*Please Reply me on rugender.na...@rsystems.com <rugender.na...@rsystems.com>*
*Title: Technical Writer * *Duration: 3 MONTHS* *Location: Valencia, CA(Los Angeles area) * *POSITION SUMMARY:* The technical writer assists with the development of labeling of medical devices. This includes but is not limited to development, writing, and editing of the product manuals, inserts, and administrative documentation from marketing requirements, engineering requirements, risk assessment reports, and production or other specifications and directions. *SPECIFIC DUTIES AND RESPONSIBILITIES:* · Assists with writing instructions for use for new medical device/software products based on specifications, prototypes, and researched gathered from subject experts. Update existing manuals, product inserts, and administrative documentation to meet customer, regulatory, legal, marketing, and engineering requirements. · Maintains documentation relating to Bioness labeling and assists with corresponding paperwork, as needed. Gathers and researches technical information, including engineering and development information, for use in documentation activities. Actively reviews and edits documents associated with product development meetings. · Plans own daily activities and prioritizes assigned tasks. Work is periodically reviewed at certain steps prior to completion, and periodically during the process depending on the type of document. Able to react to change productively and to perform other essential tasks assigned. · Administrative tasks include, but are not limited to, coordinating review/approval process, submitting Document Control requests, creating logs, and redlining documents. *EDUCATIONAL REQUIREMENTS:* · Bachelors degree or advanced degree in English, Science, or technical field to ensure accuracy of technical information regulated by the FDA and other country regulatory authorities. *EXPERIENCE:* 2-5 years related experience. Experience in the medical device or pharmaceutical industry a plus. *KNOWLEDGE, SKILLS AND ABILITIES:* · Ability to read, analyze, and interpret technical procedures, product development documentation, and governmental regulations. Strong writing, communication, and editing skills (will be asked to submit writing samples). · Proficiency in Microsoft Word, Microsoft Excel, Adobe InDesign, and Adobe Acrobat Pro software. · Working knowledge of Adobe Illustrator and PhotoShop preferred, but not required. · Solid ability to interview and evaluate information from technical experts and incorporate the information into technical documentation with an emphasis on grammatical accuracy and visual impact. · Strong organizational skills and ability to meet tight deadlines. · Ability to work both independently and as a part of a team. -- *Thanks & Regards * *Rugen Nagar* R Systems Inc 5000,Windplay Drive,El Dorado Hills,CA 95762 Desk no: *916-692-3594* Fax: 916-939-6337 [CMMi & PCMM Level 5 Company] ISO 27001 |Six Sigma Web*:* www.rsystems.com [image: cid:image001.png@01CF57D3.4811B630] *YIM/GTalk --> rugender.rgtalent* -- You received this message because you are subscribed to the Google Groups "SAP-UK" group. To unsubscribe from this group and stop receiving emails from it, send an email to sap-uk+unsubscr...@googlegroups.com. To post to this group, send email to sap-uk@googlegroups.com. Visit this group at http://groups.google.com/group/sap-uk. For more options, visit https://groups.google.com/d/optout.
