As a Validation Intern, you will gain hands-on experience in the lifecycle of product design transfer, from test protocol generation to final reporting
Job Summary
As a Validation Intern, you will gain hands-on experience in the lifecycle of product design transfer, from test protocol generation to final reporting.
You will support the engineering team in ensuring that our Medical Device OmniPod products meet strict regulatory requirements and performance specifications.
We are looking for highly motivated, performance-driven individuals to be a part of our expanding team guided by shared values who exceed customer expectations.
Matching Summary
As a Validation Intern, you will gain hands-on experience in the lifecycle of product design transfer, from test protocol generation to final reporting.
Skills & Requirements
Must-have
validation life cycle documentation
test protocol generation and execution
data analysis and root cause analysis
compliance with cGMP and ISO standards
collaboration with cross-functional teams
test automation tool development
Nice-to-have
proficiency in Microsoft Office Suite
scripting languages such as Python or SQL
familiarity with lab equipment and manufacturing systems
understanding of medical device regulations
strong attention to detail
excellent communication skills
Key Requirements
currently pursuing relevant Bachelor’s degree
basic understanding of validation methodologies
knowledge of medical device quality principles
familiarity with cGMP, GAMP 5, 21 CFR Part 11, or ICH guidelines