|Job Category||Information Technology|
|Application Deadline||July 31, 2020|
|Experience Required||3 years|
|Job Duration||1 year|
ESSENTIAL DUTIES AND RESPONSIBILITIESReview protocols and reports pertaining to clinical software changes and updatesFollow the software validation and verification protocols as outlined in the quality management systemAssess work completed against the software validation and verification requirements and ensure that gaps are identified and addressedAssess other quality documentation protocols and reports as requiredAuthor quality documents (protocols and reports)Independently execute assigned tasksAttend cross-functional team meetings to share informationKeep up-to-date with the latest technical developments in related areas, assess and integrate appropriate changes to work practices
EXPERIENCEMinimum 1-3 years in a Software Validation role
KNOWLEDGE, SKILLS AND ABILITIESBachelors Degree in Science or Engineering with software or other scientific focus, or equivalentStrong working knowledge of software validation requirements and the software lifecycleStrong working knowledge of data analysis and data mining techniques (SAS JMP or Minitab experience an asset);Demonstrated initiative and problem-solving skills; critical thinking skills;Analytical skills, creativity and innovative approach to problem solving;Ability to collaborate effectively with multidisciplinary team members and also to work independently;Willingness to work in labs, manufacturing areas, and office environments;Very strong investigational skills, drive to understand and solve problems;Propensity to continuous learning and experimentation.
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