Intermediate Engineer (Manufacturing Operations) – Point of Care (Ottawa)

Résumé du poste

The role involves supporting high-volume manufacturing operations to ensure optimal equipment performance and production yields. Responsibilities include identifying process improvements, conducting root cause analysis, and managing non-conformance investigations.

Détails du poste

Working at Abbott At Abbott, you can do work that matters, grow, and learn, care for yourself and family, be your true self and live a full life. You will have access to: Career development with an international company where you can grow the career you dream of. A company recognized as a great place to work in dozens of countries around the world and named one of the most admired companies in the world by Fortune. A company that is recognized as one of the best big companies to work for as well as a best place to work for diversity, working mothers, female executives, and scientists. The Opportunity This position is based at our Ottawa office within the Point of Care Division. We’re empowering smarter medical and economic decision making to help transform the way people manage their health at all stages of life. Our Point of Care diagnostic portfolio spans key health and therapeutic areas, including Chemistry, Electrolytes, Hematology, Blood Gases, Coagulation, Endocrinology, Cardiac Markers, Neurology, and Informatics. As a member of Component Manufacturing Engineering, you will contribute to the team’s success by supporting high volume manufacturing operations, to ensure optimal equipment performance and production yields, and implementation of continuous improvement projects. What You’ll Do Identification, development, and implementation of process improvement initiatives. Oversee material qualification activities to ensure continuity of material supply. Investigations into product and process problems, perform root cause analysis, implement changes, and develop documentation and reactions schemes. Investigations into non-conformances (NCRs) and documentation of findings and Corrective Actions in Quality Reports (QRs). Supporting manufacturing processes and equipment. There will be a mixture of process sustaining and project work, along with supporting the quality system Safeguard the environment and facilitate a healthy workplace culture Other miscellaneous duties may be required Required Qualifications Undergraduate university Degree (4-year program), or equivalent experience (Engineering, or equivalent) Two to three years related work in a manufacturing environment would be considered an asset. Familiarity with any of the following areas would be an asset: automated assembly processes, product packaging, injection molded components, experimental design and statistical process control, ISO/FDA regulations, risk management/FMEA methods, root cause analysis (6M’s/ 5 Why’s), Solidworks and statistical software packages such as Minitab and SAS JMP. 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. The annual base salary for this position ranges from $62,250.00 to $100,100.00 CAD. The salary range provided applies to Canada only and does not apply to any other locations outside of Canada. Follow your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life. Abbott is an Equal Opportunity Employer, committed to employee diversity. Connect with us at www.abbott.com, on Facebook at www.facebook.com/Abbott and on Twitter @AbbottNews and @AbbottGlobal.

Ce que vous ferez

The role involves supporting high-volume manufacturing operations to ensure optimal equipment performance and production yields. Responsibilities include identifying process improvements, conducting root cause analysis, and managing non-conformance investigations.

Exigences

Candidates must hold an undergraduate degree in Engineering or a related field. Two to three years of experience in a manufacturing environment is considered an asset.

Avantages

• Career development • International company growth opportunities

Compétences indiquées

• SolidWorks · Souhaitée
• Risk Management · Souhaitée
• Documentation · Souhaitée
• Root Cause Analysis · Souhaitée
• Process Improvement · Souhaitée

Autres compétences pertinentes

Relevées dans la description du poste. Confirmez les exigences importantes ci-dessus.

• Process improvement
• Root cause analysis
• Manufacturing operations
• Quality reports
• Statistical process control
• Automated assembly
• Injection molding
• Risk management
• FMEA
• Solidworks
• Minitab
• SAS JMP
• ISO regulations
• FDA regulations
• Material qualification
• Documentation
• FDA Regulations
• Continuous Development
• Self-Discipline
• Quality Management Systems
• Chemistry
• Arterial Blood Gas Analysis
• Automation
• Hematology
• Decision Making
• Coagulation
• Communication
• Continuous Improvement Process
• SolidWorks (CAD)
• Electrolytes
• Endocrinology
• Packaging And Labeling
• Failure Mode And Effects Analysis
• Risk Management
• Manufacturing Engineering
• Manufacturing Operations
• Manufacturing Processes
• Neurology
• SAS (Software)
• Statistical Process Controls
• Statistical Software
• Process Improvement
• Collaboration
• Investigation
• Root Cause Analysis
• JMP (Statistical Software)

Domaines d’emploi

• Engineering
• Manufacturing
• Healthcare
• Science & Research
• Manufacturing Operations Engineer
• Manufacturing Engineer (General)
• Industrial and Production Engineers
• Manufacturing Engineers
• Industrial Engineers