Qualification & Validation Senior Consultant - Guadalajara, México - PHARMA QUALITY EUROPE

PHARMA QUALITY EUROPE
PHARMA QUALITY EUROPE
Empresa verificada
Guadalajara, México

hace 4 días

Rodrigo Fernández

Publicado por:

Rodrigo Fernández

Reclutador de talento para beBee


Descripción

  • 02 years' experience in pharmaceutical industries
  • Support of development of qualification documents, user/technical requirements specifications, design qualification reports, test plans, requirementstesting traceability matrixes, qualification summary reports
  • General knowledge and support in the development of validation documents of Technical Qualification
  • General knowledge in riskbased assessment (e

g:
FMEA, HACCP)

  • General knowledge in concepts such as calibration and maintenance plans and related instructions
  • General knowledge of GMPs
  • Integrity, strong analytical skills and attention to details
  • Interest and proactivity to develop a career in this Industry
  • Native in Spanish; fluent in English (at least B2)
  • Full availability to travel
Numero de vacantes: 1

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Requisitos:


  • 02 years' experience in pharmaceutical industries
  • Support of development of qualification documents, user/technical requirements specifications, design qualification reports, test plans, requirementstesting traceability matrixes, qualification summary reports
  • General knowledge and support in the development of validation documents of Technical Qualification
  • General knowledge in riskbased assessment (e

g:
FMEA, HACCP)

  • General knowledge in concepts such as calibration and maintenance plans and related instructions
  • General knowledge of GMPs
  • Integrity, strong analytical skills and attention to details
  • Interest and proactivity to develop a career in this Industry
  • Native in Spanish; fluent in English (at least B2)
  • Full availability to
Numero de vacantes: 3


Tipo de contrato:
Determinado

Ventajas sociales o económicas

Prestaciones de ley y superiores a las de ley.

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Requisitos

Descripción

  • 2 5 years' experience in pharmaceutical industries
  • Support of development of qualification documents, user/technical requirements specifications, design qualification reports, test plans, requirementstesting traceability matrixes, qualification summary reports
  • General knowledge and support in the development of validation documents of Technical Qualification
  • General knowledge in riskbased assessment (e

g:
FMEA, HACCP)

  • General knowledge in concepts such as calibration and maintenance plans and related instructions
.

  • General knowledge of GMPs
  • Integrity, strong analytical skills and attention to details
  • Interest and proactivity to develop a career in this Industry
  • Native in Spanish; fluent in English (at least B2)
  • Full availability to travel
Estudios mínimos
Licenciado


Idiomas:

Inglés nível Alto.

  • Experiência mínima
2 años

Disponibilidad para viajar
El 80% del tiempo laboral

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