Quality Engineer Intern
Tomz Inc, Berlin, CT, United States
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:
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
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
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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:
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
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
#J-18808-Ljbffr