Valeant Pharmaceuticals International, Inc. is a diverse pharmaceutical company that is committed to focusing on our key stakeholders while delivering consistently high performance. Our values provide the overall direction for our company, and provide us with the tools necessary to rise to any challenge by leveraging our collective hard work and effort along with our unwavering competitive spirit. These values help us set goals based on our organization’s potential and what we hope it will become.
Supervises the MQA batch record audit team and batch release process; SME for QA systems. Provides training, direction, evaluation of personnel and addresses personnel issues on a timely manner. Provide technical oversight for QA systems and programs including troubleshooting and providing expert advice on system functionality to regional sites. Design and implement other quality processes as projects are assigned. Assist with other quality functions as needed. Provide support and guidance to Manufacturing departments in aspects related to and aseptic processing and quality control.
Leads performance of the team and objectives. Keys to success include proper management of product quality and compliance of employees / equipment to established quality standards, promotion of a safe and positive work environment, successful management and development of direct reports and achieving results through cross-functional relationships (i.e., Engineering, Quality, Equipment and Materials). Generate process improvements through innovative ideas and execution while meeting daily production / operational demands.
Valeant is an EEO/AA employer M/F/D/V.
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