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Location
In office (Reynosa)
Seniority
Junior · 2+ years exp
Employment
Full-Time

Confirmed on the employer's own hiring board on Nov 1, 2026. First seen by Alion on Sep 23, 2026. Essity scores A on the Alion truth index.

Overview
Company
Impact
Profile match
Essity is a Swedish hygiene and health company headquartered in Stockholm, making consumer tissue, incontinence and feminine care products, professional hygiene solutions and medical products such as wound care and compression garments. The group was spun off from SCA in 2017, sells brands including TENA, Tork, Libero, Leukoplast and JOBST, and has its North American headquarters in Philadelphia. It hires machine operators, maintenance technicians, warehouse staff, demand planners, key account managers, clinical specialists and marketing interns across Europe and the Americas.

Quality Systems Specialist

Introduction

Ensure that the processes within the QMS comply with internal and external requirements, are continually improved based on data and that deviations are properly investigated, and appropriate corrective actions are implemented.

We're looking for people who embody our values, aren't afraid to challenge, innovate, experiment, and move at a fast pace. We're always looking for ways to improve our products and ourselves. If this is you, we'd love to talk.

About the Role

The Quality Systems Specialist is responsible to create and administrate in SAP /PLM platform the technical documentation (Product and Raw materials Specifications, Prints) for all manufactured products in Reynosa PC, interacts with Legal Manufacturer in USA to require or send approvals related product changes.

What You Will Do

  • SAP / PLM_ Administrator for technical documentation (products specification/JB2. Raw materials) for all manufactured products in Reynosa.
  • Main contact between Legal Manufacturer in USA and Reynosa team related product changes process.
  • GMS (Global Management System) Administrator for QMS documents_ Reynosa & Hidalgo DC.
  • Assists associates in understanding and maintaining the QMS for Reynosa & Hidalgo DC.
  • Software validation administrator for all Reynosa processes.
  • Internal Auditor (ISO 13485:2016, FDA (21 CFR Part 820) and NOM-241-SSA1-2021 requirements).
  • CAPA/Deviation administration.
  • Monitoring trends about QMS (and reporting).
  • Training personnel on QMS.
  • Participating in internal / external regulatory and customer audits.

Who You Are

  • Bachelor’s degree in engineering field preferred.
  • 2 years of experience in related position or similar.
  • Strong knowledge of ISO 13485:2016, FDA (21 CFR Part 820) and NOM-241-SSA1-2021 requirements.
  • Excellent writing and communications skills.
  • Experience in Microsoft office and database applications /platforms.
  • Experience and great interpersonal skills for daily in-person / virtual, email, and interaction with employees.
  • Bilingual English/ Spanish.
  • Goal Oriented, Proactive, and Collaborative.
  • Proven experience with establishing and prioritizing tasks and objectives to manage time and resources appropriately.

What We Can Offer You

Our purpose, Breaking Barriers to Well-Being, provides meaning to everything we do. Join us to improve well-being for people and drive positive change for society and the environment. At Essity, you'll feel valued, empowered to grow, and challenged to achieve business results in a collaborative and open atmosphere. Innovate for Good | Excel Together | Be You with Us

Reynosa Villa Florida

#EstamosContratando #OfertaDeTrabajo #Reclutamiento #Talento

#Management Systems Specialist #Quality #TrabajoEnEquipo #DesarrolloProfesional #Innovación #Sostenibilidad

Application End Date:

07 nov 2026

Job Requisition ID:

Essity265519
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