Contractor, Technical Science Writer

Your Contribution at Lila Lila Sciences is in search of a skilled and knowledgeable Technical Science Writer / Content Creator to play a pivotal role in articulating our scientific endeavors. This position resembles that of a managing editor, where you will convert intricate scientific concepts into precise and comprehensible content, while also mentoring a …

Join our team at Integrated Resources Inc. as a Technical Writer, where you will play a crucial role in crafting and refining documentation that supports our innovative projects. You will collaborate closely with engineers, product managers, and other stakeholders to ensure that complex technical concepts are conveyed clearly and effectively. Your expertise in writing and editing will help us maintain high standards of quality in our documentation.

We are seeking a highly skilled and motivated SOP Writer III to join our dynamic team in Cambridge. The ideal candidate will play a crucial role in developing and refining standard operating procedures (SOPs) that ensure operational excellence across the organization. This is an exciting opportunity to contribute to the success of our projects through meticulous documentation and process improvement.

We are seeking a skilled and experienced Senior Medical Writer to join our dynamic team at Artech Information Systems LLC. In this role, you will be responsible for producing high-quality, scientifically accurate documents that communicate complex medical information clearly and effectively. You will collaborate with cross-functional teams to develop and deliver regulatory submissions, clinical study reports, and other essential documentation.

We are seeking a highly skilled SOP Writer III to join our dynamic team. In this role, you will be responsible for developing and refining Standard Operating Procedures (SOPs) that adhere to industry regulations and ensure operational excellence. The ideal candidate will possess a keen eye for detail and a strong understanding of technical writing principles.

Join Integrated Resources, Inc. as a Medical Writer, where you will play a pivotal role in the development of high-quality medical documentation. In this dynamic position, you will collaborate with cross-functional teams to produce regulatory documents, clinical study reports, and other materials that adhere to industry standards.

Join lilasciences as a Technical Program Manager in the vibrant city of Cambridge, MA. In this role, you will lead cross-functional teams to drive projects that enhance our innovative life sciences solutions. Your expertise will guide the successful execution of programs from inception through completion, ensuring alignment with our strategic goals.

Join us at Jobs for Humanity as we seek passionate Speakers and Writers who are ready to inspire and empower diverse communities. Your words can make a difference, driving social change and promoting inclusivity. We value creativity, originality, and the ability to engage audiences effectively.

Join Integrated Resources Inc. as a Medical Writer, where your expertise will contribute to the advancement of healthcare communications. In this role, you will create and edit high-quality scientific documents, ensuring clarity and compliance with regulatory standards. Collaborate with cross-functional teams to produce materials that effectively convey complex medical information.

Lila Sciences seeks a Life Science Program Lead based in Cambridge, MA. This position centers on guiding research programs from planning through delivery, with a focus on advancing key initiatives in the life sciences. The role involves close collaboration with teams spanning multiple scientific fields and plays a key part in supporting project success. Main responsibilities Manage project planning and oversee daily execution for life science programs Work alongside multidisciplinary teams to move research initiatives forward Track progress and help ensure programs meet their objectives What we look for Genuine interest in science and research Dedication to maintaining high standards and achieving program goals Background in working with or leading cross-functional teams

Role overview Lila Sciences uses its autonomous science platform to tackle challenges in materials discovery, from advanced structural materials and coatings for harsh environments to clean energy catalysts and carbon capture technologies. The Materials Science experimentation team moves quickly and relies on solid operational management to keep projects on track. The Materials Technical Program Manager plays a key role in maintaining this operational discipline. This position focuses on managing execution: overseeing project plans, coordinating dependencies across teams, and removing obstacles before they slow progress. The Technical Program Manager works closely with Materials Science domain leaders, who set the scientific direction, and takes responsibility for building the structure and processes that enable rapid, scalable experimentation. This role does not direct scientific research but ensures the environment supports high-velocity scientific work. It suits someone who enjoys program management in complex technical fields. What you will do Direct daily program execution for the Materials Science experimentation team by managing project plans, tracking milestones, and keeping autonomous science programs on schedule. Act as the main operational point of contact between the Materials Science team and partners in Automation, ML, and Engineering. Communicate needs, align priorities, and resolve cross-functional dependencies. Translate scientific objectives into structured workstreams that support efficient and scalable autonomous experimentation. Lead program rituals such as sprint planning, stand-ups, and retrospectives. Ensure meetings are purposeful, documentation is thorough, and follow-up actions are completed. Collaborate with domain leaders to identify blockers, risks, and interdependencies early, and drive resolution. Support delivery of commercial contracts by working with the Product & Revenue team to define, monitor, and communicate program commitments to stakeholders. Contribute to capacity planning and resource allocation in partnership with scientific leadership. Requirements Minimum 10 years of program or project management experience in materials science, advanced manufacturing, or deep tech settings. Bachelor’s degree in Materials Science, Chemistry, Chemical Engineering, or a related discipline. Proven ability to manage multiple concurrent programs in evolving, ambiguous environments. Strong motivation to build programs from the ground up; experience in early-stage startups is a significant advantage. Location Cambridge, MA, USA

Your Contribution at Lila Sciences Be a part of innovating the scientific landscape! We are on the lookout for a talented software engineer with a background in life sciences to enhance our data science team. In this role, you will collaborate closely with software engineers, laboratory scientists, and machine learning engineers to develop state-of-the-art tools for automated scientific analysis and beyond. Your expertise in web services and data engineering, particularly in Python development for scientific applications, will be crucial. If you excel in a collaborative and fast-paced environment while adhering to best practices in git, development workflows, and user-centered design, we encourage you to apply! Your Responsibilities Engage in the complete software development life cycle, concentrating on the design, implementation, and maintenance of software services. Create reusable code and libraries to enhance efficiency and scalability. Ensure development aligns with strategic objectives, facilitating software that meets broader organizational requirements. Oversee git repositories, manage the team’s Jira board and Notion Hub, advocate for best practices, assist laboratory scientists in utilizing new tools, and cultivate a collaborative development culture. Collaborate directly with scientists to identify gaps and unmet needs, crafting customized software solutions for data management, LIMS functionality, and data automation. Advocate for infrastructure as code and devise efficient deployment strategies. Produce clear, concise documentation for both engineering teams and end users. Required Qualifications A minimum of 2 years of experience in software development within a commercial environment. High proficiency in Python programming. Solid understanding of git best practices. Strong listening skills and the patience to thoroughly understand user challenges. Experience in implementing scalable software solutions. Exceptional problem-solving abilities and a team-oriented mindset. Excellent communication skills for effective collaboration with team members and stakeholders. A proactive self-starter with independent thinking capabilities and keen attention to detail. Desire to work with highly skilled and dynamic teams in a fast-paced, entrepreneurial technical setting. Preferred Qualifications A background in biological sciences. Familiarity with data science and machine learning libraries (e.g., pandas, numpy, scipy). Knowledge of modern developer tools (e.g., pydantic, pyright, uv). Understanding of Kubernetes, ArgoCD, and GitHub Actions.

Join our team as a Medical Writer III, where you will play a vital role in creating and maintaining high-quality medical documentation. You will collaborate with cross-functional teams to ensure that all materials meet regulatory and compliance standards. Your expertise will contribute to the advancement of medical information and communication within our organization.

As a Principal Medical Writer at Sobi, you will leverage your expertise in communication to spearhead a strategy-oriented approach in crafting pivotal clinical and regulatory documents. Your role will be crucial in ensuring clarity, credibility, and consistency of clinical information across submission packages and clinical programs, thereby facilitating regulatory assessment and achieving product labels that meet commercial needs.Key Responsibilities:Lead an effective strategy for authoring clinical components of regulatory submissions, ensuring that the scientific content is clear, concise, complete, credible, and compelling, aligned with regulatory document objectives.Take the lead in preparing essential clinical and regulatory documents, including those that support major regulatory submissions and responses to regulatory agencies/health authorities.Provide leadership and project coordination to cross-functional authoring teams, ensuring timely delivery, high quality, and compliance with regulatory standards for clinical documents.Collaborate with senior project staff to develop a storyboard for submissions and plan document development to optimally support the proposed prescribing information.Serve as a Product Medical Writer, offering strategic medical writing expertise and support across multiple projects within a clinical development program.Ensure that all documents meet high technical quality standards in accordance with in-house technical requirements.Mentor and develop less experienced Medical Writers.Oversee and coordinate the contributions of all Medical Writers involved in documents under your purview, including in-house consultants and Medical Writers at Contract Research Organizations (CROs).

Your Impact at Lila Sciences Lila Sciences is seeking a dynamic and visionary Director of Product, Life Sciences to lead our innovative product strategies. In this pivotal role, reporting directly to the Vice President of Life Science Product, you will be at the forefront of enhancing our therapeutic research and development capabilities, shaping the future of drug discovery, chemical synthesis, and scientific intelligence. What You'll Be Building Steer the strategic direction for developing breakthrough AI solutions in drug discovery, chemical synthesis, and molecular characterization. Convert strategic goals into comprehensive target product profiles (TPPs) and development campaigns that will empower our science and engineering teams to achieve groundbreaking innovations in life sciences. Lead customer and internal-user discovery initiatives, acting as the primary technical liaison between external customers and partners. Pinpoint and cultivate product opportunities driven by real-world discovery challenges, collaborating closely with stakeholders to ensure relevance and maximize downstream value. Transform insights into precise product requirements, acceptance criteria, and experimental plans that will guide our engineering and science teams. Oversee product execution from inception to launch, leading cross-functional teams across various disciplines including science, machine learning, automation, and software engineering. Manage resource allocations effectively (budget, compute, lab access, personnel) against a complex array of priorities. Establish clear success metrics and milestones, communicating progress to the organization, including executive leadership. What You'll Need to Succeed Advanced degree (MS, PhD, or equivalent experience) in medicinal chemistry, chemical biology, chemical engineering, biochemistry, or a related field, with a solid foundation in experimental science. 7+ years of experience in Product Management, particularly in developing new or experimental products in drug discovery, molecular profiling, machine learning, or scientific software development. In-depth understanding of drug development processes, molecular and cellular research tools, as well as wet and dry lab workflows. Experience with small molecule discovery workflows (e.g., lead optimization, ADMET profiling, synthesis planning) is highly preferred.

Your Role at Lila SciencesWe are on the lookout for exceptionally skilled Forward Deployed Engineers across various levels (Engineer, Senior Engineer, and Lead Engineer) to be a part of our dynamic team. Our FDEs are versatile professionals with a wide array of skills and specialized knowledge in one or more areas. This particular role in Physical Sciences demands a solid background in chemistry and materials science within an industrial manufacturing environment.As an FDE, you will work closely with our internal biotech and materials science teams as well as with external clients, immersing yourself in their challenges and swiftly developing solutions that enhance their research capabilities. You will utilize our AI and software platform tools to create custom features that cater to each customer’s specific needs. This role transcends conventional software development; it's a fast-paced, AI-driven engineering position where you will deploy production code in days rather than months.Your ContributionsCrafting, wrapping, and adapting specialized tools for data analysis, process optimization, molecular modeling, and more.Implementing tailored scientific workflows that connect with industrial instruments (PLCs, control software) and data systems (ERP, MES, SCADA).Establishing real-time data pipelines that convert complex scientific data into actionable insights.Designing user-friendly interfaces that make sophisticated AI/ML functionalities accessible to scientists.Engineering solutions that evolve from proof-of-concept to enterprise-wide implementation.

Lila Sciences is forming a dedicated AI safety team to address the unique risks and challenges posed by scientific superintelligence. The company seeks a Senior or Principal Technical Program Manager to guide the operational side of AI safety research, helping to shape how the team approaches complex and evolving problems. Role overview This Technical Program Manager position connects research, engineering, model development, policy, and executive leadership. The work involves translating fast-moving research into structured, accountable plans. While this is not a research role, curiosity about the technical aspects of AI safety is important. The team values clear communication and the ability to bring clarity and structure as the organization expands. What you will do Act as the primary communication link between the AI safety team and technical, research, and scientific groups. Share complex results and coordinate resource needs. Establish information flows to keep teams connected. Promote accountability within cross-functional, distributed teams, building consensus and trust through open communication and sound judgment. Support rapid experimentation and iteration by refining and applying effective program management practices. Create clear documentation and reports to communicate vision, track progress, and ensure alignment with company objectives. Accurately represent program status and risks, even in uncertain or shifting situations. Requirements Bachelor’s or Master’s degree in Computer Science, Engineering, Life Sciences, or a related discipline. Minimum of 6 years of program or project management experience in technology or life sciences. Demonstrated success in program management, leading cross-functional teams, and delivering projects. Strong analytical and problem-solving abilities, with skill in turning technical requirements into actionable plans. Excellent written and verbal communication skills, including experience preparing executive-level documents, roadmaps, and updates. Location This position is based in Cambridge, MA or San Francisco, CA, USA.

Your Impact at Lila Join our dynamic and innovative AI safety team at Lila Sciences, where we prioritize talent and agency to mitigate risks associated with scientific superintelligence. Our mission is to craft and execute a tailored safety strategy that aligns with our unique objectives and deployment methods. This role involves creating technical safety strategies, engaging with the broader scientific community, and producing critical technical documentation, including evaluations focused on risk and capability assessments. What You’ll Be Creating Design and implement capability evaluations to assess scientific risks, particularly from cutting-edge scientific models integrated with automated physical laboratories across biological and physical sciences. Lead and coordinate threat modeling sessions with both internal and external scientific experts, keeping abreast of emerging technologies and use cases. Develop and manage high-quality training and testing datasets for evaluations and safety systems. Analyze risks associated with Lila’s capabilities and their interactions with the broader ecosystem of general-purpose frontier models and specialized scientific tools. Contribute to high-quality research initiatives focused on scientific capability evaluation and restriction as needed. Assist with external communications regarding Lila’s safety initiatives. What You’ll Need to Succeed A PhD in biological sciences (e.g., molecular biology, virology, computational biology) or physical sciences (e.g., materials science, physics, chemistry, or chemical engineering), or similar experience. Proficient in scientific computing related to biological or physical sciences. Familiarity with dual-use research and dissemination issues within relevant safety, regulatory, and governance frameworks (e.g., export control, biological and chemical conventions). Exceptional communication skills to convey complex technical concepts to non-expert audiences effectively. Proven ability to lead internal and external teams in developing Lila's perspective on biological and physical risks. Demonstrated capacity to collaborate with cross-functional stakeholders (science, AI, product, policy) in a complex environment.

Your Contribution at Lila At Lila, we are assembling a highly skilled and proactive AI safety team that will collaborate with all core departments, including science, model training, and lab integration, to effectively address risks associated with scientific superintelligence. The primary mission of this team is to develop and execute a tailored safety strategy that aligns with Lila's unique objectives and deployment methodologies. This will encompass formulating technical safety strategies, engaging with the broader ecosystem, and producing technical documentation such as risk and capability assessments and safety measures. Your Responsibilities Establish the research and development strategy for Lila’s safety framework concerning biological and physical risks. Design and implement capability evaluations to identify scientific risks (both recognized and novel) arising from state-of-the-art scientific models integrated with automated physical laboratories across biological and physical sciences. Lead and coordinate threat modeling sessions with both internal and external scientific experts, including monitoring advancements in technologies and their applications. Create and curate high-quality training and testing datasets for evaluations and safety systems. Assess risks linked to Lila’s capabilities, considering interactions with the broader ecosystem of capabilities (including general-purpose frontier models and specialized scientific tools). Contribute to extensive, high-quality research initiatives when needed for scientific capability evaluation and restriction. Engage in external communications regarding Lila’s safety initiatives. Qualifications for Success A PhD in a biological sciences field (e.g., molecular biology, virology, computational biology) or a physical sciences field (e.g., materials science, physics, chemistry, chemical or nuclear engineering) or equivalent experience. Proven track record in setting research directions for open issues surrounding dual-use risks in biological and physical sciences. Experience in scientific computing within the biological or physical sciences. Understanding of dual-use research and dissemination issues in relation to relevant safety, regulatory, and governance frameworks (e.g., export controls, biological and chemical-related conventions). Excellent communication skills, capable of articulating complex technical concepts to non-specialist audiences. Demonstrated leadership capabilities in guiding teams of internal and external collaborators in developing Lila's perspective on biological and physical risks.

Lila Sciences, located in Cambridge, MA, develops technology for chemical discovery through its autonomous science platform. The company’s projects include advanced synthesis, new catalyst development, and sustainable molecular design for applications in energy and industry. The Chemistry experiment team is searching for a Technical Program Manager to coordinate complex scientific programs in close partnership with the Chemistry domain lead and teams across the organization. Role overview This position centers on managing the daily operations and long-term planning for the Chemistry experiment team. The Technical Program Manager will keep project plans up to date, monitor milestones, and help ensure scientific programs meet both deadlines and quality standards. Acting as the main point of contact between Chemistry and platform partners, such as Automation, Machine Learning, and Engineering, the role involves communicating needs, aligning priorities, and making sure dependencies are clear and managed. What you will do Maintain project plans, track progress, and ensure delivery of scientific programs on schedule and to quality expectations. Coordinate with cross-functional partners to communicate requirements, align on priorities, and track dependencies. Break down scientific goals into actionable workstreams to support scalable autonomous experimentation. Lead program routines, including sprint planning, stand-ups, and retrospectives, with a focus on purposeful meetings and clear documentation. Work with Chemistry leads to surface and address blockers, risks, and interdependencies early in the process. Support execution of commercial contracts by collaborating with the Product & Revenue team, ensuring commitments are defined, tracked, and communicated. Assist with capacity planning and resource coordination alongside scientific leadership. Requirements At least 10 years of program or project management experience in chemistry, pharmaceuticals, or deep tech sectors. Bachelor’s degree in Chemistry, Chemical Engineering, or a related discipline. Proven ability to manage several programs in complex, evolving environments. Experience building programs from the ground up and working in early-stage startups is a strong plus. Skilled in coordinating with both scientific and operational teams, and managing cross-functional groups.