Life Cycle Managment Engineer (Medical Devices) | Presencial - San José - San José

Empresa: GSB Solutions
Tu Postulación: Aún no te has postulado
Ubicación: San José, Costa Rica
Correo de empresa: *********@*******.com (Ver email)
WhatsApp:  Enviar WhatsApp
3+ in Years in Medical Device Industry
Project Management experience
Must have very good written and verbal communication skill.
Project Management Skills
Demonstrated knowledge of manufacturing principles and practices, and procedures
Knowledge of specific business practices and software and software applications
Experience in New Product Development for Medical Device Industry
Experience in Technical documentation, quality control, lay-Out, fabrication, modification, and assembly of mechanical or electrical equipment and/or components for Medical-Device
An Engineering in any specialty is required
Masters in Science is recommended
English Advanced
Actividades a realizar:
Under (e. G. Limited supervision, general direction, etc. ) and in accordance with all applicable federal, state and local laws/regulations and Corporate Johnson & Johnson, procedures and guidelines, this position:

- Can guide the EM on the Validation process, lead the draft and review of protocols and test reports
- Can offer onsite support at the EM during the execution phase of validations (IQ, OQ, PQ).
- Can draft Validation Strategy, including TMVs
- Need to determine approach to documentation to be transferred systems, flows, storage, etc.
- Should review current DHF status for products in scope.
- Can identify needed strategies and inputs from R&D & other functions.
- Plan and conduct work requiring judgment in the independent evaluation, selection, and substantial adaptation and modification of standard techniques, procedures, and criteria while devising new approaches to problems encountered
- Plan, schedule, conduct, and coordinate detailed phases of engineering work in part of a major project or in a total project of moderate scope that involves conventional engineering practice but may include a variety of complex features such as conflicting design requirements, unsuitability of conventional materials, and difficult coordination requirements.
- Update work instructions, part specifications, validation protocols, technical documents (PFMEA's, ECO's, NCRs, CAPA's), and various forms of reports and correspondence.
- Can supervise, coordinate and technically revise the work of a limited group of technicians.
- Responsible for ensuring subordinates follow all Company guidelines related to Health, Safety and Environmental practices and that all resources needed to do so are available and in good condition
- Responsible for communicating business related issues or opportunities to next management level
- Responsible for ensuring personal and Company compliance with all Federal, State, local and Company regulations, policies, and procedures
- Performs other duties assigned as needed
- Ability to work in stressful/fast paced environment
Law benefits
Courses and Certifications
San José, Costa Rica

Jornada laboral: Tiempo Completo
Tipo de empleo: Trabajo Fijo
Salario: CRC 1,500,000.00 - 2,420,000.00 Mensual
Cantidad de vacantes: 1

Experiencia Mínima: 3 años
Idiomas: Inglés Avanzado
Estudios Mínimos: Licenciatura
Sexo: Indistinto

¿Eres Apto para este Empleo?

  • Averigua tu score para esta posición y adapta tu perfil para asegurar este Empleo

  • ?/100
  • Consultar
  • ¡En camino! Nuestro motor de Inteligencia Artificial ha comenzado a analizar tu Currículum. Esto puede demorar unos minutos. Te enviaremos un correo cuando tengamos el resultado listo.
  • ¿Cómo funciona?

Empleos que podrían interesarte