Regulatory Document Management Associate - Pharma (top dollar/contract to start)

Our client, a specialty pharmaceutical firm headquartered in the RTP area, is actively recruiting for a sharp and capable document control professional for key role supporting the Regulatory Affairs department.  The company is undergoing substantial growth.  Maintaining a high quality records management system is critical.  Seek a committed and diligent professional who enjoys and understands the value of this important work.

 

The Document Management Associate will be responsible for executing in a timely, accurate and thorough manner the operational aspects of incoming and outgoing electronic and paper documents and records.  He/She will perform records processing activities, which include filing, retrieving, archiving and imaging as well as be responsible for maintaining the security and integrity of records contained in the document control rooms.

 

The ideal candidate will be a highly competent self-starter who offers smart and reliable organizational skills, astute attention to detail and excellent judgment.  2+ years of experience in the pharmaceutical industry with focus on managing documents is required.  Knowledge of GCP, GMP and GLP documentation/records mgmt important.  The company is growing and systems that worked in the past may not work for the future.  Seek savvy operational candidate who will bring ideas and improvements to the process.  Degree preferred but quality experience more important.

 

This is a 6 month contract with potential to extend.  Company will pay excellent wage to recruit and retain top candidate.  If you are interested in discussing, please send your Word resume to leef@frankelstaffing.com . Local candidates only.