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Radiopharmaceutical Associate

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Job Order #: 5510312

NOC: 2112
Employer Name:
CANADIAN ISOTOPE INNOVATIONS CORPORATION
Posted Date:
17-May-2016
Location:
SASKATOON
 
# of Positions:
1
Employment Terms:
Full Time
Length of Employment:
3 years in the first instance (40 hours/week)
Education:
University Bachelor's Degree
Experience:
3-5 Years
Apply By:
03-Jun-2016
How to Apply?:
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Employer Name:
CANADIAN ISOTOPE INNOVATIONS CORPORATION
Contact Name:
Kennedy Mang'era
Contact Email:
kmangera@isotopeinnovations.com
Employer Website:
www.isotopeinnovations.com


Description

CIIC is establishing the linear accelerators as a dependable, environmentally friendly technology for production of the isotopes molybdenum-99/Technetium-99m. To view the full job posting, visit our Newsroom at www.isotopeinnovations.com

Qualifications: A minimum BSc in pharmacy, biotechnology, chemistry or related field is required. A MSc in these fields is preferred for the non-pharmacy training. At least 2 years of exp. in the radiopharmaceutical field working with medical isotopes is required. Experience with radionuclidic extractions and separations and with technetium-99 radiolabeling of cold kits will be strongly preferred. At least 3 years of exp. in analytical chemistry techniques (thin layer chromatography, GC, HPLC, preparative HPLC, endotoxin) and instrumentation (qualification, troubleshooting and maintenance) is required. Strong experimental skills, as well as demonstrated ability to design & carry out experimental laboratory techniques is required. Experience with cGMP requirements & compliance, and with aseptic processes is required.
    
Duties: Execution of development, operational & regulatory activities related to the separation of isotopes, the radiolabeling and quality control of radiopharmaceuticals. Participation in dissolution & processing of the irradiated targets. Quality control testing of incoming materials, drug substances & drug products. Quality assurance activities including calibration of equipment, environmental monitoring, inventory of process components, preparation of SOPs, validation protocols, analytical methods validation, and validation/qualification reports. Adherence to Radiation Safety, Drug Establishment License, and cGMP regulations by maintaining complete records pertaining to all aspects of production, dispensing, quality control and equipment maintenance. Performance of delegated duties for preclinical & clinical studies.

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