Engineering Intern
CardioQuip
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- Location
- College Station, TX
- Job type
- Internship
- Posted
- Nov 6
- 2 days ago
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About the company
CardioQuip
Medical devices · 11 to 50 employees
What you'll do
- Assist engineering in the design and development of product(s)
- Assist the engineering team in the design, development, and management of our Design and Development process
- Assist in the transfer of CardioQuip products and prototypes to manufacturing
- Ensure that our current and future processes are compliant and conform to 21 CFR 820 and ISO 13485:2016
- Prepare and conduct design reviews
- Become familiar with Regulatory and FDA submission paperwork in support of product development
What you need
- Pursuing a Bachelor’s degree or graduate degree in a relevant engineering field
- Within two years of graduating with a Bachelor's degree or graduate degree in a relevant engineering field
- Completed at least 2 semesters in relevant engineering courses
- Semester interns must commit at least 20 hrs/week
- Summer interns must commit 40 hrs/week
Key skills
design and development21 CFR 820ISO 13485:2016design reviews
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Read the full posting here
Engineering Intern Con sidering y our op tions f or inte rnships? W hy n ot j oin a pr ogram w here y ou c an g ain va luable exp erience a nd m ake mea ningful cont ributions? B ased in Co llege St ation, Te xas, Card ioQuip’s Eng ineering In tern w ill col laborate w ith o ur pr oduct dev elopment a nd qu ality eng ineering te ams, a nd as sist in t he re search a nd dev elopment of b oth n ew a nd ex isting pro ducts. In add ition, u nder t he sup ervision of an R &D Eng ineer, in terns w ill a lso con tribute in t he de sign, deve lopment, a nd man agement of o ur de sign a nd dev elopment pr ocess, w hich w ill in clude dev eloping quali ty-assurance a nd de sign pri nciples t hat a re com pliant a nd co nform to 21 C FR 820, MD D/MDR, a nd I SO 13485:2016. Responsibilities U nder dir ection, Eng ineering In terns sh all: Assist engineering in the design and development of product(s) Assist the engineering team in the design, development, and management of our Design and Development process Assist in the transfer of CardioQuip products and prototypes to manufacturing Ensure that our current and future processes are compliant and conform to 21 CFR 820 and ISO 13485:2016 Prepare and conduct design reviews Become familiar with Regulatory and FDA submission paperwork in support of product development Other duties and responsibilities as assigned Requirements and Qualifications Applicant is pursuing a Bachelor’s degree or graduate degree in relevant engineering field, OR applicant is within two years of graduating with a Bachelor's degree or graduate degree in a relevant engineering field Minimum GPA Requirement: 3.25/4.0 Applicant has completed at least 2 semesters in relevant engineering courses Semester interns must commit at least 20 hrs/week, summer interns must commit 40 hrs/week Spring Interns: full and part-time R&D and Quality Engineering positions available from January to May. Apply between July 2nd and November 1st. Summer Interns: full-time R&D and Quality Engineering positions available from May to August. Apply between November 2nd and March 1st. Fall Interns: full and part-time R&D and Quality Engineering positions available from August to December. Apply between February 2nd and June 1st.