Beschreibung
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.