Descripción y detalle de las actividades
**Summary**:
The role will be pulling and analyzing Complaint Data to support Risk Management / Postproduction Control. Responsible for planning, implementing, and managing compliance of post market monitoring processes with internal and external safety, quality and regulatory standards requirements for worldwide distribution.
Experiência y requisitos
**Responsibilities**:
- Designs, implements, and maintains quality assurance protocols and methods for Analyzing Complaint Data.
- Designs methods and procedures for inspecting, testing and evaluating the precision and accuracy of post-production processes.
- Performs analysis of reports and production data to identify trends and recommend updates or changes to quality standards and procedures when necessary.
- May assure compliance to in-house and/or external specifications and standards (i.e. GLP, GMP, ISO, Six Sigma).




- Works on problems of a moderate scope where analysis of situation or data requires a review of a variety of factors.
- Normally receives general instructions on routine work and detailed instructions on new projects or assignments.
**Qualifications**:
- Professional degree in Engineering.
- Must possess 2 years of minimum experience in a FDA Regulated environment (medical industry) requirement
- Fluent in English.
Beneficios
- Confiable de vida
- Fondo de ahorro
- Seguro de gastos médicos
- Bonos anuales
**Número de vacantes** 1
**Área** Calidad
**Contrato** Permanente
**Modalidad** Presencial
**Turno** Diurno
**Jornada** Tiempo Completo
**Horario**
- Tiempo completo
- Lunes a viernes
**Estudios** Carrera con título profesional
**Inglés**Hablado: Avanzado, Escrito: Avanzado
**Disponibilidad p. viajar** No

📌 QA Engineer -b (Tijuana)
🏢 ENOVIS México, S.A. de
📍 Tijuana