Manufacturing quality assurance engineer
hoy
*about wsa*:
ws audiology combines over 140 years of experience in pioneering better solutions to help people with hearing loss. With a passion for impact, our around 12.000 employees are committed to achieving our purpose: wonderful sound for all. With brands like signia, widex, audio service, rexton and vibe, and with diverse assets across wholesale, retail, online, managed care and diagnostic solutions, we are active in over 125 markets. Going beyond together, we achieve annual revenues of around eur 2 billion.
quality assurance engineer iii
hoy
why merit?
en merit medical, nuestra misión es desarrollar dispositivos médicos innovadores que mejoren vidas. Nuestro objetivo es integrar y desarrollar a gente que quiere construir a través de trabajo duro, en equipo y comprometido, dispositivos que salvan vidas. Juntos estamos haciendo la diferencia en la vida de pacientes de todo el mundo.
essential functions performed
1. Independently evaluates, selects, and applies standard engineering techniques, procedures, and criteria, using judgment in making minor adaptations and modifications.
2. Investigates a moderate number of engineering variables in completing assignments that have clear and defined objectives.
3. Works independently on standard projects while assistance is furnished on unusual problems.
4. Responsible for risk management documentation for assigned product line(s) or processes; identifies and updates failure modes and related process/product improvements by facilitating teams and implementing required changes.
5. Reviews, approves and generates engineering change notifications (ecns) to update or generate: verification, validation, monitoring and inspection methods, procedures, and test protocols; specific to assigned product line(s) and processes and production control(s).
6. Evaluates and participates in the selection of suppliers by monitoring supplier performance, through collection and trending of data and performing supplier quality audits, as required.
7. Reviews nonconformance records (internal/external) to determine: disposition, root cause and need for corrective and preventive actions.
8. Ensures containment (identification, segregation and reconciliation) of nonconforming product has been performed, to prevent unintended use.
9. Identifies and implements any changes necessary to ensure and maintain the continued suitability and effectiveness of the quality management system through the use of: quality policy, quality objectives, audit results, analysis of data, etc.
10. Evaluates the work environment in which product is manufactured, and ensures it is adequately environmentally controlled and monitored, with sufficient personnel and safety production controls.
11. May participate in design and development activities.
12. Performs other related duties and tasks as required.
essential physical/environmental demands
- lifting - not to exceed 50 lbs. - local practice may apply.
- writing
- sitting
- standing
- bending
- vision
- color perception
- depth perception
- reading
- field of vision/peripheral
- fine motor skills
- noise
- chemical vapors
summary of minimum qualifications
- education and/or experience equivalent to a bachelor's degree in engineering or related field with five years quality engineering experience
- strong interpersonal, organizational, and verbal and written communication skills and the ability to work effectively as a team member.
- demonstrated working knowledge of 21 cfr 820 (quality systems medical devices), iso 13485, iso14791, and other medical device related standards.
- proven ability to work effectively in a team environment through conflict resolution and negotiations.
- working knowledge of statistical methodologies, quality control and manufacturing tools, such as applied statistics, lean manufacturing, six sigma, etc.
- demonstrated computer skills preferably spreadsheets, word processing, database and other applicable software programs.
preferred qualifications
- medical device experience or equivalent experience in a regulated industry.
- experience with smartcapa, oracle and crystal reports.
- experience handling deviations, investigations and capas.
competencies
- engineering variable analysis
- plans/surveys/structures/equipment
- supervisory assistance
- special projects/ecn's/prototype creation
- nc 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.
como integrante de merit, eres elegible a:
seguro de vida y gastos funerarios.
servicio médico en planta extensivo a familia.
2 días adicionales de festivo (viernes santo y navidad).
fondo de ahorro sin tope.
bono anual por resultados.
comida gratis.
academia merit - capacitación constante.
comité de responsabilidad social.
quality engineer
hoy
*main goal*
responsible to validate and verifying manufacturing systems; including process documentation, controls and optimization through the life of the product to ensure internal quality, customer satisfaction and drive automotive culture. Quality engineer seeks and promotes the quality continuous improvement of the manufacturing processes on current and transfers businesses in accordance with the quality management system.
*responsibilities*:
contribute to the sqdci metrics of the focus factory.
uses daily production data (internal and external ppm’s., etc.) to work with the operations team on developing and executing corrective actions plans to drive continuous improvement.
perform statistical studies to determine data behavior and propose actions along with the operations core team.
communicate and interact with employees in regards of customer satisfaction to build improvement commitment actions (8ds or a3s) towards automotive quality culture.
manage quality metrics such as external-internal ppm’s, customer complain.
validate manufacturing the assembly lines through the process documentation (pfmea, wis, control plan, flow chart, procedures) and ppap - when applicable - when process or product requires changes (minor or major). In case of issues in manufacturing, stop shipment or production to correct quality problems.
work with adherence to the qms in the process in order to review the changes being implemented accordingly.
maintain effective communication with customer through the follow up on complaints (8ds) to ensure customer satisfaction and improve score cards per eaton's quality system.
perform corrective actions coming from the rma process (return material authorization), drive deployment of eaton quality system.
audit and address employee actions or behavior to ensure adherence with required qms policies and procedures.
perform layered process audits (lpa) as required.
participate in apqp & ppap documentation and preparation and in continuous improvement activities as well.
train personnel in qms as required or needed.
*ehs responsibilities*
- separate hazardous waste from the common waste.
- place hazardous waste (gloves, rags, etc.) in assigned containers.
- keep clean the work área contaminant free.
- do not waste water.
- report any activity that may jeopardize my safety and the environment.
- identify and properly dispose all the chemicals that may contaminate the environment.
- ensure the correct container for the disposal of hazardous waste (identified containers and containers to prevent spills).
- report the entry of new chemicals required for maintenance purposes due to mantain a record updated and assure the compliance of the correct handling of them.
- contain oil spills and repair as necessary.
*#li-ma1*
*qualifications*:
*preferred education level*
- bachelor’s degree in industrial engineering, electronics or mechanics (or similar)
*years and area of experience required*
- 3-5 years of experience in automotive and electronic manufacturing.
*technical knowledge*
- strong knowledge on quality tools (apqp, msa, spc, ppap), 3-5 years of experience solving qa issues, implementing process controls and process improvements.
- strong knowledge of electronic standards and esd.
- strong knowledge of iso9001/iatf16949 standards and automotive practices.
*soft skills*
- strong written and verbal communication skills in english and spanish.
- highly skilled on ms project, minitab, 8d methodology & problem-solving tools.
- cqe certified by asq
- (certificate quality engineer) (preferred).
what you will get from us
eaton’s mission is to improve the quality of life and the environment through the use of power management technologies and services. We provide sustainable solutions that help our customers effectively manage electrical, hydraulic and mechanical power - more safely, more efficiently and more reliably. Making what matters work at eaton takes the passion of every employee around the world. We create an environment where creativity, invention and discovery become reality, each day. It’s where bold, bright professionals like you can reach your full potential—and where you can help us reach ours. Eaton’s 2020 revenues were $17.9 billion, and we sell products to customers in more than 175 countries. We have approximately 85,000 employees.
we make work exciting, engaging and meaningful for our employees through our dedication to tackling some of the toughest power management challenges on the planet and by never losing sight of what matters. Our culture is built on a strong commitment to practicing our core values and supporting our employees with the tools they need to succeed. We pledge to always foster a diverse and inclusive environment, including inclusion resource groups that bring together employees who share a common purpose, interest or background. In the past year, our company has received top employment recognition by th
quality engineer
hoy
*descripción y detalle de las actividades*
- quality assurance - analysis of customer data (complaints/issues). Reviewing, auditing processes. Audit the correct methods of inspection of materials and processes through the use of approved procedures to ensure their quality in all stages of manufacturing. Surveillance of calibrated equipment and calibration process. Maintain the standards according to applicable regulation and the gmp, for the quality and conformation of the product. Analyze the necessary statistics to be able to monitor the non-conforming product.costumer complaints - contribute with manufacturing during complaint investigations and investigation of reported issues.maintaining the standards according to the fda and the gmp, for the quality and conformation of the product.qms - support qms in local document control system according to global and regulatory requirements. Support qms sustaining of the global capa system according to regulatory requirement and support capa owners during all capa phases. To monitor local kpis and perform data analysis and track action items out of the management review and qit. To participate as during in process inspection audits. Support operations department with change control system. Provide the necessary training to all the personnel involved to support the needs of training system of the quality department.process validation - quality representative to review on ipl (initial production lot) finding and result. Quality representative to review validation protocols and records. Quality representative to review pfmea. Maintain updated mvp and pfmea.distribution quality assurancesupport distribution qa/sqm when needed
*experiência y requisitos*
- profess. Knowl.: gdp, statistical analysis, six sigma or similar, iso 13485, management of work teams,methodologies: presentation and training capabilities, gmp, quality controlsoft skills: communication and team playerproficient englishdesired: experience working with colleagues overseas in us, europe and asia.at least 3-5 years experience in qms of medical device manufacturer. Experience in local and global project management.
*organización*
- wsa*giro*
- medicina*actividad principal*
- manufactura y distribucion*número de empleados*
- 600- mostrar más información
*número de vacantes* 1*área* calidad*contrato* permanente*turno* diurno*jornada* tiempo completo*estudios* carrera profesional*inglés *hablado: 85%, escrito: 85%*sexo* indistinto
quality engineer
hoy
descripción y detalle de las actividades
experiência y requisitos
organización
springs window fashions de tijuana, s. de r.l. de c.v.
giro
maquiladora (export.)
actividad principal
fabricación de persianas.
número de empleados
1500
*área* ingeniería
*contrato* permanente
*turno* diurno
*jornada* tiempo completo
*horario* 7:15am a 5:15pm lunes a jueves / 7:15am a 3:15pm viernes
*estudios* carrera profesional
*inglés *hablado: 80%, escrito: 80%
*sexo* indistinto
*edad* 18 - 65 años
quality engineer
hoy
*quality engineer*
*what you’ll do*:
job summary - coordinate activities of quality auditors. - coordinate and participate in meetings related to customer complaints, participate and validate the corrective actions. - coordinate reports of corrective actions defined to solve problems reported by customer. i.e.: 8d, 5 why, or reports of part analysis. - monitoring and analysis data of process audits and statistical process controls and define the corrective actions. - prepare and review hip (product inspection sheet) and process audits. - coordinate initial investigations of customer complains. - coordination of containments of material due customer or internal issues. - participate in run of new launches. - support to complete 18 points of ppap. - participate and coordinate engineering changes applicable. - participate as owner in changes of documentation: control plan, pfmea. - follow up to material contained in mrb. Strategic context and challenges - support to production cells. - support to amg - interaction with supplier quality area, customer quality area, product engineering. Deliverables - reduce nce-p. - on time zero defect workshops. - read-across implementation (cat a). - implement locked red bin. - scrap reduction from.
*what is required*:
functional competencies - monitoring and analysis data of process audits and statistical process controls and define the corrective actions. - pfmea and control plan knowledge. - spc. - 8ds methodology. - process engineering personal characteristics enabling success - customer focused. - lack of adherence of standards education - bachelor degree. Previous experience - automotive manufacturing experience. Languages - english
*what’s in it for you*:
- attractive compensation package
- recognition awards, company events, family events, university discount options and many more perks.
- gender pay equality
autoliv is proud to be an equal opportunity employer. Autoliv does not discriminate in any aspect of employment based on race, color, religion, national origin, ancestry, gender, sexual orientation, gender identify and/or expression, age, disability, or any other characteristic protected by federal, state, or local employment discrimination laws where autoliv does business.
engineer, quality assurance ii
hoy
*date*:sep 4, 2024
*location*: tijuana, mexico, mexico, 2225
*company*:belden, inc
*belong. Believe. Be you. Belden.*
propel your career surrounded by a diverse team of innovative, goal-oriented individuals who are pursuing the next generation of connectivity solutions. At belden, you’ll participate in work that will challenge you and position you to excel. You’ll collaborate with colleagues from around the world, gaining exposure to a broad base of expertise and perspectives.
together, we’ll continue on a journey of innovation, creating a connected world and paving the way for automation. Join us and let’s build the future.
*job summary*:
sera un ingeniero en control de calidad que pueda adaptar el proceso de pruebas que utiliza para las diferentes variaciones de los productos, al tiempo que se esfuerza por lograr la calidad en cada liberaci#n delproducto, y debe ser alguien que probablemente tiene las habilidades adecuadas para ser un ingeniero en control de proceso y dar seguimiento da los indicadores de desempe#o del #rea de calidad, dara cumplimiento de est#ndares regulatorios, sera responsable del seguimiento y control de pruebas de laboratorio y equipo y pruebas de medici#n y sera responsable de la administraci#n de quejas de clientes.
*responsibilities*:
*required skills and experience*
sistema de calidad iso 9000.manejo de herramientas de calidad y manufactura esbelta.control estad#stico de procesoacciones correctivas y preventivas en 8 disciplinas.manejo de quejas de clientes.elaboraci#n y manejo de plan de control.manejo de indicadores de desempe#o.experiência en pruebas el#ctricas.conocimiento de metrolog#a y medici#n.
*let’s write the next 100 years together.*
join a global community striving to improve connectivity and security. The work we’re doing puts our people on the front lines of impacting lives and shaping the future. Propel your story of innovation by helping belden write the next chapter in ours. Shape your future at belden.
- these statements are intended to describe the general nature and level of work involved for this job. It is not an exhaustive list of all responsibilities, duties and skills required of this job.
process quality or supplier quality engineer
address:
alejandro graham bell 19285 interior a-1 y a-2, tomas alva edison, 22163 b.c., mexico
job responsibilities:
i. Process quality assurance (pqa)
* oversee process quality management operations and develop customer-centric quality production strategies.
* improve quality performance at the customer end, conduct closed-loop analysis of customer issues, and ensure alignment with customer expectations to achieve satisfaction.
* drive continuous quality improvements at local manufacturing sites and implement early warning systems for anomaly detection.
ii. Supplier quality assurance (sqa)
* supplier quality enhancement : collaborate with suppliers to achieve annual quality objectives, driving internal quality improvements to ensure compliance with material quality standards.
* quality initiatives : develop and execute targeted improvement projects based on performance metrics and quality trends.
* new product development support : monitor and resolve material-related issues during new product phases, ensuring design, mold, and supplier corrections are fully implemented.
* abnormality resolution : investigate material-related defects (incoming, in-process, and market failures), issue 8d reports, and ensure timely root-cause resolution.
* incoming material control : establish standardized inspection procedures (sip) aligned with customer requirements (iis) and ensure consistency in material specifications across internal processes.
* supplier accountability : reclaim costs from suppliers for losses caused by defective materials and ensure formal acknowledgment of resolutions.
job requirement:
* bachelor's degree or above. Safety science and engineering, automation, industrial engineering or other related major.
* related experience is preferred.
quality engineer(j48805)
process quality or supplier quality engineer
address:
alejandro graham bell 19285 interior a-1 y a-2, tomas alva edison, 22163 b.c., mexico
job responsibilities:
i. Process quality assurance (pqa)
* oversee process quality management operations and develop customer-centric quality production strategies.
* improve quality performance at the customer end, conduct closed-loop analysis of customer issues, and ensure alignment with customer expectations to achieve satisfaction.
* drive continuous quality improvements at local manufacturing sites and implement early warning systems for anomaly detection.
ii. Supplier quality assurance (sqa)
* supplier quality enhancement: collaborate with suppliers to achieve annual quality objectives, driving internal quality improvements to ensure compliance with material quality standards.
* quality initiatives: develop and execute targeted improvement projects based on performance metrics and quality trends.
* new product development support: monitor and resolve material-related issues during new product phases, ensuring design, mold, and supplier corrections are fully implemented.
* abnormality resolution: investigate material-related defects (incoming, in-process, and market failures), issue 8d reports, and ensure timely root-cause resolution.
* incoming material control: establish standardized inspection procedures (sip) aligned with customer requirements (iis) and ensure consistency in material specifications across internal processes.
* supplier accountability: reclaim costs from suppliers for losses caused by defective materials and ensure formal acknowledgment of resolutions.
job requirement:
* bachelor's degree or above. Safety science and engineering, automation, industrial engineering or other related major.
* related experience is preferred.
quality engineer(j48805)
hoy
process quality or supplier quality engineer
address:
alejandro graham bell 19285 interior a-1 y a-2, tomas alva edison, 22163 b.c., mexico
job responsibilities:
i. Process quality assurance (pqa)
* oversee process quality management operations and develop customer-centric quality production strategies.
* improve quality performance at the customer end, conduct closed-loop analysis of customer issues, and ensure alignment with customer expectations to achieve satisfaction.
* drive continuous quality improvements at local manufacturing sites and implement early warning systems for anomaly detection.
ii. Supplier quality assurance (sqa)
* supplier quality enhancement: collaborate with suppliers to achieve annual quality objectives, driving internal quality improvements to ensure compliance with material quality standards.
* quality initiatives: develop and execute targeted improvement projects based on performance metrics and quality trends.
* new product development support: monitor and resolve material-related issues during new product phases, ensuring design, mold, and supplier corrections are fully implemented.
* abnormality resolution: investigate material-related defects (incoming, in-process, and market failures), issue 8d reports, and ensure timely root-cause resolution.
* incoming material control: establish standardized inspection procedures (sip) aligned with customer requirements (iis) and ensure consistency in material specifications across internal processes.
* supplier accountability: reclaim costs from suppliers for losses caused by defective materials and ensure formal acknowledgment of resolutions.
job requirement:
* bachelor's degree or above. Safety science and engineering, automation, industrial engineering or other related major.
* related experience is preferred.
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