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Quality Engineer - Medical Device


Registada há 5 anos no SAPO Emprego 137790 ofertas anunciadas nos últimos 6 meses

Detalhe da Função

I am currently recruiting for a contract Quality Engineer to work on a 6 month contract in Bordeaux for a high profile medical device company.

They are looking for someone with experience in the following:

Essential skills required for the roles:

  • 21 CFR Part 820 Subpart G - Production and Process Controls
  • ISO 13485 - Medical Device and Quality Systems
  • Computer Software Validation (CSV) as part of manufacturing process validations.
  • Medical Device Production Part Approval Process (PPAP)
  • Unique Device Identification (UDI) is a plus
  • Process Validation experience in Medical Device, including creation and execution of protocols and reports.
  • Experience with Test Method Validation(TMV)/Measurement System Analysis (MSA), Gage R&R
  • Ability to correctly determine specifications from prints.
  • Process Flow Maps
  • Control points
  • Reaction plan to prevent non-conforming product.
  • pFMEA control for risks included in process flow map
  • Quality System remediation experience
  • Experience with process monitoring of manufacturing process using Cpk and Ppk

Please note:

Fluency in French and English required

If you you think this position is a good match for you please apply and I will be in contact ASAP to discuss in detail.

If you have any questions please contact me at (see below)

Employment Type: Contract
Duration: 5-6 months
Work Hours: Not Specified
Salary (minimum): 50.00
Salary (maximum): 60.00
Salary Currency: Euro . EUR
Salary Period: Hourly
Salary (Additional):

Pesquise também por: Quality Engineer - Medical Device



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