Beschreibung
Guten Tag,
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 6 months contract (Start 1 July).
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. Quick learner, motivated self-starter. Excellent customer service, interpersonal, communication and team collaboration skills. Able to follow change management procedures and internal guidelines
Language Proficiencies
* English and German fluent
To find out more please contact me.
Beste Grüße
Corinna Freier