Senior MES MBR Author ApolisSenior MES MBR AuthorAtlanta, GA$60–$65 / hourProvide on-site, hands-on support for manufacturing execution, including End User training and resolving issues related to Client-X master records (runtime errors, missing master data, step logic issues, signature/role issues). 2.Life Sciences industry understanding of GMP concepts: data integrity (ALCOA+), electronic signatures, validation requirements, audit trails, controlled documents, deviations/CAPA, and change control.
Senior PAS-X MES MBR Author / MES Business Analyst IconmaSenior PAS-X MES MBR Author / MES Business AnalystLithia Springs, GAProvide on-site, hands-on support for manufacturing execution, including End User training and resolving issues related to PAS-X master records (runtime errors, missing master data, step logic issues, signature/role issues). Responsibilities: The Senior MES MBR Author & Coordinator is responsible for authoring, reviewing, and coordinating end-to-end execution of electronic Master Batch Records (eMBRs) in PAS-X for GMP manufacturing.
Senior PAS-X MES MBR Author / MES Business Analyst ICONMA, LLCSenior PAS-X MES MBR Author / MES Business AnalystLithia Springs, GA$60.71 / hourProvide on-site, hands-on support for manufacturing execution, including End User training and resolving issues related to PAS-X master records (runtime errors, missing master data, step logic issues, signature/role issues). Responsibilities: The Senior MES MBR Author & Coordinator is responsible for authoring, reviewing, and coordinating end-to-end execution of electronic Master Batch Records (eMBRs) in PAS-X for GMP manufacturing.
Senior MES MBR Author TechDigital CorporationSenior MES MBR AuthorLithia Springs, GAProvide on-site, hands-on support for manufacturing execution, including End User training and resolving issues related to Client-X master records (runtime errors, missing master data, step logic issues, signature/role issues). 2. Life Sciences industry understanding of GMP concepts: data integrity (ALCOA+), electronic signatures, validation requirements, audit trails, controlled documents, deviations/CAPA, and change control.
Senior PAS-X MES MBR Author / MES Business Analyst Iconma LLCSenior PAS-X MES MBR Author / MES Business AnalystLithia Springs, GAProvide on-site, hands-on support for manufacturing execution, including End User training and resolving issues related to PAS-X master records (runtime errors, missing master data, step logic issues, signature/role issues). Responsibilities: The Senior MES MBR Author & Coordinator is responsible for authoring, reviewing, and coordinating end-to-end execution of electronic Master Batch Records (eMBRs) in PAS-X for GMP manufacturing.
Solution Author, Audit Solutions Caseware International Inc.Solution Author, Audit SolutionsAtlanta, GARemoteAs a Solution Author, you will work closely with Product Managers, Solution Architects, Developers, Quality Assurance teams, and Subject Matter Experts to design, develop, and maintain audit content and workflows within Caseware's cloud-based audit solutions. All legitimate communication from us will come from email addresses ending in @caseware.com and our open positions are always listed on reputable job boards and on our website https://jobs.lever.co/caseware .
Clinical Document Author - Remote YO AI LabsClinical Document Author - RemoteAtlanta, GeorgiaRemote$50–$80 / hourWe are seeking an experienced Medical Writer / Clinical Document Author to develop, review, and evaluate clinical and regulatory documents while ensuring scientific accuracy, regulatory compliance, and high-quality medical writing. Verify scientific accuracy using source data, TFLs (Tables, Figures, and Listings), and study documentation.
Technical Problem Author - Remote YO AI LabsTechnical Problem Author - RemoteAtlanta, GeorgiaRemoteAuthor and evaluate advanced technical problems across areas such as Aerodynamics, Materials Science, CAD/Mechanical Design, Mechanical Engineering, Circuit Design, and related disciplines . We are seeking experienced Engineering Technical Problem Authors to contribute their technical expertise to a project focused on advancing next-generation AI systems in engineering.
Solution Author, Audit Solutions CasewareSolution Author, Audit SolutionsAtlanta, GeorgiaRemoteFull timeAs a Solution Author, you will work closely with Product Managers, Solution Architects, Developers, Quality Assurance teams, and Subject Matter Experts to design, develop, and maintain audit content and workflows within Caseware's cloud-based audit solutions. All legitimate communication from us will come from email addresses ending in @caseware.com and our open positions are always listed on reputable job boards and on our website https://jobs.lever.co/caseware.
Medical Writer / Clinical Document - Remote YO AI LabsMedical Writer / Clinical Document - RemoteAtlanta, GeorgiaRemote$50–$80 / hourWe are seeking an experienced Medical Writer / Clinical Document Author to develop, review, and evaluate clinical and regulatory documents while ensuring scientific accuracy, regulatory compliance, and high-quality medical writing. Verify scientific accuracy using source data, TFLs (Tables, Figures, and Listings), and study documentation.
Technical Writer ASM Research, An Accenture Federal Services CompanyTechnical WriterAtlanta, GA$64,000–$71,700 / yearCompensation ranges for ASM Research positions vary depending on multiple factors; including but not limited to, location, skill set, level of education, certifications, client requirements, contract-specific affordability, government clearance and investigation level, and years of experience. This role collaborates closely with engineers, analysts, process and practice owners, service owners, the ITIL Specialist, and the Service and Integration Management Lead to translate complex technical, operational, and security-related information into accessible content.
QC Document Control Writer Zp Group LlcQC Document Control WriterAthens, GAKeywords: Technical Writer, Documentation Specialist, Document Control, SOP, cGMP, GDP, Quality Assurance, pharmaceutical. Piper Companies is seeking a QC Document Control Writer to support a global, industry-leading pharmaceutical organization in Athens, GA.
Medical Writer - Remote YO AI LabsMedical Writer - RemoteAtlanta, GeorgiaRemote$50–$80 / hourWe are seeking an experienced Medical Writer / Clinical Document Author to develop, review, and evaluate clinical and regulatory documents while ensuring scientific accuracy, regulatory compliance, and high-quality medical writing. Verify scientific accuracy using source data, TFLs (Tables, Figures, and Listings), and study documentation.
Senior Technical Writer - Madcap Flare & AI Expert Wolters KluwerSenior Technical Writer - Madcap Flare & AI ExpertKennesaw, GARemote$60,700–$106,000 / yearThis is an exciting opportunity for a technical writer who enjoys learning complex software, partnering with Product Managers and Subject Matter Experts, and turning complicated functionality into clear, intuitive documentation for end users. We've been recognized by employees as a European Diversity Leader in the Financial Times, as one of Forbes America's Best Employers for Diversity in 2022, 2021 and 2020 and as one of Forbes America's Best Employers for Women in 2021, 2020, 2019 and 2018.