7 systems engineer intern jobs at 5 companies in New Hampshire
1mo
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Systems Engineer
Merrimack or Westlake or Smithfield
$35-$60/hr OnsiteFull Time
Experience building developer platforms, internal tooling, IDE integration, Windows/macOS deployment, secure high-availability distributed systems, cloud (AWS/Azure/Google Cloud), CI/CD and DevOps practices; strong debugging and collaboration skills.
VS Code, GitHub Copilot, Gemini Code Assist, AWS, Azure, Google Cloud, Kubernetes
2mo
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Quality Systems Engineer
Salem, New Hampshire, United States
OnsiteFull Time
8+ YOEMaintain and improve QMS, lead internal/external audits, assess risks, drive corrective actions; Bachelor's degree in engineering/quality/manufacturing or related; 8+ years experience (6+ with Master's); proficiency with Microsoft Office and quality software.
Microsoft Office
1w
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Systems Engineering Intern IV, Summer 2027 (NH - Onsite)
Nashua or Hudson or Manchester or Merrimack
OnsiteFull Time
Must be completing senior undergraduate year and be enrolled in a graduate program before Summer 2027; eligible for US DoD security clearance; majors in EE/ECS/ME/SW or related; proficiency with Microsoft Office.
Microsoft Office
1w
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Systems Engineering Intern II, Summer 2027 (NH-Onsite)
Nashua or Hudson or Manchester or Merrimack
$46k-$63k/yr OnsiteFull Time
Currently enrolled undergraduate in EE/ECS/ME/SW or related, completing sophomore year prior to Summer 2027; U.S. person eligible for DoD security clearance; Microsoft Office proficiency; GPA 3.0 preferred.
Microsoft Office
1w
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New Hampshire Systems Engineering Intern III, (Summer 2027) Onsite
Nashua or Hudson or Manchester or Merrimack
OnsiteFull Time
Must be a U.S. person completing junior undergraduate year prior to Summer 2027 in EE/ECS/ME/SW or related, eligible for DoD security clearance, proficient in Microsoft Office; GPA 3.0+ preferred.
Microsoft Office
2w
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Quality Engineer II
Salem, New Hampshire, United States
OnsiteFull Time
Knowledge of medical device quality systems (ISO 13485, 21 CFR 820), GMP/GDP, CAPA, SPC, root-cause analysis, gage R&R, supplier quality (SCAR, MRB), process and transfer validations, and internal auditing.
ISO 13485, 21CFR Part 820, GMP, GDP, SPC, SCAR, gage R&R
1mo
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Regulatory Affairs Specialist I
Minnetonka or Portsmouth
HybridFull Time
1+ YOEBachelor's degree in science/engineering,1-3 years regulatory affairs experience in medical device industry,experience with international registrations and quality system regulations,strong communication and organization skills.