Valeant Pharmaceuticals International, Inc. is a diverse and decentralized 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 Associate Director, Regulatory Affairs – CMC, independently manages all aspects of regulatory CMC information for Valeant Pharmaceuticals products throughout their lifecycle. This includes Brand, Generics, OTC/Nutritionals, dietary supplements and medical devices. Responsible for the regulatory CMC strategy of all submissions and managing interactions with regulatory authorities on CMC issues.
Valeant is an EEO/AA employer M/F/D/V.
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