Valeant Pharmaceuticals

Process Engineer II- Tampa FL

US-FL-Tampa
Job ID
9103
Pos. Category
Global Manufacturing Supply (GMS) - Operations
Pos. Type
Full Time

Overview

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 for process development to support the introduction of new technology capital equipment into the Tampa manufacturing facility.  This position will support ongoing improvements to existing processes/products and manufacturing equipment and also the process development and project management of new Contract Manufacturing technology transfer projects.

Responsibilities

  1. Perform process design to support the introduction of new technology capital equipment into the Tampa manufacturing facility by writing and executing validation studies.  Major process development projects are planned for and executed in a period of 1 –   3 years.
  2. Perform process development and technology transfer for new products from Contract Manufacturing customers into the Tampa manufacturing facility by writing and executing validation studies. Major technology transfer projects are planned for and executed in a period of 1 – 3 years.
  3. Perform manufacturing support improvement projects such as scale- up, product hold time extensions, and other improvements to existing products.
  4. Lead capital improvement projects. Prepare business justification, prepare Capital Expenditure Requests, Implement Projects.
  5. Lead recurring conference calls with customers and issue meeting minutes.
  6. Participate in cross functional teams for investigations relating to contract manufacturing products and other Bausch and Lomb products.

Qualifications

BS in Chemical Engineering or related engineering or physical science degree. Strong engineering skills in a cGMP environment. Good oral and written communication skills. Project management skills with Project Management Professional Certification Preferred. Time management ability. Computer literate; capable of operating Microsoft Visio program.

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