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Title : SAN-Documentation Specialist I-044
State : Connecticut   Date : Sep 27, 2018
Experience Level :  
Position Type : Documentation Specialist I      
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: Meriden, CT

Job Title           : Documentation Specialist I

Duration           :  6+ months (extendable) contract on W2

Duties:
Duties may include organizing and reviewing change control and other GMP documentation. May assist with the editing of quality documents (SOP's, guidelines, validation master plans, etc.) to ensure compliance with regulator requirements. Must be able to work quickly with a high degree of accuracy.   Duties will include archival and organization of GMP documents as well as review of logbooks and temperature monitoring charts to ensure adherance to SOPs and specifications. Activation of GMP documents such as batch records and SOPs will be an additional assigned task. Other documentation duties as assigned.

Skills:
Must possess sound interpersonal and information gathering skills, being able to relate well to others at all levels throughout the organization and have the ability to work in a team environment, effectively interacting with others.  Must be proficient in Microsoft Word and Excel.

Education:
Bachelor's degree in a life-sciences related field.


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Thanks & Regards,
Vicky B
Resource Specialist (Clinical)
vicky@newageclinical.com
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