Director, SDS Authoring Services 3EDirector, SDS Authoring ServicesBethesda, MD8+ years of experience in SDS authoring, chemical regulatory consulting, product stewardship, or a related field, including 7+ years of leadership experience managing global teams and developing people leaders. Reporting to the Associate Vice President, Delivered Services, you will lead a global team responsible for delivering approximately 20,000 SDSs annually across a diverse portfolio of customers with varying service levels and turnaround expectations.
Technical Editor and Writer 2 StratAcuity Staffing Partners IncTechnical Editor and Writer 2Elkridge, MD$35–$51 / hourIn terms of professional development, Everforth Apex hosts an on-demand training program, provides access to certification prep and a library of technical and leadership courses/books/seminars once you have 6+ months of tenure, and certification discounts and other perks to associations that include CompTIA and IIBA. Everforth Apex also offers a HSA (Health Savings Account on the HDHP plan), a SupportLinc Employee Assistance Program (EAP) with up to 8 free counseling sessions, a corporate discount savings program and other discounts.
Technical Editor and Writer 2 PGS WorldwideTechnical Editor and Writer 2Elkridge, MD$30 / hourThis onsite role requires active Secret clearance, structured authoring experience, XML document tagging, MS Office and Adobe Acrobat proficiency, and the ability to work with engineers, task leads, instructors, and program teams to produce clear technical manuals for military end users. 2+ years of technical writing experience using structured authoring applications such as Arbortext, IADS Viewer, or other XML authoring software tools.
Technical Editor and Writer 2 First Tek, Inc.Technical Editor and Writer 2Elkridge, MDWrites, rewrites, develops technical manual content such as Operating Procedures, Maintenance procedures, Troubleshooting procedures, Preventive Maintenance, to communicate clearly and effectively technical information and instructions to the military end-user. Minimum of 5 years' technical writing experience with structured authoring applications, such as Arbortext, and/or IADS viewer, or other XML authoring software tools.
Technical Editor and Writer 2 DP ProfessionalsTechnical Editor and Writer 2Elkridge, MDResponsibilities: Writes, rewrites, develops technical manual content such as Operating Procedures, Maintenance procedures, Troubleshooting procedures, Preventive Maintenance, to communicate clearly and effectively technical information and instructions to the military end-user. Preferred qualifications: Minimum of 5 years’ technical writing experience with structured authoring applications, such as Arbortext, and/or IADS viewer, or other XML authoring software tools.
Engineering Tech Writer 2 Precision Resources Company IncEngineering Tech Writer 2Elkridge, MDResponsibilities: Writes, rewrites, develops technical manual content such as Operating Procedures, Maintenance procedures, Troubleshooting procedures, Preventive Maintenance, to communicate clearly and effectively technical information and instructions to the military end-user. Preferred Qualifications: Minimum of 5 years’ technical writing experience with structured authoring applications, such as Arbortext, and/or IADS viewer, or other XML authoring software tools.
Senior Manager, Medical/Regulatory Writer Immunocore Holdings PlcSenior Manager, Medical/Regulatory WriterGaithersburg, MDVacancy NameSenior Manager, Medical/Regulatory Writer Vacancy NoVN831 Employment TypeFull Time Location of roleGaithersburg, MD, Radnor, PA, Remote, US DepartmentRegulatory Affairs Key ResponsibilitiesThe Senior Manager, Medical/Regulatory Writer will be accountable for leading and overseeing the medical and scientific regulatory writing for assigned programs to support submissions from first-in-human studies through product registration. Authoring or supervising the preparation of other regulatory documents required for Health Authority submissions, including but not limited to: Clinical Summaries (Clinical Overview, ISS/ISE, PK/PD summary, Advisory Committee Briefing document), Investigator Brochure(s), DSURs, other regulatory documents including briefing documents for health authorities, responses to Health Authority questions, etc.
Technical Writer - TS/SCI with Polygraph General Dynamics Information TechnologyTechnical Writer - TS/SCI with PolygraphElkridge, WashingtonTo ensure our employees are able to protect their income, other offerings such as short and long-term disability benefits, life, accidental death and dismemberment, personal accident, critical illness and business travel and accident insurance are provided or available. To encourage work/life balance, GDIT offers employees full flex work weeks where possible and a variety of paid time off plans, including vacation, sick and personal time, holidays, paid parental, military, bereavement and jury duty leave.
Clinical Regulatory Writer, Associate Director / Manager AstraZeneca PlcClinical Regulatory Writer, Associate Director / ManagerGaithersburg, MD$133,042.40–$199,563.60 / yearOur team provides expert communications leadership to drug projects, authoring strategically important clinical-regulatory documents that align with project strategies and regulatory requirements. Essential Skills/Experience: Education/Experience required: Associate Director level: BS Life Sciences degree or simiilar, 7+ yrs medical writing experience in pharmaceutical industry or CRO.
Lead Technical Writer - Columbia, MD Rohde & Schwarz GmbH & Co KGLead Technical Writer - Columbia, MDColumbia, MDRemote$90,000–$120,000 / yearCollaborate with other departments (including internationally), such as Service Operations, Production, Program Management, and Engineering to ensure alignment and effective communication regarding project status, timeline, risk management/mitigation in deliverables, etc. The successful candidate works closely with system engineering, software development, test engineering, trainers, and customer stakeholders to translate complex technical information into clear, accurate, and user-friendly technical documentation.
Technical Writer LeidosTechnical WriterAnnapolis Junction, MarylandOversee the collection, organization, and analysis of technical information, and support the preparation, editing, and revision of a wide range of documentation for complex computer systems and network environments, including user manuals, training materials, installation guides, and other program deliverables. Collaborate closely with software developers, systems engineers, test engineers, and other technical personnel to gather source data, screenshots, and supporting media required for the development of accurate and effective technical documentation.
Technical Writer TS/SCI Polygraph LeidosTechnical Writer TS/SCI PolygraphAnnapolis Junction, MarylandOversee the collection, organization, and analysis of technical information, and support the preparation, editing, and revision of a wide range of documentation for complex computer systems and network environments, including user manuals, training materials, installation guides, and other program deliverables. Collaborate closely with software developers, systems engineers, test engineers, and other technical personnel to gather source data, screenshots, and supporting media required for the development of accurate and effective technical documentation.
Technical Writer Textron IncTechnical WriterHunt Valley, MD$71,400–$107,000 / yearTechnical Writers in the Textron Integrated Product Support Services (IPSS) group are responsible for developing technical manual documentation necessary to install, operate and support complex equipment platforms for a variety of military and commercial customers. Technical Writers develop publications work products that include: equipment description, theory of operation, operator instructions, troubleshooting procedures, maintenance instructions (remove and replace procedures), wiring list, supporting information, and Repair Parts and Special Tools Lists.