ICU Medical

ICU Medical

Manufactura de productos médicos.

Corporativo

Giro

Maquiladora (Export.)

Actividad principal

Manufactura de productos médicos.

Número de empleados

3000

Sitio Web corporativo

Información

ICU Medical connects patients and caregivers through safe, life saving, life enhancing IV therapy products, systems, and services. Since IV therapy is our only business, meeting your IV needs with quality products and consistent supply is our only concern. We are 100% focused on bringing you intuitive, patient-centric IV products and services that provide meaningful clinical differentiation, consistent innovation, and superior value. We design our products to work within your existing workflows to minimize disruption and maximize the time you spend with patients. Together, we help forge the human and emotional connections that enhance clinical experience and are the essence of outstanding quality of care. For more than three decades, we have been dedicated to a singular purpose—improving the safety and efficiency of IV therapy. With the acquisition of Hospira Infusion Systems from Pfizer in 2017, we became the only company to focus exclusively on IV therapy across the continuum of care.

11 puestos de Trabajo

Validation Engineer II

• Bachelor’s degree in Engineering required. • 3–5 years of experience in a similar position. • Manufacturing experience in the medical device industry. • Thorough understanding and broad application of technical principles, theories, and concepts within the engineering field. • Ability to clearly communicate ideas and concepts verbally and in writing in both Spanish and English. • Critical thinking. • Ability to organize resources and establish priorities. • Ability to assign tasks and responsibilities. • Basic knowledge of administration and management. • Ability to follow procedures. • Ability to interact with, develop, and motivate personnel. • Proficiency in basic computer programs (MS Office, Microsoft Project, AutoCAD, Visio, Minitab). • Ability to establish and maintain effective working relationships with employees from different departments. • Ability to work with integrity and build trust. • Intermediate problem-solving and analytical skills. • Ability to critically review and interpret technical documentation. • Ability to work accurately with attention to detail. • Ability to manage multiple priorities and meet key deadlines under pressure through effective time-management skills. • Works under general supervision, with direction provided in terms of broadly defined objectives and desired results. • Continuously monitors the progress of activities or projects and evaluates results. • Independently plans, schedules, conducts, or coordinates detailed phases of assigned tasks or projects.

Septiembre 24 2026 en Tijuana

Tooling Engineer II

Knowledge and Skills Strong knowledge of plastic part design for manufacturability, and plastic processing. Knowledge and experience with cold and hot runner high cavitation tools. Knowledge of mold manufacturing processes and their capabilities. Proficient in Solid works or similar. Working knowledge of statistical tools (e.g., Minitab) for DOE, SPC, Gage R&R, and process capability (Ppk/Cpk) analysis, including normality testing. Working knowledge of 3D scanning / CMM metrology software (e.g., ZEISS INSPECT) for dimensional verification against print and CAD models. Strong skills in project scheduling and SMART-goal based project management. Demonstrate problem analysis skills and provide solutions. Review and understand tool & product drawings, tolerance stack up, understanding molding processing documents, data collection and analysis and development of standard work instructions. Working proficiency in English (written and verbal) sufficient to prepare technical reports and deliver project updates to multi-site and global stakeholders. Strong self-management, accountability, and proactive communication — reliably reports project status without prompting. Minimum Qualifications, Education and Experience BS in Mechanical Engineering or equivalent. In lieu of a degree a combination of training and experience will be considered. Min 3 - 5 yrs. experience in the Medical Device or Engineering Industry. Scientific molding/RJG molding knowledge/training. Mold Simulation experience. Experience with Silicone Molding. Experience with IQ/OQ/PQ process validation in an FDA 21 CFR 820 / ISO 13485-regulated environment preferred. Prior experience with mold or line insourcing, technology transfer, or multi-site project coordination is a strong plus.

Octubre 07 2026 en Tijuana