Beschreibung
Technical Writer, Technical Author German, FDA, TUV,SOP, SDLC
I have a fantastic opportunity to work within the worlds largest medical device project. Due to the size of the project, I would expect contract extensions.
IMPORTANT: I require fluent English and German
Project/Department Description and responsibilities:
Quality & Compliance; 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, company 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;
- 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 Skills and Additional Details
Good knowledge of German
Good knowledge of English
Technical experience
Non-Technical profile requirements:
Accepts personal responsibility for client satisfaction; - Strong tracking, coordination and project planning skills;
ABOUT SENTINEL:
In a connected world, relationships matter. For over 15 years, our recruiters have been building networks that connect the very best technologists. No one is better placed to reach the people who can help you succeed. We can name some of the global top 10 life science companies as valued clients and what we offer goes beyond the normal scope of the client-agency-candidate relationship. With our head office in the UK and our new Swiss based office, your profile will be treated with due care and attention and matched to the best possible role. We offer advice on CV structuring, interview technique and a concierge service when finalizing your contract or permanent offer with assistance in regards to booking flights/hotels, salary simulations, advice on local culture/living expenses and information on your new employer.
We have placed Quality Engineer's, CAPA consultants, Product Development Engineers, Auditors, Regulatory Affairs professionals Validation Engineers, Technical Writers/Authors and CSV consultants across Europe and have a strong understanding of the requirements of our clients highly FDA/EUMDD/PAL regulated environments.
Technical Writer, Technical Author German, FDA, TUV,SOP, SDLC