Software Quality Assurance Visa Sponsorship Jobs in Massachusetts
Software quality assurance roles in Massachusetts are concentrated in the Greater Boston tech corridor, with employers like MathWorks, HubSpot, Wayfair, and Moderna actively hiring QA engineers. The state's dense university ecosystem and established biotech and enterprise software sectors make it one of the more active markets for visa sponsorship in this discipline.
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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
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
Software Quality Assurance Job Roles in Massachusetts
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Search Software Quality Assurance Jobs in MassachusettsSoftware Quality Assurance Jobs in Massachusetts: Frequently Asked Questions
Which companies sponsor visas for software quality assurance roles in Massachusetts?
Massachusetts employers with consistent H-1B visa sponsorship records for software quality assurance roles include MathWorks in Natick, Wayfair and HubSpot in Boston, Rapid7, and various biotech firms like Biogen and Vertex Pharmaceuticals that maintain in-house software teams. Larger consulting and technology services firms operating out of Boston, such as Accenture and Cognizant, also regularly sponsor QA engineers.
Which visa types are most common for software quality assurance roles in Massachusetts?
The H-1B is the most common work visa for software quality assurance engineers in Massachusetts, as QA roles typically qualify as specialty occupations requiring a bachelor's degree in computer science, software engineering, or a related field. F-1 OPT and STEM OPT extensions are also widely used by recent graduates from Massachusetts universities before transitioning to H-1B sponsorship.
How to find software quality assurance visa sponsorship jobs in Massachusetts?
Migrate Mate filters job listings specifically by visa sponsorship willingness, making it more targeted than general job searches. For software quality assurance roles in Massachusetts, you can browse listings from employers in the Greater Boston tech and biotech corridor who have indicated sponsorship availability. This is particularly useful for narrowing to QA-specific titles like automation engineer, SDET, or QA lead without sifting through unsponsored roles.
Which cities in Massachusetts have the most software quality assurance sponsorship jobs?
Boston and Cambridge account for the largest share of sponsored QA roles, driven by the concentration of technology companies, biotech firms, and financial services institutions in the metro area. Natick is notable for MathWorks' engineering teams. Waltham and Burlington in the Route 128 corridor also host a significant number of enterprise software and life sciences employers that regularly hire QA engineers with sponsorship.
Are there any state-specific considerations for software quality assurance candidates pursuing sponsorship in Massachusetts?
Massachusetts has a strong pipeline of international QA talent from institutions like MIT, Boston University, and Northeastern University, which means competition for sponsored roles can be meaningful, particularly in the Boston metro. The state's high concentration of regulated industries, including biotech and financial services, can elevate the technical expectations for QA roles, often requiring familiarity with compliance-driven testing frameworks, which strengthens a visa-sponsored candidate's profile.
What is the prevailing wage for sponsored software quality assurance 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.