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: 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.
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.
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
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.
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)
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.
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.