• Lead end-to-end proposal management across RFPs, RFIs, and permits throughout the Amer-APAC region, including kickoff, timeline development, stakeholder coordination, drafting, and final submission. Flex fluidly between proposal management and writing responsibilities depending on the needs, scale, and complexity of each opportunity. • Analyze procurement documents to identify key priorities, evaluation criteria, eligibility requirements, and competitive considerations, translating complex requirements into actionable proposal strategies. Partner closely with local operations, policy, finance, and other cross-functional teams across multiple countries and time zones to gather insights, align stakeholders, escalate issues, and develop high-impact offerings. • Write clear, compelling, and strategically tailored content for RFPs, RFIs, permits, and other city-facing submissions, often under tight deadlines, while owning the full review and revision cycle. Shape proposal narratives, messaging, and win themes that align with city priorities and strengthen Lime’s competitive positioning in collaboration with cross-functional stakeholders, graphic design, and content partners. • Build and improve internal proposal infrastructure, including best practices, templates, toolkits, and content libraries, to increase efficiency, consistency, and scalability across the team. Help drive continuous improvement across the proposals function, owning long-term infrastructure projects like best practices, templates, toolkits and content libraries and identifying new ways to make the team faster, sharper, and more scalable. • Support strategic market development efforts through occasional travel to key markets for pre-tender workshops, cross-functional meetings, and/or local planning sessions.

Role Description Shape the documentation foundation of a mission-critical Department of Veterans Affairs (VA) cloud platform as a Technical Writer! You'll produce, edit, and maintain the comprehensive suite of technical and operational documents supporting VA staff and millions of Veterans. The Technical Writer is responsible for the production, editing, formatting, and maintenance of all technical documentation and formal deliverables where you'll work across multiple program areas to synthesize complex technical content into clear, accurate, and professionally formatted documents suitable for both technical audiences and VA executive leadership. Qualifications - 5 years of experience in technical writing for cloud platforms, DevSecOps environments, and enterprise information technology (IT) systems - Bachelor's Degree in technical writing, English, communications, information technology, or related field Requirements - Excellent experience producing federal government technical documentation - Excellent experience producing project management plans, architecture packages, maintenance plans, assessment reports, and monthly status reports in Microsoft Word and Project formats - Excellent ability to translate complex technical concepts into clear, accurate prose accessible to non-technical stakeholders (e.g., cloud architecture, Kubernetes platform operations, DevSecOps pipelines, Risk Management Framework/security processes) - Excellent experience ensuring all deliverables meet Section 508 conformance requirements - Excellent experience tracking and reporting Information and Communication Technology (ICT) deliverable 508 status in weekly progress reports - Excellent ability to manage multiple simultaneous deliverable deadlines, track status against the Contractor Project Management Plan (CPMP), and proactively identify risks to on-time delivery - Excellent experience developing and maintaining living documents including capabilities and services catalogs, platform dependency lists, and architecture packages - Above average knowledge of SAFe Agile methodology and its documentation requirements (e.g., Sprint Retrospective Reports, Program Increment (PI) Milestone documents, PI artifacts) - Above average experience with Microsoft Office Suite (Word, Project, PowerPoint) - Above average experience with Jira and Confluence for document production, version control, and collaborative authoring - Working knowledge of cloud platform operations, AWS architecture, and VA enterprise policies to accurately document technical content - Experience supporting a federal agency - Excellent verbal and written communication skills Benefits - The annual projected pay range for this position is $75,769 - $101,809 with consideration being given to various factors including but not limited to qualifications, experience, job responsibilities, and geographic location. - Medical, dental, vision and prescription drug coverage for you and your family. - Life Insurance, short-term disability and long-term disability paid for by the Company. - Supplemental coverages including Accident, Critical Illness, and Hospital. - Additional Life insurance coverage for you and your dependents. - 401k plan with various options to select based on your retirement goals.

Role Description - Convert author-submitted manuscripts into clear, accurate, and engaging voiceover transcripts and video scripts. - Collaborate with authors to guide their manuscripts through the JoVE video creation process. - Proofread and review the video scripts to ensure scientific accuracy, clarity, and error-free content. - Interpret scientific comments, feedback, and requirements accurately and implement necessary changes with precision. - Utilize AI-assisted writing and editing tools effectively as part of the content development workflow. - Review journal protocol videos to ensure scientific accuracy and adherence to publication standards. - Assess author feedback on rough video drafts and effectively communicate required revisions to the video editing team. - Manage multiple projects simultaneously while meeting strict production timelines. - Follow established guidelines and maintain high-quality standards throughout the script development process. - Take initiative to identify and propose process improvements that enhance efficiency and content quality. Qualifications - PhD in biology, molecular biology, bioengineering, chemistry, or a related natural science discipline. - 1-3 years of experience in scientific communication, technical writing, or educational content creation. - Experience in teaching or content/curriculum development is preferred. - Strong scientific and technical vocabulary with the ability to explain complex concepts clearly. - Excellent written and verbal communication skills, with demonstrated strength in editing and proofreading. - Ability to apply AI-assisted tools in writing, editing, or content development workflows. - Strong attention to detail and ability to identify scientific inaccuracies in written and visual materials. - Strong organizational skills with the ability to multitask, prioritize, and work effectively under pressure. - Ability to follow detailed guidelines and consistently meet strict deadlines. - Ability to collaborate effectively across cross-functional production teams. - Enthusiasm for science and a willingness to learn about new research areas and visual communication methods. - A record of original research published in peer-reviewed scientific journals is strongly preferred. Benefits - A competitive compensation package. - You will make a direct impact in accelerating science research and in improving student learning in science education. - Opportunity to work with global teams and in an environment that promotes innovation and collaboration. - Our strong promotion from within culture draws a clear path to advance your career with us.

Role Description We are seeking a Freelancer Senior Medical Writer, based in Colombia for a part-time role, to provide medical and scientific expertise required for the successful completion of Excelya’s projects. - To write and edit complex medical writing deliverables (including informed consent forms, clinical study reports, clinical evaluation reports, CTD submissions) in accordance with sponsors’ and Excelya’s SOPs, guidelines and applicable legislation. - To coordinate cross-functional stakeholders and departments (including Clinical Operations, Biostatistics, Data Management, Regulatory Affairs, PV) to ensure the timely collection, review, alignment, and integration of scientific and clinical content required for the development of high-quality medical writing deliverables (including clinical study protocols, IBs, INDs). - To ensure the accuracy, consistency and regulatory compliance of all information, data and references included in the produced publications/documents, maintaining high standards of scientific quality. - To contribute to document quality control (reviewing data accuracy, formatting, appropriateness of language and compliance with industry guidelines). - To mentor and lead less experienced Medical Writers on complex projects, and to support the Principal Medical Writer with the coordination of other Medical Writers or Senior Medical Writers. - To liaise with sponsors to negotiate changes where necessary and ensure alignment on deliverables and expectations. Qualifications - Degree in Life Sciences. - At least 3 years of experience in medical writing. - Experience with writing of protocols, CSRs and CTDs. - Fluent in English. - Previous experience in CROs is a plus. - Project management and coordination skills. Benefits - High-impact projects. - Opportunities to nurture your potential. - Space to shine and push boundaries.