- Quarantine and monitor product in “on hold” status prior to disposition.
- Prepare required batch disposition documentation and provide to international markets as required to ensure current Good Manufacturing Practices compliance.
- Identify and resolve all batch record discrepancies to prevent a regulatory impact.
- Assist department supervisors in maintaining dispositioned batch records to provide an efficient and secure storage and retrieval process.
- Perform all Final Product and disposition. Following global and SOPs for release in SAP. Exercise independent judgement in every batch based on evidence provided. i.e. CAPAs and their effectiveness.
- Performing the Quality Assurance check of all batch related documents for manufacturing, production, validation, and quality assurance departments. Responsible for the final sign-off of the product being released to the market.
- Ability to exercise independent judgement and critical thinking.
Qualifications
Bachelor’s Degree in the Sciences or technical field or equivalent experience.
5 years of experience in a quality role or experience handling and reviewing documentation records.
Intermediate Microsoft Word and Microsoft Excel skills. SAP experience preferred.
3 years of experience in a GMP Environment.
Prefer experience in an aseptic manufacturing environment.
Working knowledge of Quality Assurance systems, cGMP’s, ISO 13485, CMDRs, and EMEA regulations preferred.
Competency utilizing Electronic Systems ie. Maximo and Trackwise for Quality checks.
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
QA Engineer Job Roles in Massachusetts
See all 102+ QA Engineer Jobs in Massachusetts
Sign up for free to filter by visa type, set job alerts, and find employers with verified sponsorship history.
Search QA Engineer Jobs in MassachusettsQA Engineer Jobs in Massachusetts: Frequently Asked Questions
Which companies sponsor visas for QA engineers in Massachusetts?
Several large Massachusetts employers have documented H-1B visa sponsorship histories for QA engineering roles. These include Wayfair, MathWorks, Biogen, Raytheon Technologies, and Liberty Mutual. Smaller biotech firms in the Kendall Square area and fintech companies in downtown Boston also appear in Department of Labor LCA disclosure data for QA and software quality positions.
Which visa types are most common for QA engineer roles in Massachusetts?
The H-1B is the most common visa category for QA engineers in Massachusetts, as most roles require a bachelor's degree in computer science, engineering, or a related field, meeting the specialty occupation standard. Candidates already in the U.S. on F-1 OPT or STEM OPT extensions are also actively hired, with employers filing H-1B petitions before OPT expires. The TN visa covers Canadian and Mexican nationals in qualifying engineering classifications.
How to find qa engineer visa sponsorship jobs in Massachusetts?
Migrate Mate filters job listings specifically by visa sponsorship availability, making it straightforward to find QA engineer roles in Massachusetts where employers have indicated willingness to sponsor. Because sponsorship status is often buried or omitted on general job boards, using a focused platform saves significant time. Filtering by Massachusetts and the QA engineer role on Migrate Mate surfaces the most relevant active openings.
Which cities in Massachusetts have the most QA engineer sponsorship jobs?
Boston and Cambridge account for the largest share of QA engineer sponsorship activity, driven by the concentration of biotech, software, and financial services firms. Waltham and Burlington along the Route 128 corridor host major tech and defense employers with established sponsorship programs. Worcester is a secondary market with growing healthcare IT activity, and Marlborough has notable medical device manufacturing employers.
Are there any Massachusetts-specific factors QA engineers should know about visa sponsorship?
Massachusetts employers filing H-1B Labor Condition Applications must attest to paying at least the Department of Labor prevailing wage for the QA role and geographic area. Boston and Cambridge prevailing wages are among the higher benchmarks nationally, which can work in candidates' favor for offer competitiveness. The state's heavy concentration of life sciences employers also creates demand for QA engineers with regulatory and compliance testing backgrounds, a specialization that strengthens sponsorship cases.
What is the prevailing wage for sponsored qa engineer jobs in Massachusetts?
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.