Quality Control Manager Visa Sponsorship Jobs in Massachusetts
Massachusetts quality control manager roles are concentrated in life sciences, medical devices, and defense manufacturing, with major employers like Boston Scientific, Thermo Fisher Scientific, Raytheon Technologies, and Pfizer actively hiring in Greater Boston, Marlborough, and the Route 128 corridor. The state's dense concentration of FDA-regulated industries makes QC manager positions among the more consistently sponsored roles in the region.
Find Quality Control Manager JobsOverview
Showing 5 of 103+ Quality Control Manager Jobs in Massachusetts with Visa Sponsorship
Have you applied for this role?
Have you applied for this role?
Have you applied for this role?
Have you applied for this role?
Have you applied for this role?
See all 103+ Quality Control Manager Jobs in Massachusetts with Visa Sponsorship
Sign up for free to unlock all listings, filter by visa type, and get alerts for new Quality Control Manager Jobs in Massachusetts with Visa Sponsorship.
Get Access To All JobsJob Description
The Manager, Quality Control is a key position that provides oversight of a variety of analytical functions that occur in the QC department supporting testing, and reporting of in-process, release, and stability samples. This role also ensures activities occur in an efficient and cGMP compliant manner. The role will have formal people management responsibilities.
Key Duties and Responsibilities:
- Manages various laboratory program(s)/processes within the department (assay readiness, training, sample management, data review and reporting) and serves as QC representation at triage and QC of contact for Quality Events.
- Coordinates and facilities laboratory activities to meet commitments on-time.
- Ensure lab personnel have appropriate training.
- Assist in troubleshooting of analytical methods and/or equipment as required.
- Authors, review, and/or approves data, SOPs.
- Assist in monitor, tracking and publishing lab metrics.
- Ensure all laboratory records adhere to cGMP/GDP expectations.
- Leads sub-teams working towards the goal of continuous improvement.
- May be required to lead OOS/OOT investigations/deviations and to identify corrective actions to prevent reoccurrence.
- Provide guidance to reports when issues arise. Coach and develop reports.
- Serves as T1D Cell QC representative in cross-functional, cross-departmental working teams and/or working with outside vendors to meet all laboratory needs.
Knowledge and Skills:
- Strong knowledge of US and EU cGMP regulations/guidance and some experience with regulatory agency inspections.
- Strong knowledge of analytical methodologies such as flow cytometry, cell-based assays, qPCR, ELISA, BACT, endotoxin and applying/interpretation of GMP requirements.
- Effective communication skills, both verbal and written.
- Ability to prioritize objectives from multiple projects, adhere to scheduled timelines while maintaining flexibility and attention to detail.
Education and Experience:
Bachelor's Degree in science or related discipline is required with 8 years of experience in pharmaceutical/biopharmaceutical industry, or the equivalent combination of education and experience.
Pay Range:
$117,800 - $176,800
Disclosure Statement:
The range provided is based on what we believe is a reasonable estimate for the base salary pay range for this job at the time of posting. This role is eligible for an annual bonus and annual equity awards. Some roles may also be eligible for overtime pay, in accordance with federal and state requirements. Actual base salary pay will be based on a number of factors, including skills, competencies, experience, and other job-related factors permitted by law.
At Vertex, our Total Rewards offerings also include inclusive market-leading benefits to meet our employees wherever they are in their career, financial, family and wellbeing journey while providing flexibility and resources to support their growth and aspirations. From medical, dental and vision benefits to generous paid time off (including a week-long company shutdown in the Summer and the Winter), educational assistance programs including student loan repayment, a generous commuting subsidy, matching charitable donations, 401(k) and so much more.
Flex Designation:
On-Site Designated
Flex Eligibility Status:
In this On-Site designated role, you will work five days per week on-site with ad hoc flexibility.
Note: The Flex status for this position is subject to Vertex’s Policy on Flex @ Vertex Program and may be changed at any time.
LI-Onsite
Company Information
Vertex is a global biotechnology company that invests in scientific innovation.
Vertex is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person's race, color, sex, gender identity or expression, age, religion, national origin, ancestry, ethnicity, disability, veteran status, genetic information, sexual orientation, marital status, or any characteristic protected under applicable law. Vertex is an E-Verify Employer in the United States. Vertex will make reasonable accommodations for qualified individuals with known disabilities, in accordance with applicable law.
Any applicant requiring an accommodation in connection with the hiring process and/or to perform the essential functions of the position for which the applicant has applied should make a request to the recruiter or hiring manager, or contact Talent Acquisition at ApplicationAssistance@vrtx.com
Job Description
The Manager, Quality Control is a key position that provides oversight of a variety of analytical functions that occur in the QC department supporting testing, and reporting of in-process, release, and stability samples. This role also ensures activities occur in an efficient and cGMP compliant manner. The role will have formal people management responsibilities.
Key Duties and Responsibilities:
- Manages various laboratory program(s)/processes within the department (assay readiness, training, sample management, data review and reporting) and serves as QC representation at triage and QC of contact for Quality Events.
- Coordinates and facilities laboratory activities to meet commitments on-time.
- Ensure lab personnel have appropriate training.
- Assist in troubleshooting of analytical methods and/or equipment as required.
- Authors, review, and/or approves data, SOPs.
- Assist in monitor, tracking and publishing lab metrics.
- Ensure all laboratory records adhere to cGMP/GDP expectations.
- Leads sub-teams working towards the goal of continuous improvement.
- May be required to lead OOS/OOT investigations/deviations and to identify corrective actions to prevent reoccurrence.
- Provide guidance to reports when issues arise. Coach and develop reports.
- Serves as T1D Cell QC representative in cross-functional, cross-departmental working teams and/or working with outside vendors to meet all laboratory needs.
Knowledge and Skills:
- Strong knowledge of US and EU cGMP regulations/guidance and some experience with regulatory agency inspections.
- Strong knowledge of analytical methodologies such as flow cytometry, cell-based assays, qPCR, ELISA, BACT, endotoxin and applying/interpretation of GMP requirements.
- Effective communication skills, both verbal and written.
- Ability to prioritize objectives from multiple projects, adhere to scheduled timelines while maintaining flexibility and attention to detail.
Education and Experience:
Bachelor's Degree in science or related discipline is required with 8 years of experience in pharmaceutical/biopharmaceutical industry, or the equivalent combination of education and experience.
Pay Range:
$117,800 - $176,800
Disclosure Statement:
The range provided is based on what we believe is a reasonable estimate for the base salary pay range for this job at the time of posting. This role is eligible for an annual bonus and annual equity awards. Some roles may also be eligible for overtime pay, in accordance with federal and state requirements. Actual base salary pay will be based on a number of factors, including skills, competencies, experience, and other job-related factors permitted by law.
At Vertex, our Total Rewards offerings also include inclusive market-leading benefits to meet our employees wherever they are in their career, financial, family and wellbeing journey while providing flexibility and resources to support their growth and aspirations. From medical, dental and vision benefits to generous paid time off (including a week-long company shutdown in the Summer and the Winter), educational assistance programs including student loan repayment, a generous commuting subsidy, matching charitable donations, 401(k) and so much more.
Flex Designation:
On-Site Designated
Flex Eligibility Status:
In this On-Site designated role, you will work five days per week on-site with ad hoc flexibility.
Note: The Flex status for this position is subject to Vertex’s Policy on Flex @ Vertex Program and may be changed at any time.
LI-Onsite
Company Information
Vertex is a global biotechnology company that invests in scientific innovation.
Vertex is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person's race, color, sex, gender identity or expression, age, religion, national origin, ancestry, ethnicity, disability, veteran status, genetic information, sexual orientation, marital status, or any characteristic protected under applicable law. Vertex is an E-Verify Employer in the United States. Vertex will make reasonable accommodations for qualified individuals with known disabilities, in accordance with applicable law.
Any applicant requiring an accommodation in connection with the hiring process and/or to perform the essential functions of the position for which the applicant has applied should make a request to the recruiter or hiring manager, or contact Talent Acquisition at ApplicationAssistance@vrtx.com
Quality Control Manager Job Roles in Massachusetts
See all 103+ Quality Control Manager Jobs in Massachusetts
Sign up for free to filter by visa type, set job alerts, and find employers with verified sponsorship history.
Search Quality Control Manager Jobs in MassachusettsQuality Control Manager Jobs in Massachusetts: Frequently Asked Questions
Which companies sponsor visas for quality control managers in Massachusetts?
Life sciences and medical device companies are among the most active sponsors for quality control manager roles in Massachusetts. Employers like Boston Scientific, Thermo Fisher Scientific, Pfizer, Hologic, and Raytheon Technologies have filed H-1B visa petitions for quality and regulatory roles in recent years. Contract manufacturers and clinical research organizations operating in the Greater Boston area also appear in DOL disclosure data as recurring sponsors for these positions.
Which visa types are most common for quality control manager roles in Massachusetts?
The H-1B is the most common visa for quality control managers in Massachusetts, as the role typically requires a bachelor's degree in engineering, chemistry, biology, or a related technical field, which satisfies the specialty occupation requirement. Candidates with multinational company experience may qualify for an L-1A or L-1B transfer. Professionals with extraordinary achievement in quality systems may explore the O-1 visa, though that pathway is less common for this role.
Which cities in Massachusetts have the most quality control manager sponsorship jobs?
Greater Boston, including Cambridge and Somerville, hosts the highest concentration of sponsored quality control manager positions, driven by the region's life sciences cluster. The Route 128 corridor, particularly Marlborough, Waltham, and Woburn, is another active area given its density of medical device and biotech manufacturers. Worcester also has manufacturing employers in regulated industries that periodically sponsor for quality and compliance management roles.
How to find quality control manager visa sponsorship jobs in Massachusetts?
Migrate Mate filters job listings specifically by visa sponsorship availability, making it straightforward to browse quality control manager openings in Massachusetts without sorting through roles that don't offer sponsorship. You can filter by state and job category to surface positions at life sciences, defense, and manufacturing employers across the Greater Boston area and Route 128 corridor. Searching through Migrate Mate saves significant time compared to manually verifying sponsorship eligibility employer by employer.
Are there any Massachusetts-specific considerations for quality control manager sponsorship?
Massachusetts sits in DOL wage area Region 1, which generally reflects higher prevailing wages than national averages, meaning employers must meet those thresholds when filing a Labor Condition Application for H-1B sponsorship. The state's concentration of FDA-regulated industries means many quality control manager roles require familiarity with cGMP, ISO 13485, or 21 CFR Part 820 standards, which can strengthen a candidate's case as a specialty occupation worker. Massachusetts universities like MIT, Northeastern, and UMass also supply a consistent pipeline of internationally educated engineers into these roles.
What is the prevailing wage for sponsored quality control manager 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.