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.
This position will provide quality and technical guidance for pharmaceutical and medical device products undergoing tech transfer from site to site, and/or participate in significant investigations where product non-conformances are complex. Direct modern documentation packages for new validations and control and specification limits that are representative of shelf-life limiting measures and critical-to-quality attributes. Apply statistical process control and lean six-sigma practices to validation strategies and product knowledge
Valeant is an EEO/AA employer M/F/D/V.
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