DETAILS:
- Position: Driver Helper
- Job Group: Helper
- Location: Colgate, WI 53017 – Colgate (Driver Helpers)
JOB DESCRIPTION:
UPS is hiring individuals to work as
temporary, seasonal Driver Helpers. This is a physical, fast-paced, outdoor position that involves continual lifting, lowering and carrying packages that typically weigh 25 – 35 lbs. and may weigh up to 70 lbs. It requires excellent customer contact skills and a lot of walking.
As a Driver Helper you will not drive the delivery vehicle but assist the driver in the delivery of packages.
Driver Helpers usually meet the UPS driver at a mutually agreed upon time and location each weekday (Monday through Friday) and typically do not work on weekends or selected holidays. Hours vary but usually begin after 8:00 a.m. and end before 8:00 p.m. Driver Helpers must comply with UPS appearance guidelines.
Driver Helper seasonal opportunities are typically between the Thanksgiving and Christmas holiday time period.
Job ID: WIGTE4
APPLY TO THIS POSITION
Date: Oct 17, 2011
Location: Waukesha, WI, United States
| Job Number: |
1451984 |
| Business |
GE Healthcare |
| Business Segment: |
Healthcare |
| Posted Position Title: |
Clinical Research Associate |
| Career Level: |
Experienced |
| Function |
Quality |
| Function Segment: |
Medical & Clinical Affairs |
| Location: |
United States |
| U.S. State, China or Canada Provinces: |
Wisconsin |
| City: |
Waukesha |
| Postal Code: |
53188-1696 |
| Relocation Assistance |
No |
| Role Summary/Purpose: |
The Clinical Research Associate (CRA) supports the Business Research Managers (RMs) through monitoring and coordinating of clinical research studies to ensure research is compliant with Good Clinical Practices and other applicable regulations and company procedures. |
| Essential Responsibilities |
Primary responsibilities include:
• Supports RMs in performing initial contact and participates in the assessment and selection of qualified investigators for inclusion in research.
• Supports RMs in completing Pre-Selection, Initiation, Monitoring, and Closeout site visits, or coordinate contractors in their performance of these activities as needed. Tracks required documentation from study site.
• Reviews and approves study documentation such as protocols, informed consents, amendments, case report forms, and study reports.
• Supports RMs with initiation of research and site training.
• Ensures compliant recording and reporting of any adverse events occurring during research.
• Interfaces with Regulatory Agencies as required.
• Ensures overall regulatory compliance of investigational sites with applicable regulations.
• Reviews clinical history file for completeness throughout research process.
• Assists with the coordination and conducting of the Research Review meetings.Quality Specific Goals:
1. Aware of and comply with Good Clinical Practice guidelines, the GEHC Quality Manual, Quality Management System, Quality Management Policy, Quality Goals, and applicable laws and regulations as they apply to this job type/position
2. Complete all planned Quality & Compliance training within the defined deadlines
3. Identify and report any quality or compliance concerns and take immediate corrective action as required
4. Ensure Research is executed in compliance with Good Clinical Practices and other applicable regulations and company procedures.
5. Assist with continuous improvement activities by driving the implementation of process improvement initiatives |
| Qualifications/Requirements: |
• Bachelor’s degree (or internationally recognized equivalent) in a science related field or R.N. with a minimum of 5 years experience with clinical applications, research management or regulatory affairs within the pharmaceutical or medical device industry OR minimum of 9 years progressive experience with clinical applications, research management or regulatory affairs within the pharmaceutical or medical device industry.
• Strong experience of all aspects of the clinical research process, including site selection, investigator qualifications, monitoring, protocol and report writing.
• Excellent verbal and written communication and presentation skills with the ability to communicate business issues in English in an easy to understand manner
• Strong problem solving, influencing and negotiation skills; diplomatic team player
• Ability to travel up to 20% of time for responsibilities focused on research management and up to 75% for responsibilities focused on research site monitoring. |
| Additional Eligibility Qualifications |
GE will only employ those who are legally authorized to work in the United States for this opening. Any offer of employment is conditioned upon the successful completion of a background investigation and drug screen. |
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Nearest Major Market: Waukesha
Nearest Secondary Market: Milwaukee
Job Segments: Business Process, Clinic, Clinical Research, Compliance, Engineering, Healthcare, Law, Legal, Management, Medical Device, Medical Research, Pharmaceutical, Quality, Quality Manager, Regulatory Affairs, Research, Research Associate, Science, Scientific
Apply Now
Date: Oct 15, 2011
Location: Waukesha, WI, United States
|
| Job Number: |
1448918 |
| Business |
GE Healthcare |
| Business Segment: |
Healthcare |
| About Us: |
GE Healthcare provides transformational medical technologies that are helping a new age of patient care. GE Healthcare’s expertise in medical imaging and information technologies, medical diagnostics, patient monitoring and life support systems, disease research, drug discovery, and biopharmaceutical manufacturing technologies is helping physicians detect disease earlier and to tailor personalized treatments for patients.GE Healthcare offers a broad range of products and services that are improving productivity in health and enhancing patient care by enabling healthcare providers to better diagnose and treat cancer, heart disease, neurological diseases, and other conditions. Headquartered in the United Kingdom, GE Healthcare is a $15 billion unit of General Electric Company (NYSE: GE). Worldwide, GE Healthcare employs more than 43,000 people committed to serving healthcare professionals and their patients in more than 100 countries.
GE is an equal opportunity employer. |
| Posted Position Title: |
Materials Specialist I-HC |
| Career Level: |
Experienced |
| Function |
Manufacturing |
| Function Segment: |
Materials |
| Location: |
United States |
| U.S. State, China or Canada Provinces: |
Wisconsin |
| City: |
Waukesha |
| Postal Code: |
53188-1677 |
| Relocation Assistance |
Yes |
| Role Summary/Purpose: |
Ensure an uninterrupted supply of materials to support production and sales. Work to resolve Materials issues while achieving and maintaining inventory business metrics. |
| Essential Responsibilities |
•Overall ownership of material ordering and availability
•Oracle, Xelus and Digital Cockpit expert
•Expedite part shortages
•Daily Shortage root cause investigation and resolution
•Communication with suppliers – packaging, min/max planning. PCNs, as they relate to old/existing parts
•Support material aspects of transfers, which includes Integrated Supplier Program
•Field Modification Instruction, as appropriate – ordering material, formulating schedules
•Supplier visits, as needed – internal and external
•Manage Phase In / Phase Out (NPI) to minimize obsolete material |
| Qualifications/Requirements: |
•Bachelors degree or HS diploma and 5 years experience in materials or production scheduling
•Computer proficiency
•Excellent Interpersonal Skills |
| Additional Eligibility Qualifications |
GE will only employ those who are legally authorized to work in the United States for this opening. Any offer of employment is conditioned upon the successful completion of a background investigation and drug screen. |
| Desired Characteristics |
•APICS Certification
•Oracle knowledge and experience |
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Nearest Major Market: Waukesha
Nearest Secondary Market: Milwaukee
Job Segments: Database, Healthcare, Neurology, Operations, Oracle, Patient Care, Research, Supply, Technology
Apply now
Schneider National Inc., a Green Bay trucking company, is adding 500 driving jobs as it extends its operations to the country’s booming oil-shale sector. Schneider said it is offering new service to companies in the hydraulic fracturing, or “fracking,” industry.
According to its website “Our Oil Field Services division is literally booming with full-time, permanent truck driving opportunities for both experienced truck drivers and recent truck driving school graduates (based on location).”
“We can’t always bring the driving job to you, but we can bring you to the job. If you’re a qualified truck driver who is interested in any of our Oil Field driving opportunities, but do not live in close proximity to the work area, we may be able to help. Relocation assistance options, including up to $2,500, may be available in your area. Additional opportunities as a tanker driver may also be available to qualified truck drivers holding HazMat and Tanker endorsements.”
ABOUT SCHNEIDER NATIONAL
“Schneider National was founded in 1935 and currently operates 14,000 tractors, 40,000 trailers, and has partnerships with over 6,000 carriers. Schneider drives more than five million loaded miles per day. We are utilized by two-thirds of the Fortune 500 companies. Schneider operates out of 36 locations in North America.”
