Documentation Coordinator

Descripción del Empleo:
The purpose of this position is to perform the coordination activities to ensure manufacturing documentation integrity and compliance with the cGMP. This position must comply with all Security guidelines, Environmental Health and Safety regulations and the current Good Manufacturing Practices required by the job function.1. Generates commercial and experimental Batch Records for Production.-makes copy from Bath Record Master File
-prints all applicable documentation from Documentation Control A (DCA) and SAP systems.-prints label (lot number, product code and name and adds lot additional information.-assigns seals to be placed on the final product drums (Compression, Coating and Printing) -compares all batch records documentation versus production orders and BOM/BOS to assure the documentation corresponds to the product lot. - verifies that batch records.
Requisitos:
Bachelor Degree • One (1) year of experience in manufacturing documentation or Quality Control administration in a Pharmaceutical industry• Computer knowledge is required (Word, Excel, PowerPoint, Internet)• Excellent communication verbal and written skills (English/Spanish).• Excellent analytical skills with details • Good mathematical skills
• Team Player and ability to work with people at different levels.• Typing and Filing skills• Excellent organization skills
• Self-starter and motivator.• Able to work with minimum supervision, a must.• Good proof-reading skills.
• Good knowledge of office machines, such as fax, copiers, etc.