Associate Engineer (Supplier Engineering) - Point of Care (Ottawa)

Job summary

The Associate Engineer will provide technical support to suppliers regarding material deficiencies and lead failure analysis and corrective action activities. They will also support the qualification of new materials and suppliers while ensuring compliance with quality and regulatory standards.

Job details

JOB DESCRIPTION: About Abbott Abbott is a global healthcare leader, creating breakthrough science to improve people’s health. We’re always looking towards the future, anticipating changes in medical science and technology. 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 an Associate Engineer in the Supplier Engineering group, you will have the chance to support supply continuity, supplier performance, new supplier onboarding and manufacturing improvement initiatives. What You’ll Do ​ Provide technical support and consultation to suppliers on deficiencies related to cartridge materials and components, including supplier site, specification and process changes. Support the qualifications of new suppliers, alternate suppliers, and new or modified materials through data collection, technical evaluations, risk assessments, testing activities, and documentation of qualification requirements. Lead technical activities related to failure analysis and corrective and preventive actions (CAPA) activities, both internally and with external suppliers, using structured problem-solving methodologies. Maintain and analyze reports on materials, identify trends, and support implementation of corrective actions with internal and external stakeholders. Collaborate effectively with internal teams and external suppliers to support quality, delivery, and technical objectives. Ensure work complies with Abbott quality and regulatory requirements (FDA, ISO, IVDR, DEKRA) and that deliverables meet applicable standards and procedures. Participate in process improvement initiatives and provide technical input to manufacturing and supplier-related projects. Understand and comply with applicable Environmental Health and Safety policies, procedures, rules, and regulations. Responsible for implementing and maintaining effectiveness of Quality System. Other tasks and duties as assigned. Required Qualifications Less than one year experience in an engineering role. Undergraduate University Degree in Engineering or Science with a GPA of 3.0 or higher. Co-op and/or internship experience in a related field an asset. Demonstrated success in challenging engineering, science, and related coursework. Strong analytical, technical, and problem-solving skills with the ability to exercise sound judgment and make data-driven decisions. Leadership skills demonstrated through extracurricular activities. Demonstrated ability to work independently, manage multiple priorities, and meet deadlines in a fast-paced environment. Experience analyzing manufacturing and quality data to support process improvements, risk assessments, validation activities, and continuous improvement initiatives. Strong understanding of statistical principles and methods, with proficiency in Microsoft Excel, JMP, Minitab, or equivalent statistical analysis software. Strong attention to detail with the ability to prepare accurate technical reports, investigation reports and quality documentation. Effective verbal and written communication skills as well as presentation skills, with the ability to communicate technical information and collaborate with cross-functional teams at all organizational levels. Familiarity with Statistical Process Control (SPC), Corrective and Preventive Action (CAPA), Root Cause Analysis (RCA), Failure Mode and Effects Analysis (FMEA), and quality management system requirements. The annual base salary for this position ranges from $59,250.00 to $86,900.00 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. The base pay for this position is N/A In specific locations, the pay range may vary from the range posted. JOB FAMILY: Engineering DIVISION: APOC Point of Care LOCATION: Canada > Ottawa : 185 Corkstown Road ADDITIONAL LOCATIONS: WORK SHIFT: M-F (Canada) TRAVEL: Not specified MEDICAL SURVEILLANCE: Not Applicable SIGNIFICANT WORK ACTIVITIES: Continuous standing for prolonged periods (more than 2 consecutive hours in an 8 hour day)

What you’ll do

The Associate Engineer will provide technical support to suppliers regarding material deficiencies and lead failure analysis and corrective action activities. They will also support the qualification of new materials and suppliers while ensuring compliance with quality and regulatory standards.

Requirements

Candidates must hold an undergraduate degree in Engineering or Science with a GPA of 3.0 or higher and have less than one year of engineering experience. Strong analytical skills, proficiency in statistical software, and familiarity with quality management systems are required.

Benefits

• Career development • Global company opportunities

Listed skills

• Technical Documentation · Preferred
• Problem solving · Preferred
• Regulatory Compliance · Preferred
• Data analysis · Preferred
• Root Cause Analysis · Preferred
• Cross-Functional Collaboration · Preferred

Other relevant skills

Identified from the job description. Confirm important requirements above.

• Supplier engineering
• Failure analysis
• CAPA
• Root cause analysis
• FMEA
• Statistical process control
• Risk assessment
• Technical documentation
• Data analysis
• Quality management systems
• Problem solving
• Manufacturing improvement
• Technical evaluation
• Cross-functional collaboration
• Statistical analysis
• Regulatory compliance
• Supply Chain Risk and Continuity Planning
• Ability To Meet Deadlines
• Statistical Analysis Software
• Data-Driven Decision Making
• Microsoft Excel
• Quality Management Systems
• Chemistry
• Arterial Blood Gas Analysis
• Hematology
• Medical Science
• Corrective And Preventive Action (CAPA)
• Decision Making
• Coagulation
• Communication
• Continuous Improvement Process
• Data Collection
• Electrolytes
• Endocrinology
• Failure Mode And Effects Analysis
• Leadership
• Problem Solving
• Medical Surveillance
• Minitab
• Neurology
• Presentations
• Regulatory Requirements
• Risk Analysis
• Statistical Process Controls
• Supplier Performance Management
• Process Improvement
• Environment Health And Safety
• Investigation
• Root Cause Analysis
• JMP (Statistical Software)

Job areas

• Engineering
• Healthcare
• Manufacturing
• Science & Research
• Supplier Engineer
• Supplier Quality Engineer
• Supply, Distribution and Related Managers
• Industrial Engineers