Document Control Analyst (Supply Chain) - Queretaro Site at Abbott Pediatrics

Querétaro, Querétaro, Mexico -

Full Time

Start Date

Immediate

Expiry Date

13 Jun, 26

Salary

0.0

Posted On

15 Mar, 26

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Document Control, Supply Chain, Quality Area, EPIQ System, Nonconforming Material Reports, Root Cause Analysis, Corrective Actions, CAPAs, Quality Metrics, Power BI, Advanced Excel, Dashboards, KPIs, QMS, English Proficiency, Claim Management

Industry

Hospitals and Health Care

Description

Document Control Analyst (Supply Chain) - Queretaro site in Mexico About Abbott Abbott is a global healthcare leader, creating breakthrough science to improve people’s health. We’re always looking towards the future, anticipating changes in medical science and technology. 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. Main Purpose of the role Accurately capture the nonconformities identified by the Quality area (Incoming Inspection) for raw materials or finished products in the EPIQ system. Verify that Nonconforming Material Reports (NCMR) are correctly documented, signed, and filed for audits. Provide support in root cause analysis to ensure that corrective actions are documented and closed within established timelines. Main Responsabilities Record, monitor, and file documentation of nonconforming materials (NCMR). Serve as a liaison between the Quality, Engineering, and Supply Chain departments for documenting material-related CAPAs. Report quality metrics and indicators related to recurring material issues and their impact on the production line. Document quality failures of received materials and follow up on supplier responses to ensure corrective actions are implemented at the source. Qualifications Bachelor’s Degree in Industrial Engineering or related field. 2 years of recent experience in related activities. Proficiency in Power BI and Advanced Excel. Must Experience with dashboards, metrics, and KPIs for the area. Must Document management and control (QMS). Language Proficiency: Intermediate Commands of English / Required Experience managing claims, tracking information, and learning the CAPA methodology. Qualifications Knowledge of problem‑solving tools. Experience as an Audit Champion in internal or Supply Chain audits. CAPA certification or advanced knowledge. 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.

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Responsibilities

The main purpose involves accurately capturing nonconformities for raw materials or finished products in the EPIQ system, verifying NCMR documentation, and supporting root cause analysis for corrective actions. Responsibilities include recording and filing nonconforming material documentation, serving as a liaison for CAPAs, reporting quality metrics, and following up on supplier corrective actions.