• Serve as a subject matter expert for Microsoft Word, document formatting, style management, templates, and document production best practices • Perform advanced document formatting and publishing activities, including management of complex tables, figures, references, cross-references, automated numbering, table of contents generation, and document quality control • Manage document development timelines, review cycles, and comment resolution activities to ensure high-quality deliverables are completed on schedule • Develop, maintain, and improve standardized document templates, style guides, macros, and formatting tools to support efficient document development and regulatory submissions • Partner with Medical Writing, Regulatory Operations, Clinical Development, Biometrics, Pharmacovigilance, and other functions to ensure documents are submission-ready and comply with regulatory publishing requirements • Author and coordinate the preparation of clinical, regulatory, and safety documents, including protocols, protocol amendments, clinical study reports (CSRs), investigator brochures (IBs), CTD components, and other submission-related documents.

Technical Writer Job ID 508107 Posted since 28-May-2026 Organization Digital Industries Field of work Internal Services Company Siemens Industry Software Inc. Experience level Experienced Professional Job type Full-time Work mode Remote only Employment type Permanent Any Siemens location in - United States of America We are a leading global software company dedicated to the world of computer aided design, 3D modeling and simulation— helping innovative global manufacturers design better products, faster! With the resources of a large company, and the energy of a software start-up, we have fun together while creating a world class software portfolio. Our culture encourages creativity, welcomes fresh thinking, and focuses on growth, so our people, our business, and our customers can achieve their full potential. Position Overview: Do you have an Electrical Engineering background? Do you have a talent for learning complex software and conveying that information to customers in a simple and effective manner? If yes, consider a career as an Information Developer for Siemens’ Electronic Design Automation (EDA) products. Xpedition Enterprise is the industry’s most innovative printed circuit board (PCB) design flow, providing integration from system design definition to manufacturing execution, including electrical performance analysis. Its unique technologies can reduce design cycles by 50 percent or more while significantly improving overall quality and resource efficiency. Customers can configure our software to implement their unique business processes. They can also choose from packaged SaaS solutions that meet specific, pre-defined business needs. The Xpedition tool suite combines ease-of-use and highly automated functionality to deliver industry-leading advanced technologies for creating today’s most complex PCB designs. Our writing team provides the following environment: - A shared sense of purpose, camaraderie, and humor - Training to gain knowledge in the field - DITA XML-based editing and publishing integrated with a CCMS - Agile development framework - Ability to innovate and drive workflow and product improvements Key Responsibilities: As an Information Developer, you will work closely with a talented development staff and be responsible for developing documentation for both new and proven technologies that enable customers to quickly realize value from purchasing electronic board system products. Your ability to develop real-world use cases and task-based usage information is critical to onboarding customers and ensuring their success with our products. Our global development staff and customer service teams are your partners in this endeavor. Your responsibilities include creating examples, usage flows, procedures, AI-targeted content, and other reference materials as well as opportunities for How-To video development. This skilled technical writer will document complex HyperLynx tools, coordinate documentation efforts, and contribute to a collaborative environment with significant growth potential in EDA skills. Preferred Skills: - PCB software industry knowledge, or experience working with specific PCB software tools - Experience with high‑speed PCB analysis tools that rely on detailed, constraint‑driven design methodologies - Highly technical writing experience - Excellent interpersonal skills - Outstanding investigative research skills - Multitasking or Agile project management experience - BS in a technical discipline (such as Electrical Engineering) If you have a highly technical background or are an engineer looking to develop new skills, please send both a cover letter and resume. At Siemens we are always challenging ourselves to build a better future. We need the most innovative and diverse Digital Minds to develop tomorrow’s reality. Find out more about the Digital world of Siemens here: www.siemens.com/en-us/company/jobs/ This position will be subject to U.S. export control requirements under the International Traffic in Arms Regulations (ITAR) and/or Export Administration Regulations (EAR).  Employment is contingent on either verifying the U.S. Person status or obtaining any necessary export license.  Why us? Working at Siemens Software means flexibility - Choosing between working at home and the office at other times is the norm here. We offer great benefits and rewards, as you'd expect from a world leader in industrial software. A collection of over 377,000 minds building the future, one day at a time in over 200 countries. We're dedicated to equality, and we welcome applications that reflect the diversity of the communities we work in. All employment decisions at Siemens are based on qualifications, merit, and business need. Bring your curiosity and creativity and help us shape tomorrow! Siemens Software. Transform the Everyday #LI-PLM #LI-REMOTE You’ll Benefit From Siemens offers a variety of health and wellness benefits to our employees. Details regarding our benefits can be found here: https://www.benefitsquickstart.com/siemens/index.html The pay range for this position is $90,000 - $162,000 annually with a target incentive of 3 - 5% of the base salary. The actual wage offered may be lower or higher depending on budget and candidate experience, knowledge, skills, qualifications, and premium geographic location. Equal Employment Opportunity Statement Siemens is an Equal Opportunity Employer encouraging inclusion in the workplace. All qualified applicants will receive consideration for employment without regard to their race, color, creed, religion, national origin, citizenship status, ancestry, sex, age, physical or mental disability unrelated to ability, marital status, family responsibilities, pregnancy, genetic information, sexual orientation, gender expression, gender identity, transgender, sex stereotyping, order of protection status, protected veteran or military status, or an unfavorable discharge from military service, and other categories protected by federal, state or local law. EEO is the Law Applicants and employees are protected from discrimination on the basis of race, color, religion, sex, national origin, or any characteristic protected by Federal or other applicable law. Reasonable Accommodations If you require a reasonable accommodation in completing a job application, interviewing, completing any pre-employment testing, or otherwise participating in the employee selection process, please fill out the accommodations form by clicking on this link Accommodation for disability form. If you’re unable to complete the form, you can reach out to our AskHR team for support at 1-866-743-6367. Please note our AskHR representatives do not have visibility of application or interview status. Pay Transparency Siemens follows Pay Transparency laws. California Privacy Notice California residents have the right to receive additional notices about their personal information. To learn more, click here. Criminal History Qualified applications with arrest or conviction records will be considered for employment in accordance with applicable local and state laws.

• Responsible for researching, writing, and editing materials for regulatory submission to the FDA from pre-clinical to clinical trials Phase 1 - 4 • Works collaboratively with Clinical Project Managers, Clinical Trial Associates (CTA) and other cross-functional departments • Identifies and executes timeline plans for clinical, nonclinical, and CMC • Coordinates, authors, and develops drug applications and submissions in support of clinical programs • Offers high visibility and exposure to FDA regulatory requirements, Good Clinical Practice (GCP), ICH guidelines, and/or eCTD format • Author and compile FDA and Ex-US regulatory applications and submissions • Assist in the research of scientific and regulatory information to write submission documents • Work with data management and clinical teams to review protocol development and interpret clinical trial data • Responsible for contributing to project timelines and regulatory milestones • Responsible for communication of commitments to team members • Lead multiple, concurrent projects, with support from the Principal or Regulatory Manager • Format and edit regulatory documentation for inclusion in INDs, CTAs, and other global submissions • Support on-time preparation and publication of regulatory submission documents

Role Description JoVE is seeking an experienced Peer Review Editor to coordinate our peer review process from submission to editorial decision. You will manage reviewers, oversee review quality and timelines, and ensure that manuscripts meet JoVE’s scientific rigor, ethics, and reporting standards, delivering a clear, timely, and positive experience for authors and reviewers alike. - Manage end-to-end peer review for assigned submissions (reviewer selection/invitations, review monitoring, decision preparation, and revision management). - Build, vet, and maintain a high-quality reviewer pool; track expertise coverage; build network with top reviewers for rapid, fair evaluations. - Monitor timelines and throughput (e.g., time to first decision, reviewer acceptance/turnaround); proactively unblock delays and optimize workflow. - Collaborate with JoVE Editorial and Production teams to deliver a smooth author journey from submission through publication. - Identify and implement process improvements (templates, automation, dashboards) to reduce cycle times and improve review quality. - Maintain accurate records in the manuscript system (e.g., Editorial Manager, Monday.com): reviewer activity, decisions, correspondence, and policy exceptions. Qualifications - A Bachelor’s degree in the life sciences or a related field (advanced degree a plus). - 5+ years in scholarly publishing with hands-on peer review experience. - Working knowledge of peer review models (single-blind, double-blind, open), open access workflows, and emerging trends in scholarly communication. - Proficiency with manuscript systems and workflow tools (Editorial Manager strongly preferred; comfort with automation/AI-assisted tools for efficiency). - Exceptional written communication and editorial judgment; able to synthesize complex feedback into clear, actionable decisions. - Strong organization and project management skills; thrives in a fast-paced, deadline-driven environment. Benefits - A competitive compensation package. - You will make a direct impact in accelerating science research and in improving student learning in science education. - Opportunity to work with global teams and in an environment that promotes innovation and collaboration. - Our strong promotion from within culture draws a clear path to advance your career with us.