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Emploi: technical writer - manufacturing

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job details

   . 17. novembre 2021
   . luterbach, soleure
   . life sciences
type d'emploi
   . contract
   . 16789
   . audrey bisch, bâle professionals health care & life sciences
   . 058 201 55 50
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description du poste

Do you want to work in a biotech company? Do you have experience as a Technical Writer in a GMP environment ? You should then read the following lines! 
Our client, based in Solothurn, is looking for a  Technical Writer for a 7 months contract. 
Home based but supporting the Solothurn Drug Substance manufacturing facility, this Manufacturing Sciences situation provides technical writing expertise and support to complete technical reports in support of regulatory filings and campaign completion. Solid technical understanding of bioprocessing technologies (mammalian cell culture, bioreactors, perfusion and fed-batch strategies, PAT, chromatography, UF/DF and filtration) is required. situation reports to program TT leader (the overall TT project manager) and will work with guidance from that lead to collect data from various data system (OSI Pi, SIMCA and LIMs) to populate report templates. The situation requires knowledge in working within electronic documentation management systems and knowledge of GMP documentation practices and procedures. The situation will work cross-functionally with other members of the project team in Manufacturing Science and other functions such as Quality, Engineering and Operations. 
Your Responsibilities: 
1. Drive technology report completion, cross-functional (Operations, Development, Process and Automation Engineering, QA and QC) process transfer team to ensure success in project documentation and closure.
2. Collect data from various process data systems to support report data population and be able to interpret data for initial data analysis and conclusions.
3. Provide Technical Writer and report status updates to the program TT lead and provide routine updates to other functions regarding technical report status and completion of key milestone. 
Your profile: 
BS with minimum 5 years of experience in bioprocess manufacturing process, or MS with minimum 3 years experience in upstream process
Bachelor?s or Master degree in Chemical or Bioprocess Engineering, Biochemistry, Chemistry, Biology or closely related discipline 
Do not waste any minutes, apply now!  We are looking forward to receiving your application.
Please note that only candidates with a valid work permit or who are EU/EFTA citizens will be considered.


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Post Date: 06/07/2024 / Viewed 139330 times
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