We are looking for detail-oriented Temporary Administrative Assistant for a Manufacturing site in Arden,NC to support a special short-term project focused on improving document management within our Quality Management System. In this role, you will assist in organizing, reviewing, and standardizing documentation to ensure full compliance with internal procedures and industry standards such as IATF 16949. This is a temporary, 3-month contract assignment off
We are looking for detail-oriented Temporary Administrative Assistant for a Manufacturing site in Arden,NC to support a special short-term project focused on improving document management within our Quality Management System. In this role, you will assist in organizing, reviewing, and standardizing documentation to ensure full compliance with internal procedures and industry standards such as IATF 16949. This is a temporary, 3-month contract assignment off
In this role, you will be responsible for preparing, splicing, routing, and assembling the critical wire lead and harness systems that power our advanced industrial sensors.You will translate technical schematics into high-quality physical assemblies. If you enjoy hands-on, meticulous work and take pride in quality craftsmanship, this is a fantastic opportunity to build a career with a global technology leader.Responsibilities:Precision Splicing & Assembly
In this role, you will be responsible for preparing, splicing, routing, and assembling the critical wire lead and harness systems that power our advanced industrial sensors.You will translate technical schematics into high-quality physical assemblies. If you enjoy hands-on, meticulous work and take pride in quality craftsmanship, this is a fantastic opportunity to build a career with a global technology leader.Responsibilities:Precision Splicing & Assembly
The Clinical Research Associate (CRA) serves as a sponsor-side clinical operations representative responsible for oversight of investigational sites and support of high-quality study execution across Phase 1 oncology trials (required) plus other therapeutic areas monitoring oversight a plus. This role combines traditional site monitoring responsibilities with broader sponsor oversight activities, including identification of operational and quality risks, c
The Clinical Research Associate (CRA) serves as a sponsor-side clinical operations representative responsible for oversight of investigational sites and support of high-quality study execution across Phase 1 oncology trials (required) plus other therapeutic areas monitoring oversight a plus. This role combines traditional site monitoring responsibilities with broader sponsor oversight activities, including identification of operational and quality risks, c
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