6 documentation writer jobs at 5 companies in Limerick, 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.
Senior Director, Global Scientific and Regulatory Documentation, Content Strategy
Princeton or Phoenix or Los Angeles County or Puerto Rico
$225k-$273k/yrOnsiteFull Time
Bristol Myers SquibbNew York Stock Exchange: BMY: Develops and distributes innovative medicines for serious diseases.
Leading a team of scientific writers, applying advanced regulatory documentation standards, driving content libraries and document automation, and providing scientific and customer-focused leadership.
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.
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.
EXPERIENCED AUTOMOTIVE SERVICE ADVISOR / WRITER (3+ YEARS EXPERIENCE)
Wilmington, Delaware, United States
OnsiteFull Time
Winner Automotive Group: Sells and services new and pre-owned vehicles in Delaware.
Customer-facing role requiring automotive system knowledge, telephone and documentation skills, ability to estimate service time, and promote service/maintenance to customers.
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.