Mexicali, Baja California- Beneficios de acuerdo a la LFT
- fondo de ahorro
Giro
Manufacturera
Actividad principal
Proveedor de soluciones de cuidado auditivo - Dispositivos Médicos
Número de empleados
800
Sitio Web corporativo
Aviso de privacidad
Descripción y detalle de las actividades
• Maintain Quality Records in appropriate location.
• Capture Training logs/roster for the site.
• Training Data base handling.
• CAPA facilitator.
• Responsible to archive quality records (Training files, Logs, TCR, etc).
• Audit/verify documents are compliant with GDPs.
• Responsible for the distribution of controlled copies and retrieval when needed.
• Assess/Audit of current controlled documents are posted at site level.
• Scan DHR documentation prior to ship product to LLC for digital archiving.
• Prepare records for outside storage (Iron Mountain).
• Responsible for shredding obsolete/unused documents for the site.
• Responsible for the support on document translations.
• Purchase appropriate consumables for records shipping.
Experiencia y requisitos
- Must have: Visa B1/B2 & Passport.
- Availability to travel - 30 % traveling request.
- Experience with GMP and GDP, Clean room environment.
- Medical device manufacturing environment.
- Proficient with Microsoft programs and other basic computer applications.
- Ability to communicate effectively internal and externally with co-workers, and department management in both written and verbal form.
- Provide support on NHO preparation.
- Provide support with QA departmental purchases.
- Support Internal/External audits.
- Support with admin tasks.
- Support Environmental control activities such as providing cleaning logs to the employees, ID DI water samples, etc.
Beneficios
Número de vacantes 1
Área Calidad
Contrato Permanente
Modalidad Presencial
Turno Mixto
Jornada Tiempo Completo
Horario
- Tiempo completo
- Lunes a viernes
Estudios Carrera con título profesional
Inglés Hablado: Avanzado, Escrito: Avanzado
Edad 18 - 65 años
Disponibilidad p. viajar Si