QC - Technical Writer - Skill set 2 - Normal

Vertragsart:
Vor Ort
Start:
1.7.2014
Dauer:
6 months
Von:
Michael Bailey Associates - Munich
Ort:
Solothurn
Eingestellt:
13.06.2014
Land:
flag_no Schweiz
Projekt-ID:
725624

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Technical Writer m/f

For our client, one of the leading Medical Device companies we are currently looking for a Technical Writer m/f for the Quality & Compliance department.

Your primary tasks will be:

Prepare technical & regulatory documents within established timelines that are of high quality in terms of applicable content, data interpretation, organization, clarity, accuracy, format, and consistency, with adherence to regulatory guidelines, internal guidelines/styles/processes, and SDLC standards/guidelines

Writing technical SOP's (procedures) and work instructions based on input from the different technical departments and based on available documentation/presentations related to IT Infrastructure

Your Profile:

Strong experience in regulated environments, especially in CSV and GxP

Accepts personal responsibility for client satisfaction

German and English fluent

Others:

Start: 01/07/14

End: 31/12/14 (extension possible)

Location: Central Switzerland, Kanton Solothurn

I hope that the role will be of interest to you, there is a detailed job description available on request, I understand that you may require further information before applying to the client however please feel free to apply via this website and I will answer any questions you have. I am also available for phone calls at anytime to further discuss.

Kind regards,

Frank

Pharmaceutical Recruitment Consultant

Job Code: 101042

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