- Medtronic (Minneapolis, MN)
- …in a more connected, compassionate world. **A Day in the Life** As a Technical Writer , you will support the production of customer facing product documentation, ... will support product documentation updates to comply with EUMDR, FDA and other regulatory body requirements by...Medtronic design standards. **Careers That Change Lives** As a Technical Writer , you will support the production… more
- Actalent (Columbus, OH)
- Technical Writer Needed- Urgently Hiring Actalent is currently hiring a technical writer in the Columbus area. This is a contract position for 6 months, ... Biologics, Gene Therapy, or Pharmaceutics and knowledge of GMP, regulatory ( FDA ) requirements, and understanding of aseptic...aseptic processes. Job Description We are seeking a meticulous Technical Writer to join our team. In… more
- Randstad US (Marietta, PA)
- technical writer - first shift. +...regulated safety and quality standards. - Knowledge of cGMP, FDA and other regulatory requirements and quality ... reference48863 job details job summary: - Serve as a Technical Writer dedicated to authoring, revising and...regulated safety and quality standards. - Knowledge of cGMP, FDA and other regulatory requirements and quality… more
- Abbott (St. Paul, MN)
- …Our location in St. Paul, MN currently has an opportunity for a ** Technical Writer II** professional. This individual will work under general supervision ... requirements. + Complies with US Food and Drug Administration ( FDA ) regulations, other regulatory requirements, Company policies,...plus years of progressively more responsible experience as a technical writer in a medical or high… more
- DEKA Research & Development (Manchester, NH)
- … Technical Writer : + 3+ years' experience in cybersecurity and/or regulatory + Technical writing experience in a medical device environment + Experience ... The Cybersecurity Software Technical Writer has responsibilities such as...such as the creation, review, and release of the FDA documentation for the eSTAR materials related to cybersecurity:… more
- Randstad US (Marietta, PA)
- technical writer . + marietta , pennsylvania...team in a dynamic environment. + Knowledge of cGMP, FDA , and other regulatory requirements and quality ... computer and mathematical occupations + reference1065043 job details job summary: A Technical Writer is needed for a leading pharmaceutical manufacturer in… more
- Abbott (Plano, TX)
- …routine fingersticks. **The Opportunity** We currently have an opportunity for a **Senior** ** Technical Writer ** to join our Abbott Medical Device team. This ... requirements. + Complies with US Food and Drug Administration ( FDA ) regulations, other regulatory requirements, Company policies, operating procedures,… more
- Astrix Technology (Columbus, OH)
- Sanitation Technical Writer (3rd Shift) Medical Writer Columbus, OH, US Pay Rate Low: 25 | Pay Rate High: 26 + Added - 13/08/2024 Apply for Job **_Our client ... **Pay** **: $25/hr** **Type** **: Contract to hire** **Requirements:** + Previous technical writing experience in a manufacturing setting required; 2-3 years of… more
- ManpowerGroup (Marietta, PA)
- **Biopharmaceutical Technical Writer ** **Marietta, PA** **Pay:$78,000-$85,000 annual** Visa Sponsorship? Not offered Corp-to-Corp? Not eligible Must be a US ... practices. + **Quality & Compliance:** + Ensure documents meet quality and regulatory standards. + Manage document formatting, revisions, and change requests. +… more
- Novo Nordisk (West Lebanon, NH)
- …report contains the technical merit and completeness according to regulatory expectations. The Deviation Investigator- Writer will be responsible for ... Are you ready to realize your potential? The Position The Deviation Investigator- Writer is responsible for investigating and writing of deviations to the… more
- Houston Methodist (Houston, TX)
- At Houston Methodist, the Scientific Writer position is responsible for performing a variety of tasks including preparing laboratory and clinical studies and ... publication. + Provides faculty with full lifecycle support from technical document development to preparation and submission. **QUALITY/SAFETY ESSENTIAL FUNCTIONS**… more
- MD Anderson Cancer Center (Houston, TX)
- Provides technical writing and editing of grants, publications, clinical research proposals, and clinical trial protocols. Impacts the visibility of melanoma ... projects concurrently and, through excellent communication skills, deliver high-quality technical content for both internal and external publication. 2. Demonstrated… more
- ThermoFisher Scientific (Greenville, NC)
- …perspectives are valued. **What will you be doing in this Senior Medical Writer role focused on Promotional Review work?** Provides tailored high-level support in ... regional regulations and codes of practice. In addition, the Senior Medical Writer will provide high-quality medical and scientific writing from planning and… more
- Alaka'ina Foundation Family of Companies (Frederick, MD)
- …Clinical Data Manager/ Regulatory Writer ; Quality Assurance Officer; Regulatory Scientist; Technical Writer ; Program Manager; Biomedical Science ... Regulatory , Clinical, and Technical Clinical Trial...Clinical Laboratory Improvement Amendments (CLIA), Food and Drug Administration ( FDA ), Good Clinical Practices (GCP) Good Laboratory Practices (GLP),… more
- BeiGene (San Mateo, CA)
- …protocols, and protocol amendments + Keen understanding of the key requirements for regulatory submissions as stipulated in FDA and ICH guidelines + Experience ... INDs, MAAs, and NDAs is a plus + The technical /scientific ability to critically analyze, synthesize, and present complex...+ 7+ years of relevant industry experience as a regulatory medical writer with a BA/BS degree.… more