Qualification and Validation Engineer

Vertragsart:
Vor Ort
Start:
ASAP
Dauer:
31.12.13
Von:
Harvey Nash IT Recruitment Switzerland
Ort:
Ticino
Eingestellt:
16.07.2013
Land:
flag_no Schweiz
Projekt-ID:
567938

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On behalf of our client in the Life Science industry, Harvey Nash is looking for a Qualification and Validation Engineer for a 6 month projects in various locations: Ticino, Visp area and Solothurn

The role

  • Support for the validation activities
  • Ensuring that all compliance issues and requirements are addressed
  • Create Validation Master Plans, Protocols, Summary Reports and other documentation associated with validati
  • Facilitates successful team behaviour within Quality Systems and across functional areas Manages relationships externally and internally
  • cross-functional and cross-departmental support, fostering overall effectiveness
  • implement innovation and continuous improvement within the Validation process

    Requirements

  • Preferably experience in 21 CFR 820, 21 CFR 11 and European regulations associated with the medical device industry
  • High understanding of GMP, Compliance, Validation Practices including the system development life cycle and Regulatory expectations
  • Working experience of validation computer systems for use in a FDA regulated environment
  • 2 years experience in medical devices/regulated environment
  • BSc/MSc in scientific/engineering related field or equivalent
  • Fluent English and German required, additional languages are an asset

    Are you available immediately, have experience working within a Life Science company? Please send your complete CV (Word documents preferred). For further details feel free to call me. Im looking forward to receiving your application.


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