Software Quality Engineering - Queretaro Site
Abbott
This listing was originally posted on Abbott's careers page. Formulate is an equal opportunity job aggregator and is not involved in the hiring process. Where salary information is estimated, it is derived from BLS industry benchmarks and may differ from actual compensation.
Upgrade to Pro to access the AI-generated 'Read before applying' briefing and other premium pharma intelligence.
Upgrade to Pro — $25/mo
MAIN PURPOSE OF ROLE
Summarize the main purpose of the role
MAIN RESPONSIBILITIES
We are hiring Software Quality Engineer
About Abbott
Abbott, global leading healthcare company, is investing in Mexico. We are building a manufacturing facility in Querétaro.
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.
This facility will offer 1,200 local new jobs and will be the first health manufacturing facility in Querétaro (pioneers for healthcare Hub).
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
Software Quality Engineer role purpose is work in the implementation of Electrophysiology Software Qnufacturing Practices (GMP) compliance of documental system, non-conformities, Corrective Action Preventive Action (CAPA), Complaints, Self-Inspections /Audits, Risks systems, among others Quality systems. Works closely with Quality, Manufacturing and Engineering on sustaining and projects activities to ensure compliance with the quality system requirements and achievement of Key Performance Indicators (i.e. NCMR’s, projects, etc.).
What You’ll Do
Qualifications
3 years of experience working with computer applications (MES, INFOR, Power BI, and Excel); SAP knowledge is desirable.
• 1 year of experience in Quality-related positions.
• 1 year of project management experience.
• 2 years of experience in regulated industries (pharmaceutical, food, or cosmetics).
• 2 years of experience in CSV projects, with involvement from Design Qualification through maintenance of the validated state.
• Intermediate to advanced English proficiency.
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/AIn specific locations, the pay range may vary from the range posted.
Explore related positions you might be interested in
We'll notify you when matching roles are posted.
Interviewed at Abbott?
Help others prepare — share your experience anonymously.
BIOTECHNOLOGY
Device Manufacturing
Upgrade to Pro to access AI interview prep brief and other premium pharma intelligence.
Upgrade to Pro — $25/mo