Amazing Medical Device Company URGENTLY looking to add a ENGINEERING DOC CONTROL SPECILAIST to join the team ASAP!!!
40 hours a week, Hybrid role with ONSITE 3 days a week!!!
MUST HAVE:
NICE TO HAVE
Description:
Develop and update process documentation including assembly procedures, test procedures, routers, travelers, BOMs, process flows, and process FMEAs. Assist engineering team to qualify develop Design Verification and Validation documentation (protocols).
o TrueVault (Veeva) would be the system used more.
o Trackwise (heavy change controls come from here – drug group)
o Work with drawings and specs
Top Skills Details:
Document control
Experience Level:
Intermediate Level
Actalent connects passion with purpose. Our scalable talent solutions and services capabilities drive value and results and provide the expertise to help our customers achieve more. Every day, our experts around the globe are making an impact. We’re supporting critical initiatives in engineering and sciences that advance how companies serve the world. Actalent promotes consultant care and engagement through experiences that enable continuous development. Our people are the difference. Actalent is an operating company of Allegis Group, the global leader in talent solutions.
The company is an equal opportunity employer and will consider all applications without regards to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
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