Descripción y detalle de las actividades
- plans and leads process development activities including design, prototyping, testing (verification and validation) risk management/process fmea, process characterization, and documentation. Participate in the redesign of existing processes to improve quality, utilize automated production techniques, optimize process capabilities, and product improvements in a more cost-effective manner.
- provide technical expertise in developing new assembly tooling, guidance in processing and troubleshooting.
- interface with new product development and manufacturing to understand product requirements and establish design criteria for manufacturing processes.
- interact with suppliers to define and evaluate materials and processes needed for effective execution of process development activities.
- responsible for validations, iq/oq/pq, product production within agreed upon scope, budget, timeline, and quality.
- interact with suppliers to debug problems with production parts, processes and equipment.
- interface with procurement to obtain quotations, purchase components.
- advise other engineering personnel on technical aspects of product/process design, assembly techniques and the validation of processes.
- interface with engineers, manufacturing, and lab technicians to design and develop new fixtures and tooling.
- support product related technical problems in engineering and manufacturing areas.
- develop comprehensive manufacturing strategy for all projects that will include alternate methods for component acquisition including timelines, costs, capital, expense, risk, and recommendations
- interface with suppliers and manufacturing when implementing new processes.
- coordinate with sbu planning for initial and ongoing supply, safety stock, distribution management including shelf life, and alternate suppliers for critical components
- in conjunction with quality establish aql levels for each component and incoming inspection criteria including location, method of measurement, consistent data recording, disposition.
Experiência y requisitos
- bachelor level degree in engineering
- 3+ years previous experience in related field (e.g., medical device manufacturing and assembly, disposables manufacturing processes, plastics, automation).
- strong bilingual (english/spanish) communication and presentation skills (written and verbal).
- ability to work effectively with other product development team members.
- experience in the medical industry / knowledge of iso 13485.
* the site to work is in tecate site.
Beneficios
- beneficios de acuerdo a la lft
- fondo de ahorro
- transporte
- utilidades garantizadas
- servicios medicos en planta
- comedor
- caja de ahorro
- comedor
- fondo de ahorro
- servicios médicos en planta
*número de vacantes* 1
*área* ingeniería
*contrato* permanente
*modalidad* presencial
*turno* diurno
*jornada* tiempo completo
*estudios* carrera con título profesional
*inglés*hablado: avanzado, escrito: avanzado
*disponibilidad p. viajar* si