Associate Director of Quality Assurance, Pharmaceutical Manufacturing
NE

Global leader in the development and production of life saving pharmaceuticals seeks an Associate Director of Quality Assurance to oversee QA activities within the manufacturing operations group at the company's flagship manufacturing site near Omaha, Nebraska. The Associate Director will:

Lead development, maintenance and ongoing review of quality systems within manufacturing operations plant wide
Lead a large QA team, providing daily leadership and strategic direction on the manufacturing floor.
Oversee quality investigations, deviations, and complaints, both plant wide as well as 3rd party
Develop and implement resolution plans for corrective action
Monitor and ensure third party compliance
Oversee plant quality groups to ensure site wide compliance
Perform applicable audits at supplier and 3rd party sites
Manage 3rd party documentation

Job Requirements

Bachelor's degree in a scientific discipline; chemistry, pharmaceutical science, microbiology or related discipline; advanced degree a plus
7+ years of quality assurance experience in a pharmaceutical manufacturing environment
5+ years of quality leadership experience
Progressive career growth showing documented success in pharmaceutical quality
Strong working experience with SAP, LIMS
Extensive audit, CAPA, complaints resolution experience
Strong leadership, mentoring and communications skills
The ability to decisively lead in a fast paced, highly charged pharmaceutical manufacturing environment

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