|Position Type||Full Time|
|Application Deadline||November 30, 2021|
|Experience Required||1-2 years|
|Job Duration||1 year|
MaxSys Staffing & Consulting is hiring on behalf of our client, a global leader in the medical manufacturing industry. This is an ever-growing sustainable company with no plans to slow down, so it is a great opportunity to begin a rewarding career with them. They are located in Ottawa’s west end, easily accessible by car or public transportation.
Work as an individual contributor within the Product Engineering team with a focus on semi-annual calibration of chemistry and blood gas sensors, control fluid value assignment and related root cause investigations and implementation of corrective and preventative actions.
-Support and execute semi-annual sensor calibration of the Chemistry and Blood Gas tests in the i-STAT System for Global Software Releases.
-Support control fluid value assignment testing, analysis and determination of fluid targets for internal and external (customer) use.
-Investigate non-conformances/potential non-conformance to identify root cause and corrective/preventative actions for implementation related to sensor calibration, value assignment or interference testing.
-Develop and deliver communications/status updates on investigations within and outside Product Engineering.
-Design and execute experiments and analyze/interpret data to drive to root cause.
-Create verification, validation and engineering file protocols and reports consistent with the Quality System.
-Independently execute assigned tasks by applying standard engineering theories, concepts and techniques.
-Collaborate cross functionally with individuals and teams from Operations, Project management, Supply Chain, Manufacturing Engineering, Chemistry, Quality leads and R&D.
Required Education and Experience:
-Bachelors Degree in Science or Engineering
-1-3 years in a relevant engineering or technical role is preferred.
-Experience with statistics and data analysis tools. Experience with SAS JMP and Minitab is preferred. Ability to apply mathematical concepts and statistics.
-Demonstrated understanding of non-conformance & CAPA and experience documenting quality reports in an electronic system adhering to quality system requirements.
-Experience writing validations and verifications and FMEA.
-Experience with GMP and working in an ISO and FDA regulated environment is an asset.
-Experience with LEAN Six Sigma manufacturing principles is an asset.
-Experience in a manufacturing environment is considered an important asset
-Excellent organizational and planning. Project management experience is an asset.
-Excellent oral and written communication skills and ability to interact effectively with all levels in the organization.
-Demonstrated initiative and problem-solving skills; critical thinking and analytical skills; Very strong investigational skills, drive to understand and solve problems;
-Ability to design experiments, analyze and interpret data, and document conclusions;
-Ability to collaborate effectively with multidisciplinary team members, and work independently;
-Willingness to work in labs, manufacturing areas, and office environments;
-Propensity for continuous learning and experimentation.
-Effective at dealing with a variety of people and understanding/communicating their requirements.
-Self-directed, proactive and not easily discouraged.
Please send your CV to [email protected] if you are interested