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Technical Writer
Eingestellt von Edelway
Gesuchte Skills: Sql, Client
Projektbeschreibung
Technical Writer
Edelway SA is a Swiss IT Services Consultancy. Our global multinational end-client based in the Basel/Bern area is currently looking to hire a Technical Writer on a long-term basis.
Working language: English. German is a plus.
Full time engagement at least until end of 2014 (extension possible)
Starting Date: 01.07.2014
THE ROLE:
* 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
* Perform technical writing, research, and related editing functions to prepare documents, test plans, user cases, project manuals, business proposals, reports, briefings, presentations, guidelines, and other written materials
YOUR PROFILE :
*Strong experience in similar position (5+ years)
*Strong experience in regulated environments, especially in CSV and GxP
*Strong tracking, coordination and project planning skills
*Ability to identify and implement process and/or application improvements
*Able to follow change management procedures and internal guidelines
If it sounds like your next challenge, send your CV and we will contact you shortly to discuss it further.
Keywords: Writer, Technical, SDLC, CSV, GxP, SQL, SOP, Medical Devices, Pharma, Basel, Bern, Solothurn, Schweiz, Switzerland
Edelway SA is a Swiss IT Services Consultancy. Our global multinational end-client based in the Basel/Bern area is currently looking to hire a Technical Writer on a long-term basis.
Working language: English. German is a plus.
Full time engagement at least until end of 2014 (extension possible)
Starting Date: 01.07.2014
THE ROLE:
* 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
* Perform technical writing, research, and related editing functions to prepare documents, test plans, user cases, project manuals, business proposals, reports, briefings, presentations, guidelines, and other written materials
YOUR PROFILE :
*Strong experience in similar position (5+ years)
*Strong experience in regulated environments, especially in CSV and GxP
*Strong tracking, coordination and project planning skills
*Ability to identify and implement process and/or application improvements
*Able to follow change management procedures and internal guidelines
If it sounds like your next challenge, send your CV and we will contact you shortly to discuss it further.
Keywords: Writer, Technical, SDLC, CSV, GxP, SQL, SOP, Medical Devices, Pharma, Basel, Bern, Solothurn, Schweiz, Switzerland
Projektdetails
Geforderte Qualifikationen
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Kategorie:
IT Entwicklung