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Quality Engineer
hace 4 semanas
Quality Engineer I is responsible for ensuring the safety and quality of our products and procedures through rigorous inspections, implementation of quality control measures, and identification of areas for improvement, collaborates with cross-functional teams to address quality issues, drive continuous improvement, and contribute to building high-quality products that exceed customer expectations.
Quality Engineer possess a strong background in engineering or quality assurance, attention to detail, and a proactive mindset.
- Contribute to all cost saving and safety initiatives and related CIS programs.
- Generate and maintain process requirements, specifications, validation and confirming quality documents to assure product / component conformance.
- This position can develop and manage Quality Engineering Technicians.
- Execute test method validations and Engineering Tests.
- Develop and maintain FMEA's and Control Plans.
- Perform, maintain, and sustain activities under QMS.
- CAPA, NMCRs and Customer complaints root cause investigations are completed in a timely manner.
- Coordinate and/or contribute in DHRs processes.
- Generate a weekly and monthly reports using quality objectives.
- Provides support during customer visits.
- Set detailed guidelines on what needs to be checked and what the quality standards are.
- Update the Quality Management System (QMS) with incidents, fixes and improvements.
- Audit our quality systems based on standards requirements.
- Monitor the entire production cycle and perform regular tests to identify potential malfunctions as early as possible.
- Inspect product for defects and identify the root of technical issues and recommend fixes.
- Prepare reports on malfunctions and corrective actions.
- Review quality documentation - Set and track quality assurance goals.
- Coordinate with external quality assurance auditors and technicians to ensure legal compliance.
- Work with internal teams to increase customer satisfaction by improving the quality of the products.
Experiência y requisitos
- Bachelor's degree in engineering (industrial, chemical, manufacturing or any other related).
- Ideal to have previous experience in Medical Devices / Quality System ISO 13485 - And/or is preferable required at least 2 years of experience in similar position.
- Advanced Computer skills (Minitab, Office, Word, Excel, Power Point, and/or Application Programs, Statistical Software, Databases.
Etc.).
- Capability to train and develop people.
- Knowledge of National and International Standards related to quality.
- Certification Desirable (Green Belt, Certified Lead Auditor, Certified Quality Engineer, or any other related.)
- Knowledge of ISO 14001 Environmental management System
**Número de vacantes** 1
**Área** Calidad
**Contrato** Permanente
**Modalidad** Presencial
**Turno** Diurno
**Jornada** Tiempo Completo
**Estudios** Titulo Profesional
**Sexo** Indistinto
**Disponibilidad p. viajar** No
