Quality Assurance Engineer Visa Sponsorship Jobs in Massachusetts
Massachusetts is one of the stronger states for quality assurance engineer visa sponsorship, driven by its concentration of life sciences, biotech, and software companies. Major employers like Biogen, MathWorks, and Wayfair have active QA engineering teams across Greater Boston, Waltham, and Cambridge, where demand for skilled QA talent regularly supports international hiring.
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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
Quality Assurance Engineer Job Roles in Massachusetts
See all 56+ Quality Assurance Engineer Jobs in Massachusetts
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Search Quality Assurance Engineer Jobs in MassachusettsQuality Assurance Engineer Jobs in Massachusetts: Frequently Asked Questions
Which companies sponsor visas for quality assurance engineers in Massachusetts?
Several large employers in Massachusetts have a documented history of sponsoring work visas for quality assurance engineers. These include biotech and pharma firms like Biogen, Moderna, and Takeda, software companies like MathWorks and HubSpot, and e-commerce platforms like Wayfair. Defense contractors and medical device manufacturers in the state also regularly sponsor QA engineering roles.
Which visa types are most common for quality assurance engineer roles in Massachusetts?
The H-1B visa is the most common visa category for quality assurance engineers in Massachusetts, as QA roles at technology and life sciences companies typically qualify as specialty occupations requiring a relevant bachelor's degree. Australian citizens may also be eligible for the E-3 visa, which follows a similar process but without the lottery. TN visa status is available for Canadian and Mexican nationals in qualifying engineering roles.
Which cities in Massachusetts have the most quality assurance engineer sponsorship jobs?
Greater Boston, including Cambridge and Somerville, accounts for the majority of QA engineering sponsorship activity in Massachusetts, largely due to its dense concentration of biotech, medtech, and software employers. Waltham and Burlington, along Route 128, are also significant hubs, hosting the Massachusetts offices of several large technology and life sciences companies that actively hire and sponsor international QA engineers.
How to find quality assurance engineer visa sponsorship jobs in Massachusetts?
Migrate Mate is built specifically for international job seekers and filters quality assurance engineer roles in Massachusetts by visa sponsorship availability, so you're not sifting through listings from employers who won't sponsor. The platform aggregates roles from biotech, software, and medtech companies across the state, making it easier to identify which Massachusetts employers are actively hiring QA engineers and willing to support the H-1B or other work visa processes.
Are there any state-specific considerations for quality assurance engineers seeking visa sponsorship in Massachusetts?
Massachusetts has one of the highest concentrations of FDA-regulated employers in the country, meaning QA engineers with backgrounds in medical devices, pharmaceuticals, or clinical software are particularly sought after. The state's university pipeline, including MIT, Northeastern, and UMass Amherst, also means employers here are accustomed to hiring and sponsoring international graduates. Prevailing wage requirements for H-1B petitions in the Boston metro area reflect the region's competitive compensation environment for engineering roles.
What is the prevailing wage for sponsored quality assurance 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.