Supervisor de producción para tintorería y acabado
gran empresa líder en la industria textil, está en busca de tu talento como:
zona a laborar: naucalpan, lomas verdes.
ofrecemos
* sueldo mensual
* seguro social imss
* vacaciones
* aguinaldo
* prima vacacional
* excelente ambiente laboral
* estabilidad laboral
requisitos
* escolaridad: ingeniería textil.
* experiencia mínima 5 años en el mismo puesto.
* conocimientos en matizados, formulas, acabado, teñido, máquinas de teñido, ramas).
actividades a desempeñar
* planear, verificar y programar el área de producción, así como el cumplimiento del mismo.
* supervisar que se trabaje con las prioridades.
* seguimiento de recetas programadas.
* trabajo en equipo con calidad en cuanto a los tonos de baño, para ser enviado a acabado.
* realizar proceso de matizado en conjunto con calidad y cocina de colores.
* supervisar que la rama trabaje de acuerdo con las prioridades de las recetas.
* asignación de actividades así como supervisar al personal para que se lleven a cabo.
* cargar recetas en el sistema.
* organizar el programa de producción para los siguientes turnos.
notas
no pierdas la oportunidad laboral. Postúlate por este medio o envía tu cv con el nombre de la vacante.
respondemos de manera inmediata
tipo de puesto: tiempo completo
salario: $13,000.00 al mes
horario: turno mixto
prestaciones: opción a contrato indefinido
educación: licenciatura terminada (deseable)
experiencia: producción giro textil: 5 años (deseable)
hoy
lider en producción cnc
hoy
te estamos buscando, por expansión solicitamos líder en producción cnc. ¡no lo pienses y únete a nuestro equipo de trabajo!
requisitos
* ingeniero mecánico, mecatrónica, industrial, de proceso o afín. (titulado)
* mínimo 5 años de experiencia en puesto similar
conocimiento y habilidades
* manipulación de centro de maquinado
* software mastercam x9 en adelante
* conocimiento en máquinas de 5 ejes
* plus maquinado de 5 ejes simultáneos
* software de programación cnc
* máquinas cnc
* manejo de personal 30 a 50 operadores y ayudantes a su cargo
* herramientas de corte
* suministrar a los ajustadores para la fabricación de piezas planeadas
* mantener las máquinas con un stock
* definir la mejor estrategia de maquinado para cada pieza
* asistencia en maquinados de estructuras a ajustadores sr.
* asegurar que cuenten con los archivos 3d y planos de las piezas a fabricar
* capacitar al personal
* responsable de manufactura
* cumplimiento de metas
* monitoreo de tiempos
ofrecemos
* sueldo con base a competencias desde $25,000 a $5,000
* prestaciones de ley desde el día uno
* estabilidad laboral
tipo de puesto: tiempo completo
salario: $5,000.00 - 35,000.00 al mes
horario: incluye fines de semana; turno de 10 horas
lugar de trabajo: una ubicación
hoy
why patients need you
everything we do, every day, is in line with an unwavering commitment to the quality and the delivery of safe and effective products to patients. Our science and risk-based compliant quality culture is flexible, innovative and customer oriented. Whether you are involved in development, maintenance, compliance or analysis through research programs, your contribution will directly impact patients.
what you will achieve
in your role, you have the all - important task of preparation and review of required documentation, such as good manufacturing practices, good laboratory practices (glp), good clinical practices (gcp) manuals. You will be relied on to prepare procedure manuals, quality control manuals, engineering documents, manufacturing instructions and change authorizations in accordance with company policy and government regulations. Your skills will help you implement related documentation systems, propose change control processes and coordinate the review of procedures and forms. You will also provide input on quality control procedures and r&d documentation.
as a senior associate, your knowledge and skills will contribute towards the goals and objectives of the team. Your focus and ability to meet team targets will help in completing important deliverables on time. Your innovative use of communication tools and techniques will make it easy to manage difficult issues and help in establishing consensus between teams.
it is your dedication and hard work that will make it possible for pfizer’s customers and patients to receive the medicines they need, when they need them.
how you will achieve it
* contribute to the completion of moderately complex projects.
* manage own time to meet agreed targets.
* develop plans for short-term work activities on own projects (timelines, work plans, deliverables).
* provide document technical writing, editing and design support to other team members and supported site departments.
* create, maintain and update policies, procedures, specifications, data-entry materials, training materials and other technical documents in accordance with company and site standards.
* contribute to the completion of project tasks and/or milestones related to document creation and revision. Organizes own work to meet required project task deadlines.
* collaborate with functional area and network customers, as needed, to develop new and revised documents, including providing suggestions for suitable terminology, content and format and assist in tracking each revision through the review and approval workflows.
* collect and analyze information necessary to develop documents that are easily understood, readily usable for consistency in training and performance and reflect the most effective systems to reduce misunderstanding or undesired outcomes.
* ensure good laboratory practices and safety practices within the team.
* configure master data objects with respect to approved specification.
* assist in the design and development of site style guidance and document formatting standards to meet business and end user needs. Evaluate and recommend revisions to existing standards and guidelines.
* work closely with project teams to ensure that documents are accurate, internally consistent and meet intended purpose. Prepare documents in accordance with internal standards and external regulatory guidelines.
qualifications
must-have
* bachelor’s degree and 3+ years of experience.
* strong understanding of cgmp, data integrity and alcoa principles.
* strong organizational and communication skills.
nice-to-have
* master’s degree and relevant pharmaceutical experience.
* demonstrated technical writing experience is desirable.
* strong project management skills.
pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.
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