6 documentation writer jobs at 5 companies in Wyncote, PA
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Specifications Writer
Conshohocken, Pennsylvania, United States
HybridFull Time
Array Architects: Healthcare-focused architecture and advisory firm.
5+ YOE5+ years in construction documentation and technical specifications writing; knowledge of CSI MasterFormat, specification development, technical writing, and ability to support multiple projects and teams.
SystImmune: Developing multi-specific antibodies and antibody-drug conjugates for cancer therapy
1+ YOEMaster's in life sciences or 3–4 years medical writing experience (PhD with 1+ year acceptable). Requires excellent writing, knowledge of FDA/ICH, clinical data interpretation, and experience with protocols/CSRs/major regulatory documents.
Synterex: Clinical consulting firm providing regulatory documentation and medical writing.
5+ YOERequires 5+ years of medical writing experience in CRO, biotech, or pharmaceutical settings, a relevant bachelor's degree or higher, regulatory document expertise, Microsoft applications proficiency, and strong communication skills.
Microsoft Word, Microsoft Excel, Microsoft PowerPoint, Microsoft Outlook
Battle Creek or Whitehall or Wright-Patterson Air Force Base or New Cumberland or Philadelphia or Hill Air Force Base or Fort Belvoir or Richmond
$106k-$158k/yrHybridFull Time
Defense Logistics Agency: Manages the global supply chain for the Department of Defense.
1+ YOEOne year of specialized experience equivalent to GS-12 in technical writing, editing, enterprise documentation, publication workflows, version control, records management, and stakeholder coordination.
Defense Logistics Management Standards (DLMS), Section 508, Content Management System (CMS), USA Hire, USAJOBS, Microsoft Word, PDF
Bristol Myers SquibbNew York Stock Exchange: BMY: Develops and distributes innovative medicines for serious diseases.
10+ YOEAdvanced scientific degree or equivalent experience, ~10 years regulatory documentation experience, expert writing skills for regulatory submissions, knowledge of global drug development, document management and publishing processes.
Kardigan: Developing precision medicines to treat and cure cardiovascular disease.
10+ YOE10+ years in regulatory affairs/writing or scientific communication supporting global submissions; advanced degree preferred; experience with eCTD content, briefing documents, protocols, CSRs, health authority interactions, GxP and inspection readiness; leadership of writers/vendors.