Quality Supervisor Visa Sponsorship Jobs in New York
New York's quality supervisor roles span pharmaceutical manufacturing in Long Island, food production in the Hudson Valley, and electronics and aerospace in the Capital Region. Companies like Pfizer, PepsiCo, and Northrop Grumman have sponsored quality professionals here. International candidates with quality management backgrounds find consistent demand across these sectors.
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Get Access To All JobsAt Perrigo, we are driven by our mission to Makes Lives Better Through Trusted Health and Wellness Solutions, Accessible to All. We are proud to be a Top 10 player in the European Consumer Self-Care market and the largest U.S. store brand provider of over the counter and infant formula. Dedicated to providing The Best Self-Care for Everyone, we are the people behind the brands you trust. We are Opill®, Compeed®, Solpadeine®, NiQuitin®, and many more. We Are Perrigo. We are committed to enhancing the wellbeing of our colleagues and consumers alike. We pride ourselves on fostering an inclusive, collaborative culture where each person can experience a sense of belonging.
Join us on our One Perrigo journey as we evolve to win in self-care.
Description Overview
The QA Supervisor is responsible for leading a team of Quality Assurance Inspectors that provides quality oversight for bulk manufacturing, filling, and packaging operations involved in the production of topical and suppository pharmaceutical products. This role ensures compliance with current Good Manufacturing Practices (cGMP), FDA regulations, internal quality systems, and approved procedures. The QA Supervisor serves as a key quality resource for Manufacturing, Packaging, Engineering, and Validation. Responsibilities include providing real-time quality support, maintaining quality systems, reviewing and approving quality documentation, supporting investigations, and assisting with audits and inspections to ensure product quality and regulatory compliance.
Schedule: First shift, Monday through Friday. Occasional weekend on-call support may be required. Salary: $80,000
Scope of the Role
- Supervise, coach, train, and evaluate QA Inspectors responsible for in-process oversight of manufacturing and packaging operations.
- Ensure manufacturing and packaging activities comply with cGMP requirements, FDA regulations, approved procedures, batch records, and internal quality standards.
- Review production, packaging, and quality documentation for accuracy, completeness, and compliance.
- Provide quality support to operations by addressing quality concerns, conducting risk assessments, and escalating issues when appropriate.
- Author, revise, review, and approve SOPs, Standard Work Instructions (SWIs), forms, and other controlled documents; develop new procedures and improve existing quality systems as needed.
- Lead or support investigations involving deviations, non-conformances, documentation errors, environmental monitoring excursions, and other quality events, ensuring timely implementation of corrective and preventive actions.
- Monitor compliance trends and identify opportunities for continuous improvement.
- Schedule and prioritize team activities and ensure personnel maintain required GMP qualifications and training.
- Support FDA inspections, customer audits, and internal audits while maintaining inspection readiness and assisting with remediation activities.
- Assist with quality metrics, management reviews, and other quality system initiatives.
Experience Required
- Bachelor's degree in a scientific discipline preferred; equivalent experience in a regulated manufacturing environment may be considered in lieu of a degree.
- Minimum of four (4) years of Quality Assurance experience in a regulated industry.
- Previous experience in pharmaceutical, biotechnology, medical device, cosmetics, or another FDA-regulated manufacturing environment is required.
- Demonstrated knowledge of cGMP requirements and quality systems.
- Experience reviewing manufacturing and packaging documentation, investigations, deviations, CAPAs, and change controls.
- Experience authoring and revising SOPs and other controlled documents.
- Previous supervisory or leadership experience preferred.
- Experience supporting FDA inspections and audits preferred.
- Strong written, verbal, organizational, and interpersonal skills.
- Knowledge of SAP and/or electronic quality management systems (eQMS) preferred.
Benefits
We believe our people are our greatest asset. Alongside competitive compensation, we offer benefits tailored to supporting you and your family, as well as career development opportunities to ensure you feel valued and supported, both professionally and personally.
Find out more about Total Rewards at Perrigo.
We are proud to be included in the Forbes list of "America's Best Employers by State 2024". Find out more here.
Applicants please note: To apply to this position please click the APPLY button at the bottom of the application. (The SAVE button will only save your profile information but not submit an application for this open position.) All application materials, including resumes and CVs, must be submitted in English. Thank you.
We are an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or other characteristics protected by law. #weareperrigo
At Perrigo, we are driven by our mission to Makes Lives Better Through Trusted Health and Wellness Solutions, Accessible to All. We are proud to be a Top 10 player in the European Consumer Self-Care market and the largest U.S. store brand provider of over the counter and infant formula. Dedicated to providing The Best Self-Care for Everyone, we are the people behind the brands you trust. We are Opill®, Compeed®, Solpadeine®, NiQuitin®, and many more. We Are Perrigo. We are committed to enhancing the wellbeing of our colleagues and consumers alike. We pride ourselves on fostering an inclusive, collaborative culture where each person can experience a sense of belonging.
Join us on our One Perrigo journey as we evolve to win in self-care.
Description Overview
The QA Supervisor is responsible for leading a team of Quality Assurance Inspectors that provides quality oversight for bulk manufacturing, filling, and packaging operations involved in the production of topical and suppository pharmaceutical products. This role ensures compliance with current Good Manufacturing Practices (cGMP), FDA regulations, internal quality systems, and approved procedures. The QA Supervisor serves as a key quality resource for Manufacturing, Packaging, Engineering, and Validation. Responsibilities include providing real-time quality support, maintaining quality systems, reviewing and approving quality documentation, supporting investigations, and assisting with audits and inspections to ensure product quality and regulatory compliance.
Schedule: First shift, Monday through Friday. Occasional weekend on-call support may be required. Salary: $80,000
Scope of the Role
- Supervise, coach, train, and evaluate QA Inspectors responsible for in-process oversight of manufacturing and packaging operations.
- Ensure manufacturing and packaging activities comply with cGMP requirements, FDA regulations, approved procedures, batch records, and internal quality standards.
- Review production, packaging, and quality documentation for accuracy, completeness, and compliance.
- Provide quality support to operations by addressing quality concerns, conducting risk assessments, and escalating issues when appropriate.
- Author, revise, review, and approve SOPs, Standard Work Instructions (SWIs), forms, and other controlled documents; develop new procedures and improve existing quality systems as needed.
- Lead or support investigations involving deviations, non-conformances, documentation errors, environmental monitoring excursions, and other quality events, ensuring timely implementation of corrective and preventive actions.
- Monitor compliance trends and identify opportunities for continuous improvement.
- Schedule and prioritize team activities and ensure personnel maintain required GMP qualifications and training.
- Support FDA inspections, customer audits, and internal audits while maintaining inspection readiness and assisting with remediation activities.
- Assist with quality metrics, management reviews, and other quality system initiatives.
Experience Required
- Bachelor's degree in a scientific discipline preferred; equivalent experience in a regulated manufacturing environment may be considered in lieu of a degree.
- Minimum of four (4) years of Quality Assurance experience in a regulated industry.
- Previous experience in pharmaceutical, biotechnology, medical device, cosmetics, or another FDA-regulated manufacturing environment is required.
- Demonstrated knowledge of cGMP requirements and quality systems.
- Experience reviewing manufacturing and packaging documentation, investigations, deviations, CAPAs, and change controls.
- Experience authoring and revising SOPs and other controlled documents.
- Previous supervisory or leadership experience preferred.
- Experience supporting FDA inspections and audits preferred.
- Strong written, verbal, organizational, and interpersonal skills.
- Knowledge of SAP and/or electronic quality management systems (eQMS) preferred.
Benefits
We believe our people are our greatest asset. Alongside competitive compensation, we offer benefits tailored to supporting you and your family, as well as career development opportunities to ensure you feel valued and supported, both professionally and personally.
Find out more about Total Rewards at Perrigo.
We are proud to be included in the Forbes list of "America's Best Employers by State 2024". Find out more here.
Applicants please note: To apply to this position please click the APPLY button at the bottom of the application. (The SAVE button will only save your profile information but not submit an application for this open position.) All application materials, including resumes and CVs, must be submitted in English. Thank you.
We are an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or other characteristics protected by law. #weareperrigo
Quality Supervisor Job Roles in New York
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Search Quality Supervisor Jobs in New YorkQuality Supervisor Jobs in New York: Frequently Asked Questions
Which companies sponsor visas for quality supervisors in New York?
Pharmaceutical and biotech employers on Long Island, including Pfizer and Regeneron, have sponsored quality supervisors through H-1B visa petitions. Food and beverage manufacturers like PepsiCo in Purchase and Constellation Brands upstate also appear in sponsorship records. Defense and electronics contractors including Lockheed Martin and L3Harris, both active in New York, have similarly filed for quality and manufacturing oversight roles.
Which visa types are most common for quality supervisor roles in New York?
The H-1B is the most common visa for quality supervisors in New York when the role requires a bachelor's degree in engineering, manufacturing, or a related technical field. TN visas are available to Canadian and Mexican nationals in qualifying engineering categories. Candidates already in the U.S. on OPT or STEM OPT sometimes transition to H-1B sponsorship through New York employers in regulated industries.
Which cities in New York have the most quality supervisor sponsorship jobs?
New York City and its surrounding metro area see demand from life sciences and consumer goods companies. Long Island concentrates pharmaceutical and defense manufacturing employers with sponsorship histories. The Capital Region, including Albany and Schenectady, has a strong manufacturing base tied to semiconductor and electronics production. Buffalo and Rochester in western New York also host food processing and industrial manufacturers that hire quality supervisors.
How to find quality supervisor visa sponsorship jobs in New York?
Migrate Mate filters job listings specifically by visa sponsorship availability, so you can search quality supervisor roles in New York without sorting through positions that don't offer sponsorship. The platform is designed for international candidates, making it straightforward to identify employers actively willing to sponsor. Filtering by New York state narrows results to the pharmaceutical, food production, and manufacturing sectors where sponsorship is most common for this role.
Are there any New York-specific considerations for quality supervisor visa sponsorship?
New York's concentration of FDA-regulated industries means quality supervisor roles often require familiarity with GMP and ISO standards, which can strengthen a sponsorship case by demonstrating specialized expertise. Employers filing H-1B petitions in New York must post prevailing wage notices at the worksite under Labor Condition Application rules. Candidates near university clusters like SUNY Binghamton or RPI may find employers familiar with sponsoring international graduates into quality and operations roles.
What is the prevailing wage for sponsored quality supervisor jobs in New York?
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.