- Danaher Corporation (San Diego, CA)
- …or Computer Science). + Prefer minimum of 5 years of experience as a Technical Writer creating documentation for medical devices, diagnostics, or life ... Business System (https://www.danaher.com/how-we-work/danaher-business-system) which makes everything possible. The Senior Technical Writer for Leica Biosystems creates accurate,… more
- ManpowerGroup (Durham, NC)
- …or a related field + 2+ years of experience as a Technical Writer , preferably in a pharmaceutical, biotechnology, medical device , or regulated ... Our client,within Pharma and Life Sciences is seeking a Technical Writer to join their team in Raleigh, NC. **Job Title: Technical Writer ** **Location:… more
- J&J Family of Companies (Irvine, CA)
- …of America **Job Description:** Johnson & Johnson MedTech, Electrophysiology, is recruiting an ** Medical & Technical Writer ** to join our Scientific ... journey to wellness. Learn more at https://www.jnj.com/medtech As the Medical & Technical Writer within...subject area. + Minimum of 3 years of experience medical device , diagnostics, or pharmaceutical industry with… more
- Kelly Services (Irvine, CA)
- ** Technical Writer 1** Hybrid - Onsite...position. + Technical writing knowledge in the medical device industry, preferably + Prior experience ... Kelly FSP Science and Clinical is currently seeking a Technical Writer 1 for a long-term engagement...for a long-term engagement with one of our Global Medical Device clients. This position is onsite… more
- Abbott (St. Paul, MN)
- …education and work experience. + 3 years' progressively more responsible experience as a technical writer in a medical or high technology (preferably ... for diversity, working mothers, female executives, and scientists. For years, Abbott's medical device businesses have offered technologies that are faster, more… more
- Abbott (Alameda, CA)
- …generic medicines. Our 114,000 colleagues serve people in more than 160 countries. **Senior Technical Writer ** **Working at Abbott** At Abbott, you can do work ... and scientists. **The Opportunity** We are seeking a Senior Technical Writer to lead the development of...mapping (eg, using Visio), and a deep understanding of medical device operations. The successful candidate will… more
- Kelly Services (Jacksonville, FL)
- …and Company regulations, policies, and procedures_ **_QUALIFICATIONS:_** + _Minimum of 5 years of Technical writing in the Medical device industry_ + _Must ... As a Kelly employee, you will be eligible for Medical , Dental, 401K and a variety of other benefits...quality systems._ **_DUTIES & RESPONSIBILITIES_** + **_Writes and edits technical materials such as changes in quality systems, data… more
- Sandia National Laboratories (Albuquerque, NM)
- …by job classification. What Your Job Will Be Like: We are seeking a skilled Technical Writer and Editor to join our team, responsible for the development, ... and maintenance of Joint Nuclear Weapons Publication System (JNWPS) technical publications. The JNWPS is a comprehensive system of...law. NNSA Requirements for MedPEDs: If you have a Medical Portable Electronic Device (MedPED), such as… more
- Roche (Branchburg, NJ)
- …generations to come. Join Roche, where every voice matters. **The Position** As the Principal Technical Writer , you will operate at the highest level in the ... technical writing series, providing strategic leadership and definitive regulatory...is required** . Preferred Industry Knowledge: + Knowledge of medical device , software, pharmaceutical, or biotechnology industry… more
- Adecco US, Inc. (Morristown, NJ)
- Adecco Healthcare & Life Sciences is seeking a skilled **CMC Regulatory Technical Writer II** to support a global pharmaceutical client in lifecycle management ... + Knowledge of cGMP requirements and small-molecule products; experience with aseptic or medical device products is a plus. + Proficiency in Microsoft Office… more
- Mentor Technical Group (PR)
- …the knowledge and experience to ensure compliance with pharmaceutical, biotechnology, and medical device safety and efficacy guidelines. With offices in Caguas, ... Mentor Technical Group (MTG) provides a comprehensive portfolio of...Experience: 2-5 years in a regulated industry (pharma, biotech, medical devices) with direct experience in SOP writing or… more
- GE HealthCare (Cleveland, OH)
- …and regulatory teams with documentation creation and updates, applying knowledge of medical device guidelines + Collaborate with engineering teams to develop ... You'll Need: + At least 6 years of prior experience in technical writing, preferably in the medical industry or a related area + Excellent skills in researching,… more
- GE HealthCare (Cleveland, OH)
- …and regulatory teams with documentation creation and updates; build your knowledge of medical device quality and regulatory guidelines + Develop and maintain ... + Should have at least 4 years of prior experience in technical writing, preferably in the medical industry or a related area + Aptitude to develop clinical and… more
- FocusKPI Inc. (Mountain View, CA)
- FocusKPI is seeking a UX writer or a Public health writer ...for medical devices or Software as a Medical Device (SaMD), and using a quality ... of our clients, a high-tech SaaS company. The UX writer will join a cross-disciplinary team of product managers,...Qualifications: + Bachelor's or graduate degree in English, Journalism, Technical Writing, Public Health, or related field + 5-7… more
- Danaher Corporation (Miami, FL)
- …hands-on experience and exposure in the critical area of regulatory labeling within the medical device and Life Sciences industry. Interns will work closely with ... Reagent Labeling Writer Intern Accelerating answers Are you ready to...cross-functional teams including R&D, Quality/Regulatory Assurance, and Technical Support. This position reports to the Senior Manager… more
- Saildrone (Alameda, CA)
- … device operations and characteristics, highlighting performance metrics and technical specs * Support engineers to capture how devices/sensors operate under ... The Role Saildrone is seeking a highly organized, passionate Quality and Service Document Writer to join our corporate quality team. As part of a comprehensive team,… more
- Seek Now (GA)
- …inspections mobile app (iOS/Android): tasking, guidance, offline-first workflows, and on- device quality checks. + Define requirements for reliability (spotty ... connectivity, battery constraints, device variability) and measurable app performance SLAs (startup time,...not required: experience in insurance and/or real estate. + Technical Acumen: Comfortable with APIs/SDKs, mobile analytics, and data… more
- AbbVie (North Chicago, IL)
- …medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's ... will contribute to the development and launch of exciting new drug / device combination products. As a Sr. Principal Systems Engineer, you will be responsible… more
- AbbVie (North Chicago, IL)
- …+ 10-12 years of experience (MS 8-10 years, PhD 2-4 years) ideally in the medical device , drug delivery or other regulated industry + Strong communication skills ... that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a...versatile Senior Scientist II/Mechanical Engineer to join our Injection Device Development team to help us accelerate AbbVie's combination… more
- Allied Universal (Wilmington, MA)
- …for translating, expanding, finalizing, and documenting pre-sales proposals and technical designs produced by Sales and Solutions Architecture in pre-sale ... products for the Solution Engineer are security system and construction technical drawings, including custom installation drawings and instructions, network design… more