QA Specialist in Neuchatel

veröffentlicht:
Ort
Neuchatel, Neuenburg
Sektor
Life Sciences
Jobtyp
Contract
Referenznummer
9676
Kontakt
Mayank Chaubey, Basel Professionals IT & Life Sciences
Telefon
058 201 55 50
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Stellenbeschreibung

Our client, a leading international company, with seven of world’s top 15 brands, including the world’s number one brand is looking for a

QA Specialist 

Location: Neuchatel, Switzerland

Contract: long term temporary assignment at 100%

Start date: asap

The incumbent is responsible to maintain the NC (Nonconformance) and CAPA databases, including the generations of KPIs to support the regular review meetings for these processes. 

The job holder is responsible for ensuring that the NC and CAPA are followed up with the appropriate responsible person and documented and closed out according to the process. In addition the job holder will be responsible to project manage the implementation of the new Quality systems suite, liasing with the experts from all areas covered by the system.

Responsabilities:

  • Manage the non-conformance and CAPA ( NC & CAPA) databases 
  • Follow up with responsible persons to obtain supportive documentation to ensure edequate closure of NC and CAPA and ensure all supporting records are included with NC & CAPA forms.
  • Calculate KPIs and provide input to the regular NC&CAPA review board meetings (NCRB). Record minutes for NCRB (Non conformance Review Board) meetings
  • Project manage, as business specialist, the implementation of the quality systems suite (QSS9, including the drafting of SOPS (Standard Operation Procedure) and work instructions to support the system
  • Train as specialist in the new QSS, in order to train others and administratively manage the system
  • Liaise with audit team to ensure closure of CAPA internally and externally

Requirements:

  • College/University in a relevant subject (Life Sciences, Biology, Chemistry, ecc)
  • 2-4 years of experience preferably in the area of life sciences and quality
  • Previous experience in the process of Non conformance, CAPA and/or audits, in an electronic system
  • Experience in writing quality documentation, and understanding of workflows and integrity of records is essential.
  • Fluent in English (written and spoken), fluent in French is a plus
  • Team worked and flexible

We are looking forward to receiving within your application:

  •  your CV in English
  • latest Work Certificates
  • your Motivation Letter  
  • ID/passport copy

 Apply now to be considered – Good to know you!

For more information and your application, please contact: Mayank Chaubey, Consultant Life Science Professionals,  M +41 79 513 24 13, mayank.chaubey@ch.randstad.com   

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