Valeant Pharmaceuticals

Job Listings


Here are our current job openings. Please view the details for more information, and apply from that page if you are interested.

Valeant Pharmaceuticals is an equal opportunity employer and supports workforce diversity.

Use this form to do another job search

The system cannot access your location for 1 of 2 reasons:
  1. Permission to access your location has been denied. Please reload the page and allow the browser to access your location information.
  2. Your location information has yet to be received. Please wait a moment then hit [Search] again.
Click column header to sort

Search Results

US-SC-Greenville
Effectively and efficiently set-up, troubleshoot and operate packaging lines and equipment in order to manufacture quality products per Standard Operating Procedures (SOP) and Good Manufacturing Practices (GMP)
Job ID
9766
US-SC-Greenville
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
Job ID
9763
US-SC-Greenville
The Operations Training Specialist is responsible for executing the Greenville Packaging and Accessories departments training schedule, will deliver various training programs to a wide associate base which includes Packaging/Accessory department employees and temporary employee on-boarding, will maintain associate training records within the current LMS system to ensure accurate reporting and metrics. Partner with the Training department to design and develop Packaging department training courses.
Job ID
9761
US-NJ-Bridgewater
The Accounts Payable Analyst is accountable for processing check payments, wires and ACH payments.  
Job ID
9760
US-VA-Lynchburg
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.   Provide IT support for day-to-day operations at Bausch + Lomb’s Global Distribution Center located in Lynchburg, Virginia. This position interacts with senior IT and business management on priority and direction setting, progress reporting, and issue resolution.     This position reports directly to the IT Manager, North America Distribution.    This position has no direct reports.  
Job ID
9759
US-NY-Rochester
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 Senior Quality Assurance Specialist provides support for multi-disciplinary teams engaged in new product development for Pharmaceuticals.  The role ensures that quality systems and projects are managed in compliance with global GMP standards, ISO and FDA regulations, and Valeant policies and procedures.
Job ID
9756
US-FL-Tampa
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.   Responsible to source, procure and inventory plan for direct materials and/or indirect materials and services necessary for the production of products in accordance with company policy, specifications and cGMP's. Manage supplier relationships to drive improvements in quality, total cost of acquisition and support new product development. Must be versed in subject matter for given commodities and/or services.
Job ID
9755
US-FL-Tampa
Quality Auditor III The assurance of quality product and batch records from the manufacturing departments. Evaluates quality issues with Manufacturing and Quality Assurance.
Job ID
9754
US-NJ-Bridgewater | US-NY-Rochester | US-FL-Clearwater | US-SC-Greenville
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.   Project management lead for strategic projects within the Global QA organization. Drive consistent practices that efficiently & effectively achieve desired results.   This role does not have any direct reports. 
Job ID
9753
US-SC-Greenville
The Filling Operator is responsible for controlling the filling line including parameter setup, purging, and running production according to Standard Operating Procedures, Aseptic Technique, Bill of Materials, and Batch Records. Operates the Aseptic Filling Process and equipment to aseptically fill solution product into sterilized bottles. Monitors and inspects product during the filling process and reacts to issues by making machine and process adjustments, documenting issues, and informing the appropriate personnel of mechanical, electrical, and quality issues. Maintains the APA in orderly and aseptic condition by removing culls, documenting inspection of the work area, and performing disinfection activities as directed or required. Supports all functions of the APA as needed.
Job ID
9752