Quality Assurance Expert, Pharma, CONTRACT, Switzerland

Aargau  ‐ Vor Ort
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Beschreibung

We have a 6 month Contract role available to work with a global Pharmaceutical manufacturer in the canton of Aargau, Switzerland. This is an opportunity to manage, write and lead the GMP processes of a large manufacturing site for pharmaceutical drugs.

Please see general requirements for application below:

  • German speaking (very advanced)
  • At least 5 years Quality Assurance (QA) experience within a GMP regulated environment for the pharmaceutical, generics or OTCx industry.

This managerial role holds the following responsibilities; regulatory compliance of manufacturing site, writing SOPs, training colleagues, change requests coordination, assisting with batch release and ensuring qualification of suppliers.

There is a competitive Hourly rate available for the Contract, alternative market rates are also welcome. Please note there is a job description available on request and a likelihood of the contract extending into 2016.

We hope the role will be of interest to you and understand that further information may be required before making an application to the end client, please feel free to send either your full name, contact details or a complete CV via this website and I will endeavour to get back to you with further information on the role and answer any questions you may have. Alternatively I am contactable via an open-link on LinkedIn or XING.

Best regards,

Michael Kellitt

Job Code: 105731

Key words: Quality Assurance, Quality Control, Quality Engineer, GMP, GxP, Compliance, Regulatory, Freelance, Qualitaet, Pharmaceutical, Generics, Generic Pharma, OTC, Biopharmaceutical, 6 sigma, black belt, cGMP

Michael Bailey International is acting as an Employment Business in relation to this vacancy.

Start
15/06/2015
Dauer
6 months
Von
Michael Bailey Associates - Munich
Eingestellt
02.06.2015
Projekt-ID:
915705
Vertragsart
Freiberuflich
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