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.
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Get Access To All JobsINTRODUCTION
Within our Analytical Service team, we have a functional service provider solution, which is a unique partnership that allows our customers to leverage the experience of our staff, while allowing you, the employee, to gain direct experience working onsite at a pharmaceutical/biopharmaceutical company.
As a QC Operations Analyst, you will join the Cell and Gene Therapy Department to support QC operations in a fast-paced GMP environment. The ideal candidate will have GMP lab experience and excellent organization skills. The candidate will need to be flexible to working at Boston/Cambridge depending on need.
ESSENTIAL FUNCTIONS:
- Work cross functionally with internal (facility, validation, metrology) and external (CTL, instrument vendors) teams to minimize day to day lab operations interruptions
- Identifying and creating processes that will ensure success within the QC lab
- Sample, reagent and chemical lifecycle management
- Establish, write, and update Standard Operating Procedures (SOPs) in compliance with GMP guidelines as needed in support of quality control operations
- Sets up and maintains instrumentation by working with the cross functional team (QC, QA, facility and vendors)
- Maintain QC equipment and perform regular performance verification/calibration as specified by equipment SOP
- Communicates project status to project leader
- Performs work assignments accurately, and in a timely and safe manner
Shift work applies - 2 roles:
Candidate will train M-F then convert to one of the below shifts. Flexible during manufacturing runs - if working later, will have a later start time.
- Sun – Wed 12:30 PM – 11:00 PM
- 3:30 PM – 2:00 AM (manufacturing run) at least 2x a month
QUALIFICATIONS
Education and Experience:
- Bachelor's degree in Chemical Engineering, Scientific Field, or equivalent and relevant formal academic/vocational qualification
- Previous GMP lab experience that provides the knowledge, skills, and abilities to perform the job is preferred (0-2 years industry experience)
- In some cases, an equivalency, consisting of a combination of appropriate education, training and/or directly related experience will be considered sufficient for an individual to meet the requirements of the role.
Knowledge, Skills and Abilities:
- GMP experience preferred
- Ability to understand and independently apply GMPs and/or GLPs to everyday work with regard to documentation and instrument use
- Proficient in Microsoft Excel and Word (LIMS is a plus)
- Proven problem solving and troubleshooting abilities
- Good written and oral communication skills
- Time management and project management skills
- Ability to work in a collaborative work environment with a team
- Able to lift and move objects up to 25 pounds.
PAY RANGE:
$40-$43/hr
REQUISITION DISCLAIMER:
This job posting is for a temporary role with a third-party agency partner on assignment at Vertex Pharmaceuticals (“Vertex”). The individual selected for this role will be offered the role as an employee of a third-party agency partner; compensation, medical benefits, fringe benefits and other terms and conditions of employment shall be presented by the third-party agency partner upon offer. The pay rate range provided is a reasonable estimate of the anticipated compensation range for this job at the time of posting. The actual pay rate will be based on a number of factors, including skills, competencies, experience, location and/or being pursued and other job-related factors permitted by law. In addition, this role will be eligible for overtime pay, in accordance with federal and state requirements.
By applying for this position, you agree to the Atrium Terms and Conditions and you direct Atrium to share your application materials, which may include your CV/Resume, email address or phone number, with Vertex. For more information on how Vertex handles your personal data related to your job application, please see Vertex’s Careers Privacy Notice. Agreeing to the Atrium Terms and Conditions, includes permission to use the email address and mobile phone number you provide during the application process or throughout the duration of your prospective or actual employment to notify you of job openings, profiles, articles, news, and other employment-related information, as well as to notify you of special promotions or additional products and services offered by us or our affiliates and partners (collectively, “Atrium Alerts”). Atrium Alerts may be sent by email, phone, or text message. Your personal information will be safely stored within the Atrium & Vertex databases. Atrium does not sell your personal information to third parties. Text message and data rates may apply. To OPT OUT of text messaging or to modify your communication preferences for Atrium Alerts at any time, please contact Atrium at privacyadministrator@atriumstaff.com.
If you do not agree with the Atrium Terms and Conditions, you can still complete your application for this position by emailing your resume to our team at tempstaffing@vrtx.com. Please include the job title in the subject of your email.
No C2C or Third-Party Vendors
INTRODUCTION
Within our Analytical Service team, we have a functional service provider solution, which is a unique partnership that allows our customers to leverage the experience of our staff, while allowing you, the employee, to gain direct experience working onsite at a pharmaceutical/biopharmaceutical company.
As a QC Operations Analyst, you will join the Cell and Gene Therapy Department to support QC operations in a fast-paced GMP environment. The ideal candidate will have GMP lab experience and excellent organization skills. The candidate will need to be flexible to working at Boston/Cambridge depending on need.
ESSENTIAL FUNCTIONS:
- Work cross functionally with internal (facility, validation, metrology) and external (CTL, instrument vendors) teams to minimize day to day lab operations interruptions
- Identifying and creating processes that will ensure success within the QC lab
- Sample, reagent and chemical lifecycle management
- Establish, write, and update Standard Operating Procedures (SOPs) in compliance with GMP guidelines as needed in support of quality control operations
- Sets up and maintains instrumentation by working with the cross functional team (QC, QA, facility and vendors)
- Maintain QC equipment and perform regular performance verification/calibration as specified by equipment SOP
- Communicates project status to project leader
- Performs work assignments accurately, and in a timely and safe manner
Shift work applies - 2 roles:
Candidate will train M-F then convert to one of the below shifts. Flexible during manufacturing runs - if working later, will have a later start time.
- Sun – Wed 12:30 PM – 11:00 PM
- 3:30 PM – 2:00 AM (manufacturing run) at least 2x a month
QUALIFICATIONS
Education and Experience:
- Bachelor's degree in Chemical Engineering, Scientific Field, or equivalent and relevant formal academic/vocational qualification
- Previous GMP lab experience that provides the knowledge, skills, and abilities to perform the job is preferred (0-2 years industry experience)
- In some cases, an equivalency, consisting of a combination of appropriate education, training and/or directly related experience will be considered sufficient for an individual to meet the requirements of the role.
Knowledge, Skills and Abilities:
- GMP experience preferred
- Ability to understand and independently apply GMPs and/or GLPs to everyday work with regard to documentation and instrument use
- Proficient in Microsoft Excel and Word (LIMS is a plus)
- Proven problem solving and troubleshooting abilities
- Good written and oral communication skills
- Time management and project management skills
- Ability to work in a collaborative work environment with a team
- Able to lift and move objects up to 25 pounds.
PAY RANGE:
$40-$43/hr
REQUISITION DISCLAIMER:
This job posting is for a temporary role with a third-party agency partner on assignment at Vertex Pharmaceuticals (“Vertex”). The individual selected for this role will be offered the role as an employee of a third-party agency partner; compensation, medical benefits, fringe benefits and other terms and conditions of employment shall be presented by the third-party agency partner upon offer. The pay rate range provided is a reasonable estimate of the anticipated compensation range for this job at the time of posting. The actual pay rate will be based on a number of factors, including skills, competencies, experience, location and/or being pursued and other job-related factors permitted by law. In addition, this role will be eligible for overtime pay, in accordance with federal and state requirements.
By applying for this position, you agree to the Atrium Terms and Conditions and you direct Atrium to share your application materials, which may include your CV/Resume, email address or phone number, with Vertex. For more information on how Vertex handles your personal data related to your job application, please see Vertex’s Careers Privacy Notice. Agreeing to the Atrium Terms and Conditions, includes permission to use the email address and mobile phone number you provide during the application process or throughout the duration of your prospective or actual employment to notify you of job openings, profiles, articles, news, and other employment-related information, as well as to notify you of special promotions or additional products and services offered by us or our affiliates and partners (collectively, “Atrium Alerts”). Atrium Alerts may be sent by email, phone, or text message. Your personal information will be safely stored within the Atrium & Vertex databases. Atrium does not sell your personal information to third parties. Text message and data rates may apply. To OPT OUT of text messaging or to modify your communication preferences for Atrium Alerts at any time, please contact Atrium at privacyadministrator@atriumstaff.com.
If you do not agree with the Atrium Terms and Conditions, you can still complete your application for this position by emailing your resume to our team at tempstaffing@vrtx.com. Please include the job title in the subject of your email.
No C2C or Third-Party Vendors
Quality Control Manager Job Roles in Massachusetts
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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.