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Contractor Validation Engineer (m/f/d) (EN)

[11390]
Validation (IQ/OQ/PQ), Technical Documentation, Deviations

Job title: Contractor Validation Engineer (m/f/d) Industry: Medizintechnik Skills: Validation (IQ/OQ/PQ),Technical Documentation,Deviations Start of project: ASAP Duration of the project : 6 months Project volume: 1008 Hour(s)  Location: Biel/Bienne, Switzerland Tasks: ·Validation and Qualification, IQ- OQ- PQ ·Write technical documentation ·Manage protocol, address additional condition, execute the qualification, write the report to the execution ·Handle any deviations, close the documentation correctly ·Equipment IOQ protocol development, execution, and report writing/approval ·To execute room commissioning protocols, resolve any deficiencies, and drive to report approval. ·Communicate across the organization at many levels to resolve and align the protocol output.  Qualifications: ·GDP and basic medical device validation best practices are required ·Experience on medical devices, qualification and validation, documentation ·Technical writing expertise ·Fluent in English, spoken and written ·Independent, proactive and self-starter

Job title: Contractor Validation Engineer (m/f/d)
Industry: Medizintechnik
Skills: Validation (IQ/OQ/PQ),Technical Documentation,Deviations
Start of project: ASAP
Duration of the project : 6 months
Project volume: 1008 Hour(s) 
Location: Biel/Bienne, Switzerland

Tasks:

  • Validation and Qualification, IQ- OQ- PQ
  • Write technical documentation
  • Manage protocol, address additional condition, execute the qualification, write the report to the execution
  • Handle any deviations, close the documentation correctly
  • Equipment IOQ protocol development, execution, and report writing/approval
  • To execute room commissioning protocols, resolve any deficiencies, and drive to report approval.
  • Communicate across the organization at many levels to resolve and align the protocol output. 

Qualifications:
  • GDP and basic medical device validation best practices are required
  • Experience on medical devices, qualification and validation, documentation
  • Technical writing expertise
  • Fluent in English, spoken and written
  • Independent, proactive and self-starter

 


map Biel/Bienne, Switzerland date_range ASAP update Temporary
Direct contact

Evlina Latifi

Recruitment Consultant
mail e.latifi@aristo-group.ch
phone +41 44 274 39 00


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