Quality control technician
the quality control technician provides technical support to functional areas of quality engineering, coordinating quality control inspections on products, materials, components, parts, etc. at various stages of the production process to ensure compliance with the established standards.
responsibilities
* follow up on quality reviews by reporting any anomaly.
* review main incidents of work cells to reach a team solution.
* assist the quality engineer by troubleshooting and determining actions in the process.
* recommend new or improved methods, procedures and quality standards.
* support new or improved methods, procedures and quality standards.
* support the reduction of quality events, through the audits in the work stations, ensuring the delivery of a product according to specifications.
* propose continuous improvement actions in terms of quality and efficiency of the manufacturing or inspection process.
* control non-conforming materials and supplier rejections.
* support with calibration plans of measurement equipment.
experience / qualifications
* relevant work experience or knowledge of the role.
* must be a team player able to work in a fast-paced environment with demonstrated ability to handle multiple competing tasks and demands.
* strong organization, planning and time management skills to achieve results.
* self-accountable to achieving goals and standards.
* proficient in microsoft office programs (outlook, word, powerpoint, and excel).
quality control supervisor – ppi
as a quality control supervisor you will lead a dedicated team of quality control professionals, providing guidance and support to maintain our commitment to exceptional quality.
responsibilities
* manage and supervise quality control staff to ensure adherence to quality standards and protocols.
* develop and implement quality control policies and procedures to ensure compliance with local, national, and international standards.
* conduct regular inspections and testing of products to assess quality and identify defects or areas for improvement.
* prepare reports on quality metrics, inspection results, and improvement initiatives for management review.
* provide training and mentorship to quality control staff on quality assurance processes and best practices.
* investigate quality issues and implement corrective actions to resolve non-conformities.
* work cross-functionally with production, engineering, and supply chain teams to foster a culture of quality improvement.
* ensure compliance with all relevant regulatory requirements and industry standards.
core skills / competency requirements
* strong knowledge of quality control principles, methodologies, and tools.
* experience with statistical analysis and quality improvement techniques.
* familiarity with regulatory requirements and industry standards iso.
* experience in leading and managing quality control teams.
* ability to analyze data and identify trends for continuous improvement.
education
* bachelor's degree required.
laboratory administrative specialist – vantive
resumen de responsabilidades:
* responsable de realizar actividades administrativas en laboratorio de microbiología y departamento de esterilización.
tareas y responsabilidades esenciales:
1. responsable de someter y dar seguimiento a requisiciones y órdenes de compra de laboratorio.
2. responsable de administrar la recepción de material de laboratorio, entrada a sistema como inventario, dar seguimiento a niveles de inventario y reordenar en base a programa/vigencia de material.
3. responsable de gestionar las muestras de laboratorio por parte de manufactura y post esterilización, así como su cadena de custodia hasta la disponibilidad de las muestras para ejecutar el análisis y su disposición.
4. responsable de dar seguimiento a la recepción y gestión de facturas de laboratorio, incluyendo recepción de materiales y recepción de servicios de análisis solicitados a laboratorios externos.
5. responsable de dar seguimiento a la comunicación con esterilizadoras frente a una eventualidad (e.g. cambios, no conformidades, temas de servicio y/o calidad).
6. responsable de reunir de pruebas de laboratorio y certificados de esterilización para realizar liberación de lotes.
7. responsable de realizar liberación de esterilización y liberación final de producto terminado.
8. responsable de seguimiento a la recepción de reportes de daños en material enilizadoras, recepción física de cajas dañadas en planta y administrar la disposición a material de acuerdo a los procedimientos locales aplicables.
9. dar soporte a actividades relacionadas a su posición solicitadas por departamento de control de calidad.
10. planeación y ejecución de proyectos del departamento de control de calidad asignados por gerencia.
conocimientos / habilidades / capacidades
* conocimiento en manejo de sistema sap y/o jde.
* conocimiento intermedio del idioma inglés (lectura, escritura y conversacional).
* conocimiento deseable básico de finanzas y manejo de inventarios.
* conocimiento en estándares relacionados a la manufactura de dispositivos médicos (e.g. Iso 13485, 21 cfr parte 820, mdsap).
escolaridad
* título profesional de lic. en las áreas de ciencias químicas o biológicas (incluyendo, pero no limitado a: qfb, qi, ing. Químico, ing. Bioquímico, ing. Biomédico y carreras afines).
equal opportunity employer
protective industrial products (pip) is an equal opportunity employer that is committed to diversity and inclusion in the workplace. We prohibit discrimination and harassment of any kind based on race, color, sex, religion, sexual orientation, national origin, disability, genetic information, pregnancy, or any other protected characteristic as outlined by federal, state, or local laws. This commitment applies to all aspects of employment, including hiring, recruiting, promotion, termination, compensation, benefits, training, and development opportunities. We believe that a diverse team strengthens our global success and enriches our culture.
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