Remote Senior Technical Writer Job Vacancies

3 of 3 Remote Senior Technical Writer Jobs

Senior Technical Editor (Technical Writer) with Security Clearance

Washington, Washington DC, United States
Hybrid / WFH Options
General Dynamics Information Technology
Technical Editor Senior (Technical Writer) Your Impact Own your opportunity to work alongside federal civilian agencies. Make an impact by providing services that help the government ensure the well-being of U.S. citizens. Job Description We are seeking a qualified, motivated individual to join GDIT as a Senior Technical Editor (Technical Writer … the development of contract deliverables and reports Editing functional descriptions, user manuals, special reports, or any other customer deliverables or document Conducting research and ensuring the use of proper technical terminology Preparing and maintaining operations documentation, user guides, manuals, and technical publications Preparing reports, responses, and briefings targeted to a wide range of audiences Senior Technical … processes are defined, executed, monitored, and improved Review existing processes and offer recommendations for process improvements, streamlined workflows, and simplified procedures Ensure documentation meets customer compliance and audit standards Senior Technical Editor Requirements and Qualifications: Bachelor of Arts/Science in English, Business Administration, Computer Science, Software Engineering or equivalent Knowledge of Federal documentation standards and processes Experience More ❯
Employment Type: Permanent
Salary: USD Annual
Posted:

Technical Writer/Senior Operations Analyst (MANA2) with Security Clearance

Arlington, Virginia, United States
Hybrid / WFH Options
ELS Inc
professionals that work collaboratively to provide exceptional support and solutions to our customers. We are caring, results driven, and strive to provide a meaningful work experience. Job summary: The Technical Writer/Senior Operations Analyst will support the NATO SEASPARROW Project Office (NSPO) as a key member of the meeting support and operations team. The role focuses … on executive-level engagement within a fast-paced Integrated Warfare Systems (IWS) acquisition program. The selected candidate will capture real-time strategic and technical meeting content, manage critical workflows, and enhance operational efficiency through superior communication and documentation practices. Key Responsibilities: • Attend and document classified and CUI-level meetings both virtually and on-site. • Capture and synthesize real-time … notes, action items, and decision points during executive and technical forums. • Draft executive summaries, meeting minutes, after-action reports, and stakeholder updates for leadership. • Coordinate logistics for high-level meetings, including agenda preparation, read-ahead distribution, and teleconference facilitation. • Maintain an organized action item tracker; ensure accountability and follow-up with responsible stakeholders. • Develop and format presentations and decision More ❯
Employment Type: Permanent
Salary: USD Annual
Posted:

Senior MSAT Technical Writer

Leiden, Zuid-Holland, Netherlands
Hybrid / WFH Options
Panda International
An international biopharmaceutical company is seeking an experienced Senior Technical Writer to support its cell and gene therapy initiatives-specifically focusing on CAR-T and Lentiviral Vector (LVV) programs. Based in Leiden, this position will work closely with the Global MSAT and Viral Vector teams to produce high-quality, regulatory-compliant documentation that supports process development, validation … Location: Leiden, Netherlands (Hybrid: 2-3 days onsite per week) Start Date: ASAP Contract: 6 months Language Requirement: English Key Responsibilities: Develop, review, and maintain a broad range of technical documents, including process descriptions, scientific reports, SOPs, risk assessments, comparability protocols, and deviation/investigation reports. Support the preparation of CMC sections for INDs, IMPDs, and regulatory responses. Collaborate … documentation standards, including template creation, content quality training, and best practice implementation. Candidate Profile: PhD or MSc in Life Sciences, Biotechnology, or Engineering. Minimum 7 years of experience in technical and regulatory writing within GMP environments. Background in cell and gene therapy required; direct experience with CAR-T or LVV is highly preferred. Strong ability to simplify complex scientific More ❯
Employment Type: Permanent
Salary: EUR Annual
Posted: