PDQA Manager

Organization
Actavis, Inc.
Job Location
Sunrise, FL
Job Description

Responsible and knowledgeable in:
Labeling revising and ordering and liaison with Regulatory Affairs
Product drug listing
Customer correspondence
Maintenance of chronological labeling files
Overseeing the reporting activities for Controlled Substances
Initiating of Packaging protocols (process and cleaning) inclusive of the end reports
Maintain yearly requirements; maintaining of stability requirements
Updating and maintaining CGMP and staff training requirementa
Approving and overseeing revisions to master worksheets
Managing of chronological file for submissions to Regulatory Affairs
SAP Q.A. releasing functions and Coordinate the activities of the Q.A. Supervisors (1) and Q.A. Auditors (6)
Assisting in revisions to SOPs
Perform site audit
Deputy for Q.A. Director.

Requirements:
Qualifications:
BA/BS Degree. (Master preferred). Minimum of 6 years related Supervisory/managerial
experience. Excellent written and oral command of English. Strong interpersonal and communication skills mandatory. Computer literate.Reports to: Director of QA

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