6 senior writer jobs at 6 companies in Elon, NC

2mo
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Specifications Writer
Asheville or Charlotte or Greensboro or Greenville or Jacksonville or Atlanta or Savannah or Columbia or Myrtle Beach or Charleston or Raleigh or Wilmington
OnsiteFull Time
LS3P
LS3P: N architecture, interiors, and planning firm celebrating more than 60 years of design excellence.
5+ YOEDevelop and manage project specifications; knowledge of CSI MasterFormat; proficiency with specification platforms (RIB SpecLink preferred, SpecsIntact desired); 5+ years preparing architectural specifications; strong communication and organization.
CSI MasterFormat, RIB SpecLink, SpecsIntact
3w
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Technical Writer
Morrisville or Cranberry Township or Boulder
OnsiteFull Time
NetApp
NetAppNASDAQ: NTAP: Global cloud-led, data-centric software.
8+ YOERequires 8+ years in technical writing, content strategy, knowledge management, or information architecture; leadership of complex documentation initiatives; structured authoring, content strategy, AI-assisted tools, and enterprise technology documentation.
GitHub, AsciiDoc, Markdown, AI-assisted tools
2d
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Technical Writer - 4
San Jose or Durham or Mexico City or Bangalore or Pune or Hoofddorp or Belgrade or Barcelona or Singapore or Sydney or Tokyo
HybridFull Time
Nutanix
NutanixNASDAQ: NTNX: Enterprise hybrid multi-cloud computing and software provider.
8+ YOEGraduate degree in a related field and 8+ years documenting software products; experience with structured authoring, multiple deliverables, UNIX/Linux, and cross-functional teams required.
GitHub, UNIX/Linux, DITA, XML
2mo
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Principal Medical Writer
Durham or London
OnsiteFull Time
ViiV Healthcare
ViiV Healthcare: Specialty pharmaceutical developing HIV medicines for people living with HIV and people needing HIV prevention.
5+ YOEBachelor's in life/health/scientific field, 5+ years medical or regulatory writing in pharma, 3+ years regulatory dossier and CTD experience, 3+ years independently authoring protocols and clinical study reports; strong writing, teamwork, and regulatory knowledge.
Common Technical Document (CTD), International Council for Harmonisation (ICH), Good Clinical Practice (GCP)
2mo
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Principal Medical Writer
Durham or London
OnsiteFull Time
ViiV Healthcare
ViiV Healthcare: Specialty pharmaceutical developing HIV medicines for people living with HIV and people needing HIV prevention.
5+ YOEBachelor's in life/health sciences, 5+ years medical or regulatory writing in pharma/healthcare, 3+ years regulatory dossier/CTD experience, 3+ years authoring protocols and clinical study reports.
3w
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Principal Medical Writier
Durham, North Carolina, United States
$84k-$211k/yr OnsiteFull Time
IQVIA
IQVIANYSE: IQV: Providing advanced analytics, technology solutions, and clinical research services.
7+ YOEBachelor's degree required (advanced degree preferred),7+ years medical writing experience in biopharma/CRO, knowledge of ICH/FDA/EMA guidelines, strong project and communication skills, proficiency in Microsoft Word.
Microsoft Word