Quality Release Technician- 2nd shift- Querétaro Site

Abbott Laboratories; Santiago de Querétaro; Presencial; MXN 167.000 - 246.000; Jornada completa

Descripción de la vacante

Abbott Laboratories in Querétaro is seeking a Quality Release Technician to conduct final and in-process documentation review, inspections, and release activities as part of manufacturing.

You will audit production, collect data, perform basic statistics, support verifications/validations, resolve nonconformances, and train technicians to uphold GMP and ISO 13485 standards.

Formación

• Education: Bachelor’s degree in Engineering or related field.
• 1–2 years of experience in a similar role.
• Proficiency in MS Excel, Word, and PowerPoint.
• Knowledge of GMP; ISO 13485 desirable.
• Knowledge of good documentation practices.
• Experience reviewing quality documents (e.g., batch records, certificates of analysis, inspection reports).

Responsabilidades

• Perform in-process and final product inspections against specifications and procedures, including document review of the device history record.
• Audit production operations and document inspections.
• Collect data, summarize analyses, and monitor critical-to-quality parameters.
• Assist with verifications, qualifications, and validations of equipment, product, process, and test methods.
• Maintain area release goals and control plans to prevent line downtime or backorders.
• Support documentation and resolution of nonconformances with engineering teams.
• Train and certify technicians in area procedures.
• Coordinate with team members to set priorities and tasks.
• Obtain vendor certifications and issue conformance certificates when required.

Conocimientos

MS Excel

MS Word

MS PowerPoint

Documentation practices

Quality document review

GMP knowledge

ISO 13485 knowledge

Educación

Bachelor's degree in Engineering or related field

Herramientas

MS Office

Descripción del empleo

We are Quality Release Technician

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

This position is responsible for conducting final and in process documentation review, inspection of product and final release activities in a routine basis as part of the manufacturing processes. They may also serve as area coordinators, qualified trainers and may provide assistance to engineers with quality technical support such as new product development, problem solving, resolution of nonconformances, system/services support and engineering department tasks.

What You’ll Do

• Perform in process and final product inspections against specification and procedural requirements, including documentation review of the device history record as applicable.
• Audit production operations as applicable, including documenting inspection.
• Collect data, summarize, analyze, perform basic statistical analysis, and perform process control and monitoring of critical-to-quality parameters and specifications.
• Assist in executing and documenting equipment, product, process, and test method verifications, qualifications, and validations.
• Assist and maintain area release goals are within the expected levels to avoid line down or back-order events and assist and maintain control plans for products and processes.
• Support operations and engineering teams in the documentation and resolution of nonconformances, problem solving, documentation practices and education to reduce documentation errors
• Trains and certifies technicians in the corresponding procedures for the area.
• Coordinates with area members to determine and complete work priorities and key tasks
• Requests certifications from vendors and provides certificates of conformance when required.

Required Qualifications

• Education:Bachelor's degree in Engineering or a related field (degree required).
• Experience:1 or 2 years in a similar role.
• Proficiency in computer applications (MS Excel, MS Word, MS PowerPoint).
• Knowledge of GMP, ISO 13485 is Desirable
• Knowledge of good documentation practices
• Experience reviewing quality documents ( for example batch records, certificates of analysis, inspection reports)

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.