- Olympus Corporation of the Americas (Westborough, MA)
- …within Olympus's career ladder is between Sr. Engineer and Principal Eng. The Staff Technical Writer is responsible for all aspects of documenting all related ... a Core Team Member. In this role, the Staff Technical Writer will execute all aspects of...includes labeling for both clinicians and patients that accompany medical device products that conform to the… more
- Cordis (Irvine, CA)
- …of experience in technical writing, preferably in regulatory affairs or the medical device sector. + **Knowledge:** Familiarity with medical device ... **Overview** Cordis is a pioneering medical technology company specializing in groundbreaking solutions for...keep saving lives. MedAlliance (Cordis) are currently seeking a ** Technical Writer ** to join our Regulatory Affairs… more
- Envista Holdings Corporation (Quakertown, PA)
- … Technical English controlled natural language. + Familiarity with medical device regulatory requirements for accompanying documentation. + Proficiency ... **Job Description:** The ** Technical Writer ** in the Engineering organization...instructions, and Quick Start guides for different kinds of medical products and software. This position will also assist… more
- Ultradent Products Inc (Salt Lake City, UT)
- … Medical Writer is responsible for researching, drafting and reviewing technical documentation for medical device , drug and cosmetic products, while ... the global name in oral health, is seeking a Medical Writer to join Ultradent's Clinical Evidence...Device regulations and ISO 13485. + Excellent organization, technical and writing skills. Ultradent is an Equal Opportunity… more
- Humera (Maple Grove, MN)
- …Grove, MN Medical Writer II Maple Grove, MN Humera is currently hiring a Medical Device Writer II, for our client based in Maple Grove, MN The Sr. ... Medical Writer on the Regulatory Clinical Evaluation...writing experience + Experience may include writing in a medical , pharmaceutical, medical device , clinical… more
- Integra LifeSciences (Boston, MA)
- …outcomes and set new standards of care. The Senior Quality Compliance Specialist - Technical Writer will work with Boston quality system leadership and cross ... education and years' experience in QA/Compliance within the Life Sciences Industry, preferably Medical Device Industry. + Working knowledge of medical … more
- Novo Nordisk (Lexington, MA)
- …a living. Are you ready to make a difference? The Position The Senior Medical Writer works closely with cross-functional project teams to manage preparation of ... regulatory requirements of a clinical program. Relationships The Senior Medical Writer reports to a Director of...in other settings will be considered + Specific or technical job skills: + Exceptional written and oral communication… more
- Philips (Bend, OR)
- ** Medical Writer ** You will be responsible for helping with authoring and maintaining clinical and post-market documentation such as CEPs, CERs, PMCFPs, and ... data, risk assessments, and published literature-to conduct comprehensive evaluations of medical device safety and performance, identifying potential evidence… more
- Grifols Shared Services North America, Inc (San Diego, CA)
- …of experience writing end-user software or hardware instructions. Experience in the medical device industry and working in a federally regulated environment ... regions. Grifols Diagnostic Solution is seeking an Instrument Documentation Writer in San Diego, CA. This role will be...bodies (FDA, IVDR, EUDR) and the European Union (EU Medical Device Regulation). + Deliver supporting documentation… more
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