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.

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.
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• 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