Calibration Chemist - 12 month contract
Toronto, Canada, Ontario, M1B2K9
Who we are
The opportunity
Calibration Chemist - 12 month contract
Under the direction of the functional leader, involved in developing and implementing compliant, cost-effective calibration qualification and repair procedures. Responsibilities include delivering in-house technical training, performing repairs, creating calibration SOPs, mapping protocols, initiating track wise change controls and ensuring adherence to GMP compliance.
How you’ll spend your day
- Assist in the maintenance, configuration, troubleshooting, and calibration of all controls and instrumentation in the QC Laboratory area.
- Assist in performing preventative maintenance and qualification on analytical instruments to minimize unexpected downtime.
- Support audit of Preventative Maintenance/Qualification documents produced by onsite metrology group and track RFT statistics to develop improvement strategies.
- Assist in the creation and maintenance of SOPs for the qualification of existing/new analytical instruments and ensure qualification intervals are adhered to and documented.
- Assist with updating the LIMS and SAP database to track all instrument PM and qualification intervals.
- Support project teams during design, commissioning, calibration, training and handover phases of projects.
- Responsible for managing, organizing all the documentations related to the metrology department.
- Responsible for Harmony Track wise (change control, CAPA), SOP creation, IQOQ qualification doc etc.
- Other related duties as assigned.
Your experience and qualifications
- University Degree and/or College Diploma in Chemistry, Chem. Eng., or other related discipline.
- Minimum of two (2) years of relevant experience. Preferred experience: Instrument troubleshooting and/or calibration experience an asset.
- Excellent skill/experience using Microsoft Excel
- Advanced technical knowledge and experience with a wide variety of analytical instrumentation employed in a pharmaceutical laboratory
- Knowledge of cGMP, ICH and other requirements as it relates to instrument qualification and validation.
- Exhibit good written and verbal communication skills in order to:
- Interact with a variety of Teva contacts to complete projects/tasks as needed.
- Create technically sound written protocols and procedures
- Exhibit good organizational skills and a professional attitude
- Demonstrate resourcefulness to solve problem and source technical supplies.
- Strong understanding of TWD (Harmony Trackwise), LabWare LIMS, Empower, MS Office, and other QC lab applications..
- Analytical methods and techniques common to QC Lab
- Proficient in Good Documentation Practices
- GMP, cGMP, ICH and other requirements as it relates to instrument qualification and validation.
- Key measurements to support business such as customer service, cycle time, costing, etc.
- Strong organizational and time management skills
- Ability to work well under pressure in a stressful and fast paced working environment
- Required to work independently and follow through on assignments/instructions/tasks with minimal supervision/direction
Already Working @TEVA?
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