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Quality Control Analyst I

CanniMed®, a leader in plant-based technologies, is seeking a self-driven individual to join the Quality Control (QC) team in a permanent, full-time position. The QC Analyst I performs routine and non-routine analytical testing for incoming, in-process, finished product, and stability samples, critical reagents and raw materials as needed. The QC Analyst I also reports the analytical data using the appropriate statistical techniques. Shift and weekend work will be required on a rotating basis. The QC Analyst I will report directly to the QC Lab Supervisor, and will be responsible for the following:

Primary Responsibilities

  • Perform testing as per established SOPs using analytical instrumentation such as HPLC, UPLC, GC-MS, ICP-MS, spectroscopy and associated software
  • Follow all established laboratory, regulatory, safety and environmental policies and procedures
  • Ability to author, review and update SOPs as needed
  • Ability to understand and follow complex written procedures
  • Assist with validation and qualification activities as needed
  • Must follow good documentation practices in all aspects and phases of work
  • Provide analytical reports for review in a timely manner
  • Work with other lab personnel on projects and participate in investigations
  • Maintain the safety, cleanliness and orderliness of the lab
  • Apply knowledge of cGMPs and GLPs on a daily basis
  • Demonstrate excellent written and oral communication skills
  • Demonstrate excellent organizational, analytical and problem-solving skills
  • Demonstrate detail oriented and accurate work
  • Proficient in material sampling, receipt and inventory control
  • Assist in the development of new sampling and analytical programs
  • All other duties as assigned


  • A University Degree (BSc.) in an applicable discipline (chemistry or related field)
  • Preferably a minimum of 1 year laboratory experience, in a cGMP and/or GLP setting
  • Must have strong working knowledge of Microsoft Word and EXCEL
  • Experience with method validation and knowledge of HC regulations, USP and Ph. Eur. are assets

We would like to thank all applicants for their interest but only those selected for an interview will be contacted.

How to Apply

Click on the "Apply Now" button below to proceed to the application form. Make sure you specify the title of the job you are applying for as well as all other relevant information.

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