I have a position available as a Web Application Developer. It is a full time position located in Brewster, NY.
Position Overview
As a member of the Application Development and Support team, the person will be responsible for the development and support of web based and mobile applications. The role requires interaction and coordination with teams in different time zones. The individual needs to be self-motivated, flexible, and independent.
The individual would also play a critical role in ...
Responsibilities
* Organize and manage teams of engineering personnel for the purpose of verifying and validating product designs according to FDA requirements and internal quality standards to meet project delivery commitments.
* Accountable for ensuring execution against project schedules and Testing and Validation (T&V) standards/processes
* Manage automated tools to support product development documentation and engineering process improvement
* ...
Job Ref: #1610
Location: Danbury CT
Relocation: No
Salary: High Salary
Summary: We need someone from a medical device, medical equipment, avionics, robotics type background. Electric vehicle could be a fit for example. It needs to be electro mechanical type hard equipment. Need a strong test and validation person with project management and medical equipment or something else that is highly complex.
Duties and Responsibilities:
1. ...
MICROBIOLOGIST - MUST HAVE ATLEAST 1 YR MICRO LAB EXPERIENCE (ORANGEBURG AREA, NEW YORK)
Microbiologist I
ORANGEBURG AREA, NEW YORK (ROCKLAND COUNTY)
Description: Responsible for the accurate analysis of incoming raw materials, bulk liquids and finished products utilizing Standard Operating Procedures (SOPs), Work Instructions (WIs) and Good Laboratory Practices (GLPs) and Good Manufacturing Practices (GMPs). Assures released raw materials, bulk liquids and finished products have met the required ...
Summary of Duties and Responsibilities
* Organize and manage teams of engineering personnel for the purpose of verifying and validating product designs according to FDA requirements and internal quality standards to meet project delivery commitments.
* Accountable for ensuring execution against project schedules and Testing and Validation (T&V) standards/processes
* Manage automated tools to support product development documentation and engineering process improvement
...
Responsible for the accurate analysis of incoming raw materials, bulk liquids and finished products utilizing Standard Operating Procedures (SOPs), Work Instructions (WIs), and Good Laboratory Practices (GLPs) and Good Manufacturing Practices (GMPs). Assures released raw materials, bulk liquids and finished products have met the required specification criteria prior to release. Investigate failures to determine final disposition. Maintain accurate, complete and traceable documentation related to ...
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