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 Process Engineer is responsible for developing, documenting, validating, maintaining and improving manufacturing processes, related to the manufacture, inspection and packaging of lathed intraocular lenses. Specific tasks to include: new technology and process improvements for existing manufacturing processes, lathe and milling competency, optics knowledge, leadership support for increasing product quality and process productivity enhancements, support for new process transfer into production and other projects which may be assigned by the Engineering Manager. Knowledge of cGMPs for medical devices a plus, strong technical writing skills.
8+ years related experience with two years of experience in medium to high volume manufacturing industry with experience in the medical device field preferred. Lathing and Milling competency experience and/or precision machining experience preferred.
Valeant is an EEO/AA employer M/F/D/V.