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Abbott·Pharma·6 hours ago
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Software Quality Engineering - Queretaro Site

Queretaro, MexicoMid · 2-5 yearsQuality Engineer

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Must-have skills for this role

  • gmp
  • csv
  • computer system validation
  • software validation

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Apply faster with autofill FREEThe NextRaise extension autofills your application in one click.careers.example.com/applyAutofillingFull namePriya SharmaEmailpriya.sharma@example.comPhone+49 30 1234567LocationBerlGet the extension

What you'll do

  • Work in the implementation of Electrophysiology Software Quality Systems to ensure business/plant continuity through GMP compliance
  • Support creation of software requirements, protocols, test plans, scripts, and reports to validate non product software, using the non-product software development life cycle procedure and support process validation activities, qualification, working with multidisciplinary areas
  • Identify, standardize and document software validations to meet current regulations and medical industry standards
  • Provides guidance, maintain, leads and/or develops other software quality engineers in the Non product software Lifecyle.
  • Apply the software quality methodologies to ensure that all non-product software adhere to regulations and standards
  • Works closely with Quality, Manufacturing, IT, Microbiology, Calibration, and Engineering on sustaining and projects activities to ensure compliance with the quality system requirements
  • Provide guidance and understanding of the quality management system procedures (related with software), as well as support to ensure compliance with current regulatory requirements.
  • Coordinate, approve and ensuring software requirements and compliance with CFR21, FDA and other applicable regulations

What they're looking for

  • 3 years of experience working with computer applications (MES, INFOR, Power BI, and Excel)
  • 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.

Nice to have

  • SAP knowledge is desirable.

Summarised by NextRaise from the employer’s description, which follows in full below.

Full description from employer

     

JOB DESCRIPTION:

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

  • List the main responsibilities this job position regularly performs
  • Work in the implementation of Electrophysiology Software Quality Systems to ensure business/plant continuity through GMP compliance
  • Support creation of software requirements, protocols, test plans, scripts, and reports to validate non product software, using the non-product software development life cycle procedure and support process validation activities, qualification, working with multidisciplinary areas
  • Identify, standardize and document software validations to meet current regulations and medical industry standards
  • Provides guidance, maintain, leads and/or develops other software quality engineers in the Non product software Lifecyle.
  • Apply the software quality methodologies to ensure that all non-product software adhere to regulations and standards
  • Works closely with Quality, Manufacturing, IT, Microbiology, Calibration, and Engineering on sustaining and projects activities to ensure compliance with the quality system requirements
  • Provide guidance and understanding of the quality management system procedures (related with software), as well as support to ensure compliance with current regulatory requirements. It will offer coaching and support to achieve objectives and may provide feedback or escalate situations if internal and/or regulatory requirements and policies are not met.
  • Coordinate, approve and ensuring software requirements and compliance with CFR21, FDA and other applicable regulations

 

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/A

In specific locations, the pay range may vary from the range posted.

     

JOB FAMILY:

Operations Quality

     

DIVISION:

EP Electrophysiology

        

LOCATION:

Mexico > Queretaro : Avenida FINSA 156, Lote 12

     

ADDITIONAL LOCATIONS:

     

WORK SHIFT:

Turno 1 Day Shift (Mexico)

     

TRAVEL:

Not specified

     

MEDICAL SURVEILLANCE:

Not Applicable

     

SIGNIFICANT WORK ACTIVITIES:

Not Applicable

     

     

��    

Pharma

Company

AbbottPharma
Queretaro, Mexico

Company facts come from this company's own listings. We only show what the postings themselves carry.

Sourced from Abbott's careers site·first seen 22 Sept 2026·last verified 22 Sept 2026·How we source jobs

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