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 responsible to provides quality technical support within product process in the manufacturing lines. Provides support to Quality Engineering during non conformance processes and others. This position is responsible to bring support to the manufacturing lines following costumer service techniques. .
In Abbott’s Electrophysiology (EP) business, we’re advancing the treatment of heart disease through breakthrough medical technologies in atrial fibrillation, allowing people to restore their health and get on with their lives
What You’ll Do
• Document nonconformances as appropriate and assist in the resolution of nonconformances.
• Identifies and segregates nonconforming material from the production line according to governing documents.
• Coordinates with Quality Engineer to prepare and handle the material in and out of the designated quarantine area.
• Provides support in the process related to nonconformance actions (corrective, preventive or corrections) rework or Short activities.
• Perform inspection of production operations, including documenting inspection and audit results.
• Initiate related documentation changes request.
• Document test plan protocols, test procedures, and test reports, with mentorship from the Quality Engineer.
• Collect data, summarize, analyze, perform basic statistical analysis on, and document test results
• Assist: with or perform Gage R&R studies, with the selection, installation and programming of precision measuring equipment, and assist in designing, building, and evaluation of test methods, providing improvement recommendations.
• Assist in writing, executing and documenting equipment, product, process, and test method verifications, qualifications, and validations.
• Support manufacturing lines, with clarification of documental doubts and correction of documentation errors.
• Reviews compliance of quality and manufacturing documentation such as batch records.
• Assists in the writing of Build as Risk (BAR's) and the approval process
• Provides support in the investigation process related to Manufacturing Analysis (MA) as training evidence, material expiration etc
• Assists to sets up in the and training process for the new or transferred Quality Technicians
Required Qualifications
Student of Engineering (At least 40% of degree completion) or Quality Technical Degree, engineering, quality or related fields or minimum 4 years of equivalent experience in medical devices or pharmaceutical quality control.
At least 2 years of work experience
Proficiency in computer applications (MS Excel, MS Word, MS PowerPoint).
Knowledge of Quality Systems/engineering required.
2 years of experience would be considered equivalent to 60% of credits completed in an engineering related career
Intermediate Commands of English / Required
Prefered Qualifications
Previous experience in assisting with validations, qualifications, test methods or NCMR.
Knowledge in blueprint reading and experience with sampling techniques.
Prior medical device experience.
ASQ CQT certification or equivalent.
Basic knowledge of statistical techniques/ tools.
SHIFT TA
100% on site
Apply Now
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.