Science & Research STEM OPT Jobs in New Hampshire
New Hampshire's science and research sector spans pharmaceutical manufacturing in Manchester, life sciences firms along the Route 3 corridor, and federally affiliated research institutions like Dartmouth-Hitchcock and the University of New Hampshire. F-1 students on STEM OPT can pursue roles at employers with documented OPT sponsorship history in disciplines from biomedical research to environmental science.
Find Science & Research JobsOverview
Showing 2 of 3+ Science & Research STEM OPT Jobs in New Hampshire
See all Science & Research STEM OPT Jobs in New Hampshire
Sign up for free to unlock all listings, filter by visa type, and get alerts for new Science & Research STEM OPT Jobs in New Hampshire.
Get Access To All JobsINTRODUCTION
The Senior Supplier Quality Engineer (Sr. SQE) is responsible for leading supplier quality activities across both New Product Introduction (NPI) and sustaining manufacturing operations. This role ensures supplier compliance to applicable requirements, including 21CFR, ISO 13485, and drives robust supplier qualification, development, and performance management processes.
The Sr. SQE serves as a key technical and quality liaison between DEKA, manufacturing partner and its supplier base, with primary responsibility for ensuring suppliers are capable of consistently meeting quality, regulatory, and performance expectations. This role will heavily support supplier qualification activities for NPI programs, including process validation support, and onboarding of new suppliers, while also managing sustaining supplier quality performance for production materials and services.
ROLE AND RESPONSIBILITIES
How you will make an impact as a Senior Supplier Quality Engineer:
- Lead supplier qualification activities for New Product Introduction (NPI) projects
- Perform risk-based supplier assessments aligned with product and process criticality
- Support supplier selection decisions in collaboration with Design Authority (customer), Engineering, Procurement, and Quality Assurance
- Conduct supplier audits (remote and onsite) for new and existing suppliers
- Review and approve supplier documentation including certifications, validations, and quality records
- Ensure supplier readiness for production launch, including capacity, quality systems, and process controls
- Participate in design transfer and process validation activities where supplier input is required
Sustaining Supplier Quality Management
- Own supplier quality oversight for assigned NPI projects and production suppliers
- Monitor supplier performance using quality metrics (e.g., SCARs, defects, delivery performance)
- Lead supplier corrective action activities (SCAR/CAPA) and ensure timely closure
- Conduct supplier performance reviews and drive continuous improvement initiatives
- Support containment, root cause analysis, and resolution of supplier-related quality issues
- Perform risk-based supplier re-evaluations and periodic assessments
Supplier Quality System & Compliance
- Ensure supplier compliance with applicable regulatory and quality system requirements including ISO 13485
- Maintain and improve Approved Supplier List (ASL) classification and risk-based controls
- Support external and internal audits involving supplier quality systems
- Ensure supplier quality agreements are established and maintained
- Drive adherence to change notification and supplier control requirements
Cross-Functional Collaboration
- Partner with Design Authority (customer), Procurement, Manufacturing and Engineering
- Support material nonconformance investigations and disposition decisions
- Provide supplier risk input to project teams and change control processes
- Support supply continuity and risk mitigation strategies
BASIC QUALIFICATIONS
- Bachelor’s degree in Engineering, Life Sciences, or related technical field; or equivalent experience in regulated industry may be considered in lieu of degree.
- 3–5 years of experience in Supplier Quality, Quality Engineering, or related role in medical device or regulated industry
- Strong knowledge of ISO 13485 and medical device regulatory requirements
- Experience with supplier audits, qualification, and risk-based supplier management
- Experience supporting NPI or design transfer activities strongly preferred
- Strong understanding of manufacturing processes, validation, and quality systems.
PREFERRED QUALIFICATIONS
- Experience with contract manufacturing and global supply chains
- Ability to interpret mechanical drawings (CAD files)
- Familiarity with statistical tools, risk analysis (FMEA), and CAPA systems
- Experience in lean manufacturing or continuous improvement environments
- Strong technical judgment and problem-solving skills
- Ability to lead supplier interactions and drive accountability
- Excellent communication and cross-functional collaboration skills
- Strong root cause analysis and data-driven decision-making capability
- Ability to manage multiple priorities in a fast-paced NPI and production environment
- High attention to detail and regulatory compliance mindset
- Willingness to travel both domestically and internationally to suppliers as needed, estimated to be 20% travel
PREFERRED CERTIFICATIONS
- ISO 13485 Internal Auditor certification preferred.
- ASQ certifications (CQE, CQA, or similar) are a plus.
INTRODUCTION
The Senior Supplier Quality Engineer (Sr. SQE) is responsible for leading supplier quality activities across both New Product Introduction (NPI) and sustaining manufacturing operations. This role ensures supplier compliance to applicable requirements, including 21CFR, ISO 13485, and drives robust supplier qualification, development, and performance management processes.
The Sr. SQE serves as a key technical and quality liaison between DEKA, manufacturing partner and its supplier base, with primary responsibility for ensuring suppliers are capable of consistently meeting quality, regulatory, and performance expectations. This role will heavily support supplier qualification activities for NPI programs, including process validation support, and onboarding of new suppliers, while also managing sustaining supplier quality performance for production materials and services.
ROLE AND RESPONSIBILITIES
How you will make an impact as a Senior Supplier Quality Engineer:
- Lead supplier qualification activities for New Product Introduction (NPI) projects
- Perform risk-based supplier assessments aligned with product and process criticality
- Support supplier selection decisions in collaboration with Design Authority (customer), Engineering, Procurement, and Quality Assurance
- Conduct supplier audits (remote and onsite) for new and existing suppliers
- Review and approve supplier documentation including certifications, validations, and quality records
- Ensure supplier readiness for production launch, including capacity, quality systems, and process controls
- Participate in design transfer and process validation activities where supplier input is required
Sustaining Supplier Quality Management
- Own supplier quality oversight for assigned NPI projects and production suppliers
- Monitor supplier performance using quality metrics (e.g., SCARs, defects, delivery performance)
- Lead supplier corrective action activities (SCAR/CAPA) and ensure timely closure
- Conduct supplier performance reviews and drive continuous improvement initiatives
- Support containment, root cause analysis, and resolution of supplier-related quality issues
- Perform risk-based supplier re-evaluations and periodic assessments
Supplier Quality System & Compliance
- Ensure supplier compliance with applicable regulatory and quality system requirements including ISO 13485
- Maintain and improve Approved Supplier List (ASL) classification and risk-based controls
- Support external and internal audits involving supplier quality systems
- Ensure supplier quality agreements are established and maintained
- Drive adherence to change notification and supplier control requirements
Cross-Functional Collaboration
- Partner with Design Authority (customer), Procurement, Manufacturing and Engineering
- Support material nonconformance investigations and disposition decisions
- Provide supplier risk input to project teams and change control processes
- Support supply continuity and risk mitigation strategies
BASIC QUALIFICATIONS
- Bachelor’s degree in Engineering, Life Sciences, or related technical field; or equivalent experience in regulated industry may be considered in lieu of degree.
- 3–5 years of experience in Supplier Quality, Quality Engineering, or related role in medical device or regulated industry
- Strong knowledge of ISO 13485 and medical device regulatory requirements
- Experience with supplier audits, qualification, and risk-based supplier management
- Experience supporting NPI or design transfer activities strongly preferred
- Strong understanding of manufacturing processes, validation, and quality systems.
PREFERRED QUALIFICATIONS
- Experience with contract manufacturing and global supply chains
- Ability to interpret mechanical drawings (CAD files)
- Familiarity with statistical tools, risk analysis (FMEA), and CAPA systems
- Experience in lean manufacturing or continuous improvement environments
- Strong technical judgment and problem-solving skills
- Ability to lead supplier interactions and drive accountability
- Excellent communication and cross-functional collaboration skills
- Strong root cause analysis and data-driven decision-making capability
- Ability to manage multiple priorities in a fast-paced NPI and production environment
- High attention to detail and regulatory compliance mindset
- Willingness to travel both domestically and internationally to suppliers as needed, estimated to be 20% travel
PREFERRED CERTIFICATIONS
- ISO 13485 Internal Auditor certification preferred.
- ASQ certifications (CQE, CQA, or similar) are a plus.
STEM OPT Science & Research Job Roles in New Hampshire
See all Science & Research STEM OPT Jobs in New Hampshire
Sign up for free to filter by visa type, set job alerts, and find employers with verified sponsorship history.
Search Science & Research Jobs in New HampshireScience & Research STEM OPT Sponsorship Jobs in New Hampshire: Frequently Asked Questions
Which science and research companies sponsor F-1 STEM OPT visas in New Hampshire?
Employers with active STEM OPT sponsorship history in New Hampshire's science and research sector include pharmaceutical and biotech firms in Manchester and Nashua, contract research organizations operating near the Massachusetts border, and research divisions at institutions such as Dartmouth College and the University of New Hampshire. Defense-adjacent research contractors in the Merrimack Valley corridor also file regularly for STEM-designated OPT workers in laboratory and analytical roles.
Which cities in New Hampshire have the most science and research F-1 STEM OPT sponsorship jobs?
Manchester and Nashua account for the largest share of science and research STEM OPT sponsorship activity in New Hampshire, driven by life sciences manufacturing and contract laboratory employers. Durham is notable for university-affiliated research positions at UNH. Hanover supports a smaller but consistent cluster of research roles tied to Dartmouth College and its medical center. Concord occasionally appears in state agency and environmental research filings.
How do I find science & research F-1 STEM OPT sponsorship jobs in New Hampshire?
Migrate Mate filters science and research positions in New Hampshire by verified STEM OPT sponsorship history, showing which employers have an established record of filing for F-1 STEM OPT workers in laboratory, research, and analytical roles. You can narrow results by occupation type and location within the state, which is particularly useful given that New Hampshire's sponsoring employers are concentrated in a small number of cities rather than distributed statewide.
What types of science and research roles typically qualify for F-1 STEM OPT sponsorship in New Hampshire?
Roles that commonly qualify include research scientist, analytical chemist, environmental scientist, biomedical researcher, data scientist, and laboratory technician positions where the job requires a STEM-designated degree. The role must fall under a STEM-classified Standard Occupational Classification code and the employer must be enrolled in E-Verify. New Hampshire employers most often file for positions in life sciences, environmental testing, and defense-related research and development.
Are there state-specific considerations for F-1 STEM OPT sponsorship in science and research roles in New Hampshire?
New Hampshire has no state-level visa sponsorship registry or additional filing requirement beyond federal STEM OPT rules, but the state's science and research employer base is smaller than neighboring Massachusetts, meaning fewer total sponsoring employers. Many New Hampshire research employers operate as subsidiaries of larger organizations headquartered elsewhere, so the legal entity filing the E-Verify enrollment and OPT extension paperwork may differ from the local facility name. Verifying the filing entity against OFLC records before applying is advisable.