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

The CPDC is a global leader in the discovery, development and distribution of next generation radiopharmaceuticals.  Our products are used daily for the detection and treatment of human diseases such as cancer.

As a SPECT Supervisor, you will lead a team setting that is using state-of-the art techniques and equipment to manufacture and package radiopharmaceutical products.  This role requires some night shift coverage.  Shift start times can vary between 12am and 6am.  Some weekend shifts are also required.

Duties and Responsibilities:

  • Manufacture, dispense and package all SPECT products
  • Support vacation and sick days coverage
  • Supervise the day-to day operations including but not limited to training, assigning tasks, scheduling, materials ordering
  • Supervise SPECT pharmacy including, development and execution of SOPs, launch of new products, train new staff and report to the Director, Manufacturing Operations any efficiencies and process improvements
  • Act as point of contact for customers and other departments and team members for matters related to the SPECT operations
  • Work alongside the Director, Manufacturing Operations to develop action plans for any decision-making on batch release and to troubleshoot and problem solve critical issues related to the facility
  • Work across teams to ensure that equipment is maintained and calibrated
  • Maintain documentation to fulfill all customer, facility, Provincial, Federal and applicable International regulatory requirements relating to nuclear safety and cGMP manufacturing
  • Adhere to the Health Canada GMP requirements for sterile pharmaceuticals
  • Ensure compliance with accepted radiation safety procedures for staff members and may function as Radiation Safety Officer delegate of the facility by ensuring radiation safety compliance
  • Any and all other duties that support the mission of the Centre

Qualifications:

  • Diploma in Sciences or equivalent with at least 5 years' experience in a GMP environment (pharmaceutical, radiopharmaceutical or biopharmaceutical industry)
  • Minimum 5 years of experience in Pharmaceutical Manufacturing Supervisory position
  • Previous experience with Sterile Manufacturing facilities will be considered an asset
  • Flexibility in work schedule to support a 24/7 production environment
  • 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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