Associate Director of Quality Systems, Pharmaceutical Manufacturing
NE

Associate Director of Quality Systems

Industry leading, global pharmaceutical company seeks an Associate Director of Quality Systems to ensure site-wide quality systems compliance at the company's flagship manufacturing site near Omaha, NE. The Associate Director of Quality Systems will lead the development, implementation, and on-going review of quality systems to maintain compliance with company guidelines and regulatory agency requirements. Additional duties will include:

Daily leadership of quality systems team
Oversight of computer systems quality activities including review and approval of computer systems validation plans and reports
Leadership responsibilities for the development and maintenance of site's annual quality plan, change control committee and change control process
Maintain and support supplier quality program as well as supplier compliance
Ensure and maintain site-wide validation master plan
Lead site-wide implementation of document management system

Job Requirements

Bachelor's degree in a technical discipline; chemistry, pharmaceutical science, microbiology or other applicable discipline; advanced degree a plus
7+ years experience in pharmaceutical quality in a manufacturing environment
5+ years management experience in pharmaceutical quality
Demonstrated career growth in pharmaceutical quality with an emphasis in developing and maintaining quality systems
Excellent, documented leadership skills with experience developing subordinates

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