Quality Intern
Scientia Vascular
Date: 1 week ago
City: West Valley City, UT
Contract type: Intern
About Scientia Vascular
Our mission is to save lives. Scientia Vascular is a leading innovator and manufacturer of endovascular medical devices. We use micromachining and microfabrication processes to manufacture products that provide physicians with enhanced performance for optimal outcomes for their patients.
Position Summary
Contributes to new product development by supporting Quality initiatives. The primary purpose of the role is to assist the R&D Quality Engineering group with daily responsibilities and improvement projects related to Product Development, Test Method Development, Design Controls, and Risk Assessment.
Primary Responsibilities
The Scientia Vascular culture is centered on the principals of equal opportunity for all employees. Consistent with our culture, all qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, family status, marital status, sexual orientation, national origin, genetics, disability, age, or veteran status, or any other non-merit based or legally protected grounds.
Visit our website and learn more about us at www.scientiavascular.com
Our mission is to save lives. Scientia Vascular is a leading innovator and manufacturer of endovascular medical devices. We use micromachining and microfabrication processes to manufacture products that provide physicians with enhanced performance for optimal outcomes for their patients.
Position Summary
Contributes to new product development by supporting Quality initiatives. The primary purpose of the role is to assist the R&D Quality Engineering group with daily responsibilities and improvement projects related to Product Development, Test Method Development, Design Controls, and Risk Assessment.
Primary Responsibilities
- Data checks
- Training checks on protocols and testing execution
- DV builds mock auditing /document reviews
- Risk assessment support
- Tooling qualification
- Preliminary protocol and data review for consistency
- Execution and evaluation of newly developed and revised test methods
- Ability to solve problems and work with minimal supervision
- Perform job functions in accordance with applicable GMP (Good Manufacturing Practices) and ISO guidelines
- Comply with applicable FDA and international regulatory laws/standards
- Other duties as assigned with or without accommodation
- High School diploma/GED
- Enrolled in a college level engineering or microbiology program
- Demonstrated interest in Medical Device Development, Quality Systems, Inspection, or Quality Engineering
- Computer skills including understanding of Microsoft Excel and Word
- Excellent verbal and written communication skills
The Scientia Vascular culture is centered on the principals of equal opportunity for all employees. Consistent with our culture, all qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, family status, marital status, sexual orientation, national origin, genetics, disability, age, or veteran status, or any other non-merit based or legally protected grounds.
Visit our website and learn more about us at www.scientiavascular.com
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