Centre for Probe Development and Commercialization
  • Toronto, ON, CAN
  • Full Time

The Centre for Probe Development and Commercialization (CPDC) is dedicated to fostering the development, translation, and commercialization of molecular imaging probes and associated technologies.

As a QC Technician, you will be responsible for working in accordance with company policy and within GMPs while contributing your technical expertise to support current products and develop future drugs within the CPDC portfolio. 

Duties/Responsibilities include but are not limited to:

  • Perform quality control (release & retrospective) testing of finished drug products according to standard operating procedures, including analytical chemistry and microbiological tests.
  • Conduct peer review of laboratory records as well as responsible for routine monthly environmental monitoring according to standard operating procedures.
  • Perform routine quality operations including calibration/maintenance of equipment and inventory/material management of incoming raw materials/container closures and analytical reagents, when required.
  • Plan, implement, and successfully complete assigned tasks in a timely fashion ensuring consistent high quality.
  • Conduct investigations for testing failure and non-conformances.
  • Conduct all work in accordance with CPDC SOPs and raise any deviations immediately to the attention of Management.
  • Be responsible for the general husbandry of the facility including the disposal of waste through the appropriate waste-streams.
  • Understand and work under the Health Canada and FDA GMP requirements for sterile pharmaceuticals.
  • Understand and work under the Canadian Nuclear Safety Commission regulations.
  • Support analytical method development, transfer, and validation activities
  • Author, revise, and review technical documents, including SOPs, validation documents, standard test methods according to good documentation practices and reports
  • Assist with inventory and management of Quality Control materials.
  • Adhere to CNSC and GMP regulations by maintaining complete records pertaining to all aspects of microbiological testing, routine operations, and equipment maintenance and assist in training of other colleagues.
  • Work as a member of a team to achieve all outcomes.
  • Complete all other related duties as assigned.

 

Qualifications:

  • College Diploma or B. Sc. in Engineering, Chemistry, Microbiology or a related field
  • Understanding of analytical chemistry techniques such as HPLC, GC and TLC is an asset for the role
  • 1 to 3 years of relevant experience
  • Experience working in a GMP is considered an asset
  • Ability to lift 23 kilograms required

 

Additional Details: This position requires shifts with starting times between 4am to 9am and may include work on weekends.

 

If you require accommodation for your application or interview, please contact Human Resources directly at 905.525.9140 extension 21112 or via email at careers@imagingprobes.ca

Centre for Probe Development and Commercialization
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