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Engineering Site Projects Lead - 2263

Date: Nov 25, 2022

Location: Stouffville, Ontario, CA, L4A1H5

Company: Teva Pharmaceuticals

Who are we?

Teva is a global pharmaceutical leader and the world's largest generic medicines producer, committed to improving health and increasing access to quality health solutions worldwide. Our employees are at the core of our success, with colleagues in over 80 countries delivering the world's largest medicine cabinet to 200 million people every day. We offer a uniquely diverse portfolio of products and solutions for patients and we've built a promising pipeline centered around our core therapeutic areas.  We are continually developing patient-centric solutions and significantly growing both our generic and specialty medicines business through investment in research and development, marketing, business development and innovation. This is how we improve health and enable people to live better, healthier lives. Join us on our journey of growth!

Job Description

We are currently seeking an Engineering Site Project Lead.  This is a full time opportunity, located in Stouffville Ontario. 
 

The main responsibilities include but are not limited to:

  • Create a reliability based strategy for site assets to optimize the mean time between failure and mean time to repair in a cost effective manner.
  • Research, develop and implement processes and procedures necessary to establish a Reliability Centered culture to improve equipment performance and reliability. Constantly pursue new tools and methods to make engineering and maintenance group more reliability focused, proactive work group.
  • Provide design solutions to enhance the reliability of equipment through the monitoring programs developed to enhance production utilization.
  • Perform engineering design to select appropriate equipment technology for a given process.
  • Evaluate various economic options, develop project schedule and prepare overall project impact summary, including cost benefit analysis.
  • Evaluate process control, monitoring, data acquisition and other support requirements for the manufacturing.
  • Troubleshoot problems with process equipment and implement changes as required.
  • To develop and implement Condition Based monitoring programs to identify potential equipment failures with sufficient lead time to allow for planning and scheduling of the work in a proactive manner as to reduce impact to production
  • Develop and maintain reliability related databases, including but not limited to vibration analysis, oil analysis and ultrasound analysis.
  • Coordinate with internal and external resources in relation to reliability projects ensuring that they are completed on time and are effective in identifying potential failures and that reliability insights are captured in the CMMS system for remediation.
  • Support Defect Elimination and Operational Excellence programs by providing expertise to the cross functional teams contributing to the resolution of submissions in the idea management system.
  • Conduct Failure Mode and Effects Analysis/ Reliability Centered Maintenance/ Precision installation & commissioning of critical assets to develop ideal preventive and proactive maintenance strategies and ensure that the equipment are properly installed during maintenance and engineering
  • Support of the CMMS system including asset hierarchy, master data and bill of equipment materials to provide the engineering and maintenance department the required information from a central repository
  • Development and reporting of metrics and KPIs for the Reliability Department to demonstrate cost savings and cost avoidance over time

Qualifications

  • Required  -  Bachelor’s degree in Engineering and/or other Science related field equivalent
  • 5+ years experience working in maintenance in manufacturing industry preferably pharmaceutical industry
  • 3+ years experience working in reliability/design engineering
  • Proven problem solving, project and time management skills demonstrated by previous work experience in order to manage multiple priorities in a fast paced environment
  • Advanced communication and technical writing skills: 
  • Interpersonal skills: Educates internal and external customers on facts by taking into account differences in level of understanding, needs, and expectations
  • Must be computer literate with good working knowledge of CMMS, Oracle, MS Office (Excel, Word, Project)
  • Good working knowledge of SOPs, GMPs, and cGMP’s applicable to Engineering, Operations, Manufacturing and Packaging 

Function

Engineering

Sub Function

Engineering

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Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws.