Quality Analyst Jobs in New York
Quality Analyst jobs in New York are among the most active in the country, concentrated in financial services, healthcare, pharmaceuticals, and technology across New York City, Buffalo, and Albany. Major employers with lasting presences in the state include JPMorgan Chase, Pfizer, and IBM, all of which maintain quality and compliance functions at scale. Demand runs from entry-level QA associates through senior quality engineers and quality management specialists, with particular strength in software testing, regulatory compliance, and manufacturing quality. See the openings below and apply to the ones that match your experience.
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Showing 5 of 22+ Quality Analyst jobs
Position Summary
The Quality Analyst in the STERIS Applied Sterilization Technologies (AST) Chester, NY facility is responsible for assisting in administration of the quality management system at a site to assure adherence to ISO 9001, ISO 13485, FDA 21 CFR Part 820/211, EU GMPs, ISO 17025, ISO 11137 and/or ISO 11135 and other applicable regulatory standards. The Quality Analyst leads complaint/CAPA investigations, supplier quality improvement initiatives, continuous improvement initiatives and countermeasures with the use of statistical techniques and other accepted quality principles. The Quality Analyst executes activities concerned with the development, implementation, maintenance, and continuous improvement of STERIS quality systems. The Analyst also supports production and quality operations by coordinating and performing problem-solving investigations, pre-reviews and final acceptance/run release of processing runs that contain non-conformances.
The Quality Analyst is responsible for the activities related to quality and regulatory compliance to ensure all product processing requirements are met in accordance with Customer specifications including calibrations, dosimetry results, generation of test methods, audits, scheduling, validations, record keeping and reporting.
This position requires working onsite in our Chester, NY facility from 8:00 am to 5:00 pm (or 8:30m to 5:30pm).
What You'll do as a Quality Analyst
- Coordinate day-to-day tasks and direction for Quality Technicians/Senior Quality Technicians by providing technical support, mentoring and oversight.
- Responsible for oversight of all product and/or report pre-reviews and releases conducted by Quality Technicians/Senior Quality Technicians.
- Responsible for executing product and/or report releases for all processing runs/lab samples containing a non-conformance, including management of Customer communication and leading the associated non-conformance investigations.
- Initiate and/or participate in corrective actions, problem-solving and continuous improvement activities.
- Perform internal audits at other AST facilities, including identification of non-compliances and report generation. Responsible for managing remediation of internal audit observations assigned by site Quality Manager.
- Manage creation of new quality system policies and procedures and revisions to existing policies/procedures.
- Review collected data to perform statistical analysis and recommend process changes to improve quality.
- Monitor and report on performance metrics.
- Instruct other STERIS employees in quality principles, effective corrective actions, and valid statistical techniques.
- Collaborate with other departments and facilities within the company on quality related issues.
- Lead quality system programs (i.e. calibration, maintenance, training, CAPA, complaints, non-conformances, supplier quality, management review, operational qualifications, document control, change control, risk management, etc.).
- Overall responsibilities include commitment to ensure external and internal requirements are met according to documented policies, procedures, standards and regulations.
- Perform other duties as assigned.
The Experience, Skills and Abilities Needed
Required:
- Bachelor’s degree (Scientific or related technical field)
- Minimum of 1 year of combined Manufacturing/Quality Engineering and/or Quality Systems experience.
- Minimum of 1 year of experience working in an ISO certified environment required.
Preferred:
- Minimum of 1 year experience with medical device or other regulated industries, preferred.
- Working knowledge of FDA QSR/ EUGMP regulations strongly preferred.
Other:
- Excellent problem-solving skills
- Focus on identification of potential issues and continuous improvement.
- Experience working on cross-functional teams and on own initiative.
- Demonstrated excellent organizational, oral and written communications skills.
- Must have PC experience, as well as working familiarity of desktop applications including Excel, Word, and PowerPoint.
- Ability to work in a fast-paced, regulated environment with strict deadlines.
- Mathematical skills including practical application of fractions, percentages, ratios, proportions and algebra.
What STERIS Offers
We value our employees and are committed to providing a comprehensive benefits package that supports your health, wellbeing, and financial future.
Here is just a brief overview of what we offer:
- Market Competitive pay
- Extensive Paid Time Off and added Holidays
- Excellent Healthcare, Dental and Vision benefits
- Long- and Short-Term Disability coverage
- 401(k) with a company match
- Maternity and Paternity Leave
- Additional add-on benefits / discounts for programs such as Pet Insurance
- Tuition Reimbursement and continuing education programs
- Excellent opportunities for advancement in a stable long-term career
#LI-MO1
#LI-Onsite
Pay range for this opportunity is $76,000 - $86,000. This position is eligible for bonus participation.
Minimum pay rates offered will comply with county/city minimums, if higher than range listed. Pay rates are based on a number of factors, including but not limited to local labor market costs, years of relevant experience, education, professional certifications, foreign language fluency, etc.
STERIS offers a comprehensive and competitive benefits portfolio. Click here for a complete list of benefits: STERIS Benefits
Open until position is filled.
STERIS is an Equal Opportunity Employer. We are committed to equal employment opportunity to ensure that persons are recruited, hired, trained, transferred and promoted in all job groups regardless of race, color, religion, age, disability, national origin, citizenship status, military or veteran status, sex (including pregnancy, childbirth and related medical conditions), sexual orientation, gender identity, genetic information, and any other category protected by federal, state or local law. We are not only committed to this policy by our status as a federal government contractor, but also we are strongly bound by the principle of equal employment opportunity.
Position Summary
The Quality Analyst in the STERIS Applied Sterilization Technologies (AST) Chester, NY facility is responsible for assisting in administration of the quality management system at a site to assure adherence to ISO 9001, ISO 13485, FDA 21 CFR Part 820/211, EU GMPs, ISO 17025, ISO 11137 and/or ISO 11135 and other applicable regulatory standards. The Quality Analyst leads complaint/CAPA investigations, supplier quality improvement initiatives, continuous improvement initiatives and countermeasures with the use of statistical techniques and other accepted quality principles. The Quality Analyst executes activities concerned with the development, implementation, maintenance, and continuous improvement of STERIS quality systems. The Analyst also supports production and quality operations by coordinating and performing problem-solving investigations, pre-reviews and final acceptance/run release of processing runs that contain non-conformances.
The Quality Analyst is responsible for the activities related to quality and regulatory compliance to ensure all product processing requirements are met in accordance with Customer specifications including calibrations, dosimetry results, generation of test methods, audits, scheduling, validations, record keeping and reporting.
This position requires working onsite in our Chester, NY facility from 8:00 am to 5:00 pm (or 8:30m to 5:30pm).
What You'll do as a Quality Analyst
- Coordinate day-to-day tasks and direction for Quality Technicians/Senior Quality Technicians by providing technical support, mentoring and oversight.
- Responsible for oversight of all product and/or report pre-reviews and releases conducted by Quality Technicians/Senior Quality Technicians.
- Responsible for executing product and/or report releases for all processing runs/lab samples containing a non-conformance, including management of Customer communication and leading the associated non-conformance investigations.
- Initiate and/or participate in corrective actions, problem-solving and continuous improvement activities.
- Perform internal audits at other AST facilities, including identification of non-compliances and report generation. Responsible for managing remediation of internal audit observations assigned by site Quality Manager.
- Manage creation of new quality system policies and procedures and revisions to existing policies/procedures.
- Review collected data to perform statistical analysis and recommend process changes to improve quality.
- Monitor and report on performance metrics.
- Instruct other STERIS employees in quality principles, effective corrective actions, and valid statistical techniques.
- Collaborate with other departments and facilities within the company on quality related issues.
- Lead quality system programs (i.e. calibration, maintenance, training, CAPA, complaints, non-conformances, supplier quality, management review, operational qualifications, document control, change control, risk management, etc.).
- Overall responsibilities include commitment to ensure external and internal requirements are met according to documented policies, procedures, standards and regulations.
- Perform other duties as assigned.
The Experience, Skills and Abilities Needed
Required:
- Bachelor’s degree (Scientific or related technical field)
- Minimum of 1 year of combined Manufacturing/Quality Engineering and/or Quality Systems experience.
- Minimum of 1 year of experience working in an ISO certified environment required.
Preferred:
- Minimum of 1 year experience with medical device or other regulated industries, preferred.
- Working knowledge of FDA QSR/ EUGMP regulations strongly preferred.
Other:
- Excellent problem-solving skills
- Focus on identification of potential issues and continuous improvement.
- Experience working on cross-functional teams and on own initiative.
- Demonstrated excellent organizational, oral and written communications skills.
- Must have PC experience, as well as working familiarity of desktop applications including Excel, Word, and PowerPoint.
- Ability to work in a fast-paced, regulated environment with strict deadlines.
- Mathematical skills including practical application of fractions, percentages, ratios, proportions and algebra.
What STERIS Offers
We value our employees and are committed to providing a comprehensive benefits package that supports your health, wellbeing, and financial future.
Here is just a brief overview of what we offer:
- Market Competitive pay
- Extensive Paid Time Off and added Holidays
- Excellent Healthcare, Dental and Vision benefits
- Long- and Short-Term Disability coverage
- 401(k) with a company match
- Maternity and Paternity Leave
- Additional add-on benefits / discounts for programs such as Pet Insurance
- Tuition Reimbursement and continuing education programs
- Excellent opportunities for advancement in a stable long-term career
#LI-MO1
#LI-Onsite
Pay range for this opportunity is $76,000 - $86,000. This position is eligible for bonus participation.
Minimum pay rates offered will comply with county/city minimums, if higher than range listed. Pay rates are based on a number of factors, including but not limited to local labor market costs, years of relevant experience, education, professional certifications, foreign language fluency, etc.
STERIS offers a comprehensive and competitive benefits portfolio. Click here for a complete list of benefits: STERIS Benefits
Open until position is filled.
STERIS is an Equal Opportunity Employer. We are committed to equal employment opportunity to ensure that persons are recruited, hired, trained, transferred and promoted in all job groups regardless of race, color, religion, age, disability, national origin, citizenship status, military or veteran status, sex (including pregnancy, childbirth and related medical conditions), sexual orientation, gender identity, genetic information, and any other category protected by federal, state or local law. We are not only committed to this policy by our status as a federal government contractor, but also we are strongly bound by the principle of equal employment opportunity.
See All 22 Quality Analyst Jobs in New York
Find roles in New York that match your experience and apply in just a few clicks.
Find Quality Analyst JobsQuality Analyst Jobs by City in New York
Where New York roles are concentrated, by current openings.
Quality Analyst Job Market in New York
A snapshot from current New York openings, updated as new roles post.
Who's Hiring
Top Industries Hiring
- Technology & Software
- Biotechnology & Pharmaceuticals
- Consulting & Professional Services
What New York Employers Look For
The qualifications that appear most often in quality analyst jobs across New York.
- Bachelor's degree in a relevant field such as engineering, life sciences, or business
- Experience with quality management systems including ISO 9001 or FDA 21 CFR standards
- Proficiency in test case development, defect tracking, and QA documentation practices
- Familiarity with tools such as JIRA, TestRail, or similar test management platforms
- Strong analytical skills and ability to interpret data from audits or production processes
- Professional certification such as ASQ Certified Quality Auditor or Certified Quality Engineer preferred
Quality Analyst Jobs in New York: Frequently Asked Questions
How do you become a quality analyst in New York?
Most quality analyst roles in New York require a bachelor's degree in engineering, life sciences, information technology, or a related field. New York does not issue a state license specifically for quality analysts, but employers in regulated industries such as pharmaceuticals and medical devices expect familiarity with FDA quality system regulations. Earning an ASQ certification, such as the Certified Quality Auditor or Certified Quality Engineer, strengthens a candidacy considerably and is widely recognized by New York employers.
Which companies hire quality analysts in New York?
Employers hiring quality analysts in New York right now include Curia, Lockheed Martin, and Citi, based on current listings on Migrate Mate as of August 2026. New York's concentration of financial institutions, pharmaceutical companies, and large healthcare networks means ongoing and recurring demand for quality and compliance professionals across the state.
Which New York cities have the most quality analyst jobs?
The cities with the most quality analyst openings in New York are New York, Albany, and Rensselaer. New York City dominates the distribution because of its density of financial services firms, technology companies, and hospital systems, while secondary markets like Buffalo and Albany reflect the presence of manufacturing, state government agencies, and regional healthcare networks that maintain active quality functions.
Are there remote quality analyst jobs in New York?
Yes, and more than many fields. About 60% of quality analyst openings tied to New York are remote or hybrid as of August 2026, reflecting the fact that software QA and analytical compliance work can be performed off-site. Roles focused on physical inspection, on-site auditing, or manufacturing floor quality tend to require in-person presence, while software testing and documentation-heavy positions are the most likely to be listed as remote.
How can I get hired as a quality analyst in New York with little or no experience?
The most realistic entry path is a QA associate or junior quality analyst role at a mid-size technology or healthcare company in the New York City metro. Large New York employers such as hospital networks and pharmaceutical manufacturers often run structured associate programs that accept candidates with a relevant degree but no direct QA experience. Moving laterally from a business analyst, data analyst, or compliance coordinator role is another common route. Building a portfolio of documented test cases or completing an ASQ entry-level certification gives candidates a concrete edge when applying.
Where can I find and apply to quality analyst jobs in New York?
You can find and apply to quality analyst jobs in New York on Migrate Mate, which lists current openings across the state. Search the listings to find roles that match your experience, industry background, and location preference, then apply directly to the ones that fit.
See All 22 Quality Analyst Jobs in New York
Find roles in New York that match your experience and apply in just a few clicks.
Find Quality Analyst Jobs