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Job Description Why Join Us? As a member of the Parabilis Medicines team, you will be a part of an organization dedicated to creating extraordinary medicines for diseases with urgent unmet needs, harnessing our proprietary peptide platform to transform treatment possibilities for patients. Parabilis is a clinical-stage biopharmaceutical company dedicated to unlocking high-impact protein targets long-considered undruggable. The company has developed a new class of stabilized, cell-penetrant alpha-helical peptides – Helicons™ – capable of modulating intracellular proteins that are inaccessible to traditional drug modalities. Headquartered in Cambridge, Mass., Parabilis is advancing a focused pipeline of multiple first-in-class therapies across both rare and common cancers. Its lead asset, zolucatetide (FOG-001), is a first-in-class, clinically validated direct inhibitor of the interaction between β-catenin and the T-cell factor (TCF) family of transcription factors, implicated in millions of cancer cases annually, including in colorectal cancer, desmoid tumors, hepatocellular carcinoma and a range of other Wnt/β-catenin-driven tumors. In Phase 1 clinical trials, zolucatetide produced the first-ever clinical evidence that it can directly inhibit this interaction, once previously considered "undruggable" despite its role across multiple cancer types. Parabilis is also advancing investigational degraders of ERG and ARON into clinical development for the treatment of prostate cancer, as well as progressing other preclinical programs. Backed by a recent $305 million Series F financing, Parabilis is entering an exciting phase of growth and execution. What's the opportunity? We are seeking a highly talented and self-motivated person to contribute to the development of the Computational Drug Discovery group, a strategic function in Data Science that is part of Parabilis's platform discovery engine for HeliconTM stapled-peptide drugs. The skill sets of the group includes state-of-the-art machine learning/generative AI, molecular modeling, cheminformatics and data science towards the discovery and development of HeliconTM stapled-peptide drugs. You'll be part of a data science team that is a central pillar of Parabilis's innovative discovery platform and pipelines targeting "undruggable" genes of major therapeutic interest to patients. Our data science team is an integrated team, ranging from computational biology, bioinformatics, computational drug discovery, research informatics and engineering. We work at the interface of chemistry, biology, clinical and computational sciences, and are responsible for all aspects of data science, from building the discovery pipeline to supporting and developing our discovery . Responsibilities • Provide computational expertise towards, but not limited to, ternary complex designs for degraders and other proximity-based modalities, hit-to-lead progression using multi-objective optimization, initiating new projects, new drug-target assessments and advancing drug-pipeline projects towards the clinic., • Identify, implement, and apply 3D modeling techniques for sampling HeliconTM peptide conformations in presence of a target, in ternary complex, and in different physiological environments., • Analyze and derive 3D peptide-structure relationships., • Exemplify scientific leadership by partnering across functions and working within a team of talented and passionate scientists to discover drugs., • PhD in Computational Chemistry, Protein Engineering, Chemistry, Physics, Macromolecular sciences or close-related field, • 5+ years of pharma/biotech industry experience in computational rational drug ., • Demonstrated experience with ternary complex design and understanding, peptide design or protein engineering and a good understanding of peptide structure-property relationships (e.g. helicity and amphiphilicity metrics, cell penetration)., • Demonstrated mastery of modern computational chemistry including, but not limited to, peptide folding and docking, use of co-folding foundation models, such as Boltz, structure-based design (receptor and ligand-based), scaffold hopping, docking and conformational analysis., • An understanding of modern drug discovery including, but not limited to, medicinal chemistry, multi-parametric optimization, molecular recognition principles, and the ability to adapt and translate these principles to stapled peptides., • Excellent communication and collaboration skills, with the ability to work well in a multidisciplinary environment, • Excellent organizational skills and attention to detail, with a strong passion for learning new concepts and technologies, • Expertise in one or more peptide modeling environments (e.g. ICM, Rosetta, Amber, GROMACS) and methods (enhanced sampling MD, Monte Carlo, MSM)., • Demonstrated understanding of critical assessment of molecule-property data and predictive model quality., • Demonstrated understanding of experiments behind the data that can be translated to computational analysis., • Experience with command line modeling applications., • Familiarity with cloud computing environments., • Strong scientific programming skills (Python) in a Linux environment., • Experience with enterprise research informatics systems such as Dotmatics and chemical and biological data warehouses is a plus., • Familiarity with concepts in machine learning., • Familiarity with cheminformatics techniques is a plus., • Familiarity with use of LLMs and IDEs, such as Cursor, to enhance workflows, productivity and innovation is a plus. Parabilis is a team of passionate pioneers who are trailblazing the future of precision medicine with the aim of making a meaningful difference in the lives of patients. The company is committed to promoting an inspiring and flourishing working environment for all employees across the business, in all departments, and driving innovation for patient benefit. • Growth-Minded. We're inventing a new class of medicines—one applicable to therapeutic targets that have been dreamt about, but always considered impossible to drug. Our work requires us to be curious, humble and adaptable., • In(ter)dependent.We are fiercely independent as a leader in defying the limitations of current therapeutic modalities, and interdependent as a team as we work collaboratively to shift drug discovery paradigms and provide patients with better treatment options., • Patient-focused.We are deeply focused on patient outcomes, and all energy in the company is focused on science as it translates to patient impact. As an equal opportunity employer, Parabilis values an inclusive workplace and welcomes applicants of all backgrounds and experiences. All qualified applicants will receive consideration for employment without discrimination on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability, or any other factors prohibited by law.

Job DescriptionCompany Description By working at Harvard University, you join a vibrant community that advances Harvard's world-changing mission in meaningful ways, inspires innovation and collaboration, and builds skills and expertise. We are dedicated to creating a diverse and welcoming environment where everyone can thrive. The HBS AI Institute is a global research center that provides research-driven insights, accessible to anyone in the world, on using AI and digital technologies to advance business and society. Founded on the premise that AI technology is only half the answer and that businesses must also revamp their processes to harness AI’s potential, the Institute is made up of an unbiased, multidisciplinary team of researchers and scientists, business leaders, and entrepreneurs. Job Description Job Summary: As a Senior Data Scientist, you will be a key member of the HBS AI Institute's Data Science Team, working closely with Harvard Business School (HBS) faculty and researchers on research projects in the social sciences related to business and management, digital transformation, data science and artificial intelligence. Specifically, you will be working with HBS faculty to leverage AI and investigate its implications for business and society through experimental research. You will also play a role in developing and disseminating ML and AI-based tools for the research community. Because you will act as an expert guide and resource for researchers with a wide range of abilities and knowledge relating to data methodologies and emerging technologies, a substantial component of the role is effective communication about technologies. Additionally, the ability to learn new skills on the fly, to keep up with emerging technologies, and to transition comfortably among multiple ongoing projects of varying size and complexity, are all crucial. Job-Specific Responsibilities: • Extract, clean, explore, and analyze data collected from various sources, including organizational data, public data, and experimental data, • Participate in the intake and assignment of projects in the HBS AI Institute Data Science Team, • Design and execute data science and AI experiments with partner organizations., • Create and implement a variety of models and analyses and be able to extract insights and inform strategy from them., • Create and maintain clear documentation of data files, modeling choices, rationale, results, and annotated code and readme files., • Present and explain data science methods and findings to faculty, managers and other non-technical stakeholders at HBS AI Institute., • Provide training and mentorship of other data scientists, research scientists, post-doctoral fellows, research assistants, and PhD students., • Troubleshoot complex problems and device a strategy of seeking solutions in collaboration with other data scientists., • Document and disseminate findings., • Build trust and collaboration by being present on-site and engaging directly with colleagues and various constituents., • Responsible for other duties as assigned.Qualifications Basic Qualifications: • Minimum of seven years’ post-secondary education or relevant work experience, • Master’s or PhD in one of the following disciplines: Computational Sciences in either Physics, Biology, Neuroscience, Statistics, Applied Mathematics, Computer Science or another quantitative field, • Minimum of 5 years of experience in data science or related quantitative role., • Experience with R, Python, SQL, and related languages., • Experience with AWS (RDS, EC2, S3, etc.) preferred or with Azure or Google Cloud., • Experience with supervised and unsupervised ML methods., • Advanced Statistical Expertise: Extensive experience with statistical modeling and regression analysis, including hypothesis testing and causal analysis., • Familiarity with LLM API use for research purposes. Additional Qualifications and Skills: • Ability to handle multiple projects, stakeholders and demands, • Strong team player with excellent verbal and written communication skills, • Experience with data visualization tools, • Experience prototyping products for research purposes Additional Information • Standard Hours/Schedule: 40 hours per week, • Visa Sponsorship Information: Harvard University is unable to provide visa sponsorship for this position, • Pre-Employment Screening: Identity, Education, • Other Information:, • This is a hybrid position which we consider to be a combination of remote and onsite work at our Boston, MA based campus. HBS expects all staff to be onsite a minimum of 3 days per week and departments provide onsite coverage Monday – Friday. Specific hours and days onsite will be determined by business needs and are subject to change with appropriate advanced notice., • As part of our evaluation, candidates are required to complete a take-home assignment/assessment after clearing the technical screen. This position has been determined by school or unit leaders that some of the duties and responsibilities can be effectively performed at a non-Harvard location. The work schedule and location will be set by the department at its discretion and based upon operational needs. When not working at a Harvard or Harvard-designated location, employees in hybrid positions must work in a Harvard registered state in compliance with the University’s Policy on Employment Outside of Massachusetts. Additional details will be discussed during the interview process. Certain visa types and funding sources may limit work location. Individuals must meet work location sponsorship requirements prior to employment. Salary Grade and Ranges This position is salary grade level 059. Please visit Harvard's Salary Ranges to view the corresponding salary range and related information. Benefits Harvard offers a comprehensive benefits package that is designed to support a healthy work-life balance and your physical, mental and financial wellbeing. Because here, you are what matters. Our benefits include, but are not limited to: • Generous paid time off including parental leave, • Medical, dental, and vision health insurance coverage starting on day one, • Retirement plans with university contributions, • Wellbeing and mental health resources, • Support for families and caregivers, • Professional development opportunities including tuition assistance and reimbursement EEO/Non-Discrimination Commitment Statement Harvard University is committed to equal opportunity and non-discrimination. We seek talent from all parts of society and the world, and we strive to ensure everyone at Harvard thrives. Our differences help our community advance Harvard's academic purposes. Harvard has an equal employment opportunity policy that outlines our commitment to prohibiting discrimination on the basis of race, ethnicity, color, national origin, sex, sexual orientation, gender identity, veteran status, religion, disability, or any other characteristic protected by law or identified in the university's non-discrimination policy. Harvard's equal employment opportunity policy and non-discrimination policy help all community members participate fully in work and campus life free from harassment and discrimination.

Job Description About the Team STR's Analytics and C2 Division researches and develops novel technologies to solve challenging national security problems through advanced analytics. Our team consists of passionate and motivated engineers and scientists with advanced degrees in engineering, computer science, mathematics, physics, and data science. We use our expertise and creativity to take innovative ideas from conception to mature implementation to improve mission success of our customers. The Signals Exploitation and Tracking (SET) Group in the Analytics and C2 Division focuses on applying machine learning, statistics, estimation theory, and information theory algorithms for signals exploitation, target tracking, predictive analytics, and system resource management. The Role As a Lead Research Scientist at STR, you will help develop disruptive technologies focused on signals exploitation, estimation theory, system resource management, and systems analysis. You will lead the development of cutting-edge AI/ML algorithms for novel application domains and modalities, participate on and lead project teams, and interact with customers. You will explore fascinating datasets, develop cutting-edge algorithmic techniques, and solve high-impact, unique problems for our customers. We are looking for someone to join our team onsite as this position is based primarily in the Woburn, MA office. Who you are: • MS with at least 8 years of experience, and/or PhD with at least 5 years of experience (or equivalent experience) in a scientific field such as applied math, physics, electrical engineering, computer science, or data science, • Experience building neural networks using standard deep learning tools (e.g., PyTorch, JAX, TensorFlow), including implementing new layers/network architectures, model training, hyperparameter tuning, and ablation studies, • Experience adapting novel machine learning approaches (e.g., from academic literature) to new data sets and problems, • Experience with standard data science tools such as scikit-learn, Pandas, and Matplotlib, • Proficiency in one or more programming languages: Python, C/C++, • Able to work, collaborate on, and lead multi-disciplinary teams, • Able to communicate technical foundations of models and algorithms to technical and non-technical audiences, • Active US government security clearance, • Experience applying deep learning to domains other than images/text, such as time series, discrete event sequence, or geospatial, • Experience with self-supervised machine learning, • Expertise working with time series, geospatial, and/or spatio-temporal data The salary range listed is based on external market data. Offers are based on factors, such as but not limited to, the candidate's experience, education, training, key skills/critical skills, security clearances, and prevailing market and business conditions. STR is a growing technology company with locations near Boston, MA, Arlington, VA, near Dayton, OH, Melbourne, FL, and Carlsbad, CA. We specialize in advanced research and development for defense, intelligence, and national security in: cyber; next generation sensors, radar, sonar, communications, and electronic warfare; and artificial intelligence algorithms and analytics to make sense of the complexity that is exploding around us. STR is committed to creating a collaborative learning environment that supports deep technical understanding and recognizes the contributions and achievements of all team members. Our work is challenging, and we go home at night knowing that we pushed the envelope of technology and made the world safer. STR is not just any company. Our people, culture, and attitude along with their unique set of skills, experiences, and perspectives put us on a trajectory to change the world. We can't do it alone, though - we need fellow trailblazers. If you are one, join our team and help to keep our society safe! Visit us at for more info. STR is an equal opportunity employer. We are fully dedicated to hiring the most qualified candidate regardless of race, color, religion, sex (including gender identity, sexual orientation and pregnancy), marital status, national origin, age, veteran status, disability, genetic information or any other characteristic protected by federal, state or local laws. If you need a reasonable accommodation for any portion of the employment process, email us at and provide your contact info. Pursuant to applicable federal law and regulations, positions at STR require employees to obtain national security clearances and satisfy the requirements for compliance with export control and other applicable laws.

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. #LI-Remote We value diversity and believe the unique contributions each of us brings drives our success. We do not discriminate on the basis of race, sex, religion, color, national origin, gender identity, age, marital status, veteran status, or disability status. 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). Mandatory Employer Disclosures: Notice to Illinois applicants: Applicants are not obligated to disclose expunged juvenile records or adjudication, arrest, or conviction. Notice to Connecticut applicants: OneStudyTeam may require applicants to submit to a urinalysis drug test in connection with an application for employment. Notice to Arizona, Georgia, Indiana, and North Dakota applicants: OneStudyTeam complies with applicable laws prohibiting smoking in and around places of employment. Notice to 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. Notice to Rhode Island applicants: OneStudyTeam complies with Rhode Island law prohibiting smoking in enclosed areas within places of employment. OneStudyTeam is also subject to is subject to Chapters 29–38 of Title 28 of the Rhode Island General Laws. Notice to Maryland applicants: UNDER MARYLAND LAW, AN EMPLOYER MAY NOT REQUIRE OR DEMAND, AS A CONDITION OF EMPLOYMENT, PROSPECTIVE EMPLOYMENT, OR CONTINUED EMPLOYMENT, THAT AN INDIVIDUAL SUBMIT TO OR TAKE A LIE DETECTOR OR SIMILAR TEST. AN EMPLOYER WHO VIOLATES THIS LAW IS GUILTY OF A MISDEMEANOR AND SUBJECT TO A FINE NOT EXCEEDING $100.

Job Description Zoox is on an ambitious journey to develop a full-stack autonomous vehicle system for cities. We are seeking a Staff Data Scientist to join a verification and validation team that evaluates safety-critical AI systems. You will join a team of software and data engineers that leverage methods including log data analysis, simulation, and closed-course structured testing. You'll work cross-functionally with AI software, System Design and Mission Assurance, Simulation, Sensors, and other teams to develop, execute, and iterate on validation methods and pipelines. These pipelines evaluate safety-critical systems, are highly visible, and are an important critical path element of launching our service. The ideal candidate brings a hybrid of statistical rigor and engineering mindset to drive clarity from ambiguity, establish new processes, and propel the team forward. This is a deeply technical and hands-on role where you will be expected to be a self-sufficient builder and coder, not just a manager of projects. In this role, you will: * Design Evaluation Frameworks: Architect statistical methodologies for safety-critical AI systems to form objective, rigorous conclusions about their performance and reliability. * Conduct Robust Analysis: Deliver validation evidence to support increasingly complex operations and identify potential edge-case failures. * Inform Strategy: Deliver clear, data-driven insights to development teams to guide system improvement, and to executive leadership to inform milestone-level go/no-go decisions. * Define Metrics: Drive alignment across engineering teams on performance metrics and data extraction strategies. * Lead the Lifecycle: Manage all phases of evaluation including prototyping, requirements capture, design, implementation, and validation. * Scale Pipelines: Partner with engineers to build and maintain scalable data processing and simulation pipelines, applying distributed computing to analyze petabytes of driving data. Qualifications: • MS or PhD in Statistics, Computer Science, Machine Learning, Applied Mathematics, or related quantitative field, • Proficiency in Python and SQL with experience in production-quality code, • Demonstrated expertise in statistical methodologies including hypothesis testing, power analysis, spatiotemporal modeling, Bayesian inference, and multivariate analysis., • Experience with large-scale data analysis and statistical modeling, • Proficiency with Git, unit testing, and collaborative development practicesBonus Qualifications: Hands-on experience with production machine learning pipelines: dataset creation, training frameworks, metrics pipelines * Experience with modern data processing technologies such as Apache Spark, Spark SQL, and Databricks * Experience with designing metrics and delivering actionable insights that drive business decisions There are three major components to compensation for this position: salary, Amazon Restricted Stock Units (RSUs), and Zoox Stock Appreciation Rights. A sign-on bonus may be offered as part of the compensation package. The listed range applies only to the base salary. Compensation will vary based on geographic location and level. Leveling, as well as positioning within a level, is determined by a range of factors, including, but not limited to, a candidate's relevant years of experience, domain knowledge, and interview performance. The salary range listed in this posting is representative of the range of levels Zoox is considering for this position. Zoox also offers a comprehensive package of benefits, including paid time off (e.g. sick leave, vacation, bereavement), unpaid time off, Zoox Stock Appreciation Rights, Amazon RSUs, health insurance, long-term care insurance, long-term and short-term disability insurance, and life insurance. 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 Description About the Team The Maritime Domain Awareness Group (MDA) develops and delivers advanced signal processing algorithms and techniques for airborne radar and passive optical systems. MDA fosters a culture of innovation, collaboration, and execution. We develop and analyze cutting edge algorithms for detection and exploitation of signals in high clutter and noise environments using both classical, physics-based approaches, and big data-driven artificial intelligence and machine learning (AI/ML) techniques. If you are seeking an opportunity to apply your deep technical knowledge and creativity in a fast-paced, challenging environment to make a lasting impact, we invite you to join us. The Role We are seeking a Principal Scientist to lead the development of next-generation signal processing capabilities for airborne passive optical sensing systems supporting critical national security missions. In this role, you will guide teams of scientists and engineers in designing advanced algorithms and processing architectures that enable the detection, characterization, and exploitation of targets operating in low signal-to-noise and highly cluttered environments. You will apply first-principles physics, statistical signal processing, and advanced modeling and simulation to understand complex operational environments and drive the development of end-to-end processing solutions—from raw sensor phenomenology and calibration through detection, tracking, and classification. This role requires the ability to integrate knowledge across optics, sensing phenomenology, atmospheric effects, signal processing, and machine learning to develop robust solutions that transition from research prototypes into operational systems. As a senior technical leader, you will help shape the technical vision and strategy for passive optical sensing within the organization, identifying emerging mission challenges, defining research directions, and guiding the development of technologies that address future operational needs. What You Will Do: • Lead multidisciplinary teams in the design, development, and maturation of advanced signal processing algorithms for airborne passive optical sensing systems, • Apply physics-based modeling and simulation to understand sensing phenomenology, clutter environments, and environmental effects impacting sensor performance, • Architect and develop end-to-end processing chains, including sensor modeling, calibration, detection, tracking, and target classification algorithms, • Identify and pursue novel algorithmic approaches for detecting and exploiting low-SNR signals in complex environments, • Collaborate closely with program leadership, government sponsors, and external partners to shape technical direction and align research with mission needs, • Mentor and guide scientists and engineers, helping develop the next generation of technical leaders within the organization, • Drive the transition of research algorithms into operational software and deployed capabilities, • Ability to obtain and maintain a security clearance, for which U.S. citizenship is needed by U.S. Government, • BA, or MS in Physics, Applied Mathematics, Electrical Engineering, or related technical discipline, • 10-12+ years of relevant work experience, • Expertise in two or more of the following areas:, • Signal processing, Fourier analysis, linear estimation, optimization, adaptive signal processing, AI/ML algorithm development, algorithm development, modeling & simulation, systems engineering, optics modelling, • Experience building and delivering technical briefs to peers, senior level executives, and customers, • Proficiency in one or more scientific or mathematical programming languages, such as MATLAB, Python, and C/C++, • Experienced researcher and team member who is excited to work with mission partners to leverage cutting-edge technology and research for immediate impact, • Excellent communicator and briefer, who is comfortable communicating with both technical and non-technical audiences, • Active Secret or TS/SCI Clearance, • Demonstrated leadership of complex research, development, and engineering efforts, • Experience with:, • Passive optical technologies in the defense sector, particularly airborne, downward-looking sensors, • Computer vision techniques such as feature identification/matching/tracking, optical flow, background subtraction, etc, • Interacting with decision-makers and customers to translate mission needs into an end-to-end solution The salary range listed is based on external market data. Offers are based on factors, such as but not limited to, the candidate's experience, education, training, key skills/critical skills, security clearances, and prevailing market and business conditions. STR is a growing technology company with locations near Boston, MA, Arlington, VA, near Dayton, OH, Melbourne, FL, and Carlsbad, CA. We specialize in advanced research and development for defense, intelligence, and national security in: cyber; next generation sensors, radar, sonar, communications, and electronic warfare; and artificial intelligence algorithms and analytics to make sense of the complexity that is exploding around us. STR is committed to creating a collaborative learning environment that supports deep technical understanding and recognizes the contributions and achievements of all team members. Our work is challenging, and we go home at night knowing that we pushed the envelope of technology and made the world safer. STR is not just any company. Our people, culture, and attitude along with their unique set of skills, experiences, and perspectives put us on a trajectory to change the world. We can't do it alone, though - we need fellow trailblazers. If you are one, join our team and help to keep our society safe! Visit us at for more info. STR is an equal opportunity employer. We are fully dedicated to hiring the most qualified candidate regardless of race, color, religion, sex (including gender identity, sexual orientation and pregnancy), marital status, national origin, age, veteran status, disability, genetic information or any other characteristic protected by federal, state or local laws. If you need a reasonable accommodation for any portion of the employment process, email us at and provide your contact info. Pursuant to applicable federal law and regulations, positions at STR require employees to obtain national security clearances and satisfy the requirements for compliance with export control and other applicable laws.

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 Vice President, Head of Clinical R&D (HoC) – Solid Biosciences Charlestown HQ preferred Solid Biosciences is a precision genetic medicine company focused on advancing a portfolio of gene therapy candidates targeting rare neuromuscular and cardiac diseases, including Duchenne muscular dystrophy (Duchenne), Friedreich’s ataxia (FA), catecholaminergic polymorphic ventricular tachycardia (CPVT), TNNT2-mediated dilated cardiomyopathy, BAG3-mediated dilated cardiomyopathy, and additional fatal, genetic cardiac diseases. We are advancing a diverse pipeline and delivery platform in the pursuit of uniting experts in science, technology, disease management, and care. Patient-focused and founded by those directly impacted by Duchenne, Solid’s mission is to improve the daily lives of patients living with devastating rare diseases. We are seeking a Vice President, Head of Clinical R&D to work as a strategic partner with the CMO, and other members of the Executive team to provide strategic direction and technical leadership to the clinical R&D and clinical scientist groups and is responsible for the overall management, direction and performance of Phase I-IV for drug products, including: overseeing clinical development and pharmacovigilance according to agreed-upon deadlines and budgets, clinical trial design, implementation and execution, clinical research, data analysis and management. The HoC also provide strategic direction and technical leadership to the clinical R&D and clinical scientist groups in their role to guide translational development and clinical guidance and planning for Lead and IND Candidate programs as well as for evaluation, input and direction on potential partnering/business development opportunities. The HoC works in partnership with the CMO to establish the clinical research vision and regulatory roadmap for the company including standards and policies designed to ensure the quality and outcomes of compounds under development. The HoC in collaboration with the CMO and the rest of the Executive team will have over-arching responsibility for the successful clinical development of Solid’s pipeline programs including development of a clinical roadmap for all compounds. This role will report to the Chief Medical Officer and can be based in Solid’s Corporate Headquarters located in Hood Park in Charlestown, MA or work remotely from the East Coast. Key Position Responsibilities • Provide oversight and leadership of the various functional areas: Clinical R&D (medical directors and therapeutic area heads), clinical science, medical monitoring, pharmacovigilance, • Work collaboratively with the Research function, providing input into design of preclinical trials to support drug products from Lead through candidate phase as they enter in the clinic and including but not limited to CDP development, TPP development and IND/CTA clearance along with associated activities., • Close collaboration with Patient Advocacy to ensure patient centricity from product conception, through clinical trial conduct into and through commercial launch and to work collaboratively to ensure the voice of the patient is represented in all decisions and actions and to ensure the voice of the physician is appropriately presented., • Experience managing multiple programs across multiple geographies, • Input into the development of key marketing materials., • Research and identify new opportunities and novel therapeutic opportunities that augment the company’s mission, vision, values, and goals, • Establish and maintain relationships with principal investigators and KOL’s to ensure that the Company has a clear understanding of clinician needs and requirements., • Represent and manage communication of Solid’s clinical and regulatory programs to diverse audiences including: the executive team, regulatory agencies including the FDA and EMA, investors, Board of Directors, and other key stakeholders., • To assist in communications with other pharmaceutical companies and partners to identify and implement collaborative studies, regulatory activities, and other programs that align with the company’s strategy and goals., • Attract, motivate, retain and lead a highly skilled clinical development and regulatory team., • Maintain current understanding of competitors and clinical developments in relevant therapeutic areas by attending scientific presentations and reviewing relevant literature., • Other related ad hoc duties and projects as required., • Dedicated to maintaining and or adapting our clinical R&D structure and cross functional matrix relationships that empower colleagues, leverage and optimally harness their talents and maximizes their opportunities for promotion and advancement, • Dedicated to providing a dynamic working environment for mentorship and professional growth of clinical R&D colleagues. Experience Requirements • Board Certified MD with medical research and drug development experience., • MD with regenerative medicine (such as AAV) preferred, • MD with experience in neuromuscular and or cardiovascular rare disease space preferred., • Proven leader of high potential high performing teams., • Prior experience in clinical development leadership roles (preferably global experience) across all phases of clinical studies. Demonstrated capabilities leading clinical programs to successful filing and approval in both US and globally., • Experience interacting with the FDA/EMA and knowledge of GCP clinical requirements, general regulatory requirements, and relevant regulatory guidance documents pertinent to the Company., • Excellent interpersonal and communication skills with ability to relate to both internal and external stakeholders. Ability to develop strong relationships with Executive team and Board of Directors., • Able to foster and nurture a company culture grounded in science and ethics. Key Position Attributes This role should have an expectation of 20% travel and may require significant travel on an ad hoc basis. Compensation The base compensation range for this role is: $290,000 - $400,000. Base salary offered is determined through an internal analysis utilizing a combination of factors including, but not limited to, relevant skills & experience, job location, and internal equity. Regular employees are eligible to receive both short-term and long-term incentives, including cash bonus and equity incentive opportunities, designed to reward individual performance and align incentives to Solid’s long term company performance. Benefits and Solid Advantages At Solid Biosciences we offer a highly competitive total rewards and benefits package, intended to support all aspects of our employees’ lives and well-being. Additionally, for those employees working onsite at our Hood Park Headquarters, we offer a variety of onsite resources to support those working in our offices. • Competitive Health and Dental programs with flexible plan offerings, including FSA and HSA programs, • 401(k) program participation with competitive company matched contributions, • Eligibility to participate in Solid’s Employee Stock Purchase Plan, • Mobile phone subsidy for eligible employees, • Tuition Reimbursement, • Vision Coverage, • Life Insurance, • Voluntary Pet Insurance, • Employee Discount Program on Travel, Entertainment, and Services, • Employee Assistance Programs, • Daily Subsidized Lunch Delivery (onsite @ Hood Park), • Free Onsite Full-Service Gym (onsite @ Hood Park), • Employee Parking (onsite @ Hood Park), • 12 Observed Holidays and a winter shut down, • 15-day PTO Policy and a 40-hour rollover YoY, • 40-hour Sick Policy, • 8 Hour Floating Holiday

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 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. Within AbbVie’s Biotherapeutics and Genetic Medicine (BGM) organization, our siRNA team is advancing therapeutic programs from early discovery through development, applying rigorous biology and data-driven decision making to build differentiated RNA medicines. AbbVie is seeking a Senior Scientist I with deep, hands-on expertise in siRNA therapeutic discovery to join the siRNA group within Biotherapeutics and Genetic Medicine (BGM). 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. This role is best suited for candidates with direct, hands-on experience in therapeutic siRNA discovery, where siRNA biology directly informed experimental and program-level decisions. Responsibilities • Independently lead in vitro siRNA discovery biology, including experimental strategy, assay design, execution, data analysis, and interpretation in support of active therapeutic programs., • Design, optimize, and validate fit-for-purpose assays that directly inform siRNA potency, durability, specificity, and mechanism-of-action., • Drive scientific decision making by integrating siRNA knockdown data with orthogonal readouts (protein, functional, and transcriptomic endpoints)., • Identify and resolve key biological and technical risks related to siRNA activity, delivery, and on-target effects., • Work with cross-functional partners (chemistry, delivery, bioinformatics, in vivo biology) to advance siRNA candidates through discovery milestones., • Maintain high experimental rigor and productivity while operating with minimal supervision., • Author internal technical reports and contribute as a primary author on publications and/or inventor on patents.Qualifications, • BS, MS, or PhD in Cell Biology, Molecular Biology, Biochemistry, or related field with typically 10+ years (BS), 8+ years (MS), or 0-3 years (PhD) of relevant experience., • Demonstrated, hands-on experience in siRNA therapeutic discovery is required, including ownership of in vitro siRNA studies that informed go/no-go, lead selection, or optimization decisions., • Extensive experience with mammalian cell culture and molecular biology techniques directly supporting siRNA programs, including RNA isolation, qPCR, ELISA, Western blot, and nucleic acid sequencing (NGS/Sanger)., • Proven ability to independently troubleshoot siRNA-specific challenges (e.g., variability in knockdown, assay sensitivity limits, off-target interpretation)., • Strong hands-on experience with stem-loop RT-qPCR, including assay design, optimization, validation, and data interpretation for siRNA and target mRNA quantification., • Direct experience supporting antibody-based or antibody-enabled delivery strategies, including antibody conjugates or biologics-related development., • Hands-on experience analyzing RNA-seq data generated from siRNA perturbation studies, including differential expression analysis and biological interpretation., • Experience with siRNA sequence design and optimization, including target site selection and evaluation of structure–activity relationships., • Familiarity with CNS-relevant biology and genetic medicine applications., • Working knowledge of bioinformatics tools or scripting (e.g., R, Python) to interrogate high-dimensional RNA datasets. How to Apply If you have deep, hands-on experience in siRNA therapeutic discovery and are motivated to drive rigorous, data-driven biology in support of RNA medicines, we encourage you to apply. Please submit your resume highlighting your direct contributions to siRNA programs. 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 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 with 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 your 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 of 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 This role supports the synthesis, purification, and analysis of oligonucleotides using established laboratory methods and instrumentation. The individual will work collaboratively within a chemistry team to ensure high‑quality experimental output while maintaining accurate documentation and laboratory standards. Key Responsibilities * Synthesis: Assist in the synthesis of oligonucleotides using automated synthesizers. Prepare reagents accurately, follow established protocols, and ensure proper reaction conditions are maintained throughout synthesis runs. * Purification: Perform oligonucleotide purification using techniques such as Fast Protein Liquid Chromatography (FPLC) and High Performance Liquid Chromatography (HPLC). Monitor purification processes and assess results to ensure product quality and yield. * Analysis: Conduct analytical testing to confirm the quality and identity of synthesized oligonucleotides using LC‑MS and other applicable methods. * Documentation: Maintain accurate, complete, and timely records of experiments, procedures, and results in accordance with company policies and applicable regulatory or quality standards. * Laboratory Maintenance: Support routine laboratory maintenance, including proper handling and upkeep of equipment, organization of workspaces, and adherence to safety and cleanliness requirements. * Collaboration: Work closely with senior chemists and cross‑functional team members to support ongoing projects, meet timelines, and contribute to overall team objectives. Qualifications Minimum Required Qualifications • B.S. in chemistry, biochemistry, chemical/biomedical engineering, pharmaceutical sciences, or related field with < 1 year of relevant laboratory experience., • Basic understanding of chemistry, stoichiometry, and chemical synthesis., • Comfort performing numerical calculations., • Hands-on experience with wet lab skills: pipetting, manipulating liquids, handling chemicals, and work in a laminar flow hood (familiarity with oligonucleotide synthesizers, mass spectrometry, chromatography is a plus)., • Strong attention to detail and ability to follow protocols precisely., • Excellent organizational and time-management skills., • Effective communication skills for collaborating with team members and conveying technical information clearly., • Strong problem-solving abilities and critical thinking skills., • Hands on experience in solid-phase oligonucleotide synthesis is a plus., • Familiarity with electronic lab notebooks (ELN)., • Authorization to work in the United States without restriction or sponsorship. Additional Information The position is Full Time, Monday through Friday, 8am-5pm. Candidates currently living within a commutable distance of Boston, MA, are encouraged to apply What to Expect in the Hiring Process: • 10-15 Minute Phone Interview with Regional Recruiter, • 45-60 Minute Virtual Interview with Manager and/or Group Leader, • 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

Job Description About us Eli Health is making continuous hormone monitoring possible so users can support their daily and long-term health. No more waiting days to track key biomarkers—get results you can use within minutes. Eli’s flagship product, Hormometer™, is the first instant hormone monitoring platform to deliver results from saliva to mobile app—anytime, anywhere. Developed over six years of R&D, over 2,000 product iterations, and backed by a dozen patent-pending innovations, Eli’s award-winning platform turns hormones into measurable signals you can track and improve. Just as the thermometer and glucometer have transformed health for millions, Eli’s platform is poised to be the next major evolution in tracking changes in stress, endurance, sleep, and more. About the role Eli is looking for an R&D Scientist. You will be a key member of our R&D team, helping to discover new ways to improve current and future iterations of our assay technology. Your primary responsibilities will be to: * Contribute to building a novel technology that can shape the next generation of women’s healthcare and at-home testing. * Independently design experiments with an exceptional variable control for lateral flow assay development and optimization. * Run experiments, record and analyze data, as well as interpret and present results to your team. * Find creative and innovative ways to solve R&D challenges. * Maintain high-quality work and organization while conducting experiments at a very high rate. * Exercise exceptional wet laboratory etiquette, team collaboration skills, and work ethic. This description is not exhaustive. You will have a lot of autonomy over your work as Eli’s technology and research efforts progress. About you * You have a Bachelor's or a Master's in Chemical Engineering, Bioengineering, Analytical Chemistry, Biochemistry, or a related field. * You have 2+ years of wet lab experience, including 1+ years of laboratory experience beyond the classroom. * You have 1+ years of experience leading your own projects in a wet lab environment. * You have experience working with and developing assays (keywords include: lateral flow assays (LFA), immunoassays, ELISA, In Vitro Diagnostics (IVD), point-of-care diagnostics, rapid diagnostic tests, paper-based sensors, biosensors, microfluidic, bioconjugation, nanoparticle conjugation, antibody purification). * You have experience working with bioconjugation techniques. * You are a self-starter who also enjoys collaborating and sharing knowledge and ideas. You think critically and creatively. * It is an added asset if some of your experience was at an early-stage startup or related environment (fast-paced, high-growth, innovative, small independent teams, etc.) If you don’t exactly match the description but still believe you are the right person to join the team, please reach out. We value mindset and character. Why you’ll love working at Eli * You’ll work with a group of talented and mission-driven people eager to improve lifelong health at scale. * You’ll be part of the core team developing and commercializing the first product that monitors hormonal data daily and over a lifetime. * You’ll join the early-stage startup phase and have a wide-reaching impact in a constantly evolving, fast-paced environment. * You’ll be part of a small (<25 people), high-performing, and diverse team where everything you do results in tangible impact and shapes the company’s trajectory. * You’ll be in an environment where people drive their own work, think creatively about open-ended problems, and solve them proactively. * You’ll get health insurance (medical, dental, vision, and more) to ensure you and your family stay physically and mentally at your best. * You’ll have flexibility over your schedule and vacations. We seek to hire great people, then give them the autonomy and space they need to achieve their goals. * Although our office and R&D facilities are in Montreal, we have a distributed team. We prioritize asynchronous workflows and minimize meetings to focus on the work itself. * You and your +1 will have unlimited free access to the Bota Bota spa in Montreal to recharge. How to apply Sounds like you? Please apply using this link:. Please note that we will not review applications made through other platforms. We look forward to learning about you!

Job DescriptionRole Location: Waltham, MA The Company We are Alloy Therapeutics - a biotechnology ecosystem company empowering the global scientific community to make better medicines together. Through a community of partners, we democratize access to pre-competitive tools, technologies, services, and company creation capabilities that are foundational for discovering and developing therapeutic biologics. The company facilitates affordable, non-exclusive access to the entire drug discovery community from academic scientists, small and medium biotech, to the largest biopharma. At Alloy, we believe our industry should compete on getting the best drugs to patients as quickly as possible, not exclusive access to the best platforms. As a reflection of our relentless commitment to the scientific community, we reinvest 100% of our revenue in innovation and access to innovation. MAY THE BEST DRUG WIN. Alloy has evolved from a startup into a global biotechnology infrastructure company operating 11 divisions across 5 research sites in 4 countries on 3 continents. Our model - Integrated Independence - combines centralized capabilities with entrepreneurial operating divisions. Successful members thrive in our shared culture of accountability, deliberate trust, and open communication. As a team we aspire to work together to exceed expectations and collectively contribute across the global organization to always maintain our nimble, startup culture. At Alloy, we have an ethos of “Mentorship-By-Apprenticeship” in all of our positions. We strive to have workers in the office when needed to interact organically and face-to-face. Of course, as a lab-based operation, our cells and animals grow 7 days a week, 365 days per year. We respect and value our colleagues for their hard work that requires them to be in the lab every day. We ask our people who have more flexible accommodations, like this position, to appreciate their colleagues who have less flexibility. We are all one team! The Role We are seeking a hands-on scientist with strong expertise in LC–MS to lead bioanalytical characterization of oligonucleotide therapeutics, focusing on DMPK and biological interpretation. This LC–MS-focused role involves generating and interpreting data on oligonucleotide exposure, stability, metabolism, protein binding, and structural integrity to answer DMPK-relevant questions and link analytical findings with PK/PD and biological activity. Key Responsibilities • LC–MS–Driven Bioanalysis: Develop and execute LC–MS/MS and LC–HRMS methods for quantitative and structural analysis of oligonucleotides in biological matrices. Design and perform stability, degradation, and Metabolite Identification (MetID) studies to support DMPK. Provide a higher throughput or automated protein binding data (LC-MS Proteomics) ., • Exposure & Disposition: Apply LC–MS and other methods to assess oligonucleotide–protein interactions, binding, and disposition, interpreting how stability, metabolism, and chemical modifications influence systemic and tissue exposure., • DMPK & Biological Integration: Interpret LC–MS data within a DMPK context, collaborating with cross-functional teams to link findings with PK, PD, and biological readouts (e.g., target knockdown, gene expression)., • Data Analysis & Communication: Perform quantitative LC–MS data analysis, troubleshoot analytical issues, and clearly communicate analytical and DMPK insights to inform decision-making.Required Qualifications, • Ph.D. or M.S. in Analytical Chemistry, Pharmaceutical Sciences, Biochemistry, or a related field., • 3+ years (Ph.D) or 10+ years (M.S.) of post-academic experience, • Demonstrated experience with LC–MS and high-resolution MS (HRMS) oligonucleotides bioanalysis, including stability, MetID, and protein binding studies., • Comfort working cross-functionally in a discovery environment.Preferred Qualifications, • Experience with chemically modified oligonucleotides and/or conjugates., • Ability to interpret LC–MS data in a DMPK and biological context., • Exposure to PK/PD concepts and molecular biology-based analytical technologies (e.g., qPCR, ddPCR).Key Skills & Competencies, • LC–MS/MS and LC–HRMS (core expertise), • Oligonucleotide exposure, stability, metabolism, and protein binding, • DMPK-relevant data interpretation, • Strong troubleshooting ability and scientific judgment Compensation • Competitive base and equity compensation commensurate with level of experience and independence, • 401(k) company matchHealth & Family, • Generous personal and family medical, dental and vision benefits with 100% of premiums and deductibles covered, • Company-paid disability (STD, LTD) and life insurance, • Paid parental leave, • Family planning support up to $45,000 (e.g., IVF/PGT, adoption, surrogacy, egg retrieval)Unique Perks, • Unlimited PTO (paid time off) and flexible schedules, • Annual stipend for continuing education with commitment to your career through individualized professional development plan Additionally, this role is eligible for equity compensation, reflecting our commitment to shared success as we work together to make better medicines. We are proud to offer competitive compensation and benefits, aiming to support our team’s professional and personal well-being. If you have any questions about pay or benefits, we’re here to help. Alloy Therapeutics is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, national origin, sex, sexual orientation, gender identity, veteran status, disability, or other legally protected status. If you are unable to submit an application because of incompatible assistive technology or a disability, please contact us at . We will make every effort to respond to your request for disability assistance as soon as possible. Powered by JazzHR A1y1zprA3i

Job DescriptionTitle: Scientist Location: Cambridge, MA Duration: 07 Months Job Summary Key Responsibilities • Develop, qualify, and troubleshoot chromatographic (GC, HPLC/UPLC) and LCMS based methods for the identification, characterization, and impurity profiling of oligonucleotides, siRNAs, and their formulations, as well as raw material related analytical methods and other methods as needed., • Understand and apply advanced scientific principles, theories, concepts, practices and standards to process and analytical development. Provide analytical support for investigations leading by quality, manufacturing, supply chain., • Perform testing of late development siRNA candidates and their formulations for their characterization. Author method development and qualification reports and SOPs for test methods., • Evaluate suitability of new methods and oversee method qualification and validation in the external contract testing labs., • Author and review analytical sections in regulatory submission documents., • Apply strong technical knowledge of organic and analytical chemistry to support laboratory investigations (deviations/OOS/OOT), as needed., • May serve as a primary contact person for cross-departmental needs or projects and be accountable for key deliverables., • PhD in Chemistry, Biochemistry or related disciplines with 0-4 years industry experience, Master's degree with > 5 years related industry experience or Bachelor's degree with > 8 years related industry experience respectively, with demonstrated chromatographic separation, method development / qualification and structure elucidation expertise., • Experience with HPLC/UPLC and LCMS-based analytical method development desired., • Hands-on experience with oligonucleotides, proteins, or peptides is a plus., • Familiarity with instrument troubleshooting and software including Empower, MassHunter, and UNIFI preferred. Knowledge of GxP requirements and application of statistical methods in the analytical laboratory is a plus., • Strong interpersonal skills, communication, and collaboration.#TB_PH #ZR #RESCIE1 #Linkd Why TalentBurst? At TalentBurst, we deliver more than talent, we deliver outcomes. We partner with you to move quickly and connect you to opportunities aligned with your skills and long term growth. Backed by precision, transparency, and results, we connect top talent with leading organizations through trusted partnerships. We offer competitive compensation and comprehensive benefits, including medical, dental, vision, and retirement options. TalentBurst is an equal opportunity employer committed to an inclusive and diverse workforce. Company 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 Cambridge, MA (In-person) 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’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 mission-driven, multidisciplinary LNP Scientist to join our Deliveromics Platform Development team to advance the next generation of non-viral delivery technologies. In this role, you will design and develop novel ionizable lipids, engineer ligand-conjugated lipid nanoparticle formulations, support Deliveromics in vivo screening, and evaluate performance using both in vitro assays and in vivo animal models. You will be responsible for experimental planning and execution, data analysis and interpretation, and the clear communication of results. As one of the earliest scientific hires at an emerging techbio company, you will have the opportunity to shape platform development, collaborate across disciplines, and contribute directly to transformative delivery solutions for genetic medicines. This is a full-time, in-person position based in Cambridge, MA. Responsibilities: * Lead the discovery and development of innovative ligand-LNP delivery technologies, with a focus on improving biological performance, biophysical properties, and in vivo targeting. * Design and develop novel ionizable lipids, ligand-conjugated LNP formulations, and related chemistries for targeted delivery applications. * Develop, optimize, and implement high-throughput assays to evaluate LNP systems, including stability, delivery efficiency, and critical quality attributes, in both in vitro and in vivo models. * Design and execute experiments at the intersection of chemistry, molecular biology, and formulation science, including spatial or sequencing-based readouts when appropriate. * Independently plan, execute, and analyze experiments while also overseeing work performed by supporting scientists. * Stay current with emerging research, technologies, and competitive landscapes across lipid nanoparticles, nucleic acid delivery, targeted therapeutics, automation, and gene editing modalities. * Collaborate closely across chemistry, biology, and automation scientists within the Deliveromics Platform group to troubleshoot challenges and integrate new methods into the screening and development pipeline. * Analyze and interpret experimental data using rigorous quantitative and statistical frameworks; generate high-quality reports and provide actionable insights that inform design decisions and platform direction. * Establish and maintain complete, well-organized documentation, including protocols, SOPs, experimental records, and data summaries to ensure reproducibility and compliance. * Drive process and platform innovation, contributing to technology transfer efforts as workflows mature toward automation, scale, and production readiness. Qualifications: Required: * PhD in Chemistry, Bioengineering, Biomedical Engineering, Biochemistry, Biophysics, or a related field. Exceptional candidates with substantial relevant experience will also be considered, regardless of degree. * Hands-on experience with ionizable lipids, LNP formulation, RNA/LNP nanoparticle preparation, targeted delivery systems, or related technologies, with a strong track record in industry or academia. * Deep expertise in the design, synthesis, purification, and characterization of novel ionizable lipids, lipid conjugates, lipid-like compounds, or related molecular platforms. * Practical experience with lipid biology, LNP formulation development and optimization, and in vitro and/or in vivo assays assessing delivery performance. * Strong problem-solving skills, meticulous attention to detail, and a high level of experimental rigor. * Excellent written and verbal communication skills with the ability to collaborate effectively across diverse scientific and technical teams. * A resourceful, adaptable, and emotionally intelligent team member who thrives in a fast-paced, cross-functional environment. * Ability to work onsite five days per week at our Cambridge, MA location. Nice to have: * Prior experience working with non-human primate models will be a strong plus. * Experiences with nucleic acid chemistry (mRNA, ASO, and siRNA, etc.). * Basic coding skills (e.g., Python, R, or MATLAB). * Hands-on experience troubleshooting liquid-handling platforms or automated lab systems. 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. Equal Opportunity Employer: GT Biosciences is an Equal Opportunity Employer. We celebrate diversity and are committed to fostering an inclusive, supportive environment for all employees. All qualified applicants will be considered without regard to race, color, religion, national origin, age, sex, marital status, ancestry, physical or mental disability, veteran status, gender identity, or sexual orientation. 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 DescriptionZurich Instruments is a technology leader in advanced test and measurement instruments and in control electronics for quantum computing. Our products are used in many challenging research fields by scientists all over the world and by leading high-tech companies worldwide. We help advance science and build the next generation of quantum computers. As an Application Scientist, you will be part of our marketing and sales team in Boston. With the opportunity to apply your technical expertise to solve new technical challenges, you will be making a significant contribution to the success of our fast-growing company. This is a great chance to transition directly from an academic path into a role within a dynamic company environment that allows you to stay at the cutting edge of technology. Your responsibilities • Provide quantum solutions to ensure scientific and commercial success, • Provide application-specific customer support, including onsite system integration, • Maintain and establish customer contacts to secure future sales and support market growth, • Represent Zurich Instruments at trade shows, engage with opinion leaders and work with leading quantum researchers across the US, • Produce marketing material, including presentations, product documentation, and videosYour profile, • PhD or Master’s in Physics, Electrical Engineering, or Computer Science with a relevant background in Quantum Computing, • Solid scientific track record with practical lab experience, including RF/microwave signal generation and measurement, • Programming experience with scientific instrumentation, preferable with Python, • Sales experience or a keen interest in developing your skills in this area

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. Position Summary We're looking for a Product Development Scientist to support the development and commercialization of new products across our growing portfolio of beverages and fruit-based foods. This role sits at the intersection of front-end innovation and commercial execution and is ideal for someone who is comfortable in ambiguity and in the rigor of scale-up and commercialization. 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 • Own and execute product innovation projects from concept through commercialization, ensuring consumer relevance, technical feasibility, and business viability, • Translate consumer insights into rapid prototypes and product mock-ups to influence project decision-making and direction, • Develop agile product development methods and systems to accelerate time to launch, • Tap into external partners (ie. vendors, suppliers) to accelerate prototyping and execution, • Leverage supplier relationships and AI tools to forecast trends, map white space, and assess competition, • Partner with Marketing and Consumer insights to develop consumer testing plans, • Communicate with external co-manufacturing partners ensuring timelines and qualification plans align across businesses, • Deliver work in support of business continuity, quality monitoring, productivity, and cost and product optimization initiatives, • Design and execute sensory testing to validate formula changes and ingredient swap outs, • Plan and execute bench-top, pilot plant, and plant trials documenting results and next steps, • Collaborate cross-functionally with Marketing, Insights, QA, Operations, and Finance, • Brings both a passion for consumer co-creation and strong technical execution, • Builds strong working relationships with cross-functional partners, • Navigates ambiguity by turning ideas into actionable plans, • Hands on and resourceful, with a drive to quickly build, test, and iterate, • Balances speed and rigor, making thoughtful, timely decisions, • Adapts quickly based on new learnings and shifting priorities, • Takes ownership of outcomes and follows through on complex challenges, • Works relentlessly to anticipate obstacles and creates plans to overcome them, • 3-5 years of new product development experience with a proven track record of launching food and/or beverage products from concept through commercialization, • A Bachelor's degree in food science, Chemistry, Chemical Engineering, or related fields., • Comfort guiding actions of external partners (suppliers, service vendors, co-manufacturers, labs), • Strong communication skills and ability to translate technical information to non-technical audiences, • Ability to manage multiple projects simultaneously, • Strong analytical skills and ability to translate data into decisions, • Basic knowledge of food safety, GMPs, regulatory requirements, and quality systems, • General knowledge of food & beverage processing and filling equipment, • Willingness to travel up to 15% based on project requirements, • Preferred Qualifications, • Experience in fruits and vegetables food and beverage, • Experience with rapid prototyping and agile innovation approaches, • 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: 40 hours of paid volunteer time for all non-union employees, • 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 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.

statistics & Mathematicsdata handlingdata collectingdata analysis and modelingdata visualizationdata clesningprogrammingAbout micro1micro1 connects domain experts to the development of frontier AI models. Real-world expertise is turned into training data, evaluations, and feedback loops that improve how models perform. AI labs and enterprises use micro1 to train models and build reliable AI agents through advanced evaluations and reinforcement learning environments. Experts contribute directly to how AI systems learn, reason, and perform across domains like finance, healthcare, engineering, and more. Our platform identifies and vets top talent through an AI recruiter, enabling high-quality contributions at scale.Our goal is to enable 1 billion people to do meaningful work by applying their expertise to AI. We’ve raised $40M+ in funding, and our AI recruiter has powered over 1 million AI-led interviews as our global network of experts grows into the human intelligence layer for AI. Job Title: Data Scientist Job Type: Contractor Location: Remote Job Summary: Join our customer's team as a Data Scientist and play a pivotal role in transforming data into actionable insights that drive business growth. You will leverage your expertise in statistics, mathematics, and programming to tackle challenging data problems, ensuring clean, robust, and insightful analyses. This is an exciting opportunity to work in a dynamic, expert-driven environment that values clear communication and innovative thinking. Key Responsibilities: • Collect, clean, and preprocess diverse data sets to ensure integrity and readiness for analysis., • Develop, validate, and implement statistical models to extract actionable insights from complex data., • Conduct exploratory data analysis to identify trends, patterns, and opportunities for business improvement., • Present findings and recommendations through compelling data visualizations and reports, tailored for technical and non-technical stakeholders., • Collaborate closely with team members to design and execute end-to-end data projects, from ideation to delivery., • Continuously improve analytical methodologies and automation processes to enhance data workflows., • Communicate effectively in both written and verbal formats, ensuring clarity and impact of data-driven recommendations. Required Skills and Qualifications: • Expertise in statistics, mathematics, and data analysis techniques., • Proven experience in collecting, handling, and cleaning large, complex data sets., • Proficiency in programming languages such as Python, R, or similar for data manipulation and modeling., • Strong data modeling skills with experience in building and validating predictive models., • Advanced ability to visualize data using tools like Tableau, Power BI, or related libraries., • Meticulous attention to detail and commitment to data quality at every stage., • Excellent written and verbal communication skills, with an emphasis on clarity and precision. Preferred Qualifications: • Experience working in a remote, cross-functional, or customer-focused team environment., • Background in developing and deploying machine learning solutions in production settings.

Job DescriptionJob Title: Senior Associate Scientist Job Location: Cambridge, MA 02142 Job Duration: 8 months+ Shift: Standard Payrate: $40-$46/ hr on W2 Skill set – Oligonucleotide synthesis and downstream processing, Analytical HPLC/LCMS/UV-vis Justification: Summary of Key Responsibilities • Hands-on lab support and process development for the chemical synthesis and downstream processing of oligonucleotide-based drug substance, • Synthesis of oligonucleotides up to 11 mmol scale, • Downstream processing of oligonucleotides including prep-HPLC, Ultrafiltration, annealing, concentration and Lyophilization, • In process analytical testing including AX-HPLC, IPRP-HPLC, LCMS, UV-vis, • Technical support for optimization of contract manufacturing processesQualifications:, • BS in Chemistry with 3+ years lab experience, preferably in an industrial setting., • Basic understanding of analytical techniques (pH, osmolality, conductivity measurement, HPLC, LC-MS etc.). Related hands-on experience is preferred. Knowledge of oligonucleotide manufacture process including phosphoramidite chemistry, chromatography, ultrafiltration etc. is a plus., • Experience in record-keeping and excellent laboratory documentation practice, are required. Strong commitment to high laboratory and scientific standard; ability to maintain a safe, clean, and orderly laboratory work environment; assist in routine lab and equipment maintenance., • Good communication skills are a must for this position. The successful candidate must be a responsible and proactive individual who is able to work as a team player in a highly dynamic environment with aggressive timelines.#sczr2

Our client, a leading global pharma company, is seeking a Senior Data Scientist (AD) to lead the development of advanced analytics and AI solutions that drive strategic decisions across Marketing, Sales, Medical, and Market Access. This role focuses on Marketing Mix Modeling (MMM), resource allocation, and machine learning–based personalization to improve commercial performance and investment efficiency. • Location: ONSITE, Cambridge, MA, • Salary: to 250K + bonus and incentives, • NO SPONSORSHIP RESPONSIBILITIES: • Lead development and deployment of Marketing Mix Models (MMM) to quantify channel level promotional impact, • Measure ROI across field force, digital, media, speaker programs, and patient initiatives, • Build resource allocation and optimization frameworks to guide commercial investment decisions, • Support annual brand planning, scenario modeling, and in year budget reallocation, • Drive the long term data science and AI vision for commercial analytics, • Serve as a strategic partner to Insights, Marketing, and Access teams, • Translate brand objectives into scalable analytical solutions and machine learning pipelines, • Guide stakeholders through insight activation and integration into workflows, • Provide technical leadership on analytical tools, model governance, and responsible experimentation, • Collaborate with and mentor a high performing team of data scientists, • Manage external analytics partners to ensure alignment and delivery Requirements: • 7+ years in analytics or data science, including 4+ years leading data science products, teams, or programs, • Experience in pharma or biotech, specifically with Marketing Mix Modeling and commercial optimization, • Strong command of statistical modeling, supervised/unsupervised learning, A/B testing, and time series forecasting, • Experience deploying data science solutions in a commercial environment, • Proficiency in Python, R, SQL, Snowflake; familiarity with Power BI, Tableau, or similar tools, • Proven experience with omnichannel analytics, marketing optimization, and machine learning pipelines, • Excellent communication and stakeholder influencing skills Preferred Skills • Master’s degree in Data Science, Statistics, Engineering, Computer Science, Business Analytics, or related field, • Experience building proprietary data products or commercial decision engines

Supports downstream process development through purification and characterization of viral vectors, biologics, or recombinant proteins. Responsibilities include executing purification techniques such as CsCl density gradient ultracentrifugation, affinity and ion-exchange chromatography, and tangential flow filtration, while operating AKTA systems for purification runs. The role involves experimental execution, data analysis, process optimization, sample characterization, and maintaining GMP/GLP-compliant documentation. Requires hands-on purification experience, strong technical understanding of protein/viral vector purification principles, attention to detail, and effective collaboration with cross-functional teams.

Location: China Job Responsibilities: 1.Independently conduct literature searches, develop synthetic routes, and draft project proposals. 2.Independently complete small-scale process research for drug synthesis; coordinate with and guide the pilot plant team for process transfer. 3.Collaborate with quality research personnel to support analytical activities. 4.Independently prepare documentation for regulatory submissions. 5.Perform other duties assigned by leadership. Qualifications: 1.Ph.D. in Organic Chemistry, Total Synthesis, Peptide Synthesis, or related fields. 2.Proficient in route scouting, small-scale process development, and pilot-scale scale-up. 3.Demonstrated ability to systematically record experimental data and prepare technical reports. 4.Skilled in using automated screening tools (e.g., high-throughput reactors) and analytical instruments (HPLC, LC-MS, etc.). 5.Strong learning agility, execution capability, resilience, and teamwork spirit; excellent communication and collaboration skills.

Location: China Job Responsibilities: 1.Lead feasibility assessment, dosage form design, formulation screening, process development, and optimization for 505(b)(2) NDAs and first-in-class innovative drugs. 2.Track clinical needs in key therapeutic areas to drive formulation innovations achieving enhanced efficacy/reduced toxicity. 3.Monitor global innovations in clinical-stage modified-release drugs; translate novel technologies/research concepts into R&D strategies. 4.Deepen expertise in formulation science while integrating cross-disciplinary knowledge (clinical pharmacology, medicinal chemistry, biopharmaceutics) for clinically driven drug development. 5.Establish in vitro-in vivo correlations (IVIVC) by analyzing pharmaceutical data and PK studies to link formulation properties with clinical outcomes. 6.Document experimental records; author regulatory submission documents ensuring data integrity and ALCOA+ compliance. 7.Execute assigned tasks: due diligence for in-licensed projects, novel technology platform assessments, literature reviews, e-journal editing, and technical training. Qualifications: 1.Ph.D. in Pharmaceutics, Pharmaceutical Sciences, or related field. Preferred: Experience with complex dosage forms (e.g., complex injectables, modified-release oral systems, inhalation products). 2.Comprehensive expertise in drug development with advanced technical proficiency; demonstrated ability to design scientifically sound studies and solve complex formulation challenges. 3.Proficient in literature mining (English journals/patents) with strong capability to extract, synthesize, and implement technical insights. 4.Intellectual curiosity and self-driven learning agility; embraces innovative/high-challenge tasks. 5.Hands-on experience with:Formulation equipment (e.g., fluid bed dryers, hot-melt extruders)、DoE-based formulation screening、Technical report writing. 6.Strong ethics, resilience in fast-paced environments, and collaborative mindset with excellent cross-functional communication skills.

Senior / Staff / Sr. Staff Engineer About SDIRA Samsung SDI Research America (SDIRA), based in Cambridge, MA, is one of several newly established global battery R&D centers created to foster cutting edge research and pioneer the development of Samsung’s next-generation cell technologies. The location is close to world-renowned universities and start-up companies, enabling unique collaborative research within a strong North American ecosystem of battery development expertise. Responsibilities • Join as a core member of the growing research team at SDIRA!, • Lead internal and external R&D projects with well-defined goals and milestones. Work closely with the internal team as well as professors, national laboratory researchers, and/or students to guide progress on external collaborations, create accountability, and solve for obstacles., • Execute on experimental activities independently or in lean, fast moving teams. Projects may involve active material synthesis, material characterization, electrode formulation, cell assembly process refinement, cell prototyping and testing, and cell performance modeling., • Propose new areas of research and methodologies to enhance understanding of technology gaps. Keep up to date on the latest literature and competitors to contextualize progress., • Spearhead the design and setup of new laboratory capabilities., • PhD degree in Mechanical, Chemical, Electrochemical Engineering, Chemistry or Materials Science, or similar technical field, • 5+ years of combined academic and industrial experience in battery cell and materials R&D. Level based on years of relevant experience. Industry practice in battery development is highly valued, • Expertise in materials development, electrochemical analysis, cell failure analysis and materials characterization techniques, • Expertise in cell prototyping with emphasis on tailoring component properties and refining assembly or test methods to optimize performance at relevant scales, • Knowledge of cell manufacturing processes and the impacts of design and material selection on commercial viability, • Demonstrates engineering judgement that enables the greatest impact while pushing the boundaries of current understanding, • Demonstrates inventiveness in solving technical, logistical or programmatic obstacles, • Prioritizes execution while acknowledging risks and taking steps for mitigation, • Creates frameworks and documentation to enhance communication and generate order from complexity, • Prioritizes working within a cohesive team: supports others across projects and functions, invests in “infrastructure” and processes that enhance the efficiency of the team, champions a “one team” approach to collective success

Our Boston based biotechnology client is seeking a highly skilled Senior or Principal Scientist to lead the development, transfer, and validation of bioassay methods supporting innovative gene therapy programs. This role is ideal for a scientifically driven professional who thrives in a dynamic, collaborative environment and is motivated by impactful work in clinical-stage development. This position requires 2-3 days per week onsite in Boston, MA. About the Role The incumbent will be responsible for establishing and managing biological potency assays used for release and stability testing. This position also oversees CRO activities for both GMP and non-GMP sample testing, ensuring high-quality execution and regulatory compliance. You will collaborate closely with cross-functional teams, contribute to analytical CMC documentation, and support regulatory submissions. This is a high-impact role with opportunities to influence analytical strategy and drive scientific excellence. Key Responsibilities • Lead development, transfer, and validation of biological assays for release and stability testing., • Manage laboratory investigations, OOS assessments, and data trending; support manufacturing investigations., • Execute development studies for process and product characterization, including comparability assessments., • Draft, review, and approve SOPs, protocols, reports, and analytical documentation for internal and external QC labs., • Support preparation of analytical CMC content for regulatory submissions, including data summaries and trend analyses., • Collaborate effectively with internal stakeholders and manage external CRO relationships. Skills and Expertise • Strong technical expertise and hands-on experience with cell-based potency assays., • Familiarity with statistical analysis tools (e.g., JMP, Prism, PLA 3.0) is an asset., • Excellent technical writing skills for analytical CMC documents, including change controls, SOPs, protocols, and reports., • Solid understanding of regulatory guidance and GMP requirements for analytical method lifecycle management., • Highly organized, detail-oriented, and capable of strategic thinking., • MS or PhD in Biological Sciences or related field, with a minimum of 10 years of biotech/pharma industry experience., • Extensive hands-on experience in analytical method development, validation, and clinical-stage sample testing., • Strong background in analytical documentation within a regulated environment., • Proficiency in cell-based assays, ddPCR, and ELISA is required., • Experience with HPLC/UPLC or CE-SDS is a plus., • Demonstrated project management, problem-solving, and organizational skills., • Experience managing CDMO/CRO partnerships is required., • Excellent written and verbal communication skills, with the ability to present findings to diverse stakeholders.

Title: Scientist Location: Cambridge, MA Duration: 6 months Must have- candidates with a focus on pepProduct/protein analytical development and antibody characterization experience. Key Responsibilities: • Develop, qualify, and troubleshoot chromatographic (GC, HPLC/UPLC) and LCMS based methods for the identification, characterization, and impurity profiling of oligonucleoProducts, siRNAs, and their formulations, as well as raw material related analytical methods and other methods as needed., • Perform testing of late development siRNA candidates and their formulations for their characterization., • Apply strong technical knowledge of organic and analytical chemistry to support laboratory investigations (deviations/OOS/OOT), as needed. Qualifications: • PhD in Chemistry, Biochemistry, or related disciplines with 0-4 years industry experience, master’s degree with > 5 years related industry experience or bachelor’s degree with > 8 years related industry experience respectively, with demonstrated chromatographic separation, method development / qualification, and structure elucidation expertise. Experience: • Experience with HPLC/UPLC and LCMS-based analytical method development desired., • Hands-on experience with oligonucleoProducts, proteins, or pepProducts is a plus., • Familiarity with instrument troubleshooting and software including Empower, MassHunter, and UNIFI preferred.

JOB DETAILS:- Position Title: Scientist III, Cellular Biology and Automation Length of Contract: 6 months Location/Site: 200 Sidney st. Cambridge MA - 100% on-site What are the top 3-5 skills, experience or education required for this position: • BS, MS in cell biology, molecular biology, biochemistry, or equivalent, with 5+ years of experience., • Experience within cellular models for drug discovery. Experience with neural or microglial models preferred., • Experience with primary, iPSC, complex cell models, and immortalized cell culture., • Expertise and interest in cell biology and assay development, • Also preferred is industrial experience in early drug discovery including the identification of small molecules and/or biologic reagents, to validate targets and as leads toward the identification of human clinical candidates. Description In this position you will design and perform both routine and complex cell culture work to contribute to research in drug discovery to treat neurological diseases. Using both manual and automated means, you will collaborate with other scientists to develop iPSC derived cellular models, and prepare materials for in vitro research work. Microfluidic cell cloning, CRISPR, cell line generation, and protein analysis are other responsibilities. Automating these processes using advanced robotics will be a key goal and responsibility. Identifying and evaluating new technologies and methods will also be a component of the successful candidate’s responsibilities. Key Responsibilities Include • Scaleup and maintenance of cultured cells by automated and manual means, • Scaleup and maintenance of immortalized cell lines, • Tracking and distribution of fresh and cryopreserved cell resources to collaborators, • Adaptation of cell culture methods to lab automation, • Collaborate with groups within and beyond Discovery Neuroscience at both the Cambridge Research Center and other sites, requiring a full understanding of the uses to which cultured materials will be put, • Collaborate on method development for differentiation of iPS cells to models of neurological disease, • Derivation and characterization of CRISPR KO pools and clones, • Help maintain cell line inventory system, • Proactively monitor new external developments in cell culture and automation, and incorporate this into individual projects, • Understand and adhere to corporate standards regarding code of conduct, safety, appropriate handling of materials, etc. Qualifications Required Skills and Educational Requirements: Basic: • BS, MS in cell biology, molecular biology, biochemistry, or equivalent, with 5+ years of experience., • Experience within cellular models for drug discovery. Experience with neural or microglial models preferred., • Experience with primary, iPSC, complex cell models, and immortalized cell culture., • Expertise and interest in cell biology and assay development, • The successful candidate must be highly collaborative, enjoying a dynamic, multi-disciplinary project team environment. Desired Skills: • Preference will be given to candidates with expertise in the use of automated cell culture robotic hardware and software, particularly the Sartorius CompacT SelecT. Training or interest in software and hardware engineering is a plus., • Experience with basic molecular biology, protein characterization, ICC, transfection/transduction of mammalian cells, • Also preferred is industrial experience in early drug discovery including the identification of small molecules and/or biologic reagents, to validate targets and as leads toward the identification of human clinical candidates. EEO: “Mindlance is an Equal Opportunity Employer and does not discriminate in employment on the basis of – Minority/Gender/Disability/Religion/LGBTQI/Age/Veterans.” Thank You

About BOSTONGENE: BostonGene is redefining cancer patient care and drug development through the integration of omnimodal data and artificial intelligence. Built and validated through an extensive real-world clinical testing network, BostonGene’s Foundation Model of cancer and the immune system integrates genomic, transcriptomic, and immune data with clinical outcomes to generate biologically grounded, actionable insights. These insights enable biopharma partners to design and de-risk trials, identify novel targets, and optimize therapeutic response prediction across all stages of development while simultaneously improving patient care through clinically integrated innovation. Position Overview BostonGene is seeking a bench Scientist to join our R&D next-generation sequencing (NGS) team in our laboratory located in Waltham, MA. This candidate will support assay development and technical transfer in collaboration with immunology, production, and bioinformatics teams. The candidate will be expected to support NGS protocols, such as RNA and DNA isolation from tissue, cell-free DNA isolation from plasma, library preparation, QC, and other lab processes. The role will primarily require laboratory bench work (70-80%) in a BSL-2 laboratory. Key Responsibilities: • Perform assay and product development experiments of NGS workflows, including WGS, WES, and liquid biopsy assays for internal and external collaborators, • Troubleshoot and support the technical transfer of workflows to the production lab., • Maintain detailed and accurate records in LIMS, ELN, and in compliance with laboratory protocols and regulatory requirements., • Assist in the development of laboratory SOPs and batch records., • Execute and assist with validation studies, bridging studies, and technical reports., • Stay informed on emerging technologies and trends in NGS to support innovation in assay development. Qualifications: OR B.S. with 6–10 years of hands-on experience. (The job title will be commensurate with experience.) • Strong experience in nucleic acid extraction (DNA/RNA) from FFPE, blood, or other clinical samples., • Proficiency in NGS library prep (short-read and/or long-read), including WGS and WES., • Excellent problem-solving and troubleshooting skills., • Strong organizational skills with the ability to manage sample tracking, documentation, and inventory. Preferred Skills & Experience: • Experience working with liquid biopsy samples (cfDNA/ctDNA, cfRNA, or exosomes)., • Familiarity with NGS QC metrics and analysis tools., • Understanding of assay validation in regulated environments (GCLP, ISO)., • Demonstrated experience in SOP development and process documentation., • Strong verbal and written communication skills, with the ability to work effectively in cross-functional teams., • Proven ability to work in a dynamic, fast-paced environment with shifting priorities., • Self-motivated and accountable, with a collaborative mindset. Additional Information • Ability to stand for prolonged periods and perform repetitive tasks inherent to laboratory work.

Senior Scientist, Toxicology — Cambridge, MA Our Cambridge based biotech client is looking for a highly motivated Senior Scientist in Toxicology to help shape the preclinical safety strategy for oligonucleotide programs across all stages of development. This role provides the chance to influence discovery, development, and regulatory decision‑making while working closely with cross‑functional teams. Key Responsibilities • Serve as Study Director for non‑GLP and GLP toxicology studies in rodent and non‑rodent species, • Manage CRO relationships, protocol development, and study execution, • Act as a subject matter expert on nonclinical safety topics, • Prepare and review safety pharmacology and toxicology reports, • PhD in toxicology, pharmacology, or related field with 3+ years of industry experience or BS/MS with 10+ years of experience; DABT preferred, • Experience with nonclinical development of antisense oligonucleotides or siRNA, • Strong understanding of GLP requirements and global regulatory guidelines (ICH, FDA, etc.), • Proven experience managing CROs and leading GLP/non‑GLP studies, • Excellent communication, organizational skills, and ability to thrive in a fast‑paced environment About Stratacuity: Whether you are seeking a career change or simply interested in becoming part of our network, you will appreciate the ethics guiding each Stratacuity team member. We build lasting relationships with exceptional biopharmaceutical talent and take great care to protect your personal information. Upon receiving your inquiry, you may be directly contacted by a Stratacuity team member to discuss your career goals. We will not share your information with anyone without your direct prior consent. PROVEN SCIENTIFIC PLACEMENT™ Stratacuity is an Equal Employment Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, age, sexual orientation, gender identity, national origin, disability, protected veteran status, or any other characteristic protected by law. Stratacuity will consider qualified applicants with criminal histories in a manner consistent with the requirements of applicable law. If you have visited our website in search of information on employment opportunities or to apply for a position, and you require an accommodation in using our website for a search or application, please contact us.

Erdogan Lab at Boston University Medical Campus is seeking a highly motivated Postdoctoral Associate to join an NIH-funded interdisciplinary research program investigating how neuro-immune responses and interactions shape pain, infection, and tissue repair in barrier tissues in the oral cavity. Erdogan Lab, in the Department of Translational Dental Medicine at Boston University Henry M. Goldman School of Dental Medicine, operates at the interface of neurobiology, immunology, and microbiology, combining in vivo disease models, genetic and chemogenetic manipulations, systems-level profiling, advanced imaging, and translational approaches. Our overarching goal is to define how sensory neurons respond to and interact with immune and microbial signals in dental and oral tissues and to translate these insights into pain management strategies and minimally invasive therapies. Erdogan Lab is highly collaborative, with active partnerships across Boston’s leading academic and research institutions. Key Responsibilities • Design, execute, and lead independent and collaborative, hypothesis-driven research at the intersection of neuroimmunology and oral biology, • Utilize in vivo models of dental injury, infection, and chemogentic approaches, • Integrate molecular, cellular, and systems-level approaches (e.g., flow cytometry, imaging, transcriptomics), • Analyze complex datasets, including transcriptomic and microbiome data, • Lead projects from experimental design through publication, • Mentor trainees and contribute to a dynamic, team-oriented lab environment Required Qualifications • PhD, MD/DDS/PhD or equivalent doctoral degree in immunology, neuroscience, microbiology, oral biology, or a related discipline, • Ability to work both independently and as part of a collaborative team, • A creative and rigorous scientist with a strong track record of research productivity, • Excited to tackle mechanistic, translational, cross-disciplinary questions, • Comfortable with (or eager to learn) in vivo biology and complex experimental systems, • Preferred: Experience in neuroimmunology, pain biology, host–microbe interactions, imaging, or transcriptomics Candidates with clinical training in dentistry (DDS/DMD) with substantial research experience are encouraged to apply. Please submit CV, cover letter, and contact information for three references to: Alecha Pantaleon For inquiries: PI Dr. Ozge Erdogan () Boston University is an equal opportunity employer and is committed to building a diverse and inclusive academic community.

About the Company A soon to launch Third Rock Ventures company is seeking an experienced Peptide Scientist to lead peptide design efforts supporting discovery-stage therapeutic programs. This role will focus on peptide SAR, data interpretation, and lead optimization, working closely with project leadership and cross-functional teams. Responsibilities • Lead and design strategies for peptide therapeutics to support early discovery programs, • Drive structure–activity relationship (SAR) efforts and guide molecule optimization, • Manage and oversee work conducted at external CRO partners, including peptide synthesis, analytics, and related studies, • Review and interpret experimental data to inform molecule design and program strategy, • Present program updates and recommendations to project teams, • Partner closely with project leads and cross-functional teams (biology, pharmacology, DMPK, CMC) to advance programs, • Help define external study plans, timelines, and priorities to support program milestones Qualifications • PhD in chemistry, chemical biology, peptide science, or related field, • Significant experience in therapeutic peptide discovery, • Expertise in metabolic or endocrine indications, • Demonstrated ability to guide molecule design and SAR strategy, • Track record of contributing to advancement of discovery programs, • Experience managing external CRO collaborations, • Strong communication skills and ability to present scientific strategy to multidisciplinary teams Required Skills • Experience in therapeutic peptide discovery and optimization, • Ability to guide peptide design and SAR strategy, • Strong communication skills, • Experience managing external CRO collaborations, • Ability to present scientific strategy to multidisciplinary teams Location • With offices in Boston, San Francisco and Shanghai, the ability to work from one of these locations, but we are open to remote employment for exceptional individuals able to work collaboratively and effectively Equal Opportunity Statement We are committed to diversity and inclusivity.

Scientist/Senior Scientist – Cell Biology (Diabetes) Company Overview GC Therapeutics is the first genome-wide cell landscape exploration company using an integrated synthetic biology and AI-driven platform for cell programming. Its patent-pending and proprietary pluripotent stem cell differentiation technology platform TFome™ was developed in Professor George Church’s lab, a pioneer in synthetic biology, and allows for the development of unique cell therapies with significantly streamlined manufacturing, improved cell quality, efficiency and speed. GC Therapeutics is based in Cambridge, MA. For additional information, please visit ___ Job Purpose GC Therapeutics is seeking a highly motivated Scientist or Senior Scientist for its diabetes program. This role focuses on conducting genetic screens to identify factors that drive iPSC differentiation into therapeutic cell populations relevant to diabetes as well as establishing assays for molecular and functional characterization. The ideal candidate will have deep expertise in developmental biology, iPSC differentiation and assay development and will contribute to the advancement of the diabetes programs. The role demands hands-on experimental work with cell culture, strategic project planning and cross-functional collaboration to accelerate therapeutic development. Duties and Responsibilities • Culture and maintain iPSC lines and relevant primary cells, including preparation of media, passaging, cryopreservation, and routine quality assessments., • Conduct genetic screens on iPSCs to optimize differentiation protocols for diabetes-relevant therapeutic cell populations., • Design, execute and optimize differentiation workflows using principles of synthetic biology and stem cell biology., • Develop, establish and run molecular, phenotypic and functional assays to characterize differentiated cell populations (e.g. flow cytometry, PCR, fluorescence microscopy, ELISA and other relevant readouts)., • Perform, analyze and interpret experimental data, ensuring comprehensive documentation of methodologies and outcomes., • Troubleshoot differentiation and screening workflows to improve hit rate, throughput and robustness., • Maintain a detailed laboratory journal, summarize results, and create presentations for meetings., • Maintain accurate and complete records, ensuring compliance with documentation management systems., • Collaborate effectively across the GC Therapeutics team to achieve strategic goals. General Laboratory Roles: • Responsible for experimental design, data generation, analysis, and communication of results to supervisor, and team members., • Provide scientific and technical guidance to junior staff, collaborators, or contract research organizations (CROs) for defined projects., • Maintain organized and detailed laboratory journal, summarize results, and create presentations for internal group meetings., • Stay current on relevant scientific literature, emerging technologies and advancements in the field., • Exemplify scientific curiosity and deep expertise with relevant literature and cutting-edge technologies to advance research directions., • Work with other members of the research team and within GCTx to accomplish company goals., • Follow all safe laboratory practices and company policies. Experimental Techniques: Cellular Biology: • Perform cell engineering on iPSCs to screen factors for synthetic biology-based differentiation., • Design and execute synthetic biology-based differentiation of iPSCs., • Optimize iPSC-derived differentiation for therapeutic cell products., • Utilize techniques such as PCR, molecular cloning and plasmid isolation., • Characterize target cell types using next-generation sequencing methods (e.g. library preparation for bulk and single cell RNA-seq) and other gene expression analysis techniques. Qualifications Essential Qualifications: • Ph.D. degree in stem cell biology, cell biology, bioengineering, biochemistry, or related discipline and 5+ years of laboratory work experience in academia or industry., • Strong expertise in cell culture expertise, particularly for iPSCs and cell types relevant to diabetes., • Deep knowledge of development biology and stem cell differentiation principles as applicable to diabetes., • Proven experience in cell-based assay development and molecular biology laboratory techniques., • Strong work ethic with the ability to perform tasks independently and lead junior staff effectively., • Proficient in analysis, presentation, and documentation of scientific data and scientific reports., • Effective communicator with excellent interpersonal skills., • Strong project management and organizational skills and ability to prioritize and multitask., • Ability to work in a laboratory environment approximately 75% of the time including occasional weekend hours. Additional Preferred Qualifications: • Experience in genome editing or high throughput genetic library screening., • Skill to perform animal studies, including rodent handling, dosing., • Ability to analyze next generation sequencing or other genome-scale datasets., • Proven track record and strong publications in stem cell or developmental biology., • Knowledge of R, Python and FlowJo. Pay Range $120,000 - $145,000 (This range reflects the base salary only and does not include additional compensation such as annual bonus and equity awards, which are part of the total compensation package.) Disclosure Statement: The range provided is based on what we believe is a reasonable estimate for the base salary pay range for this job at the time of posting. This role is eligible for an annual bonus. Some roles may also be eligible for overtime pay, in accordance with federal and state requirements. Actual base salary pay will be based on a number of factors, including skills, competencies, experience, and other job-related factors permitted by law. At GC Therapeutics, our generous competitive benefits package also include generous PTO, paid holidays, Medical, Dental, Vision, 401(k), Life and Disability Insurance and transportation subsidy. Equal Opportunity Workplace: GC Therapeutics is an equal opportunity employer. We provide equal employment opportunities to all applicants for employment and existing employees without regard to ancestry, national origin, place of birth, race, color, gender, sexual orientation, marital status, pregnancy, religion, age, disability, gender identity, results of genetic testing, service in the military or otherwise to the full extent of all federal, state and local laws. GC Therapeutics’ equal employment opportunity policy applies to all terms and conditions of recruiting, hiring, placement, training, compensation, transfer, leave of absence, employment, promotion, layoff and termination of employment.

Senior Scientist, Discovery – Cambridge, MA Our Cambridge based biotech client is seeking a highly motivated and detail‑oriented Senior Scientist is sought to join a fast‑paced and collaborative Discovery team in Cambridge, MA. This role offers the opportunity to make a visible impact on an innovative RNA‑editing pipeline by identifying high‑value targets and driving hands‑on experimental validation. The ideal candidate is scientifically curious, adaptable, and comfortable working across multidisciplinary teams to design, execute, and analyze experiments that advance discovery efforts. This role requires 5x per week onsite in Cambridge, MA. Responsibilities • Develop and execute strategies to identify and validate RNA‑editing targets using a range of in vitro and in vivo assays., • Evaluate disease targets based on clinical and genetic evidence, unmet need, RNA‑editing suitability, and commercial potential., • Identify RNA editing sites that enhance protein expression or activity., • Establish and run cell‑based assays to support target discovery and validation., • Prepare clear, detailed study summaries and present findings to cross‑functional teams., • Collaborate closely with research colleagues to ensure timely execution of experiments and data generation., • Maintain accurate electronic lab notebook records and update documentation such as SOPs and batch records., • PhD in Biological Sciences, Biochemistry, Molecular Biology, Pharmaceutical Sciences, or a related field., • 2+ years of relevant post‑graduate experience in academia or industry., • Strong background in RNA biology and regulation; experience in target search and evaluation is a plus., • Hands‑on experience with cell‑based assays such as RT‑qPCR, ELISA, MSD, or western blotting., • Excellent documentation habits and attention to detail., • Strong analytical and troubleshooting skills., • Proficiency with Microsoft Office and GraphPad Prism., • Experience in RNA regulation., • Willingness to perform hands‑on laboratory work., • Familiarity with in vitro assays for target discovery and validation., • Proactive, communicative, and highly collaborative working style.

THE OPPORTUNITY We’re looking to hire a Principal Scientist to join the R&D team. The ideal candidate will bring a strong background in organic chemistry, medicinal chemistry, biochemistry or material science along with proven success in early-stage drug discovery. In this role, you will: • Develop novel small molecules, peptides, or proteins for cutting-edge application, • Lead research programs focused on new molecule discovery, high-throughput screening, target validation, and assay development., • Drive research conception, planning and execution of studies that support our R&D projects, spearheading them from proof-of-concept to product validation., • Continuously refine experimental plans to enable data-driven decision-making and accelerate the transition from concept to market-ready products., • Stay apprised of new biochemistry, bioengineering and chemistry trends and implement new technologies that further enhance capabilities, • Develop and present new project concepts to expand our pipeline of innovative solutions., • Provide feedback, coaching, and mentorship to 1-3 team members, fostering a culture of innovation and leadership within the organization. Who You Are • You hold a PhD, MD, MD/PhD, or PharmD in Chemistry, Biochemistry, Chemical Engineering, or a related field., • You possess extensive knowledge of current techniques in chemistry or biochemistry, with hands-on experience in their application., • You are intensely focused on driving discoveries from the lab to the market, ensuring that concepts are not just theoretical but are translated into tangible, impactful products., • You have a deep curiosity and a passion for tackling challenging problems in a dynamic, fast-paced environment., • You bring high intensity and discipline to your work, and are excellent in creating structure for ambiguous problems ADDITIONAL INFORMATION • This position is hiring for an immediate start, • This position is in-office 5 days a week in our Cambridge, Massachusetts office, • The salary for this position is commensurate with experience

Skill set – Oligonucleotide synthesis and downstream processing, Analytical HPLC/LCMS/UV-vis • Hands-on lab support and process development for the chemical synthesis and downstream processing of oligonucleotide-based drug substance, • Synthesis of oligonucleotides up to 11 mmol scale, • Downstream processing of oligonucleotides including prep-HPLC, Ultrafiltration, annealing, concentration and Lyophilization, • In process analytical testing including AX-HPLC, IPRP-HPLC, LCMS, UV-vis, • Technical support for optimization of contract manufacturing processes Qualifications • BS in Chemistry with 3+ years lab experience, preferably in an industrial setting., • Basic understanding of analytical techniques (pH, osmolality, conductivity measurement, HPLC, LC-MS etc.). Related hands-on experience is preferred. Knowledge of oligonucleotide manufacture process including phosphoramidite chemistry, chromatography, ultrafiltration etc. is a plus., • Experience in record-keeping and excellent laboratory documentation practice, are required. Strong commitment to high laboratory and scientific standard; ability to maintain a safe, clean, and orderly laboratory work environment; assist in routine lab and equipment maintenance., • Good communication skills are a must for this position. The successful candidate must be a responsible and proactive individual who is able to work as a team player in a highly dynamic environment with aggressive timelines.

Meet Life Sciences is representing a clinical-stage oncology biotech seeking a Medical Director / Senior Medical Director to support the clinical development of oncology programs. This role will focus on the design, execution, and oversight of clinical trials, including contributing to clinical strategy, serving as primary Medical Monitor, supporting regulatory submissions, and collaborating with cross-functional teams. The position will provide 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 client’s Cambridge, MA office. This role would require a candidate to work on-site 3 times per week. Key Responsibilities • Clinical Trial Support: Provide medical expertise to support the lead physician/scientist in 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: Partner 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 our client 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 the medical leadership team with 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 the clinical development function. Qualifications Required • MD with board certification in Oncology, Hematology-Oncology, or a related specialty. Preferred • Clinical development experience, with a focus on late-stage trials, preferably as a Medical Monitor., • Experience working in cross-functional team environments., • Strong understanding of oncology drug development, clinical endpoints, and regulatory pathways., • Clinical practice experience or experience as an investigator., • Strong communication skills., • Effective collaboration skills with the ability to interact with internal and external stakeholders., • High ethical standards and commitment to scientific rigor.

Key Responsibilities • Develop and optimize core robotic algorithms: including motion planning, navigation control, and perception fusion (e.g., SLAM, sensor fusion for LiDAR/vision/IMU)., • Implement kinematic/dynamic modeling: such as trajectory generation, force control, and enhancing algorithm robustness in dynamic environments., • Algorithm integration and testing: integrate algorithms with hardware systems, perform simulation (e.g., using ROS, Gazebo, MuJoCo), and deploy/debug on physical robots., • Education: Bachelor’s, Master’s, or Ph.D. degree in Robotics, Computer Science, Automation, or related fields., • Programming skills: Proficiency in C++/Python, with experience using ROS, OpenCV, and PyTorch/TensorFlow., • Theoretical foundation: Solid knowledge of robotics theory (kinematics, control systems, optimization) and sensor processing (LiDAR, vision, IMU)., • Practical experience: Hands-on experience in motion control, SLAM, or path planning; familiarity with reinforcement learning frameworks is a plus., • Publications in top conferences (e.g., RSS, CoRL, ICRA, IROS, NeurIPS), or practical experience in multi-robot systems/human-robot collaboration., • Experience in training/deploying large-scale AI models in robotics.

COMPANY OVERVIEW AIRNA is a biotechnology company with a mission to be the leading RNA editing company delivering precision therapies to patients with rare and common diseases. AIRNA is harnessing advances in genetics to develop transformative RNA-editing medicines that improve human health. Our proprietary platform is based on groundbreaking research by pioneers of the field and company co-founders Thorsten Stafforst (University of Tübingen) and Jin Billy Li (Stanford University) and enables optimal potency, safety, and delivery. AIRNA is advancing a robust pipeline of therapeutic candidates that are designed to provide functional cures for severe or chronic diseases by repairing harmful genetic variants or introducing beneficial variants promote optimal health. AIRNA has raised $245 million in financing from a world-class syndicate of investors including Arch Venture Partners, Forbion, Venrock Healthcare Capital Partners, RTW Investments, Nextech Invest, and ND Capital. We value teamwork, resilience, excellence, human, and health, and have a diverse team at both our headquarters in Cambridge, MA and our research operations in Tübingen, Germany. POSITION SUMMARY: We are seeking a highly motivated Analytical Biomarker Scientist to support biomarker discovery and translational research using advanced mass spectrometry platforms. The successful candidate will develop, validate, and apply LC-MS–based assays for proteomics, metabolomics, and lipidomics to enable biomarker identification, pharmacodynamic assessment, and disease mechanism studies in preclinical and clinical samples. This role requires strong expertise in sample preparation, LC-MS method development, data analysis, and biomarker interpretation within a multidisciplinary research environment. Assay Development & Analytical Work • Develop and optimize LC-MS/MS assays for proteomics, metabolomics, and lipidomics., • Design and execute quantitative and qualitative biomarker assays in biological matrices (plasma, serum, tissue, CSF, etc.)., • Perform sample preparation workflows including protein digestion, metabolite extraction, and lipid isolation., • Operate and maintain high-resolution and triple-quadrupole LC-MS systems., • Identify and validate protein, metabolite, and lipid biomarkers relevant to disease biology and drug response., • Support preclinical and clinical biomarker studies including pharmacodynamic and mechanistic endpoints., • Process and analyze LC-MS data using appropriate bioinformatics and statistical tools., • Perform quantitative analysis and biomarker data interpretation., • Maintain data quality and ensure reproducibility of assays., • Work closely with cross-functional teams including biologists, clinicians, and computational scientists., • Contribute to study design and experimental strategy for biomarker discovery projects., • Present results at internal meetings and external scientific conferences., • Support manuscript preparation and regulatory documentation when applicable. QUALIFICATIONS Education • PhD in Analytical Chemistry, Biochemistry, Proteomics, Metabolomics, or related field, • Hands-on experience with LC-MS/MS instrumentation., • Expertise in proteomics workflows (protein extraction, digestion, peptide analysis)., • Experience with metabolomics and/or lipidomics assays., • Experience analyzing complex biological samples., • Experience with high-resolution MS platforms (e.g., Orbitrap, Q-TOF)., • Knowledge of biomarker discovery pipelines in translational research., • Experience with quantitative MS methods such as MRM/PRM., • Familiarity with bioinformatics tools for omics data analysis., • LC-MS method development, • Proteomics / metabolomics / lipidomics, • Biomarker discovery and validation, • Sample preparation and assay optimization, • Data analysis and statistical interpretation, • Cross-functional collaboration LOCATION: AIRNA has a hybrid work model, and the role will be based in AIRNA’s corporate headquarters in Cambridge, MA ~3 days per week. COMPENSATION: $120,000 - $155,000

Duration: 6 months Contract, strong chances of extension Job Description: Position Overview: In this position you will design and perform both routine and complex cell culture work to contribute to research in drug discovery to treat neurological diseases. Using both manual and automated means, you will collaborate with other scientists to develop iPSC derived cellular models, and prepare materials for in vitro research work. Microfluidic cell cloning, CRISPR, cell line generation, and protein analysis are other responsibilities. Automating these processes using advanced robotics will be a key goal and responsibility. Identifying and evaluating new technologies and methods will also be a component of the successful candidate’s responsibilities. Key Responsibilities Include: • Scaleup and maintenance of cultured cells by automated and manual means., • Scaleup and maintenance of immortalized cell lines., • Tracking and distribution of fresh and cryopreserved cell resources to collaborators., • Adaptation of cell culture methods to lab automation., • Collaborate with groups within and beyond Discovery Neuroscience at both the Cambridge Research Center and other sites, requiring a full understanding of the uses to which cultured materials will be put., • Collaborate on method development for differentiation of iPS cells to models of neurological disease., • Derivation and characterization of CRISPR KO pools and clones., • Help maintain cell line inventory system., • Proactively monitor new external developments in cell culture and automation, and incorporate this into individual projects., • Understand and adhere to corporate standards regarding code of conduct, safety, appropriate handling of materials, etc. Qualifications: Basic: • BS, MS in cell biology, molecular biology, biochemistry, or equivalent, with 5+ years of experience., • Experience within cellular models for drug discovery., • Experience with neural or microglial models preferred., • Experience with primary, iPSC, complex cell models, and immortalized cell culture., • Expertise and interest in cell biology and assay development., • The successful candidate must be highly collaborative, enjoying a dynamic, multi-disciplinary project team environment. Desired Skills: • Expertise in the use of automated cell culture robotic hardware and software, particularly the Sartorius CompacT SelecT. Training or interest in software and hardware engineering is a plus., • Experience with basic molecular biology, protein characterization, ICC, transfection/transduction of mammalian cells., • Also preferred is industrial experience in early drug discovery including the identification of small molecules and/or biologic reagents, to validate targets and as leads toward the identification of human clinical candidates. 1. About US Tech Solutions: US Tech Solutions is a global staff augmentation firm providing a wide range of talent on-demand and total workforce solutions. To know more about US Tech Solutions, please visit ___. 2. Equal Employment Opportunity (EEO) Statement: US Tech Solutions is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran. 3. AI Statement: By applying, you acknowledge that AI-assisted tools may be used during hiring. Recruiter Details: Name: Ishan Atre email: Job #: 26-11175

Job Description About the ALS Therapy Development Institute The ALS Therapy Development Institute (ALS TDI) is the world's leading nonprofit biotech focused exclusively on discovering and developing effective treatments for amyotrophic lateral sclerosis (ALS). Our multidisciplinary team integrates in vivo pharmacology, molecular biology, and clinical insights to accelerate ALS therapy development from bench to bedside. Position Summary We are seeking a highly motivated scientist to join our preclinical pharmacology team. The successful candidate will bring a broad and robust technical skill set largely focused on in vivo techniques. This position is responsible for developing new animal models of ALS and performing preclinical pharmacology studies to evaluate the safety, efficacy, and mechanism of action of experimental drugs. Key Responsibilities • Design, execute, and interpret pharmacology studies including tolerability, PK/PD, and efficacy to evaluate therapeutic candidates., • Perform aseptic surgical procedures in rodents such as stereotaxic ICV and intrathecal injections and osmotic pump implantations., • Develop and conduct phenotypic, behavioral, and functional assays to assess drug efficacy and characterize disease progression., • Generate and characterize novel ALS models using transgenic approaches, viral vectors, and CRISPR-based genome editing, • Design and manage transgenic mouse breeding strategies to investigate genetic interactions., • Write grant proposals, manuscripts, presentations, and reports to communicate experimental findings., • Prepare and maintain standard operating procedures (SOPs) and ensure all studies comply with IACUC, animal welfare, and biosafety requirements., • Mentor and train junior staff in experimental techniques, data analysis, and scientific problem solving. Required • PhD in neuroscience, pharmacology, molecular biology, or related field, • Strong publication record with at least two first-author papers, • Hands on experience with rodent models, behavioral assays, and stereotaxic surgery, • Background in mouse model development, transgenic strategies, or genetic engineering, • Strong foundation in experimental design and statistical analysis, • Postdoctoral or industry experience in drug discovery or translational research, • Work in ALS or related neurodegenerative diseases, • Experience with transgenic colony management, genotyping, and breeding strategies, • Experience with histology, immunohistochemistry, or imaging-based analyses, • Work with non-rodent models (zebrafish, Drosophila, C. elegans), • Exposure to gene therapy, antisense oligonucleotides, or biologics, • Familiarity with pharmacology studies and drug discovery workflows, • Proficiency with coding and AI based tools, • A mission-driven environment focused on accelerating therapies for ALS patients., • A collaborative, cross-functional research setting with access to advanced technology platforms., • A competitive salary and benefits package commensurate with experience and level., • Opportunities for scientific growth and contribution to high-impact research. Job Posted by ApplicantPro

Job DescriptionCompany Description About AbbVie 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 including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at . Follow @abbvie on LinkedIn, Facebook, Instagram, X and YouTube. Job Description We are seeking a highly motivated Associate Scientist to support the development of in vivo pharmacology assays and models for psychiatry drug discovery. The successful candidate will work with behavioral, neurochemical, and electrophysiological technologies to assess circuit-level dynamics relevant to psychiatric indications with an emphasis on depression. This role is an excellent opportunity to be part of a dynamic and collaborative team focused on investigating circuit dysfunction in psychiatric disorders. Key Responsibilities • Perform in vivo experiments leveraging a variety of assays and circuit-based technologies to advance drug development in psychiatry, • Support and assist with development and execution of survival surgery experiments (e.g. stereotactic surgeries), • Independently generate precise, reliable and reproducible data in a timely manner and keep detailed experimental records, • Analyze data and present results to project teams and other cross-functional teams, • Help design studies, research new models and disease areas of interest Qualifications, • Bachelor’s Degree with typically 3 or more years’ experience or Master’s Degree (no additional experience)., • Hands-on experience with rodent handling, various dosing routes and tissue collection methods., • Enthusiasm for performing lab-based research to drive discovery efforts in psychiatric disorders, • Ability to analyze and critique results, noting significant deviations, • Strong communication and collaboration skills to work effectively within a multidisciplinary team, • Desired Qualifications, • Extensive hands-on experience with rodent models for depression, anxiety and/or other psychiatric disorders, • Direct experience with neurocircuit-based approaches especially electrophysiology (e.g. EEG), • Prior experience in drug discovery, particularly in Psychiatry 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 Are you highly motivated, hard-working, and seeking to join a growth-focused consulting & engineering firm? Are you looking for a company that will invest in your development and grow your professional skills? If so, consider a career with Apex! Powered by record sales, extraordinary client retention, strategic acquisitions, and an entrepreneurial spirit, Apex Companies is one of the fastest growing engineering and environmental consulting firms in the US. We were recently recognized by the Zweig Group as one of the fastest growing firms in the AEC industry. We take pride in providing our clients with exceptional service and have earned numerous awards for project excellence. We continue to grow, and we want you to grow with us. Our Northeast Division is a well-respected and award-winning group where career development, training, and mentoring co-exist with diverse civil, environmental, water resources, and traffic/transportation projects in a fast-paced and challenging work environment. We're seeking a dynamic Wetland Scientist to join our growing team. Key Responsibilities Include but are not limited to: • Conduct wetland and regulated resource delineations in Massachusetts in accordance with federal, state, and local regulations, • Perform natural resource surveys and field investigations, including vegetation, wildlife, water, soils, site conditions, and habitat assessments, • Prepare and maintain field documentation, data collection records, and scientific analyses consistent with regulatory programs and technical guidance, • Support the preparation of project narratives, impact assessments, alternatives analyses, and supporting documentation for permit applications, • Assist with local, state, and federal permitting efforts, including coordination with agencies and project teams, • Utilize GPS and mapping tools to document field conditions and support project deliverables, • Collaborate with engineers, ecologists, designers, and GIS/mapping staff to support integrated, solutions‑based client services, • Contribute to technical reports, regulatory filings, and client deliverables with a high level of accuracy and professionalism, • Support biological monitoring, protected species reviews, and environmental compliance efforts as applicable, • Bachelor's degree in Environmental Science, Ecology, or a related field, • 3 years of experience conducting wetland and regulated resource delineations, both independently and as part of a team, • Massachusetts experience required; experience in other New England states a plus, • Willingness to travel up to 50% regionally, • Familiarity with wetlands and native plant identification, • Basic knowledge and use of GPS equipment, • 38‑hour USACE Delineation Training, • Experience with GIS and/or FieldMaps, • Experience with natural resource surveys and methodologies, including vegetation, wildlife, water, soils, site characteristics, and habitat assessments, • Knowledge of routine permitting requirements for wetlands, waters, floodplains, and buffer zones within inland and coastal/tidal ecosystems, • Experience with USACE NC/NE Regional Supplement and state wetland and environmental resource programs (MassDEP Wetlands & Waterways, CT Inland Wetlands, etc.), • State wetland and waters permitting experience in MA and CT required; RI preferred, ME and NH preferred, • Strong technical writing skills, including field documentation and scientific data collection in accordance with regulatory programs and technical guidance, • Strong communication skills and a collaborative, team‑oriented approach when working with design/engineering, ecologists, and mapping teams, • Strong computer skills, including Microsoft Word, Excel, PowerPoint, Teams, and Outlook Why you'll love working for us: • Company-subsidized medical and dental., • Company-paid life, short, and long-term disability., • 401k match, tuition assistance, and more., • Cross-training and the ability to work on a variety of projects., • Performance-based bonuses or other incentives., • Working with the best and brightest in the industry., • 2,000+ employee national firm with 70+ locations across the US. #LI-BS1 Apex Job Title: Scientist 2 - Project Scientist Req ID: 11436 Annual Expected Pay Range$65,000—$85,000 USD We believe in equality for all and celebrate the diversity and differences of our employees, customers, and communities. We do not discriminate based on gender, race or color, ethnicity or national origin, age, disability, religion, sexual orientation, gender identity or expression, veteran status, or any other applicable characteristics protected by law. Apex aims to make apexcos.com accessible to all users. If you have a disability or special need that requires accommodation to navigate our website or complete the application process, please contact or (301) 417-0200. Likewise, feel free to reach out to us if you would like to view or discuss Apex policy related to equal employment opportunity or have any related concerns. EO/AA/VEV/Disabled Employer TO ALL RECRUITMENT AGENCIES: Apex Companies does not accept unsolicited agency resumes. Please do not forward resumes for any of our job postings to our career's sites, or to any employees of Apex Companies or affiliates. Apex Companies is not responsible for any fees related to unsolicited resumes.

Job Description Salary Band: $160,000-$220,000 Location: Downtown Boston, MA (In-Office Minimum 3 Days/week) Position Summary Antares Therapeutics is seeking an enthusiastic and self‑motivated Senior Scientist/Principal Scientist, Toxicology to join the Nonclinical Development group and support nonclinical safety assessment activities from discovery through IND‑enabling stages across the Antares pipeline. The successful candidate will play a key role in the design, execution, and interpretation of nonclinical safety studies, working both hands‑on in the laboratory and in close collaboration with external CROs. This role requires scientific independence, strong technical expertise in in vitro and in vivo safety assessment, and effective cross‑functional collaboration in a fast‑paced, matrixed environment. Key Responsibilities • Serve as a nonclinical safety representative on cross‑functional Discovery and Development project teams, supporting program progression through IND‑enabling stages., • Design, execute, and troubleshoot nonclinical safety studies, including hands‑on assay execution, data generation, and interpretation. Up to 40% of time in the lab., • Support the oversight of GLP and non‑GLP nonclinical safety studies conducted at CROs, including active involvement in troubleshooting assay‑ and study‑related challenges., • Work in the laboratory to establish and run in vitro safety assays, with an emphasis on New Approach Methodologies (NAMs)., • Analyze and interpret study data, contributing to study reports, regulatory documentation, and IND‑supporting materials under guidance., • Collaborate closely with Pharmacology, DMPK, and other functional teams to support exploratory and mechanistic safety studies., • Identify and communicate potential safety findings and actively contribute to discussions on risk assessment, data interpretation, and next‑step recommendations., • Ph.D. or M.S. in Toxicology or a related scientific discipline., • Minimum 5+ years of industry experience in pharma or biotechnology focused on nonclinical safety assessment., • Demonstrated ability to work independently while contributing scientific expertise within cross‑functional teams., • Experience supporting nonclinical safety programs from discovery through IND‑enabling stages., • Hands‑on experience with one or more of the following:, • In vitro 3D models, • In vitro safety screening platforms, • Familiarity with NAM‑based approaches for safety assessment., • Proactive, collaborative, and scientifically curious., • Positive, flexible attitude with the ability to thrive in a matrixed, fast‑paced biotech environment.

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 Key Responsibilities • Function as a principal investigator, generating original technical ideas & search or development strategies., • Generate new scientific proposals & lead those efforts., • Anticipate & critically evaluate scientific or regulatory advances or competitive threats & respond with appropriate new strategies., • Independently responsible for project science with area of expertise on 1 or more project teams., • Primary author of publications, presentations, regulatory documents & /or primary inventor of patents., • Present at leading scientific conferences., • Understand & adhere to corporate standards regarding code of conduct, safety, appropriate handling of materials, controlled drug & radioactive compounds, GxP compliance, & animal care., • Mentor a team & evaluate performance.Qualifications Education & Experience Must possess a MS in Pharmaceutical Science, Chemistry, Chemical Engineering or other related field & 3 years as a drug product formulation scientist working with a pharmaceutical company. Of industry work experience required, must have 3 years: (i) performing design development, leading projects & providing innovation of (a) multi particulate system (mini tablets, drug layering), (b) modified release formulation with ASD, (c) bi-layer/tri-layer tablets, & (d) other nonconventional oral delivery systems; (ii) managing clinical supply manufacturing & other activities to support clinical studies at different stages; (iii) performing GMP activities for both documentation & manufacturing activities; (iv) supporting regulatory filings, including authorizing, reviewing & approving; (v) conducting DOE & performing statistical analysis for pharmaceutical drug product development; & (vi) using PBPK modeling as a tool to guide formulation development. Alternatively, would accept PhD in Pharmaceutical Science, Chemistry, Chemical Engineering or other related field & 1 year as a drug product formulation scientist working with a pharmaceutical company. Of industry work experience required, must have 1 year: (i) performing design development, leading projects & providing innovation of (a) multi particulate system (mini tablets, drug layering), (b) modified release formulation with ASD, (c) bi-layer/tri-layer tablets, & (d) other nonconventional oral delivery systems; (ii) managing clinical supply manufacturing & other activities to support clinical studies at different stages; (iii) performing GMP activities for both documentation & manufacturing activities; (iv) supporting regulatory filings, including authorizing, reviewing & approving; (v) conducting DOE & performing statistical analysis for pharmaceutical drug product development; & (vi) using PBPK modeling as a tool to guide formulation development. Work experience may be gained concurrently. Will accept reasonable combination of education, training & work experience. Additional Information Salary Range: $164,439.50 - $236,500.00 per year. Apply online at or send resume to . Refer to Req ID: REF49787Q 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 and long-term incentive programs. AbbVie is committed to operating with integrity, driving innovation, transforming lives, serving our community, and embracing diversity and inclusion. It is AbbVie’s policy to employ qualified persons of the greatest ability without discrimination against any employee or applicant for employment because of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information, gender identity or expression, sexual orientation, marital status, status as a protected veteran, or any other legally protected group status. 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 DescriptionSalary: About Aura: Aura Biosciences is a clinical-stage biotechnology company focused on developing precision therapies for solid tumors that aim to preserve organ function. Our lead candidate, bel-sar (AU-011), is currently in late-stage development for primary choroidal melanoma and in early-stage development in other ocular oncology indications and bladder cancer. Aura Biosciences is headquartered in Boston, MA. Our mission is to grow as an innovative global oncology company that positively transforms the lives of patients. For more information, visit aurabiosciences.com. Follow us on X (formerly Twitter) @AuraBiosciences and visit us on LinkedIn. Position Summary: Aura is seeking an experienced and highly collaborative Senior QC Scientist to support late-stage product development and drive Process Excellence initiatives. This role is critical to ensuring analytical readiness for commercial manufacturing through strong partnership with Contract Development and Manufacturing Organizations (CDMOs) and cross-functional internal teams. The ideal candidate is a seasoned analytical chemist with deep expertise in method validation, transfer, optimization, and troubleshooting in a cGMP-regulated pharmaceutical environment. This individual thrives in complex, fast-paced settings and brings both technical depth and the ability to influence and collaborate across organizations. Key Responsibilities Analytical Method Life Cycle Management & Validation • Lead analytical method activities to CDMOs, including transfer as appropriate, validation and authoring validation protocols and reports., • Manage and review work performed under method validation protocols, method performance, and any required third party activities., • Provide on-site technical readiness support and serve as SME during validation campaigns., • Troubleshoot and resolve technical challenges related to method life cycle management and validation in partnership with CDMO and internal stakeholders., • Monitor and trend analytical method performance in collaboration with Analytical Development (AD)., • Support quality systems activities, including change controls, deviation investigations, CAPAs, OOS investigations, and method improvements., • Perform statistical analyses to support method validation, qualification studies, and critical material qualification., • Author and review GMP documentation, including:, • Method transfer protocols and reports, as required, • Validation protocols and reports, • Test methods and best-practice documents, • Maintain comprehensive documentation of validation and transfer activities., • Partner closely with Analytical Development, MS&T, Quality Assurance, and external testing laboratories., • Lead training for new analytical methods at external labs and support QC analysts in execution, data analysis, and technical review. Subject matter expertise in analytical methods relevant to biologics and/or advanced therapeutics, including but not limited to: • qPCR, • ELISA, • Potency assays Qualifications • B.Sc., M.Sc., or Ph.D. in Analytical Chemistry, Pharmaceutical Sciences, or related scientific discipline, • Minimum of 10 years of pharmaceutical industry experience, with significant exposure to cGMP manufacturing and late-phase method validation, • Demonstrated expertise in:, • Analytical method validation and lifecycle management, • Process validation support, • Technology transfer and troubleshooting, • Proficiency in statistical software (e.g., JMP or equivalent), • Strong communication, negotiation, and stakeholder management skills, • Ability to operate independently, prioritize dynamically, and succeed in a fast-paced environment, • Willingness to travel to CDMO sites as needed Salary & Benefit Information: Salary Range: $150,000/yr - $215,000/yr (Placement within the listed range depends on many factors including, but not limited to: geographic location, degree, years of experience, and internal company equity) Health insurance with FULL premium coverage 401K with company match Employee Stock Purchase Program (ESPP) Competitive paid time off (PTO) Company-paid short & long-term disability insurance and life insurance

Job Description At Editas Medicine, we are pioneering the possible. Our mission and commitment is to translate the power and potential of the CRISPR/Cas12a and CRISPR/Cas9 genome editing systems into a robust pipeline of medicines for people living with serious diseases around the world. Our goal is to discover, develop, manufacture, and commercialize transformative, durable, precision genomic medicines for a broad class of diseases. Why Choose Editas? At Editas Medicine, we’re a team of passionate problem solvers, harnessing the power and potential of CRISPR gene editing to transform the future of medicine. Driven by a shared purpose to serve people living with serious diseases, we succeed together through collaboration, mutual respect, and innovation. If you want to be part of a team where your voice is heard and respected, where you can operate at the forefront of gene editing, and push the boundaries of what’s possible in medicine, come join us and become an Editor! Decoding The Role: Editas Medicine is seeking an accomplished Scientist to join our In Vivo Discovery Team to bolster our assay development group and support our pharmacology efforts. The Sci I will be integral to pipeline development by centralizing our molecular/biochemical assay development activities in support of existing targets, and spearheading research, onboarding and qualification of new assays to support new indications. Characterizing Your Impact: As Scientist I in the In Vivo Discovery Team, you will: • Generate high quality and reproducible data that will allow us to conclusively determine whether a disease program will move forward to the next stage of development., • Be an integral contributor to the evaluation of novel therapeutic targets and help expand Editas drug pipeline, • Design, optimize and qualify assays to quantify the functional impact of therapeutic gene editing in vivo and in vitro., • Examine gene and protein expression in vivo and in vitro, • Complete timely experimental documentation and reports, • Demonstrate command of our standard lab techniques, instrumentation and software, • Show good organization and sharing of data at group meetings, • Demonstrate successful and independent troubleshooting of assay development The Ideal Transcript: To thrive in this role, you’ll need: Qualifications • B.S. w/ 6+ years, M.S. w/ 4+ years of experience or Ph.D. in cell biology, molecular biology, bioengineering, or a related field, • Industry experience in molecular biology or a related field is highly desirable, • Extensive experience in biochemical and cell-based assay development including design, execution and qualification., • Extensive experience in molecular and cell biology techniques: ELISA, Western blotting, MSD, flow cytometry, RT-ddPCR, quantitative PCR, biochemical/cell-based assays to measure metabolites and enzymatic activity (colorimetric, fluorometric and luminescence-based)., • Extensive experience in mammalian cell culture and transfections, • Experience working with CRISPR, non-viral (LNP) and/or viral (AAV, lentivirus) delivery vectors is a plus, • Knowledge of genetic diseases, gene-editing and gene therapy, • Experience with in vitro or in vivo pharmacology and assay qualification, • Experience with primary hepatocytes and advanced in vitro hepatocyte culture such as 3D-organoid culture or liver-on-a-chip, • An ability to work in a dynamic, fast-paced, team-oriented, and multidisciplinary environment, • Self-motivated and results-driven with excellent attention to detail, • Ability to independently design, execute and evaluate protocols to drive assignments to completion Benefits Editas provides a comprehensive array of benefits to all employees, including a Blue Cross Blue Shield PPO Medical Plan, a company-funded Health Savings Account, Dental and Vision Insurance, Life and Disability Insurance, Dependent Care Account, Tuition Reimbursement, 401(k) plan with company match, Employee Assistance Plan, Wellness Programs, and a flexible Paid Time Off policy. Salary Range: $132,000 - $145,000 Pay Transparency Editas Medicine is committed to transparency and accuracy in our hiring practices. The anticipated salary range for each position is posted within the role. The final salary offer will be determined based on a comprehensive assessment of the candidate's qualifications, including education, training, and relevant experience. Additional factors such as external market conditions, the role's criticality, and internal equity will also be considered. Editas Medicine's compensation philosophy ensures fair and equitable pay practices. Aspire to be an Editor? We invite you to apply and join us at the forefront of innovation and be a key contributor to realizing Editas Medicine's mission of developing transformative medicines for people living with serious diseases.

Job DescriptionAt 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 seeking a Senior Machine Learning Scientist to join the Sensor Intelligence Group (SIG), a cross-functional team collaborating across WHOOP Labs, Firmware, and Data Science. This role is central to developing and scaling machine learning systems that power the most foundational health features at WHOOP. You’ll enable next-generation AI coaching at Whoop, developing robust algorithms for constrained edge and cloud environments,ultimately delivering meaningful and personalized coaching to millions of members.RESPONSIBILITIES: * Research, architect, and develop ML systems for member coaching distributed between edge hardware and the cloud * Collaborate with machine learning and edge ML engineers to translate prototypes into production * Partner with product and user experience teams to ensure consistent user experience in bandwidth-constrained environments and to align with member impact and health insights goals * Contribute to architectural decisions and mentor team members in ML best practices QUALIFICATIONS: * Bachelor's degree in Computer Science, Electrical/Computer Engineering, Applied Mathematics, or a related field; Master’s or PhD degree preferred * 5+ years of experience as a Machine Learning Scientist or similar role with a focus on applied research, preferably related to voice and/or text-based conversational systems * Experience training, fine-tuning, and deploying state-of-the-art deep learning architectures to production * Experience with time-series foundation models and self-supervised training approaches * Experience pre-training and fine-tuning small language models and/or building natural language understanding (NLU) models than run on resource-constrained targets * Experience with cloud platforms (AWS or GCP) and familiarity with modern MLOps practices such as CI/CD, model versioning, monitoring, and observability * Strong communication and collaboration skills across cross-functional teams * Strong commitment to embracing and leveraging AI tools in day-to-day tasks, ensuring AI-assisted work aligns with the same high-quality standards as personal contributions This role is based in the WHOOP office located in Boston, MA. The successful candidate must be prepared to relocate if necessary to work out of the Boston, MA office. Interested in the role, but don’t meet every qualification? We encourage you to still apply! At WHOOP, we believe there is much more to a candidate than what is written on paper, and we value character as much as experience. As we continue to build a diverse and inclusive environment, we encourage anyone who is interested in this role to apply. WHOOP is an Equal Opportunity Employer and participates in E-verify to determine employment eligibility. 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. The WHOOP compensation philosophy is designed to attract, motivate, and retain exceptional talent by offering competitive base salaries, meaningful equity, and consistent pay practices that reflect our mission and core values. At WHOOP, we view total compensation as the combination of base salary, equity, and benefits, with equity serving as a key differentiator that aligns our employees with the long-term success of the company and allows every member of our corporate team to own part of WHOOP and share in the company’s long-term growth and success. The U.S. base salary range for this full-time position is $150,000 - $215,000 Salary ranges are determined by role, level, and location. Within each range, individual pay is based on factors such as job-related skills, experience, performance, and relevant education or training. In addition to the base salary, the successful candidate will also receive benefits and a generous equity package. These ranges may be modified in the future to reflect evolving market conditions and organizational needs. While most offers will typically fall toward the starting point of the range, total compensation will depend on the candidate’s specific qualifications, expertise, and alignment with the role’s requirements.

Job Description Position Summary: TScan Therapeutics is a clinical-stage biotech seeking to revolutionize life-changing therapeutics for patients by identifying novel T cells and epitopes. We are looking for an experienced researcher to join our team as Principal Research Associate/Associate Scientist in the Molecular Assembly team, supporting our novel target identification and validation workflow in house. The ideal candidate should have relevant experience in cloning techniques and enjoy a fast-paced, collaborative, and vibrant culture. A team player with a sense of urgency will thrive in this role. Responsibilities: • Collaborate with other scientists to design and build various constructs and vectors in support of target/TCR discovery efforts., • Assemble large libraries of peptides, TCRs, etc. using specialized cloning protocols., • Perform medium- to high-throughput cloning experiments to support discovery efforts in target identification and validation., • Analyze and interpret cloning and screening data (e.g., sequencing, functional assays) to guide construct design and optimization., • Troubleshoot complex cloning and library construction challenges and propose scalable solutions., • Lead group efforts towards technology development and improvement., • Implement and optimize high-throughput workflows, including automation where applicable., • Train co-workers on molecular cloning techniques., • Maintain accurate and well-documented experimental records (e.g., ELN) to ensure data integrity and reproducibility. Requirements: • PhD with 0-2+ years of industry experience; Master’s degree with 5-7+ years of relevant lab experience, preferably in the biopharmaceutical or biotechnology industry., • Hands-on experience in a variety of molecular cloning techniques, including Gibson Assembly, Golden Gate Assembly, Gateway recombination, etc.; experience constructing large-scale libraries is desirable., • Highly organized with very strong attention to detail., • Demonstrated ability to manage multiple projects and meet deadlines in a fast-paced environment., • Ability to work both independently and collaboratively and adapt quickly to changing priorities., • Scientific creativity, critical thinking, and problem-solving skills., • Excellent written and verbal communication skills, with the ability to document experiments in an organized and timely fashion and to present scientific data to coworkers., • Familiarity with sequence analysis tools, NGS, and basic bioinformatics workflows preferred., • Knowledge of immunology concepts, especially TCR biology and antigen recognition, is preferred.