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Automation Engineer

Teva Pharmaceuticals
Stouffville, Canada, Ontario, L4A1H5
$70K-$75K a year (estimated)
Full-time

The opportunity

We are seeking a talented individual to join our dynamic team as an Automation Engineer. In this role, you'll play a pivotal part in designing, optimizing, and troubleshooting processing equipment to ensure our manufacturing processes operate at peak efficiency.

The responsibilities will include but are not limited to :

  • Performs specialized activities related to design, commissioning, performance improvement, and troubleshooting of computer control assisted processing equipment.
  • Provides and develops design / approval of hardware, software, and controls for computer assisted equipment.
  • Evaluates / implements process control, process monitoring, data acquisition and other support requirements for manufacturing.

packaging constraints, utilities, sensors and controllers, vision based algorithm, equipment calibration)

  • Implements software / hardware changes and upgrades, understands impact of actions to Manufacturing and Facilities and process.
  • Implements modification / change control procedures and protocols.
  • Programs PLC and HMI application for automated process equipment, capable of troubleshooting and demonstrates knowledge of instrumentation and controls.
  • Development of Standard Operation Procedures (SOPs), Preventive Maintenance (PM’s), and calibration forms.
  • Provides support to the calibration group and assists with the existing calibration program when required.
  • Provides support to Project Engineers regarding related departmental activities specifically to process control and automation.
  • Provides project management for all assigned projects and assignments.
  • Prepares detailed capital project requests, equipment procurement specifications and vendor’s contracts as per overall guidelines.
  • Coordinates with vendor for inspection and testing of new equipment, supervises the installation and commission of equipment.
  • Provides all necessary inputs to the Qualifications Group for IQ / OQ / PQ of new equipment and facility.
  • Ensure the system is operating as per qualified requirements and maintained in a robust state while conforming to our change management system.
  • Meets all deadlines associated with projects as directed, including all reports and documentation as directed.
  • Ensures Director of Engineering is kept up-to-date on project schedules.
  • Conforms to the principles of cGMP and to conform to all relevant departmental and other company standard operating procedures.
  • Works as a member of a team to achieve all outcomes.
  • Performs all work in support of our Corporate Values and demonstrates a strong and visible support of our values.
  • Performs all work in accordance with all established regulatory and compliance and safety requirements.

Your experience and qualifications

  • Bachelor’s degree or higher in Chemical / Electrical Engineering, or Technologist
  • Minimum 5 years of experience in the design / build / programming troubleshooting and maintenance of control systems.
  • Professional Engineer licensed or in the process of being licensed
  • Familiar with GMP, FDA, ISO requirements and Validation concepts and protocols.
  • Strong PLC and HMI programming skills; must have proven hands on experience in PLC / HMI logic programming and troubleshooting systems in a pharmaceutical or biopharmaceutical manufacturing facility.
  • Knowledge in automation technology (Cobots, Robots, Vision systems, AGV, automated warehouse)
  • Strong knowledge of process control and machine automation in pharmaceutical manufacturing facility.
  • Understanding of cGMP software quality system principles and sanitary equipment design requirements.
  • Working knowledge of word processing, spreadsheet, and database management software. Cad design would be an added benefit.
  • Strong communication skills.
  • 27 days ago
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