INTERNSHIP DETAILS

Quality Engineer Intern

CompanyTomz Corporation
LocationBerlin
Work ModeOn Site
PostedApril 21, 2026
Internship Information
Core Responsibilities
The Quality Engineer Intern will support quality design and development activities throughout the product development process. They will also assist in sustaining manufacturing operations, including risk management, validation strategies, and audit preparation.
Internship Type
full time
Salary Range
$22 - $23
Company Size
139
Visa Sponsorship
No
Language
English
Working Hours
40 hours
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About The Company
ISO 13485:2016 Certified & FDA Registered TOMZ Corporation was founded in 1988 and is a leader in the manufacturing of precision components for major medical device, healthcare and laboratory diagnostics. We have been able to maintain private ownership and operation since inception and will continue into the next generation. With 200,000+ square feet, our facilities across Connecticut, Indiana and Minnesota house state of the art, validated CNC Lathe/Mill/Wire EDM, Finishing, Passivation/Anodize, Inspection, to Package & Label. We are truly your "one stop shop."​ TOMZ understands and works closely with our customers to provide the best engineering services, product, for the best price, with the best delivery. TOMZ Corporation is headquartered at 47 Episcopal Rd. Berlin, CT.
About the Role

Summary of Position:

TOMZ is looking for a highly motivated Quality Engineer Intern who is eager to apply what they have learned and join our team in Berlin, CT!  Reporting to the Quality Engineering Manager, this internship will support activities related to Quality Design & Development control and assurance during the Product Development Process (PDP). The intern will assist with ongoing design and development efforts, as well as provide support for sustaining manufacturing and product distribution.

 Essential Functions:

  • Assist in the development and execution of Quality Plans for product design and development projects
  • Support engineering teams in creating and updating Risk Management documentation based on project needs
  • Help develop risk-based validation strategies and contribute to verification and validation (V&V) activities. 
  • Assist with operational and process qualifications for manufacturing processes.
  • Support test method development and participate in validation activities to assess effectiveness.
  • Help implement inspection plans for incoming, in-process, and final products.
  • Assist in developing sampling plans and documenting test and inspection methods.
  • Participate in design reviews as a Quality Engineering representative (as appropriate).
  • Support audit preparation and activities for customers and regulatory agencies.
  • Assist with supplier and vendor qualification activities, including audits and assessments.
  • Contribute to quality best practices and continuous improvement initiatives
  • Apply basic problem-solving skills to help identify and resolve quality issues
  • Support compliance with the Quality Management System and training requirements
  • Assist in the development of Quality Agreements for external customers
  • Follow all TOMZ Quality Management System requirements
  • Perform other duties as assigned

Qualifications:

  • Currently pursuing a bachelor’s degree in Engineering, Quality, Manufacturing, Life Sciences, or a related field 
  • Basic understanding of engineering or quality principles through coursework or projects 
  • Strong attention to detail and organizational skills 
  • Effective written and verbal communication skills 
  • Ability to work both independently and in a team environment 
  • Proficiency in Microsoft Office (Excel, Word, PowerPoint) 
  • Preferred:
  • Exposure to quality systems, such as Quality Management Systems (QMS), GDP, or GMP 
  • Familiarity with risk management concepts (e.g., FMEA) 
  • Knowledge of validation concepts (IQ/OQ/PQ) or test method validation 
  • Experience with data analysis or problem-solving tools (e.g., root cause analysis, 5 Whys) 
  • Previous internship, co-op, or project experience in a manufacturing or regulated environment 
  • Interest in medical device, manufacturing, or regulated industries

 Education:

  • Currently pursuing a Bachelor’s degree in Engineering (e.g., Mechanical, Biomedical, Industrial), Quality Engineering, Manufacturing Engineering, Life Sciences, or a related field
  • Junior or Senior standing preferred

Experience:

Required

  • No prior professional experience required
  • Hands-on experience through coursework, academic projects, or lab work
Key Skills
Quality EngineeringRisk ManagementProduct Development ProcessVerification And ValidationManufacturing ProcessesTest Method DevelopmentInspection PlansSampling PlansAudit PreparationSupplier QualificationRoot Cause AnalysisMicrosoft OfficeData AnalysisQuality Management SystemsFMEAGMP
Categories
EngineeringManufacturingHealthcareScience & Research