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About Abbott
Abbott is a global healthcare leader creating breakthrough science to improve peoples health. Were 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:
The Opportunity
This position works out of our Ottawa Ontario location in the Point of Care Diagnostics division. Were empowering smarter medical and economic decision making to help transform the way people manage their health at all stages of life. Every day more than 10 million tests are run on Abbotts diagnostics instruments providing lab results for millions of people.
What Youll Do
Coordinate Component Investigation Returns (CIRF) from Assembly and conduct investigations of returned components.
Alert SQA and CSE of issues that cannot be resolved by IQC.
Generate appropriate disposition of material after investigation is finalized and approved.
Generate Exception Reports when components are not within specification following the CAPA process.
Investigate Exception Reports assigned to the IQC department
Inspect all incoming parts using current documents (TP SW MAT) molded components (covers bases clips) paper components (boxes cartons pouches) rubber components (BPG Diaphragm) labels foils and barrier film.
Lead Gage R & R studies for IQC and supplier gages.
Support Component Engineering in doing the measurements of new parts for CTQ studies and other items as required.
Support the inspection of new material and other identified existing material used in production as required.
Work from Alert List and Priority list to ensure Production needs are met.
Participate in 5s (Quality Organization tools) Lean initiatives and projects Participate in documentation creation review and the DCP process
Understand and comply with EHS policies procedures and guidelines.
Safeguard the environment and facilitate a safe and healthy workplace culture.
Other miscellaneous duties as may be required
Required Qualifications
High School Diploma
3 to 6 years of experience in manufacturing in a regulated environment is an asset.
Ability to plan organize and prioritize own daily work to meet established schedule.
Demonstrated problem-solving and trouble-shooting skills.
Detail-oriented and ability to multi-task.
Ability to clearly concisely and accurately convey communications.
Ability to form and develop interpersonal professional relationships; display socially and professionally appropriate behavior.
Ability to work independently and in groups.
Demonstrated leadership skills Connaissances / Knowledge:
Knowledge of quality control within a regulated cGMP environment;
Certification as an investigator and resolution planner in the CAPA system is an asset.
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 on Facebook at and on Twitter @AbbottNews and @AbbottGlobal.
The base pay for this position is
N/AIn specific locations the pay range may vary from the range posted.
Required Experience:
Senior IC
Full-Time