Posted in General Business 30+ days ago.
Type: Full-Time
Diagnostica Stago, Inc., (DSI) is an industry leader in the science of hemostasis and thrombosis. Stago provides the total commitment of global resources and responsiveness, coupled with cutting edge technology and reliability. DSI is dedicated to continually developing and providing the very best hemostasis products, technical support, and services.
Summary: Manages all regulatory and quality assurance systems within the DSRV manufacturing division to meet the regulatory and quality requirements as defined in the company quality manual, ISO 9001, ISO 13485, 21 CFR 829, 21 CFR 600 series, European Medical Devices Regulations, and other regulatory standards, as applicable.
Job Duties: • Acts as the designated management representative. Skills: Education & Requirements: • Associates Degree required; Bachelor's degree from a four-year college or university preferred and three to four years related experience and/or training in a medical device manufacturing environment required. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, citizenship, disability or protected veteran status.
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Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities. |
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