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 Sr. Validation Engineer-Process Validation will be subject matter expert and provide leadership in validation of products and components at the Greenville site.
In addition, the Sr. Validation Engineer-Process Validation will lead the Media Fill program (execution schedule and investigations).
The Sr. Validation Engineer-Process Validation shall be able to manage consultants and mentor validation engineers and validation technicians.
The Sr. Validation Engineer-Process Validation will serve as a backup of the Validation Supervisor, mentoring co-workers, approving protocols, and managing consultants among others
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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.