L3Harris is dedicated to recruiting and developing high-performing talent who are passionate about what they do. Our employees are unified in a shared dedication to our customers’ mission and quest for professional growth. L3Harris provides an inclusive, engaging environment designed to empower employees and promote work-life success. Fundamental to our culture is an unwavering focus on values, d...
L3Harris is dedicated to recruiting and developing high-performing talent who are passionate about what they do. Our employees are unified in a shared dedication to our customers’ mission and quest for professional growth. L3Harris provides an inclusive, engaging environment designed to empower employees and promote work-life success. Fundamental to our culture is an unwavering focus on values, d...
Job DescriptionAbout the Company
Protego Bio is a clinical-stage biotechnology company based in San Diego, California, focused on developing first-in-class small-molecule therapeutics that target protein misfolding diseases. By restoring protein stability and function through novel pharmacological chaperones, Protego aims to transform the treatment of rare and systemic diseases with significant unm...
Job DescriptionExport control scope experience related to Nuclear/Defense Technical Document writing & Document conversion.
Technical Documents
Attend pre-job brief or other supporting meetings in advance of technical writing being performed
Perform technical writing review of text-based documents as per applicable discipline process
Collaborate with document owners and content creators on content...
Job DescriptionGrant Writer needed to identify funding opportunities, develop competitive proposals, coordinate cross‑departmental input, and ensure compliance with all federal, state, and local requirements. The ideal candidate is a strategic thinker, exceptional writer, and detail‑driven project manager who thrives in deadline‑driven environments and has proven experience securing grants of...
Job DescriptionPurpose:
Responsible for supporting clients’ missions, strategic goals, and operational objectives. Identifies and analyzes relevant client opportunities and threats. Contributes new ideas, improvements, methods to serve client needs, and initiatives that advance the Firm’s success.
Key responsibilities include:
Identifies, analyzes, and tracks grant programs, legislation, re...
Job DescriptionThe Clinical Regulatory Writing team provides expert communications leadership to drug projects and authors strategically important clinical-regulatory documents that are label focused and align with project strategies, regulatory requirements, and communications best-practices. We support the Company’s core therapeutic areas in all phases of clinical development. Our vision is to ...
Technical Editor Open
Technical Editor Open
Job DescriptionHTRI seeks someone to edit and format technical documents, including electronic rendering of schematics and graphics; create, manage, and revise software documentation projects.
Principal Responsibilities
Edit (both online and hard copy) and format documents, including electronic rendering of supporting graphics. Ensure consistency and quality of documents that reflect corporate i...
Technical Writer Open
Technical Writer Open
Bathing Brands is a well-established, growing organization in the sauna, steam, and experiential bathing space. We don’t just build products—we make them easy to understand, install, and enjoy, and that starts with clear, well-crafted documentation.As we continue to grow, we’re looking for a Technical Writer to take the lead on the written content behind our products throughout their lifecycl...
Technical Writer Open
Technical Writer Open
Job DescriptionJob Title: Quality Control Investigation Writer
Location: High Point, NC 27265
Duration: 12 Months - Contract
Pay Rate: $20.00 - $36.00/hr w2
Position Summary:
The Quality Control (QC) Investigation Writer is responsible for leading, authoring, and coordinating laboratory investigations within the Quality Control department in support of GMP-regulated pharmaceutical manufacturing ...
BHE GT&SJOB DESCRIPTIONBHE GT&S has an exciting opportunity as a Technical Specialist/Senior Technical Specialist (Civil Technical Services) at our White Oaks General Office location in Bridgeport, WV.RESPONSIBILITIESLead planning, design, procurement, and construction activities for pipeline, compression, and civil/structural projects across the BHE GT&S system. Provide technical oversight, engine...
Technical Writer Open
Technical Writer Open
Technical WriterWork Mode: OnsiteLocation: Onsite, four days per week – Kohler, WIOpportunitySupports the development, review, and execution of technical communication deliverables for kitchen and bath products, including publications, labels and packaging, and animations. Works under the guidance of experienced Technical Communications team members to gather information, draft content, follow es...
Job DescriptionContract Technical Writer – CAPA/SOP Remediation
Location: Raleigh, NC (On-site)
Pay Rate: $40–$47/hour
Engagement Type: Contract
Schedule: Monday-Friday 8am-5pm
Duration: Initial 6–8 weeks with strong potential for extension
Openings: 2
Overview
We are seeking multiple Contract Technical Writers to support a high-priority documentation remediation initiative at a regulated man...
Job DescriptionThe ideal candidate will be responsible for creating and writing various types of user documentation, including how-to guides, manuals, references, or instructions. This candidate should have strong communication skills which enable them to explain complicated concepts in a simple manner. This individual will also meet with customer representatives frequently in order to understand r...
Technical Writer Open
Technical Writer Open
Job DescriptionPosition Summary
The Technical Writer serves as a bridge between customers, product management, and software engineering. This position is responsible for documenting product requirements, creating customer-facing documentation, and supporting product delivery from concept through implementation. This role works closely with stakeholders, development, QA, support, and product teams t...
Job DescriptionSUMMARY/OBJECTIVE:
The Technical Writer is responsible for leading Quality Management System (QMS) documentation activities within Operations. This role will partner closely with Manufacturing, Packaging, Warehouse, Facilities, and Quality Assurance teams to draft, revise, route, and maintain controlled documentation in support of compliant GMP operations. This position serves as a k...
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