|Application Deadline||May 31, 2020|
|Experience Required||1 year|
|Job Duration||1 year|
ESSENTIAL DUTIES AND RESPONSIBILITIES:Create and execute efficient experimental strategies using DOE methods to identify potential design improvements.Independently execute assigned tasks by applying standard engineering theories, concepts and techniquesDocument results of experiments in a manner consistent with the Quality System.Create verification, validation and engineering file protocols and reports consistent with the Quality System.Keep up-to-date with the latest technical developments in related areas, assess and integrate appropriate changes to work practices.Experience with GMP and in working in an ISO and FDA regulated environment is an asset. Experience with LEAN Six Sigma manufacturing principles is an asset.Superior analytical and problem solving skills: experience with statistics.Organizational and leadership skills. Project management experience is an asset.
KNOWLEDGE, SKILLS AND ABILITIES:Bachelors Degree in Science or Engineering with Chemical, Biochemical or Mechanical Engineering focus, or equivalent (If this education is from outside of Canada, a Canadian Equivalency must have been completed)1-3 years in an engineering or technical role is preferred.Experience in a manufacturing environment is considered an important asset.Experience working in an ISO and FDA regulated environment is an asset.Experience with LEAN Six Sigma manufacturing principles is an asset.Demonstrated initiative and problem-solving skills; critical thinking skills;Ability to design experiments, analyze and interpret data, and document conclusions;Willingness to work in labs, manufacturing areas, and office environments;Very strong investigational skills, drive to understand and solve problems;Ability to apply mathematical concepts and statistics.Excellent organizational, planning and scheduling skills.Good oral/written communication skills.
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