QC Analyst Level 1

3 weeks ago

Markham, Ontario, Canada SGS Full time
Job Summary

We are seeking a highly skilled QC Analyst Level 1 to join our team at SGS. As a key member of our analytical laboratory, you will be responsible for executing and performing testing as per methods, following the company's Standard Operating Procedures, Deviations and Change Control programs and cGMP guidelines.

Key Responsibilities
  • Execute and perform testing as per methods, following the company's Standard Operating Procedures, Deviations and Change Control programs and cGMP guidelines.
  • Ensure that work order documentation is complete in every aspect and all results are entered into Lab Book.
  • Execute daily work determined by supervisor in order to maintain efficient work flow to assure completion of scheduled tasks and meet established due dates.
  • In case of testing failure, immediately report to the Department Manager before proceeding any further with the test. Assist in the failure investigations as instructed. Do not discard any solutions or glassware that was used during testing.
  • Ensure that equipments are maintained in good order, perform calibrations and qualifications as required, volumetric/test solutions and mobile phase preparations are checked.
  • Record findings in standardized format, keeping all records and analyst notebook in good order. Prepare reports and record data in timely manner.
  • Prepare and standardize Test solutions, Standard solutions and Volumetric solutions.
Requirements
  • Education: Chemistry or Science related field
  • Experience: over 5 to 7 years of laboratory testing experience with demonstrated ability to complete more complex role/duties
  • Maintain workbench area clean and organized ensuring spills are immediately cleaned; disposal is according to laboratory procedures, glassware is appropriately handled and lab solutions are replaced.
  • Assist in the resolution of routine, as well as non-routine technical problems.
  • Adhere to the principles of 5S at the work stations and fume hoods.
  • Ability to step in when the Supervisor is not available to be able to answer technical queries as well as help fellow Analysts.
  • Perform routine and more complex analysis/testing of pharmaceutical finished products/raw materials.
  • Conduct testing using instruments HPLC,UPLC and Dissolution obtaining accurate results.
  • Conduct calibration and preventive maintenance of instruments/testing apparatus ( HPLC, GC, Dissolution, Thermometer, Oven, etc.) for compliance and accurate testing results.
  • Prepare and generate reports for method verification, validation and transfers.
  • Ability to execute method verifications, validations, transfers based on signed protocols.

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