Description
My client a well known pharmaceutical company is looking for candidate to work within their Quality & Compliance/IT division in Solothurn. They are looking to recruit a Technical Writer on a 5 months contract (Start asap).Project/Department Description and responsibilities
* Quality & Compliance
* IT Infrastructure
Primary Tasks and responsibilities
* 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, J&J 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
Non-Technical profile requirements
* Strong experience in regulated environments, especially in CSV and GxP
* Accepts personal responsibility for client satisfaction
* Strong tracking, coordination and project planning skills
* Establishes and manages engagement objectives, expectations and quality plan
* Ability to identify and implement process and/or application improvements * Strong analytical and problem-solving skills
* Must be able to work on multiple simultaneous tasks with limited supervision
* Able to follow change management procedures and internal guidelines
Language Proficiencies
* English and German fluent
To find out more please contact me on or
Beste Grüße
Corinna Freier