## Plastics Engineer IApplyremote type: Onsitelocations: Reynosa, TAMPS, MEXtime type: Full timeposted on: Posted Todaytime left to apply: End Date: June 19, 2026 (30+ days left to apply)job requisition id: R **Plastics Engineer I**At **Fresenius Medical Care**, we are the global leader in kidney care, committed to improving the lives of patients with chronic kidney disease. Our mission is to deliver high-quality, innovative products, services, and care across the entire healthcare journey.Guided by our vision—**“Creating a future worth living. For patients. Worldwide. Every day.”**—we work with purpose and compassion, supported by a global team of over 110,000 employees.Within our **Care Enablement** segment, we develop and provide life-sustaining medical products, digital health solutions, and therapies that empower clinical teams and improve patient outcomes. Our **FME Reignite** strategy drives transformation through innovation, efficiency, and sustainable growth.Our values guide how we work:* **We Care** for our patients, each other, and our communities* **We Connect** across teams and borders to deliver excellence together* **We Commit** to doing things the right way—growing with purpose and leading kidney care with integrity and innovationAt our Reynosa plant in Mexico, we are committed to the highest standards in the production of disposable medical products for dialysis treatments. With a dedicated team of more than 3,000 employees across four manufacturing sites, the plant focuses on manufacturing essential components such as hemodialysis disposables, peritoneal dialysis (PD) disposables, hemodialysis (HD) machines, and PD cycler machines.By utilizing advanced technologies to ensure the highest standards in dialysis product manufacturing, we’re not only driving innovation—we’re also creating meaningful change for patients worldwide. Join our passionate team and be part of this global impact.As a **Plastics Engineer I**, you will validate new systems and maintain the validated state of existing systems used to manufacture components, tubing, and resins in the plastics area. You may also support cost-saving projects, process improvements, and cross-functional validation/engineering initiatives. In addition, you will coordinate, review, and evaluate the work of plastics engineering technicians.**Responsibilities:*** Lead engineering project implementations in the molding area, coordinating activities to meet schedule commitments.* Maintain 100% training compliance per the applicable curriculum.* Follow and ensure compliance with current GMP and documentation practices, keeping local procedures updated and compliant.* Identify and verify machine/peripheral equipment manuals, drawings, and dimensional reports for protocol development.* Develop and execute equipment validation protocols (IQ/OQ).* Develop and execute engineering studies per task/project by defining tests that challenge physical/mechanical characteristics per specifications/drawings; document per established procedures.* Support training and execution/verification of physical test methods, from method design through release.* Perform and verify periodic process/equipment reviews in a timely manner and document per effective procedures.* Support Engineering on implementation, innovation, new equipment development, and improvements.* Reconcile material generated during engineering study and validation runs.* Maintain, scan, and archive physical validation/study documentation and peripheral equipment manuals.* Keep the validation list updated per current validation procedures.* Support development of detailed modules/instructions for specific manufacturing process tasks. • Perform annual reviews, temporary deviations, and activities related to engineering project implementation.* Create Change Control Notifications (CCN) and required supporting documentation for process/support document updates.* Create Document Management Change (DMC) for administrative updates and organizational chart revisions.* Train Plastics and Quality personnel prior to executing validation protocols, engineering changes/module creation, and procedure changes.**Qualifications:*** Engineering degree (Industrial preferred).* 2+ years of experience in IQ/OQ/PQ validation schemes.* 2+ years generating, executing, and reporting engineering studies.* 1+ year developing modules, engineering changes, and temporary process deviations.* Medical industry experience desirable; plastics area experience desirable.* 1+ year using basic measurement devices (caliper, micrometer, etc.).* Continuous improvement tools experience (Ishikawa, 5 Whys, DMAIC, etc.).* Strong computer skills required; SPC experience preferred.* Intermediate MS Office; Minitab, Visio, Project.* Bilingual (English/Spanish).**Our Offer for You:**There is a lot you can discover at Fresenius Medical Care, regardless of the field of expertise or level of experience—everything is dedicated to supporting your professional journey.• Whether in front of or behind the scenes, you help make better medicine available to more people worldwide • Individual opportunities for self‐determined career planning and professional development • A corporate culture that encourages innovative thinking—finding the best solution together, not just the fastest one • A team of committed professionals with diverse skills, talents, and experiences • The strength of a successful global corporation combined with the collegial culture of a mid‐sized company#J-18808-Ljbffr