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 incumbent will be responsible for the leadership and management of the implementation of Materiovigilance activities associated with EU- Medical Device Regulations (EU-MDR) across the Valeant company. As such, the incumbent will be a key contributor the EU-MDR project management team. The incumbent will lead the implementation of process improvements regarding complaint handling, medical device reporting and global complaint handling strategies.
This position will supervise direct reports.
Internal customers/business partners:
External customers/business partners:
Valeant is an EEO/AA employer M/F/D/V.
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