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Location: CHA Cambridge Hospital Work Days: Sun - Thurs 11:15 - 07:15 am w/ wknd rotation, on-call Category: Medical Technologist Department: Hematology Job Type: Full time Work Shift: Night Hours/Week: 40.00 Union Name: CH Laborers 380 Lab Up to $10,000 Sign on Bonus for ASCP certified Medical Technologists!!! Bonus is based on experience & shift The CHA laboratory provides everything from routine blood and urine tests to special tissue evaluation. Summary: Through the utilization of applied theories, principles, and practices of clinical laboratory technology, performs and reports tests in a manner to promote the efficient operation of the laboratory and provide effective patient care. Job Purpose: Performs and reports laboratory testing in a manner to promote the efficient operation of the laboratory and effective patient care. Duties and responsibilities include: *performs and evaluates Quality Control *performs testing in Chemistry and Diagnostic Immunology *participates in proficiency testing *troubleshooting and resolves basic instrument problems *receives and processes a variety of laboratory specimens and utilizes the Meditech computer system for data entry; computerized worksheets and instrument interfaces are used in the performance of testing *performs both STAT and routine testing in an accurate and timely manner *assists the manager in the development of new methods and evaluating cost feasibility as required *trains new employee in department procedures and policies *participates in department meetings *works with fellow staff members to analyze workflow processes and conduct QI audits *on-call coverage responsibilities Qualifications: Minimum education: BS MT required Registration/certification as MT or MLS (ASCP) or equivalent NCA, AMT or HEW highly preferable at time of hire. Will consider a candidate who will take and pass certification exam at the next opportunity examination is offered. Keywords: Med Tech, Clinical Lab Scientist In keeping with federal, state and local laws, Cambridge Health Alliance (CHA) policy forbids employees and associates to discriminate against anyone based on race, religion, color, gender, age, marital status, national origin, sexual orientation, gender identity, veteran status, disability or any other characteristic protected by law. We are committed to establishing and maintaining a workplace free of discrimination. We are fully committed to equal employment opportunity. We will not tolerate unlawful discrimination in the recruitment, hiring, termination, promotion, salary treatment or any other condition of employment or career development. Furthermore, we will not tolerate the use of discriminatory slurs, or other remarks, jokes or conduct, that in the judgment of CHA, encourage or permit an offensive or hostile work environment. Cambridge Health Alliance brings Care to the People - including your neighbors, friends and family. Our local hospitals and care centers serve our vibrant, diverse communities, and play an integral role in improving health. As passionate advocates for the underserved, we actively partner with our communities to take on challenging public health issues, and conduct important research to help reduce barriers to care. We believe that everyone deserves access to high quality, convenient health care. This is why our employees believe in where they work and why many build long, rewarding careers at CHA. Healthcare is changing rapidly. CHA has a strategic plan that charts a proactive course for our future. It is built on a vision of equity and excellence for everyone, every time. It also recognizes that our workforce is our most valuable asset and prioritizes competitive salaries, benefits and professional development opportunities for employees. The strategic plan is changing the way we provide care and improving the health and experience of our patients; we are looking for smart, committed, compassionate people who want to be part of making our vision of better health and equity a reality. At CHA, you can believe in where you work and go home every day knowing you made a difference. Join our team and help us bring Care to the People.

Job Description About Us: The ALS Therapy Development Institute (ALS TDI) is a leading non-profit biotechnology company dedicated to discovering and advancing effective treatments for amyotrophic lateral sclerosis (ALS). At ALS TDI, we are driven by our mission to find therapies that can make a real difference for patients living with ALS. Position Overview: We are seeking a motivated and detail-oriented Associate Scientist to join our Translational Research team. In this role, you will support the development of cell-based models of ALS and contribute to chemical and genetic screening efforts aimed at identifying novel drug targets and therapeutic candidates. This is a unique opportunity to work in a collaborative, mission-driven environment and contribute to impactful ALS research. Key Responsibilities: • Develop and characterize patient-derived and genome-edited induced pluripotent stem cell (iPSC) lines and their differentiated derivatives., • Assist in cellular phenotype discovery and screening assay development., • Support screen automation and implementation of high-content analysis techniques., • Collaborate with team members to execute experiments and analyze data., • Present findings to the research team and contribute to ongoing project discussions. Minimum Qualifications: • Education: BS/BA in Molecular and Cell Biology or a related discipline., • Experience: Proven experience with mammalian cell culture and general molecular and cellular biology techniques., • Preferred Skills: Background in neurobiology, stem cell biology, cellular immunology, genome editing, cell-based assay development, laboratory automation, or high-content cell analysis., • Attributes: Strong organizational and communication skills, attention to detail, and the ability to work both independently and collaboratively on multiple projects. Why Join Us? • Be part of a passionate and innovative team dedicated to making a difference in the lives of ALS patients., • Collaborate in a cutting-edge research environment with opportunities for professional growth and development., • Contribute to impactful scientific discoveries that bring us closer to effective ALS treatments. What We Offer We offer a comprehensive benefits package designed to support your well-being and growth. Enjoy unlimited PTO, a generous holiday schedule, and a casual, collaborative work environment. Benefits include medical, dental, and vision coverage, HRA for out-of-pocket expenses, Health and Dependent Care FSAs, company-paid Life, AD&D, and Short- and Long-Term Disability insurance, and a retirement plan with company match. Additional perks include tuition reimbursement, MBTA pass, and gym access. ALS-TDI is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. Job Posted by ApplicantPro

Job DescriptionSalary: The Company: Newleos Therapeutics is an innovative, fast-growing biotech startup dedicated to transforming the treatment of mental health conditions through evidence-based interventions and novel therapeutics. Our current focus includes programs in Generalized Anxiety Disorder (GAD), Social Anxiety Disorder (SAD), and Substance Use Disorders (SUDs). We aim to accelerate the development of next-generation therapies by combining clinical rigor with cutting-edge clinical science. Position Overview: We are seeking a Medical Director to provide clinical and scientific leadership for one of our core programs in GAD, SAD, or SUD. This role is ideal for a psychiatrist or physician-scientist with experience in clinical trials who is eager to contribute to early-stage development, help shape trial strategy, and collaborate with cross-functional teams in a startup environment. The Medical Director will work closely with the Chief Medical Officer (CMO), Clinical Operations, Regulatory Affairs, and Clinical Pharmacology teams to ensure clinical excellence, safety oversight, and scientific integrity across program activities. This position is based in Back Bay, reports to the CMO, and supports a weekly hybrid work schedule with 3 days (Mon, Tues, Wed) in the office and 2 days (Thurs & Fri) remote. Responsibilities: • Serve as medical lead for one assigned clinical program (GAD, SAD, or SUD)., • Provide medical and scientific input into the design, execution, and interpretation of clinical trials., • Contribute to the development of clinical protocols, investigator brochures, and regulatory submissions., • Monitor trial conduct and patient safety, including review of adverse events and emerging efficacy data., • Participate in clinical study team meetings, investigator meetings, and interactions with external key opinion leaders (KOLs)., • Support data analysis, interpretation, and publication of clinical trial results., • Collaborate with internal and external partners, including CROs, investigators, and scientific advisors., • Stay current with scientific and therapeutic developments in psychiatry., • Contribute to the strategic development of future programs and new indications. Qualifications: • MD or equivalent medical degree., • Minimum 25 years of clinical experience, with at least some exposure to clinical research or clinical trials (industry, academic, or CRO setting)., • Strong interest in psychiatry, anxiety disorders, and substance use disorders., • Board-certified or board-eligible in Psychiatry or Neurology, • Experience in clinical development or medical monitoring for psychiatric indications., • Previous involvement in early-phase trials (Phase III) and interactions with regulatory agencies., • Strong analytical and problem-solving skills; ability to translate scientific insights into clinical strategy., • Entrepreneurial mindset and comfort working in a startup or small-company environment. Newleos Therapeutics is proud to be an Equal Opportunity Employer. Our goal is to have a diverse workforce. We do not discriminate on the basis of race, age, color, religion, national origin, gender, sexual orientation, gender identity or expression, veteran status or disability or any other status protected under federal, state or local law. All employment is decided on the basis of qualifications, merit and business need.

Job DescriptionCrossbow Therapeutics is seeking a highly motivated and detail-oriented Associate Scientist – Protein Sciences to join our Antibody Development Team in Cambridge, MA. This individual will contribute to the development and characterization of therapeutic antibodies for both therapeutic applications and research initiatives. This role provides the opportunity to work collaboratively with cross-functional teams to produce, purify, and analytically characterize antibodies and fusion proteins. The ideal candidate will possess a solid foundation in biochemistry or a related field, along with hands-on experience in protein analytical techniques, production, and purification. If you are passionate about protein science and eager to make a significant contribution, this role offers a dynamic opportunity to contribute to innovative therapeutic developments.Essential Duties and Responsibilities: • Perform production of recombinant monoclonal and bispecific antibodies, and other proteins using mammalian protein expression systems (e.g., CHO, HEK293)., • Implement various chromatography methods (affinity, IEX, SEC, HIC, MMC) for the purification of antibodies and other proteins., • Conduct comprehensive analyses to assess protein purity and quality using SDS-PAGE, UV/Vis spectroscopy, HPLC tools, and other relevant analytical methods., • Operate and maintain AKTA FPLC systems and analytical HPLC instruments to ensure efficient workflow., • Address and resolve technical challenges that arise in protein analytical and purification workflows, ensuring high-quality results., • Work with the team to develop and implement sophisticated analytical methods (HPLC, BLI, ELISA, etc.) for the characterization of antibodies and other proteins., • Document and maintain precise records of laboratory activities using an electronic laboratory notebook (Benchling) and communicate findings clearly through written reports and presentations., • Actively stay informed about advancements in protein analytical, production, and purification technologies to continuously enhance methodologies., • Provide technical and resourcing support to other functional groups as needed.Requirements, • Bachelor's degree + 6 years with relevant experience, Master's + 3 years in Biochemistry, Molecular Biology, or a related field., • Demonstrated hands-on expertise in mammalian expression systems, including CHO and HEK293., • Demonstrated expertise in protein purification, with the ability to independently design and execute purification strategies with minimal supervision; proficiency with ÄKTA chromatography systems is required., • Proficiency in chromatography techniques relevant to antibody and bispecific protein production, including Protein A affinity chromatography, ion exchange chromatography (IEX), and size exclusion chromatography (SEC); experience with mixed-mode chromatography or HIC is a plus., • Experience producing complex biologics, such as bispecific antibodies, multispecific proteins, or engineered antibody formats., • Solid understanding of protein biochemistry and developability considerations, including purity, aggregation, and stability., • Working knowledge of protein analytical techniques, with a strong interest and aptitude to expand skills in this area., • Experience using Agilent HPLC systems for protein analytics., • Ability to work independently and manage experiments end-to-end, including experimental planning, execution, troubleshooting, and documentation., • Strong organizational and data analysis skills, with attention to detail and reproducibility., • Effective written and verbal communication skills for cross-functional collaboration., • This position requires on-site work 5 days per week at our office in Harvard Square, Cambridge, Massachusetts. Additional Knowledge, Skills and Abilities, • Experience with therapeutic antibody developability assessments is a plus., • Excellent problem-solving skills complemented by keen attention to detail., • Ability to thrive both independently and collaboratively in a fast-paced environment., • Flexibility to adapt to changing plans., • Strong communication and organizational skills to support effective teamwork.The Benefits of Working at Crossbow, • We offer a competitive compensation that includes an annual discretionary bonus and equity package, allowing you to have a stake in our long-term success., • Base salary will be commensurate with experience and in the range of $105,000-$130,000 for an Associate Scientist., • Take care of your physical and mental health through our subsidized medical, dental and vision insurance programs., • Enjoy work and life with our flexible paid time off program, annual holidays including a Winter Break and sick time., • Utilize our tuition reimbursement program to further your education. Note to Recruiters: Please be aware that we do not accept unsolicited resumes and kindly request that you do not contact our team regarding this job posting. If a resume is submitted to a Crossbow team member without a prior agreement, we will not be obligated to pay any referral or placement fees.

Job Description About Us: GT Biosciences is a seed-stage techbio startup building Deliveromics, the first AI-powered, high-throughput, multiplexed in vivo data engine for cracking the design rules of drug delivery. Founded by MIT PhDs and an MIT professor, backed by top-tier investors, we’re creating next-generation, non-viral, cell-type-specific delivery vehicles. We’re a small, fast-moving, science-obsessed team on a mission to make routine in vivo cell reprogramming possible. We value transparency and collaboration, and seek teammates who thrive in an open, cooperative environment and want to grow together with the team and the company. Job Description: GT Biosciences is seeking a highly mission-driven, multidisciplinary Spatial Biology Scientist to join our Platform Development Team and help advance our Deliveromics platform. In this role, you will work closely, day-to-day, with teammates across biology, chemistry, and engineering to turn complex spatial and sequencing workflows into robust, automated, and scalable systems. You will contribute hands-on to a transformative technology aimed at enabling systematic, cell-specific drug delivery in vivo. This is a full-time, in-person position based in Cambridge, MA. Responsibilities: * Optimize in-situ barcode sequencing workflows for robust, reproducible, high-quality data. * Design experiments at the chemistry-biology interface to advance spatial readout performance. * Analyze results quantitatively, document findings clearly, and provide recommendations that guide platform development. * Ensure accurate record-keeping (e.g., protocols, SOPs, experimental records) * Troubleshoot technical challenges and integrate new methods across teams. * Apply statistical tools to assess quality, identify variability, and drive optimization. * Help scale workflows from benchtop prototypes to automated, production-ready systems. Qualifications: Required: * PhD in Bioengineering, Biomedical Engineering, Biochemistry, Biophysics, or related field. Exceptional candidates with equivalent experience will be considered. * Hands-on expertise in developing novel tools and methods for spatial biology, spanning FISH, RNAscope, MERFISH, in situ sequencing, spatial transcriptomics, and spatial proteomics. * Basic coding skills (e.g., Python, R, or MATLAB). * Experience operating and troubleshooting optical imaging systems (confocal or fluorescence microscopy). * Practical knowledge of tissue processing workflows (fresh-frozen and FFPE prep, cryosectioning, antigen retrieval). * Strong problem-solving skills, attention to detail, and experimental rigor. * Clear communicator who collaborates well across scientific and technical teams. * Resourceful, adaptable team player who thrives in fast-paced, cross-functional environments. * Available to work onsite full time. Nice to have: * Experiences with nucleic acid chemistry (mRNA, ASO, and siRNA, etc.). * Experiences with drug delivery systems (lipid nanoparticles, polymer nanoparticles, AAV, etc.). * Experience with image analysis pipelines or software tools (e.g., ImageJ or CellProfiler). * Prior experience working with mouse and non-human primate tissues. * Familiarity with NGS or single-cell sequencing workflows such as scRNA-seq, ATAC-seq, or related methods. * Hands-on experience troubleshooting liquid-handling platforms or automated lab systems. * Relevant work experience in similar roles across academia, industry, or core facilities, particularly in spatial biology, imaging, or sequencing-heavy environments. What we offer * Competitive salary and equity. * Flexible, generous health benefits. * Work with a small, world-class team that values rigorous science and candid collaboration. * Opportunity to work with experts from diverse scientific backgrounds. We don't expect anyone to know everything. We learn together, support each other, and get better every day! If you are ready to make an impact, we would love to hear from you.

Job Description (Associate) Director, Clinical Scientist (Remote) Key Responsibilities • Provide scientific and strategic leadership in the planning and execution of clinical trials, including protocol development, study design, and data analysis., • Author and review clinical protocols, ICFs, CSRs and regulatory documents, • Collaborate closely with cross-functional teams, including Clinical Operations, Regulatory Affairs, Biostatistics, and Medical Affairs, to ensure the successful conduct of clinical studies., • Interpret clinical data, prepare study reports, and contribute to regulatory submissions and presentations for internal and external stakeholders., • Support investigator meetings, advisory boards and data monitoring committee meetings, • Stay current with emerging scientific literature, competitive landscape, and regulatory requirements relevant to Immuneering’s oncology therapeutic area., • Support the development of clinical development plans and contribute to the strategic direction of ongoing and future programs., • Work closely with CRO’s and have a can do, proactive biotech mindset. Qualifications & Education · PhD, PharmD, RN, or MD in a relevant scientific discipline (e.g., biology, pharmacology, medicine). · Minimum of 5-8 years of experience in clinical development within the pharmaceutical or biotechnology industry. · Direct Phase 3 oncology clinical trial experience required. · Demonstrate experience authoring and reviewing clinical documents. · Demonstrated strong experience in clinical trial execution and data interpretation. · Strong analytical, organizational, and communication skills. · Deep understanding of oncology clinical development, endpoints and regulatory expectations. Technical / Soft Skills · Excellent cross-functional communication and stakeholder management. · Ability to work collaboratively in a fast-paced, team-oriented environment. · Must be a strong champion of our Values: All in, Data Rules, Care, Humble, Own It (Accountable) Physical Demands/ Working Conditions The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of the job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Requires prolonged sitting, some bending, stooping, and stretching. Requires eye-hand coordination and manual dexterity sufficient to operate a keyboard, photocopier, telephone, calculator, and other office equipment. Requires the ability to perform essential job functions with or without reasonable accommodation. No significant lifting is associated with the role. While extensive travel is not anticipated with this role, it is possible to perhaps up to 15% at times. Requires prolonged sitting, some bending, stooping, and stretching. Requires eye-hand coordination and manual dexterity sufficient to operate a keyboard, photocopier, telephone, calculator, and other office equipment. Requires normal range of hearing and eyesight to record, prepare and communicate appropriate reports. No significant lifting is associated with the role. Immuneering is an equal opportunity employer. We are committed to creating a diverse and inclusive workplace where all employees are treated with fairness and respect. We do not discriminate on the basis of race, ethnicity, color, religion, gender, sexual orientation, age, disability, or any other legally protected status. Our hiring decisions and employment practices are based solely on qualifications, merit, and business needs. We encourage individuals from all backgrounds to apply and join us in our mission. Job Offers: Immuneering uses the Immuneering.com domain and email addresses for all official communications. If you received communication from any other domain, please consider it spam. Note to Recruitment Agencies: We appreciate your interest in finding talent for Immuneering but please be advised that we do not accept unsolicited resumes from recruitment agencies. All resumes submitted to Immuneering without a prior written agreement in place will be considered property of Immuneering, and no fee will be paid in the event of a hire. Thank you for your understanding.

Job DescriptionCompany Description AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at . Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok. Job Description AbbVie’s global Information Research (IR) group has a mission to unlock information that makes cures possible. Within IR, the Enterprise Knowledge Accelerator (EKA) team is the trusted knowledge partner for clients in R&D and the Corporate Business & Strategy Office (CBSO). EKA drives innovation and enhances knowledge-sharing across the value chain, for better and faster decisions that impact advancement in our pipeline. The team is a global organization, with presences at the Lake County, Illinois headquarters and Boston, Massachusetts areas (US), as well as the Ludwigshafen site (Germany). Leveraging cutting-edge technologies and scientific expertise, we deliver industry-leading capabilities to harness insights from published content for high-impact decision-making. Our team possesses the scientific and technical expertise to utilize and provide guidance on a wide range of knowledge sources, ensuring high-quality answers for our clients. The Senior Data Scientist will join the Solutions for Published Insights and Client Enablement (SPICE) team, supporting AbbVie’s R&D, CBSO and other business functions enterprise wide. SPICE provides business partnership, resource consultancy, ad-hoc research support for business-critical questions, knowledge and insights mining and analysis, as well as designing and building innovative self-service solutions for insights generation from published resources and internal knowledge. This includes literature, patent, conference, news, clinical trial, and competitive intelligence data such as competitor pipelines. As a Senior Data Scientist on the Solutions for Published Insights & Client Enablement (SPICE) team, you will serve as the lead data scientist focused on advancing AbbVie’s competitiveness by driving Therapeutic Modality Knowledge & Intelligence Solutions. You will lead the creation of new methods and algorithms for extracting, harmonizing and proactive monitoring of knowledge on emerging therapeutic approaches, critically evaluate new technologies and scientific advances, and integrate them into impactful business solutions, to set AbbVie up for future success in a competitive landscape. You will play a critical role in identifying and filling strategic knowledge gaps around emerging therapeutic modalities—including genetic medicines, innovative biotherapeutics, and RNA therapies—through the design and implementation of innovative GenAI-based and agentic knowledge solutions. Your leadership will enable AbbVie to leverage high-value insights extracted, harmonized, and integrated from literature, patents, news, and competitor intelligence. In this role, you will collaborate cross-functionally with other EKA/IR and business teams to develop and deploy AI-powered and data science solutions that support AbbVie’s pipeline strategy, corporate strategy, and R&D initiatives. The position requires a strong background in both science and technology, and the ability to rapidly learn and adapt to new scientific advances in therapeutic modalities and information technology (such as generative AI solutions and AI agents), given the dynamic and expanding landscape. Responsibilities * Conceive, design, and implement advanced AI-powered published insights solutions (incl. agentic workflows) that address significant scientific and strategic trends and knowledge gaps in therapeutic modalities. * Develop and deliver innovative, high-quality intelligence solutions that systematically extract, analyze, summarize, integrate and proactively monitor key knowledge about novel therapeutic modalities (such as gene/cell therapies and innovative RNA or antibody-based drugs) to address urgent scientific and business needs. * Apply broad expertise in knowledge & information science, Generative AI/NLP, data warehousing, and software development to build robust data pipelines and analytical workflows for large and complex published (often unstructured) data, including literature publications, patents, news/press releases, and competitor pipelines. * Demonstrate deep knowledge of pharmaceutical R&D, drug development, and therapeutic modality trends * Operate with high autonomy and productivity, proactively tackling complex problems and driving multiple projects with minimal supervision. * Pursue and evaluate relevant external and internal leads in novel modalities, new technologies, and data sources—rapidly incorporating new findings into project strategies and generate novel, actionable insights for R&D and business strategy. * Collaborate cross-functionally with scientific, corporate strategy, and other R&D teams to ensure solutions meet real-world needs, fill knowledge gaps, and democratize access to key intelligence. * Mentor or supervise junior data & information scientists * Stay at the forefront of emerging trends, methodologies, and technologies that can advance therapeutic modality & competitor intelligence at Abbvie. * Author high-impact presentations and publications, communicating findings to diverse audiences. * Ensure adherence to AbbVie’s standards of compliance, data security, GxP, and code of conduct. * Achieve great results, while overwhelmingly demonstrating key AbbVie values and behaviors. Qualifications Required: • PhD (with 4+ years relevant experience) in life sciences (biology, pharmacology, chemistry, biotechnology, bioinformatics, pharmacy, medicine, biomedical data science, or related). Equivalent experience considered at Master's (10+ years) or Bachelor's (12+ years) level., • Deep knowledge of emerging therapeutic modalities, such as biotherapeutics (ADCs, mAbs, multispecific antibodies, cell therapies, etc.), different types of degraders, gene therapies (AAV, lentiviral, CAR-T, CRISPR, etc.), RNA therapies (mRNA, siRNA, ASO), as shown in recent industry advances, • Demonstrated leadership in designing and delivering creative technology solutions that advance business and scientific objectives; proven ability to translate complex scientific/business questions into actionable, large-scale information solutions., • Solid background in programming, informatics, and data science. Proficiency in Python required., • Hands-on expertise with extraction and integration of knowledge from literature, patents, competitive intelligence databases (e.g., Citeline, Cortellis), and news/press release sources., • Competence in using GenAI models for knowledge extraction (including prompting, pitfalls, etc.)., • Ability to rapidly learn and adapt to new advances in therapeutic modalities and information technologies and balancing multiple projects with shifting priorities., • Strong analytical, organizational, and problem-solving skills, with superior attention to detail and high degree of reliability and integrity., • Excellent written and oral English communication skills; proven ability to present complex concepts clearly to scientists, non-scientific audiences and different leadership levels, • Pharmaceutical industry experience., • Experience working in fast-paced, dynamic, multidisciplinary, and collaborative settings and global teams., • Familiarity with data engineering, software development principles, relational databases and SQL (e.g., Oracle, Hadoop) as well as common formats/APIs (REST, XML, JSON, Python libraries like Pydantic)., • Experience with embedding Gen AI models in larger Python-based workflows to automate knowledge extraction tasks., • Basic understanding of agents and agentic workflows (MCP, A2A). Additional Information Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law: * The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future. * We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees. * This job is eligible to participate in our short-term incentive programs. Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company’s sole and absolute discretion, consistent with applicable law. AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled. US & Puerto Rico only - to learn more, visit US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:

Job Description Who are we? A strategic and trusted insurance partner, Berkshire Hathaway Specialty Insurance (BHSI), provides a broad range of commercial property, casualty and specialty insurance coverages and outstanding service to customers and brokers around the world. Part of Berkshire Hathaway’s insurance operations, we bring our solutions to market with our stellar brand name, top-rated balance sheet, and the expertise of our global team of professionals, who exude excellent capabilities and strong character. We are a values-based organization where respect, integrity, excellence, collaboration, and passion define who we are and how we do business. We value diversity of backgrounds, experience, and perspectives and strive to foster an inclusive environment that enables all our team members to bring their best selves to work. We are one team committed to building a culture where every teammate has the opportunity to contribute and be recognized. Want to be part of the team building the finest property, casualty and specialty lines insurance company in the world? Learn more about our unique culture and history. Job Opportunity: Berkshire Hathaway Specialty Insurance (BHSI) has an exciting opportunity for Data Scientist / Senior Data Scientist to join the Catastrophe Engineering and Analytics (CAT E&A) team. CAT E&A is an innovative and versatile technical team conducting catastrophe risk research and development and providing complex quantitative metrics that inform underwriting decisions across multiple lines of business. The successful candidate will be responsible for identifying and applying cutting-edge data science techniques to build a better view of the risk for multiple perils. You will work across functional areas and perils within the team, supporting the development of models for various natural catastrophes, natural hazards, building vulnerability, and man-made risks such as cyber, casualty, among others. In addition, you will conduct in-depth evaluation of vendor models, research and develop internal views of exposure and risks, consult on account-specific risk analyses, and develop internal tools to facilitate account underwriting decision-making and other related activities. Duties & Responsibilities: • Evaluate and develop insights into large and diverse data sets from claims, hazard models, structural analysis, geospatial sources, and various other public/proprietary datasets., • Develop and maintain expertise in advanced data science, machine learning, and artificial intelligence techniques, and their application to understanding risk., • Work with domain experts across teams and perils to enhance our use of available data., • Propose and execute innovative solutions to insurance problems that directly impact BHSI underwriting decisions. Qualifications, Skills and Experience: • Ph.D. or M.S. in data science, civil engineering, atmospheric science, actuarial science, computer science, mathematics, or a related field, • 3-6 years of industry experience is preferred and required for the Senior Data Scientist level role, • Advanced knowledge of probability theory, statistics, and machine learning methods is required, • Practical experience in insurance, catastrophe model development, cyber and casualty risk modeling, and/or exposure data collection is preferred, • Experience applying advanced statistical techniques and machine learning to large data sets, especially in areas of structural performance, natural catastrophe hazard, building exposure data, geospatial data, or insurance claims data, • Familiarity with large language models (LLMs), retrieval-augmented generation (RAG), and their application in data-driven workflows is a plus, • Strong written and verbal communication skills, • Strong programming skills in Python (preferred), R, and SQL, • Experience and understanding of relational and non-relational databases preferred, • Comfort working within git-based version-control environments, • Experience with Databricks or other cloud-based data and analytics platforms preferred, • Highly motivated, detail oriented, and team player BHSI Offers: • A competitive package and exciting growth opportunities for career-oriented teammates., • A dynamic, action oriented, and thoughtful environment centered on always doing the right thing for our customers, teammates, and our other stakeholders., • A purposely non-bureaucratic organization that embraces simplicity over complexity and emphasizes individual excellence in a team framework., • Benefits that support your life and well-being, which include:, • Comprehensive Health, Dental and Vision benefits, • Disability Insurance (both short-term and long-term), • Life Insurance (for you and your family), • Accidental Death & Dismemberment Insurance (for you and your family), • Flexible Spending Accounts, • Health Reimbursement Account, • Employee Assistance Program, • Retirement Savings 401(k) Plan with Company Match, • Generous holiday and Paid Time Off, • Tuition Reimbursement, • Paid Parental Leave The base salary range for this position in Atlanta, GA, Boston, MA, or San Ramon, CA is $100,000 to $160,000, along with annual bonus eligibility. Total compensation for a candidate is determined by their relevant skills, location, and experience. We value our teammates – both their capabilities and character – as demonstrated by our amazing culture. NOTE: Compensation will be commensurate with experience. This job description is not intended to be all-inclusive. Team Member may perform other related duties as negotiated to meet the ongoing needs of the organization.

Job DescriptionAbout Skyhook Bio: Skyhook accelerates the discovery and development of differentiated therapeutics by accessing vast biological design spaces previously intractable with current state of the art technologies. Our differentiated platform employs efficient AI-guided design, synthesis, and functional screening of diverse programmable biomolecule libraries at unprecedented speed and scale. About the Role: We are seeking an innovative, self-motivated, and team-oriented Machine Learning Scientist with a passion for working at the intersection of human and synthetic biology. In your role, you will be responsible for developing deep-learning methods and models to design functional proteins as well as analyze large proprietary data sets from high-throughput functional assays. As a member of a growing and engaged team, you will have the opportunity to take part in leading innovative research and development and work with a highly skilled multidisciplinary team in a fast-paced startup environment. Key Responsibilities: • Train and deploy deep neural network models using public and proprietary protein sequence, structure, and function data, • Establish automated processes to continuously evaluate and improve our protein design methodology, • Apply and develop deep-learning models to learn from large experimental datasets, • Build and maintain database infrastructure for long-term data storage and versioning on AWS, • Collaborate closely with experimental and computational scientists to develop integrated experimental/in silico pipelines, including for NGS data analysis, • Develop efficient, high-quality code, and data pipelines, • Present computational approaches and results to colleagues in regular update meetings Required Qualifications:, • PhD in Computer Science, Machine Learning, Computational Biology, Biophysics, Bioinformatics, Statistics, or related field. 2+ years industry experience in pharma or biotech R&D preferred. Position leveling will be commensurate with experience, • Strong foundation in machine learning, including model development, training, evaluation, and application to large-scale biological datasets, • Experience with exploratory data analysis, statistical analysis, and data visualization to interpret experimental results and guide modeling decisions, • Proficiency in modern ML frameworks such as PyTorch or TensorFlow, and writing efficient, well-structured, and maintainable code (Python required), • Experience working with cloud-based ML workflows and data pipelines, • Strong analytical and problem-solving skills; comfortable working in a dynamic, collaborative startup environment, • Clear written and verbal communication skills, with the ability to explain technical concepts to diverse audiences Preferred Qualifications:, • Experience with protein-focused ML models and tools (e.g., ESM, AlphaFold, or related frameworks), • Experience designing or improving ML infrastructure and data pipelines, including cloud-based training, inference, data versioning, automation, and deployment (AWS preferred)

Job DescriptionDescription: GeoEngineers USA, PC is seeking a Senior Environmental Engineer, Scientist, or Geologist for our Boston office. Responsibilities of this position include providing technical leadership on environmental investigation and remediation projects; planning and managing environmental data (soil, sediment, groundwater indoor air, and/or soil vapor) collection efforts; managing remedial construction oversight; evaluating and interpreting environmental data; performing engineering and scientific analysis and evaluation; preparing cleanup documents including work plans, reports, and design submittals (design drawings, specifications, and engineers estimate); managing projects; developing and supporting client relationships; business development; and mentoring junior staff. Essential Duties and Responsibilities • Play a key role working closely with Principals/Associates in developing and supporting client relationships, business development activities, preparing Statements of Qualification (SOQ), and competing for new project opportunities., • Serve as a technical leader for clients and project staff, providing guidance on all phases of remediation projects including planning, permitting, investigation, design, remedial construction, project/regulatory closeout, and long-term monitoring., • Plan and manage field explorations and environmental data (soil, sediment, groundwater, indoor air and/or vapor) collection efforts. Field explorations may include drilling and test pitting to collect soil samples, sediment grab sampling and coring, and monitoring well installation and collection of groundwater samples., • Evaluate and interpret field and laboratory environmental data, perform engineering/scientific analysis and evaluation, and develop solutions to complex problems., • Evaluate the fate and transport of environmental contaminants in various media including soil, sediment, groundwater, indoor air and/or soil vapor, and develop conceptual site models to evaluate contaminant exposure pathways to receptors., • Develop solutions to environmental problems by evaluating different and applicable remedial technologies to meet the requirements of the Massachusetts Contingency Plan (MCP)., • Prepare MCP documents, remedial investigation work plans, sampling and analysis plans, data reports, remedial investigation/feasibility study (RI/FS) reports, cleanup action plans, and remedial action completion reports., • Prepare design documents, engineering calculations, and permit applications., • Perform management and oversight of remedial construction involving remedial excavation and design, installation, and operations and maintenance of in-site remediation systems and site restoration activities., • Mentor and train junior staff., • Bachelor’s or master’s degree in civil/environmental engineering, geology, or environmental science. Master’s degree preferred., • 10+ years of environmental consulting or related professional experience., • Licensed engineer and/or Licensed Site Professional (LSP) is a plus., • Working knowledge of environmental regulations, including the MCP, and how to apply them., • Skilled in managing environmental field investigation (soil, sediment, groundwater, indoor air, and/or soil vapor) and cleanup construction projects., • Ability to independently prepare and lead proposals, work plans, data reports, remedial investigation/feasibility study (RI/FS) reports and design (design drawings, specifications, and engineers estimate)., • Working knowledge of Local, State, and Federal permitting processes applicable to environmental cleanup projects., • All candidates are subject to completing a background check, and reference check., • Ability to perform physical duties, including use of personal protective and respiratory equipment and occasional lifting., • Able to perform consistent work on a PC., • Ability to travel for short-term and long-term assignments as needed. Travel will typically not exceed 10%. At GeoEngineers, investing in our people is a top priority. In addition to competitive and equitable pay, we are proud to offer a wide range of benefits to support employees and their families, including healthcare (with travel benefit for care not locally available), 401(k) with company match, short-term and long-term disability, life insurance, wellbeing benefits, paid vacation and sick time and paid holidays, among others. View our full listing of benefits here. Our Commitment to Belonging at GeoEngineers When people feel they can bring their whole selves to work, that they have a voice and are supported and respected, it creates trust and a feeling of belonging— employees then flourish, grow their careers, and do the best work of their lives. A culture of belonging allows our employees to thrive and our company to prosper. This is a journey, and we are committed to doing the work, learning and evolving as we go. GeoEngineers is proud to be an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to age, ancestry, color, family or medical care leave, gender identity or expression, genetic information, marital status, medical condition, national origin, physical or mental disability, political affiliation, protected veteran status, race, religion, sex (including pregnancy), sexual orientation, or any other characteristic protected by applicable laws, regulations, and ordinances. GeoEngineers is also committed to working with and providing reasonable accommodation to individuals with physical and mental disabilities. If you need special assistance or accommodation while seeking employment, please contact Human Resources at or by phone at (425) 861-6000. We will then make a determination regarding your request for reasonable accommodation on a case-by-case basis. We welcome and encourage individuals from all backgrounds and experiences to apply for openings on our team. We would love for you to join us! We care about your privacy. Read GeoEngineers’ Privacy Notice for details on our personal data policies. Requirements:

Job Description Company Overview We are the only AI-native biotech, pioneering small and large molecule therapeutics discovery by integrating massive multimodal data, frontier AI models, and high-throughput lab automation into an infrastructure for AI-enabled drug discovery. We hire top 1% talent to join our interdisciplinary team of scientists, engineers, researchers, operators, innovators, drug developers, business professionals, and technologists. Join us to build the world's first AI infrastructure for tech-enabled drug discovery and to deliver a pipeline of diverse drug modalities for all major disease areas. As an AI Research Scientist II at 1910 you will be expected to roll up your sleeves as an Individual Contributor (IC) by keeping up with relevant scientific literature, prototyping promising methods, and contributing to our active drug design campaigns by applying 1910's productionized AI/ML models. Role Description • Propose and prototype AI and Machine Learning solutions that address use cases in 1910's design pipeline, • Apply productized AI and Machine Learning models to advance 1910's active drug design campaigns with minimal support from senior members of the AI Research Team, • Write and publish peer reviewed scientific articles with minimal support from senior members of the AI Research Team, • Periodically presenting recent AI research at internal journal clubs, • Work cross-functionally with scientific colleagues, being a subject matter expert in how AI and Machine Learning can be used to answer cheminformatics and bioinformatics questions, • Keep up-to-date on cutting-edge research in the AI for drug discovery space Qualifications • PhD in a relevant discipline (Computer Science, Biology, Chemistry, etc.), • 2 years of relevant industry experience (AI, Drug Discovery, etc.), • A strong understanding of statistics and classical machine learning methods (SVM, RF, etc.), • Industry experience training and deploying cutting edge deep learning methods (Transformers, Graph Neural Networks, etc.), • Wet lab validation of at least 1 AI-driven drug discovery initiatives, • Demonstrated experience writing clean, maintainable, production-quality Python code, with examples available in code repositories, • Familiarity with MLOps and DevOps best practices, • Exposure to distributed computing (Microsoft Azure, HPC Cluster, etc.), • Strong track record of publications of individual research in top-tier AI journals and conferences, • Ability to demonstrate business value related to developed AI and Machine Learning solutions in biology and medicinal chemistry related to your modeling efforts, • Ability to work effectively in a fast-paced startup environment with evolving projects and shifting priorities driven by business needs, • Excellent written and verbal communication skills, including the ability to create clear documentation for roadmaps, proposals, and related materials #LI-Onsite Diversity and Inclusion (1910's Promise) At 1910, we believe that a diverse, equitable, and inclusive workplace furthers relevance, resilience, and longevity. We encourage people from all backgrounds, ages, abilities, and experiences to apply. 1910 is proud to be an equal-opportunity workplace and is an affirmative action employer. We are committed to equal employment opportunity regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity, or Veteran status. If, due to a disability, you need an accommodation during any part of the interview process, please let your recruiter know. While 1910 supports visa sponsorship, sponsorship opportunities may be limited to certain roles and skills. Benefits and Perks • Competitive compensation package, • Above market benefits, • Generous vacation and parental leave, • Super cool team building activities, • Great colleagues

Job Description Company Overview We are the only AI-native biotech, pioneering small and large molecule therapeutics discovery by integrating massive multimodal data, frontier AI models, and high-throughput lab automation into an infrastructure for AI-enabled drug discovery. We hire top 1% talent to join our interdisciplinary team of scientists, engineers, researchers, operators, innovators, drug developers, business professionals, and technologists. Join us to build the world's first AI infrastructure for tech-enabled drug discovery and to deliver a pipeline of diverse drug modalities for all major disease areas. As an AI Research Scientist I at 1910 you will be expected to roll up your sleeves as an Individual Contributor (IC) by keeping up with relevant scientific literature, prototyping promising methods, and contributing to our active drug design campaigns by applying 1910's productionized AI/ML models. Role Description • Propose and prototype AI and Machine Learning solutions that address use cases in 1910's design pipeline, • Apply productized AI and Machine Learning models to advance 1910's active drug design campaigns with the support of senior members of the AI Research Team, • Write and publish peer reviewed scientific articles with the support of senior members of the AI Research Team, • Periodically presenting recent AI research at internal journal clubs, • Learn how a molecule processes through the drug discovery process, • Work cross-functionally with scientific colleagues, being a subject matter expert in how AI and Machine Learning can be used to answer cheminformatics and bioinformatics questions, • Keep up-to-date on cutting-edge research in the AI for drug discovery space Qualifications • PhD in a relevant discipline (Computer Science, Biology, Chemistry, etc.), • A strong understanding of statistics and classical machine learning methods (SVM, RF, etc.), • Experience training and deploying cutting edge deep learning methods (Transformers, Graph Neural Networks, etc.), • Demonstrated experience writing clean, maintainable, production-quality Python code, with examples available in code repositories., • Familiarity with MLOps and DevOps best practices, • Exposure to distributed computing (Microsoft Azure, HPC Cluster, etc.), • Ability to work effectively in a fast-paced startup environment with evolving projects and shifting priorities driven by business needs, • Excellent written and verbal communication skills, including the ability to create clear documentation for roadmaps, proposals, and related materials Nice to Haves • An understanding of how a molecule progresses through the drug discovery process, • Relevant industry experience via internship and co-op (AI, Drug Discovery, etc.) #LI-Onsite Diversity and Inclusion (1910's Promise) At 1910, we believe that a diverse, equitable, and inclusive workplace furthers relevance, resilience, and longevity. We encourage people from all backgrounds, ages, abilities, and experiences to apply. 1910 is proud to be an equal-opportunity workplace and is an affirmative action employer. We are committed to equal employment opportunity regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity, or Veteran status. If, due to a disability, you need an accommodation during any part of the interview process, please let your recruiter know. While 1910 supports visa sponsorship, sponsorship opportunities may be limited to certain roles and skills. Benefits and Perks • Competitive compensation package, • Above market benefits, • Generous vacation and parental leave, • Super cool team building activities, • Great colleagues

Job Description R&D Partners is seeking to hire an Associate Scientist II in Cambridge, MA. Your main responsibilities as an Associate Scientist II: · Support processing activities for oligonucleotide manufacturing under guidance from senior staff · Execute laboratory-scale and pilot-scale processes to support research and in-house material needs · Perform routine in-process analytical tests (e.g., pH, conductivity, UV, basic chromatography) · Assist in the preparation, execution, and documentation of non-GMP manufacturing runs · Follow established SOPs and batch records in a cGLP laboratory environment What we are looking for in an Associate Scientist IIn: · BS in Chemistry, Chemical Engineering, Biochemistry, or a related scientific discipline. · 0–2 years of laboratory experience (academic, co-op, internship, or industrial experience acceptable). · Basic familiarity with analytical techniques such as pH, conductivity, HPLC, or LC-MS is preferred. · Strong attention to detail and commitment to high-quality laboratory documentation · Willingness to learn regulated laboratory practices and manufacturing workflows Why Choose R&D Partners? As an employee, you have access to a comprehensive benefits package including: • Medical insurance – PPO, HMO &, • Dental & Vision insurance, • 401k plan, • Employee Assistance Program, • Long-term disability, • Weekly payroll, • Expense reimbursement, • Online timecard approval Pay Scale: $77,642 – $97,066Dependent on Experience) R&D Partners is a global functional service provider and strategic staffing resource specializing in scientific, clinical research & engineering. We provide job opportunities within major pharmaceutical, biopharmaceutical, biotechnology, and medical device companies. R&D Partners is an equal-opportunity employer. If you are interested in applying to this exciting opportunity, then please click ‘Apply’ or to speak to one of our specialists visit the ‘Contact Us’ page. R&D Partners is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. R&D Partners is acting as an Employment Agency in relation to this vacancy. By submitting this application, you confirm that you've read and understood our privacy policy, which informs you how we process and safeguard your data - Company DescriptionR&D Partners is a national staffing firm focused in the areas of: Scientific, Clinical Research and Engineering. Our team offers well over 200 years of combined staffing experience providing consulting, direct hire & outsourcing solutions with our west coast offices in San Francisco, Redwood City and San Diego, CA and our east coast offices located in Harrisburg, PA and Tampa, FL. The cornerstone of our success: a knowledgeable and experienced recruiting team. Our life sciences recruiters, clinical research recruiters and engineering recruiters are uniquely specialized. After a detailed assessment of our clients’ needs, we can then identify appropriate candidates utilizing our established network of professionals. R&D Partners takes a proactive approach to recruiting, establishing relationships with experienced passive candidates so when the time is right, we can combine our candidates’ talents with our clients’ opportunities.R&D Partners is a national staffing firm focused in the areas of: Scientific, Clinical Research and Engineering. Our team offers well over 200 years of combined staffing experience providing consulting, direct hire & outsourcing solutions with our west coast offices in San Francisco, Redwood City and San Diego, CA and our east coast offices located in Harrisburg, PA and Tampa, FL.\r\n\r\nThe cornerstone of our success: a knowledgeable and experienced recruiting team.\r\n\r\nOur life sciences recruiters, clinical research recruiters and engineering recruiters are uniquely specialized. After a detailed assessment of our clients’ needs, we can then identify appropriate candidates utilizing our established network of professionals. R&D Partners takes a proactive approach to recruiting, establishing relationships with experienced passive candidates so when the time is right, we can combine our candidates’ talents with our clients’ opportunities.

Job Description About Us Catalyst Labs is a specialized talent partner with a focus on recruiting top-tier engineers across Software, Data, and AI-driven domains. We are deeply embedded in our clients’ technical hiring operations. We collaborate directly with Founders, CTOs, and Heads of AI at Tier 1 VC backed startups, scale ups and enterprise tech like Palatir, who are driving the next wave of applied intelligence from model optimization to productized AI workflows. We take pride in facilitating conversations that align with your technical expertise, creative problem-solving mindset, and long-term growth trajectory in the evolving world of intelligent systems Our Client: A fast-growing technology company that embeds top engineering talent directly into customer environments to solve high-impact operational and data challenges. They help enterprises rapidly build and scale mission-critical applications that drive measurable business outcomes. The company bootstrapped to generate $25M in revenue and raised $6.7M in total funding, supporting its continued growth and expansion. Location: Hudson Yards, NY Work type: Full time, Hybrid (travel required 10 to 30% of the time) Overview This role is centered around partnering directly with customers to solve their most valuable and complex problems. As a Forward Deployed Software Engineer, you will work hand-in-hand with stakeholders to design, build, and maintain high-impact applications that drive real business change. Your day-to-day work involves understanding mission-critical objectives, transforming enterprise data into operational workflows, and delivering tools that executives and frontline teams rely on to make informed decisions. You’ll move fast rapidly iterating, building systems from scratch, and enabling organizations to modernize their operations at exceptional speed. Beyond writing code, you will play a key role in reshaping how entire teams operate by delivering powerful, data-driven solutions that directly influence business outcomes. Key Responsibilities * Work closely with customer stakeholders to understand their most critical business objectives and translate them into high-impact technical solutions. * Architect, develop, and maintain applications that operationalize enterprise data and drive measurable business outcomes. * Build end-to-end workflows using large structured and unstructured datasets in production environments. * Iterate rapidly, often building systems from scratch, to help customers transform their operations at exceptional speed. * Collaborate directly with executives, operators, and cross-functional teams to deploy tools that meaningfully improve business processes. * Own projects autonomously taking full responsibility for delivery, implementation, and long-term success. * Embed with customer teams as needed, providing both technical expertise and on-the-ground support. * Travel to client sites as required (typically 10 to 33%) to support implementations and ensure successful adoption. * Work hybrid/on-site at company offices (London, New York, Washington D.C., or Denver) and at customer locations during key phases of deployment. Qualifications Required * Bachelor’s or Master’s degree in Computer Science or a related field. * 1 to 5 years of experience as a fullstack engineer, data engineer, or FDE * Strong analytical and problem-solving skills, with the ability to break down complex challenges and deliver practical, production-ready solutions. * Proficiency in Python and/or TypeScript. * Demonstrated experience building applications that leverage large datasets in real-world production environments. * Proven track record of delivering measurable outcomes through codewhether as a software engineer, data scientist, or technical analytics lead. * Ability to work independently and own outcomes end-to-end while also collaborating effectively with technical and non-technical stakeholders. * Excellent communication and interpersonal skills to work closely with customers and internal teams. * Willingness to travel for customer implementations (10 to 33% depending on project). * Enthusiasm for working hybrid-in-person at one of the company’s office locations and onsite with customers. Preferred * Experience working with Palantir Foundry and/or AIP. * Experience delivering production ML or LLM-based solutions. * Experience building production React frontend applications. * Familiarity with Spark, distributed computing, or large-scale data processing frameworks. Note: We adhere to strict data protection policies to ensure that your information is secure and only shared with potential employers with your explicit consent to ensure your confidentiality throughout the hiring process

Job Description Xometry (NASDAQ: XMTR) powers the industries of today and tomorrow by connecting the people with big ideas to the manufacturers who can bring them to life. Xometry's digital marketplace gives manufacturers the critical resources they need to grow their business while also making it easy for buyers at Fortune 1000 companies to tap into global manufacturing capacity. Xometry is an on-demand manufacturing marketplace that leverages machine learning (ML) techniques to predict the manufacturing cost of machined parts and produce automated buy it now prices on Xometry.com. Customers love our instant quoting engine, and that engine depends on Xometry's ML team and technology. We need a strong data scientist leader to manage our ML & data science research & development and evolve the services that make up the backbone of Xometry's business. The successful candidate will bring experience as a data scientist and machine learning leader working for a company where "AI" is considered core to the company's success. They should have experience bringing new ML models to the market as part of an online platform. They should be comfortable leading a technical team, working with product and executive stakeholders with excellent communication and stakeholder management skills - particularly when bridging technical and non-technical audiences. We have a lot of ideas on how we can improve these systems. We need help connecting these ideas to business metrics, prioritizing them with input from stakeholders into a roadmap, executing efficiently from research to bringing ML models to market, and providing proactive communication on the vision/direction and status of the work. Responsibilities: • Serve as a strategic leader as part of our data science & machine learning team, with responsibility for Xometry's pricing strategy, • Build collaborative relationships with key stakeholders; set priorities aligned to business goals; communicate analysis, strategies, timelines, and work of the data science & machine learning team, and gain buy-in from executive leadership, • Incorporate internal and external feedback to iterate and evolve ML models, • Practice outcome-oriented/KPI-driven team management: Define metrics that lead to business goals and report on the outcomes of your efforts, • Lead complex, cross-team projects to deliver on our product & ML strategy, with a singular focus on driving business results, • Play a crucial role in exploring new machine learning opportunities, researching and performing proof of concepts, and bringing new machine learning and AI solutions into Xometry's platform, • Develop and implement machine learning models that improve Xometry's ability to predict cost, price, and sourcing options for our customers and suppliers., • Responsible for leading the evaluation of emerging technologies, identifying areas for improvement, and developing new features while ensuring the reliability and scalability of Xometry's platform, • Lead the exploration of emerging AI and machine learning technologies and develop proof-of-concepts to assess their potential impact on Xometry's platform, • Collaborate with cross-functional teams to gather requirements, prioritize features, and define technical solutions based on the latest innovations, • Monitor machine learning models and AI performance and troubleshoot issues as they arise, • 8+ years experience developing and implementing machine learning algorithms, ideally within an online marketplace, • Excellent understanding of scalable architectures and thrive working in Agile environments, • Recognized expertise in the areas of marketplace optimization and pricing theory, • Ability to apply and implement research concepts, ultimately in production quality code, • Experience defining clear, testable research hypotheses, including intended impact on the business, • Deep knowledge of design of experiments, online experimentation approaches at scale, • Ability to formulate and advocate for R&D objectives and results to multi-functional team members including executive business leadership and product management, • Experience with your machine learning models running in a real production environment, • Experience in end-to-end model development and deployment lifecycle i.e., from prototyping to model development and putting models into production, • Strong experience with Python/R, forecasting methodologies, machine learning and statistics,, • Experience with SQL and cloud technologies like Snowflake, Google BigQuery, Databricks, presto etc.,, • Strong fluency in Python and SQL, experience with Tensorflow, PyTorch, Airflow and data warehouse, • PhD in a quantitative field (or BS/MS with equivalent work experience), • Mission-driven, positive attitude, and ability to motivate others #LI-Hybrid Xometry is an equal opportunity employer. All applicants will be considered for employment without attention to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran, or disability status. For US based roles: Xometry participates in E-Verify and after a job offer is accepted, will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S.

Job DescriptionWho We AreButcherBox is a certified B Corp headquartered in Boston, and honored to be celebrating our second year in a row on Inc.'s list of Best Workplaces. At ButcherBox, we believe in better. That’s why we deliver 100% grass-fed, grass-finished beef, free-range organic chicken, pork raised crate-free, and wild-caught seafood directly to our members’ doors. All of our products are humanely raised or wild-caught and never given antibiotics or added hormones ever. We’re working to build a world that’s better for all, and we’re inviting everyone to come along. For us, better means treating our planet with respect. It means improving the lives of animals and the livelihoods of farmers. It means never cutting corners when it comes to doing business. Ultimately, it means better meals, enjoyed together. Our team is made up of people who collaborate and support one another. We’re always looking for outstanding people to join our mission! About The Role We are seeking a Senior Data Scientist to uncover critical member insights from our marketing, operational, and financial data, driving smarter decisions and delivering exceptional offers, products, and services. The primary focus will be statistical analysis, high-quality predictive modeling, and end-to-end development of AI and ML systems integrated with our eCommerce platform, customer portal, and internal applications. The ideal candidate will work from our Watertown, MA two day a week. Responsibilities •Partner cross-functionally with Marketing, Operations, Product, and Engineering teams to translate business needs into data-driven solutions •Perform advanced analysis and modeling using Python and Spark SQL •Own projects from ideation and stakeholder engagement through production deployment and impact measurement •Provide analytical thought leadership, propose new data experiments, and identify opportunities for measurable impact •Champion data quality, reproducibility, and scalable code using best practices in version control (GitHub) and cloud infrastructure (Azure) •Mentor junior Data Scientists, Data Engineers, and Analytics Engineers to develop their technical and business acumen •Present complex findings and actionable recommendations to diverse audiences, including senior leadership Requirements •7+ years of proven experience solving complex business problems with analytics, statistical analysis, and coding (Python, R, SQL) •Advanced knowledge of statistical modeling: linear/multivariate models, hypothesis testing, time series analysis •Familiarity with causal inference methods: instrumental variables, diff-in-diff, fixed effects regression, synthetic controls, double ML •Track record of delivering robust, production-grade data solutions in a cloud environment •Strong communication skills—able to translate results and recommendations for non-technical stakeholders •Hands-on experience with large datasets, cloud platforms (Azure), and version control (GitHub) •Demonstrated commitment to code quality and reproducible research Preferred Qualifications •Evidence of using analytics to influence business strategy and drive measurable outcomes •Experience solving marketing, subscriber growth, or operational problems in e-commerce or similar domains •Experience in personalization modeling and reinforcement learning •Success mentoring and developing data science talent •Interest in sustainability, food systems, or mission-driven work aligning with ButcherBox values •Ability to commute to Watertown, MA at least once a weekWhat We OfferOur Values We are a mission-driven company and strive to embody our values in every step of the process. ButcherBox is driven by relentless improvement, accountability, humility, and customer obsession. We want our workplace to be one of growth and learning where everyone can be safe/comfortable to show up as their authentic self to work. Anyone who loves our products and goals is welcome here! We are proud to be an equal opportunity employer aspiring to incite positive change in the pastures, the fulfillment centers, the office, and the world. Benefits•Health: medical, dental, vision, and life insurance, an employer-funded HSA, and short & long-term disability benefits•Financial: 401(k) with generous employer match•Annual bonus based on company performance•Time off: unlimited paid time off policy, 20 weeks parental leave, an executive team that encourages a good work/life balance•Personal growth: Annual Learning & Development stipend, and access to a range of personal and professional coaching solutions through BetterUp•Food: a free Custom Classic ButcherBox each month and weekly lunch reimbursement•Others: reimbursement for wellness activities, an exceptional EAP, fertility benefits, life insurance and more ButcherBox is an equal opportunity employer committed to fostering a diverse, inclusive environment at all steps in the hiring process. Every qualified applicant will receive consideration without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws. We are happy provide reasonable accommodations during our hiring process. Please click here if you need to request an accommodation for your interview. ButcherBox does not use artificial intelligence (AI) tools in any part of our hiring process. If you would like more information about how your data is processed, please contact us.

Job DescriptionFocusKPI is seeking smart, curious, technically savvy, and experienced candidates to join our cutting-edge internal data science team. The data science team at FocusKPI builds models and machine learning algorithms that power all our clients' ad-tech/mar-tech products at scale, develops methodologies and tools to precisely and effectively measure market and campaign effects, and researches in-house and public data sources for insights into consumer spending behavior. In this role, you'll spearhead the company's advanced predictive modeling and analytics to elevate its analytical capabilities. In addition, you'll be expected to play an essential role in executing the R&D agenda and delivering products on time and to high quality for different businesses. Work Location: Remote - anywhere in the US Duration: Full-time position Pay Range: $90k+/annum Responsibilities: • Support clients' modeling needs, including maintenance, enhancement of existing measurement and targeting solutions, and timely, high-quality delivery., • Developing innovative and automated solutions for custom needs, leveraging appropriate AI/ML/statistical tools., • Mine large consumer datasets in the cloud environment to support ad hoc business and statistical analysis., • Provide analytical/statistical support for marketing test design, campaign measurement, and market insights to clients and stakeholders., • Communicate methodologies and results to management, clients, and other non-technical stakeholders.Qualifications:, • An advanced degree in Computer Science/Statistics/Mathematics/ Economics, or related fields, requires advanced training in data modeling and analytics., • Ph.D. degree in statistics/mathematics, engineering, computer science, economics, or a related field, • Deep understanding and solid knowledge of the fundamentals of statistical reasoning and ML models., • Experience with causal inference, marketing mix models (MMM), and multi-touch attribution models is highly valued and mandatory to have, • An added advantage is familiarity with deep learning, natural language processing (NLP), computer vision, and generative AI., • Skilled in conceptualizing complex business problems and designing practical, effective modeling and analytical solutions to address them., • Proficiency in common programming languages such as Python and SQL., • Experienced and comfortable working with standard big data tools, including cloud platforms, database technologies, and parallel processing frameworks., • Entrepreneurial, highly self-motivated, collaborative, keen attention to detail, willing and capable to learn quickly, and effectively prioritize and execute tasks in a demanding environment. FocusKPI Hiring Team Founded in 2010, FocusKPI, Inc. (FocusKPI) is a data science and technology firm specializing in predictive analytics practice and methodologies. FocusKPI is a US company headquartered in Silicon Valley, California, with an East Coast office in Boston, Massachusetts. NOTICE: Please be aware of fraudulent emails regarding job postings, job offers and fake checks. FocusKPI's recruiting team will strictly reach out via @focuskpi.com email domain. If you have received fraudulent emails now or in the past, please report it to . The domain @focuskpijobs.com is fraudulent and not related to FocusKPI. Please do not not reply or communicate to anyone with @focuskpijobs.com. Powered by JazzHR CAPzX1fQDM

Job DescriptionSalary: $152,000 - $183,000 TheSenior Scientist, Research position is a key member of the Genomics Platform team and will be involved in bioinformatics analyses of genomics and multi-omics datasets to support our drug discovery and therapeutic development at Visterra. Reporting to the Executive Director of Research, this person will play a lead role in developing and applying advanced computational approaches to analyze and interpret genetics, genomics and multi-omics datasets to support our drug development decisions. We are seeking an experienced bioinformatician to develop and adapt data-driven approaches to analyze single cell multi-omics, spatial transcriptomics, genetics and other high-content datasets to aid target identification, disease characterization and mechanism-of-action studies to derive biological insights supporting drug candidate discovery and development. Responsibilities • Develop and implement advanced machine learning and computational strategies, including deep learning, graph-based methods, and probabilistic modeling, to extract insights genomics datasets, including single-cell, spatial and genetic modalities., • Collaborate with internal and external scientists and clinicians to drive insights from multi-omic data, supporting novel therapeutic development., • Develop new bioinformatics strategies efforts to address key target identification questions on underlying biological mechanisms of disease., • Leverage and extend best practices from genomics, statistics, and data science to process and analyze internal and public multi-omics data and derive biological insights that will impact program strategy., • Manage existing high-dimensional data resources and ingest new public and internal datasets for use by team members., • Clearly communicate complex data findings to colleagues and senior management., • Engage in research discussions, proactively suggesting innovative solutions to impact discovery and clinical programs., • Stay current with advancements in computational biology by reviewing literature, evaluating new technologies, and implementing relevant methodologies., • Present research findings at conferences and publish in scientific journals., • Participate in research team meetings, and proactively suggest new ways to impact programs from discovery through the clinic., • Maintain expertise in the field by staying current with relevant literature, proactively evaluate new technologies, and implement in-house where appropriate. Requirements • PhD. in Computational Biology, Bioinformatics, Computer Science, or a related field with 4+ years of experience, or a M.S. with 10 years of relevant experience., • Expertise in single-cell genomics (scRNA-seq), spatial transcriptomics, genetics or other large-scale multi-dimensional genomics analyses., • Deep experience implementing workflows to process high-throughput -omics data and performing downstream analyses that generate biological insights., • Proven track record of evaluating and using public biology databases, with an understanding of how to utilize large datasets to drive discovery and development, • Deep understanding in computational single cell toolsets such as Seurat, Scanpy, and other relevant methods., • Strong programming skills in Python and/or R for bioinformatics applications., • Familiarity with cloud computing services, such as AWS, is, • Excellent collaboration and interpersonal skills for multi-disciplinary teamwork., • Strong problem-solving abilities, analytical thinking, and intellectual curiosity., • Exceptional written and verbal communication skills, with the ability to present complex ideas clearly to diverse audiences., • Passion for developing computational technologies for biological research and translating findings into therapeutic applications in precision medicine and translational research. Management responsibilities: This position may include supervisory responsibilities. Travel: Possible travel to local and national conferences Company Visterra is a clinical stage biotechnology company committed to developing innovative antibody-based therapies for the treatment of patients with kidney, immune-mediated and other hard-to-treat diseases. Our proprietary technology platform enables the design and engineering of precision antibody-based product candidates that specifically bind to, and modulate, key disease targets. Applying this technology to disease targets that are not adequately addressed by traditional therapeutic approaches, we are developing a robust pipeline of novel therapies for patients with unmet needs. Visterras pipeline has multiple clinical-stage assets and one approved therapeutic, sibeprenlimab. As a member of the Otsuka family of companies, we are uniquely positioned as a small, dynamic, nimble and innovative organization where individuals and teams are empowered to make big impacts while benefiting from the support, strength, stability and long-term perspective of a 100-year-old global company. Visterra has approximately 105 employees and is located in Waltham, Massachusetts.

Job Description About General Fluidics General Fluidics is a clinical diagnostics startup developing the AxessTM platform, a breakthrough point-of-care system that delivers laboratory-grade performance across clinical chemistry, hematology, and immunoassays from a single blood sample. By integrating three “gold standard” analytical technologies into one compact instrument, we are transforming how clinicians access and act on diagnostic data. Learn more at generalfluidics.com. The Role We are seeking a highly motivated Senior Research Associate to join our R&D team and help expand our menu of diagnostic assays for veterinary and human health applications. This is an R&D-focused laboratory role—ideal for a scientist who thrives on experimental design, assay development, and hands-on instrumentation work. You will design, troubleshoot, and interpret experiments where answers are unknown, not simply execute QC protocols. Onsite presence 5 days per week at our Watertown, MA offices is a requirement for this role. Reporting to the VP of Assay Development, you will work closely with engineers and scientists to optimize assay and instrument performance, generate data for analytical validation, and accelerate our path to regulatory clearance and product launch. This role is best suited for a junior scientist with prior industry experience and self-starter who can work independently under mentorship, with the drive to solve problems in a fast-paced, startup environment. Key Responsibilities • Design, develop, and validate clinical chemistry, hematology, and immunoassays on the AxessTM point-of-care instrument., • Independently plan and execute experiments to optimize assay and instrument performance, collaborating closely with engineers on system integration., • Perform data analysis and statistical evaluation to guide assay development and regulatory submissions., • Author experimental protocols, R&D reports, and supporting documentation., • Support quality assurance through calibration, control protocols, and proficiency testing., • Work safely with human and animal blood specimens in compliance with biosafety regulations. Qualifications • Bachelor’s, Master’s, or PhD in biotechnology, biomedical engineering, chemistry, physics, or related field., • 3-6 years of prior industry R&D experience (not academic lab or QC/manufacturing), • Experience designing and interpreting experiments, analyzing data, and troubleshooting unexpected results., • Hands-on laboratory skills: pipetting, assay development, reagent preparation, use of biosafety cabinets., • Familiarity with clinical instrumentation (e.g., flow cytometry, hematology analyzers, clinical chemistry, immunoassays) strongly preferred., • Exposure to diagnostic assay development, validation, or instrumentation is a plus., • Comfortable in a dynamic startup environment: onsite presence, ownership mentality, willingness to push projects forward outside a strict 9–5., • Excellent communication skills, with the ability to clearly present scientific concepts and data. Who You Are • Curious, creative, and excited to tackle open-ended scientific questions., • Thrives on independence but values mentorship and collaboration.

Job DescriptionCompany Summary:Atavistik Bio is a privately-held clinical stage biotechnology company accelerating the discovery and development of transformative precision allosteric therapeutics to address serious unmet patient needs. Our proprietary AMPS™ platform allows us to rapidly unlock functional cryptic pockets across a broad range of target classes to accelerate the development of groundbreaking medicines. We have rapidly established an emerging pipeline of allosteric therapeutics with the potential to achieve superior efficacy and tolerability profiles by leveraging the power of allostery. Atavistik Bio is led by an experienced team of drug hunters with a proven track record of developing marketed small molecule therapies and supported by top-tier investors, including The Column Group, Nextech Invest, Lux Capital, and Regeneron Ventures. Positions Summary: We are seeking a strategic and dynamic Principal Scientist with deep expertise in hematologic malignancies in cell and in vivo models, to join our R&D group and work with an enthusiastic team of highly skilled scientists in a fast-paced environment. Reporting to the VP, Head of Biology, this individual will be responsible for leading the biology and translational research strategy for small molecule drug candidates. The ideal candidate will have extensive experience in studying the biology behind hematologic malignancies, drug development, biomarker identification, and the ability to work cross-functionally in a dynamic environment.Key Responsibilities: • Work closely with broader drug discovery scientific team to progress compounds from screening to preclinical animal models., • Work with CRO and academic partners on a wide-range of drug discovery efforts including cell-based screening and primary patient cell-based assays., • Partner with CROs and academic partners to design and execute in vivo PK/PD and efficacy models., • Develops and executes the translational science strategy in collaboration with the Clinical Development organization., • Designs and implements translational research plans to identify and validate biomarkers for patient selection strategy, treatment response, and disease progression., • Clearly communicates the biology, translational research strategy, data, and other information to employees, company leadership, and external stakeholders including key opinion leaders, board members, and investors., • Supports the preparation of regulatory documents, including IND submissions, clinical study protocols, and reports., • Drafts and submits data for scientific publications and presents our research and development programs at scientific conference and to regulatory agencies.Required Qualifications:, • PhD. in Biology with 5+ years of experience in industry, with a strong focus on drug discovery in hematologic malignancies., • Strong interpersonal skills and ability to build strong collaborative relationships in a cross-functional environment is a must., • Deep knowledge of preclinical in vivo models of hematologic malignancies, in particular myeloproliferative neoplasms., • Ability to think strategically with consideration of translational proof of concept, competitive landscape, and optimal patient populations.

Job Description Xometry (NASDAQ: XMTR) powers the industries of today and tomorrow by connecting the people with big ideas to the manufacturers who can bring them to life. Xometry's digital marketplace gives manufacturers the critical resources they need to grow their business while also making it easy for buyers at Fortune 1000 companies to tap into global manufacturing capacity. Xometry is seeking a Senior Data Scientist to our sourcing team. The ideal candidate will have a passion for using machine learning tools and techniques to construct, optimize, and evaluate predictive models that predict the likelihood of different business outcomes. Additionally, this person will use their knowledge of probability and statistics to make defensible statistical inferences from data. Responsibilities: • Use data science and machine learning principles to develop effective predictive models, • Write software to prepare, clean, and sample data for use in developing predictive models, • Use cloud resources (e.g., Amazon Web Services) to prepare and process data, • Query and extract data from databases (Snowflake), • Use data analysis and visualization tools (examples include SQL, Python, Jupyter Notebooks, and Looker) to inform the business strategy, • Relentlessly iterate solutions within a fast-paced environment where ambiguity is the norm, • Solve challenging, uncharted problems, • Bachelor's degree required; degree in applied math, computer science, natural sciences or engineering preferred, • M.S. or Ph.D. in a related field highly desired, • 5+ years of experience with machine learning, statistical modeling, and optimization techniques, • Fluent in Python (pandas, numpy, SciPy, and scikit-learn preferred), • Proficient in linear algebra and statistics, • Familiar with scientific software principals, e.g. versioning systems, reproducibility, • Experience in the manufacturing industry is desired #LI-Hybrid Xometry is an equal opportunity employer. All applicants will be considered for employment without attention to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran, or disability status. For US based roles: Xometry participates in E-Verify and after a job offer is accepted, will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S.

Job Description At Klaviyo, we value the unique backgrounds, experiences and perspectives each Klaviyo (we call ourselves Klaviyos) brings to our workplace each and every day. We believe everyone deserves a fair shot at success and appreciate the experiences each person brings beyond the traditional job requirements. If you're a close but not exact match with the description, we hope you'll still consider applying. Want to learn more about life at Klaviyo? Visit careers.klaviyo.com to see how we empower creators to own their own destiny. We're looking for someone who thrives at the intersection of data and product — someone who brings solid analytical skills, experience with experimentation, and curiosity to uncover insights that shape product strategy. You should be comfortable working with SQL and R or Python, designing and analyzing A/B tests, and translating data into actionable recommendations for product teams. Please note this is a hybrid role that requires 3 days/week in our Boston office. Fully remote candidates will not be considered at this time. What You'll Do • Partner with product and engineering teams to evaluate product opportunities through A/B testing, data analysis, and customer insights, • Contribute to the design, implementation, and analysis of experiments — ensuring correct setup, sufficient power, and clear interpretation of results, • Conduct exploratory analyses to uncover patterns in customer behavior and product usage that inform product strategy, • Define and track product and customer metrics to measure success, and help build dashboards and reporting that make insights accessible to product managers and stakeholders, • Collaborate with data engineering to ensure data pipelines and DBT models are accurate, reliable, and well-structured for downstream use, • Communicate insights in a clear, compelling way to cross-functional partners, making data actionable for product decisionsWho You Are, • You have 3-4 years of experience in product analytics, data science, or applied statistics, preferably in a SaaS or product-focused environment, • You hold a degree in a quantitative field such as Statistics, Mathematics, Computer Science, Economics, or Engineering, • You are proficient in SQL and have experience using either Python or R for data analysis, • You have hands-on experience with A/B testing and statistical analysis, and are motivated to grow into more advanced methods over time, • You bring strong business intuition and curiosity, and can translate questions into structured analytical approaches, • You're a clear communicator who can frame findings for both technical and non-technical audiences, • You enjoy working cross-functionally and are energized by using data to improve customer outcomesWhy You'll Love This Role, • Gain hands-on experience influencing product direction through experimentation and analytics, • Build your expertise in product data science with mentorship and collaboration from senior data scientists, • Join a company where data science is a core part of the product development lifecycle Our salary range reflects the cost of labor across various U.S. geographic markets. The range displayed below reflects the minimum and maximum target salaries for the position across all our US locations. The base salary offered for this position is determined by several factors, including the applicant's job-related skills, relevant experience, education or training, and work location. In addition to base salary, our total compensation package may include participation in the company's annual cash bonus plan, variable compensation (OTE) for sales and customer success roles, equity, sign-on payments, and a comprehensive range of health, welfare, and wellbeing benefits based on eligibility. Your recruiter can provide more details about the specific salary/OTE range for your preferred location during the hiring process. Base Pay Range For US Locations:$88,000—$132,000 USD Get to Know Klaviyo We're Klaviyo (pronounced clay-vee-oh). We empower creators to own their destiny by making first-party data accessible and actionable like never before. We see limitless potential for the technology we're developing to nurture personalized experiences in ecommerce and beyond. To reach our goals, we need our own crew of remarkable creators—ambitious and collaborative teammates who stay focused on our north star: delighting our customers. If you're ready to do the best work of your career, where you'll be welcomed as your whole self from day one and supported with generous benefits, we hope you'll join us. AI fluency at Klaviyo includes responsible use of AI (including privacy, security, bias awareness, and human-in-the-loop). We provide accommodations as needed. By participating in Klaviyo's interview process, you acknowledge that you have read, understood, and will adhere to our Guidelines for using AI in the Klaviyo interview Process. For more information about how we process your personal data, see our Job Applicant Privacy Notice. Klaviyo is committed to a policy of equal opportunity and non-discrimination. We do not discriminate on the basis of race, ethnicity, citizenship, national origin, color, religion or religious creed, age, sex (including pregnancy), gender identity, sexual orientation, physical or mental disability, veteran or active military status, marital status, criminal record, genetics, retaliation, sexual harassment or any other characteristic protected by applicable law. IMPORTANT NOTICE: Our company takes the security and privacy of job applicants very seriously. We will never ask for payment, bank details, or personal financial information as part of the application process. All our legitimate job postings can be found on our official career site. Please be cautious of job offers that come from non-company email addresses (@klaviyo.com), instant messaging platforms, or unsolicited calls.By clicking "Submit Application" you consent to Klaviyo processing your Personal Data in accordance with our Job Applicant Privacy Notice. If you do not wish for Klaviyo to process your Personal Data, please do not submit an application. You can find our Job Applicant Privacy Notice here and here (FR).

Job Description Grow with Welch's! Welch's is on a journey towards our bold ambition of being the global-leader of convenient, good for you fruit-based food and beverages. To turn this goal into a reality we need you and other exceptionally talented, agile, and innovative individuals who are eager to contribute to something extraordinary! At Welch's, we're not just offering a job; we're inviting you to be a part of a vibrant, authentic, and inclusive culture where you not only belong, but also have the opportunity to unleash the best, most authentic version of you. Grow with Welch's! Welch's is on a journey towards our bold ambition of being the global-leader of convenient, good for you fruit-based food and beverages. To turn this goal into a reality we need you and other exceptionally talented, agile, and innovative individuals who are eager to contribute to something extraordinary! At Welch's, we're not just offering a job; we're inviting you to be a part of a vibrant, authentic, and inclusive culture where you not only belong, but also have the opportunity to unleash the best, most authentic version of you. Position Summary: Welch's is modernizing its R&D digital ecosystem through the implementation of a new ERP and an upgraded Product Lifecycle Management (PLM) system. As a Senior Scientist Product Systems on the R&D team, you will play a pivotal role in designing, building, and validating PLM functionality, ensuring that product data, formulation workflows, and specification structures are accurate, scalable, and aligned with business needs. During the implementation phase, you will serve as a technical lead representing R&D in enterprise design discussions, system configuration, and cross-functional testing. Once the new PLM system is successfully deployed and stable, your role will expand to include creation and stewardship of product, ingredient, formula, and analytical specifications within the PLM system. This role is ideal for a highly technical, detail-oriented scientist who excels in digital tools, structured data, formulation workflows, and cross-functional problem-solving. Where You'll Work: This role will be based out of our Waltham, MA headquarters where you will be immersed in a dynamic workplace where innovation thrives and collaboration is key. Our company in-office schedule is designed to maximize collaboration & relationship building balanced with flexibility and well-being with 3 days in office and Thursdays/Friday being remote, flex days. What You'll Do: • Serve as a core R&D technical lead in the implementation of Welch's new PLM and ERP systems., • Translate R&D formulation workflows, product data needs, and technical requirements into system logic and configuration., • Lead R&D's execution of system testing, including writing test scripts, validating data structures, and troubleshooting issues., • Partner with IT, Supply Chain, Quality, and external vendors to design and refine digital workflows that reflect R&D processes accurately and efficiently., • Support customization and build activities to ensure PLM functionality meets R&D's operational needs., • Identify and drive improvements in data governance, workflow efficiency, and system usability across the R&D organization., • Develop training materials, processes, and user guidance to support system adoption within R&D., • After ERP/PLM stabilization, become a primary author and steward of product, formula, ingredient, and analytical method specifications in the new PLM system., • Create and maintain high-quality, audit-ready specifications with strong attention to metadata, version control, and technical accuracy., • Collaborate with Product Development, Quality, Supply Chain, and Operations to gather accurate inputs and finalize specifications., • A technically strong scientist with experience in formulation, analytical methods, product development, or structured product data., • A systems thinker who enjoys understanding how digital workflows, product data, and technical processes fit together., • Exceptionally organized and detail-oriented, with a natural ability to create accurate technical documentation and manage structured data., • Skilled at breaking down complex R&D processes and translating them into clear system requirements and digital workflows., • A collaborative partner who communicates clearly and effectively across IT, Quality, Supply Chain, Operations, and R&D., • Comfortable working in an environment undergoing major digital transformation—able to bring structure, clarity, and problem-solving when processes are evolving., • A proactive troubleshooter who can identify root causes, propose solutions, and improve how systems and data function., • Someone who enjoys supporting others, creating training materials, and helping teams adopt new tools and workflows., • Bachelor's degree in Food Science, Chemistry, Engineering, Information Systems, or related fields., • 5+ years of experience in PLM, ERP, product data systems, digital transformation, or R&D systems roles within food, beverage, consumer goods, or related manufacturing sectors., • Hands-on experience leading system implementations or upgrades., • Strong technical documentation skills and comfort working in structured, data-driven environments., • Ability to work cross-functionally (IT, FSQ, Supply Chain, Operations), influence without authority, and drive alignment across technical teams., • Strong critical thinking and troubleshooting skills, with the ability to diagnose workflow or system issues quickly., • Experience training others, developing user documentation, or supporting digital tools is beneficial., • Organization with a bold, clear purpose & vision for the future, • Inclusive Culture: Be a part of an inclusive workplace where you not only belong but also have the opportunity to be the best version of yourself, • Passionate Community: You are encouraged to have a voice, share your opinions, and have individual impact on the success of the business, • Hybrid work model: Flexible & collaborative work environment to maximize well-being & success, • Paid Time Off and Holidays: Available immediately for you to enjoy time away from the office to rest and recharge, • Paid Volunteer Time Off: Enjoy time away from the office to rest and recharge, • Development & Advancement: Access to LinkedIn Learning as well as both formal and informal opportunities to develop and grow your career, • Compensation Package Consisting of Competitive Base Salary and Annual Incentive Plan (Bonus), • 401K plan with Generous Company Match, • Flexible Benefits from your first day: Choose the benefits that meet your needs and preferences:, • Health, Dental & Vision Insurance, • Health Savings Accounts, • Life and accident insurance, • Employee Assistance Programs, • Tuition reimbursement program, • Additional benefits available through Perks at Work #LI-Hybrid Welch's is an Equal Employment Opportunity Employer. We are committed to the prevention of employment discrimination based on race, religion, color, sex, gender identity, national origin, age, marital status, disability and/or military or veteran status, sexual orientation or any other action covered by federal or applicable state/local laws. Welch's offers more than just a job - it's an opportunity to grow, innovate, and make a global impact with a passionate community.

Job Description At OneStudyTeam (a Reify Health company), we specialize in speeding up clinical trials and increasing the chance of new therapies being approved with the ultimate goal of improving patient outcomes. Our cloud-based platform, StudyTeam, brings research site workflows online and enables sites, sponsors, and other key stakeholders to work together more effectively. StudyTeam is trusted by the largest global biopharmaceutical companies, used in over 6,000 research sites, and is available in over 100 countries. Join us in our mission to advance clinical research and improve patient care. One mission. One team. That's OneStudyTeam. As a Senior Data Scientist, you will play a pivotal role in advancing Reify Health's data-driven solutions for clinical trials. In this position, you will drive the development of statistical models and machine learning algorithms to improve patient enrollment and trial management. You'll work in a highly regulated healthcare data environment, ensuring compliance with privacy standards while innovating on predictive analytics. This role involves close collaboration with cross-functional teams (especially ML Engineering) to translate complex data insights into practical, impactful tools for the clinical research community. What You'll Be Working On • Site Randomization Forecasting: Develop/enhance forecasting models for site randomization and enrollment trends, enabling better planning and resource allocation across trial sites., • Patient Matching/Ranking Algorithms: Support projects to build algorithms that intelligently match patients to (or rank patients for) appropriate clinical trials, enhancing recruitment efficiency and patient inclusion., • Develop Other Advanced Statistical Models: Create and refine predictive models (Bayesian inference, regression analysis, time-series forecasting) to address other key clinical trial challenges and improve decision-making., • AI Monitoring and Bias Detection: Implement processes to monitor machine learning models in production, detecting bias or performance drift and ensuring models remain fair, accurate, and compliant., • Data Pipeline & Tooling Development: Build and optimize data pipelines and analytical workflows using tools like AWS Athena, Redshift, SageMaker, and dbt, enabling scalable model training and deployment., • Regulatory Compliance in Data Science: Ensure all data science practices align with HIPAA, GDPR, and other privacy regulations, integrating compliance considerations into model development and data handling., • Cross-Functional Collaboration: Work closely with machine learning engineers, product managers, and other stakeholders to integrate models into products and clearly communicate insights and recommendations. What You Bring to OneStudyTeam, • Education: Master's or Ph.D. in Statistics, Data Science, Computer Science, or a related quantitative field (or equivalent professional experience)., • Experience: 5+ years of hands-on data science or analytics experience, preferably in a healthcare, clinical research, or other highly regulated data environment., • Statistical & ML Expertise: Strong foundation in statistical modeling and machine learning techniques, including experience with Bayesian methods, regression analysis, and time-series forecasting., • Model Monitoring & Fairness: Proficiency in evaluating model performance and bias, with the ability to implement AI monitoring tools and bias mitigation strategies to ensure ethical and reliable outcomes., • Technical Toolset: Advanced programming skills in Python (with libraries such as scikit-learn, PyMC, mlforecast, etc.) and SQL, as well as familiarity with data transformation tools like dbt., • Cloud & Data Infrastructure: Hands-on experience with cloud-based analytics and ML services, especially AWS tools (Athena for querying, Redshift for data warehousing, SageMaker for model development/deployment)., • Regulated Data Handling: Experience working with sensitive healthcare or clinical trial data under regulations like HIPAA and GDPR, demonstrating a deep commitment to data privacy and security best practices., • Collaborative Communication: Excellent teamwork and meticulous verbal/written communication abilities, with a track record of partnering with engineering and product teams to translate data science work into actionable business solutions. Note: OneStudyTeam is unable to sponsor work visas at this time. If you are a non-U.S. resident applicant, please note that OneStudyTeam works with a Professional Employer Organization. As a condition of employment, you will abide by all organizational security and privacy policies. This organization participates in E-Verify (E-Verify's Right to Work guidance can be found here).

Job Description Flexcompute is architecting the next generation of multi-physics simulation. We are moving beyond legacy solvers to build a platform defined by speed and physical fidelity. We are seeking a Computational Scientist to lead the development of our new structural mechanics solver. We prioritize fundamental understanding over tool proficiency. We are looking for an architect who can derive the governing equations from first principles and implement them into a robust numerical framework. About Flexcompute We are a “Physics Intelligence” company making hardware innovation as easy as software. Our solvers (Flow360, Tidy3D) are not just faster; they are effectively instant, reducing simulation times from days to minutes using massive GPU parallelism and proprietary algorithms. • Intellectual Density: We maintain an exceptionally high talent bar. Our team of ~90 includes over 50 PhDs from MIT, Stanford, and top research labs. You will work alongside peers who will challenge your thinking and elevate your work daily., • Impact: Our technology is currently used to design optical interconnects, 3D chiplets, quantum computing chips, eVTOL aircraft, and next-gen wind turbines. You are building the “math engine” that drives real-world engineering breakthroughs., • Education: Ph.D. in Applied Mechanics, Physics, Applied Mathematics, or a related field., • Deep Physics Intuition: You possess an intuitive grasp of continuum mechanics—elasticity, plasticity, contact mechanics, and wave propagation. You can predict how a structure should behave before the simulation runs., • Advanced Numerical Analysis: You have a theoretical mastery of numerical PDEs. You can mathematically prove the consistency, stability, and convergence of a scheme. You understand the trade-offs between implicit/explicit integration and various spatial discretizations., • Strong General Programming: Proficiency in at least one high-level language (C++, Python, Julia, Rust, or Fortran) with a focus on algorithmic efficiency. You understand data structures, computational complexity (Big O), and how to write maintainable research code., • Interest in learning High-Performance Computing (HPC) and GPU architecture., • Experience with C++ for scientific computing., • Exposure to multi-physics coupling (fluid-structure interaction, thermal-stress). Key Responsibilities • Solver Formulation: Derive and implement governing equations for structural mechanics, ensuring thermodynamic consistency and physical accuracy across linear and non-linear regimes., • Numerical Architecture: Design the core numerical framework. You will determine the optimal discretization strategies (FEM, DG, IGA, etc.) to balance stability, accuracy, and computational cost., • Algorithmic Development: Specific language is secondary to code quality. You will write clean, modular, and efficient algorithms to solve large-scale systems of equations., • Collaborative Autonomy: We operate with high trust. You own your module, but you have immediate access to world-class experts in electromagnetics and fluid dynamics for cross-domain problems., • Continuous Learning: We host regular internal seminars where team members teach each other—from “Advanced Linear Algebra” to “GPU Memory Hierarchies.”, • Compensation: Competitive salary + meaningful equity in a fast-growing startup., • Well-being: Comprehensive Medical, Dental, and Vision insurance; 401(k); and a gym/fitness allowance., • Environment: A flat hierarchy where the “best idea wins,” regardless of job title.

Job DescriptionCompany Description Zai Lab is a patient-focused, innovative, commercial-stage, global biopharmaceutical company based in China and the United States. We are dedicated to discovering, developing, and commercializing best-in-class and first-in-class therapies that address medical conditions with significant unmet needs in oncology, immunology, neuroscience, and infectious disease. Guided by innovation and driven by purpose, our mission is to leverage our expertise and resources to make a lasting, positive impact on human health worldwide. Zai Lab’s global team of 2,100 talented professionals includes industry leaders and professionals dedicated to advancing novel therapies to patients. With headquarters in Cambridge, Massachusetts, and Shanghai, and teams in the U.S., China and Europe, we collaborate across time zones to deliver meaningful impact where it’s needed most. Founded in 2014 by Dr. Samantha Du, Zai Lab was purpose-built to become a leading global biopharma, combining scientific innovation, operational scale, and strong execution. Our global pipeline features ZL-1310, a DLL3 antibody-drug conjugate (ADC) with best-in-class and first-in-class potential in small cell lung cancer, now in clinical trials. At the same time, our R&D team is progressing several other global programs into the clinic, including ZL-1503, a bispecific IL-13/IL-31 antibody for atopic dermatitis, and ZL-6201, an LRRC15 ADC for solid tumors. In China, we’ve earned a reputation as a partner of choice for leading global biopharmaceutical companies, leveraging our proven commercial infrastructure and clinical trial capabilities to accelerate market access to our innovative products. Due to its large population, China is the second largest pharmaceutical market in the world. Our unique business model combines in-licensed assets with strategic partnerships, leveraging our in-house research capabilities to build a regional portfolio of late-stage, potential best-in-class and first-in-class therapies. Today, with eight products on the market in China, we are delivering meaningful impact for patients and building opportunities for talented professionals to shape the future of medicine. Zai Lab is publicly traded with dual-primary listings on both the Nasdaq Stock Market and the Hong Kong Stock Exchange, underscoring our commitment to transparency, global reach, and long-term growth. Job Description The Medical Director will support the clinical development of oncology programs, focusing on the design, execution, and oversight of clinical trials. Responsibilities include independently contributing to and executing on the clinical strategy, serving as Medical Monitor, supporting regulatory submissions, and collaborating and leading cross-functional teams. The role provides scientific and medical input to ensure the successful conduct of clinical trials and advancement of oncology assets. This role reports to the VP, Clinical Development, Oncology and is based in our Cambridge, MA office. • Clinical Trial: Provide medical expertise to support the leading physician/scientist for the design and execution of oncology clinical trials. Collaborate with clinical operations to ensure trials are conducted in alignment with scientific objectives, patient safety standards, and regulatory requirements., • Medical Monitoring: Serve as Medical Monitor for assigned clinical trials, ensuring patient safety, protocol compliance, and medical oversight. Review safety data, participate in data monitoring activities, and act as the primary medical contact for study teams and investigators., • Cross-functional Collaboration: Work with regulatory affairs, clinical operations, pharmacovigilance, biostatistics. medical affairs, and commercial teams to align clinical and business objectives, often across multiple time zones., • External Representation: Represent Zai Lab in interactions with investigators, key opinion leaders, regulatory authorities, and external collaborators., • Data Analysis & Interpretation: Analyze clinical trial data and real-world evidence to identify trends, assess efficacy and safety signals, and support data-driven decision-making. Collaborate with cross-functional teams to translate findings into actionable insights that inform clinical strategy, regulatory submissions, and program advancement., • Regulatory Support: Support the preparation of regulatory documents, participate in health authority interactions, and contribute to risk management planning and mitigation strategies throughout the development lifecycle., • Business Development Support: Support medical leadership team to to support licensing opportunities, partnerships, and due diligence activities., • Scientific Support: Maintain up-to-date knowledge of oncology trends, the competitive landscape, and regulatory changes to inform clinical strategy and contribute to clinical development function.Qualifications REQUIRED • Clinical development experience, with a focus on late-stage trials, preferably as a Medical Monitor, • Experience in cross-functional team environments, • Understanding of oncology drug development, clinical endpoints, and regulatory pathways., • Clinical practice experience or experience as an investigator, • Strong communication skills., • Effective collaboration skills to effectively interact with internal and external stakeholders., • High ethical standards and commitment to scientific rigor. Additional Information The pay range for this position at commencement of employment is expected to be between $257K and $299K/year; however, base pay offered may vary depending on multiple individualized factors, including market location, job-related knowledge, skills, and experience. The total compensation package for this position may also include other elements, including a sign-on bonus, restricted stock units, and discretionary awards in addition to a full range of medical, financial, and/or other benefits (including 401(k) eligibility and various paid time off benefits, such as vacation, sick time, and parental leave), dependent on the position offered. Details of participation in these benefit plans will be provided if an employee receives an offer of employment. If hired, employee will be in an “at-will position” and the Company reserves the right to modify base salary (as well as any other discretionary payment or compensation program) at any time, including for reasons related to individual performance, Company or individual department/team performance, and market factors. At Zai Lab, we are proud of the gender diversity of our company and our promotion of women in biotech. We have achieved gender base pay equity at all levels, 59% of our employees are women and 53% of our management positions are held by women. We are committed to the health of patients and our planet. That’s why our environmental protection, social responsibility, and corporate governance strategy, called “Trust for Life,” is integrated within our business. Disclaimer: This description is not intended to be construed as an exhaustive list of duties, responsibilities, or requirement for the position. All personnel may be required to perform duties outside of their normal responsibilities from time to time, as needed. All qualified applicants will receive consideration for employment without regard to race, sex, color, religion, sexual orientation, gender identity, national origin, protected veteran status, or based on disability. Zai Lab is committed to protecting the privacy and security of the information we collect and to being transparent about the purposes for which we use your information. We have a Privacy Notice which sets forth our policies and practices for handling the information we collect and use in the employment context. Privacy Notice available upon request.

Job Description Company Description The Ikigai platform unlocks the power of generative AI for tabular data. We enable business users to connect disparate data, leverage no-code AI/ML, and build enterprise-wide AI apps in just a few clicks. Ikigai is built on top of its three proprietary foundation blocks developed from years of MIT research - aiMatch, for data reconciliation, aiCast, for prediction, and aiPlan, for scenario planning and optimization. Our platform enables eXpert-in-The-Loop (XiTL) for model reinforcement learning and refinement, at scale. Rooted in academia, Ikigai also offers unmatched educational support that upskills workforces and transforms organizations into AI-driven ones. Ikigai Academy has already trained over 6000 students from 90+ countries on topics like “No Code AI” and “Time Series Forecasting”. Role Description: We are seeking a Data Scientist who thrives at the intersection of data transformation, analytics, and implementation. In this role, the Data Scientist will partner directly with clients to prepare, clean, and transform their data so it can seamlessly integrate with our aiCast platform. This Data Scientist will help customers unlock the value of their data—building pipelines, dashboards, and forecasts—and in many cases, own the end-to-end implementation from ingestion through delivery. This Data Scientist position is centered on data engineering, applied analytics, and client enablement. You’ll play a key role in helping customers get from raw data to actionable insights. Responsibilities: * Collaborate with client teams to understand their data sources, structures, and business requirements. * Design and implement data transformation pipelines to prepare data for aiCast ingestion. * Build reporting and dashboarding solutions to help clients interpret and act on their data. * Develop forecasting and analytics workflows to extend client use cases beyond data prep. * Support end-to-end solution delivery—covering extraction, transformation, validation, and deployment—when applicable. * Troubleshoot data quality issues and provide recommendations for improved structures or processes. * Partner with internal engineering and success teams to ensure smooth implementations and knowledge transfer. Qualifications: * At least 1-3 years of experience in a data role, preferably with enterprise clients * Associate’s or Bachelor’s degree in a relevant field (e.g., Computer Science, Statistics, or Applied Mathematics) preferred * Proficiency in Python, including libraries like NumPy and Pandas for data transformation. * Working knowledge of SQL for querying and joining datasets (intermediate level). * Experience building ETL/ELT pipelines or similar data processing workflows. * Familiarity with data visualization, reporting, or dashboarding tools. * Strong problem-solving skills with a focus on client outcomes and practical implementation. * Ability to work with incomplete or messy data and structure it for usability in production systems. * Excellent communication skills for translating technical work into business impact. Preferred Skills: * Knowledge of data transformation (e.g. using python Pandas library) database management, data integration, or data visualization is a plus * Experience with forecasting techniques or applied time-series analytics. * Background in client-facing or consulting roles where you owned implementation delivery. * Understanding of software engineering best practices (version control, testing, deployment). Ikigai Labs is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person's race, color, sex, gender identity or expression, age, religion, national origin, ancestry or citizenship, ethnicity, disability, military or protected veteran status, genetic information, sexual orientation, marital or familial status, or any other personal characteristic protected under applicable law. Powered by JazzHR sfmsCHcJWY

Job Description We are currently seeking a Lead Scientist / Engineer with a PhD in Systems & Control, Biomedical Engineering, Applied Mathematics, or a related quantitative field, and 5–6+ years of experience in applied modeling and estimation. This role will function as a senior member of the company’s algorithm team. It will involve designing and implementing Etiometry’s next-generation physiologic risk and treatment-prediction algorithms. The position will require close collaboration with Etiometry’s data science, product, and clinical teams to translate physiologic and clinical requirements into real-time decision support tools deployed in the ICU. Responsibilities * Lead the design, implementation, and validation of algorithms that predict patient trajectories and responses to interventions (e.g., fluids, vasoactives, ventilator changes). * Extend Etiometry’s existing ODE-based physiologic models with advanced estimation methods (e.g., Kalman filters, Bayesian inference, particle filters). * Integrate data-driven approaches (e.g., neural networks, probabilistic ML, hybrid mechanistic/ML frameworks) with classical physiology-based models. * Translate physiologic and clinical requirements into quantitative risk indices for FDA-regulated software. * Work with real-world ICU data, including physiologic waveforms, vital signs, and laboratory values. * Mentor junior scientists and collaborate with engineers, clinical experts, and regulatory affairs to bring models from research → cleared product. Basic Qualifications * PhD in Systems & Control, Biomedical Engineering, Applied Mathematics, Electrical/Mechanical Engineering, or a related field. * 5–6+ years of experience (industry or postdoctoral) in applied modeling, estimation, or control systems. * Strong background in dynamical systems & ODE/PDE modeling. * Strong background in state estimation techniques (Kalman filters, stochastic processes, Bayesian methods). * Working knowledge of machine learning (neural networks, probabilistic ML, data-driven system identification). * Proficiency in scientific computing in Python (NumPy, SciPy, PyTorch, TensorFlow). * Strong communication and organization skills. * Proven ability to work in cross-disciplinary teams and translate theory into applied solutions. Desired Qualifications * Experience working with clinical monitoring data (ICU waveforms, vital signs, laboratory data, EHR integration). * Familiarity with computational physiology or biomedical modeling. * Knowledge of medical device software lifecycle (IEC 62304, FDA 510(k)). * Experience mentoring junior scientists or leading research projects. About Etiometry Etiometry is the market leader in predictive analytics for the Intensive Care Unit. Our system leverages real-time patient data to provide clinicians with actionable information that improves care for the most vulnerable patients. In use at some of the best medical institutions across three continents, the Etiometry Platform has a proven track record in improving outcomes while reducing hospital costs. Our next generation of algorithms will go beyond monitoring risk to forecasting how treatments will affect patient physiology — giving clinicians foresight to guide critical interventions. By joining Etiometry, you will be at the forefront of clinical innovation, working with a passionate team of engineers and scientists with the mission of transforming the delivery of critical care. You will become an integral part of a dynamic team whose work will directly impact patients worldwide and shape the future of ICU analytics.

Job DescriptionWe are seeking a highly skilled and experienced Data Scientist to join our Perception Verification and Validation team. The team is responsible for verifying and validating the perception stack of our autonomous driving system. The candidate will work closely with other data scientists, perception engineers, and systems engineers to develop datasets and metrics to quantify the performance of our perception system. The candidate will also help define key performance metrics that will enable perception engineers to directly measure the impact of new features on both the overall Perception stack as well as end-to-end system behavior.In this role, You will... • Define key performance metrics that will help perception engineers to measure the impact of new features on the perception stack and the end-to-end system behavior, • Create and maintain datasets used to evaluate the perception stack and end-to-end driving performance., • Analyze large scale metric results to identify patterns and insights about perception failure modes. Present results and insights to leadership., • Design and implement statistical methods to quantify uncertainty in our performance and validation metrics.Qualifications, • Master's or PhD degree in Statistics, Mathematics, Computer Science, or a related field, • Proficient using data query languages (SQL and/or Spark/scala) to quickly build complex yet efficient data queries at scale and using Python to build production-quality code, • Basic experience with autonomous driving, safety-critical systems, or computer vision systems., • Proficient in exploratory data analysis (EDA) and data visualization to understand and present trends and their implications for the business., • Background in statistical modeling and analysis; including experience making data-driven decisions that connect point and uncertainty estimates to business impact.Bonus Qualifications, • Skilled at using AI tools to improve development efficiency and quality., • Experience with experiment design and statistical comparisons (A/B testing, parametric/non-parametric statistics, etc.)

Job Description At Klaviyo, we value the unique backgrounds, experiences and perspectives each Klaviyo (we call ourselves Klaviyos) brings to our workplace each and every day. We believe everyone deserves a fair shot at success and appreciate the experiences each person brings beyond the traditional job requirements. If you're a close but not exact match with the description, we hope you'll still consider applying. Want to learn more about life at Klaviyo? Visit careers.klaviyo.com to see how we empower creators to own their own destiny. We're looking for someone who thrives at the intersection of data science and product development, someone who pairs deep statistical rigor with product intuition, and can fluidly move between building complex models in R or Python and advising product leaders and executives on strategic decisions. You should be just as comfortable designing and validating a causal inference framework as you are communicating its implications to stakeholders across the company. Please note that this is a hybrid role that requires 3 days/week in our Boston office. Fully remote candidates will not be considered at this time. What You'll Do: • Partner with product and engineering teams to identify and evaluate high-impact product opportunities through rigorous experimentation, causal inference, and predictive modeling, • Lead the design, implementation, and analysis of experiments — including A/B tests and multivariate tests — ensuring sufficient power, correct statistical methods, and actionable recommendations, • Conduct statistical research projects to uncover patterns in customer behavior, evaluate product performance, and identify causal relationships — using methods such as Mixed Effects Models, Difference-in-Differences, clustering algorithms, and time series analysis to guide product strategy and decision-making., • Define the right product and customer metrics to measure success, and build scalable, self-serve analytics tools and dashboards that enable product managers and cross-functional stakeholders to make data-informed decisions independently., • Collaborate with data engineering to define and implement reliable data pipelines and DBT models that ensure clean, well-structured, and trustworthy data for downstream analysis and self-serve use., • Communicate insights clearly and persuasively to cross-functional stakeholders, from product teams to executive leadershipWho You Are, • You have 7+ years of experience in data science, product analytics, or applied statistics, preferably in a B2B SaaS or product-focused environment, • You hold a degree in a quantitative field such as Statistics, Mathematics, Computer Science, Economics, or Engineering, • You are highly proficient in SQL and either Python or R, and comfortable using DBT for analytics engineering, • You have deep expertise in experimentation and statistical analyses., • You bring strong business intuition and the ability to translate ambiguous questions into clear analytical plans, • You work with speed and focus, balancing analytical rigor with the urgency and iteration cadence of product development, • You are a compelling communicator who can frame complex statistical findings into product-relevant insights, • You thrive in cross-functional settings and are energized by using data to drive product decisions that improve customer outcomesWhy You'll Love This Role, • Influence the direction of a high-impact product area and help define how success is measured, • Work alongside a world-class data team where experimentation and modeling are first-class tools, • Join a company where data science is embedded in the product development lifecycle, not siloed as reporting support, • Be part of a culture that values intellectual rigor, collaborative problem-solving, and continuous learning We use Covey as part of our hiring and / or promotional process. For jobs or candidates in NYC, certain features may qualify it as an AEDT. As part of the evaluation process we provide Covey with job requirements and candidate submitted applications. We began using Covey Scout for Inbound on April 3, 2025. Please see the independent bias audit report covering our use of Covey here Massachusetts Applicants: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability. Our salary range reflects the cost of labor across various U.S. geographic markets. The range displayed below reflects the minimum and maximum target salaries for the position across all our US locations. The base salary offered for this position is determined by several factors, including the applicant's job-related skills, relevant experience, education or training, and work location. In addition to base salary, our total compensation package may include participation in the company's annual cash bonus plan, variable compensation (OTE) for sales and customer success roles, equity, sign-on payments, and a comprehensive range of health, welfare, and wellbeing benefits based on eligibility. Your recruiter can provide more details about the specific salary/OTE range for your preferred location during the hiring process. Base Pay Range For US Locations:$142,400—$213,600 USD Get to Know Klaviyo We're Klaviyo (pronounced clay-vee-oh). We empower creators to own their destiny by making first-party data accessible and actionable like never before. We see limitless potential for the technology we're developing to nurture personalized experiences in ecommerce and beyond. To reach our goals, we need our own crew of remarkable creators—ambitious and collaborative teammates who stay focused on our north star: delighting our customers. If you're ready to do the best work of your career, where you'll be welcomed as your whole self from day one and supported with generous benefits, we hope you'll join us. AI fluency at Klaviyo includes responsible use of AI (including privacy, security, bias awareness, and human-in-the-loop). We provide accommodations as needed. By participating in Klaviyo's interview process, you acknowledge that you have read, understood, and will adhere to our Guidelines for using AI in the Klaviyo interview Process. For more information about how we process your personal data, see our Job Applicant Privacy Notice. Klaviyo is committed to a policy of equal opportunity and non-discrimination. We do not discriminate on the basis of race, ethnicity, citizenship, national origin, color, religion or religious creed, age, sex (including pregnancy), gender identity, sexual orientation, physical or mental disability, veteran or active military status, marital status, criminal record, genetics, retaliation, sexual harassment or any other characteristic protected by applicable law. IMPORTANT NOTICE: Our company takes the security and privacy of job applicants very seriously. We will never ask for payment, bank details, or personal financial information as part of the application process. All our legitimate job postings can be found on our official career site. Please be cautious of job offers that come from non-company email addresses (@klaviyo.com), instant messaging platforms, or unsolicited calls.By clicking "Submit Application" you consent to Klaviyo processing your Personal Data in accordance with our Job Applicant Privacy Notice. If you do not wish for Klaviyo to process your Personal Data, please do not submit an application. You can find our Job Applicant Privacy Notice here and here (FR).

Job DescriptionSenior Scientist, Cardiometabolic Health At WHOOP, we’re on a mission to unlock human performance and healthspan. WHOOP empowers members to perform at a higher level through a deeper understanding of their bodies and daily lives. WHOOP is hiring a Senior Scientist, Cardiometabolic Health to lead research that expands our understanding of cardiometabolic physiology and supports evidence‑based product innovation. You will design and execute rigorous research (observational, interventional, and prospective), contribute to scientific dissemination, and partner across internal and external stakeholders to drive meaningful health insights at scale.Responsibilities • Design and lead real-world and clinical research studies, including observational, retrospective, prospective, and interventional designs, ensuring methodological rigor and scientific integrity., • Develop and execute statistical analysis plans, including use of mixed models, causal inference, and other advanced methods, to generate insights on cardiometabolic health and behavior change., • Conduct and interpret analyses of large-scale time-series physiological and wearable data to uncover meaningful patterns and health outcomes., • Prepare IRB submissions and oversee compliance when applicable to support ethical and regulatory standards in research execution., • Communicate research findings through peer-reviewed publications, scientific presentations, white papers, internal briefs, and cross-functional knowledge sharing., • Establish and manage academic and industry research partnerships to support validation studies, innovation initiatives, and scientific advancement., • Collaborate with internal stakeholders across Marketing, Data Science, Enterprise, and Product teams to translate research into product and business impact., • Mentor junior scientists, fostering a culture of scientific rigor, curiosity, and collaboration within the Performance Science team.Qualifications, • Advanced degree (PhD, MD, PharmD, or equivalent) in life sciences, public health, biostatistics, physiology, cardiometabolic health, biomedical data science, or related discipline., • 5+ years of post‑graduate experience with a strong record of publications and independently led research., • Demonstrated experience designing and executing clinical research and real‑world studies; familiarity with IRB processes and clinical trial frameworks., • Advanced proficiency in Python, R, and/or SQL for data extraction, statistical analysis, and visualization of wearable and biomedical datasets., • Experience working with large‑scale time‑series physiological or wearable data., • Ability to communicate scientific insights effectively with both technical and non‑technical audiences., • Excellent organizational skills, attention to detail, and ability to manage multiple projects., • Experience collaborating with academic partners, healthcare systems, or consortiums.

Job Description Hi, we're Oscar. We're hiring a Senior Data Scientist to join our Data team. Oscar is the first health insurance company built around a full stack technology platform and a relentless focus on serving our members. We started Oscar in 2012 to create the kind of health insurance company we would want for ourselves—one that behaves like a doctor in the family. About the role: The Senior Data Scientist, Advanced Risk Modeling, is a senior individual contributor role focused on utilizing advanced machine learning (ML) and artificial intelligence (AI) methodologies on modern ML platforms. This role will build and deploy sophisticated models to help solve complex business problems specifically within Oscar's risk adjustment domain. You will report into the Director of Data. Work Location: This is a remote position, open to candidates who reside in: Boston, MA. You will be fully remote; however, our approach to work may adapt over time. Future models could potentially involve a hybrid presence at the hub office associated with your metro area. #LI-Remote Pay Transparency: The base pay for this role is: $158,400- $207,900 per year. You are also eligible for employee benefits, participation in Oscar's unlimited vacation program, company equity grants, and annual performance bonuses. Responsibilities: * Conduct in-depth data analysis and advanced feature engineering using large, complex healthcare datasets to create robust predictors. * Design, develop, and validate advanced ML/AI models (e.g., regression/classification, deep learning, NLP, gradient boosting, LLM experimentations) to solve complex clinical and business problems within the risk adjustment domain. * Leverage modern ML Ops platforms (e.g., Vertex AI) and data science best practices to efficiently train, test, deploy, and maintain production-level models. * Build and maintain the supporting data systems, analytics, and monitoring infrastructure required for complex, production-level AI/ML systems. * Research, develop, and evaluate new AI applications using cutting-edge techniques, including LLM models and agentic frameworks, to solve critical business challenges in risk adjustment. * Work closely with business stakeholders, engineering teams, and product managers to gain a deep understanding of business operations and technical systems. * Build strong partnerships to foster close, effective integrations between data science, engineering, product, and business units. * Partner with leaders to identify high-impact opportunities, translate complex business challenges into data science solutions, and ensure successful model implementation within business workflows. Requirements: * 4+ years of industry or other quantitative technical fields (which may include academia). * 3+ years of work experience working with SQL, R, and/or Python to query, manipulate and analyze data * 3+ years experience building data models, using more advanced analytics methods, statistical modeling, and/or data processing Bonus points: * Advanced degree in a quantitative or technical field * Experience in the healthcare, finance and/or insurance industries This is an authentic Oscar Health job opportunity. Learn more about how you can safeguard yourself from recruitment fraud here. At Oscar, being an Equal Opportunity Employer means more than upholding discrimination-free hiring practices. It means that we cultivate an environment where people can be their most authentic selves and find both belonging and support. We're on a mission to change health care -- an experience made whole by our unique backgrounds and perspectives. Pay Transparency: Final offer amounts, within the base pay set forth above, are determined by factors including your relevant skills, education, and experience. Full-time employees are eligible for benefits including: medical, dental, and vision benefits, 11 paid holidays, paid sick time, paid parental leave, 401(k) plan participation, life and disability insurance, and paid wellness time and reimbursements. Artificial Intelligence (AI): Our AI Guidelines outline the acceptable use of artificial intelligence for candidates and detail how we use AI to support our recruiting efforts. Reasonable Accommodation: Oscar applicants are considered solely based on their qualifications, without regard to applicant's disability or need for accommodation. Any Oscar applicant who requires reasonable accommodations during the application process should contact the Oscar Benefits Team () to make the need for an accommodation known. California Residents: For information about our collection, use, and disclosure of applicants' personal information as well as applicants' rights over their personal information, please see our Privacy Policy.

Job DescriptionSalary: $170,000 - $220,000 Acrivon(NASDAQ: ACRV)is a clinical stage biopharmaceutical company discovering and developing precision medicinesutilizingits proprietary GenerativePhosphoproteomicsAP3 platform. The platform allows the company to interpret and quantify compound specific, drug-regulated pathway activity levels inside the intact cell in an unbiased manner, yielding terabytes of proprietary data and delivering rapid, actionable insights. The GenerativePhosphoproteomicsAP3 platform iscomprisedof a growing suite of powerful,internally-developedtools, including the AP3 Data Portal,converting multimodal data into structured data for generative AI analyses, the AP3 Kinase Substrate Relationship Predictor and the AP3 Interactome.These distinctive capabilities enable the company to go beyond the limitations of traditional drug discovery, as well as current AI-based target-centric drugdiscovery, andrapidly design highly differentiated compounds with desirable pathway effects through intracellular protein network analyses and advance these agents into the clinic for streamlined development. Acrivonis currently advancing its lead program, ACR-368 (also known asprexasertib), a selective small molecule inhibitor targeting CHK1 and CHK2 in a potentially registrational Phase 2b trial for endometrial cancer. The company has received Fast Track designation from the Food and Drug Administration, or FDA, for the investigation of ACR-368 as a monotherapy based onOncoSignature-predicted sensitivity in patients with endometrial cancer. The FDA has granted a Breakthrough Device designation for the ACR-368OncoSignatureassay for the identification of patients with endometrial cancer who maybenefitfrom ACR-368 treatment. In addition to ACR-368,Acrivonis alsoleveragingits proprietary GenerativePhosphoproteomicsAP3 platform for developing its co-crystallography-driven, internally discovered pipeline programs. These include ACR-2316, the companys second clinical stage asset, a novel, potent, selective WEE1/PKMYT1 inhibitor designed for superior single-agent activity through strong activation of not only CDK1 and CDK2, but also of PLK1 to drive pro-apoptotic cell death, asobservedin preclinical studies against benchmark inhibitors. The Phase 1 trial of ACR-2316 is advancing with enrollment in the first three dose-escalation cohorts completed. Drug target engagement wasobservedat DL1 and 2 using the companys clinical mass-spectrometry-based AP3 profiling, with evidence of approximate dose proportionality based on plasma pharmacokinetic analyses, and initial clinical activity with tumor shrinkageobservedat DL3. In addition, the company is advancing a preclinical program directed against an undisclosed cell cycle regulatory target. Our global teamoperatesout of two leading life science clusters, Watertown, MA andMediconVillage in Lund, Sweden. Position Overview: The Principal Scientist/ Associate Director/Directorwill be a key member ofAcrivonTherapeutics Clinical Development team andassistour clinical science effortsto: • Support thedevelopmentoftwoclinical stageassets currentlybeingevaluated in cancer patients(ACR-368and ACR-2316), • Drivereal-time analysis and monitoring ofemerging clinical data (bothsafety and clinical activity), • Bea key contributor in all the futureclinicalstudies that will beexecutedbyAcrivonin terms of design,data collection,datainterpretation, and visualization of data summaries withvarious typesofgraph plotsfor corporate presentations Location: The position reports to the Chief Medical Officer andwill be based out of the corporate headquarters in Watertown, MA. Duties and Responsibilities: • Collaborate within the Clinical Development Team on the review, analysis, and interpretation of study results and assureappropriate datareview,accuratedata reporting,timelyand complete query closure, database quality and integrity, safetyeventand protocol deviation oversight, and tracking andtimelyreporting of study related samples, reports, and procedures., • Support the leadership team through the development ofpowerfulpresentations to communicate study data results (e.g.waterfall, swimmer, and spider plots) to internal (e.g.board) and to external audiencesin visually clear and appealing manneron behalf of the Company., • Help support database control and integrity, data and sample tracking documents and processes, periodic reporting updates, regulatory responses, query issuance and tracking, and adherence to GCP and company standards., • Work closely with the medical monitor toassurehe/she is informed of pertinent study information., • Proactivelyidentifyany study or program challenges by reviewing andmonitoring ofemerging clinical data related to safety, efficacy, protocol deviations, site performance, and query management., • Develop and implement sound solutions to any identified issuesin collaboration with the clinical study team andClinical Research Organizations., • Conduct literature reviews as needed for the interpretation of study data and development of next stepsor improvements to workflow., • In collaboration with internal/external experts and stakeholders on biostatistics, clinical pharmacology, translational medicine, clinical operations, and data management, contribute to trial design including clinical protocols, ICF and CRF design, study procedures manuals, data review plans, statistical analysis plans, IRT, data entry guidelines, and medical monitoring and risk management plans., • Support the development ofadditionalprogram documents including pharmacy manuals, study procedures manuals, clinical SOPs, safety, and deviation tracking, and SIV materials., • Support the development of clinical sections for various regulatory documents such as INDs, clinical study reports, investigator brochures, annual reports and updates, and NDAs., • Serve as a clinical science representative on cross-functional teams as assigned. Qualifications: • Advanced degree ina lifescience field(PhD, or PharmD)., • Aminimum of4years (Principal),7years(Associate Director), or 10 years (Director)relevant clinical research experience in pharmaceutical and/or biotech companiesor from a clinical trial organization(direct translational experienceisdesirable)., • Experience in execution and interpretation of early,mid, andlatestageoncology clinical studies,with vast experience with diverse trial endpoints includingthose with translational/biomarkerandqualityoflifeassessments., • Experience managing and tracking clinical data and critically reviewing study documents with exceptional attention to detail and ability to analyze and interpret clinical data., • Experience working with and managing CRO(s); experience working in joint research collaborations desirable., • Outstanding oral and written communication skills and swift ability to work efficiently with a multi-disciplinary clinical team at different geographical locations and (US) time zones., • Demonstrably strong IT skills, including command of the Microsoft Office Suite, SharePoint, Egnyte, Zoom, MS Teams, etc., • Deepexpertisewith one or more data visualization platforms (e.g.Spotfire, Tableau, Prism,etc)to develop key clinicalgraphs,e.g.heatmaps,waterfall, spider, and swimmer plots, and variations thereof,in a timely manner.Experience with a programming language (e.g.R, Python, SAS) is desirable but notrequired.

Job Description Company Overview We are the only AI-native biotech, pioneering small and large molecule therapeutics discovery by integrating massive multimodal data, frontier AI models, and high-throughput lab automation into an infrastructure for AI-enabled drug discovery. We hire top 1% talent to join our interdisciplinary team of scientists, engineers, researchers, operators, innovators, drug developers, business professionals, and technologists. Join us to build the world's first AI infrastructure for tech-enabled drug discovery and to deliver a pipeline of diverse drug modalities for all major disease areas. As an AI Research Scientist III at 1910 you will be expected to roll up your sleeves as an Individual Contributor (IC) by keeping up with relevant scientific literature, prototyping promising methods, and contributing to our active drug design campaigns by applying 1910's productionized AI/ML models. Role Description • Propose and prototype AI and Machine Learning solutions that address use cases in 1910's design pipeline, • Independently apply productized AI and Machine Learning models to advance 1910's active drug design campaigns, • Independently write and publish peer reviewed scientific articles and mentor junior AI Researchers with their work, • Periodically presenting recent AI research at internal journal clubs, • Work cross-functionally with scientific colleagues, being a subject matter expert in how AI and Machine Learning can be used to answer cheminformatics and bioinformatics questions, • Keep up-to-date on cutting-edge research in the AI for drug discovery space, • Manage junior AI Research Scientists including having weekly 1:1s, and regular performance reviews Qualifications • PhD in a relevant discipline (Computer Science, Biology, Chemistry, etc.), • 3+ years of relevant industry experience (AI, Drug Discovery, etc.), • A strong understanding of statistics and classical machine learning methods (SVM, RF, etc.), • Industry experience training and deploying cutting edge deep learning methods (Transformers, Graph Neural Networks, etc.), • Wet lab validation of at least 2 AI-driven drug discovery initiatives, • Demonstrated experience writing clean, maintainable, production-quality Python code, with examples available in code repositories, • Familiarity with MLOps and DevOps best practices, • Exposure to distributed computing (Microsoft Azure, HPC Cluster, etc.), • Strong track record of publications of individual research in top-tier AI journals and conferences, • Ability to demonstrate business value related to developed AI and Machine Learning solutions in biology and medicinal chemistry related to your modeling efforts, • Ability to work effectively in a fast-paced startup environment with evolving projects and shifting priorities driven by business needs, • Excellent written and verbal communication skills, including the ability to create clear documentation for roadmaps, proposals, and related materials Nice to Haves • Past experience managing junior AI Research Scientists #LI-Onsite Diversity and Inclusion (1910's Promise) At 1910, we believe that a diverse, equitable, and inclusive workplace furthers relevance, resilience, and longevity. We encourage people from all backgrounds, ages, abilities, and experiences to apply. 1910 is proud to be an equal-opportunity workplace and is an affirmative action employer. We are committed to equal employment opportunity regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity, or Veteran status. If, due to a disability, you need an accommodation during any part of the interview process, please let your recruiter know. While 1910 supports visa sponsorship, sponsorship opportunities may be limited to certain roles and skills. Benefits and Perks • Competitive compensation package, • Above market benefits, • Generous vacation and parental leave, • Super cool team building activities, • Great colleagues

Job DescriptionJob Title: Research - Associate Scientist II Location: Cambridge, MA Duration: 12 Months Job Summary • Seeking a motivated Associate Scientist to join the Process Sciences group, supporting the development and execution of oligonucleotide manufacturing processes for siRNA therapeutics., • This entry-level role is ideal for a recent graduate or early-career scientist looking to gain hands-on experience in processing, manufacturing, and process development of oligonucleotide therapeutics within a collaborative, fast-paced environment., • The Associate Scientist I will work closely with senior scientists and engineers to execute laboratory operations, collect and document data, and support process optimization and technology transfer activities., • Support processing activities for oligonucleotide manufacturing under guidance from senior staff., • Execute laboratory-scale and pilot-scale processes to support research and in-house material needs., • Perform routine in-process analytical tests (e.g., pH, conductivity, UV, basic chromatography)., • Assist in the preparation, execution, and documentation of non-GMP manufacturing runs., • Follow established SOPs and batch records in a cGLP laboratory environment., • Support drafting and revision of SOPs, batch records, and technical documentation., • Operate laboratory and analytical equipment after appropriate training., • Accurately document experimental work following good documentation practices (GDP)., • Collaborate with cross-functional teams including Process Development, Analytical Sciences, and Manufacturing., • BS in Chemistry, Chemical Engineering, Biochemistry, or a related scientific discipline. 0–2 years of laboratory experience (academic, co-op, internship, or industrial experience acceptable)., • Basic familiarity with analytical techniques such as pH, conductivity, HPLC, or LC-MS is preferred. Strong attention to detail and commitment to high-quality laboratory documentation., • Willingness to learn regulated laboratory practices and manufacturing workflows., • Ability to work collaboratively, follow instructions, and manage time effectively. #ZRCompany DescriptionFounded in 2002 by three former Monster.com executives; TalentBurst is an award-winning full-service Staffing Firm working directly with Fortune 500 companies in the US and Canada. We specialize in Contract and Contract to Permanent roles across many industries and have direct/contractual relationships with all our clients. Please visit our website or come meet us at our offices in Natick, MA, Miami, FL, Christiansburg, VA, Vineland, NJ, Houston, TX & downtown San Francisco, CAFounded in 2002 by three former Monster.com executives; TalentBurst is an award-winning full-service Staffing Firm working directly with Fortune 500 companies in the US and Canada. We specialize in Contract and Contract to Permanent roles across many industries and have direct/contractual relationships with all our clients. Please visit our website or come meet us at our offices in Natick, MA, Miami, FL, Christiansburg, VA, Vineland, NJ, Houston, TX & downtown San Francisco, CA

Job Description Senior Scientist III (iPSC-Derived Gut Models) Cambridge, MA (Lab Based Position) Pay Rate: $70 -77/hr W2 This 24+ Month Contract Position Has A Tentative Start Date of 2/2/26 Role Overview: We are seeking a hands-on Scientist with strong experimental biology expertise to advance iPSC-derived gut models for evaluating combination therapies for inflammatory diseases (e.g., IBD). Working closely with DAGS, Immunology, and Pharmacology colleagues, the contractor will culture and differentiate human iPSCs into intestinal lineages (e.g., epithelial monolayers and 3D organoids/enteroids), establish microphysiological systems, and design and execute combination therapy studies. The successful candidate will optimize functional assays, perform dose–response and matrixed combination experiments, analyze synergy/antagonism, and deliver clear, actionable data packages to cross-functional teams. Required Qualifications: • MS with 5+ years or PhD with 1–2+ years of relevant experience in molecular/cellular biology, immunology, pharmacology, or related field, • Proven ability to execute and troubleshoot functional assays; experience running dose–response studies and quantitative assay analysis, • Strong documentation, data analysis, and presentation skills; success working in collaborative, cross-functional settings, • Following aseptic processes Preferred Qualifications • Direct experience with iPSC-derived intestinal models, including 3D organoids, 2D monolayers, Transwells, and/or gut-on-chip systems, • Expertise in barrier function assays (TEER, permeability), imaging-based analyses, and cytokine profiling, • Experience with automation, liquid handling, and high-throughput assay development, • Background in inflammatory disease biology and prior industry experience in preclinical combination testing or pharmacology Job Description: The Merck Genome Sciences (GS) iPSC disease modeling group within the Department of Data, AI, and Genome Sciences (DAGS) partners with Immunology and cross-functional teams to evaluate therapeutic strategies based on human-relevant models. Our mission is to build and apply robust iPSC-derived systems to understand mechanisms in human disease and to test mono- and combination therapies under controlled, scalable in vitro conditions. We leverage genetic and pharmacological perturbations in iPSC-derived gut models to inform therapeutic combination design and prioritization. The contractor is expected to work both independently and collaboratively in a dynamic early discovery environment. • Ensure compliance with safety practices and proper maintenance of cell lines, reagents, and equipment. Johnson Service Group, Inc. (JSG) is a North American leader in the staffing and consulting services industry, with over 35 years of experience investing in people and companies. Johnson Service Group (JSG) is an Equal Opportunity Employer. JSG provides equal employment opportunities to all applicants and employees without regard to race, color, religion, sex, age, sexual orientation, gender identity, national origin, disability, marital status, protected veteran status, or any other characteristic protected by law. Company DescriptionOur people and culture make JSG a great place to work. JSG’s mission is to empower people, help our clients reach their goals, and hire motivated individuals. Johnson Service Group, Inc. (JSG) is a North American leader in the staffing and consulting services industry, with 40 years of experience investing in people and companies. We are always looking for great people to join our team—we want to see your success here at JSG! We can be found locally in more than 30 offices throughout the United States and Canada. JSG continues to work diligently to offer our clients and candidates world-class service and diversified offerings to fit their evolving needs. We offer medical, dental, vision, life insurance options, 401(k), weekly pay, and more. Johnson Service Group (JSG) is an Equal Opportunity Employer. JSG provides equal employment opportunities to all applicants and employees without regard to race, color, religion, sex, age, sexual orientation, gender identity, national origin, disability, marital status, protected veteran status, or any other characteristic protected by law.Our people and culture make JSG a great place to work. JSG’s mission is to empower people, help our clients reach their goals, and hire motivated individuals.\r\n\r\nJohnson Service Group, Inc. (JSG) is a North American leader in the staffing and consulting services industry, with 40 years of experience investing in people and companies. We are always looking for great people to join our team—we want to see your success here at JSG! We can be found locally in more than 30 offices throughout the United States and Canada. JSG continues to work diligently to offer our clients and candidates world-class service and diversified offerings to fit their evolving needs.\r\n\r\nWe offer medical, dental, vision, life insurance options, 401(k), weekly pay, and more.\r\n\r\nJohnson Service Group (JSG) is an Equal Opportunity Employer. JSG provides equal employment opportunities to all applicants and employees without regard to race, color, religion, sex, age, sexual orientation, gender identity, national origin, disability, marital status, protected veteran status, or any other characteristic protected by law.

Job DescriptionScholar Rock is a biopharmaceutical company that discovers, develops, and delivers life-changing therapies for people with serious diseases that have high unmet need. As a global leader in the biology of the transforming growth factor beta (TGFβ) superfamily of cell proteins and named for the visual resemblance of a scholar rock to protein structures, the clinical-stage company is focused on advancing innovative treatments where protein growth factors are fundamental. Over the past decade, the company has created a pipeline with the potential to advance the standard of care for neuromuscular disease, cardiometabolic disorders, cancer, and other conditions where growth factor-targeted drugs can play a transformational role. Scholar Rock is the only company to show clinical proof of concept for a muscle-targeted treatment in spinal muscular atrophy (SMA). This commitment to unlocking fundamentally different therapeutic approaches is powered by broad application of a proprietary platform, which has developed novel monoclonal antibodies to modulate protein growth factors with extraordinary selectivity. By harnessing cutting-edge science in disease spaces that are historically under-addressed through traditional therapies, Scholar Rock works every day to create new possibilities for patients. Learn more about the company’s approach at ScholarRock.com and follow @ScholarRock and on LinkedIn. Summary of Position: The Medical Director, reporting to the VP, Clinical Research, will be a member of the early development team, accountable for driving clinical development activities for product candidates from IND through Proof-of-Concept. The successful candidate will be responsible for providing medical leadership for clinical development activities of follow-on indication(s) for apitegromab as well as new product candidates, in alignment with corporate strategy. This position requires a highly motivated physician scientist with hands-on expertise in advancing product candidates to deliver life-changing medicines.Position Responsibilities: • Deliver clinical development plan for assigned pipeline products from IND through Proof-of-Concept, • Provide medical leadership for clinical development activities of pipeline product candidates, including new indication assessment, • Collaborate with other members of the development and preclinical research teams to contribute to building a collaborative culture and improving effectiveness of the development team, • Engage with external scientific and clinical trial experts, health authorities, and consultants, to develop scientifically robust development plans, • Drive scientifically robust evaluation of new opportunities, including disease area assessment, landscape analysis, evaluation of development and regulatory pathways, and development of study concepts, • Provide strategic guidance and support to the early development team, including hands-on authoring, for the development of clinical development plans, study protocols, investigator brochures, regulatory documents, publications, etc., • Provide medical leadership and input in cross-functional team activities, including business development activities, non-clinical development, quality assurance, clinical operations, biostatistics, regulatory affairs and drug safety, • Responsible for medical oversight of clinical trials, including medical monitoring of studies, adverse event reporting, and patient safety for all clinical trials across a development program., • Provide medical and scientific leadership in data analysis and interpretation, maintaining integrity, scientific rigor, and transparency, • Work within compliance to all applicable GCP/ ICH regulationsCandidate Requirements:, • MD, MD/PhD, or equivalent, based in greater Boston, • Strong critical thinking skills, with ability to synthesize complex information, and exceptional communication skills, both verbal and written, • 5+ years of experience in the biopharmaceutical clinical development function, with 3+ years of clinical development leadership experience; neuromuscular or rare disease experience preferred but not required, • Highly organized, outcome-oriented, self-motivated team player with strong interpersonal skills and effective conflict management skills, • Experience in innovative clinical study design, analysis of clinical data, publications, and working knowledge of biostatistics and pharmacokinetics/pharmacodynamics, • Understanding of the drug development process from pre-IND through BLA, • Experience interacting with health authorities in the US and EU, • In-depth knowledge of ICH-GCP and other application regulatory guidelines, • Ability to travel domestically and internationally (~15%)Scholar Rock is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.

Job Description Medical Technologist / Clinical Laboratory Scientist Location: Boston VA Medical Center (VAMC) Employer: Emerging Tech Employment Type: Full-Time / Contract Position Overview Emerging Tech is seeking experienced Medical Technologists / Clinical Laboratory Scientists to support laboratory operations at the Boston VA Medical Center. This role is ideal for professionals passionate about laboratory science and committed to delivering accurate, timely diagnostic results in service of our nation’s veterans. The Medical Technologist will perform a full range of clinical laboratory testing in support of patient diagnosis, treatment, and disease prevention while ensuring compliance with Department of Veterans Affairs standards and policies. Key Responsibilities • Perform complex laboratory tests, analyses, and procedures across assigned laboratory sections such as hematology, chemistry, microbiology, and blood bank., • Operate, calibrate, and maintain laboratory instrumentation while adhering to quality control and quality assurance standards., • Analyze, validate, and interpret test results, identify discrepancies, and take appropriate corrective action., • Accurately document and report laboratory data in accordance with VA regulations and laboratory protocols., • Collaborate with physicians, nurses, and laboratory personnel to support efficient workflows and high-quality patient care., • Comply with all safety, infection control, and regulatory requirements including CLIA, CAP, and VA standards., • Bachelor’s degree in Medical Technology, Clinical Laboratory Science, or a related scientific field., • ASCP or AMT certification as a Medical Technologist (MT) or Medical Laboratory Scientist (MLS) preferred., • Minimum of 1 year of clinical laboratory experience in a hospital or healthcare setting., • Strong analytical skills, attention to detail, and proficiency with laboratory equipment and laboratory information systems., • Ability to work independently and as part of a multidisciplinary healthcare team. Powered by JazzHR SUtANRuoKU

Job Description Aquinas Consulting is currently looking for a HYBRID Senior Data Engineer for our high growth technology partner as they continue commercializing and scaling their insurtech platform. In this role, you will be responsible for collecting, managing, and converting raw data into information that can be interpreted by Data Scientists and Business Analysts for future usage. Our partner is under a Fortune 5 global organization, where you will work cross functionally with senior leadership to continuously improve and support the functionality of its data-driven initiatives. Senior Data Engineer Job responsibilities: • Work on data model designs and ERD documentation to support new data sets and systems implemented around the organization., • Identify operational data gaps and recommend data driven solutions to address those gaps in a secure, performant and reliable manner., • Perform in-depth analysis of existing data load, analytics, and visualization code to ensure accuracy of data flow., • Create data tools for analytics and data scientist team members that assist them in building and optimizing our product into an innovative industry leader., • Bachelor’s or Master’s Degree in Computer Science/Engineering (or related field) or equivalent working experience, • 5 + years of demonstrated professional software or data engineering experience with specialization in data modeling and business intelligence., • 3 + years have experience with Microsoft Azure, specifically with concentration in ETL processing via Data Factory., • Near expert knowledge of the SQL Server stack (2016+), ETL and Transact SQL (TSQL)., • Experience with relational database modeling, star schemas and Data Warehousing., • Deep working knowledge of Python and modeling datasets for dashboards for BI visualization tools such as Power BI / SSRS / Tableau is a plus. Please note: Applying to this role is an agreement to have your information entered into our database and acknowledgement that a recruiter will reach out to you either by phone, email, and/or text message regarding this and similar job opportunities. Aquinas Consulting is a woman and minority owned company headquartered in Milford, CT that provides Engineering, Information Technology (IT), and Manufacturing staffing solutions throughout the US. We take pride in 20 years of service to our clients, our hiring managers, our consultants, and our local community. Aquinas is an affirmative action, equal opportunity employer and committed to considering all qualified applications without regard to race, genetic information, sex, age, color, religion, national origin, veteran status, disability or any other characteristic protected by law.

Job DescriptionCompany Description The work we do at Eurofins Professional Scientific Services matters, and so do our employees. At Eurofins PSS, we put a focus on your professional growth. We provide our employees the ability to break into the biopharmaceutical industry and grow from the bottom up. We have the supportive teams and tools available to invest in you while also affording you work-life balance and a competitive benefits package. Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies. If you’re looking for a rewarding career, a place to call home, apply with us today Job Description We are seeking a highly skilled, passionate, and motivated scientist to join our Neuroscience team. Our team uses cell culture systems to understand neurodegenerative diseases like Alzheimer’s Disease, Parkinson’s Disease and Amyotrophic Lateral Sclerosis and search for drugs to treat these diseases. We are looking for someone to support these efforts by maintaining cell cultures and performing assays and is eager to expand their scientific skillsets. Key Responsibilities include but are not limited to: • Perform cell-based functional assays in support of neuroscience drug discovery projects., • Provide technical support to project teams to achieve critical research objectives and timelines., • Perform hands-on laboratory work, including routine cell and biochemistry assays:, • Prepare solutions and culture media., • Maintain multiple cell lines, including primary neuronal cultures., • Measure biochemical or functional parameters in cells using techniques like microscopy, live fluorescence imaging, immunocytochemistry, calcium imaging, morphology, and live/dead cell assays., • Perform biochemical assays such as AlphaScreen, ELISA, MSD, and SDS-PAGE., • Process data generated from these assays and report findings under supervision., • Accurate recording of all practical work: completion of electronic lab notebook to meet quality standards., • Maintaining a tidy and efficient laboratory environment and ensuring health and safety standards are met.Qualifications Minimum Required Qualifications: • B.S. degree in Biological Sciences (Molecular Biology, Biotechnology, Immunology, Biochemistry, Neuroscience, or a similar field) with 4-6 years of relevant laboratory experience., • Demonstrated experience with aseptic technique and mammalian cell culture (experience with iPSCs is a plus)., • Competence in molecular biology laboratory methods, procedures, and techniques, e.g. qPCR, Western Blotting and immunofluorescence., • Demonstrated understanding of biology lab safety requirements., • Excellent written and verbal communication, work planning, data analysis, troubleshooting, and record-keeping skills with strong attention to detail., • Ability to multitask and prioritize tasks to meet deadlines., • Ability to work independently and as a part of a team, self-motivation, adaptability, and, • Background and interest in neurodegenerative disease research, including Alzheimer’s disease, Parkinson’s disease, and ALS., • Hands on experience with iPSCs and neuronal differentiation., • Experience with electronic laboratory notebook (ELN) documentation., • Authorization to work in the United States indefinitely without restriction or sponsorship. Additional Information What to Expect in the Interview Process: • 10-15 Minute Phone Screen with the Recruiter, • 45 Minute Virtual Interview with Hiring Manager What we offer: • Excellent full-time benefits, including comprehensive medical coverage, dental, and vision options, • Life and disability insurance, • 401(k) with company match, • Paid vacation and holidays, • Yearly goal-based bonus & eligibility for merit-based increases Apply today and join a team that’s making a difference in science every day. Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Job Description Arcaea is building a new ingredient toolset for the beauty and personal care industry - one rooted in biotechnology with the aim of delivering radical performance and unparalleled sustainability that will also present new opportunities for storytelling. We're hiring an Associate Scientist to contribute to the development and evaluation of innovative hair care products. This role focuses on executing scientific protocols, performing efficacy testing, and providing data-driven insights to support product claims. The ideal candidate is a detail-oriented researcher with a strong foundation in laboratory techniques and a passion for hair science. WHAT YOU'LL DO • Conduct standardized Testing Procedures (SOPs) for product efficacy using consumer-relevant predictive assays., • Design robust experiments, perform comprehensive data analysis, and present findings to help guide product direction., • Evaluate the performance of formula prototypes and raw materials through rigorous bench testing., • Develop simplex formulas to screen new ingredients and assess their functional benefits within hair care applications., • Utilize microscopy, spectroscopy, and mechanical/thermal analysis to characterize hair properties and the effects of various products., • Manage the preparation and standardized treatment of hair substrates for consistent and reproducible testing., • Conduct literature reviews to stay current on hair science, competitor products, and ingredient innovations., • Maintain laboratory equipment and ensure a clean, safe, and efficient working environment.WHAT WE SEEK, • BS in Chemistry, Chemical Engineering, Materials Science, Biochemistry, or a related scientific discipline., • 1–3 years of experience in a personal care laboratory setting, with a strong preference for hair care., • Proven experience in cosmetic product efficacy testing or claims substantiation., • Proficiency in mechanical testing, surface analysis, or thermal analysis. Experience with delicate, hands-on laboratory tasks and precise measurements is essential., • Proficiency in searching and interpreting scientific literature. Experience with image analysis and statistical software is a plus., • Strong knowledge of hair care product categories and consumer needs., • Exceptional attention to detail and a conscientious approach to data integrity. Agency and Third Party Recruiter Notice: Agencies that submit a resume to Arcaea must have a current executed Arcaea Agency Agreement executed by the Director, People Operations. In addition Agencies may only submit candidates to positions for which they have been invited to do so by an Arcaea Recruiter. All resumes must be sent to the Arcaea Recruiter under these terms or they will not be considered. If you have a disability under the Americans with Disabilities Act or similar law, or you require religious accommodation, and you wish to discuss potential accommodations related to applying for employment at our company, please contact . Arcaea participates in E-verify to determine employment eligibility. Disclaimer: This job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee.

Job DescriptionParallel Squared Technology Institute (PTI) is a non-profit research institute developing technologies, reagents, and computational tools to increase the sensitivity and throughput of protein analysis, with a specific focus on single-cell proteomics. We are applying these innovations to societally-relevant areas of biomedical research. As part of these efforts, we are developing new approaches to study protein dysfunctions in Alzheimer’s and related neurodegenerative diseases. Summary of PositionWe are seeking scientist and senior scientist candidates to help drive our efforts to use single-cell proteomics to understand the causes of Alzheimer’s and related neurodegenerative diseases. Ideal candidates will have expertise in the molecular mechanisms of neurodegeneration and direct, hand-on experience in single-cell analysis, computational biology, and brain tissue handling. Candidates will have the opportunity to work as part of an interdisciplinary team in multiple areas, including on NIH-funded projects, using proteomic technologies developed at PTI to discover new molecular mechanisms of neurodegeneration in Alzheimer’s and related disorders. Day-to-day responsibilities include designing and carrying out experiments to isolate and profile single cells from brain tissue, computationally analyzing large-scale single-cell proteomics datasets, preparing manuscripts and presentations, mentoring junior scientists, and regular meetings with collaborators in and outside of PTI. Candidates will initially work on ongoing projects but will have the opportunity to design and lead their own projects as well. Candidates with less than 1 year of postdoctoral experience will be considered for the scientist position and those with more than 1 year of experience will be considered for the senior scientist position. About PTIPTI is a nonprofit, focused research organization (FRO) established through Convergent Research. FROs aim to accelerate progress across science and technology by tackling large-scale problems with the potential to unlock existing bottlenecks in specific research areas. PTI aims to achieve a 100-1000x increase in the scale of proteomic analysis. To do so, we are developing new technologies and approaches for mass spectrometric proteomics. This includes molecular barcodes, termed “mass tags” that enable sample multiplexing, as well as computational approaches for increasing the sensitivity of protein analysis. We aim to apply these advances in societally-relevant areas, with a specific focus on neurodegenerative disease. To do so, we are collaborating with leaders in neurodegenerative disease from around the world. To learn more about PTI’s approach for studying neurodegenerative disease, please visit this page. To learn more about our technology for increasing the throughput of protein analysis, please visit here. Researchers at PTI have the opportunity to work within an interdisciplinary team of mass spectrometrists, chemists, computational analysts, and biologists to push the boundaries of protein analysis. PTI supports professional development through educational opportunities such as travel to conferences workshops. Members of PTI receive industry-level resources to lead research projects and have the opportunity to disseminate their discoveries and innovations through high-visibility publications, presentations, and submissions to public data portals. Responsibilities: • Design and execute research projects using single-cell proteomics to understand the molecular mechanisms of neurodegeneration in Alzheimer’s and related disease., • Computationally analyze large-scale, single-cell proteomic datasets to identify new molecular mechanisms of disease., • Collaborate with external laboratories, brain banks, and tissue repositories on sample procurement., • Prepare human brain tissue samples for proteomic analysis using methods and technologies developed at PTI., • Help junior scientists gain expertise in experimental techniques used at PTI, analyzing and interpreting experimental results, recording data in laboratory notebooks, and writing up and presenting research results., • Make regular presentations within PTI and to collaborators., • Prepare manuscripts related to project outcomes and grant applications for external funding., • Demonstrate a commitment to diversity, inclusion, and cultural awareness through actions, interactions, and communications with others., • Other duties as assigned.Qualifications:, • PhD Neuroscience or a related field., • Direct, hands-on experience in preparing human brain tissue for downstream analyses., • Direct, hands-on experience with single cell analysis., • Excellent communication and interpersonal skills, record keeping ability, and attention to detail.Preferred Qualifications, • Experience in high throughput or automated tissue sample collection, preparation, and analysis, particularly with human brains., • Experience with mass spectrometry proteomics., • Fluency in R or Python, particularly in the context of single-cell analysis.We offer:, • An opportunity to change the world and work with some of the smartest and the most talented experts from different fields., • Excellent medical, dental, and vision insurance with many $0 premium options for you and your family with several national and regional providers. Most employees have more than 20 plan options to choose from., • Company-paid group life, AD&D, long- and short-term disability insurance, • 15 days PTO + 10 sick days per year, • 18 company holidays + your birthday off, • $5,000 per year educational reimbursement

Job Description Quantum Talent Network, US – General Interest Boston, MA, USA - Hybrid Riverlane’s mission is to master quantum error correction (QEC) and unlock a new age of human progress. From advances in material and climate science, to complex chemistry simulation for new drug design, quantum computers will help humanity solve some of its most important challenges. But without QEC, the industry’s defining technical challenge, such breakthroughs can never be achieved. Riverlane is the world leader in QEC technology. QEC is a complex problem that requires a range of skills, talent and passion. We recently raised $75 million to accelerate our cutting-edge R&D. We partner with many of the world’s leading quantum computing companies and governments to accelerate their path to utility-scale quantum computers. We’re making remarkable progress and growing fast. Join us! Why Riverlane? As world-leaders in QEC, there’s nowhere quite like Riverlane. Our incredible, cross-disciplinary teams are made up of talented and curious people with diverse backgrounds in physics, math and computer science. As we continue to grow, we’re keen to connect with exceptional talent who share our passion for using cutting-edge science and engineering to solve complex problems that will truly make an impact. Interested in working at Riverlane, but can’t find the perfect role? Apply here! What you will do Whether you want to contribute to cutting-edge research and publications, deliver engaging talks at conferences, come up with novel designs, file patents or support customers to get up to speed with the latest QEC technology, the possibilities are endless. Responsibilities will vary depending on the role, but as a Riverlane employee you can look forward to: • Meaningful, high-impact, technically complex and challenging work, at the cutting-edge of quantum technology: solving QEC, quantum computing’s defining challenge, • Collaboration with world-class experts, • A truly special and unique culture that values curiosity, creativity, and collaboration, in a fun and rewarding environment, • Competitive compensation packages and flexible work arrangements What we look for We look for curious, ambitious, and humble individuals who are excited by the unknown. If you love solving challenging problems and thrive in collaborative, fast-paced environments, where your contributions will really make an impact, you’ll fit right in! You might be: • A Physicist or Researcher exploring new quantum architectures or algorithms, including expertise in QEC or qLDPC, • An Engineer - hardware or software - working on everything from embedded systems and compilers to AI/ML, infrastructure, verification, digital design/FPGA/RTL design, or system integration, • A Data Scientist or Mathematician developing advanced models, simulations, or quantum-inspired algorithms What we value • Technical excellence and scientific curiosity, • Open, collaborative communication, • Resilience and adaptability - scaling deep tech is hard, • Integrity, humility, and a growth mindset What can you expect from us Permanent employees enjoy a comprehensive benefits package that includes: • An annual bonus scheme, private medical insurance, life insurance and 401K contributions, • Equity, so that our team can share in the long-term success of Riverlane, • Generous paid time off, and enhanced family leave, • A diverse work environment that brings together experts in many fields (including software and hardware development, quantum information theory, physics and maths) and over 20 different nationalities, • A learning environment that encourages individual, team and company growth and learning, including training and conference budgets How to register your interest If you’re excited by Riverlane’s mission to enable utility-scale quantum computing by solving QEC, and want to work on meaningful, high-impact work then please register your interest by uploading your CV and a short cover letter by clicking 'Apply Now’. Your cover letter should explain what kind of position you are interested in, and outline what key skills and experience you feel you can bring. Please Note We review general interest applications regularly, but we’re only able to respond when there’s a clear match with an upcoming opportunity. If you see a specific role that aligns with your experience, we encourage you to apply directly - it’s the best way to ensure your application is reviewed promptly. Thank you for your interest in Riverlane and for taking the time to connect with us. If you have any queries, please contact . Everyone is welcome at Riverlane. We are an equal opportunities employer and encourage applications from eligible and suitably qualified candidates regardless of age, disability, ethnicity, gender, gender reassignment, religion or belief, sexual orientation, marital or civil partnership status, or pregnancy and maternity/paternity. Women and other underrepresented groups may be less likely to apply for a role unless they meet all or nearly all of the requirements. If this applies to you, we still encourage you to apply - you may be a great fit, even if you don’t meet every single qualification. We’d love to hear from you.

Job DescriptionAt Lendbuzz, we believe financial opportunity should be more personalized and fair. We develop innovative technologies that provide underserved and overlooked borrowers with better access to credit. From our employees to our dealers, partners, and borrowers, we’ve built a company and a culture around a resolute belief in the promise and power of diversity. We value independent and critical thinking. We are seeking a highly skilled and motivated AI Research Scientist with a PhD in relevant field to lead our initiatives in conversational AI and agentic AI systems. In this role, you will drive the research direction, technical strategy, and execution of next-generation intelligent agents across the organization. You will work closely with engineering, product, and leadership teams to develop, evaluate, and deploy innovative AI capabilities that power real-time, high-impact user experiences. This position is a hybrid role based in Boston, MA, requiring 3 days onsite.Key Responsibilities: • Research Leadership & Technical Direction, • Lead research and development for conversational AI, agentic AI, and multi-step reasoning systems, • Explore and prototype novel architectures, algorithms, and interaction paradigms across text, voice, and multi-modal interfaces, • Develop agent frameworks including prompt architectures, retrieval systems (RAG), planning modules, and tool orchestration pipelines, • Build robust real-time systems including voice streaming, low-latency inference, and continuous context tracking, • Design, fine-tune, and deploy LLM-based and multi-modal models using internal infrastructure, REST APIs, and microservices, • Run systematic experiments to evaluate model quality, reliability, reasoning, and user experience, • Analyze conversational data, agent behavior traces, and performance metrics to guide iterative improvements, • Build and curate high-quality datasets for training and evaluation, including preprocessing, labeling workflows, and data governance, • Ensure data accuracy, reproducibility, and rigor across the research lifecycle, • Partner with product teams to translate research into production features, • Work with engineering teams to ensure reliability, safety, and performance of deployed models, • PhD in Artificial Intelligence, Computer Science, Machine Learning, or a related technical field, • Prior research experience with Machine Learning / AI required, • Strong proficiency in Python, with experience in ML frameworks (e.g., PyTorch) and data tooling (NumPy, Pandas, Scikit-learn), • Demonstrated experience in NLP, LLMs, conversational AI, or machine learning research, • Strong problem-solving skills and ability to operate independently while driving complex research initiatives, • 2+ years of research or applied ML experience in conversational agents, LLM systems, or real-time AI applications, • Experience deploying models or research prototypes to cloud environments

Job DescriptionCompany Description AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at . Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok. Job Description At AbbVie, we are dedicated to solving some of the world’s most complex and serious diseases. Our mission is to develop and deliver advanced therapeutics that change lives. We are looking for talented, passionate, and driven individuals to join our Biotherapeutics and Genetic Medicine (BGM) team. As a Senior Scientist in our siRNA group, you will be part of an innovative team focused on advancing RNA-based therapies that have the potential to revolutionize patient care. AbbVie is looking for a Senior Scientist I to join our siRNA group within the Biotherapeutics and Genetic Medicine (BGM) department. This role will involve designing and executing innovative experimental approaches to address key scientific challenges related to oligonucleotide therapeutics. The successful candidate will drive scientific innovation, identify new methods and techniques, and collaborate across functions to support the development of novel RNA-based therapies. Responsibilities • Lead research efforts within a cross-functional team to advance new therapeutic targets for siRNA-based pipeline development., • Design and execute in vitro and in vivo proof-of-concept studies to evaluate siRNA library and characterize lead compounds for the target engagement and therapeutic benefits., • Design and execute structure-activity-relationship (SAR) studies for lead optimization, including optimization of siRNA sequence, chemical modification patterns, conjugation sites and linkers, etc., • Provide scientific leadership and expertise in candidate nomination and pipeline development., • Work independently and maintain a high level of productivity in the laboratory, ensuring efficiency and scientific rigor., • Analyze and interpret multidisciplinary data to generate actionable conclusions and guide future experimental directions., • Collaborate and effectively communicate results with key stakeholders and cross-functional teams throughout the organization., • Contribute as a primary author to scientific publications, presentations, and/or as a primary inventor of patent applications., • Mentor and support junior scientists within the team.Qualifications, • BS, MS, or PhD in chemistry, molecular biology, biochemistry, or related field with typically 10+ years (BS), 8+ years (MS), or 0-3 years (PhD) of experience., • Demonstrated expertise in siRNA therapeutics, including library design, screening and characterization of SAR., • Demonstrated expertise for siRNA candidate nomination and pipeline development., • Extensive hands-on experience and techniques for molecular and RNA biology, including cell culture, RNA extraction, RNA quantification (RT-PCR, qPCR, ddPCR), next-generation sequencing (NGS) library preparation, protein assays (ELISA, Western Blot, JESS), flow cytometry and other biomarker quantification., • Experience in assay development and high-throughput screening for siRNA target identification and validation, mechanism of action studies, biodistribution and biomarker analysis is a plus., • Strong understanding of ex-hepatic delivery of siRNA is highly desirable., • Proven ability to develop, troubleshoot and refine assays to enhance sensitivity, reproducibility, and throughput., • Highly self-motivated and capable of thriving in a fast-paced, collaborative team environment. How to Apply If you are passionate about advancing RNA-based therapeutics and have a track record of success in cell and molecular biology, we encourage you to apply! Please submit your resume outlining your relevant experience and why you would be a great fit for this position. Additional Information Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law: * The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future. * We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees. * This job is eligible to participate in our short-term incentive programs. Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company’s sole and absolute discretion, consistent with applicable law AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled. US & Puerto Rico only - to learn more, visit US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:

Job DescriptionAbout UsCrescent Biopharma’s vision is to build a world leading oncology company bringing the next wave of therapies for cancer patients. The Company’s clinical-stage pipeline includes its lead program, a PD-1 x VEGF bispecific antibody, as well as novel antibody-drug conjugates. By leveraging multiple modalities and established targets, Crescent aims to rapidly advance potentially transformative therapies either as single agents or as part of combination regimens to treat a range of solid tumors. For more information, visit and follow the Company on LinkedIn and X. Position OverviewCrescent is seeking a Senior Scientist, Bioanalysis to manage bioanalytical activities supporting preclinical and clinical programs. This individual will partner with internal teams and CROs to design, validate/transfer, and oversee bioanalytical assays (e.g., ligand-binding and LC–MS/MS), managing sample analysis, data quality control, interpretation, and reporting to generate high-quality concentration data supporting PK. Responsibilities include planning and authoring bioanalytical documents (plans, protocols, reports), ensuring data integrity and regulatory compliance (GLP/GCP), and managing the operational aspects of outsourced work (budgeting, SOWs, audits, and sample logistics). Responsibilities • Assist in the development and execution of bioanalytical (BA) strategies to meet current and future regulatory and scientific requirements., • Manage the implementation of bioanalytical contracts/SOW, plans, and reports., • Oversee day-to-day operations of CROs: coordination of shipments of test article, necessary reagents and samples, protocol and data review, provide technical assistance, and report review., • Work with internal and external subject matter experts and other relevant disciplines to manage and resolve scientific, technical or quality issues and improve study consistency, quality, efficiency and effectiveness., • Coordinate the bioanalysis activities for individual preclinical/clinical programs to ensure alignment of BA data deliverables., • Contribute to regulatory documents (i.e. IND, CTA, BLA etc.), providing high-quality bioanalytical content and responses to queries., • Conduct scientific audits of CROs in collaboration with the QA department., • Instill and adhere to GLP and GCP regulations, relevant SOPs, protocols, policies and safety procedures.Education & Experience, • PhD or MS in Chemistry, Pharmaceutical Sciences, Pharmacokinetics or related discipline with a minimum of 5 years of industry or related experience., • Strong understanding of bioanalytical technology and methods both for small and large molecules and peptides., • Proven experience managing external CROs (SOWs, timelines, budgets, data review) with excellent organizational and project-management skills., • Well-grounded in drug-development practices—data-driven decision making; contribution to protocols, bioanalytical plans/reports, and clinical study reports., • Ability to work in a dynamic team-oriented environment as demonstrated by participating in and contributing to cross-functional teams., • Small molecule DMPK experience is a plus.What We Offer, • Opportunity to join a mission-driven team where you'll contribute to impactful work, take on varied responsibilities, and grow quickly in a dynamic environment., • Competitive compensation, including base salary, performance bonus, and equity., • 100% employer-paid benefits package., • Flexible PTO., • Two, one-week company-wide shutdowns each year. We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.

Job DescriptionCompany Description The work we do at Eurofins matters, and so do our employees. At Eurofins, we put a focus on your professional growth. We provide our employees the ability to break into the biopharmaceutical industry and grow from the bottom up. We have the supportive teams and tools available to invest in you while also affording you work-life balance and a competitive benefits package. Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies. If you’re looking for a rewarding career, apply with us today! Job Description The Bioreactor Process Development Scientist will support upstream Drug Substance Process Development (DS PD) activities with a strong focus on mammalian cell culture, bioreactor operations, and preparation of critical upstream materials. This role is highly hands‑on, working within tissue culture suites and bioreactor bays to ensure smooth execution of experimental and operational workflows. The scientist will contribute to media preparation, consumables readiness, experimental sampling, and bioreactor manipulations that enable successful process development studies. Key responsibilities include preparing custom tubing assemblies, supporting cell culture media manufacturing, executing routine bioreactor sampling and analytics, and documenting experimental observations in real time. This role requires strong aseptic technique, operational precision, and the ability to work both independently and collaboratively within a fast‑paced development environment. Due to the nature of cell culture work, participation in a rotating weekend coverage schedule is expected. Responsibilities • Support upstream DS PD activities by preparing and organizing critical consumables for use in tissue culture suites and bioreactor bays., • Prepare custom tubing sets and assemblies used in bioreactor operations; package and sterilize assemblies via autoclaving as instructed., • Assist with the preparation and aliquoting of pre-made cell culture media., • Provide periodic support to cell culture media manufacturing operations as needed., • Perform routine bioreactor manipulations, including sampling, metabolite analysis, cell counts, and media exchanges, during weekday operations., • Participate in rotating weekend coverage to support ongoing cell culture and bioreactor studies., • Record real-time observations, data, and measurements following established procedures, work instructions, job aids, and SOPs., • Maintain high standards of safety and compliance with all applicable local, state, federal, and company EHS guidelines.Qualifications Basic Qualifications • B.S. with 2+ years of relevant experience, or M.S. with 0+ years of experience in a biology-, chemistry-, or engineering-focused discipline., • Prior experience working in a BSL1+ wet laboratory environment., • Demonstrated proficiency in aseptic technique and hands-on work in biosafety cabinets., • Strong foundation in mammalian cell culture., • Experience operating bioreactors, peristaltic pumps, and TPE tube welders., • Strong organizational skills with the ability to manage time, prioritize tasks, and troubleshoot experimental issues., • Excellent written and verbal communication abilities., • Ability to design experiments, interpret data, maintain accurate records, and follow procedural documentation., • Ability to work independently and collaboratively; demonstrates motivation, adaptability, and a positive, team-oriented attitude., • Experience working with stem cells in a BSL2+ environment., • Familiarity with electronic lab notebook (ELN) documentation systems., • Authorization to work in the United States indefinitely without restriction or sponsorship. Additional Information The position is full-time, Monday through Friday, with rotating work on weekends (2-4 hours per day). Candidates currently living within a commutable distance of Boston, MA are encouraged to apply. • Comprehensive medical coverage, dental, and vision options, • Life and disability insurance, • 401(k) with company match, • Paid vacation and holidays Apply today and join a team that’s making a difference in science every day. Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Job DescriptionCompany Description AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at . Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok. Job Description At AbbVie, we are dedicated to solving some of the world’s most complex and serious diseases. Our mission is to develop and deliver advanced therapeutics that change lives. We are looking for talented, passionate, and driven individuals to join our Biotherapeutics and Genetic Medicine (BGM) team. As a Senior Scientist in our siRNA group, you will be part of an innovative team focused on advancing RNA-based therapies that have the potential to revolutionize patient care. AbbVie is looking for a Senior Scientist I to join our siRNA group within the Biotherapeutics and Genetic Medicine (BGM) department. This role will involve designing and executing innovative experimental approaches to address key scientific challenges related to oligonucleotide therapeutics. The successful candidate will drive scientific innovation, identify new methods and techniques, and collaborate across functions to support the development of novel RNA-based therapies. Responsibilities • Lead research efforts within a cross-functional team to advance new therapeutic targets for siRNA-based pipeline development., • Design and execute in vitro and in vivo proof-of-concept studies to evaluate novel extrahepatic, targeted siRNA delivery platforms across multiple pipeline programs., • Design and execute receptor expression profiling, ligand–receptor binding, internalization, and trafficking assays., • Evaluate functional delivery and target knockdown in receptor-positive cells and tissues., • Provide scientific leadership and expertise in candidate nomination and pipeline development., • Work independently and maintain a high level of productivity in the laboratory, ensuring efficiency and scientific rigor., • Analyze and interpret multidisciplinary data to generate actionable conclusions and guide future experimental directions., • Collaborate and effectively communicate results with key stakeholders and cross-functional teams throughout the organization., • Contribute as a primary author to scientific publications, presentations, and/or as a primary inventor of patent applications., • Mentor and support junior scientists within the team.Qualifications, • BS, MS, or PhD in chemistry, biology, biochemistry, pharmacology or related field with typically 10+ years (BS), 8+ years (MS), or 0-3 years (PhD) of experience., • Demonstrated expertise in siRNA candidate nomination and pipeline development., • Demonstrated experience in drug delivery platforms, receptor biology and targeted delivery., • Hands on experience of uptake, trafficking, and functional delivery assays., • Extensive hands-on experience and techniques for molecular and RNA biology, including cell culture, RNA extraction, RNA quantification (RT-PCR, qPCR, ddPCR), next-generation sequencing (NGS) library preparation, protein assays (ELISA, Western Blot, JESS), flow cytometry and other biomarker quantification., • Experience in assay development and high-throughput screening for siRNA target identification and validation, mechanism of action studies, biodistribution and biomarker analysis is a plus., • Proven ability to develop, troubleshoot and refine assays to enhance sensitivity, reproducibility, and throughput., • Highly self-motivated and capable of thriving in a fast-paced, collaborative team environment. How to Apply If you are passionate about advancing RNA-based therapeutics and have a track record of success in cell and molecular biology, we encourage you to apply! Please submit your resume outlining your relevant experience and why you would be a great fit for this position. Additional Information Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law: * The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time ofthis posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location,and we may ultimately pay more or less than the posted range. This range may be modified in the future. * We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees. * This job is eligible to participate in our short-term incentive programs. Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of anybonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's soleand absolute discretion unless and until paid and may be modified at the Company’s sole and absolute discretion, consistent with applicable law. AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled. US & Puerto Rico only - to learn more, visit US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more: