Quality Engineer Empleos | Belden, Inc (San Nicolas de los Garza)

Nuevo

Quality IVS Projects Engineer

This role ensures regulatory compliance, supports validations, strengthens techn...

Ubicación

Costa Rica , Cartago

Salario:

No proporcionado

Coloplast

Fecha de expiración

Hasta nuevo aviso

Requisitos

Bachelor’s degree in chemical, Industrial, Electronic, Biotechnology, Electromechanical Engineering, or a related field
A minimum of 5 years of experience in medical device manufacturing with strong QA expertise
English proficiency at B2 level or higher
Strong analytical and data interpretation skills
Demonstrated ability to work effectively with cross‑functional and cross‑site teams
Ability to manage multiple priorities in a fast‑paced environment
Availability to travel approximately 20–25 days per year

Responsabilidades

Defines project requirements, coordinates execution, and ensures that all deliverables meet regulatory, quality, and timeline expectations
Ensures full compliance of project activities with global medical device regulations—including MDSAP, MDR, ISO 13485, and FDA requirements—as well as the Coloplast Management System
Supports internal and external audits through expert knowledge and documentation readiness
Oversee the creation, maintenance, and training of quality documentation for IVS projects. Responsibilities include managing DMRs, specifications, test methods, risk assessments, and change control activities in accordance with corporate and local requirements
Provides oversight for validations related to processes, equipment, software, and test methods, ensuring alignment with regulatory and procedural standards. The role approves protocols and reassesses validations as needed due to risk, regulatory, or process changes, and leads investigations to resolve abnormal test results
Owns non-conforming events and CAPAs related to IVS projects
Leads process and product risk management activities by identifying, evaluating, mitigating, and documenting risks. The engineer also supports the definition of specifications for legacy products and communicates risk status and KPIs to key stakeholders
Coordinates sample collection for design verification testing and ensure proper testing execution through Production and the QA Laboratory
The role maintains accurate and compliant quality documentation for IVS projects and supports Quality Management Review (QMR) requirements
The engineer provides backup support to QA team members when necessary and makes quality‑related decisions within the authorized training scope, ensuring continuity of quality operations across the site

Lo que ofrecemos

Medical insurance
asociation
gym
cafeteria subsidy
free transportation

Tiempo completo

Nuevo

Sr compliance, QA Engineer

As Sr compliance QA Engineer, you will combine responsibilities in CAPA, Complai...

Ubicación

Costa Rica , Cartago

Salario:

No proporcionado

Baxter

Fecha de expiración

Hasta nuevo aviso

Requisitos

Minimum of 4 years of experience in manufacturing processes, quality systems, regulatory compliance, and GMPs within Baxter or in companies producing healthcare devices
Validated knowledge of ISO 9001, ISO 13485, PMD Law, CMDR, MDSAP, CFR 21 and the Manufacturing Maturity Program (CMMI)
Validated experience in auditing systems and certification as an Internal Auditor
Knowledge and experience in Sterility Assurance
University training in Engineering (Production, Industrial, Chemical, Systems, Electrical, Electronics, Electromechanics) or related career
Equivalent experience in production environments with Quality Systems in the medical device manufacturing industry

Responsabilidades

Own the Complaints, CAPA, Risk Management, Hold and Corrective Actions systems, as well as their critical metrics and participation in local, regional and corporate forums
Implement the Internal Audit Program and follow up on corrective and preventive actions
Assess the regulatory alignment of processes and systems
Ensure they follow applicable directives and standards
Coordinate the system for change oversight, making sure changes stay in sync with regulatory requirements
Ensure evaluations of complaint samples, manufacturing investigations, and coordination with Product Surveillance within defined timeframes
Facilitate root cause analysis and ensure complete documentation in CAPA processes
Implement and maintain the risk system, assessing and controlling risks and leading residual risk
Ensure the accurate execution of the Hold process and the corrective field actions (FCA)
Maintain effective communication with productive areas and lead actions to reduce complaints

Lo que ofrecemos

Apoyo a las padres
Educación continua/ Desarrollo profesional
Salud de los empleados y Beneficios de bienestar
Tiempo libre pagado
2 días al año para ser voluntario

Validation Quality Engineer - Innovation Value Stream

Leads the IVS project quality and validation activities, providing technical dir...

Ubicación

Costa Rica , Cartago

Salario:

No proporcionado

Coloplast

Fecha de expiración

Hasta nuevo aviso

Requisitos

Bach. degree in an Engineering field, such industrial, electrical, mechanical, etc.
Understanding and Knowledge of the quality system standards ISO 13485 and ISO 9001.
Experience in regulated industries such MDSAP, MDR, FDA, and corporate QMS requirements (e.g., medical device industry).
Experience with Microsoft Office package (Word, Excel, PowerPoint, Outlook).
Knowledge in statistical techniques and software applications such as JMP, Minitab, etc.
Min. 6-10 years of experience in quality, innovation and validation roles.
Fluent in both spoken and written English
B2+ English level

Responsabilidades

Leads the IVS project quality and validation activities, providing technical direction, ensuring alignment with quality and regulatory standards, and driving successful project execution across cross‑functional teams, ensures product safety, reliability, and compliance with internal and external quality requirements.
The role includes developing and implementing quality control processes, performing risk assessments, and supporting Operations in alignment with the Coloplast Quality Management System.
It also involves executing and maintaining processes, equipment, software, and test method validations throughout their lifecycle.
Validation & Test Method Activities
Quality Assurance & Risk Management
Documentation, Training & Compliance
Audits, Continuous Improvement & Collaboration

Sr Engineer, Quality

This is where your work makes a difference. At Baxter, we believe every person—r...

Ubicación

Costa Rica , Cartago

Salario:

No proporcionado

Baxter

Fecha de expiración

Hasta nuevo aviso

Requisitos

English Language Proficiency
Applying tools for problem solving
Management of statistical concepts for data analysis (trend analysis, control charts, Pareto, among others)
Application of tools for data visualization (Excel, Power BI, Minitab, among others)
Learning agility
Motivation and development of others
Very good analytical/statistical problem-solving skills
Data-driven decision-making
Collaboration (partnership and good interpersonal relationships)
Excellent communication, planning, organization and execution skills, as well as prioritization of their activities

Responsabilidades

Ensures that evaluations of complaint samples are accomplished satisfactorily, conducts the manufacturing investigation of the complaint, and establishes effective communication with Product Surveillance to ensure that the complaint system is completed within the defined timeframes
Work as a team with staff from other areas to define the root cause of non-conformities, ensuring that all elements of the CAPA process are clearly detailed (where applicable)
Ensures that the risk system is implemented in the plant and performs analyses that allow the risk to be evaluated, controlled and identified, as well as handling the residual risk (when applicable)
Ensure the Hold and FCA process (when applicable)
Collaborate with the realization of periodic meetings of Quality Data Review and Management Review
Evaluates, develop and improves procedures related to their areas of responsibility
Keeps track of quality indicators and makes action plans for improvement
Hold regular meetings with your staff to maintain adequate communication and information among your team members
Ensures accurate communication with the production areas about the main problems of product complaints
Actively participates in projects to reduce market complaints

Tiempo completo

Nuevo

Customer Quality Engineer

Ensure the processing, trend analysis and management of customer complaints rela...

Ubicación

France , Pluvigner

Salario:

No proporcionado

Baxter

Fecha de expiración

Hasta nuevo aviso

Requisitos

Master's degree (or equivalent) in a technical field (mechanics, electronics, engineering, data science, industrialization) or any field offering a strong foundation in data analysis
A minimum of 2 years' experience in technical problem management, data analysis, technical customer relations, or product support is a plus
Ability to analyze complex technical problems
Proficiency in coordinating multidisciplinary teams
Excellent written and oral communication skills
Organizational skills, rigor, and a strong customer service orientation
Analytical skills (e.g., understanding trends, interpreting data)
Knowledge of or interest in problem-solving tools (5M, 8D, etc.) and project management tools
Autonomy and strong synthesis skills
Proactive approach

Responsabilidades

Manage and analyze customer complaints, including leveraging field information and providing support for the review of returned parts
Lead trend analyses to meet global and local requirements for tracking and resolving defects, and maintain a high level of customer satisfaction
Actively contribute to cross-functional action plans aimed at continuous product improvement, whether related to design, production, suppliers, or customer service
Ensure clear and regular communication between all teams involved in Product Care activities to guarantee a systemic and aligned approach
Produce structured and reliable reports for internal and external clients to maintain trust and uphold quality commitments

Lo que ofrecemos

Apoyo a las padres
Educación continua/ Desarrollo profesional
Salud de los empleados y Beneficios de bienestar
Tiempo libre pagado
2 días al año para ser voluntario

Tester QA / Quality Assurance Engineer

Buscamos un/a Tester QA con experiencia en entornos digitales y trabajo con rele...

Ubicación

Spain , Sabadell

Salario:

38300.00 EUR / Año

SCI - Serviclients

Fecha de expiración

Hasta nuevo aviso

Requisitos

Titulación de Grado Universitario o FP Superior
Experiencia previa en desarrollo de software o testing/QA en entornos digitales, incluyendo web, aplicaciones o plataformas
Experiencia trabajando en entornos cambiantes y con modelos de releases frecuentes
Conocimientos avanzados de Git y experiencia en gestión de repositorios y flujos de trabajo con Gitflow
Experiencia en metodologías ágiles, especialmente SCRUM
Manejo habitual de herramientas de gestión y documentación como JIRA y Confluence
Capacidad de organización, priorización, comunicación y coordinación en entornos con varios proyectos simultáneos
Enfoque práctico y resolutivo para la gestión de incidencias y el aseguramiento de la calidad

Responsabilidades

Coordinar el testing asociado a las releases mensuales del entorno digital
Identificar, registrar y priorizar incidencias detectadas tras las salidas a producción
Asegurar la calidad global de las entregas, manteniendo una visión transversal del ecosistema digital
Colaborar con equipos de desarrollo, producto y negocio para garantizar releases estables
Supervisar múltiples proyectos en paralelo, organizando prioridades y posibles riesgos
Impulsar buenas prácticas de control y seguimiento de calidad en entornos ágiles
Actuar con mentalidad resolutiva ante incidencias en producción, facilitando una respuesta rápida

Tiempo completo

Innovation Project Engineer

The Senior IVS Project Engineer is responsible for ensuring the completion of IV...

Ubicación

Costa Rica , Cartago

Salario:

No proporcionado

Coloplast

Fecha de expiración

Hasta nuevo aviso

Requisitos

University degree in Industrial Engineering, Quality, Production, Supply Chain, or equivalent
Minimum 3 years of experience in medical device manufacturing with a deep knowledge of project management methodologies and standards
Able to work at a high level with minimal supervision
Experience leading multidisciplinary teams
Proven ability to solve problems creatively
Strong familiarity with project management software tools, methodologies, and best practices
Proven ability to successfully complete projects according to defined scope, budget, and schedule
Excellent numerical skills and understanding of data analysis
Minimum English level B2+ in reading, writing, and conversation
Able to travel approximately 20-25 days per year

Responsabilidades

Responsible for analyzing and defining the scope of projects within IVS Project Management, Global Quality
Ensure the successful completion of the project within the scope, schedule, and budget
Establish and maintain project governance, standards, methodologies
Ensure project status and relevant decisions within the project are communicated to all team members and stakeholders
Ensure standardized templates, tools, and systems, that are effective and continuously maintained together with the PM & PMO community in CP
Coordinate and manage local projects
Monitor and manage resources and budgets across portfolio
Responsible for reporting status, KPIs, risks, and issues to the Head of Project Office and the Steering Committee
Provide regular reporting to senior leadership on portfolio performance, risks, and benefits realization
Regular engagement of key stakeholders to align on expectations and needs

Senior Service Technician

When you become a Commercial Service Technician at Carrier, you become part of a...

Ubicación

Vietnam , Hanói

Salario:

No proporcionado

Beretta Clima Italia

Fecha de expiración

Hasta nuevo aviso

Requisitos

Graduated from an engineering university related to HVAC systems: HVAC Engineer
Have at least two years of experience working as a same position
Ability to communicate in English
Know how to use computers and have reporting skills

Responsabilidades

Performing maintenance, repair, and warranty of chiller/VRF systems in the Northern region
Improving service quality and ensure customer satisfaction

Quality Engineer

Belden, Inc

Ubicación:
Mexico , San Nicolas de los Garza

Categoría:
Control de Calidad

Tipo de contrato:
No proporcionado

Salario:

Descripción del trabajo:

Responsabilidades:

Requisitos:

Información adicional:

Oferta publicada:
24 de diciembre de 2025

¿Buscas más oportunidades? Busca otras ofertas de trabajo que coincidan con tus habilidades e intereses.

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Quality IVS Projects Engineer

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Quality Engineer

Belden, Inc

Ubicación:Mexico , San Nicolas de los Garza

Categoría:Control de Calidad

Tipo de contrato:No proporcionado

Salario:

Descripción del trabajo:

Responsabilidades:

Requisitos:

Información adicional:

Oferta publicada:24 de diciembre de 2025

¿Buscas más oportunidades? Busca otras ofertas de trabajo que coincidan con tus habilidades e intereses.

Empleos similares para Quality Engineer

Quality IVS Projects Engineer

Sr compliance, QA Engineer

Validation Quality Engineer - Innovation Value Stream

Sr Engineer, Quality

Customer Quality Engineer

Tester QA / Quality Assurance Engineer

Innovation Project Engineer

Senior Service Technician

Ubicación:
Mexico , San Nicolas de los Garza

Categoría:
Control de Calidad

Tipo de contrato:
No proporcionado

Oferta publicada:
24 de diciembre de 2025