Author Jobs
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TekWissen ®-Charlotte
as possible—with your needs in mind. Because of our unique structure, your goals align with our goals.
Position: AEM Author
Location: Malvern, PA or Charlotte, NC
Duration: 6 Months
Job Type: Temporary Assignment
Work Type: Hybrid
Pay Rate: $ 55-55...
Pacer Group-Malvern (PA)
Contractor – Analyst (AEM - Author)
Perform all the authoring operations by leveraging the content management system (CMS) to edit, upload, delete, and manage content used online.
Manages development of content and asset requirements to execute...
Godevico Publishing-United States
Company Description
Godevico Publishing is redefining the self-publishing experience by enabling individuals from all walks of life to transform their ideas into income through accessible and easy-to-use publishing solutions. We empower authors...
Writers Work-New Orleans
Technical Web Content
Our growing New Orleans tech company seeks a seasoned technical scribe to bridge the gap between intricate software architecture and user comprehension. We aren't just documenting code; we're crafting user journeys. As our...
Bethesda (MD)
Requisition ID: 2026-4749
Job Summary:
Artemis is seeking a full-time Writer and Author (Print Journalism) to capture and share the powerful stories of innovation, compassion, and service that define the Walter Reed National Military Medical...
icims.com -
Writers Work-Philadelphia
Technical Writer
Our Philadelphia-based organization is experiencing substantial growth, and we're seeking a versatile Technical Writer to bolster our documentation efforts. This is a remote opportunity ideal for an individual passionate about...
Entourage Consulting LLC-Bethesda (MD)
Writer and Author
Place of Performance: Bethesda, Maryland
General Description:
Writer and Author (Print Journalism) shall capture and share the powerful stories of innovation, compassion, and service that define the institution. This role requires...
jobvertise.com -
Medasource-Raleigh
to ensure compliance with FDA and applicable regulatory requirements.
• Author and manage change controls related to SOP updates and manufacturing process improvements.
• Edit batch records and manufacturing documentation as needed.
• Initiate, investigate...
University of Louisville-Louisville
for a second year, contingent upon satisfactory performance & funding availability. The fellow will benefit from direct mentorship, opportunities for first-author publications, hands-on experience developing NIH grant applications, & interdisciplinary...
Thermo Fisher Scientific-Raleigh
a proven track record in authoring clinical regulatory documents; ideally they will also bring the versatility to author and support preclinical regulatory documents as part of a broader regulatory writing portfolio.
Essential Functions:
• Serves...
University of Louisville-Louisville
for a second year, contingent upon satisfactory performance & funding availability. The fellow will benefit from direct mentorship, opportunities for first-author publications, hands-on experience developing NIH grant applications, & interdisciplinary...
Thermo Fisher Scientific-Greensboro
a proven track record in authoring clinical regulatory documents; ideally they will also bring the versatility to author and support preclinical regulatory documents as part of a broader regulatory writing portfolio.
Essential Functions:
• Serves...
Meet Life Sciences-Bridgewater (NJ)
Oversee and manage multiple projects at the same time, driving CSV deliverables
/n
• Author CSV documents, including Validation Plans and Summary Reports
/n
• Assist with or co-author requirements, URS/FRS, IQ/OQ/PQ protocols, specifications, and other...
Thermo Fisher Scientific-Charlotte
a proven track record in authoring clinical regulatory documents; ideally they will also bring the versatility to author and support preclinical regulatory documents as part of a broader regulatory writing portfolio.
Essential Functions:
• Serves...
Integrated Resources, Inc ( IRI )-United
upstream and downstream process development programs.
/n
Manage analytical activities performed by CROs and support analytical transfers to CROs and CMOs.
/n
Review analytical data and reports supporting GMP manufacturing activities.
/n
Author...
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