We are seeking a highly motivated individual as a QA Sr. Document Control Administrator in our
Quality Assurance department. This is an excellent opportunity for someone to learn and grow in
their GMP Document Control experience. 

Description: 

Under Quality Management, the individual will be responsible to lead support efforts for
Quality master files to include: 

Administer corporate document control processes and issues 
Identify and implement document control process improvements to ensure compliance with
regulatory requirements 
Maintain the document change control process for Quality records 
Coordinates the routing, review, approval and distribution of documents 
Edits documents to ensure standard formats are used 
Maintains master history files in record room 
Maintain Master Equipment database and physical files 
Maintain Contract Manufacturing Master Records and physical files 
Maintain Contract Cell Processing Center Matrixes 
Coordinate and conduct training of department processes and electronic document management
systems 
Coordinate period review of controlled documents 
Assist with research and retrieval of controlled documents