|Quality Engineer IV|
o A Bachelor’s Degree in a relevant field, typically science or engineering.
o 7 – 10 years of product development/design controls experience.
o Experience with medical device Regulation 21 CFR Part 820, Part 803 and applicable international quality standards and regulations including ISO 13485:2016, Canadian MDR, and EU Medical Device Regulation or regulations with transferrable requirements.
o Expert understanding and application of appropriate medical device regulations, requirements and standards
o Cross functional team experience
o Communication in an organized and knowledgeable manner, delivering clear requests for information, demonstrating flexibility in prioritizing and completing tasks and communicating potential conflicts to a supervisor
o Manage time working on multiple projects simultaneously
SRG is an Equal Opportunity Employer - All qualified applicants will receive consideration without regard to race, color, religion, gender, national origin, age, disability, veteran status, or any other factor determined to be unlawful under applicable law.
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