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Title : SA-Validation Specialist II-242
State : Pennsylvania   Date : Jan 11, 2019
Experience Level :  
Position Type : Validation Specialist II      
Description
This position is for a leading pharmaceutical company. Below are the details of the engagement. If you are available and interested please send me your updated word resume & your expected hourly rate on W2 ASAP.
Looking forward to hearing from you soon.

Work Location:  Swiftwater, PA


Job Title:  Validation Specialist II


Duration:  12+ months (extendable) contract on W2



Position Summary:


Responsible for development and execution of improvement projects for Biologics Manufacturing. Responsibilities include determining project scope, use of lean/FMEA/statistical and other methods to perform preliminary options analysis, change control development and execution, commissioning and qualification documentation development and execution, validation documentation development and execution, project tracking and completion activities. Experience: 3 to 6 years. Skills: Ability to interact with end users to gather business requirements and information to be translated into project requirements and deliverables. Ability to interface between operations and support functions, and is expected to work effectively with partner functions such as Quality and Manufacturing Technology. Must possess strong analytical and communication skills. Experience writing and reviewing documents following Good Documentation Practices. Experience working in a cGMP environment required; biologics or pharmaceuticals preferred. Must be proficient in use of Microsoft Outlook, Word, and Excel; experience with Microsoft Project, Trackwise, and statistical analysis software (SAS, jmp) preferred.


Qualifications :

Bachelor's Degree in Science, Engineering, or another technical field.



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Many Thanks,   

Sree Kanth
Associate Recruitment Manager
Sree@newageclinical.com

NewAgeSys, Inc.
Direct: 609-945-1736 Fax: 609-228-4079
600 Alexander Rd, Suite 3-3 
Princeton , NJ 08540 
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