441 empleos de Ingeniería

Engineer III

Merit Medical

SUMMARY OF MINIMUM QUALIFICATIONS • Education equivalent to a Bachelor’s Degree in Engineering or technical field related to the department of assignment or industry with five 5 years previous related experience (title degree is required). • Advanced English level • Ability to apply analytical skills and scientific technical principles in problem solving and development. • Demonstrated computer skills preferably spreadsheets, word processing, database and other applicable software programs. • Strong interpersonal and organizational skills and the ability to work effectively as a team member. • Working knowledge of United States and international standards as applicable to the department. • Strong experience in material changes , including risk assessments, validations, and supporting documentation. • Experience leading low- to medium-impact projects , ensuring compliance with scope, timelines, and regulatory objectives. • Knowledge and experience in validations within the medical device industry , including the development and execution of IQ, OQ, and PQ protocols . • Experience developing and executing validation strategies for product, process, or material changes. • Knowledge of ISO 13485 requirements and practical application within a regulated environment. • Knowledge of European Medical Device Regulation (MDR) requirements, preferably with direct involvement in related projects. COMPETENCIES • Scientific techniques/evaluation/selection/application • Scientific variable analysis • Plans/surveys/structures/equipment • Supervisory assistance • Special projects/ECN's/prototype creation • NCMR causes/corrective actions/dispositions COMMENTS Infectious Control Risk Category II: The risk category explains whether or not employees are likely to come into contact with blood or body fluids while performing their jobs. Risk category II states employment and procedures that may require exposure.

Octubre 19 2026 en Tijuana

Labeling Engineer

Merit Medical

SUMMARY OF MINIMUM QUALIFICATIONS • Education and/or experience equivalent to a Bachelor’s Degree in Engineering or technical field related to the department of assignment or industry with five years previous related experience. • 3–5+ years of experience in labeling, document control, regulatory, quality, or manufacturing engineering • Experience with IFUs, UDI, packaging artwork, and ECO processes • Strong knowledge of FDA, ISO 13485, and EU MDR requirements • Experience using Oracle ERP and NiceLabel (preferred) • Bilingual English–Spanish • BS Engineering or equivalent • Ability to apply analytical skills and scientific technical principles in problem solving and development. • Demonstrated computer skills preferably spreadsheets, word processing, database and other applicable software programs. • Strong interpersonal and organizational skills and the ability to work effectively as a team member. • Working knowledge of United States and international standards as applicable to the department. COMPETENCIES • Scientific techniques/evaluation/selection/application • Scientific variable analysis • Plans/surveys/structures/equipment • Supervisory assistance • Special projects/ECN's/prototype creation • NCMR causes/corrective actions/dispositions COMMENTS Infectious Control Risk Category II: The risk category explains whether or not employees are likely to come into contact with blood or body fluids while performing their jobs. Risk category II states employment and procedures that may require exposure.

Octubre 19 2026 en Tijuana

Sr. NPI Engineer

Amphenol TCS de México, S.A. de C.V.

Key Responsibilities 1. Lead New Product Introduction (NPI) activities from design handoff through manufacturing qualification, production ramp-up, and handover to Operations. 2. Drive manufacturing readiness, ensuring equipment, tooling, fixtures, documentation, materials, quality controls, and resources are ready to support product launch. 3. Collaborate closely with Product Engineering, Project Management, Quality, Manufacturing, Materials, Automation, Test Engineering, and Operations. 4. Review product designs and technical requirements to ensure Design for Manufacturability (DFM) and production readiness. 5. Develop and maintain NPI project plans, milestones, risks, action trackers, and deliverables to ensure execution against committed timelines. 6. Lead and execute PFMEA, Process Flow, Control Plan, IQ/OQ/PQ, capability studies, MSA/Gage R&R, pilot builds, PVT, and First Article Inspection (FAI) activities. 7. Define and validate manufacturing processes, equipment, tooling, fixtures, test methods, and inspection requirements. 8. Identify manufacturing risks and drive corrective actions, root-cause analysis, and continuous improvement. 9. Support process capability, yield, cycle time, OEE, quality, and cost improvement initiatives during qualification and ramp-up. 10. Coordinate with suppliers and contract manufacturers to ensure equipment, tooling, material, and process readiness. 11. Lead technical knowledge transfer and manufacturing process transfers between global manufacturing sites when required. 12. Own and maintain key manufacturing documentation, including Process Flow, Standard Operating Procedures/Work Instructions, PFMEA, Control Plan, qualification reports, and Product History Records. 13. Provide technical leadership and guidance to NPI Engineers, technicians, and cross-functional teams during product launches. 14. Communicate project status, risks, recovery plans, and escalations effectively to engineering and management teams.

Octubre 16 2026 en Mexicali