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Documentation Specialist-cGMP

New Brunswick, NJ · Biotech/Pharmaceutical

ProStaff Solutions is looking for Documentation Specialist-cGMP to work with a pharmaceutical company in New Brunswick, NJ.

Contract to Hire  $20-$25 hourly DOE

Provide administrative support within Office of Data Reliability (ODR).  To assist in the finalization of ODR audits to include worksheet finalization and other audit documentation.
•             To assist in documentation and provide support to ODR audits.
•             To assist in follow ups on audit closures across the departments.
•             To maintain the documentation with the department which is traceable for future reference and review.
•             Assist in CDRO Board Meeting and inter/intra department presentations.
•          
•             Order and maintain office goods for ODR.
•             Retrieve and archive various forms of documentation.
•             Adhere to the Environmental, Health and Safety programs and associated programs.
•            

Qualifications:
 Associates or Bachelor's degree

RECENT Graduates preferred

Skills:
Must have hands on experience in using Microsoft Excel, Word, PowerPoint and Project.
Experience in Microsoft Visio is preferred.



Physical Requirements:
Must be able to move documentation binders and files (up to 20 lbs.) to storage racks by lifting them manually and organizing. 




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