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.
The Quality Assurance Specialist I/II provides Quality support for site activities involving pharmaceutical product development. The role ensures that quality systems and projects are managed in compliance with cGMP standards and applicable FDA regulations, as well as company policies and procedures.
Valeant is an EEO/AA employer M/F/D/V.
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To learn more please read Valeant’s Job Offer Fraud Statement.