Reporting to the Director, this position directly leads and coordinates the work activities and execution of the cleaning validation program and all cleaning validation activities for all three (3) Teva Canada locations in accordance with established schedules, timelines and priorities ensuring a high standard of performance and efficiency. This position is responsible for providing expertise and guidance to Teva Canada sites on Cleaning Validation issues/concerns and to ensure adherence to validation procedures.
University degree in Science, Engineering or related discipline
Minimum three (3) years Cleaning Validation experience
Technical expertise working with Microsoft Word, Excel, PowerPoint, Adobe Reader, Outlook Applications, LIMS, Trackwise Harmony and Knowledge Tree
Working knowledge of GMP/GLP regulations and other Regulatory requirements for Canadian, US and EU markets, WHMIS, and Safety Precautions
Knowledge of Manufacturing and Packaging processes in a Pharmaceutical environment
Time management and organizational skills to multi-task and determine priorities
Provide a leadership style that encourages high quality work, team participation and personal development
The individual in this role will spend some time (approx. 10%) in a manufacturing, packaging and laboratory environment and will have exposure to auditory influences
Some travel to other Teva sites (10%) required
If you are a current Teva employee, please apply using the internal career site available on "Employee Central". By doing so, your application will be treated with priority. You will also be able to see opportunities that are open exclusively to Teva employees. Use the following link to search and apply: Internal Career Site
The internal career site is available from your home network as well. If you have trouble accessing your EC account, please contact your local HR/IT partner.