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 scope of this position is directly related to global complaint management and adverse event reporting responsibilities for all company medical device products as assigned.
The position will include interaction and communication with doctors and patients as well as internal business stakeholders.
Primary responsibility is to support the global reporting obligations and the management of communication between manufacturer, distributors and competent authorities for all medical device complaint related activities, including assistance of and/or submission of medical device event reports in accordance with applicable local laws and regulations.
-Research and Development
-Design Quality Assurance
-External Manufacturing Quality Assurance.
-Manufacturing Site Quality Assurance
-Physicians (including physician’s staff)
-Audit/Inspection Organizations (FDA, Notified Bodies, International Regulatory Agencies)
Valeant Pharmaceuticals International, Inc. is committed to leveraging the talent of a diverse workforce to create great opportunities for our business and our people. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status.
Job Applicants should be aware of job offer scams perpetrated through the use of the Internet and social media platforms.
To learn more please read Valeant’s Job Offer Fraud Statement.