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 Surgical Regulatory Affairs Director is responsible for regulatory development of surgical devices. The Director Regulatory Affairs will provide leadership and expertise to develop and execute regulatory submission strategies and policies for the product portfolio for the US
Responsibilities may include but are not limited to:
Oversee the development of product regulatory strategies
Develop appropriate SOPs, processes and procedures to ensure compliance with regulations
Provides directional guidance to the business on how to prepare products for approval
Review and provide input on departmental policies and procedures
Oversee the preparation of U.S. submissions
Ability to read, analyze and interpret associated regulations
Supervise direct reports: Yes
Scope of Position: Support all North America – Surgical sites.
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