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Essity seeks a Quality Systems Specialist to create and administer technical documentation in SAP/PLM for Reynosa products, coordinating with the USA legal manufacturer for approvals related to product changes.
You will act as QMS administrator for Reynosa & Hidalgo DC, support associates, oversee software validation, CAPA/deviations, and participate in audits while ensuring compliance with ISO 13485:2016, FDA 21 CFR Part 820, and NOM-241-SSA1-2021.
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.
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.
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