We are hiring a finishing operator for a client in Morrisville. Wonderful work environment and ability to sit or stand at station. Attention to detail and fine detailing work critical.Responsibilities:- Fine detailing work- sanding- drilling- minor computer keyboardingWorking hours: 4:00 AM - 1:00 PMSkills:- Team work attitudeEducation:High SchoolExperience:1-4 yearsQualifications:- Fine detailing work experience- Manual dexterity and fine motor skills A
We are hiring a finishing operator for a client in Morrisville. Wonderful work environment and ability to sit or stand at station. Attention to detail and fine detailing work critical.Responsibilities:- Fine detailing work- sanding- drilling- minor computer keyboardingWorking hours: 4:00 AM - 1:00 PMSkills:- Team work attitudeEducation:High SchoolExperience:1-4 yearsQualifications:- Fine detailing work experience- Manual dexterity and fine motor skills A
The CNC Operator is responsible for setting up, programming, and operating woodworking CNC machines (currently Biesse) to fabricate and modify plywood components with a high degree ofaccuracy. This role plays a critical part in maintaining product quality through precise machining and inspection processes.Responsibilities:* Read and interpret engineering drawings, blueprints, charts, and work orders to determine machining operations and optimal sequencing
The CNC Operator is responsible for setting up, programming, and operating woodworking CNC machines (currently Biesse) to fabricate and modify plywood components with a high degree ofaccuracy. This role plays a critical part in maintaining product quality through precise machining and inspection processes.Responsibilities:* Read and interpret engineering drawings, blueprints, charts, and work orders to determine machining operations and optimal sequencing
The Contract Clinical Study Manager provides operational leadership, coordination, and oversight for assigned clinical studies. This role supports the successful execution of study activities in accordance with ICH/GCP guidelines, applicable regulatory requirements, company SOPs, study protocols, and study-specific plans. The Contract Clinical Study Manager works closely with internal cross-functional teams, CROs, vendors, investigators, and study site per
The Contract Clinical Study Manager provides operational leadership, coordination, and oversight for assigned clinical studies. This role supports the successful execution of study activities in accordance with ICH/GCP guidelines, applicable regulatory requirements, company SOPs, study protocols, and study-specific plans. The Contract Clinical Study Manager works closely with internal cross-functional teams, CROs, vendors, investigators, and study site per
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
Position OverviewOur client is seeking a reliable and motivated Material Handler (Forklift Certified) to join their operations team. This is a full-time, temp-to-hire position where you can showcase your skills and potentially secure a long-term role with an industry leader. The primary function of this role is to operate a forklift, pull and stage orders, and load and unload trucks.- Schedule: Full-time, Monday through Friday, 7:30 AM to 4:30 PM.- Lunch B
Position OverviewOur client is seeking a reliable and motivated Material Handler (Forklift Certified) to join their operations team. This is a full-time, temp-to-hire position where you can showcase your skills and potentially secure a long-term role with an industry leader. The primary function of this role is to operate a forklift, pull and stage orders, and load and unload trucks.- Schedule: Full-time, Monday through Friday, 7:30 AM to 4:30 PM.- Lunch B
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