What AbbVie Has to Offer: Our work can—and does—have a tangible, lasting impact on millions of people. But it’s not just the results that matter. How we achieve them matters, too. Leading with purpose, we work to build a more sustainable future for generations to come. We do that by putting our expertise, resources and talent to work to make a real difference for patients, communities and our world.
Job Details
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok.
This role is responsible for complaint trending, product performance quality presentation and complete Preventive Risk Assessment (PRA) for trend evaluation of complaints, for Breast Implants and Electromechanical Medical Devices (EMD).
MAJOR RESPONSIBILITIES
- Responsible for complaint trending and product quality review, which includes evaluating “as reported” complaints signals and conducting failure analysis on “as analyzed” complaint investigations in PRAs for Breast Implants and EMDs.
- Review the historical records of medical devices and document them properly in the system.
- Request the required documents from the appropriate personnel to carry out the review of DHRs and FIs.
- Support the process of reviewing the records of medical devices by identifying opportunities for improvement.
- Maintain constant communication with the Post Market Quality Assurance department to fulfill the requested requirements. Additionally, communicate with the Device Analysis Laboratory if needed, should any requirements arise.
- Host monthly Product Performance meeting to present product return data, complaint trending and confirmed failure analysis.
- Support OMR preparation material for DHR and DAL info.
- Ensure regulatory compliance of activities carried out in the work area: applicable Procedures, Standards, and Regulations.
- Guarantee compliance with corporate and legal EHS (Environmental, Health and Safety) requirements by adhering to internal policies and procedures. Likewise, ensure compliance through the adoption of strategies, internal controls, communication, and necessary training
- Carry out all other duties inherent to the position and those assigned by the immediate supervisor.
- Bachelor’s degree in engineering (mechanical, industrial, electrical).
- English level at least B2+ (C1 preferred)
- CQ
- E is a plus
- Microsoft, Visio, Power BI
- At least 3 years of experience in the medical device industry related to Quality activities, preferably involving complaint handling and experience with electromechanical products.
- Valid US visa with at least 9 months remaining before expiration
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.
US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html
US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
https://www.abbvie.com/join-us/reasonable-accommodations.html
Together, we break through We believe the paths we take to achieving our breakthroughs matter. At AbbVie, every one of our 50,000 employees is a... Read more