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Our client, Pharmaceutical Development is seeking a Sr. Scientist to join their team. As a Sr. Scientist, you will be part of the Pharmaceutical Development team supporting laboratory-based biologics drug product development. The ideal candidate will have strong technical problem-solving, disciplined Good Documentation Practices (GDP), and the ability to communicate scientific results clearly across cross-functional partners, which will align successfully in the organization. Job Title:Sr. Scientist Location:San Diego, CA Pay Range:$43 What's the Job? • Contribute to the setup, operation, maintenance, and routine troubleshooting of laboratory instruments; support method development and draft related procedures, reports, SOPs, and best-practice documentation., • Independently execute assigned experiments and, as experience permits, plan or lead smaller, well-defined studies supporting phase-appropriate formulation and drug product process development., • Analyze and interpret experimental data, identify trends or atypical results, draw scientifically supported conclusions, and recommend next steps within defined project parameters; escalate complex issues as appropriate., • Draft study plans, development reports, technical memos, and other scientific documentation with review from more experienced colleagues or management as appropriate., • Collaborate with project management, quality assurance, analytical, R&D, non-clinical, manufacturing, and external partners to support development activities, technology transfer, and clinical material production. What's Needed? • Experience with LC and iCiEF is required., • Hands-on experience with state-of-the-art bioanalytical methods and characterization in a biologics drug product laboratory, including UPLC or HPLC (SEC, RP, HIC, IEX/CEX, CAD preferred), charge variant analysis, particle analysis, CE-SDS, and other physical-property characterization., • Strong understanding of biochemical and physical properties of therapeutic biologics (proteins and related modalities) and commonly used protein quantification and characterization approaches., • Ability to analyze testing results, recognize trends and out-of-trend or atypical data, and summarize findings with scientifically supported conclusions and recommendations within defined parameters., • Strong technical writing skills and demonstrated Good Documentation Practices (GDP) with disciplined laboratory record keeping in a pharmaceutical or similarly regulated environment. What's in it for me? • Work on meaningful, laboratory-based biologics drug product development using modern analytical instrumentation and methods., • Build confidence by executing experiments independently and contributing to study planning and optimization as you grow., • Strengthen your scientific communication by drafting clear study documentation and presenting results and recommendations to the project team., • Collaborate with internal and external partners to support development activities, technology transfer, and clinical material production., • Join a fast-paced team environment where you can prioritize multiple work items and drive progress with accuracy and efficiency. If this is a role that interests you and you'd like to learn more, click apply now and a recruiter will be in touch with you to discuss this great opportunity. We look forward to speaking with you! About ManpowerGroup, Parent Company of: Manpower, Experis, Talent Solutions, and Jefferson Wells. ManpowerGroup® (NYSE: MAN), the leading global workforce solutions company, helps organizations transform in a fast-changing world of work by sourcing, assessing, developing, and managing the talent that enables them to win. We develop innovative solutions for hundreds of thousands of organizations every year, providing them with skilled talent while finding meaningful, sustainable employment for millions of people across a wide range of industries and skills. Our expert family of brands – Manpower, Experis, Talent Solutions, and Jefferson Wells – creates substantial value for candidates and clients across more than 75 countries and territories and has done so for over 70 years. We are recognized consistently for our diversity - as a best place to work for Women, Inclusion, Equality and Disability and in 2023 ManpowerGroup was named one of the World's Most Ethical Companies for the 14th year - all confirming our position as the brand of choice for in-demand talent.

Currently, We are looking for entry-level software programmers, Java Full stack developers, Python/Java developers, Data analysts/Data Engineers/ Data Scientists, Machine Learning engineers for full time positions with clients.

Job Description KAYGEN is an emerging leader in providing top talent for technology-based staffing services. We specialize in providing high-volume contingent staffing, direct hire staffing and project-based solutions to companies worldwide ranging from startups to Fortune 500 and Managed Service Providers (MSP) across a wide variety of industries. JOB TITLE -Scientist 2 LOACTION -San Diego California 92130 Duration - 12 months with possible extension We are seeking two highly motivated and detail-oriented Technical Data Associates to support a product data refresh initiative within the Reagent Product Management team. The ideal candidate must have hands-on flow cytometry experience and independent flow cytometry data analysis skills, including the ability to interpret dot plots and histograms, evaluate data quality, apply gating strategies, and prepare accurate customer-facing figures. Key Responsibilities • Review and analyze flow cytometry data for customer-facing technical materials., • Interpret dot plots, histograms, staining patterns, and flow cytometry results., • Independently identify data-quality issues, inconsistencies, and missing information., • Apply appropriate gating strategies and maintain consistent plot formatting., • Prepare accurate technical/product figures., • Write and update concise figure descriptions based on experimental data., • Follow established SOPs, templates, naming conventions, and formatting standards., • Enter and maintain technical information in internal product-data systems., • Maintain accurate documentation, project trackers, record status, and review items., • Work with Product Management, R&D, Technical, and Quality teams., • Identify opportunities to improve data quality, consistency, and workflow efficiency.Required Technical Skills MUST HAVE: • Hands-on Flow Cytometry experience., • Independent flow cytometry data analysis experience., • Ability to interpret dot plots and histograms., • Experience with gating and plot formatting., • Experience with at least one:, • FlowJo, • BD FACSDiva, • FCS Express, • Equivalent flow cytometry analysis software., • Ability to recognize data-quality issues and inconsistencies., • Strong Excel skills and experience maintaining large data trackers., • Ability to follow SOPs, templates, naming conventions, and quality requirements., • Strong attention to detail. At KAYGEN, people are at the heart of everything we do. We foster a diverse, inclusive, and employee-driven culture where every individual is valued, empowered, and encouraged to bring their authentic self to work. Our candidate-first approach means we are committed to understanding your career goals and connecting you with opportunities that align with your aspirations, skills, and potential. Whether you're taking the next step in your career or searching for your dream opportunity, KAYGEN is more than a staffing partner—we're a community dedicated to helping you grow, succeed, and thrive. Join us and discover a place where your talent is recognized, your ambitions are supported, and your future is built alongside a team that invests in your success every step of the way. Our team of experienced staffing experts will work with you to find you the best opportunity. For more information, please visit us at www.kaygen.com. Benefits: • Free Healthcare Insurance, • 401(k) Retirement Plan, • Free Life Insurance, • Sick Time OffAchieve your Kaizen by clicking here. A unique and exclusive talent community supported by KAYGEN, that includes programs like:, • Mentorship Program, • Certifications, • Referrals, • Family and Wellness benefits, • Continuous Growth and Career Development

Job DescriptionDescription: Position Title: Scientist Reporting to: Associate Director, ASO Strategy Research Location: San Diego, CA 92121 Employment: Full-time Salary range: $90K - $120K n-Lorem Foundation Though n-Lorem is pioneering a novel non-profit model, to provide personalized experimental ASO treatments for free, for life to patients with the rarest of mutations (nano-rare), we are functionally a biotechnology company. We have a large and growing portfolio of ASO medicine discovery programs, ASO medicines in development and multiple clinical programs. With a seasoned leadership team and strategic partnerships, the n-Lorem Foundation provides the framework, funds and access for nano-rare patients who are amenable to our technology to receive personalized ASO medicines for free, for life. We hope that you will consider joining us as we strive to change the world, one nano-rare patient at a time. If you are a professional with strong biotechnology experience and would like to join a cohesive, experienced team committed to the belief that we can change the world one patient, one family at a time, we may have a position for you. Job Overview We are seeking a highly motivated Scientist to join our dynamic and innovative Discovery and Research team focused on developing novel antisense therapies for nano-rare diseases. Reporting to the Associate Director, ASO Strategy Research, the successful candidate will play a key role in advancing novel ASO strategies, conducting mechanism-of-action studies, and contributing to next-generation ASO designs. This role will contribute to the development and validation of novel ASO approaches by conducting rigorous in vitro experiments, integrating molecular biology with cell biology, and collaborating across cross-functional teams. This is an exciting opportunity to help build the future of personalized ASO therapeutics in a mission-driven, fast-paced, and innovative environment. Key Responsibilities • Execute, troubleshoot and analyze in vitro screening experiments supporting ASO design, optimization, and mechanistic understanding., • Execute, troubleshoot, and analyze in vitro screening experiments within our pipeline to evaluate potential clinical compounds., • Work closely with cross-functional teams to ensure smooth communication and alignment, contributing to the strategic advancement of our research goals., • Plan and conduct molecular and cellular biology experiments to advance our understanding of antisense oligonucleotide, • Adapt quickly to evolving priorities and provide timely updates and clear communication on research progress., • Collaborate with internal teams to design and execute experiments that will inform decision-making and drive progress in the development of novel therapeutics., • Maintain accurate electronic laboratory records, analyze and communicate results, develop reproducible procedures, and collaborate across the team to meet program timelines.Requirements:, • US work authorization is required., • Bachelor (BSc) or Master’s degree (MSc) or equivalent experience in oligonucleotide research and discovery. 2+ years of industry experience is strongly preferred., • Drug discovery experience is strongly preferred., • Demonstrated hands-on proficiency in qPCR, including RNA isolation, cDNA preparation, assay setup, data analysis, and troubleshooting., • Strong experience with protein analysis techniques, including Western blot and ELISA., • Experience with molecular cloning, including PCR, primer design, plasmid construction and preparation, bacterial transformation, and sequence verification., • Experience in culturing and transfecting mammalian cell lines, fibroblasts, and iPSC-derived cells is strongly preferred., • A proven track record of working in a highly collaborative, team- and mission- oriented environment. Track record of accomplishments, including publications in top-tier scientific journals is preferred., • Strong experience in performing high-throughput screening assays and data analysis., • Excellent interpersonal skills, with a proven ability to build and maintain effective working relationships within teams and with external partners., • Ability to manage assignments in a fast-paced, rapidly changing environment., • Strong ability to collaborate effectively within a team., • Self-starter with a high level of motivation, and a willingness to take initiative and embrace new challenges. n-Lorem offers a competitive benefits package including medical, dental, vision, 403(b) and four (4) weeks paid vacation. n-Lorem is a small foundation with an extraordinary mission, to provide hope and potentially help to nano-rare patients today. Every employee in our organization is a significant contributor to this mission. We know that our work could have a profound impact on the life of a patient today. For more information on n-Lorem, please visit our website www.nlorem.org

Job Description Location: San Diego, CA Job Type: Full-Time Salary $110,000 - $120,000 Position Overview We are seeking a Scientist II to support the development, optimization, and maturation of molecular methods for clinical next-generation sequencing (NGS) assays. This is a hands-on, bench-focused individual contributor role: executing the experiments that move nucleic acid extraction and library preparation methods from feasibility toward robust, automation-ready processes suitable for transfer to clinical lab operations. Working closely with senior scientists and process engineers, the Scientist II will run structured experiments, generate and analyze high-quality data, and contribute to the optimization of buffer formulations, reaction conditions, and process parameters that drive method performance and stability. The role is well suited to a scientist with strong molecular biology fundamentals and solid bench execution who is ready to grow toward independent method development in a rigorous, quality-oriented environment where methods are actively evolving. Key Responsibilities • Execute bench experiments that advance library preparation methods from feasibility toward production-ready performance., • Prepare and test buffer formulations and reaction conditions, and contribute to method optimization by generating and analyzing systematic, well-controlled data., • Execute systematic experiments, and perform data analysis to characterize method performance., • Run stability and robustness studies per established protocols, and summarize results clearly., • Support the transfer of bench methods including hands-on protocol execution, method-comparison runs, and troubleshooting., • Contribute to reagent QC by executing QC assays., • Support tech transfer and analytical validation activities through bench execution, troubleshooting, and documentation., • Maintain rigorous, well-organized experimental records (electronic lab notebook), generate clear data summaries and technical reports, and contribute to process and design documentation., • Collaborate with assay development, process engineering, automation, quality, and clinical operations to advance methods from feasibility through production. Qualifications Required: • BS in Molecular Biology, Biochemistry, Chemistry, or a related field with 3+ years of relevant laboratory experience; or MS with 2+ years; or a PhD in a relevant field., • Solid molecular biology and biochemistry fundamentals, with hands-on experience in library preparation and workflows., • Demonstrated bench proficiency in core techniques, with accurate, reproducible execution and strong attention to detail., • Working familiarity with structured experimental design and data analysis., • Rigorous, well-organized record-keeping and the ability to generate clear technical data summaries., • Ability to execute independently on assigned experiments and manage parallel bench work in a fast-moving, early-stage environment. Preferred: • Experience with low-input or other challenging workflows., • Hands-on experience with liquid handling platforms., • Exposure to a regulated or quality-driven environment and familiarity with design controls., • Programming or scripting experience (Python, R) for data analysis or experimental workflows., • Familiarity with QC metrics and data interpretation., • Comfort operating in a stealth-stage, resource-constrained environment where the development roadmap is actively evolving. Why Join Us • Influence the foundational technologies and strategies of a company poised to shape the future of clinical genomics and healthcare., • Work in a dynamic, collaborative environment where innovation and scientific rigor are deeply valued., • Join a seasoned and multidisciplinary team tackling high-impact problems at the intersection of science and engineering., • Competitive compensation and equity package, comprehensive benefits, and flexibility to support work-life integration.

Job Description Scismic is supporting a global consulting company that fosters a highly collaborative and inclusive culture, encouraging creativity, growth, and innovation. With a team of over 1,000 professionals across 50 global markets, the organization partners with world-class clients to solve complex business challenges across diverse industries. The company values a “builder’s mindset,” empowering employees to create new solutions, develop lasting impact, and grow their careers in a supportive environment. The company is seeking an exceptional Senior Data Scientist with deep expertise in Natural Language Processing and Large Language Models to join the consulting practice. You'll work directly with Fortune 500 clients to solve complex business challenges using state-of-the-art AI technologies across diverse industries. Ideal Candidate Profile You combine academic rigor with practical engineering skills and exceptional client communication abilities. You will work end-to-end from project initiation through client delivery, comfortable both building sophisticated algorithms and presenting findings directly to clients. You excel at automating repetitive tasks and developing reusable frameworks that scale across multiple engagements. You should be comfortable implementing cutting-edge research while translating complex technical concepts into actionable business strategies. Strong presentation skills and the ability to build trust with senior executives are essential. Equal Opportunities Our mission is to create a positive and entrepreneurial environment where talented people thrive on creativity. We celebrate inclusivity and are committed to providing an inclusive environment for our employees. We do not tolerate discrimination or harassment of any kind and are committed to building an agency where everyone is welcome, and every voice is heard. We are proud to be an equal opportunity employer. In order to comply with equal pay and salary transparency laws in various locations, we believe the target range of base compensation in all locations within the United States for this role is $155k-$240k. Actual compensation is influenced by a wide array of factors including but not limited to skill set, level of experience, and location. In addition to medical, dental and vision coverage, we offer a generous unlimited PTO plan, 401k program and comprehensive benefits plan. Additional perks and benefits include a month-long sabbatical, active employee advocacy groups, globally driven inclusivity initiatives, wellness days, summer Fridays and learning and development programs for our employees. Responsibilities: • Lead client workshops and discovery sessions to identify NLP opportunities, • Develop and present technical proposals to C-level executives, • Manage multiple client projects simultaneously while maintaining quality and timelines, • Design and implement novel NLP solutions for complex business problems, • Architect scalable solutions for processing and analyzing large text corpora, • Build custom language models tailored to each client's unique industry challenges, • Automate repetitive analytical tasks and develop reusable algorithmic frameworks, • Mentor junior data scientists and provide technical guidance on NLP projects, • Develop automated content analysis, document processing, and customer insight systems, • Create scalable text analytics platforms that drive measurable business outcomes, • Work across retail, finance, healthcare, and media sectors, • Translate complex AI capabilities into clear business value propositionsTechnical Environment:, • Languages: Python (primary), R, SQL, potentially C++ for optimization, • ML Frameworks: PyTorch, TensorFlow, Hugging Face Transformers, • Infrastructure: Kubernetes, Docker, cloud platforms (AWS/GCP/Azure), • Tools: MLflow, Weights & Biases, Apache Airflow, Spark, Vector databasesRequired Qualification:, • PhD in Computer Science, Computational Linguistics, Statistics, Mathematics, Economics, Econometrics, or related quantitative field, • Minimum 5 years of professional experience in data science, machine learning, or related roles, • Advanced NLP expertise: Deep understanding of transformer architectures, attention mechanisms, and modern NLP techniques, • Large Language Model proficiency: Hands-on experience with LLM fine-tuning, prompt engineering, RLHF, and deployment at scale, • Programming mastery: Expert-level Python, with strong knowledge of PyTorch/TensorFlow, Hugging Face ecosystem, • MLOps & Infrastructure: Experience with model deployment, monitoring, and scaling in production environments, • Experience writing production code and ensuring well-managed software delivery, • Experience with foundation models (GPT, BERT, T5, LLaMA, etc.), • Knowledge of retrieval-augmented generation (RAG) systems, • Understanding of model compression techniques (quantization, distillation, pruning), • Experience with evaluation metrics and benchmarking for language modelsPreferred:, • Experience in consulting or client-facing technical roles, • Knowledge of specialized domains (healthcare NLP, legal AI, financial text analysis), • Cloud platform expertise (AWS SageMaker, Google Cloud AI, Azure ML), • Open-source contributions to major ML/NLP librariesBenefits:, • Hybrid work environment with home and office schedule (2+ days in office per week) and work from anywhere weeks, • Comprehensive health benefits (healthcare, vision, dental, pet, home, and auto insurance), • Generous time off policies (unlimited paid time off, wellness days, national holidays, summer Fridays), • Four-week sabbatical every five consecutive years of employment, • Exceptional parental leave benefits, • Global mentorship and networking programs, • Monthly cell phone reimbursement, • 401k savings and employee stock purchase plan, • Volunteer hours (20 hours annually) for designated non-profit partner and personal choice, • Globally driven inclusive initiatives (Employee Advocacy Groups, equity committee), • Career growth opportunities (multi-day customized trainings for each level)Equal Opportunities:, • Our mission is to create a positive and entrepreneurial environment where talented people thrive on creativity. We celebrate inclusivity and are committed to providing an inclusive environment for our employees. We do not tolerate discrimination or harassment of any kind and are committed to building an agency where everyone is welcome, and every voice is heard. We are proud to be an equal opportunity employer., • In order to comply with equal pay and salary transparency laws in various locations, we believe the target range of base compensation in all locations within the United States for this role is $155k-$240k. Actual compensation is influenced by a wide array of factors including but not limited to skill set, level of experience, and location., • In addition to medical, dental and vision coverage, we offer a generous unlimited PTO plan, 401k program and comprehensive benefits plan. Additional perks and benefits include a month-long sabbatical, active employee advocacy groups, globally driven inclusivity initiatives, wellness days, summer Fridays and learning and development programs for our employees.

Job Description Overview We are seeking a highly motivated and skilled Scientist to join our Protein Sciences team and contribute to both day-to-day operations and the advancement of Protein Science workflows. This position will focus on the design, optimization, and execution of transient transfection processes at various scales for antibody and protein production in mammalian expression systems. The successful candidate will leverage expertise in biophysical characterization and biochemical modification to evaluate key protein attributes. This position will report to the Associate Director of Protein Sciences and work closely with scientists in the Antibody Discovery, Antibody Engineering, Protein Sciences, and Project Management teams. The ideal candidate will drive innovation through process refinement, high-throughput automation, and growing proficiency of chemical conjugation techniques. This role offers the opportunity to work in a fast-paced, collaborative research environment, where creative solutions and a strong scientific approach are key to success. AlivaMab Biologics is a rapidly growing leader in the discovery of human antibody therapeutics, trusted by top-tier pharmaceutical and biotechnology companies to deliver panels of drug-quality human antibodies. We deliver on our partners' design goals, from simple to extraordinarily challenging, through collaborative access to our scientists' creativity and experience combined with proven technologies, including the AlivaMab® Mouse suite of transgenic mice. We excel in the rapid and efficient delivery of molecularly diverse therapeutic antibody candidates, well-characterized for function, kinetics, and developability, with expanding capabilities for engineering advanced modalities, including multispecifics, single-domain human VH antibodies. Our organization is dedicated to creating a healthier world through partnerships that bring better medicines to patients faster, and we recognize our success starts with hiring people who share our passion for science. Responsibilities • Independently design, execute and optimize transient transfection workflows for antibodies and proteins in various mammalian expression systems, • Troubleshoot and refine current Protein Science processes, for throughput, quality, and efficiency, as needed, • Design and conduct small to mid-scale antibody purification by affinity, ion-exchange or other chromatographic methods from hybridoma and recombinant expression, • Perform antibody characterization (SDS-PAGE and SDS-cGE, SEC-HPLC, SEC-MALS) for quality control and support developability assessment of antibodies for stability, purity and other relevant biophysical properties, • Explore, enable, and execute the development of automated high throughput processes to support antibody production workflows on Bravo, and other platforms, • Develop expression and purifications methods for antibodies, difficult-to-handle proteins and optimize platform processes for higher production yields and product stability, including VLP production, • Develop a strong understanding of current protein chemical conjugation techniques, and work to optimize and validate them for research applications, • Effectively maintain meticulous records of lab activities using electronic notebook (Benchling); communicate findings clearly through written reports and presentations to support project progression and scientific decision-making, • Manage multiple projects independently demonstrating strong self-motivation, effective time management, and the ability to consistently meet project deadlines, • Demonstrate attention to detail and scientific judgment essential for guiding data-driven decisions, • Drive innovation and project success by providing creative solutions to protein science challenges, taking initiative to explore new ideas and approaches while collaborating effectively within the team and cross-functionally in a fast-paced research environment Qualifications • Ph.D. in Biochemistry, Chemistry, Molecular Biology, Protein Engineering, or a related field with a minimum of 1-3 years of industry experience or MS with minimum of 5-7 years of direct industry experience is required, • Proven hands-on experience with multiple mammalian expression platforms is required, • Proficiency with AKTA instrumentation, demonstrating a broad range of standard and unique antibody purification (e.g., affinity, ion exchange, HIC and SEC) and QC techniques is required, • Demonstrated track record of generating high-quality recombinant proteins for biophysics or assay development in a timely manner, • Experience with SDS-PAGE or SDS-cGE, SEC-HPLC, SEC-MALS, and mass spectrometry-based methods for antibody analysis, • Experience with therapeutic antibody developability assessment is a plus, • Excellent troubleshooting and problem-solving capabilities are required, • Self-motivated team player with excellent record keeping as well as written and verbal communication skills, • Extraordinary attention to detail, planning, and organizational skills are required, • Creative thinker who demonstrates initiative and a desire to collaborate in an exciting and fast-paced research environment About AlivaMab Biologics AlivaMab Biologics sets its partners’ antibody discovery programs on the fastest and most de-risked path through discovery and development. Trusted by top-tier pharmaceutical and biotechnology companies, AMB delivers drug-quality, fully human antibodies on exceptional timelines. AMB achieves its partners’ design goals, from simple to extraordinarily challenging, through the generation and function-first screening of large, molecularly diverse panels of antibodies. AMB focuses on rapid and efficient delivery of antibodies, characterized for function, kinetics and developability, and engineering for alternative formats, including multi-specifics and CARs. The AMB team’s experience and passion for antibody drug discovery and development combined with the use of trusted, proven technologies, including Ablexis' AlivaMab® Mouse platforms, ensure the highest probability of success. AlivaMab Biologics provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to religion, race, creed, color, sex, sexual orientation, gender identification, alienage or citizenship status, national origin, age, marital status, pregnancy, disability, veteran or military status, predisposing genetic characteristics or any other characteristic protected by applicable federal, state or local law. Salary Range: $118,000 - $145,000 annually This range represents AlivaMab Biologics' good-faith estimate of the base compensation for this position at the time of posting. Offered title and compensation will account for factors such as experience, education, and comprehensiveness of qualifications. The salary range excludes bonuses, equity, health benefits, PTO, other benefits, or any other forms of compensation that may be part of the total compensation package. #LI-DNI

Job Description About Artiva: We are a clinical-stage biotechnology company focused on developing natural killer (NK) cell-based therapies. Our mission is to develop effective, safe, and accessible cell therapies for patients with devastating autoimmune diseases. We aim to develop therapies that patients and physicians can utilize in a community setting. Our lead product candidate, AlloNK®, is a non-genetically modified, cryopreserved NK cell therapy being evaluated in combination with B-cell targeted monoclonal antibodies (mAbs). We believe the compelling cell killing properties of NK cells, when combined with mAbs for targeting, creates an opportunity to generate potentially transformative therapies. For more information, visit www.artivabio.com. Job Summary: The Associate Scientist, Process Development Analytics will be responsible for completing analytical testing in support of the development of off-the-shelf, allogeneic, natural killer (NK) cell-based therapies. Operating in a cross-functional and dynamic environment, the individual will work closely with the Analytical and Process Development teams to transfer and conduct characterization testing to support Process Development activities. The ideal candidate should have a proven track record of conducting analytical testing for cell therapy products. Duties/Responsibilities: • Conduct routine in-vitro testing to support Process Development experiments and enhance process and product understanding., • Analyze data, interpret results, trend data and maintain detailed records., • Provide data for technical reports, standard operating procedures, and regulatory submissions in support of process development activities., • Manage assay transfer from internal Artiva functional groups to Process Development as needed. • Identify assay and process issues, investigate root cause, and drive troubleshooting through to resolution., • Coordinate activities within a collaborative work environment across functional teams to support process development as well as the characterization of Artiva’s products., • Train Process Development personnel on analytical testing procedures as needed. Requirements: • B.S. with 8+ years or M.S in a biological field with a minimum of 5+ years of relevant laboratory experience., • Hands-on experience (equipment and software) with flow cytometry, plate readers, and automated cell counters required., • Experience with functional assays is a plus, • Strong organizational, recording keeping, time management, and communication skills are required., • Previous exposure to analytical testing in a Pharma/Biotech, regulated (GxP) environment is preferred., • Experience in cell therapy, immunology, or oncology is strongly preferred. In addition to a great culture, we offer: • A beautiful facility, • An entrepreneurial, highly collaborative, and innovative environment, • Comprehensive benefits, including:, • Medical, Dental, and Vision, • Group Life Insurance, • Long Term Disability (LTD), • 401(k) Retirement Plan, • Employee Assistance Program (EAP), • Flexible Spending Account (FSA), • Paid Time Off (PTO), • Company paid holidays, including the year-end holiday week, • Our recognition program, Bonus.ly, is where you can trade in points earned for things you want. If all this speaks to you, come join us on our journey! Base Salary: $ 112,000 - .$129,000 annually. Exact compensation may vary based on level, skills and experience.

Job DescriptioniQuasar is seeking to fill an Data Scientist/Machine Learning Engineerin San Diego, CA. At iQuasar, we strive to provide the next generation of cutting-edge technologies. Our growth means exciting career opportunities for talented professionals in engineering, software development, and other key areas. We offer competitive compensation and benefits, including Health, Vision, and Dental Insurance, a matching 401 (k) plan, and other benefits given below, excellent training, and a vibrant working environment. Our employees are exceptional, giving us a competitive advantage by innovating solutions with a strong sense of mission and integrity. One of our clients in San Diego, CA, needs a Data Scientist for a full-time position. Position: Data Scientist (Machine Learning Engineer) Location: San Diego, CA Clearance Level: Secret JOB DESCRIPTION: iQuasar is seeking a highly motivated Data Scientist/Machine Learning Engineer to join our dynamic AI team. In this role, you will leverage machine learning algorithms and software engineering skills to contribute to diverse AI-based projects related to resource planning for ship maintenance, marine transportation, and climate/environmental informatics. Work will involve developing machine learning models that deliver predictive insights and analytics for robust, web-based full-stack AI applications spanning both government (DoD, DoT, NOAA, etc.) and commercial domains. Responsibilities: • Write code to extract and pre-process training data sets, handling disparate data formats and APIs., • Research, select, and develop appropriate ML/DL algorithms and models to tackle AI problems across disparate data domains (Navy, Transportation, Environmental Sciences, Healthcare, Public Safety, etc.)., • Work with the TRABUS Data Science team to deliver scalable AI solutions involving LLMs, RAG, prompt engineering, computer vision, and NLP tools., • Work alongside other AI/ML and DevOps engineers to establish automated AI workflows that continuously provide inferences/predictions., • Develop validation and test routines to measure and evaluate the quality of predictions.Required Qualifications, • 2+ years' programming experience in Python, • Completed coursework in Machine Learning, Deep Learning, Algorithm Design, and Data Science, • Knowledge of Python libraries such as Pandas, scikit-learn, Keras, TensorFlow, and/or PyTorch, • Good understanding of databases and API-based data ETL operations, • Strong knowledge of Linux or Unix-like OS., • Excellent coding skills in Python, ability to handle and analyze large data sets/streams, and familiarity with web frameworks such as Fast API, Django and Flask., • Experience handling git repositories., • US citizenship and the ability to obtain and maintain a final DoD adjudicated Secret ClearancePreferred Qualifications, • Strong knowledge of DevOps tools and practices., • Experience working with cloud platforms such as AWS, Azure, or Google Cloud., • Familiarity with agile development methodologies and continuous integration/continuous deployment (CI/CD) pipelines., • Proficiency in MS Office Applications, • Strong written and oral communication skills, • Attention to detail, procedural compliance, and the ability to manage multiple duties simultaneously while meeting deadlines, • Experience working in Agile environments, • DoD adjudicated secret clearanceEDUCATION:, • Bachelor's degree (Master's degree preferred) in Computer Science/Engineering/Data Science or other STEM related discipline.

Job Description We are seeking a highly motivated and rigorous Scientist to join the Analytical Development team to support the development, optimization and validation of molecular analytical methods for Kenai Therapeutic’s programs from early development through to commercial launch. The Scientist will work closely within the CMC team to consistently deliver quality data by maintaining continuous operations of extraction, manipulation and analysis of genetic material using various molecular biology techniques. The candidate will have expertise in molecular biology based analytical assay design and development, data analysis and presentation, robust experience with molecular biology related instrumentation operation and maintenance, and good documentation practices for project execution in a fast-paced biotech environment. This role is on-site in San Diego, CA and reports to the Director of Analytical Development. Responsibilities • Lead assay design, development and qualification/validation of molecular biology assays such as ddPCR, qPCR, etc., • Independently design, plan, troubleshoot and execute all aspects of laboratory daily activities, including instrument setup, sample preparation, assay execution and data analysis using industry standard software packages., • Maintain and manage cell lines/banks used in analytical assay development work., • Implement scientifically sound design strategies and establish standardized work templates., • Design and perform phase appropriate assay robustness studies following regulatory guidelines., • Generate, analyze, interpret and present scientific data in cross-functional meetings., • Maintain detailed records of executed lab work and reported results and data interpretation using electronic lab notebooks., • Apply statistical data analysis techniques using JMP, GraphPad Prism etc., to support experimental design and data interpretation., • Prepare assay development/technical reports, protocols, standard operating procedures and other relevant documents following industry standard documentation practices., • Conduct risk/gap assessments for method development and optimization at various phases of program lifecycle., • Ensure assays are fit-for-purpose and aligned with phase-appropriate regulatory expectations by exhibiting a strong understanding of regulatory principles for cell therapy industry as applicable to analytical development and validation activities., • Keep current on relevant scientific literature, new technologies/capabilities and support their implementation, as appropriate., • Partner with Process Development, Quality, Research teams and external CRO’s and vendors to ensure analytical readiness for clinical milestones., • Support method transfers, qualification and validation of assays in GMP environments to support drug product release and lifecycle management., • Demonstrate excellent written, verbal and interpersonal communication skills. Requirements Required Qualifications • Ph.D. in Immunology, Cell Biology, Neuroscience or related field with 2-3 years or M.S. with 6+ years of analytical development relevant industry experience., • Strong analytical skillset with deep expertise in various molecular biology assay development techniques, analysis, and data interpretation., • Hands-on experience with cell handling of suspension/adherent cultures of mammalian cells in BSC operations., • Strong understanding of ICH guidelines for analytical method development and validation and phase appropriate method lifecycle management., • Extensive experience in operating and maintaining advanced PCR, spectroscopic and molecular instruments including Qiagen, ThermoFisher, Biorad platforms etc. and their associated softwares such as QuantStudio, QX Manager, Quantasoft for operations and data analysis., • Familiarity with advanced statistical approaches for assay development and validation using JMP, Prism or equivalent tools., • Scientifically strong technical writing skills., • Good understanding of cell therapy product development and characterization., • Excellent organization and time management skills to work independently and balance multiple tasks and projects., • Ability to clearly analyze and communicate scientific findings and development rationale., • Ability to work in a small, fast-paced cross collaborative environment with strong listening, communication and collaboration skills. Preferred Qualifications • Experience supporting clinical programs from early phase to commercialization., • Working experience with mammalian cell culture, flow cytometry assays and cell-based assays., • Experience in assay transfers between CDMO’s and CRO’s and internal teams., • Prior experience in a startup or early-phase biotech environment. Benefits Additional Detail: The salary range for this position is $110,000 USD to $135,000 USD annually. This salary range is an estimate, and the actual salary may vary based on experience and/or the Company’s compensation practices. Kenai Therapeutics is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.

Job DescriptionSenior Scientist – Biomarker Development Kelly® Science & Clinical is seeking a Senior Scientist – Biomarker Development for a contract-to-hire position at a cutting-edge client in San Diego, CA. If you're passionate about bringing the latest scientific discoveries to life and are ready to take the next step in your career, trust The Experts at Hiring Experts. Pay: $130-170k Schedule: Remote M-F Overview Our Client is an industry-leading, clinical-stage biotherapeutics company that's leading the way in developing breakthrough neuroprotective therapeutics for highly prevalent, blinding diseases that currently have no good therapeutic alternatives. Using novel approaches, our Client is advancing first-in-class and best-in-class protein therapeutics and gene therapy solutions poised to significantly impact patients' lives. In this role, you will join a growing team as a Senior Scientist focused on biomarker development and testing, spanning research through early clinical development. You will help define fit-for-purpose biomarker plans for both gene therapy and small molecule therapeutic candidates, develop and qualify the assays that support those plans, and oversee execution of clinical testing through internal and external laboratories — including evaluating how a given drug impacts its target biomarker across both small molecule and biologic programs. Responsibilities: • Design, develop, and optimize molecular and protein-based assays for quantitation of therapeutic proteins, target engagement markers, and pharmacodynamic markers, including refinement of assay conditions, sample volume requirements, and matrix interference., • Evaluate emerging biomarker technologies and analytical approaches based on their ability to address meaningful development questions., • Manage and review assay development plans, qualification protocols, qualification reports, and SOPs., • Assist in the maintenance of critical reagents, qualification of new materials, lot-to-lot bridging, and reference standard lifecycle., • Oversee clinical biomarker sample testing at CRO partners, including sample logistics and chain of custody, data review, and vendor performance management., • Define sample collection, processing, shipping, and storage requirements for each sample type., • Serve as the biomarker representative and point of contact on internal teams, providing strategic biomarker input to program-level decision making based on the specifics of each assay or output of testing., • Author biomarker sections of clinical protocols, laboratory manuals, or other regulatory documents as needed., • Maintain accurate and detailed experimental notes in an electronic laboratory notebook or other report systems.Qualifications:, • MS with 6+ years, or PhD with 3+ years, of experience in a laboratory setting performing or managing molecular and/or cell-based experiments., • Hands-on experience developing and qualifying ligand-binding assays, with demonstrated proficiency in ELISA and MSD electrochemiluminescence methods, including troubleshooting sensitivity, background, matrix, and interference issues., • Experience overseeing or collaborating on in vitro and in vivo assay design to test gene therapy, small molecule, or protein products., • Experience taking assays from early development through qualification and into use for nonclinical or clinical sample testing., • Direct or CRO management experience involving sample testing procedures., • Preferred: experience supporting programs across multiple stages of clinical development and contributing biomarker content to IND or other regulatory submissions., • Prior experience documenting laboratory results in written or electronic laboratory notebooks and writing formal study reports., • Proven problem-solving skills with the ability to adapt to shifting priorities and deadlines., • Excellent verbal and written communication skills, including a strong command of written English for scientific writing., • Strong interpersonal skills and the ability to work and communicate effectively within the organization., • High personal integrity and strong work ethic., • Ability to operate with substantial latitude in a fast-paced environment.What happens next: Once you apply, you'll proceed to next steps if your skills and experience look like a good fit. But don't worry – even if this position doesn't work out, you're still in our network. That means our team of expert Science & Clinical recruiters will have access to your profile, making your opportunities limitless. p#1 As part of our promise to talent, Kelly supports those who work with us through a variety of benefits, perks, and work-related resources. Please note: The following benefits reflect Kelly's general offerings. Eligibility may vary by assignment, location, and job type. Kelly offers eligible employees voluntary benefit plans including medical, dental, vision, telemedicine, term life, whole life, accident insurance, critical illness, a legal plan, and short-term disability. As a Kelly employee, you will have access to a retirement savings plan, service bonus and holiday pay plans (earn up to eight paid holidays per benefit year), and a transit spending account. In addition, employees are entitled to earn paid sick leave under the applicable state or local plan. Click here for more information on benefits and perks that may be available to you as a member of the Kelly Talent Community. Why Kelly® Science & Clinical? Kelly Science & Clinical is your connection to premier scientific and clinical companies looking to hire industry experts just like you. Our team creates expert talent solutions to solve the world’s most critical challenges. Every day, we match science professionals with dream jobs that fit their skills, interests, and career goals-it’s the way we think job searching should be. Nearly 100 percent of our science recruiters have a professional background and education in science, so we know a thing or two about the science market and how to get your expertise noticed. About Kelly Work changes everything. And at Kelly, we’re obsessed with where it can take you. To us, it’s about more than simply accepting your next job opportunity. It’s the fuel that powers every next step of your life. It’s the ripple effect that changes and improves everything for your family, your community, and the world. Which is why, here at Kelly, we are dedicated to providing you with limitless opportunities to enrich your life-just ask the 300,000 people we employ each year. Kelly is committed to providing equal employment opportunities to all qualified employees and applicants regardless of race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, age, marital status, pregnancy, genetic information, or any other legally protected status, and we take affirmative action to recruit, employ, and advance qualified individuals with disabilities and protected veterans in the workforce. Requests for accommodation related to our application process can be directed to the Kelly Human Resource Knowledge Center. Kelly complies with the requirements of California’s state and local Fair Chance laws. A conviction does not automatically bar individuals from employment. Kelly participates in E-Verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S. Kelly may use AI-powered tools during the recruitment and hiring process. For full details, including how Kelly uses AI, your rights, and how to request a reasonable accommodation, visit the Recruitment Artificial Intelligence Notice.

Job Description Job Title: Analytical Chemist — Protein, RNA & Lipid Characterization (Ph.D.) Location: San Diego Job Type: Full-Time About Us: A new stealth-mode biotech focused on in vivo gene editing. Job Summary: We are seeking a highly skilled Analytical Scientist to join our team in a hands-on, lab-based role. The successful candidate will be responsible for developing, validating, and executing analytical methods for the characterization of proteins, RNA, and lipids central to our lipid nanoparticle (LNP) gene editing platform. This role requires deep expertise in LC/MS and complementary analytical techniques, with the ability to independently design experiments, troubleshoot complex analytical challenges, and deliver high-quality data to support research, process development, and regulatory submissions. The Analytical Scientist will serve as a subject matter expert across the organization on bioanalytical methodologies. Title and salary commensurate with experience. Key Responsibilities: • Design, develop, optimize, and validate analytical chemistry methods for the characterization of proteins (e.g., Cas9, antibody constructs), mRNA, gRNA, and lipid components using LC/MS (intact mass, peptide mapping, oligonucleotide analysis, lipidomics)., • Perform routine and non-routine hands-on analyses in the laboratory; operate, maintain, and troubleshoot LC/MS instrumentation (e.g., Q-TOF, Orbitrap, triple quadrupole) and associated sample preparation workflows., • Develop and execute orthogonal analytical chemistry methods including but not limited to HPLC/UPLC (RP, SEC, IEX, HILIC), capillary electrophoresis, UV/Vis spectrophotometry, and fluorescence-based assays., • Characterize LNP drug product attributes including lipid composition and ratios, encapsulation efficiency, RNA integrity, protein identity and purity, and post-translational or chemical modifications., • Support formulation development, process development, and stability studies by providing timely, high-quality analytical data and interpretation., • Author and review analytical methods, protocols, technical reports, and SOPs to support research activities and future regulatory filings., • Analyze and interpret complex mass spectrometry datasets; present findings to cross-functional teams and contribute to program-level decision-making., • Evaluate and implement new analytical technologies, software tools, and workflows to improve throughput, sensitivity, and data quality., • Collaborate closely with formulation scientists, biologists, process development, and CMC teams to ensure analytical needs are met across programs., • Maintain laboratory equipment, consumable inventories, and ensure compliance with safety and data integrity standards. Qualifications: • D. in Analytical Chemistry, Biochemistry, Chemistry, Pharmaceutical Sciences, or a related field with 5+ years of industry experience; or M.S. with 8+ years of relevant industry experience, or B.S. with 10+ years of relevant experience., • 3+ years of industry or postdoctoral experience in bioanalytical method development and characterization of biopharmaceuticals, nucleic acids, or lipid-based drug products., • Extensive hands-on experience with LC/MS platforms (Q-TOF, Orbitrap, or triple quadrupole) for protein, oligonucleotide, and/or lipid analysis., • Proficiency in chromatographic techniques (RP-HPLC, SEC, IEX, HILIC) and associated data analysis software (e.g., MassLynx, Xcalibur, Empower, BioPharma Finder, UNIFI)., • Strong understanding of protein characterization (intact mass, peptide mapping, glycosylation, disulfide mapping) and/or nucleic acid analysis (RNA integrity, modification mapping, sequence confirmation)., • Demonstrated ability to independently design experiments, interpret complex datasets, and communicate results clearly in written and oral formats., • Strong problem-solving skills and ability to manage multiple projects in a fast-paced environment. Preferred Qualifications: • Experience with lipid nanoparticle characterization and/or lipidomics by LC/MS., • Familiarity with mRNA and guide RNA analytical characterization (e.g., capillary electrophoresis, IP-RP-HPLC, LC/MS-based modification analysis)., • Experience supporting GMP or GLP analytical activities, method validation per ICH guidelines (Q2/Q14), or contributing to regulatory submissions., • Knowledge of gene therapy or gene editing product development and associated analytical expectations., • Experience with mass spectrometry-based quantitative assays (e.g., MRM/SRM for lipid or protein quantitation). Benefits: • Competitive salary, equity, and benefits package., • Opportunities for professional growth and development., • Fast-paced collaborative and innovative work environment. How to Apply: Interested candidates should submit their resume and a cover letter detailing their relevant experience. To be considered for the role, applicants must be: • Eligible to work in the United States for any employer without sponsorship., • Able to work onsite in the lab located in San Diego., • A direct candidate and not from a third party, i.e. staffing agency. Salary Range: $110,000 - $140,000

Job Description About the job Mercor connects elite creative and technical talent with leading AI research labs. Headquartered in San Francisco, our investors include Benchmark, General Catalyst, Peter Thiel, Adam D'Angelo, Larry Summers, and Jack Dorsey. Position: LLM Research Scientist (Pre-training & Computer Vision & Adversarial Robustness) Type: Contract Compensation: $100–$120/hour Location: Remote Role Responsibilities • Train image classifiers and generative image models from scratch. Fine-tune open-weight language models., • Optimize models with limited data, compute, and model-size budgets., • Enhance model robustness to adversarial inputs and conversations., • Compress models to meet size and latency constraints without losing accuracy., • Diagnose and resolve training issues effectively. Qualifications Must-Have • 3+ years of machine learning research experience (PhD research counts)., • Strong experience with PyTorch, JAX, TensorFlow, or similar ML frameworks., • Degree from a top-100 university, experience at a FAANG or comparable AI company, or equivalent research track record through publications or impactful open-source contributions. Preferred • Experience in scaling laws and training-efficiency research., • Knowledge of curriculum learning and data ordering., • Skills in model evaluation, uncertainty estimation, and model calibration., • Expertise in data augmentation and synthetic data for robustness. Application Process (Takes 20–30 mins to complete) • Upload resume, • AI interview based on your resume, • Submit form Resources & Support • For details about the interview process and platform information, please check: https://talent.docs.mercor.com/welcome, • For any help or support, reach out to: support@mercor.com PS: Our team reviews applications daily. Please complete your AI interview and application steps to be considered for this opportunity. #hiringmercor

Job DescriptionClearNote Health is an early cancer detection company focused on the development and commercialization of non-invasive epigenomic tests to detect cancer through a standard blood draw, earlier than existing methods and when the disease is still treatable. Leveraging its novel liquid biopsy technology, ClearNote Health is initially focused on high-mortality cancers with the greatest need for early detection, starting with pancreatic and ovarian cancers. Position Summary: We are seeking a Bioinformatics Scientist I/II/Senior to play a pivotal role in designing algorithms to identify early-stage cancer in cell free DNA from plasma. In this high-impact position, you will work as part of a collaborative team to analyze epigenomic and genomic features from cell free DNA and develop classification algorithms for early cancer detection. You’ll contribute across the full lifecycle—from experimental design and data analysis to production-ready code and results presentation to cross-functional teams. Key Responsibilities: • Design and analyze experiments using ClearNote’s epigenomics platform, • Develop and apply machine learning techniques tailored to the platform’s unique data characteristics, • Analyze clinical genomics data to train models that make clinically relevant predictions (e.g., cancer detection from epigenomic profiles), • Apply appropriate statistical methods to support rigorous, scientifically sound decision-making, • Evaluate and recommend software tools for epigenomic data analysis, • Write clean, maintainable code following software engineering best practices, • Present findings clearly, concisely, and quantitatively to cross-functional stakeholders, • Communicate hypotheses, data insights, and experimental designs to colleagues, collaborators, and advisors, • Embody and uphold ClearNote’s core values—visionary, pioneering, truth-seeking, driven, honest and considerate communication, and a commitment to diversity—while operating with transparency and integrityQualifications:, • PhD or equivalent experience in Biophysics, Genetics, Genomics, Biochemistry, Molecular Biology, or a related field with a strong computational focus, • Experience working with genomics technologies, preferably with cell free DNA, • Ability to interpret biological data quantitatively using principles of molecular biology and biochemistry, • Proficiency in statistical methods for supervised machine learning including logistic regression, random forest, and XGBoostExperience developing neural network models, particularly multi-layer perceptrons (MLPs), • Familiarity with deep learning approaches for genomic/epigenomic data (e.g., DNA sequence models or foundation models) is a plus, • Understanding of common parametric and non-parametric statistical tests, • Strong programming skills in Python and/or R, • Experience using Git for version control in a collaborative environment (branching, merging, pull requests), • Strong communication skills — both written and verbal — with the ability to explain complex concepts to cross-functional teams, • Experience with relational databases and SQL is a plus, • Experience with AWS services, particularly EC2 and Batch, is a plusThe anticipated salary range for this position is $125,000 to $180,000. The actual salary will be dependent on various factors that may include experience level, knowledge, skills, and abilities. Come join us in addressing large healthcare needs through precision epigenomic medicine! ClearNote Health is an exciting life science company that is reinventing non-invasive molecular diagnostic testing using next generation epigenomic technologies. We are passionate and dedicated to discovering and developing medicines that will make a significant difference in cancer and other epigenomic-driven diseases. Our technologies provide novel insight and quantitation of human health and disease, with our focus on precision medicine applications improving both clinical and health system outcomes. Our company was founded based on pioneering work in the Stanford laboratory of Stephen Quake, with advisors from Stanford and UCSF. We look for extraordinary lifelong learners with a passion and growth mindset for these areas, and for combining biological ingenuity with AI and data analysis. Led by a team with decades of experience bringing products from concept to market, we are an equal opportunity employer and value diversity at our company. We provide generous benefits to all employees including stock options. We are building a world-class company, based in San Diego and San Mateo. Our commitment to Diversity, Equity, Inclusion, and Belonging: We celebrate diversity in perspectives and backgrounds, and this is reflected in our innovation, our mission, and values. Our differences make us unique, help us innovate, and allow us to persevere. We strive to achieve representation and inclusion and redefine the possible in patients living longer lives. Powered by JazzHR 1sPtpmnTKi

Job Description Arrowhead Pharmaceuticals, Inc. (Nasdaq ARWR) is a commercial stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead therapies trigger the RNA interference mechanism to induce rapid, deep, and durable knockdown of target genes. RNA interference, or RNAi, is a mechanism present in living cells that inhibits the expression of a specific gene, thereby affecting the production of a specific protein. Arrowhead's RNAi-based therapeutics leverage this natural pathway of gene silencing. Arrowhead is focused on developing innovative drugs for diseases with a genetic basis, typically characterized by the overproduction of one or more proteins that are involved with disease. The depth and versatility of our RNAi technologies enables us to potentially address conditions in virtually any therapeutic area and pursue disease targets that are not otherwise addressable by small molecules and biologics. Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates. Arrowhead's corporate headquarters is in Pasadena, CA with research and development teams in Madison, WI & San Diego, CA, and a state of the art manufacturing facility in Verona, WI. Our employees are nimble, science-driven innovators who are collaborating to bring new therapies to patients in need. The Position The Senior Scientist will contribute to the integration of human genetics, multi-omics datasets, and real-world clinical data to generate human evidence supporting therapeutic development. This role will work at the intersection of translational genetics, computational biology, and real-world evidence (RWE) analytics to support target validation, patient stratification, clinical endpoint evaluation, and indication prioritization across Arrowhead therapeutic programs. The successful candidate will collaborate closely with the Translational Genetics & Data Science team as well as cross-functional partners including Real-World Evidence, Clinical Development, Translational Medicine, and Discovery Biology. The role will leverage large-scale biobank datasets, electronic health records (EHR), and other clinical datasets to translate human data into actionable insights supporting drug discovery and development. This position will play an important role in converting Arrowhead's growing access to biobank data and established computational pipelines into high-value insights that inform therapeutic strategy and precision medicine approaches. This role is onsite 5 days a week in San Diego. Responsibilities • Integrate human genetics, multi-omics datasets, and real-world clinical data to generate evidence supporting therapeutic target validation and indication prioritization, • Analyze large-scale biobank and population datasets to identify genetic associations and disease mechanisms relevant to Arrowhead therapeutic programs, • Collaborate with the Real-World Evidence (RWE) team to analyze clinical datasets including electronic health records (EHR), claims databases, registries, and longitudinal cohort data, • Conduct statistical and computational analyses to characterize disease progression, patient heterogeneity, and treatment outcomes using real-world datasets, • Translate genetic findings and clinical observations into hypotheses that inform biomarker strategies, patient stratification, and clinical trial design, • Develop scalable analytical workflows to integrate genetics, omics, and clinical data sources, • Work collaboratively with cross-functional teams including Discovery Biology, Clinical Development, Translational Medicine, and Data Science to support program decisions, • Present results to internal stakeholders and contribute to internal reports, project discussions, and scientific publications, • Manage multiple projects simultaneously and communicate progress and findings effectively to project teams and leadership, • Adhere to data governance and compliance standards when working with sensitive clinical datasets Requirements • PhD in Biostatistics, Statistical Genetics, Epidemiology, Bioinformatics, Computational Biology, Biomedical Data Science, or a related quantitative discipline, • 3+ years of experience in human genetics, biomedical data science, or real-world data analytics, • Strong experience leveraging AI/LLMs to accelerate end-to-end research workflows, including coding, data analysis, literature synthesis, and report generation, with demonstrated improvements in efficiency and output quality., • Experience working with biobank-scale datasets and real-world data sources such as EHR, claims databases, registries, or population cohorts, • Strong background in statistical genetics, epidemiology, or observational data analysis, • Experience integrating genetics, omics, and clinical datasets, • Proficiency in R or Python for large-scale data analysis, • Excellent problem-solving, analytical, and communication skills, • Ability to work effectively in a fast-paced, collaborative, and cross-functional research environment Preferred • Post-doc and industry experience, • Experience analyzing large-scale population genetics datasets such as UK Biobank, FinnGen, All of Us, or Genomics England, • Familiarity with analytical frameworks including phenome-wide association studies (PheWAS), Mendelian randomization, causal inference methods, and survival analysis, • Experience working with real-world clinical data models such as OMOP / OHDSI, • Experience collaborating with clinical development or real-world evidence teams, • Experience applying machine learning or advanced statistical methods to biomedical datasets, • Strong interest in translating human data into actionable insights for drug development California pay range $145,000—$165,000 USD Arrowhead provides competitive salaries and an excellent benefit package. Candidates must have current, valid authorization to work in the country where this role is located. California Applicant Privacy Policy

Job Description We are seeking a highly experienced Senior Data Scientist to lead advanced analytics, machine learning model development, and data-driven decision support within a Department of Defense (DoD) program environment. This role involves architecting and deploying end-to-end data solutions that enhance operational effectiveness, readiness forecasting, and mission-critical insights for Navy enterprise systems.Key ResponsibilitiesDesign, develop, and deploy predictive models, natural language processing (NLP), and optimization algorithmsLead data ingestion, cleaning, transformation, and exploratory analysis from diverse structured and unstructured data sourcesCreate interactive dashboards and visualizations to communicate analytical findings to technical and non-technical audiencesCollaborate with cross-functional teams including software engineers, data engineers, and subject matter expertsTranslate mission needs into analytical frameworks, model requirements, and implementation strategiesValidate and tune models for performance, explainability, and operational relevanceAuthor technical reports, white papers, and decision briefings for stakeholders and senior leadershipMinimum QualificationsU.S. Citizenship with an active or interim Secret clearanceBachelor's degree in Data Science, Computer Science, Statistics, Mathematics, or related field (Masters preferred)10+ years of professional experience in data science and leadership or senior technical roleSecurity+ CertificationProven experience with:Python, R, SQL, and Spark for data analysis and modelingMachine learning libraries such as scikit-learn, TensorFlow, PyTorch, or XGBoostData visualization tools like Power BI, Tableau, or PlotlyCloud platforms (AWS, Azure, or Google Cloud) and MLOps workflowsExperience working with DoD or federal data systems, including handling controlled unclassified information (CUI)Additional Preferred QualificationsExperience developing AI/ML solutions in support of Navy or defense logistics, sustainment, or readiness analyticsFamiliarity with DoD data governance, data labeling, and ethical AI guidelinesStrong understanding of model operationalization, A/B testing, and production monitoringKnowledge of data engineering concepts including ETL pipelines, data lakes, and data mesh architecturesAgile/Scrum experience or certifications (e.g., Certified Scrum Master, SAFe Practitioner)Ability to mentor junior data scientists and lead cross-disciplinary technical teams

Job Description Invivoscribe is an industry pioneer and global leader in precision oncology diagnostics. For more than 30 years we have driven international standardization of molecular and flow cytometry testing and expanded access to advanced cancer therapies worldwide. Our mission is simple and unwavering: Improving Lives with Precision Diagnostics ® We are seeking a Quality Control Scientist I. The QC Scientist I serves as a technical subject matter expert related to QC processes and procedures and QC representative for projects, product release, field actions, and post-market activities. This role involves applying scientific principles to quality control statistical data analysis, technical investigations, process improvement, and ongoing QC technical support. Headquartered in San Diego, with operations across North America, Europe, and Asia, Invivoscribe develops and manufactures a comprehensive portfolio of molecular and flow cytometry assays, reagents, controls, and bioinformatics tools under ISO 13485 design control. Our products and services support more than 700 clinical laboratories in over 160 countries. Core Responsibilities • Develops, improves and validates QC testing methods and processes., • Generates QC validation protocols and reports., • Supports transfer and implementation of new or modified test methods into routine QC operations., • Effectively creates, implements, maintains and improves the Standard Operating Procedures (SOPs), acceptance criteria, and other QC related documents., • Ensures that QC procedures accurately reflect current quality testing procedures, validated methods, product requirements, and applicable quality system requirements., • Designs, implements, and maintains statistical quality control and post-market surveillance activities., • Performs analysis and trending of QC data to identify shifts, trends, outliers, recurring issues, and opportunities for improvement, and recommends appropriate corrective, preventive, or improvement actions., • Develops and maintains QC metrics, reports, and visualizations to support technical review and testing process continuity., • Identifies opportunities to improve QC efficiency, reliability, consistency, throughput, and data integrity through automation and technology.Leads or provides technical assistance, including FMEA, for investigations involving NCMRs, PDs, CAPAs, product complaints and other quality events, including the designs and executes technical studies. Core Requirements • M.S. degree in a scientific discipline and, typically, 4+ years of experience in biotechnology, chemistry, or pharmaceutical QC laboratory to include 4+ years of molecular biology experience in a GMP regulated industry. Equivalent combination of education and experience will be considered. Advanced degree preferred., • Substantial experience with development, validation, optimization, troubleshooting, or implementation of laboratory test methods or technical processes., • Sound experience in molecular biology and/or molecular diagnostic testing in a GMP-regulated environment., • Substantial experimental skills with 3500xl Dx, ABI 7500 Dx, MiSeq Dx, BioTek plate fluorometer, QiaCube, 2100 Bioanalyzer, TapeStation, LabChip Gx, NanoDrop Spectrophotometer, iBright, single and multichannel pipettes., • High level proficiency in statistical quality control and application of statistical methods to laboratory, manufacturing, or quality data., • High level proficiency with medical device quality and regulatory requirements including QSR and ISO quality system standards, the IVD Directive and the IVD Regulation., • High level proficiency of GMP QC environment, including use of SOPs, MBRs, QCACs, QTPs, PSs and Oracle systems., • Experience with laboratory automation, automated liquid handling, automated data analysis tools, or process automation. Why Join Us At Invivoscribe, you will join a mission-driven global organization advancing the future of precision oncology. You will have the opportunity to shape major scientific and commercial partnerships that impact patients around the world. We offer: • Competitive compensation and performance incentives, • Comprehensive global benefits, • A collaborative, innovation-driven culture, • The opportunity to make a significant global impact in precision medicine If you are a persistent scientist with an aptitude for complex problem solving and a drive for continuous improvement, we look forward to speaking with you. Invivoscribe is an Equal Opportunity Employer.

Job Description ABOUT GENALYTE At Genalyte, we’re revolutionizing diagnostic testing to empower a healthier future. Genalyte is a San Diego-based diagnostics company developing the Merlin platform, a novel photonic ring resonator-based system designed to deliver rapid, multiplexed diagnostic results. We believe that timely and accurate health insights shouldn’t be a luxury, but a necessity. We are driven by a vision where advanced diagnostic capabilities are accessible, efficient, and seamlessly integrated into healthcare. Genalyte is more than just a laboratory; we are advocates for health empowerment, dedicated to providing insights that can transform lives and communities. WHY WORK FOR US Joining Genalyte at this pivotal pre-commercial stage means your work will have real, visible impact — on our technology, our culture, and ultimately on how diagnostic testing is delivered to patients. Regardless of your role, you'll be part of a collaborative team working closely with leadership to build something meaningful from the ground up. Genalyte offers competitive compensation including base salary, significant equity participation, and a comprehensive benefits package. This is a rare opportunity to grow alongside a high-impact company at a genuinely exciting moment in its journey. POSITION SUMMARY We are seeking a hands-on Scientific Data Scientist/Biostatistician to join our team to provide statistical analysis of complex data sets to support development of new assays and validation of clinical data. Proficiency in data analysis with a strong foundation in data validation, descriptive statistics, regression modeling and data visualization. Eager to collaborate with multidisciplinary research teams to clean datasets, generate accurate statistical outputs and support the development of new assays and validation of existing assays. ESSENTIAL FUNCTIONS & RESPONSIBILITIES These may include but are not limited to: Data management: Design, build, and maintain robust data pipelines and automated workflows to ingest, clean, and process raw experimental data Data Analysis and Modelling: Analyzing large-scale diverse datasets using advanced statistical modeling to evaluate study results Cross-Functional Collaboration: Translate complex biological questions into quantitative hypotheses, working closely with wet-lab scientists and R&D teams Insight Communication: Create clear data visualizations, dashboards, and technical reports to communicate findings to both technical and non-technical stakeholders ADDITIONAL FUNCTIONS & RESPONSIBILITIES Study Support: Help design research experiments and validation protocols with appropriate sample sizes to meet acceptance criteria. Provide a statistical analysis plan and expected calculations to achieve the goals of the study Regulatory Reporting: Create data tables, figures and summary reports to share findings with the internal regulatory group and regulatory agencies in support of 510(k) submissions Data Privacy: Handle experimental, clinical, and patient-related data in compliance with HIPAA and applicable data privacy and security policies, maintaining strict confidentiality of sensitive research and regulatory information EDUCATION, EXPERIENCE, KNOWLEDGE, SKILLS & ABILITIES Ph.D. or Master’s degree in Data Science, Bioinformatics, Computer Science, Statistics, or a related STEM field + 2yrs experience Programming: Advanced proficiency in Python or JMP (and core scientific libraries like pandas, NumPy, SciPy). Data cleaning and validation, format conversion, merging and sorting of complex, multi-factor data Data Science: Expertise in statistical analysis, experiment design, regression, clustering, and predictive modeling Insight Communication: Excellent verbal and written communication skills with the ability to explain complex quantitative results to scientists and executive leadership Organization: Strong project management skills and an ability to thrive in a fast-paced, matrixed biotech environment Collaboration: Working with cross-functional teams (research, validation, clinical, regulatory) to interpret results Prior experience in medical devices, diagnostics (IVD), or healthcare technology in a regulated environment (CLSI, FDA guidance, 510(k), etc ) is highly preferred TRAVEL REQUIREMENTS Minimal; occasional travel for industry conferences, partner meetings, or regulatory interactions (<10%). PHYSICAL REQUIREMENTS & WORK ENVIRONMENT This is a primarily office-based role in San Diego, CA. Occasional visits to laboratory and engineering environments may be required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. COMPENSATION The base salary range for this role is $105,000 - $120,000 per year. Individual pay may vary based on job-related skills, experience, and relevant education or training. In addition to base salary, this role includes meaningful equity participation, eligibility for the annual target bonus plan, and a comprehensive benefits package (health, dental, vision, and flexible time off policy). EQUAL EMPLOYMENT OPPORTUNITY Genalyte, Inc. is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, or any other legally protected characteristic. We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses and identifying potential inconsistencies or verification signals in application materials based on available information. 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 DescriptionHeadquartered in San Diego, Mulligan Funding serves as a leading provider of working capital (Up to $10M) to the small and medium-sized businesses that fuel our country. Since 2008, we have prided ourselves on our collaborative, innovative, and customer-focused approach. Enjoying a period of unprecedented growth, driven by the combination of cutting-edge technology, human touch, and unwavering integrity, we are looking to add to our people first culture, with highly motivated and results-oriented professionals, to push the limits of what’s possible while creating value for all of our partners. At Mulligan, we are transforming small business lending by replacing legacy processes with fast, intelligent, AI-driven decisioning. Backed by 18 years of proprietary credit data and deep risk expertise, our production-grade AI agents are already running in active credit and underwriting workflows. As we expand this AI-first approach across Sales, Customer Lifecycle, Finance, and Capital Markets, we offer an uncommonly rich environment for emerging data scientists. By stepping directly into the center of these efforts, you won't just observe modern machine learning—you will gain hands-on experience with advanced, industry-leading tools and complex technical architectures while contributing directly to our mission of scaling AI across the organization. Designed for ambitious graduates eager to solve real-world financial and risk challenges, the Data Scientist I Management Trainee role places you alongside senior leads in Credit & Pricing Strategy and Portfolio Analytics. In this position, your analytical rigor, SQL-based deep dives, and credit policy impact evaluations will directly inform key strategic decisions and drive our continuous growth. You will: • Perform SQL queries and complex data aggregations to support credit strategies and portfolio monitoring., • Conduct deep-dive quantitative analyses to evaluate credit policy changes and lending performance., • Collaborate with cross-functional teams including Risk and Operations to present analytical findings. Present analytical opportunities for business improvement , influence stakeholders with data backed strategies. • Work with data vendors in pushing data boundaries.Qualifications & Requirements, • Education: Bachelor’s degree in Mathematics, Statistics, or a related Quantitative field (must be in top 10% of graduating class)., • Technical Skills: Strong proficiency in SQL and Python for complex data aggregation and analysis., • Aptitude: High capacity for analytical reasoning and a solid quantitative background., • Location: San Diego, CA (On-site / Hybrid collaboration near business headquarters). A reasonable estimate of the base salary range for this role is $82,800 to $90,000 per year. In determining final compensation within the base range, Mulligan Funding considers a variety of factors, including market data, relevant experience, skills, and past performance. Mulligan Funding is an Equal Opportunity Employer (EOE) and takes great pride in building a diverse work environment. Qualified applicants are considered for employment without regard to age, race, religion, gender, national origin, sexual orientation, disability or veteran status. We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses and identifying potential inconsistencies or verification signals in application materials based on available information. 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 This position requires an ACTIVE DoD security clearance. Applicants who do not currently hold an active clearance will not be considered. At PMAT, we work on mission critical systems that directly support the warfighter, designing, building, and securing modern digital capabilities across cloud, data, and software environments. Our teams tackle complex, real-world challenges where delivery matters more than theory, and innovation is driven by curiosity, collaboration, and purpose. In this role, you’ll contribute to Naval Operational Architecture (NOA), working alongside engineers and operators to deliver resilient, forward-leaning solutions in support of national defense. About the role: PMAT is seeking a highly experienced and motivated Senior Software Engineer to contribute to the integration of AI capabilities into expeditionary systems, including sensor kits, UxS, C2, and TAK. The successful candidate will play a key role in enhancing the capabilities of expeditionary systems through innovative and cutting-edge technologies. Daily tasks can vary from hands on keyboard to technical discussions, including but not limited to, maintaining real-time Zenoh data mesh in Rust, creating frontend React applications in JavaScript, working with AI engineers to integrate machine learning models, converting data between standard tactical message formats, or providing subject matter expertise in discussions with senior management. Responsibilities: • Collaborate with cross-functional teams to understand and address the Navy's operational challenges integrating artificial intelligence into expeditionary systems., • Design, develop, and implement software for tactical applications, • Test software at field experiments to ensure performant and high-quality data flow between tactical systems, including sensors, UxS, and C2, • Collaborate with machine learning engineers and domain experts to analyze data and integrate machine learning solutions into existing systems., • Collaborate with data engineers to monitor data pipelines and analytics to ensure accuracy, reliability, and robustness., • Stay updated with the latest advancements in data architecture to propose and implement innovative solutions., • Work closely with systems engineers to connect data pipelines with operational systems, • Provide technical expertise and contribute to the development of long-term technology strategies within the Department of the Navy. About Us: PMAT is an innovative small business founded with a passion for developing forward-leaning solutions from exceptional people that increase the mission's capability. We focus on designing and building impactful digital solutions that utilize modern cloud, data, and software concepts. Our passion is working on complex and progressive challenges such as edge platform computing, containerizing legacy platforms, distributed data platforms, or heterogeneous data analysis. We recruit, retain, and foster a team motivated to pursue passions, investigate new ways of doing things, and embody an innovative and entrepreneurial spirit. We believe in being curious about every element of a problem and experiment relentlessly. We foster continuous learning in an environment that encourages positive collaboration and expands our capabilities. We tap into collective intelligence, acknowledging that the most brilliant people may not be in the room. Above all else, we believe that delivering and demonstrating is more potent than a sheet of paper. We are passionate about mission-centric design and delivering effective capabilities to and for the warfighter. Whether you’re an experienced engineer or just beginning your career, you’ll work alongside experts who are committed to solving mission-critical problems. If you’re passionate about using your skills to make a real difference, apply today and become part of a team that’s shaping the future of defense technology! Required Skills and Experience: • At least 10 years experience working as a business analyst, data analyst, data scientist, data engineer, database administrator, geospatial analyst, geospatial engineer, IT specialist, machine learning engineer, software engineer, or system administrator., • Familiarity with containerization technologies (e.g., Docker, Kubernetes)., • Expert programming skills in Python, • Intermediate programming skills in Rust or Go, • Experience designing or normalizing tactical data to common standards, • Experience with multiple data formats, e.g., CSV, JSON, XML, Parquet, ORC., • Familiarity with event streaming libraries and platforms, e.g., Apache Kafka, AWS Kinesis, RabbitMQ, ZeroMQ, or Zenoh., • Experience with troubleshooting tactical systems, • Experience deploying, monitoring, and improving tactical data pipelines, • Strong problem-solving and analytical skills., • Passion for staying updated with the latest advancements in tactical data architecture., • Excellent communication skills and the ability to work effectively in a collaborative team environment. Preferred Skills and Experience: • Experience integrating systems with Tactical Assault Kit (TAK) ecosystem., • Familiarity with data pipeline frameworks and libraries, e.g., AirByte, Apache Airflow, dbt, Apache Iceberg, Snowflake., • Experience with adding and retrieving data from Geographic Information Systems (GIS), e.g., ArcGIS, PostGIS., • Expertise in Elasticsearch, Redis, S3, PostgreSQL, or other data stores., • Understanding of cybersecurity principles in the context of tactical applications., • Previous experience working with government agencies or military organizations., • Master of Science in Computer Science, Data Science, Geography, Math, Machine Learning, or Statistics Education and Certification Requirements: • Bachelor’s Degree or Equivalent Experience Citizenship and Clearance requirements: • U.S. Citizenship required, • No dual citizenship, • Active DOD Secret security clearance is required, • TS/SCI Eligible security clearance preferred Location/Address: • 100% On-site, • San Diego, CA, NAVWAR, • Arlington, VA, • Colorado Springs, CO, • Charleston, SC, • Denver, CO, • Note: If San Diego is not your primary duty station, then you will be required to travel to San Diego for at least 5 weeks a year for team meetings and administrative tasks. Travel & Passport: • 10%, CONUS and OCONUS Work Environment: PMAT offices as needed. In some cases, work in a government facility may be required. Travel may be required for customer engagement, team coordination, and potentially for business development. PMAT is an equal-opportunity employer. We believe in hiring a diverse workforce and sustaining an inclusive, people-first culture. We are committed to non-discrimination on any protected basis, such as disability and veteran status, or any other basis covered under applicable law. #CJ

Mentor other data scientists and analysts, and contribute to technical standards, data governance, and MLOps best practices. Perform large-scale data processing and analysis using Python, SQL, Databricks, Spark, and distributed computing across structured and unstructured datasets. Evaluate and inte

As a Senior Data Scientist at Shopmonkey, you will be a part of a globally distributed team working closely with your product and engineering counterparts.We are looking for a generalist who thrives across the full project lifecycle — from statistical modeling and data analysis to experimentation

Experience with data visualization and analyst-facing tooling (Tableau, Power BI, D3. Binary Defense offers competitive medical, dental and vision coverage for employees and dependents, a 401k match which vests every payroll, a flexible and remote friendly work environment, as well as training oppor

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The Senior Environmental Scientist is responsible for planning and implementing field activities, evaluating laboratory data and measurements collected during field work and preparing technical documents under the direction of a Project Manager. The Senior Environmental Scientist will also provide s

Job Description The Senior Manager, Clinical Contracts will ensure the successful negotiation and ongoing management of clinical trial-related agreements and serve as the key liaison between Clinical Operations, Legal, Finance and Accounting departments. This role involves but is not limited to generating, reviewing, finalizing and tracking contracts and budgets, and managing cross-functional communication. This individual will be expected to support the clinical team in the planning, execution and control of contracts. The ideal candidate tasks effectively and applies critical thinking to resolve challenges while maintaining clear communication. ESSENTIAL FUNCTIONS AND RESPONSIBILITIES • Provide comprehensive contract lifecycle management., • Work closely with Clinical Operations, Legal, Finance, and other internal and external stakeholders to support the timely initiation, contractual term review, negotiation, risk assessment, execution and administration or contracts., • Manage tracking of contracts, amendments and budgets, and provide updates to the project and cross-functional teams., • Serve as point person for contracts with internal and external stakeholders., • Support RFx and Vendor Management activities., • Support internal oversight of site payment management., • Establish contracting SOPs and guidance documents., • Active participation in team meetings for the purpose of expediting contracts to execution., • Build and maintain strong relationships with external customers, investigators, and vendors., • Facilitate contract actions and processes independently and effectively in a dynamic environment with competing priorities., • Respond promptly and professionally to inquiries from internal team members and external vendors., • Strong analytical and contract administration skills, verbal and written communication skills., • Identify and implement process improvements to enhance efficiency and accountability., • Ensure compliance with SOPs and regulatory guidelines, addressing QA and audit requests as needed.EDUCATION, EXPERIENCE, KNOWLEDGE, SKILLS AND ABILITIES, • Bachelor’s degree required., • 8+ years of contract management experience within the biotechnology or pharmaceutical industry preferred. Experience within academia or a Clinical Research Organization (CRO) may also be considered based on the overall strength and relevance of the candidate's background., • Clinical Site Budget experience necessary., • Strong experience with global Phase 1-3 clinical trials. Oncology clinical trial experience preferred., • Grant Plan experience a plus., • Good knowledge of ICH-GCP, pharmaceutical related regulations and laws., • Ability to thrive in a fast-paced growing company with minimal direction and ability to adjust to changing priorities., • Proficiency in Microsoft Excel at an Intermediate level required. In addition to a competitive base salary ranging from $170,000 to $182,000, we offer stock options, restricted stock units, a stock purchase plan (ESPP) and a target bonus. Janux also provides a comprehensive benefits package for our employees and their families, which includes medical, dental, vision, and supplemental disability insurance. Relocation assistance may also be available. Please note that the base salary range is a guideline, and individual total compensation will vary based on factors such as qualifications, skill level, competencies, internal equity, and work location. Job Type: Full-time Benefits:· Annual bonus program· Incentive stock option plan· 401k plan with flat non-elective employer contribution· Comprehensive medical insurance with 90-100% employer-paid premiums· Dental and vision insurance· HSA, FSA, and supplemental insurance plans (life, disability, accident, critical illness, hospital indemnity)· Unlimited PTO· Generous holiday schedule; includes summer and winter company shutdown· Relocation assistance Schedule:· Monday to Friday Work authorization:· United States (Required) Additional Compensation:· Annual targeted bonus % Work Location:· Onsite in our San Diego office preferred; hybrid arrangements may be considered with approval and require a minimum of three days per week onsite. EQUAL OPPORTUNITY EMPLOYER:Janux Therapeutics, Inc. is an equal opportunity employer that is committed to providing a work environment free of harassment and discrimination based upon a protected category, as well as an environment free from retaliation for protected activity. Notice to Recruiters and Third-Party AgenciesThe Talent Acquisition team manages the recruitment and employment process for Janux. To protect the interests of all parties involved, Janux will only accept resumes from a recruiter once a fully-executed search agreement is in place. Agencies are hereby specifically directed not to contact Janux employees directly in an attempt to present candidates. Janux will consider any candidate for whom an Agency and/or Recruiter has submitted an unsolicited resume to have been referred, free of any charges or fees.Salary range and description Application questionsStandard Application Questions • Are you 18 years of age or older?, • Do you have proof of right to work in the United States?, • Will you now or in the future require Visa sponsorship?, • Are you able to relocate to San Diego and/or report in office 5 days per week?, • (Hybrid jobs ONLY) If you are not able to relocate and/or report to office daily, are you willing to travel to San Diego on a monthly basis or as needed?, • Please note your desired compensation (refer to job post for the salary range), • Please note your desired pronounDistributions: all applicationsClinical Scientist Questions, • Which therapeutic areas do you have experience in, and approximately how many years have you worked in each?, • What phases of clinical studies do you carry experience in?, • Which clinical and regulatory documents have you worked on, and what was your role in their preparation?Distributions: all applications We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses and identifying potential inconsistencies or verification signals in application materials based on available information. 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.

Description Ignite your curiosity. Solve the unsolvable. At Leidos, we do more than write code—we decode the unknown. Our San Diego-based research and engineering team takes on some of the nation’s toughest defense challenges using advanced signal processing, ocean remote sensing, and high-performance computing. We’re seeking a Software Engineer / Computer Scientist who enjoys solving complex problems and pushing the limits of performance. In this role, you’ll work alongside a multidisciplinary team of scientists and engineers with expertise in hydrodynamics, physics, acoustics, and signal processing to build impactful software that turns massive, complex data sets into meaningful insight. If you are motivated by innovation, energized by collaboration, and excited to see your work support real-world missions, this could be the right opportunity for you. What You’ll Do • Collaborate with scientists and engineers to design, develop, and optimize advanced algorithms for next-generation radar, optical, and infrared sensor systems., • Build scalable, high-performance backend systems for scientific computing in distributed environments., • Integrate, refactor, and improve scientific codebases to increase efficiency and scalability., • Translate and optimize existing code for GPU/CUDA acceleration and parallel or distributed execution., • Test, document, maintain, and enhance complex software in Linux/Unix environments., • Contribute in a collaborative environment that values technical excellence, creativity, and continuous growth. Required Qualifications • Bachelor’s degree in Computer Science, Applied Mathematics, Physics, or a related field with 4+ years of backend software development experience, or a Master’s degree with 2+ years of experience. Equivalent experience may be considered in place of a degree., • U.S. citizenship and the ability to obtain a Top Secret clearance; active Top Secret clearance preferred., • Strong expertise in C/C++ backend software development, including large-scale, performance-critical applications., • Experience with high-performance computing, parallel and distributed processing, and technologies such as MPI., • Hands-on experience with GPU/CUDA programming and optimization., • Familiarity with AI/ML and LLM concepts and algorithms., • Strong foundation in advanced mathematics or physics, with the ability to translate theory into practical software solutions., • Proficiency in Linux/Unix development environments., • Experience with scientific programming, algorithm development, and system-level problem-solving., • Solid understanding of software engineering principles and best practices., • Strong written and verbal communication skills, including software documentation. Preferred Qualifications • Active Top Secret clearance., • Familiarity with Agile development, object-oriented design, and modern software architecture., • Experience with Git, GitLab, MATLAB, and Fortran., • Knowledge of multithreaded or shared-memory application development. SUBSEAMSS If you're looking for comfort, keep scrolling. At Leidos, we outthink, outbuild, and outpace the status quo — because the mission demands it. We're not hiring followers. We're recruiting the ones who disrupt, provoke, and refuse to fail. Step 10 is ancient history. We're already at step 30 — and moving faster than anyone else dares. September 23, 2026 For U.S. Positions: While subject to change based on business needs, Leidos reasonably anticipates that this job requisition will remain open for at least 3 days with an anticipated close date of no earlier than 3 days after the original posting date as listed above. Pay Range $87,100.00 - $157,450.00 The Leidos pay range for this job level is a general guideline only and not a guarantee of compensation or salary. Additional factors considered in extending an offer include (but are not limited to) responsibilities of the job, education, experience, knowledge, skills, and abilities, as well as internal equity, alignment with market data, applicable bargaining agreement (if any), or other law. About Leidos Leidos is an industry and technology leader serving government and commercial customers with smarter, more efficient digital and mission innovations. Headquartered in Reston, Virginia, with 47,000 global employees, Leidos reported annual revenues of approximately $16.7 billion for the fiscal year ended January 3, 2025. For more information, visit _. Pay and Benefits Pay and benefits are fundamental to any career decision. That's why we craft compensation packages that reflect the importance of the work we do for our customers. Employment benefits include competitive compensation, Health and Wellness programs, Income Protection, Paid Leave and Retirement. More details are available at _. Securing Your Data Beware of fake employment opportunities using Leidos’ name. Leidos will never ask you to provide payment-related information during any part of the employment application process (i.e., ask you for money), nor will Leidos ever advance money as part of the hiring process (i.e., send you a check or money order before doing any work). Further, Leidos will only communicate with you through emails that are generated by the Leidos.com automated system – never from free commercial services (e.g., Gmail, Yahoo, Hotmail) or via WhatsApp, Telegram, etc. If you received an email purporting to be from Leidos that asks for payment-related information or any other personal information (e.g., about you or your previous employer), and you are concerned about its legitimacy, please make us aware immediately by emailing us at _. If you believe you are the victim of a scam, contact your local law enforcement and report the incident to the _. Commitment to Non-Discrimination All qualified applicants will receive consideration for employment without regard to sex, race, ethnicity, age, national origin, citizenship, religion, physical or mental disability, medical condition, genetic information, pregnancy, family structure, marital status, ancestry, domestic partner status, sexual orientation, gender identity or expression, veteran or military status, or any other basis prohibited by law. Leidos will also consider for employment qualified applicants with criminal histories consistent with relevant laws. #Featuredjob

Bachelor's degree in Data Science, Statistics, Economics, Mathematics, Computer Science, Engineering, Operations Research, or a related quantitative field; Master's degree or PhD preferred. Utilize Databricks and approved AI-assisted tools to accelerate data science workflows while maintaining stron

At ONI, we are driven by a profound mission: to propel scientific discovery and combat diseases by granting everyone the ability to visualize, comprehend, and share the intricate microscopic details of life. Our revolutionary Nanoimager stands at the forefront of advancing cellular studies on a molecular level, making substantial contributions to the evolution of scientific knowledge. We dedicate ourselves to broadening the realms of human potential, and we are actively seeking an enthusiastic and devoted Field Application Scientist to join our pioneering team. We believe in the power of relentless curiosity and the pursuit of excellence, and we invite you to join us in shaping the future of scientific exploration and healthcare breakthroughs. As a Field Application Scientist at ONI you will: • Demonstrate the value of ONI's technology suite to potential customers through in-person demonstrations at customer sites across multiple application spaces, • Deliver high-quality customer experience by maintaining cutting-edge imaging method expertise, operating as a peer to customers, • Create product awareness by engaging with the scientific community, answering technical questions, delivering presentations and demonstrations to showcase ONI's products at conferences, webinars, seminars, and other industry events, • Work closely with the Sales team to understand the status and details of each opportunity in the sales funnel, and providing scientific insights during pitches and meetings with potential customers, • Design and conduct experiments at customer's sites or in ONI's laboratory, to highlight how ONI's technology suite can solve specific challenges and meet their needs, • Assist customers in the setup and operation of products by conducting demonstrations and training sessions, both remotely and on-site, to ensure customers can effectively utilize ONI's products, • Provide ongoing hands-on support and guidance to customers, serving as a primary point of contact for technical inquiries, support requests, troubleshooting, and issue resolution, • Facilitate the packing & shipping of components, instruments and products to customer base and internal users using couriers, • Work with global logistics team to coordinate shipments and liaise with external and internal customers on a daily basis, • Maintain accurate records of customer interactions, demonstration outcomes, technical issues, and resolutions in Salesforce, • Generate regular reports on customer feedback, product performance, and customer success metrics for Product and Marketing teams to assess and improve customer satisfaction Essential Skills: • Characterized and performed data analysis of biological samples using relevant fluorescence microscopy techniques, • Designed protocols for preparation of samples in fluorescence in situ hybridization (FISH), immunohistochemistry or fluorescence microscopy., • Conducted physical demonstrations and presentations of innovative Life Science technologies to technical audiences, • Balanced and prioritized multiple projects in parallel and at different phases, • Worked as part of a multidisciplinary scientific team, • Sample preparation for fluorescence microscopy, fluorescence in situ hybridization (FISH) or immunohistochemistry, • Data analysis of microscopy data, • Identifying appropriate use cases for each type of microscopy experiments, • Commercial acumen and understanding of capital equipment sales process in life science industry, • Verbal and written scientific communication, • Presentation skills, • PhD in life sciences Desired Skills: • Built data science algorithms for image analysis, • Used super resolution microscopy for biological research, • CRM systems, ideally Salesforce, • Sample preparation for super-resolution microscopy, • At least 2 years in a commercial FAS role with at least 2 year in laboratory and related disciplines preferred. $100,000 - $115,000 a year At ONI, we understand that a fulfilling career involves more than just challenging work - it's about enjoying a well-rounded experience. When you become a part of our team, you not only contribute to groundbreaking research but also enjoy a range of benefits designed to enhance your life both inside and outside the workplace. As an equal opportunity employer, we prioritize fairness and respect, ensuring every team member thrives regardless of their background. But that's not all - our perks include: • Competitive Compensation We recognize and reward your talent. Enjoy a competitive salary that reflects your expertise and contributions, ensuring your hard work is recognized., • Flex PTO plus 11 federal holidays and 4 dedicated wellbeing days., • 401K via ADP, • Life Insurance, • Medical, • Dental, • Vision, • Perks at Work: Enjoy exclusive discounts and deals through our perks at work program, adding value to your everyday life. If you are driven by innovation, eager to make a significant impact in the realm of scientific and medical research, and possess the skills and passion we are looking for, we invite you to apply and be a part of our mission to improve our understanding of the details of life.

A healthier future. It's what drives us to innovate. To continuously advance science and ensure everyone has access to the healthcare they need today and for generations to come. Creating a world where we all have more time with the people we love. That's what makes us Roche. The Opportunity As a Senior Field Applications Specialist (Sr. FAS) Mass Spectrometry, you will be a key member of our Customer Support team and the primary scientific and technical authority for Roche's novel automated mass spectrometry solution, the cobas i601, in customer laboratories within the Core Lab space. Because fully automated mass spectrometry is a transformative, novel technology in a clinical market accustomed to traditional LC-MS/MS workflows, you will play a critical role in bridging the gap between complex analytical chemistry and automated routine testing. You will be responsible for building customer confidence, facilitating pre-sales technical adoption, delivering robust clinical training, and guiding labs through assay validation and regulatory compliance. As a Senior Field Applications Specialist Mass Spectrometry, you will: • Drive Scientific Adoption & Market Trust: Consult with clinical laboratory directors, pathologists, and LC-MS specialists to communicate the fundamental science, reliability, and operational advantages of automated mass spectrometry over traditional manual LC-MS/MS systems., • Pre-Sales Technical & Consultative Support: Partner with the commercial sales team as a subject matter expert. Lead technical presentations, address deep analytical and methodology concerns (e.g., ion suppression, matrix effects, mass accuracy, sensitivity), demonstrate menu expansion, and guide potential buyers through the transition to automated mass spec., • Method Validation & Regulatory Compliance: Guide lab personnel through assay implementation, verification, and validation protocols (CLSI guidelines, CAP, CLIA, ISO requirements) to ensure full regulatory compliance and seamless go-live status., • Build & Maintain Key Relationships: Build and maintain strong, collaborative relationships with key stakeholders, ensuring high customer satisfaction and positioning Roche as a long-term partner in clinical diagnostic excellence., • System Implementation & Application: Assist with the installation of mass spec instrumentation, automated front-end sample prep, and software applications in customer labs. Validate system performance to ensure it consistently meets or exceeds manufacturer specifications., • Deliver Comprehensive Training: Deliver on-site training to laboratory personnel on the operation, routine maintenance, theory of mass spectrometry, quality control (QC), calibration strategies, and automated data interpretation., • Advanced Technical Troubleshooting: Act as the primary on-site resource for resolving complex analytical, software, and hardware issues related to mass spectrometry and automated sample handling. Perform root cause analysis to minimize downtime., • Voice of Customer Feedback: Collect critical feedback on product performance, software usability, and workflow bottlenecks, relaying insights back to R&D and commercial leadership to drive continuous platform improvement., • Operational Execution: Follow Roche protocols, maintain accurate records in Roche's CRM system, and handle administrative duties (travel, expense reporting) promptly. This is a field-based role - overnight travel within a designated territory West Coast (San Diego/ Los Angeles) is expected > 80% of the time, depending on regional customer implementation and pre-sales needs. A company vehicle is provided with this position. Who You Are: • Bachelor's degree in Medical Technology, Information Technology, Computer Science, Chemistry, Biology or Clinical Laboratory or equivalent work experience., • 3 + years of experience implementing and evaluating complex laboratory, IT products, medical diagnostic equipment, reagents and/or systems. Preferred Qualifications • 3+ years of direct, hands-on experience operating, maintaining, and troubleshooting mass spectrometry platforms (LC-MS/MS) in a clinical, reference, or diagnostic laboratory setting., • In-depth understanding of mass spectrometry fundamentals, including triple-quadrupole systems, ionization techniques (ESI/APCI), chromatographic separations, sample preparation techniques, and quantitative data analysis., • Demonstrated ability to communicate complex scientific concepts to technical and non-technical stakeholders (lab directors, technicians, procurement teams)., • Advanced Degree: Master's or Ph.D. in Analytical Chemistry, Biochemistry, or related clinical science with a focus on LC-MS/MS., • Clinical Certifications: Medical Laboratory Scientist/Technologist (ASCP/AMT) or Board Certification in Clinical Chemistry / Toxicological Chemistry., • Regulatory Expertise: Strong working knowledge of clinical laboratory regulatory standards (CLIA, CAP, FDA, CLSI validation guidelines) specifically as they apply to clinical mass spectrometry and laboratory-developed tests (LDTs) / IVDs., • Sales Collaboration: Prior pre-sales support, application consulting, or customer-facing experience explaining novel diagnostic platforms., • Automation Knowledge: Experience with automated liquid handling, integrated automated front-end sample preparation, or automated clinical chemistry/immunoassay systems (e.g., cobas platforms)., • Troubleshooting Excellence: Proven track record of independently diagnosing complex analytical, chromatographic, or hardware issues., • Consultative Drive: Exceptional interpersonal, coaching, and stakeholder management skills with a passion for driving paradigm shifts in clinical lab operations. Relocation benefits are not available for this job posting The expected salary range for this position based on the primary location of California is $80,300.00 - $149,100.00. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law. This position is eligible to earn incentive compensation that is calculated and paid in accordance with the applicable Incentive Compensation Plan for the role. This position also qualifies for the benefits detailed at the link provided below. Roche is an equal opportunity employer. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company's policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws.

Would you enjoy being a part of a rapidly growing organization within Deloitte? Do projects that involve managing corporate governance, legal entity simplification and reviewing governance structures excite you? Deloitte's Tax Technology Consulting, Legal Business Services ("LBS") assists clients with all aspects of reporting and process for business as usual, as well as triggering and regulatory events. The Legal Entity Management team specifically focuses on corporate document assessments, annual compliance and management of corporate data. Additionally this team will be leading the review of governance structures, corporate changes, legal entity simplification, as well as central coordination combined with local, on the ground experience with jurisdictions around the world. Bring your expertise and client service skills to Deloitte. Work you'll do As a Senior Consultant in Legal Entity Management, your focus will be enabling our clients annual governance process with an emphasis on United States compliance, you will also support the review of governance structures, assessments of corporate documents and management of corporate data. You will be client facing, working with Deloitte Partners, Staff and Associates, on Legal Entity Management (LEM) projects and engagements. As a part of the practice you will proactively identify, pursue and execute on continuous service improvements through technology and process improvements. Responsibilities include structuring, running, and playing an execution role in the delivery of our United States Legal Entity Management operate services developing eminence and thought leadership materials in the field of Legal Entity Management and, more broadly, legal innovation monitoring the performance of LEM engagement delivery teams advising on proposals advising, planning and preparation for Board of Directors' and stockholders' meetings. Assisting with formation, maintenance, and dissolution of legal entities, including legal entity corporate compliance activities, such as annual meetings, appointment of directors and officers, powers of attorney, annual reports, document preparation, etc. Qualifications Required Ability to perform job responsibilities within a hybrid work model that requires US Tax professionals to co-locate in person 2-3 days per week 3+ years of relevant legal/legal entity management experience, corporate legal secretarial experience, or alternative legal service industry experience Bachelor's degree in technology, legal, business, accounting or other related fields Experience with entity management lifecycle including annual compliance and event driven activities including regular filings, drafting consent, associated entity management activities, etc. Experience with legal technology and its application in the legal entity management space or in the contract lifecycle management field Experience with Microsoft Office and other technology skills including, but not limited to, Excel, PPT, Visio, Power BI, Tableau Limited immigration sponsorship may be available Ability to travel up to 50%, on average, based on the work you do and the clients and industries/sectors you serve One of the following active accreditations obtained, in process, or willing and able to obtain: Licensed CPA in state of practice/primary office if eligible to sit for the CPA If not CPA eligible: Licensed attorney Enrolled Agent PMP (Project Management Certification) Contract & Commercial Management (CCM) Certification Program Certified Financial Analyst (CFA) PMI Agile Certified Practitioner (Project Management Institute-ACP) Certified Change Management Professional (CCMP) Certified Business Analysis Professional (CBAP) Procurement/Legal Procurement or SAS Certified Data Scientist. Paralegal Certification with a 4-year degree Other Technical Certifications: Six Sigma (Black Belt and Green Belt) Microsoft Certified Solutions Developer (MCSD) Contract & Commercial Management (CCM) Certification Program, PMI Agile Certified Practitioner (Project Management Institute-ACP) DocuSign (Workflow Manager, E-signature, CLM, etc.) iCertis Thomson Reuters (Legal Tracker, High Q, or Contract Express) Preferred: Attorney's barred in a US jurisdiction Experience in legal entity management, preferably in the context of the financial services industry Aptitude and commitment to continue to learn various IT platforms and additional software skills Lean Six-Sigma and/or Project Management Professional certification Knowledge of and working experience with Legal Entity Management databases and other complementary systems Experience maintaining legal entity records and optimally experience evaluating and remediating records The wage range for this role takes into account the wide range of factors that are considered in making compensation decisions including but not limited to skill sets; experience and training; licensure and certifications; and other business and organizational needs. The disclosed range estimate has not been adjusted for the applicable geographic differential associated with the location at which the position may be filled. At Deloitte, it is not typical for an individual to be hired at or near the top of the range for their role and compensation decisions are dependent on the facts and circumstances of each case. A reasonable estimate of the current range is $107,925 to $205,000. You may also be eligible to participate in a discretionary annual incentive program, subject to the rules governing the program, whereby an award, if any, depends on various factors, including, without limitation, individual and organizational performance. Deloitte is committed to providing reasonable accommodations for people with disabilities. If you require a reasonable accommodation to participate in the recruiting process, please direct your inquiries to the Global Call Center (GCC) at USTalentCICInbox@deloitte.com.

We are seeking an experienced analytical research and development scientist with a proven record of sustained laboratory achievement and innovation to join our growing CMC group at ORIC Pharmaceuticals. The candidate will be part of cross-functional teams providing analytical leadership on projects, working closely on a shared mission to bring new therapeutics to cancer patients. The successful candidate will report to the Associate Director of Analytical Sciences and will be responsible for: • Management of outsourced and in-house research activities. Function as a subject matter expert for tech transfer/development of processes to external vendors (contract development and manufacturing organizations/contract testing organizations, CDMOs/CTOs). Create and execute plans for external projects by providing technical guidance, strategic and tactical direction, and oversight to ensure the product requirements are designed and delivered appropriately and in a timely manner for all stakeholders and customers across all stages of drug development, from clinical to commercial., • Independently lead and oversee analytical method development, validation, solid state characterization, release/stability testing, data review and trending, retest/shelf-life extensions and NDA enabling activities at CDMOs and in-house., • Manage GMP manufacturing and product characterization activities at external partners, including preparation and review of analytical methods, Method Validation Protocols, Method Validation Reports, Stability protocols, and CoAs; work closely with process colleagues to propose/justify specifications for RSMs, IPCs, intermediates, and API based upon batch history data and analytical control strategy., • Manage and provide technical guidance during investigations/quality events at CDMO and CROs in collaboration with quality., • Author and review development/technical reports, technical data packages, and relevant sections in health authority filings (including INDs, NDAs, annual reports, and any other regulatory interactions), and contribute to regulatory filing strategy., • Prepare presentation materials and clearly communicate research results to manager, and at internal/external meetings., • Work cross-functionally with Regulatory, Quality, Clinical supply, and Process chemistry colleagues., • Maintain oversight of batch genealogy, stability, and test results to ensure all information is appropriately archived, readily available, and is transformed into useful knowledge and understanding., • Communication excellence in managing projects and deliverables, including budget planning, oversight in partnership with cross-functional colleagues, periodic organization and documentation of progress and accruals, and contract/PO/invoice coordination with finance. Qualifications: • Ph.D. in analytical chemistry or relevant field with 7-10+ years of relevant hands-on pharmaceutical/biotech industry experience, or equivalent, in the field of new drug discovery and development., • Demonstrated problem-solving skills, scientific curiosity, passion, critical thinking, and ability to quickly adapt and shift focus as needed., • Demonstrated ability to take initiative, ownership, problem identification, problem solving and strategic input. A proven record of sustained laboratory achievement and innovation., • Experience in process chemistry aspects of new drug development, including fate and purge studies, specification setting and justification, and other aspects required to build a control strategy, assembling data, and authoring an NDA for a small molecule commercial product is a must., • Extensive hands-on experience and mechanistic understanding of analytical technologies including UHPLC, GC, LC-MS, GC-MS, SFC, dissolution, disintegration, wet chemistry, DSC, TGA, PSD, XRPD, spectroscopic and compendial methods., • Proven track record of Person-in-Plant (PIP) oversight and a history of working within a late-stage commercial company are highly preferred., • Awareness and knowledge of cross-functional activities such as toxicology and clinical development., • Demonstrated ability to work independently and efficiently in a collaborative, fast-paced, integrated, multidisciplinary team environment that includes work internally and with external partners, such as research organizations/Universities, and CDMOs., • Experience in writing and reviewing product specifications, method validation protocol/reports, analytical methods, development reports, risk assessments, release, and stability., • Working understanding of all ICH and regulatory guidance. A strong attention to detail and demonstrated prior experience working in lab, GLP, and cGMP environment., • Scientific excellence as demonstrated by publications, presentations, and leadership/engagement in the scientific/professional community., • Hybrid, or remote work is negotiable. The anticipated base salary for candidates who will work on-site at our San Diego location is between $170,000-$185,000 per year. The final rate offered to a successful candidate will be dependent on several factors that may include, title, type and length of experience within the role, type and length of experience within the industry, education, geography, and other job-related factors. This position is not eligible for H-1B visa sponsorship. ORIC Pharmaceuticals, Inc. is an equal opportunity employer. ORIC does not discriminate based on race, color, religion, gender, sexual orientation, gender identity, age, national origin, disability status, protected veteran status, or any other legally protected characteristics.

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