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Senior Quality Analyst, DEA - Cranbury NJ

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Taro in USA
 
Senior Quality Analyst, DEA
 
Job Overview
 
Monitor use of DEA 222 order forms and electronic forms (CSOS) for compliance with DEA requirements; assist with development & revision of procedures to ensure accurate documentation, traceability, & accountability relating to controlled dangerous substances to minimize risk of diversion; provide support with DEA audits internally and externally to ensure that procedures are followed & documented, required reports are filed, and inventories are reconciled. As a site SME, oversee and monitor open non-conformances to ensure all activities are completed in a timely manner.
 
Requirements:
 
Associate’s degree in Chemistry, Microbiology, Biology, or Pharmacy or foreign educational equivalent and 8 years of quality compliance/assurance experience in the pharmaceutical industry with knowledge of regulations for DEA, GMP, ICH and FDA guidelines. Must be willing to work extended hours to resolve urgent issues, as required.
 
PLEASE NOTE: ALL JOB OPPORTUNITIES ARE ELIGIBLE FOR INCENTIVES OFFERED UNDER THE EMPLOYEE REFERRAL PROGRAM
 
Submit Resumes Via Email Only to: Susanne.Foulds@Taro.com. Please include salary requirements. Taro Pharmaceuticals U.S.A., Inc., 3 Skyline Drive, Hawthorne, NY 10532.