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 the Bridgewater, NJ External Manufacturing.
The position has no supervisory responsibilities.
The position will include routine interaction and communication with internal business stakeholders (Quality, Compliance, Supply Chain, R&D, Regulatory and Commercial) and external business partners (External Manufacturing groups).
The Senior External Manufacturing Quality Specialist will support compliant execution of quality-related activities, including but not limited to, new quality system/methodologies implementation, training, CAPA, change management, problem solving, product and process development, acceptance activities.
This position will also work directly with Valeant Finished Good (FG)/External Manufacturing (EM) suppliers, as well as medical device/Pharmaceutical product manufacturing facilities, to provide sustaining quality and compliance leadership and routine support related to current commercialized products
In addition the position is responsible for developing Product Annual Reports and measure, and report key quality metrics to drive quality and efficiency.
Internal Customers/Business Partners:
External Customers and Business Partners:
Valeant is an EEO/AA employer M/F/D/V.
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.