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

The Centre for Probe Development and Commercialization (CPDC) is a leading provider, on a global basis, of next-generation radiopharmaceuticals that are used daily for the detection and treatment of human diseases such as cancer. 

Radiopharmaceuticals are perishable products that require just-in-time manufacturing on a daily or weekly basis to ensure supply demands are met without interruption.  CPDC's success in the radiopharmaceutical industry results from the ability of our talented and committed staff to develop and manufacture high quality products, while adhering to international regulations governing nuclear safety, transportation of dangerous goods and pharmaceutical manufacturing.

The ideal candidates will have experience working in a Pharmaceutical Quality Control Laboratory, performing Chemical Potency and Impurities analysis (HPLC, TLC, GC, etc.) and/or microbiology tests such as sterility testing.

This position requires fixed evening, night or early morning shifts and work over weekends, e.g. Thursday to Monday.

Duties/Responsibilities include:

  • Quality control testing of materials and finished drug products (radiopharmaceuticals) including chemical, biological and microbiological tests using various analytical techniques such as HPLC, GC, TLC, bacterial endotoxin testing, sterility testing, bioburden testing, etc. according to standard operating procedures
  • Monthly environmental monitoring of cleanrooms according to standard operating procedures
  • Peer review of laboratory records
  • Conducting investigations for testing failure and non-conformances
  • Author, revise, and review technical documents, including SOPs, validation documents, standard test methods according to good documentation practices and reports
  • Support analytical method transfer and validation activities as required
  • Adhere to CNSC and GMP regulations

Qualifications:

  • College Diploma or B. Sc. in Chemistry, Microbiology or a related field with 3 years of relevant experience working in a GMP or ISO environment is required
  • Experience routinely executing chemistry techniques such as HPLC, GC and TLC is required for this role
  • Experience working with sterile products is considered an asset
  • Ability to lift 23 kilograms required

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

We thank all those who apply but only candidates selected for interviews will be contacted

Centre for Probe Development and Commercialization
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