Protein engineering jobs in New York, New YorkCreate job alerts

Job Description Neion Bio is harnessing nature’s best molecular factory, the chicken egg, to make medicine affordable, accessible, and resilient. Using cutting edge genetic engineering and stem cell technology, we create “living bioreactors”, which act as fully autonomous 3D biomolecular printers, operating on existing industrial-scale infrastructure. Our platform can rapidly and scalably produce almost any protein, provide national resilience to drug shortages and de-risk complex supply chains, and ultimately take advantage of novel biological environments to solve unmet medical needs. We are on a mission to reimagine the way in which complex biological molecules are produced to transform human health. At Neion Bio you will play a pivotal role in an early-stage, fast-growing company, working alongside leading scientists and entrepreneurs. You will have the opportunity to participate in the enormous potential upside while having a huge impact on the world. We are looking for a talented molecular biologist on the RA, SRA or scientist level experienced with the engineering, production and purification of viral vectors, including lentivirus, adenovirus and AAV. Key Responsibilities: • Perform cloning of large viral genomes, design and run PCR, qPCR, RT-PCR assays to quantify viral transgene and transcription, • Perform transfections on primary cells, immortalized cells, and animal tissues, • Design, manufacture, purify, characterize, validate and test a range of viral vectors, at small and large scale, • Assess efficiency of workflows through cellular assays and NGS sequencing approaches, • Extract DNA, RNA, protein from animal tissue, • Conduct experiments and work on research problems, • Maintain excellent electronic laboratory records, • Work on project milestones, • Attend lab meetings, prepare reports and presentations on the progress of projects Requirements • BA/MS/PhD in biological sciences, bioengineering, molecular biology, genetics, or any science related field, or equivalent experience, • Experience with cloning, transfecting, producing, purifying, characterizing, validating and testing of a range of viral vectors including adenovirus, lentivirus, AAV, • Experience with ultracentrifugation for viral purification, • Experience with resin and column based viral purification methods, • Strong aseptic techniques and GLP procedures, • Experience in genome engineering, cloning, DNA amplification, PCR, NGS, transfections, and other molecular biology skills, • Exceptional organizational skills with the ability to effectively manage time and priorities, • Strong written and oral communication skills, as well as creative problem-solving skills, • Curious, eager, and hardworking Preferred qualifications: • Experience with viral capsid engineering by rational design or directed evolution, • Extensive experience with and knowledge of adenoviral vectors, • Experience with viral capsid library engineering Benefits Compensation: base salary is expected to be $90-130K depending on experience, with additional bonus compensation, equity compensation, and benefits including health insurance, dental insurance, vision insurance, and 401(k).

Job Description Neion Bio is harnessing nature’s best molecular factory, the chicken egg, to make medicine affordable, accessible, and resilient. Using cutting edge genetic engineering and stem cell technology, we create “living bioreactors”, which act as fully autonomous 3D biomolecular printers, operating on existing industrial-scale infrastructure. Our platform can rapidly and scalably produce almost any protein, provide national resilience to drug shortages and de-risk complex supply chains, and ultimately take advantage of novel biological environments to solve unmet medical needs. We are on a mission to reimagine the way in which complex biological molecules are produced to transform human health. At Neion Bio you will play a pivotal role in an early-stage, fast-growing company, working alongside leading scientists and entrepreneurs. You will have the opportunity to participate in the enormous potential upside while having a huge impact on the world. We are looking for a talented scientist with knowledge and passion for ambitious synthetic biology projects and advanced genome engineering for biomanufacturing in living vertebrates. We will be building tools and methodologies for in-vivo vertebrate genome engineering, and will develop workflows to manipulate large DNA fragments and genomes. You will work with a talented group of engineers and biologists committed to developing disruptive, novel protein production technologies. We are specifically looking for a scientist experienced with in vivo delivery and integration of multi-Kb transgenes, and experienced with large serine recombinases. Key Responsibilities: • Platform development:, • Innovate and iterate on Neion Bio’s transgenic animal platform, • Develop and improve methods for DNA assembly, integration, editing, screening, • Develop and validate novel vertebrate genetic engineering approaches, • Assist in building and optimizing molecular and cellular tools for DNA/RNA delivery and perform high-throughput screens of these tools, including LNPs, VLPs, AAVs, lenti- and adenoviral vectors, electroporation and/or chemical transfection in cell culture, organ explants, live embryos and animals, • Characterize and quantify genome editing events using various molecular assays, • Scientific housekeeping:, • Analyze data, generate figures, report results., • Present findings at R&D meetings, • Maintain a thorough and detailed electronic lab notebook, • Maintain a clean and organized laboratory environment Requirements • PhD/MS in synthetic biology, bioengineering, molecular biology, genetics or related field is required, or 3+ years hands-on expertise in genomic manipulation and cell biology, • Understanding and extensive hands-on experience with current precision editing techniques, covering the design, optimization and verification of edits made with CRISPR-Cas9/HDR and Prime Editing, • Hands-on experience with recombinases and integrases, or other large construct integration methods, • Experience with in-vivo delivery of large payloads for genomic integration, • Experience with avian or mammalian cell culture, DNA/RNA transfection, bacterial culture, recombinant DNA cloning techniques, primer design and PCR, qPCR, gel electrophoresis, nucleic acid extraction and purification, • Self-motivated, proactive, works well under pressure and deadlines, detail-oriented, • Enthusiasm for learning new skills and taking on new responsibilities, • Strong written and oral communication skills, as well as creative problem-solving skills, • Strong emotional intelligence and passion for building relationships across all levels of an organization., • Enjoys the fast-paced startup environment and teamwork Preferred Qualifications: • High throughput screening experience or automation methods, • Experience with viral vector design, optimization and use, • Experience with -omics based analysis of cells culture, • Experience with development of gene therapy tools, • Experience with flow cytometry, immunostaining, and fluorescent microscopy, • Experience with dPCR and/or NGS library preparation Benefits Compensation: base salary is expected to be $110-150K depending on experience, with additional bonus compensation, equity compensation, and benefits including health insurance, dental insurance, vision insurance, and 401(k).

Job Description The Role Output has built a biological reasoning model that understands biology at the scale and complexity life actually operates. Our model independently learned the principles of molecular interactions, opening up drug treatments that were previously impossible. We're already generating therapies that traditional approaches cannot reach. The hardest problems in both AI and biology are being solved here, and there is room for you to own one. Output is currently in stealth, operated by a team of repeat founders and biotech veterans with multiple exits in AI x Bio, and backed by top-tier VCs including Y Combinator. You own the feedback loop between Output's models and the lab. You go deep into specific biological problems, translate what the biology requires into priorities for data and modeling, and manage through CRO partners the experimental cycle that validates model outputs and generates new data. You will own the active learning cycle between Output's models and experimental validation: designing experiments, managing CRO partners for synthesis and testing, interpreting results, and feeding them back to improve the models You will dive into specific biological problem areas, developing the expertise needed to translate nuanced biological requirements into priorities for data construction, modeling, and evaluation You will manage CRO relationships for peptide and molecular synthesis, biological assays, and experimental testing, designing each campaign to generate maximally informative data You will collaborate with the engineering team to design and build biology-specific agent skills and workflows, encoding your biological expertise into tools that automate experimental decision-making You will work closely with the model and data teams, identifying biological phenomena the models should be sensitive to and ensuring that experimental findings shape what and how the models learn You will stay current with biological literature and experimental methods, continuously identifying new biological problems and translating them into opportunities for model development About You You have a PhD in computational biology, biophysics, structural biology, molecular biology, or a related biological field with 3+ years of post-doctoral or industry research experience You have deep understanding of protein biology, protein-ligand interactions, and how sequence and structure relate to biological function You have experience designing biological experiments and working with CROs for synthesis and experimental validation You have experience working with protein language models or machine learning applied to biological sequences and structures You have strong programming skills in Python, with experience building computational pipelines and analysis tools You can move between the language of biology and the language of machine learning: you understand what models need from data and what experimental results mean for model development You are comfortable going deep into unfamiliar biological problem areas and rapidly developing the expertise needed to guide modeling and experimental decisions Bonus Points You have structural biology expertise, including protein structure analysis and structure-function relationships You have experience with active learning or iterative experimental design in a computational biology or drug discovery setting You have hands-on wet lab experience You have experience across multiple therapeutic modalities, including peptides You have experience building tools or writing code that automates biological analysis workflows Our Values ❤️ Heart: We foster a culture of ownership. We are assembling a team of individuals who are passionate and take pride in their contributions. 🏆 Excellence: We have an unwavering commitment to excellence and continuously challenge ourselves to reach the highest standards. 🚀 Practicality: We value practicality and results-oriented thinking. We are committed to making a tangible impact on the lives of patients and the broader community. 📣 Honesty: We place a high value on honesty and directness. We firmly believe in addressing issues as they arise, in an open and transparent manner. 🎮 Fun: We believe that life is too short to not have fun. Our goal is to create a workplace that is fun, engaging, rewarding and fulfilling. What We Offer We encourage new and different ideas, creativity and contrarian thinking Healthy feedback focused environment to help you strive - leadership will have high expectations, regularly share constructive feedback, support you and help you grow, and welcome receiving feedback and ideas from you You own your day-to-day management. What we care about is that we all hit our milestones Competitive salary and equity in a growing, well-funded startup Excellent medical, dental, and vision coverage Compensation Range: $120K - $250K

Job Description Summary The Field Service Engineer (FSE) is responsible for the installation, maintenance, troubleshooting, and repair of Hudson Lab Automation systems and devices at customer sites. This customer-facing role is essential to ensuring product reliability, customer satisfaction, and long-term success with Hudson’s lab automation solutions. Key Responsibilities • Install, troubleshoot, repair, and maintain the full range of Hudson Lab Automation systems and devices., • Provide rapid response to customer support requests, including initial triage and troubleshooting of reported product issues., • Accurately and promptly document service case activities, issues, and resolutions., • Collaborate with Sales partners to deliver best-in-class customer service., • Train customers in routine operation of hardware and software., • Develop customer relationships though proactive and collaborative communication to ensure customer engagement, customer referrals, and overall customer success with our products., • Regularly author service documentation and contribute knowledge base articles for technical support and servicing and troubleshooting techniques., • Complete ongoing training and development for continuous improvement and further expansion of service skills and delivery., • Manage and maintain field service spare parts and a service inventory accurately. Required Skills • Ability to troubleshoot complex issues in a timely manner., • Proactive and collaborative approach to customer-focused issue resolution., • Excellent written and verbal communication skills, with the ability to explain technical and non-technical information to customers and colleagues at multiple organizational levels., • Strong organizational and time management skills, ensuring achievement of tasks and objectives, and completion of all aspects of service call handling and documentation., • Exceptional customer service skills with the ability to communicate sensitive information to customers and to address interpersonal conflict appropriately and with a professional demeanor. Qualifications • Bachelor’s degree in electromechanical technology, life sciences, engineering, or related field, or equivalent certification and experience in lieu of degree., • Minimum of 2 years of experience in a field service or customer-facing support role., • Experience with laboratory automation products strongly preferred, including robotics, liquid handling systems, protein crystallization instruments, and colony pickers., • Knowledge of computer communications protocols (TCP/IP, RS232)., • Ability to travel weekly to customer sites, including >50% domestic overnight travel and occasional international travel., • Position based at headquarters in New Providence, New Jersey, • Valid driver’s license. What We Offer • Competitive compensation that includes bonus eligibility., • Comprehensive benefits package, including medical, dental and vision insurance, plus 401(k) retirement plan.

JOB SUMMARY Iambic Therapeutics is seeking a Software Engineer to join the NeuralPLexer team, focusing on the engineering systems that enable machine learning research to translate into robust, scalable workflows for drug discovery. This role sits directly alongside ML scientists and emphasizes co-development: helping design, implement, and harden the workflows used to train, evaluate, and apply models on structural (e.g., protein–ligand complexes), affinity, and synthetic data. You will play a key role in turning research code into reliable, reusable systems—without being responsible for core model development. This is a remote position based on the US East Coast. KEY RESPONSIBILITIES Work embedded with ML scientists to co-develop and refine model training and evaluation workflows Translate experimental research code into maintainable, well-structured, and reusable systems Build and expand benchmarking systems for running models on structural and affinity datasets, computing metrics, and supporting reproducible evaluation Enable rapid iteration by developing tooling and interfaces that expose new capabilities to researchers Contribute to the ongoing development and productization of NeuralPLexer Collaborate with platform and infrastructure engineers on scaling workflows where needed, without owning core infrastructure Perform code reviews and actively mentor best practices in software engineering across the team Improve reliability, clarity, and reproducibility of ML workflows and supporting systems Communicate technical work effectively across a cross-functional research and engineering team QUALIFICATIONS Required 8+ years of software engineering experience (or equivalent), ideally in ML-adjacent or data-intensive environments Strong Python skills and demonstrated rigor in software engineering practices (testing, versioning, code quality) Experience working closely with ML practitioners or in research-driven environments Experience building or supporting ML workflows, data pipelines, or evaluation systems Ability to operate in partially defined, research-heavy environments and bring structure to evolving codebases Strong collaboration skills and comfort with pair programming and iterative development Preferred Experience with scientific or computational research environments Familiarity with structural biology, chemistry, or molecular modeling workflows Exposure to cloud-based systems (e.g., AWS, Kubernetes) and/or HPC Experience working with large-scale or heterogeneous datasets ABOUT IAMBIC THERAPEUTICS Iambic is a clinical-stage life-science and technology company developing novel medicines using its AI-driven discovery and development platform. Based in San Diego and founded in 2020, Iambic has assembled a world-class team that unites pioneering AI experts and experienced drug hunters. The Iambic platform has demonstrated delivery of new drug candidates to human clinical trials with unprecedented speed and across multiple target classes and mechanisms of action. Iambic is advancing a pipeline of potential best-in-class and first-in-class clinical assets, both internally and in partnership, to address urgent unmet patient need. Learn more about the Iambic team, platform, pipeline, and partnerships at _. MISSION & CORE VALUES Our mission is to deliver better medicines through innovations in AI-based discovery technologies. The culture and work at Iambic Therapeutics are profoundly strengthened by the diversity of our people and our differences in background, culture, national origin, religion, sexual orientation, and life experiences. We are committed to building an inclusive environment where a diverse group of talented humans work together to discover therapeutics and create technologies. PAY AND BENEFITS We offer industry leading competitive pay, company paid healthcare, flexible spending accounts, voluntary life insurance, 401K matching, and uncapped vacation to our team. We are in a brand-new state-of-the art facility in beautiful San Diego with an onsite gym, dining, and easy access to great places to live and play.

Our Why At Dotmatics At Dotmatics, we believe science, data, and decision-making must be deeply intertwined for innovation to thrive. Our Portfolio includes Luma, LumaLab Connect, ELN Platform, Graphpad Prism, Geneious, SnapGene, Protein Metrics, OMIQ, FCS Express, LabArchives, NQuery, EasyPanel, MStar, SoftGenetics and Virscidian. We have a vision for a new Lab of the Future that will change the future of scientific research. We have created the world’s most comprehensive digital science platform – best-of-breed software applications already used by more than 2 million scientists, together in a single ecosystem united by a powerful, flexible enterprise data platform. This is not flat data buried away in digital graveyards. This is dynamic, multi-dimensional decision-making. Scientific enterprises need a new level of effectiveness to achieve tomorrow’s breakthroughs. Illness will not wait. The biosphere will not wait. We are tireless in our vision, because the time for innovation is now. Shaping the Future of Science At Dotmatics Our global team of more than 800 colleagues are dedicated to supporting our customers in over 180 countries. Together, with our scientific community of users, we accelerate scientific innovation in order to make the world a healthier, cleaner, and safer place to live. You’ll join a collaborative, global team pushing the boundaries of scientific innovation. Your ideas and efforts will have a tangible impact, accelerating scientific progress and discovery. We offer a dynamic, remote-friendly environment that fosters high integrity and collaboration, empowering you to excel. Dotmatics is a company built by scientists, for scientists. Combined, we are now the world’s largest cloud-based scientific research R&D platform. We need your help to keep growing and pioneering the future. We are Science Driven. We are Customer Centric. We are Better Together. What do we need Dotmatics is seeking a Staff Engineer to join our team. We are building the most powerful R&D AI-Powered platform in the world. Luma is an AI-Native Multimodal Research Platform for Scientific Intelligence, Luma fits the way our customers “do science”. It allows scientists to streamline scientific research with adaptive R&D workflows driven by AI and seamless data integration. As a Staff Engineer, you will be responsible for driving improvements in reliability, performance, and operability while helping to hire, mentor, and grow a world-class engineering team. You are curious and have some working knowledge of using AI in your everyday work or in your own personal projects, and be motivated to find new ways to use AI in software development. This is a remote position, located in Mass. There will be some travel required to the office in Boston for team meetings and working sessions. In this role you will • Define and drive system architecture for services within a Node.js/TypeScript ecosystem., • Contribute to and improve engineering standards, patterns, and best practices for distributed systems, observability, and reliability., • Architect and implement serverless and event-driven data processing pipelines for high-volume scientific data., • Guarantee the scalability, maintainability, and security of software solutions., • Provide technical guidance to Software Engineers, conduct code reviews, and raise the bar for design, code quality, and operational excellence., • Help shape user interfaces that are intuitive and accelerate scientific research., • Collaborate with other teams to build scientific solutions on top of a best-in-class scientific data engine. We are looking for candidates with 12+ years experience in engineering preferably in a SaaS environment, and ideally with a degree in Computer Science, Software Engineering, or equivalent. You will be curious and inquisitive question the why and how!! The key skills we are looking for • Strong engineering background with Node.js and React., • Proven experience designing and implementing distributed, event-driven systems and high-level web applications., • Experience implementing automated testing platforms, unit tests, and integration tests., • Professional experience with PostgreSQL and building/consuming RESTful APIs., • Hands-on experience with AWS in production environments and a solid understanding of Kubernetes for orchestrating workloads., • Proficiency with CI/CD tools such as GitHub Actions and AWS CodePipeline., • Knowledge of Agile software development practices. You may also have experience in • Setting technical direction, leading cross-team initiatives, and levelling up other engineers., • Background in complex data pipelines and scaling., • Message-based architectures (e.g., Kafka)., • Deployment technologies like Terraform., • Exposure to AWS and/or GCP or designing systems portable across multiple cloud providers., • Building Windows applications., • Building scalable distributed systems using Kubernetes and other cloud-native technologies., • Experience within Life Sciences or R&D data management. Total Rewards Dotmatics utilises a national market-based approach to base pay benchmarking and pay band development. The candidate's final starting pay is based on job-related skills, experience, job specific qualifications & location. In addition to base salary, Dotmatics has implemented a total rewards strategy, which is the combination of compensation, benefits and recognition. Certain positions are also eligible for variable pay; your recruiter will discuss the full compensation package details. Other Total Rewards Offered • Medical, Dental, Vision, Insurance, • Health Spending Accounts, • Wellness Benefits (Mental Health Apps and Fitness Perks), • Company-paid Life and Disability Insurance, • 401k Retirement Plan (with 4% company match; immediate vesting), • Flexible Time off Plan (for US exempt employees) This is the range that we, in good faith, believe is the range of possible compensation for this role at the time of this posting. We may ultimately pay more or less than the posted range. This range may be modified in the future. Starting Base Pay Range $142,445—$163,811 USD Research shows us the_ and imposter syndrome can get in the way of meeting outstanding candidates, so please don’t hesitate to apply — we’d love to hear from you. By submitting your application, you agree that Dotmatics may collect your personal data for recruiting, global organization planning, and related purposes. Dotmatics _ explains what personal information we may process, where we may process your personal information, our purposes for processing your personal information, and the rights you can exercise over Dotmatics use of your personal information. Dotmatics is an equal opportunity employer. We are a welcoming place for everyone, and we do our best to make sure all people feel supported and connected at work.

Location: Pearl River, NY Manager, GMP Facility and HSE Readiness is a pivotal operational leadership role responsible for maintaining our Pearl River manufacturing facility in a state of GMP compliance, equipment readiness, and workplace safety excellence. You will lead a team of two maintenance technicians while orchestrating facility operations across GMP cleaning, equipment asset care, and HSE leadership. Your meticulous attention to detail, proactive problem-solving, and hands-on approach will ensure our manufacturing environment meets the highest standards of regulatory compliance and operational integritydirectly enabling Sanofi to deliver life-saving medicines to patients worldwide. Main Responsibilities • GMP Facility & Cleaning Operations (primary focus):, • Ensure the manufacturing facility is maintained in a GMP-ready and safety-ready state at all times, • Oversee and coordinate GMP cleaning operations of all manufacturing areas in compliance with cleaning procedures and validation requirements, • Partner with third-party cleaning contractor to ensure thorough execution of cleaning activities, with attention to detail including rust, cleaning residue, paint integrity, floor conditions, and other facility deficiencies, • Conduct regular facility walkthroughs to identify and remediate GMP and safety deficiencies, • Maintain cleaning logs, records, and documentation in compliance with GMP requirements, • Ensure environmental monitoring requirements are supported and met within the manufacturing facility, • Equipment Asset Care & Maintenance:, • Directly manage two dedicated maintenance technicians focused on asset care and equipment readiness, • Ensure all manufacturing equipment is clean, calibrated, and current with preventive maintenance (PM) schedules, • Partner with the Maintenance team to define scope of work, planning, and execution of maintenance shutdowns, • Maintain equipment status boards and asset care records to ensure full traceability and GMP compliance, • Proactively identify equipment reliability risks and drive resolution through appropriate channels, • Support equipment qualification activities (IQ/OQ/PQ) and change control processes as needed, • Review and close preventive and corrective workorders as they pertain to the manufacturing floor, • Execute and complete corrective and preventive actions (CAPAs) as applicable, • Health, Safety & Environment (HSE) - 25-50% of role:, • Champion a culture of safety across the manufacturing shopfloor, • Ensure safe work practices are understood, followed, and reinforced among all team members and contractors, • Manage and coordinate work permitting processes (e.g., confined space, hot work, lockout/tagout), • Lead and sustain 5S implementation and continuous improvement across manufacturing areas, • Conduct safety walkthroughs, hazard assessments, and near-miss investigations, • Ensure compliance with all applicable HSE regulations, site policies, and Sanofi standards, • Serve as a key point of contact for HSE topics on the manufacturing shopfloor, • Team Leadership & Collaboration:, • Lead, develop, and manage two dedicated asset care maintenance technicians, • Collaborate cross-functionally with Maintenance, Quality, and Manufacturing teams, • Coordinate with cleaning contractor management to ensure GMP and safety standards are consistently met, • Participate in deviation investigations related to facility, equipment, or cleaning deficiencies, • Support regulatory inspections and internal audits related to facility and equipment readiness About You Basic Qualifications Bachelor's degree in engineering, Biology, Life Sciences, or related field required or 5+ years of equivalent experience in a GMP biopharmaceutical or pharmaceutical manufacturing environment. 5+ years of experience in GMP equipment maintenance, asset care, or reliability programs in a biopharmaceutical or pharmaceutical manufacturing environment. Demonstrated experience managing facility readiness, equipment maintenance, or asset care programs Proven experience implementing and sustaining 5S methodology in a manufacturing environment. Experience coordinating with maintenance teams and/or third-party contractors Familiarity with HSE programs including safe work practices, permitting, and safety compliance Technical Knowledge: Working knowledge of cGMP regulations (21 CFR Parts 210, 211) and GMP cleaning requirements Understanding of environmental monitoring principles and practices in a manufacturing setting Knowledge of preventive maintenance, calibration programs, and equipment qualification Experience with 5S implementation and workplace organization Familiarity with work permitting systems and HSE compliance requirements Soft Skills: Strong attention to detail and commitment to GMP and safety standards Proactive problem-solving and facility management skills Effective leadership and team development capabilities Strong communication and cross-functional collaboration skills Ability to manage multiple priorities in a fast-paced manufacturing environment Continuous improvement mindset with hands-on approach Preferred Qualifications: Experience in vaccine, biologics, or recombinant protein manufacturing OSHA 30-hour certification or equivalent HSE training Experience managing third-party cleaning or maintenance contractors Knowledge of cleaning validation principles Lean Manufacturing or Six Sigma training Physical Requirements: Ability to work in a manufacturing environment including cleanroom gowning requirements Regular walking and standing during facility inspections and shopfloor activities Occasional lifting up to 35 lbs Flexibility to respond to facility or equipment issues outside of standard business hours Why choose us? • Bring the miracles of science to life alongside a supportive, future-focused team., • Discover endless opportunities to grow your talent and drive your career, whether it's through a promotion or lateral move, at home or internationally., • Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact., • Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention and wellness programs and at least 14 weeks' gender-neutral parental leave., • Shape the future of medicine and vaccine delivery with cutting-edge technology, ensuring seamless launches and a resilient global supply., • Power industry-leading performance by leveraging digital, data, and AI-driven innovation at speed and scale, • Transform lives worldwide by delivering life-changing treatments anywhere, anytime. Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; marital, domestic partnership or civil union status; sex, gender, gender identity or expression; affectional or sexual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law.

Eikon Therapeutics is a new biopharmaceutical company employing revolutionary technology at the intersection of chemistry, engineering, computation, and biology to discover novel treatments for life-threatening diseases. Eikon's discovery platform is built on groundbreaking innovations from its founders (Nobel Prize, 2014), culminating in the creation of microscopes which enable real time, molecular-resolution measurements of protein movement in living cells, thereby unlocking otherwise intractable classes of proteins as drug targets. We are currently seeking an experienced leader for the clinical operations role of Director, Clinical Study Management within Clinical Study Management. The Director will manage all aspects of clinical operations study management for assigned Eikon clinical studies, and be responsible for exquisite inhouse execution of all such clinical trials and oversight of requisite clinical vendors. The role will also support the systematic pursuit of optimal performance, efficiency, and quality across the assigned clinical studies. Adherence to Good Clinical Practice (GCP), local and global policies and procedures to conduct high quality, inspection ready studies is essential. The Director is responsible for trial quality and audit responses and completion of CAPAs. The position has multiple stakeholder touch points within Clinical Research & Development (CR&D) staff and important interactions with, inter alia, Quality Assurance (QA), Finance, Regulatory, Clinical Supplies, Business Development and Legal in a matrix-based organization. This role will require a minimum of 3 days a week of onsite presence (or more as business needs require) in either of our Jersey City, New Jersey or Millbrae, California offices to ensure effective management and high-performance delivery of clinical studies. You are agile of mind, systematic, and a collaborative leader with global oncology clinical development experience and a passion for advancing patient care. You possess a deep understanding of clinical trial regulations, guidelines, and the principles of GCP, ensuring compliance throughout the clinical trial process. • In collaboration with senior clinical operations management, build and lead inhouse clinical operations study management teams responsible for delivery of assigned clinical studies., • Manage clinical study management personnel across assigned clinical studies., • Ensure that compliance, quality and timeline objectives are met for all assigned studies., • Work collaboratively in a matrix organization with all internal stakeholders to deliver company clinical trial objectives on time, on budget, and with high quality., • Work with the CR&D Functional Area (FA) leads, as appropriate, to accelerate enrollment and drive high quality., • Take responsibility for any assigned clinical trial audits, working closely with the Clinical Quality Assurance group., • Represent Clinical Study Management in process workstreams and initiatives., • Effectively solve problems and use judgment relating to national and international regulations, guidelines, investigator interactions, and timelines., • Effectively manage resources to ensure appropriately skilled and high performing staff members are assigned to support the effective execution of the portfolio and achieve CR&D objectives., • Responsible for ensuring appropriate scientific and operational training for staff members., • Serve as a talent magnet and develop, coach, and retain top talent in the clinical program team., • Set clear performance standards and holds self and organization accountable for achieving results with flawless execution., • Embrace metrics and performance standards (KPIs) to drive continuous improvement in execution., • 12+ years of relevant experience with a Bachelor's degree or 10+ years of relevant experience with a Master's Degree with a demonstrated working experience in clinical study management within the biotechnology, pharmaceutical, or healthcare industry., • Relevant experience managing international clinical studies and programs in oncology., • Proven track record of contribution to and delivery of clinical trials that support global regulatory submissions, clean regulatory inspections and product approvals or marketing authorizations., • Relevant management experience in a clinical trial setting with the ability to service and collaborate with different CR&D stakeholders in a matrix organization., • Demonstrated situational leadership, independence, problem solving abilities, self-motivation, resourcefulness and ability to work in a fast-paced team environment., • Relevant management expertise should cover management of budget, resources, headcount, processes (and controls), productivity, quality and project delivery., • A complete understanding of ICH GCP and Global/Regional/Local regulatory requirements is required., • Strong communication skills requiring proficiency in written and spoken English., • Strategic thinking and high emotional intelligence., • Process improvement mindset and experience., • Strong leadership that will attract, motivate, inspire, develop and retain talented staff., • In addition, leadership skills that enable and drive alignment with the goals, purpose and mission of our company. At Eikon, employee compensation also includes bonus and equity compensation, in addition to several generous benefit programs, including: • 401k plan with company matching, • Medical (premiums covered by Eikon at 95%), dental and vision insurance (premiums covered by Eikon at 100%), • Mental health and wellness benefits, • Weeklong summer and winter holiday shutdowns, • Generous paid time off and holiday policies, • Life/AD&D Insurance (premiums covered by Eikon at 100%) and optional supplemental employee-paid life/AD&D policies, • Enhanced parental leave benefit, • Daily subsidized lunch program when on-site The expected salary range for this role is $203,000 to $221,350 depending on skills, competency, and the market demand for your expertise. Eikon is proud to be an equal opportunity employer and will consider all qualified applicants for employment.

Analyze and interpret diverse foodomics datasets (DNA sequences, protein sequences/structures, chemical structures & bioassays, nutrition, sensory, formulation, food manufacturing, etc. Basic qualifications MSc in Chemical Engineering, Food Engineering, Nutrition, Computer Science, Bioinformatics,

Job Description About Neion Bio: Neion Bio is harnessing the world's best protein factory to create a world of healthy abundance. Our vision is to expand accessibility and affordability of therapeutics, transforming human health globally. Through pushing the boundaries of genetic engineering, we’re using living bioreactors to produce highly valuable complex proteins using existing industrial-scale infrastructure. Our platform can rapidly and scalably produce almost any protein, provide national resilience to drug shortages and de-risk complex supply chains, and ultimately provide a new environment for novel therapeutics to solve unmet medical needs. Role Summary: We are seeking an adaptable and organized Avian Caretaker who is motivated by the ethical care of animals and will contribute to the growth of Neion’s research program. This role is based in NYC and involves hands-on care and handling of chickens and quail and collecting samples. This position reports to the Head of Avian Sciences and will require one weekend day shift, as part of a 5-day work schedule (Sunday to Thursday) to ensure continuity of care and study execution. Key Responsibilities: • Aviculture: Must be comfortable safely handlingchickens and quail in a research setting.Requires working with small flocks at all stages of development from egg collection, incubation and the successful hatching and growth of chicks and chickens, • Biosecurity: Must be comfortable working in full Personal Protective Equipment (PPE) and observing standard operating protocols (SOPs) to protect avian health, • Culture of Care: Contribute to ensuring the health and environmental, nutritional and social enrichment of our flocks, • Record Keeping: Maintain timely and accurate animal and study records, • Regulatory Compliance: Help to ensure that research areas and records meet and exceed IACUC and USDA inspection requirements, • Supportive care and intervention: Productively communicate with veterinary and animal care staff and promptly report and respond to emergent conditions Requirements • 2+ years experience providing hands-on animal care in a research, small animal clinical, farm or zoological setting is critical, including direct hands-on avian experience, • Prior experience incubating and hatching eggs and production of chicken across all life stages would be beneficial, • Undergraduate or an associate degree in animal, biological or veterinary technical sciences or related fields, • This position requires working in PPE for up to 3 hours at a time, and occasionally moving equipment up to 50 lbs., • Attention to detail is important to ensure that biosecurity and care SOPs are followed, • Interest in learning new veterinary and laboratory techniques is valued at Neion, • Ability to operate with quiet confidence and competence, individually and as part of a team to promote a culture of care, • Communicate effectively with supervisor and Neion team members, as well as external veterinary and care staff, • Attuned to regulatory and procedural compliance to ensure that SOP’s are followed to promote animal welfare, biosecurity, and data integrity, • Excellent interpersonal skills and ability to communicate information accurately, clearly, and concisely to ensure understanding., • Ability to follow established work schedules, and record information accurately and in a timely manner, • Excellent judgment, time management, and observation skills to complete tasks in a timely manner, and ability to prioritize tasks to accomplish daily and weekly assigned duties. Benefits Compensation: base salary is expected to be $60-70K depending on experience, with additional bonus compensation, equity compensation, and benefits including health, dental, vision insurance, and a 401k plan.