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Job DescriptionPayrate: $20.00 - $22.00/hr. Summary: The Associate will support Discovery Protein Science by carrying out established molecular-biology, cloning, DNA-production, and sequencing workflows in a collaborative laboratory environment. The role will help project teams produce high-quality DNA reagents, including plasmid DNA, linear expression cassettes (LECs), and sequence-verified constructs. The individual will follow established procedures, maintain accurate records in internal systems, and contribute to routine laboratory operations under appropriate guidance. Key Responsibilities: • Execute DNA-production workflows, including Maxipreps, Gigapreps, and 96-well plasmid DNA minipreps using automation equipment., • Quantify DNA using 96-well instrumentation, such as NanoDrop and Lunatic., • Perform PCR to generate LECs for cell-free expression and other project-supported workflows., • Conduct molecular-cloning activities, including ligation, transformation, colony picking, minipreps, and work with multiple E. coli strains., • Support high-throughput sequencing workflows, including initial sequencing and sublot sequence reverification., • Document experimental procedures, observations, and results accurately in internal LIMS and electronic laboratory systems., • Maintain laboratory readiness through media preparation, reagent and consumable inventory management, kit and restriction-enzyme tracking, and liquid-nitrogen tank refilling., • Collaborate with scientists and cross-functional partners to meet project timelines and shifting research priorities., • Follow all applicable laboratory safety, sterile-technique, and operational-compliance requirements. Basic Qualifications: • An associate or bachelor’s degree in biology, biotechnology, chemistry, or a related scientific discipline is preferred., • Up to two years of laboratory, academic laboratory, internship, or related technical experience; relevant coursework or training may be considered., • Careful attention to detail and ability to follow written laboratory procedures accurately and consistently., • Clear written and verbal communication skills., • Basic proficiency with computer applications, including Microsoft Office., • Ability to work effectively in a collaborative team environment. Preferred Qualifications: • Experience in plasmid preparation, PCR, bacterial transformation, or related molecular-biology workflows., • Familiarity with liquid-handling automation equipment, such as Viaflow, Hamilton, or comparable systems., • Exposure to laboratory-information-management systems or electronic laboratory notebooks is a plus., • Awareness of sequencing workflows and sequence-verification concepts is a plus., • Experience or interest in supporting laboratory inventory, reagent preparation, and routine equipment upkeep., • Demonstrated problem-solving skills in a fast-paced research environment. Top 3 Must-Have Skill Sets: • Foundational Molecular Biology Skills:, • Basic laboratory training or experience with PCR, DNA purification, plasmid preparation, or molecular cloning., • Willingness to learn bacterial transformation, colony picking, and miniprep processes using established procedures., • Accurate Laboratory Execution:, • Ability to perform routine DNA-preparation and DNA-quantification tasks accurately after training., • Comfort using pipettes and basic laboratory equipment; experience with multichannel pipettes or automated tools is a plus., • Ability to support sequencing submission and sample-tracking activities after training., • Attention to Detail and Teamwork:, • Ability to maintain accurate records and enter information into internal laboratory systems after training., • Ability to follow protocols, manage assigned tasks, and ask for guidance or escalate issues when needed., • Collaborative communication with scientists, operations staff, and team members. Pay Transparency: The typical base pay for this role across the U.S. is: $20.00 - $22.00 /hr. Non-exempt positions are eligible for overtime at a rate of 1.5 times the base hourly rate for all hours worked in excess of 40 in a work week, or as required by state or local law. Final offer amounts, within the base pay set forth above, are determined by factors including your relevant skills, education and experience. Full-time employees are eligible to select from different benefits packages. Packages may include medical, dental, and vision benefits, health savings accounts with qualified medical plan enrollment, 10 paid days off, 3 days paid bereavement leave, 401(k) plan participation with employer match, life and disability insurance, commuter benefits, dependent care flexible spending account, accident insurance, critical illness insurance, hospital indemnity insurance, accommodations and reimbursement for work travel, and discretionary performance or recognition bonus. Sick leave and mobile phone reimbursement provided based on state or local law. Consent to Communication and Use of AI Technology: By submitting your application for this position and providing your email address(es) and/or phone number(s), you consent to receive text (SMS), email, and/or voice communication whether automated (including auto telephone dialing systems or automatic text messaging systems), pre-recorded, AI-assisted, or individually initiated from Aditi Consulting, our agents, representatives, or affiliates at the phone number and/or email address you have provided. These communications may include information about potential opportunities and information. Message and data rates may apply. Message frequency may vary. You represent and warrant that the email address(es) and/or telephone number(s) you provided to us belong to you and that you are permitted to receive calls, text (SMS) messages, and/or emails at these contacts. You also acknowledge and agree to Aditi Consulting LLC’s use of AI technology during the sourcing process, including calls from an AI Voice Recruiter. AI is used solely to gather data and does not replace human-based decision-making in employment decisions. Calls may be recorded. Consent is not a condition of purchasing any property, goods, or services. You may revoke your consent at any time by replying “STOP” to :messages or by contacting privacy@aditiconsulting.com. For information about our collection, use, and disclosure of applicant's personal information as well as applicants' rights over their personal information, please see our Privacy Policy #AditiConsulting #26-05996

Job Description Job Title: Scientist II Pay Rate: Up to $62/hr. W2 Job ID: 368 Location: Alameda California 94502 Duration: 6 Months Shift: 8am-5pm Possibility to extend or convert: This is to cover for a resource who is on temporary leave. There is possibility for extension. The team likely will have a FTE role open early next year that they would consider this person for. Interview Process: 1 round: 1 hour long virtual panel interview Notes - candidate ideally will be comfortable explaining cell culture and cell viability assays. Industry experience is preferred. Academia will be considered. Nice to have: CellTiter-Glo. This is a BSL2 lab, the molecules they will be working with are considered hazardous because they are new chemicals, they are not high risk. Some of the reagents they work with are considered caustic but they have standard protections. Education: • BS/BA degree in related discipline and a minimum of four years of related experience; or,, • MS/MA degree in related discipline and a minimum of two years of related experience; or,, • Equivalent combination of education and experience. Experience: · Extensive hands-on experience with basic molecular and biochemical techniques (RNA, PCR, western blot, ELISA, fluorescent imaging) and cell biology techniques (mammalian cell culture, phenotypic assays) are highly desirable. · Proficient in use of GraphPad Prism and MS Excel, Word, PowerPoint. · Drug discovery experiences are highly desirable. Knowledge/Skills: · General knowledge of cellular, biochemical, and molecular techniques, theories, and practices. · General understanding of how the individual experiments fit within a larger research program to meet organizational goals. · General understanding and application of scientific principles, theories, and concepts in field of specialty and other related disciplines. · Complete understanding of the goals of the experiments and how they fit into the overall program. · Applies extensive scientific and technical expertise in area of specialty. · Ability to effectively capture data and results. · Strong communication skills, excellent work ethics, self-motivated and work effectively both in a team environment and independently. · Computer proficiency including MS Word, MS PowerPoint and MS Excel required. • Education, • BS/BA in Biology, Cell Biology, Molecular Biology, Biochemistry, or related scientific discipline plus 4+ years of relevant industry experience, OR, • MS degree in a related scientific discipline plus 2+ years of relevant industry experience, • PhD candidates will not be considered, • Mammalian Cell Culture - Extensive hands-on experience maintaining and working with mammalian cell lines in a biotech or pharmaceutical drug discovery environment., • Cellular / Viability Assays - Direct experience performing cell viability assays, routine screening assays, and evaluating compound activity., • ELISA and/or AlphaLISA Assays - Experience performing, troubleshooting, and analyzing plate-based assays., • Drug Discovery Experience - Prior experience supporting small-molecule drug discovery programs is required., • Data Analysis & Reporting - Ability to analyze experimental results, generate dose-response curves, and communicate findings effectively. Strong Plus: • Western blot experience, • Experience with high-throughput or routine screening workflows, • GraphPad Prism proficiency SUMMARY/JOB PURPOSE: The successful candidate will be highly motivated, comfortable in a dynamic and energetic team-based environment, and passionate about discovering new cancer therapeutics. This role involves development of cell-based functional assays, and evaluation of small molecule inhibitors in those assays to support oncology drug discovery projects. This job requires reliable execution of experiments, interpretation and analysis of data, and problem solving. The ideal candidate will have good lab practices and be able to multi-task. The candidate must have good organizational skills, communication, and teamwork skills as well as flexibility and versatility to meet tight deadlines in a dynamic, fast-moving environment. ESSENTIAL DUTIES AND RESPONSIBILITIES: · Works independently to plan, design, and perform research experiments to support oncology drug discovery programs. · Analyzes and interprets scientific data under general supervision. · Maintains and operates scientific apparatus to perform research experiments. · May develop new methodologies and laboratory protocols in conducting general research duties within assigned area of responsibility. · Prepares and organizes data for presentation. Presents data and reports on project status at individual, group, and departmental research meetings. · Maintains familiarity with current scientific literature relevant to the research experiments or program. · Maintains laboratory notebook in a complete, consistent, and concise manner in accordance with company intellectual property policies and practices. • Adheres to good health and safety practices and compliance with applicable EH&S safety rules and participates in mandatory safety training programs. · Other responsibilities as assigned WORKING CONDITIONS: · Environment: primarily working in laboratories or in office · Exposures encountered, such as hazardous materials, extreme cold. · Travel not required

Job Description Job Title: Protein Expression & Purification Scientist Location: Alameda, CA Type: 12 month contract Compensation: $50-55/hour depending on qualifications Contractor Work Model: Onsite Hours: 40 hours/week Overview We are seeking a Protein Expression & Purification Scientist to support drug discovery programs through the design, expression, purification, and characterization of recombinant proteins. This hands-on laboratory role requires expertise in molecular biology, protein expression systems, and chromatographic purification methods, with opportunities to contribute across multiple research initiatives in a fast-paced discovery environment. Responsibilities • Design, clone, and optimize expression constructs using molecular biology techniques, including PCR, primer design, sequence verification, and recombinant cloning strategies., • Execute recombinant protein expression workflows using baculovirus expression vector systems (BEVS) in insect cells and E. coli expression platforms., • Generate, amplify, and optimize baculovirus stocks to support protein production objectives., • Perform high-throughput small-scale expression screening to evaluate constructs, expression conditions, and protein yield., • Purify recombinant proteins using affinity, ion exchange, and size-exclusion chromatography techniques., • Optimize expression, culture, and purification parameters to improve protein yield, purity, and overall quality., • Conduct analytical characterization using SDS-PAGE, Western blotting, SEC, and related protein analysis methods., • Document experimental procedures, results, and observations in accordance with laboratory documentation standards., • Analyze data, troubleshoot technical challenges, and recommend improvements to workflows and experimental strategies., • Communicate scientific findings and project updates effectively with cross-functional team members. Requirements Required Qualifications • Bachelor's degree in Biochemistry, Molecular Biology, Structural Biology, or a related scientific discipline with 3+ years of relevant industry experience; or Master's degree with 1+ year of relevant industry experience., • Strong expertise in molecular biology techniques, including cloning, vector design, construct optimization, and sequence verification., • Experience with PCR, primer design, restriction enzyme-based cloning, and recombination-based cloning methods., • Demonstrated experience expressing recombinant proteins in BEVS/insect cell systems and E. coli expression systems., • Experience with high-throughput small-scale protein expression screening., • Proficiency in protein purification using chromatographic techniques, including affinity, ion exchange, and size-exclusion chromatography., • Experience performing protein analytical characterization using SDS-PAGE, Western blotting, SEC, and related techniques., • Strong analytical, troubleshooting, and problem-solving skills., • Ability to independently manage experiments while collaborating effectively within multidisciplinary teams., • Strong organizational, documentation, and scientific communication skills. Preferred Qualifications • Experience with biophysical characterization techniques such as LC-MS, SPR, MST, SEC-MALS, nanoDSF, or mass photometry., • Experience with protein purification method development and process optimization., • Familiarity with electronic laboratory notebooks, including Benchling., • Experience supporting protein production activities within a drug discovery or biopharmaceutical research environment. Benefits System One, and its subsidiaries including Joulé, ALTA IT Services, and Mountain Ltd., are leaders in delivering outsourced services and workforce solutions across North America. We help clients get work done more efficiently and economically, without compromising quality. System One not only serves as a valued partner for our clients, but we offer eligible employees health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan. System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law. Ref: #568-Clinical

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: AI Safety Practitioner Type: Contract Compensation: $60–$70/hour Location: Remote Role Responsibilities • Evaluate AI-generated responses for safety, factual accuracy, policy compliance, and overall quality., • Review content involving misinformation, political persuasion, self-harm, violence, cyber, biosecurity, and other sensitive domains., • Apply and refine evaluation rubrics for RLHF, SFT, and AI safety benchmarking., • Identify unsafe outputs, hallucinations, reasoning failures, and policy violations., • Provide structured feedback to improve model alignment and safety performance., • Collaborate with AI researchers and safety teams on ongoing evaluation initiatives. Qualifications Must-Have • Bachelor's degree or higher in Journalism, Communications, Psychology, Sociology, Public Policy, Law, Biology, Chemistry, Computer Science, or a related discipline., • 5+ years of professional experience in AI Safety, Trust & Safety, journalism, public policy, scientific research, security, or a related field., • Excellent written English, critical thinking, and analytical reasoning skills., • Ability to consistently evaluate nuanced and policy-sensitive scenarios. Preferred • Experience with AI Safety, RLHF, SFT, Trust & Safety, or AI evaluation., • Familiarity with safety policies, content moderation, or evaluation rubric development., • Experience reviewing complex, high-risk, or ambiguous content. 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.

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: AI Safety Practitioner Type: Contract Compensation: $60–$70/hour Location: Remote Role Responsibilities • Evaluate AI-generated responses for safety, factual accuracy, policy compliance, and overall quality., • Review content involving misinformation, political persuasion, self-harm, violence, cyber, biosecurity, and other sensitive domains., • Apply and refine evaluation rubrics for RLHF, SFT, and AI safety benchmarking., • Identify unsafe outputs, hallucinations, reasoning failures, and policy violations., • Provide structured feedback to improve model alignment and safety performance., • Collaborate with AI researchers and safety teams on ongoing evaluation initiatives. Qualifications Must-Have • Bachelor's degree or higher in Journalism, Communications, Psychology, Sociology, Public Policy, Law, Biology, Chemistry, Computer Science, or a related discipline., • 5+ years of professional experience in AI Safety, Trust & Safety, journalism, public policy, scientific research, security, or a related field., • Excellent written English, critical thinking, and analytical reasoning skills., • Ability to consistently evaluate nuanced and policy-sensitive scenarios. Preferred • Experience with AI Safety, RLHF, SFT, Trust & Safety, or AI evaluation., • Familiarity with safety policies, content moderation, or evaluation rubric development., • Experience reviewing complex, high-risk, or ambiguous content. 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.

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: AI Safety Red Teamer Type: Contract Compensation: $70–$84/hour Location: Remote Role Responsibilities • Design adversarial prompts to stress-test frontier AI models., • Identify jailbreaks, unsafe behaviors, hallucinations, and policy failures., • Evaluate model robustness across misinformation, cyber, biosecurity, fraud, political content, and other sensitive domains., • Document vulnerabilities and contribute to safety benchmarking and red-teaming reports., • Collaborate with AI researchers to improve model alignment, robustness, and safety. Qualifications Must-Have • Bachelor's degree or higher in Computer Science, Cybersecurity, Journalism, Communications, Psychology, Biology, Chemistry, Public Policy, or a related discipline., • 5+ years of professional experience in AI Safety, AI Red Teaming, Trust & Safety, cybersecurity, investigative journalism, life sciences, or a related field., • Strong analytical reasoning, prompt design, and written communication skills., • Experience designing adversarial prompts or evaluating frontier AI systems. Preferred • Experience with AI Red Teaming, RLHF, SFT, AI Alignment, or Trust & Safety., • Familiarity with jailbreak testing, prompt engineering, or adversarial evaluation methodologies., • Expertise in one or more grey-area domains, including cyber, biosecurity, political content, misinformation, or scientific safety. 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.

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: AI Safety Practitioner Type: Contract Compensation: $60–$70/hour Location: Remote Role Responsibilities • Evaluate AI-generated responses for safety, factual accuracy, policy compliance, and overall quality., • Review content involving misinformation, political persuasion, self-harm, violence, cyber, biosecurity, and other sensitive domains., • Apply and refine evaluation rubrics for RLHF, SFT, and AI safety benchmarking., • Identify unsafe outputs, hallucinations, reasoning failures, and policy violations., • Provide structured feedback to improve model alignment and safety performance., • Collaborate with AI researchers and safety teams on ongoing evaluation initiatives. Qualifications Must-Have • Bachelor's degree or higher in Journalism, Communications, Psychology, Sociology, Public Policy, Law, Biology, Chemistry, Computer Science, or a related discipline., • 5+ years of professional experience in AI Safety, Trust & Safety, journalism, public policy, scientific research, security, or a related field., • Excellent written English, critical thinking, and analytical reasoning skills., • Ability to consistently evaluate nuanced and policy-sensitive scenarios. Preferred • Experience with AI Safety, RLHF, SFT, Trust & Safety, or AI evaluation., • Familiarity with safety policies, content moderation, or evaluation rubric development., • Experience reviewing complex, high-risk, or ambiguous content. 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.

Job DescriptionAbout Nosis Bio: Nosis Bio is a well-funded biotech startup exclusively focused on cell-specific delivery of RNA therapeutics. We are an all-scientist team of biologists, chemists, and machine learning experts that believe targeted extrahepatic delivery is the only thing preventing RNA therapies from becoming the standard-of-care for most chronic diseases. We combine deep expertise in receptor biology, generative AI, and high throughput in vivo data generation to exponentially accelerate the development of RNA therapeutics for new tissues. We are addressing a major unmet need across the industry and actively partner with pharmaceutical companies, research institutions, and biotech. About the Role: We are seeking a Research Associate I / II / Snr RA to conduct molecular biology-based assays to evaluate the pharmacokinetics (PK) and pharmacodynamics (PD) properties of therapeutic candidates. The successful candidate will have hands-on experience with various high throughput molecular biology assays and will work closely with multidisciplinary teams to support various drug discovery project Core Responsibilities ● Execute routine molecular biology workflows including RNA/DNA extraction, cDNA synthesis, PCR/RT-qPCR, ddPCR ● Prepare reagents, buffers, and master mixes; maintain clean work practices (RNase-free technique) ● Perform sample processing from diverse matrices (cells, tissues, biofluids) including homogenization, lysis, cleanup, quantification, and normalization ● Maintain accurate, real-time documentation in our electronic lab notebook, including protocols, deviations, and raw data traceability ● Conduct data QC and basic analysis (standard curves, ddCt, acceptance criteria), and summarize results clearly for team review ● Support assay development/optimization: primer/probe evaluation, thermal gradient optimization, input range testing, inhibition checks, and repeatability testing ● Maintain mammalian cell cultures (immortalized, engineered, and primary cells) using aseptic technique, including thawing, passaging, cryopreservation, cell counting/viability assessment, and routine mycoplasma testing; plate and prepare cells for downstream assays ● Use automated liquid handlers and other lab automation to increase throughput and reproducibility of plate-based assays; help develop, program, and validate new protocols on these instruments, including verifying accuracy and precision against manual methods ● Manage inventory for molecular and cell biology consumables; coordinate ordering; monitor reagent lot changes and qualify new lots when needed ● Troubleshoot core lab equipment (qPCR/ddPCR instruments, plate readers, centrifuges, biosafety cabinets), escalating service needs appropriately ● Coordinate cross-functionally to ensure samples are collected, labeled, stored, and transferred correctly ● Share results across company with clear context, controls, and interpretation What we’re looking for: Ability to work on site in our lab spaces located in the California Bay Area – Research park at Marina Village (Alameda, CA) Motivated and proactive with strong problem-solving skills. Team-oriented and open to collaboration across scientific disciplines. Title is dependent on academic and professional experience – we recruit diverse backgrounds including those with academic, non-profit, and industry experiences! RA I – Undergraduate degree 0-2 yrs industry, or similar experience RA II – BS with 2-4 years or MS with 0-2 years of industry, or similar experience Snr RA -- BS with 4+ years or Ms with 2+ years of industry, or similar experience

Job Description Senior Staff AI Engineer, Agentic AI Location: Bay Area - Oakland, CA Employment Type: Full-time Experience: 8–15 years Focus: Agentic AI, Scientific Reasoning, AI Harnesses, Tool Use, Memory, Evaluation Systems About Our Client Our client is building the first AI-native operating system for materials science. Their platform helps scientists, chemists, and R&D teams reason through complex scientific problems using AI-native workflows, proprietary scientific data, and agentic systems designed for real-world research environments. The company is working with a uniquely valuable scientific data foundation, including trillions of proprietary scientific tokens that are not available anywhere else. This creates a rare opportunity to build AI systems that understand how scientists think, work, and make decisions. About the Role Our client is hiring a Senior Staff AI Engineer to own the technical direction of the agentic AI harness at the center of the platform. This is the most senior hands-on individual contributor role on the Agentic AI team. This person will define how the product evolves from a chat-based experience into an agentic-first platform where AI agents can reason, plan, use tools, remember context, evaluate outcomes, and operate across the full scientific workflow. This is a true 0-to-1 role. You'll build the orchestration, tool use, memory, planning, and reasoning layer for production agent systems while helping lead two junior engineers on the AI harness. You'll also partner closely with product and ML leadership to expand agent capabilities across every surface of the platform. What You'll Do Own the technical direction for the agentic AI harness Build and expand production agent systems for scientific and chemistry workflows Design orchestration, tool use, memory, planning, and evaluation layers for agentic systems Help shift the platform from a chat-style interface into an agentic-first experience Build tools and sub-agent personas that reflect how chemists think and work Integrate frontier reasoning models into the application Expand agent capabilities across scientific workflows and product surfaces Contribute to potential fine-tuning programs for domain-specific scientific reasoning Make agent behavior observable, measurable, and reliable through tracing and evaluation systems Evaluate agent performance against real scientific tasks Drive agent reliability to the level where customers can trust agents to act with increasing autonomy Provide technical leadership to junior engineers on the AI harness team Partner closely with product, ML, and engineering leadership on roadmap and architecture What We're Looking For 8–15 years of experience in AI engineering, software engineering, ML engineering, or related technical roles Staff-level or Senior Staff-level experience setting technical direction, not just executing tasks Experience building sophisticated production agent systems from inception through scale Experience building an agent harness or similar agentic infrastructure Hands-on experience with low-level agentic frameworks such as LangGraph, LangChain, or equivalent tools Strong full-stack programming experience across Python, React, TypeScript, or similar technologies Deep understanding of LLMs, agent orchestration, tool use, memory, planning, evaluation, and production reliability Ability to design systems that move beyond chat into autonomous or semi-autonomous workflows Strong judgment around system architecture, model behavior, observability, and product safety Experience working in a startup, or a background combining big tech experience with startup execution Ability to lead technically while remaining deeply hands-on Technical Environment Relevant technologies and concepts include: Python LangGraph LangChain Agentic frameworks Frontier LLMs, including GPT-4, Claude, and similar models Braintrust Tracing and evaluation systems RAG React TypeScript Tool use Memory systems Agent orchestration Scientific reasoning systems Preferred Background Our client is especially interested in candidates with: A degree in science, engineering, computer science, or a related technical field Master's or PhD from a strong technical university Scientific background or professional exposure to chemistry, physics, biology, materials science, or mechanical engineering Experience fine-tuning reasoning models Experience building AI systems for scientific reasoning Experience working with proprietary datasets or domain-specific AI systems Experience mentoring or leading junior engineers while staying hands-on Why This Opportunity Own the agentic AI layer at the center of an AI-native scientific platform Build agent systems for real chemistry and materials science workflows Work with proprietary scientific data that no one else has access to Help define how scientists and AI reason together Move a platform from chat-based AI into agentic-first workflows Partner directly with product and ML leadership on company-defining technical direction Step into a Senior Staff-level role with broad technical ownership and meaningful product influence Build at the intersection of frontier LLMs, agentic systems, scientific reasoning, and enterprise R&D Ideal Candidate Profile The ideal candidate is a Senior Staff-level AI engineer who has already built production agent systems and knows what it takes to move them beyond version one. They are deeply hands-on, technically opinionated, and capable of setting direction across agent orchestration, memory, tool use, evaluation, tracing, and product integration. They understand that reliable agent behavior requires more than model calls — it requires systems, feedback loops, observability, and strong product judgment. This person should be excited by the opportunity to build AI systems that help scientists reason, discover, and work in fundamentally new ways.

Job DescriptionTITLE: eCommerce Operations Engineer (contractor) Groundbreaking advances in synthetic biology achieved at Client X allow us to create products that are better and safer for humans and more sustainable for the planet. The Digital group is charged with creating connected experiences and back-end services to catapult our consumer brands to global significance and impact. Up from three at the start of the year, today we support nine exciting brands: Biossance, Pipette, Costa Brazil, Purecane, OLIKA, Terasana, Rose, Inc., JVN Hair, and Eco Fabulous The compute ecosystem for the consumer business consists of Shopify, custom Shopify apps, Boomi, Salesforce Marketing Cloud, Zendesk, Domo, NetSuite, and other third-party and internally created software. We will also launch our largest brand, Biossance, in different languages in 2021, the first step in a global e-commerce expansion. We are hiring an engineer who is passionate about delivering operational excellence. You know how to deal with ambiguity and prioritize your tasks in a fast-paced environment. The impact of this role is highly visible to our senior business leaders. You will lead mission-critical integrations and crisis management for our eCommerce stores. You have the knowledge and confidence to advise others on the best practices in operations and develop a roadmap with our team for our future operations’ growth. Responsibilities: • Develop and support Integrations between Shopify, Boomi, NetSuite, and Salesforce., • Enforce and improve eCommerce operations policies including change management, user governance, data access control, and incident management., • Communicate with business stakeholders, collect requirements, and collaborate with overseas developers to continuously improve our eCommerce systems., • Monitor the health status of our eCommerce systems and email marketing campaigns through analytics and key metrics. Immediately address any risks that impact our live operations., • On-call for emergency operation issues., • Use your passion, skills, and wisdom to bring our digital platforms to their full potential in the best customer experience and growth for our brands. Required Qualifications:, • Bachelor’s degree., • Ten (10+) years related experience in system engineering and integration., • Five (5+) years of experience in project management in system integration., • Five (5+) years in enforcing and improving software change management in live operations., • Excellent communicator who explains technical details in nontechnical language., • Solid understanding of cybersecurity., • Demonstrated ability to work as part of a cross-functional team and willingness to take on responsibilities outside primary job description when necessary., • Proficient with MS Office, Google Suite, and Jira. Preferred Qualifications:, • Experience in Shopify, Google Analytics, Google Search Console, and Google Tag Management is highly preferred., • Experience with Accessible Rich Internet Applications (ARIA) is a big plus.

Job DescriptionPosting Title: eCommerce Operation Engineer Groundbreaking advances in synthetic biology achieved at Amyris allow us to create products which are better and safer for humans and more sustainable for the planet. The Digital group is charged with creating connected experiences and back-end services to catapult our consumer brands to global significance and impact. The eCommerce platform for the consumer business consists of Shopify, Boomi, Salesforce Marketing Cloud, Zendesk, Domo, NetSuite, and other third-party and internally-created software. We will also launch our largest brand, Biossance, in different languages in 2021, the first step in a global e-commerce expansion. The impact of this role is highly visible to our senior business leaders. You will lead mission-critical integrations and crisis management for our eCommerce stores. Responsibilities: • Develop and support Integrations between Shopify and Boomi, • Enforce and improve eCommerce operations policies including change management, user governance, data access control, and incident management using escalations and Vendor support when needed, • Communicate with business stakeholders, collect requirements, and collaborate with developers to continuously improve our eCommerce systems., • Monitor the health status of our eCommerce systems and email marketing campaigns through analytics and key metrics. Immediately address any risks that impact our live operations., • On-call for emergency operation issues., • Use your passion, skills, and wisdom to bring our digital platforms to their full potential in the best customer experience and growth for our brands. Qualifications:, • Bachelor’s degree, • 5+ years related experience in Full Stack development., • 3 to 5 years in enforcing and improving software change management in live operations., • 3 or more years’ experience in project management in system integration., • Excellent communicator who explains technical details in nontechnical language., • Solid understanding of cybersecurity., • Demonstrated ability to work as part of a cross-functional team and willingness to take on responsibilities outside primary job description when necessary, • Assertive, adaptable, and demonstrates initiative in a fast-paced environment with competing priorities, • Proficient with MS Office, Google Suite, and Jira, • A customer focus, a strong drive for results, and a collaborative team player, • Experience with Accessible Rich Internet Applications (ARIA) is a big plus.

Job DescriptionCompany Description About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on LinkedIn, Facebook, Instagram, X and YouTube. Job Description *Hybrid 3x per week in Lake County, IL, Florham Park, NJ or San Francisco, CA. Purpose: • Lead global pipeline medical affairs strategy and develop compelling differentiation across the lifecycle, leveraging distinctive insights from the market to shape AbbVie TA pipeline, • Shape initial value and evidence strategy and initiate Ev Gen plans, leveraging insights from payors, patients, and physicians. Direct pipeline execution team, ensuring pull through of strategy to Enterprise Research MSLs, • Collaborate with counterparts in International TAs, Global Therapeutic Area BU and Development, • Represent TA in pipeline governance, where aligned with TA BU Head, • Interface with Operations and Medical Engagement teams to operationalize pipeline strategy Responsibilities: • Lead and oversee pipeline (including BD) medical, value and evidence strategy development across all disease areas within TA to serve both US and International markets for all indications/ brands up to 24-36 months pre-launch (in any geography), • Drive compelling differentiation of medical, value and evidence strategy from discovery, leveraging distinctive insights from US and International markets, • Coordinate across TAs to ensure that TA-level pipeline strategies coalesce into a coherent AbbVie pipeline strategy, • Ensure HCP, Patients and Payor insights are incorporated into the developments programs to accelerate and differentiate clinical and commercialization strategies (e.g., streamlined patient data collection, patient finding), • Co-create the Brand strategy for all assets and ensure US and International market insights are embedded in the brand strategy, • Represent medical affairs in pipeline-related governance, serving as the single point of contact for commercial and development counterparts, • Serve as final decision maker (pre-BU head) for all pipeline-related strategy and decisions, • Manage pipeline resources effectively, redirecting pipeline team to enterprise critical assets along the lifecycle as needed, starting as early as discovery, • Ensure effective handover to US and International inline/ launch teams, onboarding with relevant TAs to share insights/ approach/ etc. from pipeline strategy efforts and minimizing duplication of effort across pipeline and inline teams, • Lead cross-functional gap assessment and Integrated Evidence Planning (IEP) and collaborate with Value and Evidence, • Define strategy for enterprise research MSLs in US and affiliates, leveraging pipeline insights to develop priorities and shape tactical plans, • Coordinate with pipeline execution group in US Medical Engagement to drive execution, • Collaborate with US Medical Engagement to track impact-focused KPIs and re-shape pipeline strategy based on impact or best practicesQualifications, • M.D., or equivalent advanced degree in a relevant scientific discipline (e.g., oncology/hematology), • 15+ years of experience in the pharmaceutical or biotechnology industry, with a focus on oncology, specifically hematology, • Demonstrated expertise in clinical development, regulatory requirements, and commercialization of oncology therapies, • Proven leadership experience in medical affairs, including managing direct and indirect reports, cross-functional teams and influencing strategic direction at the senior executive level, • Strong scientific knowledge of solid tumor biology, clinical trial design, biomarker development, and emerging treatment modalities (e.g., immuno-oncology, targeted therapies, precision medicine), • Proven ability to work cross-functionally and collaborate effectively with clinical development, regulatory, commercial, and other business functions, • Exceptional communication skills, with experience presenting complex scientific information to both technical and non-technical stakeholders Preferred Qualifications: • Familiarity with advanced cancer treatment modalities such as CAR-T therapies, combination therapies, and immuno-oncology, • Strong publication and scientific communication track record in oncohematology, including contributions to peer-reviewed journals and major oncology conferences, • Experience in managing global medical affairs activities across multiple geographic regions (focus on Global strategy and US region) Physical Requirements: • Ability to travel domestically and internationally (up to 25-30%). Additional Information Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law: The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future. We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees. This job is eligible to participate in our long-term incentive programs. Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company’s sole and absolute discretion, consistent with applicable law. AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled. US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more: https://www.abbvie.com/join-us/reasonable-accommodations.html

Job DescriptionCompany Description About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on LinkedIn, Facebook, Instagram, X and YouTube. Job Description The Biologics CMC Development organization at AbbVie has a long and rich history of biologics development, leveraging comprehensive end-to-end CMC capabilities to advance complex biologic therapies, such as bi-specifics and novel modalities, from discovery through human clinical studies and eventual licensure. The Cell Line Development (CLD) Innovation Group is seeking a Senior Scientist I to join a talented and collaborative team developing next-generation CHO cell line platforms for the production of recombinant antibodies and complex biologics. This is a hands-on, laboratory-focused role for a versatile molecular biologist who will independently drive expression-optimization projects across both the vector and the host cell — from experimental design through execution and data interpretation. The successful candidate will design and test vector constructs, engineer host cells, conduct transfection and clone-generation campaigns in CHO cells, and apply a deep theoretical understanding of recombinant protein expression to improve titer in stable cell lines. This is not a single-technique position: the role spans the full set of levers that govern expression, and the candidate is expected to think, read, and propose, then carry the work out at the bench with a high degree of independence. Responsibilities: • Independently conceive ideas and designs to investigate CHO expression technical improvements across both vector and host cell., • Design and test dozens of vector constructs in recombinant stable CHO cell lines for increased mAb titer. Rapidly execute the associated transfections, screening, and clone-characterization studies to generate decision-quality data., • Employ a variety of hands-on laboratory techniques, including transfection, aseptic CHO cell culture, DNA gene copy number analysis, RNA expression analysis (ddPCR / RT-qPCR), mAb titer measurement, cell engineering to knock in/out target genes., • Operate and interpret data from core CLD instrumentation, including Octet (BLI titer), ViCell, CloneSelect Imager, microfluidic clone-screening platforms such as the Beacon, flow cytometry. Share responsibility for equipment maintenance., • Apply a rigorous theoretical and practical understanding of recombinant protein expression from the genome to the protein — including genomic loci, epigenetics, transcription, mRNA stability, translation, the organelles and secretory machinery involved, and the engineering constraints specific to industrial CHO cell line development., • Author and co-author cell line development technical reports and present data to the group and to leadership; contribute scientific insight to project teams., • Collaborate closely with cell culture, analytical, purification, and bioinformatics colleagues to meet project timelines, and adhere to corporate standards for code of conduct, safety, materials handling, and good documentation practices. Qualifications Required: • Senior Scientist I: BS with a minimum of 10 years, or MS with a minimum of 8 years of experience is strongly preferred, or PhD with no minimum years’ experience, in molecular biology, cell biology, biochemistry, or a related discipline., • Demonstrated ability to read the literature, review external sources, and gather inputs to synthesize technically sound ideas and design proper experimental controls., • Demonstrated ability to independently analyze experimental data, draw appropriate conclusions, and communicate them to a wide audience., • Demonstrated proficiency with designing and implementing vector improvements to increase recombinant antibody expression levels in stable CHO cells., • Proficiency with Geneious Prime or similar software for designing and annotating DNA vectors, primers, and probes, and performing sequence alignments., • Proficiency with most or all of the following techniques and instrumentation: transfection, aseptic mammalian cell culture, Octet, ViCell, CloneSelect Imager, and microfluidic clone-screening platforms such as the Beacon., • Demonstrated ability to learn, understand, and master new experimental techniques, and to multi-task and work within timelines., • Strong scientific communication skills — verbal, written, and data presentation — with detailed daily digital lab notebook record-keeping proficiency., • A candidate who combines hands-on wet-lab depth with the ability to think alongside the team and then execute independently. Preferred: • While we welcome all candidates with a genuine passion for CHO cell line development, we strongly prefer those who bring hands-on, industry cell line development experience in a CMC / drug-substance environment over candidates with purely academic or cell-culture-development-only backgrounds., • Candidates with substantial experience developing CHO expression platform improvements in an industrial/CMC setting., • Possess a demonstrated and genuine passion for getting the most mAb titer out of recombinant CHO cells., • Previous experience performing cellular analyses using flow cytometry., • Proficiency with cell engineering to knock in / knock out target genes using CRISPR/Cas or other suitable tools. Additional Information Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law: • The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future., • We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees., • This job is eligible to participate in our short-term incentive programs. Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company’s sole and absolute discretion, consistent with applicable law. AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled. US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more: https://www.abbvie.com/join-us/reasonable-accommodations.html

Job DescriptionTitle: Web DeveloperLocation: Lisbon, Portugal (100% remote)Duration: Contractor Groundbreaking advances in synthetic biology achieved at Amyris allow us to create products that are better and safer for humans and more sustainable for the planet. The Digital group is charged with creating connected experiences and back-end services to catapult our several consumer brands to global significance and impact. Today, we serve Biossance, Pipette and Purecane. Among other projects, we are building two new brands that will launch later this year. We are creating a clean cosmetics line in partnership with Rosie Huntington-Whitely to launch on a new Rose, Inc. platform. We are creating a clean hair care brand, JVN Hair, in partnership with Jonathan Van Ness. We seek a talented, experienced web developer to help optimize our browsing and shopping experiences to drive consumer happiness, retention, and revenue. Our stack includes Shopify, custom Shopify apps, Boomi, Azure Cloud, Salesforce Marketing Cloud, Zendesk, Domo, NetSuite, and other third party and internally created software. The Web Developer will work proactively to recommend solutions to enhance functionality, performance, and extensibility of our sites and tech stack. This role partners closely with our brand teams on technical aspects of web related projects and collaborates with project managers & business stakeholders on priorities, feasibility, and timelines. Responsibilities: • Create and maintain beautiful, mobile-friendly user interfaces for Amyris.com and our various brands sites., • Develop strong relationships to collaborate effectively with designers, marketers, product managers, and developers to establish and implement their design vision., • Maintain up-to-date documentation of design solutions., • Explain potential opportunities and project risks to management., • Assist the project managers with time and budget estimations., • Contribute to the development/evolution of the Digital team., • Gain a deep understanding of our products and the customer experience to think and speak from the customer viewpoint., • Use your passion, skills and wisdom to bring our digital platforms to their full potential in service of the best customer experience and growth for our brands. Qualifications:, • Deep knowledge to create responsive websites., • Bachelor’s degree or equivalent experience, ideally in computer science or a related field, • At least 3 years of Front-End Development (HTML/CSS), • Experience with REST APIs, both client and server-side., • Experience working with modern front-end frameworks like React and AngularJS., • Expert in creating full CSS and HTML layouts., • Proven ability to deliver quality code within scope, budget and deadlines., • Demonstrate consistent follow-through on internal assignments and initiatives., • Experience with Agile methodology, • Be pleasant to work with!, • Ability to ask appropriate questions and communicate effectively to a broad range of people including users, designers, executives, marketers, producers, and technical staff., • Can translate complex user requirements and functional specifications into a tangible design for the design and technology team., • Experience with table-free, standards compliant CSS layouts., • Attention to detail and a strong sense of organization., • An understanding of different web applications and the design constraints of each platform., • Willing to learn, share knowledge and take leadership from industry experts., • Experience with Jira., • Strong communication, interpersonal, analytical and problem-solving skills, • A customer focus, a strong drive for results, and a collaborative team player, • Experience with Shopify and better yet Shopify apps development, • Experience with other elements of our architecture such as Google Analytics, Boomi, Domo, Salesforce Marketing Cloud, Klaviyo, HubSpot, NetSuite, and Microsoft Azure Cloud a plus

Job Description Direct Counsel is partnering with a distinguished American international law firm to find a midlevel associate with 1–5 years of patent prosecution experience in biotechnology. The ideal candidate will have an advanced degree—preferably a Ph.D.—in a life sciences field such as molecular biology, immunology, biochemistry, or cell biology. This position involves working closely with emerging companies on patent prosecution and strategic IP counseling, particularly in cutting-edge areas like antibodies, DNA/RNA therapeutics, chemical biology, and gene-editing technologies. Qualifications: 1–5 years of biotech patent prosecution experience Advanced degree (Ph.D. preferred) in a life sciences discipline USPTO Registration Number (Patent Bar membership) is required Candidates must pass the patent bar exam either prior to joining or within the first 12 months of employment

Job Description Crusoe is on a mission to accelerate the abundance of energy and intelligence. As the only vertically integrated AI infrastructure company built from the ground up, we own and operate each layer of the stack — from electrons to tokens — to power the world's most ambitious AI workloads. When you join Crusoe, you join a team that is building the future, faster. We're in the midst of the greatest industrial revolution of our time. The demand for AI compute is boundless, and power is a bottleneck. We're solving that — with an energy-first approach that makes AI infrastructure better for the world and faster for the people innovating with AI. We're looking for problem-solving, opportunity-finding teammates with a sense of urgency, who believe in the scale of our ambition and thrive on a path not fully paved — people who want to grow their careers alongside a team of experts across energy, manufacturing, data center construction, and cloud services. If you want to do the most meaningful work of your career, help our customers and partners advance their AI strategies, and be part of a high-performing team that believes in each other, come build with us at Crusoe. About This Role: Crusoe Cloud is revolutionizing high-performance computing by offering sustainable, low-cost GPU compute power. As a Cloud Support Engineer, you'll play a crucial role in empowering our customers to leverage this technology for groundbreaking advancements in fields like AI/ML, physics simulations, and computational biology. You will be the primary point of contact for technical support, ensuring our customers can seamlessly utilize Crusoe Cloud to achieve their goals. This role directly impacts Crusoe's mission by enabling our customers to accelerate their research and development, contributing to a more sustainable future. You will be involved in exciting projects, working with cutting-edge technologies and collaborating with a talented team to solve complex challenges. The ideal candidate is a highly motivated and experienced technical professional with a passion for customer success, a deep understanding of cloud technologies, and a commitment to Crusoe's values. This is a full-time position. What You’ll Be Working On: Customer Support: Provide exceptional technical support to customers via Zendesk, meeting SLAs and maintaining high CSAT (95%+). On-Call Rotation: Participate in a 24/7 on-call rotation to ensure timely resolution of critical issues. Troubleshooting: Diagnose and resolve issues related to VMs, hardware failures, and scaling tests using CLI and internal tools. Alert Triage and Maintenance: Manage alert triage, prepare for maintenance windows, and conduct node delivery testing. Collaboration: Work closely with SRE, Networking, and Storage teams from initial triage to root cause analysis (RCA) delivery. Global Teamwork: Adhere to global team collaboration and handoff processes for ticketing and on-call procedures. Knowledge Sharing: Develop onboarding/training materials, knowledge base documentation, and standard operating procedures (SOPs). What You’ll Bring to the Team: Education/Experience: Bachelor's degree in IT, Computer Science, Engineering, or a related field, or 2+ years of equivalent technical experience. Linux Proficiency: Strong command-line interface (CLI) skills in Linux environments. Version Control: Proficiency with Git for code management and collaboration. Customer Support Experience: 2+ years of experience in a customer support role, ideally within cloud, storage, or networking environments. Cloud Technologies: Experience with container orchestration (e.g., Kubernetes), workload management (e.g., Slurm, Terraform), and monitoring tools (e.g., Grafana). Public Cloud Knowledge: Familiarity with other public cloud platforms (e.g., AWS, Azure, GCP). Communication Skills: Excellent communication and customer service skills, including the ability to prioritize competing escalations. Bonus Points: Cloud Expertise: Deep understanding of specific cloud platforms and services. Automation Skills: Experience with automation tools and scripting languages. Problem-Solving Abilities: Demonstrated ability to analyze complex technical issues and develop effective solutions. Passion for Sustainability: A strong interest in contributing to a more sustainable future through technology. Benefits: Competitive compensation and equity packages Restricted Stock Units Paid time off, paid holidays & leave of absence programs Comprehensive health, dental & vision insurance Employer contributions to HSA account Paid parental leave Paid life insurance, short-term and long-term disability Professional development & tuition reimbursement Mental health & wellness support Commuter benefits (parking & transit) Cell phone stipend 401(k) Retirement plan with company match up to 4% of salary Volunteer time off Global travel insurance & emergency assistance Daily meals allowance Additional perks & programs specific to location Compensation Range Compensation will be paid in the range of up to $120,000-$140,000 + Bonus. Restricted Stock Units are included in all offers. Compensation to be determined by the applicant's knowledge, education, and abilities, as well as internal equity and alignment with market data. Crusoe is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, religion, disability, genetic information, pregnancy, citizenship, marital status, sex/gender, sexual preference/ orientation, gender identity, age, veteran status, national origin, or any other status protected by law or regulation.

Job DescriptionTITLE: NetSuite Senior Solution ArchitectLOCATION: Fully Remote (USA) Groundbreaking advances in synthetic biology achieved at Client X allow us to create products that are better and safer for humans and more sustainable for the planet. The Digital group is charged with creating connected experiences and back-end services to catapult our consumer brands to global significance and impact. Up from three at the start of the year, today we support nine exciting brands: Biossance, Pipette, Costa Brazil, Purecane, OLIKA, Terasana, Rose, Inc., JVN Hair, and EcoFabulous We are seeking a Senior Solution Architect who can work with Cross Functional key stake holders and Implement Leading Practices in the Retail Industry Responsibilities: • Provide leadership and help to scope, gauge, and deliver large Complex NetSuite projects., • Analyze and architect solutions for business requirements which may include complex configurations and/or technical components, • Define detail functional requirements for automations and integrations to NetSuite, • Work with technical teams to design and test automations and integrations, • Perform quality reviews of deliverables developed by other team members, • Collaborate with Brand Product Managers to facilitate on time project delivery, • Create and maintain project documents, including project plans, solution approaches, functional and technical requirements and specifications and can present them to Business Key Stakeholders, • Participate in project planning and supporting tasks to manage expectations, maintain timeline and meet goals for project deliverable., • Work with Cross Functional departments like Sales Ops, Consumer Ops, Finance and Supply Chain, • Work with our B2B and B2C 3PL Partners, • Participate in Daily Scrum meetings as we are in the 2-week sprint planning process, • Production Support during critical business functions such as Month End, Quarter End, Year End and Holiday/Peak Season, • Review team progress to ensure compliance with work program and professional standards. Educate internal and external key Stakeholders on NetSuite Leading Industry Practices Required Qualifications:, • Bachelor’s or master’s degree in a related field, • 7+ years of relevant professional experience to include NetSuite ERP Retail industry solution implementation and/ or administration, • Strong Experience In shared service model with NetSuite Inventory Management, Order to Cash, Procure to Pay, Design to Build and Record to Report Business Process Areas, • Strong verbal and written communication as well as presentation skills., • Skillset with analysis and the ability to develop processes and methodologies Preferred Qualifications:, • NetSuite ERP Consultant and/or other NetSuite Certification a Plus, • Techno Functional Experience desired, • Logistics Industry Domain Experience desired, • Omnichannel Customer Experience desired

Job DescriptionThe Fountain Group is currently seeking a Senior Automation Scientist for a prominent client of ours. This position is located in South San Francisco, CA. Details for the position are as follows: • Pay: $67-76.97/hr., • 6-month assignment with possibility for extension or conversion based on performance and budget. Responsibilities: • Develop, implement, and optimize automated laboratory workflows to support preclinical DMPK studies and bioanalytical assays., • Operate, program, and troubleshoot automated laboratory equipment, including Hamilton, Echo (Labcyte), and GBG platforms., • Support automation of immunoassays, peptide stability, protein binding, sample preparation, cell culture maintenance, and cell-based assays., • Collaborate with scientific, engineering, IT, and software teams to integrate robotic systems and improve laboratory workflows., • Analyze scientific data, maintain data integrity, update SOPs, and provide training and technical support to laboratory staff. Qualifications: • Bachelor’s degree in Engineering, Automation Sciences, Computer Science, Biology, Chemistry, or a related field., • Hands-on experience with Hamilton, Echo (Labcyte), and GBG platforms, including programming, method development, and troubleshooting., • Experience with laboratory automation, liquid handlers, dispensers, washers, centrifuges, and automated workflows.Preferred Qualifications:, • Experience in pharmaceutical, biotechnology, or bioanalytical laboratory environments., • Familiarity with robotic scheduling systems, such as HighRes BioSolutions, Biosero, or Thermo Momentum., • Experience developing SOPs, implementing automation workflows, and using electronic laboratory notebooks., • Programming experience with VB, C#, LabVIEW, or similar languages., • Experience with electromechanical design, assembly, or laboratory automation integration.If you are interested in hearing more about the position, please respond to this posting with your resume attached. Please forward this posting to any friends or colleagues as we do offer a Referral Bonus for any candidate hired. By applying for this job, you agree to receive calls, AI-generated calls, text messages, or emails from and its affiliates, and contracted partners. Frequency varies for text messages. Message and data rates may apply. Carriers are not liable for delayed or undelivered messages. You can reply STOP to cancel and HELP for help. You can access our privacy policy at Privacy Policy

Job Description Aptask Global Workforce (AGW) is seeking an Associate Scientist - Onsite position with a Global Biotechnology Company located in South San Francisco, CA. This is a 12+ month contract opportunity. The Associate Scientist will perform routine biochemical and cell-based assays to generate reliable, reproducible data. This person will follow established protocols, maintain clear experimental records, help troubleshoot assay or equipment issues, and communicate results to the project team. Responsibilities: • Execute routine biochemical and cell-based assays according to established protocols, • Prepare reagents, samples, and assay materials; operate high-throughput laboratory equipment and assay instruments, • Record, organize, and review experimental data, and communicate results and observations to the team, • Analyze assay data and contribute to summaries, presentations, and reports, • Identify and troubleshoot routine experimental or equipment issues, seeking guidance when needed, • Follow laboratory procedures for safety, documentation, and data quality, • Coordinate day-to-day assay materials and activities to support timely execution Requirements: • Bachelor's degree in biology, molecular and cell biology, biochemistry, or a related field, • At least 2 years of relevant laboratory experience, • Experience with cell culture, running assays, and data analysis, • Experience following experimental protocols and documenting laboratory work Desired skills: • Master's degree with 5 years of relevant experience, or bachelor's degree with 10 years of relevant experience, • Industry experience in a biopharmaceutical or biotechnology setting, • Experience with high-throughput laboratory instruments, such as Echo liquid dispensers and Multidrop dispensers, • Familiarity with data analysis tools such as GraphPad Prism and Genedata Screener, • Experience with biochemical and cell-based assay execution, data analysis, or troubleshooting Pay range: up to $30.32 per hour Only candidates available and ready to work directly as Aptask Global Workforce (AGW) employees will be considered for this position. If you have the described qualifications and are interested in this exciting opportunity, apply today! Aptask Global Workforce (AGW) ApTask Global Workforce (AGW) is a certified Minority and Veteran workforce solutions company. AGW delivers operational, clinical, lab and professional talent with a strong focus on healthcare and life sciences. The company supports clients with reliable staffing, program expertise and a commitment to quality, speed and consistent delivery. Benefits of working with ApTask Global Workforce include: • Medical, • Dental, • Vision, • Sick Pay (for applicable states/municipalities) Our team stays close to the process and is here to guide you every step of the way. To learn more, please visit our website https://www.agwtalent.com/. ApTask Global Workforce is an Equal Opportunity Employer. Candidates will receive consideration without regard to their race, color, religion, sex, sexual orientation, gender identity, national origin, disability or status as a protected veteran.

Job DescriptionTITLE: Senior Network EngineerLOCATION: Emeryville, CAPOSITION: Full time Client X, a leader in synthetic biology is seeking a well experienced senior network engineer to join our IT infrastructure team in a very fast paced, growth company. Client X has a large data and application footprint in multiple geographies and is continuing to see rapid growth. The right candidate will express a keen interest in developing data communications and network designs to help Client X scale and grow with demand using cutting edge designs and topology. The engineer will oversee all aspects of data communications between on-premises, SaaS and public cloud technologies utilizing a diverse set of tools to maintain operational stability, secure transmission and agility of our data flow. We are looking for a motivated, independent engineer who can learn technologies quickly, and who can translate needs across teams – including communicating with stakeholders who are not experts in software infrastructure. This position offers flexibility to design new systems from the ground up – and to have a real impact on Client Xs’ ability to deliver synthetic organisms. Responsibilities: • This role is a standard network engineering role with concentration on LAN/WAN and Security; emphasis on Cisco and cloud., • Assess, design, implement, troubleshoot, and document Cisco networks and related systems., • Cisco switch, router and firewall maintenance, upgrades, configuration, and deployment., • Develop both high-level and detailed implementation and test plans for Cisco technologies related to various types of environments., • Work with the infosec team to design and develop secure network architectures., • Develop, implement, and maintain HA/DR for all data circuits and paths., • Develop documentation as it relates to the necessary requirements, and assist with or develop Client X’s technology solutions., • Write assessment and design reports, and present them to Director of Technology., • Provide knowledge transfer and informal training to Technology Group. Qualifications:, • Active CCNP or higher-level certification in Routing and Switching is strongly preferred, but SME level knowledge is essential with or without the CCNP, • Experience with Cisco VoIP, a huge plus, • LAN/WAN design experience desired, • Working knowledge of standard OSI layer protocols, • Skills in one or more of the following areas a plus: Cisco Data center technologies, Network security (Firewall, VPN, etc.), Cisco ISE, Cisco WLAN, • Experience with Cisco ASA Firewalls and other Datacenter Technologies, • Experience with public cloud-based networking technologies (AWS, GCP, Azure, etc.), • Certifications in multiple technology areas are a significant plus, • VPN/IPSEC and other tunneling protocol experience, • Strong consultative skill set to include communications with varying levels of customer personnel as well as the ability to identify and help close new opportunities within existing clients, • SDWAN with design and deployment experience, • Must be able to work with practice lead to coordinate scheduling to meet customer needs, sometimes juggling multiple projects at one time, • Bachelor’s Degree in Computer Science, Information Technology, or related field - advanced degree or professional certifications a plus, • 6+ year of experience leading, designing, building and operating large hybrid cloud infrastructure; or equivalent combination of post-bachelor’s education and experience

Job DescriptionBiointron is a leading Contract Research Organization (CRO) specializing in antibody discovery, expression, and optimization services for the biotech and pharmaceutical industry. We provide high-throughput, fast-turnaround services and innovative solutions to our clients, including some of the largest global healthcare and pharma companies. As a Business Development Manager, you will play a vital role in supporting the company’s growth efforts by identifying potential business opportunities, building relationships with clients, and assisting in the sales process. You will work closely with senior business development team members, contributing to achieving the company’s strategic goals and expanding our market presence. Responsibilities: • Develop and implement strategies to identify new business opportunities within the biotech, pharmaceutical, and healthcare sectors. Conduct market research to analyze trends, spot potential clients, and identify new partnerships., • Build and maintain strong relationships with key decision-makers in client organizations. Support lead generation, prospect new clients, and assist in outreach through emails, calls, and social media campaigns. Act as a first point of contact for inquiries and manage the client relationship process from initial contact to contract negotiations., • Assist in crafting and delivering sales pitches for our services, including custom antibody discovery, protein expression, and other offerings. Help prepare sales presentations, proposals, and responses to requests, ensuring alignment with client needs., • Support in negotiating and securing client contracts, ensuring they align with company business goals. Work to develop long-term partnerships to expand our service offerings and market reach. Work closely with R&D, marketing, and operations teams to align business development strategies with company capabilities. Provide valuable input into product development based on market insights and customer feedback., • Track and report on business development progress, goals, and KPIs. Contribute to the development of company strategies and business plans, ensuring that activities are aligned with organizational objectives., • Maintain up-to-date records in the CRM system, track business development activities, leads, and opportunities. Ensure timely follow-up and accurate reporting on client interactions and pipeline progress.Qualifications:, • Master’s degree in Life Sciences, Molecular Biology, or a related field (PhD is a plus)., • 1-3 years of experience in business development, sales, marketing, or a related field (internships or academic projects in business development or sales within the biotech/pharma industry are a plus)., • Experience in business development, preferably within the biotechnology or pharmaceutical industries., • Familiarity with antibody discovery, protein expression, and related services., • Excellent communication and negotiation skills., • Strong analytical, organizational, and problem-solving abilities., • Proven track record of meeting or exceeding sales targets and business growth goals., • Bilingual English/Mandarin required. Location: Remote in San Francisco Bay Area, CA

Job Description OPPORTUNITY Mammoth Biosciences is seeking a Senior Software Engineer I, Research Informatics, to join our Computational team. This is an impactful group of bioinformaticians and software engineers that supports Mammoth's therapeutic CRISPR gene-editing programs from discovery through IND-enabling studies. As part of the Computational team, you’ll help build and run the analysis pipelines, model and manage the data those programs generate, and develop the internal tools scientists use to design experiments and interpret results. An ideal candidate will work at the intersection of software engineering and biology. You’ll be responsible for managing and improving the systems the research organization depends on every day: the data warehouse and models that connect assay results to decisions, the internal web applications scientists use to launch analyses and access their data, and the cloud infrastructure everything runs on. KEY RESPONSIBILITIES • Design and own relational data models and pipelines that drive scientific decisions, working in the context of existing production systems including Benchling, • Define and refine how data is ingested, modeled, and made queryable, • Collaborate with wet-lab scientists to build right-sized internal analysis tools, • Design and improve the web applications scientists use to launch analyses and access data, • Maintain the cloud infrastructure and automation tooling the research org runs on, • Work directly with Computational team members and biologists to understand scientific needs, then troubleshoot and improve the relevant pipelines and systems, • Enable responsible and reproducible use of AI across the company, • Document systems and decisions to improve reproducibility and engineering standardsREQUIRED QUALIFICATIONS, • Bachelor's, Master's, or PhD degree (or equivalent combination of education and experience) in computer sciences or biological field, • 7+ years of professional software engineering experience (5 years with Master's or 3 years with PhD) in the life sciences or related industry, • Strong proficiency in Python, • Hands-on experience with AWS services (e.g. S3, Batch, RDS, EC2, Lambda) and containerized deployment (Docker), • Experience with web development tools (ReactJS, HTML, CSS), • Experience in SQL, designing relational data models and working with production databases, • Experience with AI coding tools, • Experience working with scientists, preferably in genomics (with NGS data) or related field, • Proficiency with git-based collaborative development, code review, automated testing, and CI/CD, • Ability to work onsite 2x/per week at our Brisbane HQPREFERRED QUALIFICATIONS, • Experience with workflow orchestration systems (Prefect, Nextflow, CWL, Airflow), • Experience with LIMS/ELN data modeling, preferably Benchling, • Experience building and operating data pipelines or ETL systems, and comfort owning them end to end, • Experience with analytics engineering tooling (DBT) and data warehouse design, • Track record of building tools used by scientists or other non-engineer users, and of translating ambiguous requirements into working software, • Demonstrated ability to work independently in a small team where priorities shift and everyone wears many hats, • Background -- or real interest -- in the underlying biology, and the communication skills to work directly with bench scientists, • Infrastructure-as-code experience (Terraform), • Thoughtful, productive use of AI coding tools, and a considered point of view on where they help and where they do notBENEFITS, • Company-paid health/vision/dental benefits, • Unlimited vacation and generous sick time, • Company-sponsored meals and snacks, • Wellness, caregiver and ergonomics benefits, • 401(k) with company matching Actual base salary will be determined by relevant professional experience, applicable skills, and internal equity. THE COMPANY Mammoth Biosciences is a biotechnology company that leverages its proprietary ultracompact CRISPR systems to develop long-term curative therapies for genetic diseases. Founded by CRISPR pioneer and Nobel laureate Jennifer Doudna and Trevor Martin, Janice Chen, and Lucas Harrington, the company's ultracompact proteins are designed to enable in vivo gene editing in difficult-to-reach tissues utilizing both nuclease applications and new editing modalities beyond double-stranded breaks, including base editing and epigenetic editing. The company is building out its pipeline of potential in vivo gene editing therapeutics and capabilities and has partnerships with leading pharmaceutical and biotechnology companies to broaden the reach of its innovative and proprietary technology. Mammoth's deep science and industry experience, along with a robust and differentiated intellectual property portfolio, have enabled the company to further its mission to transform the lives of patients and deliver on the full promise of CRISPR technologies. It is our policy and intent to provide equal opportunity to all persons without regard to race, color, religion, political affiliation, sex/gender (including gender expression/identity, pregnancy, childbirth and related medical conditions), marital status, registered domestic partner status, sexual orientation, age, ancestry, national origin, veteran status, disability, medical condition, genetic characteristics, and/or any other basis protected by law. This policy covers all facets of employment including, but not limited to: recruitment, selection, placement, promotions, transfers, demotions, terminations, training, and compensation. Mammoth Biosciences requires that all employees be vaccinated against COVID as a condition of at-will employment, with exceptions for medical or religious reasons in compliance with local, state, and federal law. 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 DescriptionCompany Description About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on LinkedIn, Facebook, Instagram, X and YouTube. Job Description AbbVie is searching for an in-house Senior Counsel for our Patent Prosecution group, part of AbbVie’s Intellectual Property, Transactions, and Innovation legal team. This position will support AbbVie’s immunology pharmaceutical products and be based in our offices in Waltham, MA, North Chicago, IL, or South San Francisco, CA, with a hybrid work model (on site 3+ days/week). Acting individually and in cross-functional teams, the in-house Senior Counsel will develop and implement intellectual property strategies for AbbVie’s products and product candidates. Responsibilities: • Maximize AbbVie’s competitive position through creation and implementation of intellectual property strategies, • Provide legal advice and counsel to cross-functional R&D and business teams on a variety of IP-related matters, • Draft, file, and prosecute strategically useful patent applications worldwide both directly and through management of outside counsel, • Challenge and defend patents in IPR, opposition, interference, and other post-grant proceedings, • Conduct prior art searches, analyze third-party patent positions, and conduct due diligence to support business development activitiesQualifications, • JD degree from an accredited law school, state bar admission enabling in-house practice (specific state not required), and registration to practice before the USPTO, • 5+ years of experience practicing patent law as an attorney or patent agent at a law firm and/or life sciences company, including substantial U.S. and foreign patent prosecution, • Technical background relevant for pharmaceutical patent prosecution, such as:, • Experience with small molecule and/or biological pharmaceutical discovery & development, and/or, • Technical degree in relevant field, such as molecular biology, biotechnology, biochemistry, biology, chemistry, chemical engineering, or biomedical engineering, • Strong legal, analytical, communication, collaboration, and people skills, • Demonstrated ability to manage complex projects to meet deadlines Additional Information Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law: • The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future., • We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees., • This job is eligible to participate in our long-term incentive programs. Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company’s sole and absolute discretion, consistent with applicable law. AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled. US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more: https://www.abbvie.com/join-us/reasonable-accommodations.html

Job DescriptionCompany Description Eurofins Scientific is a network of independent companies providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work to ensure the products they supply are safe, their ingredients are authentic, and labelling is accurate. Eurofins is dedicated to delivering testing services that contribute to the health and safety of society and the planet, and to its corporate responsibility to protect the environment and ensure diversity, equity, and inclusion across the entire network of Eurofins companies. With more than 20 U.S. locations, Eurofins Built Environment Testing offers Industrial Hygiene (IH) and Indoor Air Quality (IAQ) services to protect health in built environments. Clients include consultants, industry, real estate, healthcare, government, and homeowners. Services cover a wide range of tests, including asbestos (PLM/TEM), mold, bacteria, VOCs, allergens, Legionella, radon, lead, silica, and more. Job Description Eurofins Built Environment Testing is searching for an Asbestos Analyst in Emeryville, CA. The Analyst primarily performs analysis of bulk samples using PLM for asbestos. Analyst prepares and analyzes environmental samples according to scientific methodology in compliance with company Quality Assurance programs and SOP’s, and must be knowledgeable of both job-specific routine and complex analyses. The analyst validates and reviews data for accuracy, and enters laboratory data into the LIMS that ultimately generates required reports to clients. Schedules sample workload according to due dates and sample hold times, and must be knowledgeable of the job-specific laboratory testing equipment, requiring the exercise of discretion and judgment in its operation. Asbestos Analyst responsibilities include, but are not limited to, the following: Prepare and analyze aerobiological and environmental samples for asbestos. Accurately enters and reports analytical data using the LIMS Performs independent data reviews for other analysts’ work Performs analysis of reference materials, proficiency samples and other quality control samples as needed Maintains client service and provides technical support as needed Assists the QA manager in development, implementation and data collection of QA processes for the different analytical tests Performs confirmation of lab results as needed by client services personnel Performs and completes all analytical testing and Quality Assurance related tasks as needed Assists in pursuing, receiving and maintaining necessary laboratory accreditations Maintains and updates all necessary Training and QA documents onsite as necessary Coordinates and manages projects according to their rush status and due time for timely delivery Assists co-workers on analytical questions, as necessary Participates in Lean initiatives as needed Follows company policies and procedures and ensures that coworkers are doing the same Manages and maintains the inventory of re-sale supply items and laboratory consumables and takes necessary steps to re-order supplies as needed Manages and disposes analyzed samples as needed Provides training support for relevant analytical services (i.e. mycology, bacteriology, asbestos, ect) as needed Recommends and coordinates sample transfer as necessary Establishes and maintains laboratory stock culture and reference samples Performs root cause analysis and implements corrective actions for errors and issues as necessary Maintains all equipment properly and co-ordinates servicing of all equipment used in the laboratory, as needed Routinely communicates available capacity to Regional Manager Supports other departments within the lab (mycology, asbestos, bacteriology, and other) when appropriate and as needed Other responsibilities as deemed necessary by the Supervisor/Manager Qualifications Basic Minimum Qualifications: 0-1+ years of experience performing asbestos microscopy using Polarizing Light Microscope (PLM) Bachelor’s degree in microbiology, biology, geology or a closely related science Previous work experience in a fast-paced, production or food service environment preferred Authorization to work in the United States indefinitely without restriction or sponsorship Professional working proficiency in English is a requirement, including the ability to read, write and speak in English The ideal candidate would also possess: 8 units of Geology courses preferred General regulatory requirements knowledge Knowledge of computers, spreadsheets, and databases Strong computer, scientific, and organizational skills Additional Information Compensation Range: $23-$27 per hour depending on level of experience and qualifications. Position is full-time, with possible weekends and overtime as needed. Candidates must be available to work Monday - Friday, 8:00am to 5:00pm. Eurofins Environment Testing (USA) provides a compensation range for informational purposes, the actual base compensation may vary based upon, but not limited to, relevant experience and skill set, base compensation of internal peers, business sector, and geographic location. We offer excellent full-time benefits including comprehensive medical coverage, life and disability insurance, 401(k) with company match, paid holidays and vacation, personal days, and dental and vision options. We support your development! Do you feel you don’t match 100% of the requirements? Don’t hesitate to apply anyway! Eurofins companies are committed to supporting your career development. We embrace diversity! Eurofins network of companies believe in strength and innovation through diversity, being an Equal Opportunity Employer. We prohibit discrimination against employees or applications based on gender identity and/or expression, race, nationality, age, religion, sexual orientation, disability, and everything else that makes employees of Eurofins companies unique. Sustainability matters to us! At Eurofins, we believe sustainability is at the heart of everything we do. Guided by our vision to be the Global Leader in “Testing for Life,” our mission to contribute to a healthier and safer world, and our core values, we are building a strong foundation for Environmental, Social, and Governance (ESG) initiatives. Eurofins’ commitment to sustainability begins within our own companies through a shared responsibility to people and the planet. With climate change posing an imminent threat, Eurofins and its many companies recognize their duty to proactively reduce or offset the environmental impact of essential operations while also helping our clients do the same—serving as a true ESG Enabler. Find out more in our career page: https://careers.eurofins.com/ Company description: Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in discovery pharmacology, forensics, advanced material sciences and agroscience contract research services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products. In over 35 years, Eurofins has grown from one laboratory in Nantes, France to 61,000 staff across a decentralised and entrepreneurial network of ca. 900 laboratories in 61 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products. In 2025, Eurofins generated total revenues of EUR 7.296 billion, and has been among the best performing stocks in Europe over the past 20 years. Eurofins USA Environment Testing is a Disabled and Veteran Equal Employment Opportunity employer.

Job Description About OmniAb OmniAb provides our pharmaceutical industry partners access to the most diverse antibody repertoires and cutting-edge screening technologies to enable discovery of next-generation therapeutics. We leverage our state-of-the-art technologies to facilitate the discovery of best-in-class antibodies. OmniAb consists of dynamic, collaborative and innovative team members that are passionate about contributing to the technological frontier of drug discovery and to the advancement of global human health. Together, with our partners, we are enabling the discovery of next-generation therapeutics. About OmniAb’s xPloration® Discovery System OmniAb’s xPloration offers superior screening and cell recovery compared to other single cell profiling technologies. Its high throughput enables the discovery of rare cells potentially missed by other systems or approaches. Its rapid laser-based recovery process paired with next-generation sequencing enables further mining of immune repertoires for potential hit expansion. xPloration supports various assay formats and is valuable for high-throughput B cell screening within the growing OmniAb partner ecosystem. About This Role We’re seeking a Field Application Scientist to serve as a trusted technical partner to biotech, pharmaceutical, and academic customers, delivering pre- and post-sales scientific support that drives successful evaluation, adoption, and use of the xPloration platform. This person will be an important member of the xPloration technical support team that focuses on customer enablement (both remote and on-site) while also doing some internal applications development. • Externally this person will serve as a confident, friendly, and scientifically rigorous representative of xPloration and OmniAb - leading customer demos, trainings, and technical troubleshooting., • For internal applications, this person will help expand and validate workflows, develop training materials, and translate field feedback into scalable improvements that broaden xPloration adoption across a larger audience. This individual will collaborate closely with our Sales and Science teams to ensure a seamless customer experience. The ideal candidate has a strong technical background in assay development, high-throughput screening, antibody discovery, instrument hardware support, and good customer service and communication skills. This role reports to the Senior Field Application Scientist. This is an onsite or remote position based out of our Emeryville headquarters and will require 50% to 75% domestic and international travel. This is a full-time position, and the office hours are between 8am to 5pm local time. What You’ll Do • Plan and execute on-site and virtual demos and technical evaluations in close partnership with the xPloration Sales team., • Lead customer onboarding and training, including best practices, workflow setup, experimental design guidance, and interpretation of results., • Provide expert, scientist-to-scientist technical support and troubleshooting - staying calm, confident, and solution-oriented during high-stakes or challenging demo and partner environments., • Develop enablement tools and technical content including protocols, SOPs, training decks, demo scripts, FAQs, troubleshooting guides, and demo-ready datasets., • Execute validated solutions to improve and expand on xPloration workflows, use cases, and performance to partners and customers., • Capture and synthesize customer feedback, recurring technical issues, workflow needs, and emerging applications; communicate actionable insights to Sales, Product, R&D, and Service teams to improve the customer experience and inform product development., • Maintain high-quality documentation and operational rigor (e.g., CRM notes, training records, experiment documentation, and escalation summaries)., • Educate potential customers and partners on the benefits, differentiators, and applications of our screening technology., • Communicate effectively across the company and externally, representing OmniAb at customer sites, relevant scientific conferences and trade shows., • Other duties as required. What You Bring • Bachelor’s degree in Bioengineering, Molecular Biology, Cell Biology, Biochemistry, or a related field with 5+ years of relevant industry experience., • MSc in a relevant field and 2+ years of relevant industry experience., • Proven success in a customer-facing scientific role (e.g., Field Applications Scientist, Applications Scientist, Technical Support Scientist) delivering trainings, demos, and technical troubleshooting., • Hands-on experience with mammalian cell culture, cell-based assays, high-throughput screening, flow cytometry or imaging-based analysis, and/or molecular biology workflows, • Strong experimental and analytical instincts with the ability to design experiments, interpret data, isolate variables, and recommend next steps under real-world constraints., • Excellent communication and teaching skills with the ability to build credibility quickly and represent OmniAb/xPloration with professionalism and warmth., • Strong record-keeping and organizational skills, capable of prioritizing effectively and managing a diverse workload., • A proactive, customer service-oriented mindset in regards to building trusted partner relationships and shared success., • Willingness and ability to travel up to 75% of the time. Nice To Have • MSc or PhD in a relevant field., • Familiarity with antibody discovery pipelines, single B-cell screening and sequencing concepts., • Track record creating scalable enablement assets such as training programs, onboarding checklists, troubleshooting playbooks, or application notes., • Comfort with data handling and visualization tools (e.g., Excel, GraphPad Prism, R/Python) and strong documentation discipline. Our total rewards package includes an annual base and variable compensation, target bonus, equity, refresh grants, ESPP, comprehensive health plans, immediate 401k matching, PTO, sick leave, paid parental leave, commuter benefits, wellness stipend, education reimbursement and more! The base compensation range for this position is $140,000 - $160,000 per year. The range provided is an estimate. Actual compensation may vary based on skills, experience, education, location, and other factors permitted by law. At OmniAb, we value diversity and strive to create an inclusive environment for everyone. We welcome a variety of experiences, skills, and perspectives within our organization and encourage individuals from diverse backgrounds to apply. We’re proud to be an Equal Opportunity Employer, and we will consider all qualified applicants based on merit and business need. We do not discriminate due to any non-merit-based factors or legally protected classes under federal, state, or local law.

Job Description Software Guidance & Assistance, Inc., (SGA), is searching for an Automation Specialist for a contract assignment with one of our premier Pharmaceutical clients in South San Francisco, CA. Responsibilities : Looking for a versatile Automation Specialist to work within the Complex in vitro Systems (CiS) Laboratory, where we design, develop, and characterize complex in vitro models (CIVM) to support the larger Development Sciences, Research, and Translational Medicine departments of the firm. In particular, the individual will be working in a cross functional team dedicated to providing technical expertise to automate scaling, processing, and assays using CIVMs. Currently the CIVMs include 3D multicellular models consisting of organoids and spheroids with aspiration to automate microfluidic organ-on-chip technologies. Our CIVM assays are developed to support both discovery and preclinical development portfolios broadly through multiple contexts of use, including safety, disposition, biomarker development, and pharmacodynamic responses. As part of the CiS Technologies team that establishes, qualifies, executes and maintains innovative, state-of-the-art technologies / platforms, we are looking for someone who will help us drive process and data integration and focus on advancing the operational capabilities of our automation and liquid handling systems. • In this laboratory-based role your impact will include:, • Work in a dynamic and innovative team to pioneer automation of CIVM culture (e.g. organoids, iPSC models, etc.) and assays., • Collaborate with scientists to translate manual cell culture and assay experiment processes into new automated workflows, including programming, testing, qualification and execution., • Qualify and execute automated CIVM culture and assays on our integrated liquid handling system, • Perform regular maintenance tasks and dry tests to ensure the readiness and sterility of the automation platforms, • Drive the integration of data management, analysis pipelines and data automation by aligning with internal and external stakeholders., • Train and support team members in formalizing Python development practices, including version control, collaborative workflows, and AI tool integration, with a focus on biology applications., • Document and report all relevant processes using SOPs, and share capabilities with colleagues in and outside the group in presentations, open door sessions and lab tours., • This position is laboratory-based and will include: sitting or standing for extended periods, performing repetitive tasks such as cell culture, pipetting and labeling tubes, performing techniques involving a high degree of manual dexterity and physical activity, flexibility as to work schedule (i.e. may need variation in hours worked and timing of those hours which may include weekend/holiday work as needed only), work with potentially hazardous materials including, but not limited to chemotherapeutics, biological hazards, and human primary cells., • The ideal candidate will design, develop, operate, and maintain automated protocols and systems for complex cell culture and assay process scale up. The successful candidate will work closely with other automation specialists and biologists at the firm to ensure regular maintenance of instrumentation and perform quality control of automated systems and equipment. They will also collaborate with a team of external vendors, data engineers, and software developers to implement automation best practices and proper process metadata tracking with Laboratory Information Management Systems (LIMS) integration. Importantly, the candidate will have direct experience translating lab experiments developed by individual scientists into automation-ready protocols that can run repeatedly at scale. Required Skills:, • PhD with 0-3 years of experience or Masters with 4-6 years of experience in biomedical engineering, chemical engineering, mechanical engineering, biomaterials, immunology, pharmacology, cellular or molecular biology, toxicology, pharmaceutical sciences, or a related field is required., • Must have experience in automation of cell culture in either academia, pharmaceutical/biotechnology industries, or contract research organizations., • Experience with automation and/or implementation of CIVMs is a plus., • Experience operating, programming, and integrating automation instrumentation and peripherals including but not limited to liquid handling platforms (e.g. Hamilton, Biomek, Opentron, BioTek washers), automated incubators, centrifuges, analyzers, and imagers., • Experience working with Python and/or C# and enjoy solving challenges systematically by using your analytical and technical skills, • Experience with integrating instrument and process quality control (QC) data with LIMS tools, • Track record of translating hands-on cell culture work into automated protocols, • Experience troubleshooting automation systems & workflows and ability to prioritize in a multi-user and multi-application environment., • Coordinating with external vendors and service providers for hardware/software modifications, driver requests, and system maintenance., • Maintain comprehensive technical documentation for automation systems, procedures, and troubleshooting guides to ensure knowledge transfer and system maintainability., • Passionate about collaborating in a cross-functional team in a multicultural environment., • Strong communication skills and ability to efficiently interact with scientists with different backgrounds and limited experience with automation., • Strong organizational skills, attention to detail, ability to prioritize tasks, interact professionally and present data to all levels of staff and external partners is required Preferred Skills:, • Experience with automation scheduling software (e.g. GreenButtonGo, Thermo Momentum, HiRes Cellario, etc.) is highly preferred, • Hands on experience with primary cell cultures in 3D is a plus (could be organoids, layered cultures, or spheroid work), • Hands on experience with at least several cellular assays (cell viability, flow cytometry, gene expression analysis, high content screening, 3D imaging analysis, biomarker quantification, transepithelial electrical resistance (TEER), etc.) is of advantage By applying for a job with SGA, you agree to allow SGA to process your application for this and future opportunities in accordance with our Privacy Policy. Also, to ensure timely processing, you agree to be contacted by our AI recruiter via email, text, or phone. Message frequency varies and data rates may apply, but you can reply STOP to any SMS message to opt-out of texts and may contact SGA at info@sgainc.com to opt-out of AI communications. The choice not to engage with AI will not adversely impact your consideration for placement. AI is not used to make any hiring determinations. SGA is a technology and resource solutions provider driven to stand out. We are a women-owned business. Our mission: to solve big IT problems with a more personal, boutique approach. Each year, we match consultants like you to more than 1,000 engagements. When we say let's work better together, we mean it. You'll join a diverse team built on these core values: customer service, employee development, and quality and integrity in everything we do. Be yourself, love what you do and find your passion at work. Please find us at https://sgainc.com/ . SGA is an Equal Opportunity Employer and does not discriminate on the basis of Race, Color, Sex, Sexual Orientation, Gender Identity, Religion, National Origin, Disability, Veteran Status, Age, Marital Status, Pregnancy, Genetic Information, or Other Legally Protected Status. We are committed to providing access, equal opportunity, and reasonable accommodation for individuals with disabilities in employment, and our services, programs, and activities. Please visit our company EEO page to request an accommodation or assistance regarding our policy. #LI-RJ1

Job DescriptionCompany Description About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on LinkedIn, Facebook, Instagram, X and YouTube. Job Description The Associate Director, Regulatory Affairs US Advertising and Promotion-Oncology is responsible for setting strategy and leading cross-functional, multidisciplinary, therapeutic teams, and executes multidivisional initiatives. The Associate Director envisions the future by using global marketplace, technology and business knowledge, collects and analyzes issues and trends that affect the business. This individual identifies and acts upon cross-organization or cross-business opportunities and possesses and leverages broad industry knowledge. Responsibilities: • Make decisions and plans for operations (workflow, assignments, staff development) within area of responsibility with minimal direction. Sets strategy and leads cross-functional/multidisciplinary therapeutic teams and multidivisional initiatives., • Maintains and evaluates productivity metrics to project current and future business needs, • Aligns and maintains effective communication channels with key Medical, Marketing, Regulatory, Legal and Public Affairs counterparts. Identifies areas of improvement in process/policy, develops recommendations/plan, and leads initiatives., • Assists in the management of the departmental budget, identifies and communicates budgetary needs to Operations and Finance, and identifies and projects current and future expenditures and business needs., • Collects and analyzes issues/trends that affect business to identify and act on cross-organization or cross business opportunities. Effective use of knowledge of global marketplace, technology and business levels., • Operates independently, with recognition of when to consult departmental senior concerning risks. In absence of Director, is responsible for day-to-day operations. Responsible for departmental initiatives, which have significant impact on both internal and external customers., • Encourages innovation and holds employees accountable for delivering on their goals; recognizes, mentors, rewards and recommends promotion for staff members based on their performance, results, and development., • Exhibits solid understanding of regulations, and guidance of regulatory authorities, political and legal climate and industry practices related to advertising and promotions to assist in meeting organizational goals. Possesses and leverages broad industry knowledge, • Develops and implements complex processes and projects and develops and delivers strategic presentations for senior management, • Identifies areas of improvement in process, policy, develops recommendations/plan and leads initiatives, • This role will work a hybrid work schedule (3 days in office, 2 days remotely) from our Mettawa, IL; South San Francisco, CA; Florham Park, NJ or Irvine, CA AbbVie headquarters Significant Work Activities: Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hr day) is required Qualifications • Minimum bachelor’s degree (or equivalent) in science (biology, chemistry, microbiology, immunology, medical technology, pharmacy, pharmacology), is required. Master’s, Ph.D or Pharm D preferred., • You should also possess:, • Associate Director: 8+ years of pharmaceutical experience with a Bachelor's, 5+ years with a Pharm D plus relevant ad promo experience. Oncology experience is preferred., • The candidate must have a solid understanding of regulatory advertising and promotion regulations, having had direct responsibility in this area., • Experience working in a complex and matrix environment, • Strong communication skills, both oral and written, • Experience in management capacity preferred Additional Information Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law: • The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future., • We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees., • This job is eligible to participate in our long-term incentive programs. Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company’s sole and absolute discretion, consistent with applicable law. AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled. US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more: https://www.abbvie.com/join-us/reasonable-accommodations.html

Job Description Crusoe is on a mission to accelerate the abundance of energy and intelligence. As the only vertically integrated AI infrastructure company built from the ground up, we own and operate each layer of the stack — from electrons to tokens — to power the world's most ambitious AI workloads. When you join Crusoe, you join a team that is building the future, faster. We're in the midst of the greatest industrial revolution of our time. The demand for AI compute is boundless, and power is a bottleneck. We're solving that — with an energy-first approach that makes AI infrastructure better for the world and faster for the people innovating with AI. We're looking for problem-solving, opportunity-finding teammates with a sense of urgency, who believe in the scale of our ambition and thrive on a path not fully paved — people who want to grow their careers alongside a team of experts across energy, manufacturing, data center construction, and cloud services. If you want to do the most meaningful work of your career, help our customers and partners advance their AI strategies, and be part of a high-performing team that believes in each other, come build with us at Crusoe. About This Role: Crusoe Cloud is revolutionizing high-performance computing by offering sustainable, low-cost GPU compute power. As a Cloud Support Engineer, you'll play a crucial role in empowering our customers to leverage this technology for groundbreaking advancements in fields like AI/ML, physics simulations, and computational biology. You will be the primary point of contact for technical support, ensuring our customers can seamlessly utilize Crusoe Cloud to achieve their goals. This role directly impacts Crusoe's mission by enabling our customers to accelerate their research and development, contributing to a more sustainable future. You will be involved in exciting projects, working with cutting-edge technologies and collaborating with a talented team to solve complex challenges. The ideal candidate is a highly motivated and experienced technical professional with a passion for customer success, a deep understanding of cloud technologies, and a commitment to Crusoe's values. This is a full-time position. What You’ll Be Working On: Customer Support: Provide exceptional technical support to customers via Zendesk, meeting SLAs and maintaining high CSAT (95%+). On-Call Rotation: Participate in a 24/7 on-call rotation to ensure timely resolution of critical issues. Troubleshooting: Diagnose and resolve issues related to VMs, hardware failures, and scaling tests using CLI and internal tools. Alert Triage and Maintenance: Manage alert triage, prepare for maintenance windows, and conduct node delivery testing. Collaboration: Work closely with SRE, Networking, and Storage teams from initial triage to root cause analysis (RCA) delivery. Global Teamwork: Adhere to global team collaboration and handoff processes for ticketing and on-call procedures. Knowledge Sharing: Develop onboarding/training materials, knowledge base documentation, and standard operating procedures (SOPs). What You’ll Bring to the Team: Education/Experience: Bachelor's degree in IT, Computer Science, Engineering, or a related field, or 2+ years of equivalent technical experience. Linux Proficiency: Strong command-line interface (CLI) skills in Linux environments. Version Control: Proficiency with Git for code management and collaboration. Customer Support Experience: 2+ years of experience in a customer support role, ideally within cloud, storage, or networking environments. Cloud Technologies: Experience with container orchestration (e.g., Kubernetes), workload management (e.g., Slurm, Terraform), and monitoring tools (e.g., Grafana). Public Cloud Knowledge: Familiarity with other public cloud platforms (e.g., AWS, Azure, GCP). Communication Skills: Excellent communication and customer service skills, including the ability to prioritize competing escalations. Bonus Points: Cloud Expertise: Deep understanding of specific cloud platforms and services. Automation Skills: Experience with automation tools and scripting languages. Problem-Solving Abilities: Demonstrated ability to analyze complex technical issues and develop effective solutions. Passion for Sustainability: A strong interest in contributing to a more sustainable future through technology. Benefits: Competitive compensation and equity packages Restricted Stock Units Paid time off, paid holidays & leave of absence programs Comprehensive health, dental & vision insurance Employer contributions to HSA account Paid parental leave Paid life insurance, short-term and long-term disability Professional development & tuition reimbursement Mental health & wellness support Commuter benefits (parking & transit) Cell phone stipend 401(k) Retirement plan with company match up to 4% of salary Volunteer time off Global travel insurance & emergency assistance Daily meals allowance Additional perks & programs specific to location Compensation Range Compensation will be paid in the range of up to $145,000 - $170,000 + Bonus. Restricted Stock Units are included in all offers. Compensation to be determined by the applicant's knowledge, education, and abilities, as well as internal equity and alignment with market data. Crusoe is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, religion, disability, genetic information, pregnancy, citizenship, marital status, sex/gender, sexual preference/ orientation, gender identity, age, veteran status, national origin, or any other status protected by law or regulation.

Job DescriptionAbout Tahoe Therapeutics Tahoe Therapeutics is a biotechnology company working on building the ground truth for biological superintelligence. Our Mosaic platform is the first to make in vivo data generation scalable, with single-cell resolution, allowing us to map how drugs affect patient-derived cells in the body across a wide range of biological contexts. We are building the world’s largest in vivo single-cell perturbation atlas and using it to train multimodal foundation models that learn the context-dependent nature of gene function, disease progression, and drug response. By combining cutting-edge machine learning with the most biologically relevant datasets ever assembled in drug discovery, our mission is to find better drugs, faster and bring them to more patients who need them. Your role With Tahoe-100M, we solved one of the fundamental bottlenecks in building a virtual model of the cell: generating massive, perturbation-rich, single-cell datasets that capture real biological causality. With Tahoe-x1, we removed the second bottleneck: creating a modern platform for rapid iteration on model architectures and designs in a cost-efficient manner and at scale. At Tahoe, we embody a simple philosophy: build in the open, shoot for the moon, and we’re looking for people who want to push the frontier of what’s possible. As a Senior Machine Learning Engineer, you will play a leading role in designing the next generation of foundation models of gene regulatory networks powered by Tahoe’s large scale single-cell datasets such as Tahoe-100M and beyond. This role is well-suited for someone with a strong background in machine learning and statistics, and an interest in applying cutting-edge breakthroughs in ML to meaningful problems in drug discovery. We are looking for non-incremental thinkers with the skills to help build models that can make a real impact on drug discovery. Qualifications - Required • Solid Engineering and Computer Science fundamentals, ideally with a degree in CS, Math, or equivalent experience., • Exceptional engineering skills to iterate quickly on data processing and training pipelines, • Experience in building, testing, training, and deploying modern neural network architectures such as Transformers., • Experience with frameworks like PyTorch, Tensorflow, Keras, JAX and the ability to write hardware optimized code for distributed trainingQualifications - Desirable, • Experience with distributed deep learning using frameworks such as HF Accelerate, Deepspeed, Composer, TorchTitan, Megatron etc., • Experience with training large neural networks on multiple compute nodes.Key Responsibilities, • Stay at the forefront of ML and computational biology research and rapidly adopt state-of-the-art techniques to train AI virtual cell models on our massive single cell datasets., • Work together with ML Scientists to develop the next generation of compute optimized models like Tahoe-x1.Benefits, • Unlimited Paid Time Off (PTO)., • Monthly Lunch budget, • One-time Office set up budget, • US Employees: HMO Kaiser Platinum and PPO Anthem Gold medical as well as vision and dental plans for both the employee and dependents. This position requires on-site presence at our South San Francisco office a minimum of three days per week. We welcome applicants who require visa sponsorship and provide work authorization support for qualified candidates. 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 CoreWeave is The Essential Cloud for AI™. Built for pioneers by pioneers, CoreWeave delivers a platform of technology, tools, and teams that enables innovators to build and scale AI with confidence. Trusted by leading AI labs, startups, and global enterprises, CoreWeave combines superior infrastructure performance with deep technical expertise to accelerate breakthroughs and turn compute into capability. Founded in 2017, CoreWeave became a publicly traded company (Nasdaq: CRWV) in March 2025. Learn more at www.coreweave.com. What You'll Do: AI is transforming how medicines are discovered, how diseases are diagnosed, and how care is delivered. Pharmaceutical companies, biotechs, medical device makers, payers, and health systems are moving AI from research into regulated production: training foundation models on genomic, molecular, and imaging data, running large-scale protein structure prediction and molecular dynamics, and deploying clinical and operational LLMs under strict privacy and validation requirements. Building these systems demands extraordinary compute, and it demands infrastructure that can meet the compliance bar of a regulated industry. As a GTM Solution Specialist for Healthcare & Life Sciences, you open new market opportunities with the world's leading pharma, biotech, and healthcare organizations, and drive the initial adoption of CoreWeave's Essential AI cloud with the earliest customers building AI-native drug discovery and clinical programs. You feed what you learn directly into the product roadmap, and you equip the broader sales and solution architecture teams with the domain knowledge and deal frameworks to win in HCLS. About the role: As a GTM Solution Specialist for Healthcare & Life Sciences, you sit at the front edge of CoreWeave's go-to-market motion for an industry where AI is compressing decade-long discovery timelines into years. This is a market-creation role: you take CoreWeave's AI platform into accounts where foundation model training, genomics pipelines, and clinical AI deployment are becoming infrastructure-defining decisions, win the first HCLS customers, and build the repeatable narratives and playbooks the rest of the field uses to scale. You are the connective tissue between computational science and clinical AI teams and CoreWeave's product and infrastructure roadmap, translating what early customers need around petabyte-scale biological data pipelines, regulated workload isolation, and validated environments into the priorities that make CoreWeave the essential AI cloud for healthcare and life sciences. In this role, you will: • Own the commercial and technical strategy for net new customer wins in HCLS AI, where foundation model training, genomics and imaging pipelines, and regulated AI deployment are the primary buying triggers., • Drive new business opportunities at pharmaceutical companies, techbio and biotech firms, medical device makers, payers, and health systems where GPU compute bottlenecks, biological data pipeline complexity, or compliance requirements are barriers to accelerating AI development on CoreWeave., • Build deep expertise across the HCLS AI stack (protein structure prediction and generative chemistry, molecular dynamics, genomics and multi-omics pipelines, medical imaging models, and clinical and operational LLMs), using CoreWeave's AI platform as the substrate that makes AI-native discovery and clinical AI economically viable., • Translate customer requirements around PHI handling, HIPAA and GDPR compliance, GxP validation, data residency, and model governance into specific product feedback that shapes CoreWeave's roadmap for regulated industries., • Develop deal structures, technical playbooks, and benchmark narratives that help sales and SA teams accelerate opportunities where training scale, pipeline throughput, and compliance posture are key evaluation criteria., • Engage directly with heads of computational science, AI platform leads, CIOs, and research IT as the authoritative voice on GPU cluster architecture, secure AI infrastructure, and the compute decisions that separate research pilots from production-scale discovery and clinical programs., • Design the commercial framework for large-scale HCLS infrastructure deals, including cluster reservation models, capacity commitments, and dataset storage SLAs, to support multi-year strategic partnerships., • Partner with product, infrastructure, and ecosystem teams, including NVIDIA (BioNeMo, Clara, MONAI, Parabricks), scientific software ISVs, and data platform providers, to maintain a competitive edge across active and prospective HCLS deployments.Who You Are:, • 10+ years of experience in technical business development, solutions architecture, or systems engineering within healthcare, life sciences, or AI infrastructure, with a track record of applying that expertise to drive customer outcomes and revenue., • 5+ years working directly with pharma, biotech, or healthcare organizations on GPU infrastructure, scientific computing, or ML platform architecture in a customer-facing or deal-shaping capacity., • Deep understanding of HCLS AI workloads: protein structure prediction, molecular dynamics and generative chemistry, genomics and multi-omics pipelines, medical imaging, and clinical NLP, and the infrastructure demands each creates., • Working knowledge of the regulatory and privacy landscape governing healthcare and life sciences (HIPAA, GDPR, GxP and computer system validation, FDA expectations for AI/ML-enabled products) and how it shapes cloud adoption, vendor selection, and deal structure., • Proven experience managing the full commercial lifecycle of complex technical deals exceeding $10M in contract value, including multi-stakeholder negotiation, technical due diligence, and deployment planning., • Technical proficiency in cloud-native AI infrastructure including Kubernetes, high-speed storage systems (NVMe, object storage, parallel filesystems), and high-performance networking (InfiniBand, RDMA) as applied to large-scale training and scientific computing clusters., • Demonstrated ability to build trusted relationships with senior computational science, engineering, and infrastructure decision-makers at pharma, biotech, and healthcare organizations.Preferred:, • Direct experience at or selling into leading HCLS organizations (global pharma, techbio and AI-first drug discovery companies, genomics platforms, medical imaging or device leaders, or major health systems and payers)., • Familiarity with NVIDIA's healthcare and life sciences ecosystem, including BioNeMo for biomolecular foundation models, Parabricks for genomics, and MONAI and Clara for medical imaging, at both a technical and commercial level., • Background supporting large-scale scientific computing, structure-based drug discovery pipelines, or clinical AI deployment in a validated environment., • Advanced technical degree (MS or PhD in Computational Biology, Bioinformatics, Computer Science, or equivalent) or MBA with a strong technical foundation in AI/ML systems, and a demonstrated ability to operate at the intersection of technical architecture and commercial strategy.Wondering if you're a good fit? Wondering if you're a good fit? We believe in investing in our people, and value candidates who can bring their own diversified experiences to our teams, even if you aren't a 100% skill or experience match. Here are a few qualities we've found compatible with our team. If some of this describes you, we'd love to talk. • You understand the HCLS AI stack end-to-end: you know how sequencing reads and molecular structures become training tensors, how foundation models compress years of wet-lab iteration into weeks of compute, and how to explain both to a Chief Scientific Officer and a CFO in the same meeting., • You are fluent in where the industry is heading: you follow how biomolecular foundation models, AI-native drug discovery, and clinical LLMs are reshaping R&D and care delivery, and you can speak credibly about it to computational scientists and executives alike., • You are an expert at navigating "The Room": you have a proven ability to manage multi-stakeholder technical evaluations at HCLS organizations without losing momentum, earning trust from computational scientists, research IT, compliance, and procurement in the same deal cycle.Why CoreWeave? At CoreWeave, we work hard, have fun, and move fast! We're in an exciting stage of hyper-growth that you will not want to miss out on. We're not afraid of a little chaos, and we're constantly learning. Our team cares deeply about how we build our product and how we work together, which is represented through our core values: • Be Curious at Your Core, • Act Like an Owner, • Empower Employees, • Deliver Best-in-Class Client Experiences, • Achieve More Together We support and encourage an entrepreneurial outlook and independent thinking. We foster an environment that encourages collaboration and enables the development of innovative solutions to complex problems. As we get set for takeoff, the organization's growth opportunities are constantly expanding. You will be surrounded by some of the best talent in the industry, who will want to learn from you, too. Come join us! The base salary range for this role is $177,000 to $237,000. The starting salary will be determined based on job-related knowledge, skills, experience, and market location. We strive for both market alignment and internal equity when determining compensation. In addition to base salary, our total rewards package includes a discretionary bonus, equity awards, and a comprehensive benefits program (all based on eligibility). What We Offer The range we've posted represents the typical compensation range for this role. To determine actual compensation, we review the market rate for each candidate which can include a variety of factors. These include qualifications, experience, interview performance, and location. In addition to a competitive salary, we offer a variety of benefits to support your needs. The benefits below reflect our US-based offerings for full-time employees; for roles in other locations, benefits vary and are shared during the hiring process. These include: • Medical, dental, and vision insurance - 100% paid for by CoreWeave, • Company-paid Life Insurance, • Voluntary supplemental life insurance, • Short and long-term disability insurance, • Flexible Spending Account, • Health Savings Account, • Tuition Reimbursement, • Ability to Participate in Employee Stock Purchase Program (ESPP), • Mental Wellness Benefits through Spring Health, • Family-Forming support provided by Carrot, • Paid Parental Leave, • Flexible, full-service childcare support with Kinside, • 401(k) with a generous employer match, • Flexible PTO, • Catered lunch each day in our office and data center locations, • A casual work environment, • A work culture focused on innovative disruption California Applicants California Consumer Privacy Act Equal Opportunity & Accommodations CoreWeave is an equal opportunity employer, committed to fostering an inclusive and supportive workplace. All qualified applicants and candidates will receive consideration for employment without regard to race, color, religion, sex, disability, age, sexual orientation, gender identity, national origin, veteran status, or genetic information. As part of this commitment and consistent with the Americans with Disabilities Act (ADA), CoreWeave will ensure that qualified applicants and candidates with disabilities are provided reasonable accommodations for the hiring process, unless such accommodation would cause an undue hardship. If reasonable accommodation is needed, please contact: careers@coreweave.com. Export Control Compliance This position requires access to export controlled information. To conform to U.S. Government export regulations applicable to that information, applicant must either be (A) a U.S. person, defined as a (i) U.S. citizen or national, (ii) U.S. lawful permanent resident (green card holder), (iii) refugee under 8 U.S.C. § 1157, or (iv) asylee under 8 U.S.C. § 1158, (B) eligible to access the export controlled information without a required export authorization, or (C) eligible and reasonably likely to obtain the required export authorization from the applicable U.S. government agency. CoreWeave may, for legitimate business reasons, decline to pursue any export licensing process.

Job DescriptionQualifications: Education Minimum Requirement: " Bachelor s degree in Engineering, Automated Sciences, Computer Science, Biology, Chemistry or equivalent with scientific expertise with laboratory equipment in the development and execution of bioanalytical assays Required Experience and Skills: Hands-on experience with Hamilton, Echo (Labcyte), and GBG platforms, including method development, troubleshooting, and day-to-day operation of automated workflows. Experience programming and operating automated laboratory equipment such as liquid handlers, dispensers, washers, centrifuges, and related instrumentation. Strong problem-solving skills and the ability to independently identify and resolve technical issues. Ability to generate, analyze, and interpret scientific data produced on automated platforms. Strong communication and collaboration skills, with experience working effectively across scientific, engineering, software-focused teams. Must be self-sufficient and able to hit the ground running Preferred Experience and Skills: " Integrating robotic system schedulers (e.g. High Resolution BioSolution, Biosero, Thermo Momentum) " Working in pharmaceutical or biotech company and/or laboratory experience " Implementing Client automation workflows and authoring operations SOPs " Microsoft programming languages (VB, C#, labview or equivalent) " Electro-Mechanical design/assembly skills " Use of electronic laboratory notebooks Responsibilities: The automation scientist in DMPK at South San Francisco will be responsible for driving the implementation of automated workflows to support pre-clinical studies. The Scientist will work collaboratively with other team members in a fast-paced environment to operate automated laboratory equipment and systems to support various DMPK assays. This specific position is a 6-month contract, and the individual should possess knowledge of the principles and concepts of various biological assays as they pertain to method development and sample testing using various liquid handlers and laboratory equipment. They should have a propensity towards technology. The successful candidate will play a crucial role in laboratory automation and modernization, providing input into the optimization of experimental methods with laboratory equipment and automation using state-of-the-art robotic systems. " Support the design, planning, and execution of robust automation strategies to support the DMPK group in SSF " Work jointly with department members, IT, and across functional teams to implement automation workflows, support lab instrumentation and robotic platforms, and develop Client data handling and analysis workflows " Contribute to the development of automated workflows to support assays such as immunoassay (IA), peptide stability, protein binding, automated sample preparation for plasma and tissue drug concentration analysis, cell culture maintenance & cell-based assays " Map and integrate all the workflows for efficient use of automation and space " Develop/update operations SOPs " Troubleshoot errors, maintain, and update instruments " Train and support scientists in automation workflows & platforms Manage data integrity through automated processes " Collaborate to identify, evaluate, and recommend Client and cutting-edge automation and assay strategies to drive our discovery programs, including machine learning and artificial intelligence

Job DescriptionAbout DeepOrigin Deep Origin is building ambitious science in a fast-moving environment, combining AI and physics-based methods with wet-lab biology to advance drug discovery. The people who thrive here are accountable, adaptable, rigorous, humble, and direct. Across roles, we look for: • Ownership through to the result. An experiment isn't done until the data are analyzed, the conclusion is written down, and whoever needs it next has it., • Judgment under incomplete information. You resolve what you need to know, commit to a defensible course of action, and revise when the evidence warrants it., • Exacting about the work, unguarded about yourself. You hold data to a standard that survives scrutiny, and you drop your own interpretation when someone shows you better evidence., • Transparency as a working habit. You surface problems while they are cheap to fix, and you explain your results so chemists, engineers, and computational colleagues can act on them. About the role We are hiring a hands-on Senior Research Associate to build and run the cell-based assays and engineered cell lines behind our drug discovery programs. You will work day to day with a senior scientist in R&D, owning bench execution while helping shape assay strategy. Your core work: maintaining mammalian cell lines, engineering them with RNP-based CRISPR (knockouts and knock-ins), generating validated stable lines, and turning them into robust functional assays. The data you generate feeds directly into AI and physics-based compound design, so quality and reproducibility matter as much as throughput. Applicants must be authorized to work for any employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time. Requirements • Bachelor's or Master's degree in biology, cell biology, bioengineering, biochemistry, immunology, or a related discipline, or an equivalent combination of education and experience., • Relevant hands-on laboratory experience, • Demonstrated mammalian cell culture experience with strong aseptic technique, including routine maintenance of multiple lines in parallel., • Hands-on experience with CRISPR gene editing: knockout generation, and ideally knock-in, with validation of edited clones., • Experience with transient transfection, and with generating and validating stable cell lines, including clonal selection and banking., • Experience executing at least one cell-based assay readout, such as flow cytometry, plate-based viability, reporter, or proliferation assays., • Ability to analyze data, assess assay quality, communicate findings clearly, and work in a collaborative, multidisciplinary setting., • Commitment to laboratory safety, research integrity, accurate documentation, and responsible handling of biological materials.Nice to have qualifications, • Hands-on RNP-based CRISPR knockout and knock-in using Lonza Nucleofector platforms (4D-Nucleofector or equivalent), including program and buffer selection for the target cell type., • Experience with high-throughput or automated assay platforms, including 96- or 384-channel electronic pipetting systems and benchtop pipetting robots (INTEGRA VIAFLO, MINI 96, VOYAGER, ASSIST PLUS or comparable), and multimode plate readers., • Experience developing or optimizing BRET, TR-FRET/HTRF, or related proximity-based assay formats ., • Molecular biology bench skills: construct and primer design, cloning, qPCR or digital PCR, Western blot., • Drug discovery experience in biotech or pharma, including work on a target-to-lead or lead-optimization program., • Familiarity with assay qualification concepts: design of experiments, dose-response analysis, curve fitting, acceptance criteria, and statistical assessment of assay variability., • Experience with neuronal or other CNS-relevant cell models. ., • Experience with multiplexed editing, including triple knockouts or combined knockout and knock-in lines.Key responsibilities Mammalian cell culture • Culture, expand, and maintain mammalian cell lines under strict aseptic technique; monitor health, viability, density, and passage history., • Maintain cryopreserved stocks, run mycoplasma and identity checks, and keep accurate lineage records. Genome engineering • Optimize RNP-based CRISPR/Cas editing in mammalian cell lines: single and double knockouts., • Design and execute targeted knock-in strategies, including donor design, delivery optimization, and editing-efficiency assessment., • Genotype and validate edits by sequencing, qPCR or digital PCR, and protein-level readouts. Stable cell line generation • Perform transient transfections to test constructs quickly, optimizing reagent, nucleic acid amount, and harvest timing, and confirming expression before committing to a stable line., • Generate stable lines using viral and non-viral delivery; perform clonal selection, expansion, functional validation, and banking., • Characterize clones for expression level, assay performance, and stability over passage. Cell-based assay development • Develop, optimize, and run functional assays: plate-based, reporter and proximity-based assays; flow cytometry; and other cellular functional readouts., • Optimize seeding density, stimulation conditions, dose range, incubation time, controls, and acceptance criteria to improve sensitivity, dynamic range, and reproducibility., • Prepare test articles, reagents, controls, and assay plates according to established protocols and study plans . Data, documentation, and communication • Analyze dose-response data, fit curves, assess assay quality (Z', signal window, variability), and flag trends, outliers, and deviations., • Keep complete, timely records in the electronic lab notebook, consistent with data-integrity expectations., • Present results at team meetings and contribute figures and data to technical reports. Lab operations • Troubleshoot routine assay and culture problems, escalate significant deviations, and partner with colleagues to improve method robustness and transferability., • Support reagent preparation, inventory, equipment upkeep, sample tracking, and safety compliance., • Manage assigned work to agreed timelines. Working conditions This is a primarily onsite, laboratory-based position in South San Francisco. The role involves regular use of standard laboratory equipment and PPE, work with biological samples and research reagents, prolonged standing or sitting, repetitive hand motions, and moving laboratory supplies up to approximately 25 pounds, with reasonable accommodation as needed. Occasional work outside standard business hours may be required for time-sensitive experiments. Travel is minimal. Benefits • Competitive compensation package with meaningful equity., • Comprehensive health, dental, and vision coverage., • Annual team gatherings and company events., • Free lunch, snacks, beverages, and onsite gym access (for in-office employees).

Job DescriptionJoin a Global Leader in Workforce Solutions – Net2Source Inc. Who We Are Net2Source Inc. isn't just another staffing company, we're a powerhouse of innovation, connecting top talent with the right opportunities. Recognized for 300% growth in the past three years, we operate in 34 countries with a global team of 5,500+. Our mission? To bridge the talent gap with precision—Right Talent. Right Time. Right Place. Right Price. Title: Scientist - III (Senior) (#MSD1JP00004008) Location: 213 E. Grand Avenue, South San Francisco, CA 94080 USA Duration: 06+ Months Contract Pay Rate: $76.97/Hr on W2 Shift: Mon-Friday (8am-5pm) – 40 Hours/Week Education Minimum Requirement: • Bachelor's degree in Engineering, Automated Sciences, Computer Science, Biology, Chemistry or equivalent with scientific expertise with laboratory equipment in the development and execution of bioanalytical assays Required Experience and Skills: • Hands-on experience with Hamilton, Echo (Labcyte), and GBG platforms, including method development, troubleshooting, and day-to-day operation of automated workflows., • Experience programming and operating automated laboratory equipment such as liquid handlers, dispensers, washers, centrifuges, and related instrumentation., • Strong problem-solving skills and the ability to independently identify and resolve technical issues., • Ability to generate, analyze, and interpret scientific data produced on automated platforms., • Strong communication and collaboration skills, with experience working effectively across scientific, engineering, software-focused teams., • Must be self-sufficient and able to hit the ground running Preferred Experience and Skills: • Integrating robotic system schedulers (e.g. High Resolution BioSolution, Biosero, Thermo Momentum), • Working in pharmaceutical or biotech company and/or laboratory experience, • Implementing Client automation workflows and authoring operations SOPs, • Microsoft programming languages (VB, C#, labview or equivalent), • Electro-Mechanical design/assembly skills, • Use of electronic laboratory notebooks Responsibilities: The automation scientist in DMPK at South San Francisco will be responsible for driving the implementation of automated workflows to support pre-clinical studies. The Scientist will work collaboratively with other team members in a fast-paced environment to operate automated laboratory equipment and systems to support various DMPK assays. This specific position is a 6-month contract, and the individual should possess knowledge of the principles and concepts of various biological assays as they pertain to method development and sample testing using various liquid handlers and laboratory equipment. They should have a propensity towards technology. The successful candidate will play a crucial role in laboratory automation and modernization, providing input into the optimization of experimental methods with laboratory equipment and automation using state-of-the-art robotic systems • Support the design, planning, and execution of robust automation strategies to support the DMPK group in SSF, • Work jointly with department members, IT, and across functional teams to implement automation workflows, support lab instrumentation and robotic platforms, and develop Client data handling and analysis workflows, • Contribute to the development of automated workflows to support assays such as immunoassay (IA), peptide stability, protein binding, automated sample preparation for plasma and tissue drug concentration analysis, cell culture maintenance & cell-based assays, • Map and integrate all the workflows for efficient use of automation and space, • Develop/update operations SOPs, • Troubleshoot errors, maintain, and update instruments, • Train and support scientists in automation workflows & platforms Manage data integrity through automated processes, • Collaborate to identify, evaluate, and recommend Client and cutting-edge automation and assay strategies to drive our discovery programs, including machine learning and artificial intelligence Why Work With Us? We believe in more than just jobs—we build careers. At Net2Source, we champion leadership at all levels, celebrate diverse perspectives, and empower you to make an impact. Think work-life balance, professional growth, and a collaborative culture where your ideas matter. Our Commitment to Inclusion & Equity Net2Source is an equal opportunity employer, dedicated to fostering a workplace where diverse talents and perspectives are valued. We make all employment decisions based on merit, ensuring a culture of respect, fairness, and opportunity for all, regardless of age, gender, ethnicity, disability, or other protected characteristics. Awards & Recognition • America's Most Honored Businesses (Top 10%), • Fastest-Growing Staffing Firm by Staffing Industry Analysts, • INC 5000 List for Eight Consecutive Years, • Top 100 by Dallas Business Journal, • Spirit of Alliance Award by Agile1 #LS01

Job DescriptionCompany Description Eurofins Scientific is a network of independent companies providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work to ensure the products they supply are safe, their ingredients are authentic, and labelling is accurate. Eurofins is dedicated to delivering testing services that contribute to the health and safety of society and the planet, and to its corporate responsibility to protect the environment and ensure diversity, equity, and inclusion across the entire network of Eurofins companies. With more than 20 U.S. locations, Eurofins Built Environment Testing offers Industrial Hygiene (IH) and Indoor Air Quality (IAQ) services to protect health in built environments. Clients include consultants, industry, real estate, healthcare, government, and homeowners. Services cover a wide range of tests, including asbestos (PLM/TEM), mold, bacteria, VOCs, allergens, Legionella, radon, lead, silica, and more. Job Description Eurofins Built Environment Testing is looking for an experienced TEM Asbestos Analyst in our Emeryville, CA location. Relocation assistance may be available for the right candidate. The Analyst performs analysis of bulk and air for asbestos mineral fibers using TEM -Transmission Electron Microscopy. Analyst prepares and analyzes environmental samples according to scientific methodology in compliance with company Quality Assurance programs and SOP’s, and must be knowledgeable of both job-specific routine and complex analyses. The analyst validates and reviews data for accuracy, and uploads laboratory data into the LIMS that ultimately generates required reports to clients. Schedules sample workload according to due dates and sample hold times, and must be knowledgeable of the job-specific laboratory testing equipment, requiring the exercise of discretion and judgment in its operation. Responsibilities: • Prepare and analyze environmental samples for asbestos using TEM microscopy., • Adherence to EPA, NVLAP, ELAP, OSHA, and NIOSH standards for asbestos identification, • Accurately enters and reports analytical data using the LIMS, • Performs independent data reviews for other analysts’ work, • Performs analysis of reference materials, proficiency samples and other quality control samples as needed, • Maintains client service and provides technical support as needed, • Assists the QA manager in development, implementation and data collection of QA processes for the different analytical tests, • Performs confirmation of lab results as needed by client services personnel, • Performs and completes all analytical testing QA related tasks as needed, • Assists in pursuing, receiving and maintaining necessary laboratory accreditations, • Maintains and updates all necessary Training and QA documents onsite as necessary, • Co-ordinates and manages projects according to their rush status and due time for timely delivery, • Assists co-workers on analytical questions, as necessary, • Participates in Lean initiatives and projects when called upon, • Follows company policies and procedures and ensures that coworkers are doing the same Secondary Duties: • Manages and maintains the inventory of re-sale supply items and laboratory consumables and takes necessary steps to re-order supplies as needed, • Manages and disposes analyzed samples as needed, • Trains new asbestos testing Analysts as needed, • Recommends and coordinates sample transfer as necessary, • Establishes and maintains laboratory reference samples, • Performs root cause analysis and determines and implements corrective actions for errors and issues as necessary, • Maintains all equipment properly and co-ordinates servicing of all equipment used in the laboratory, as needed, • Routinely communicates available capacity to Regional Manager, • Supports other departments within the lab (mycology, asbestos, bacteriology, and other) when appropriate and as needed, • Other responsibilities as deemed necessary by the Supervisor/ManagerQualifications Basic Minimum Qualifications: • 1+ years of experience performing asbestos microscopy, • Must have an undergraduate degree in Geology, Biology or related science, or TEM Asbestos training course, • Experience utilizing a Transmission Electron Microscope preferred, • Authorization to work in the United States indefinitely without restriction or sponsorship., • Professional working proficiency in English is a requirement, including the ability to read, write and speak in English Additional Information Compensation range: $23 - $27 per hour depending on qualifications and experience. • Position is Full-time Monday - Friday , 8AM - 5PM shift with overtime or weekend work as needed., • Candidates currently living within a commutable distance of Emeryville, CA or are willing to relocate are encouraged to apply. Eurofins Environment Testing (USA) provides a compensation range for informational purposes, the actual base compensation may vary based upon, but not limited to, relevant experience and skill set, base compensation of internal peers, business sector, and geographic location. As a Eurofins employee, you will become part of a company that has received national recognition as a great place to work. We offer excellent full-time benefits including comprehensive medical coverage, life and disability insurance, 401(k) with company match, paid holidays, paid time off, and dental and vision options. We support your development! Do you feel you don’t match 100% of the requirements? Don’t hesitate to apply anyway! Eurofins companies are committed to supporting your career development. We embrace diversity! Eurofins network of companies believe in strength and innovation through diversity, being an Equal Opportunity Employer. We prohibit discrimination against employees or applications based on gender identity and/or expression, race, nationality, age, religion, sexual orientation, disability, and everything else that makes employees of Eurofins companies unique. Sustainability matters to us! At Eurofins, we believe sustainability is at the heart of everything we do. Guided by our vision to be the Global Leader in “Testing for Life,” our mission to contribute to a healthier and safer world, and our core values, we are building a strong foundation for Environmental, Social, and Governance (ESG) initiatives. Eurofins’ commitment to sustainability begins within our own companies through a shared responsibility to people and the planet. With climate change posing an imminent threat, Eurofins and its many companies recognize their duty to proactively reduce or offset the environmental impact of essential operations while also helping our clients do the same—serving as a true ESG Enabler. Find out more in our career page: https://careers.eurofins.com/ Company description: Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in discovery pharmacology, forensics, advanced material sciences and agroscience contract research services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products. In over 35 years, Eurofins has grown from one laboratory in Nantes, France to 61,000 staff across a decentralised and entrepreneurial network of ca. 900 laboratories in 61 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products. In 2025, Eurofins generated total revenues of EUR 7.296 billion, and has been among the best performing stocks in Europe over the past 20 years. Eurofins USA Environment Testing is a Disabled and Veteran Equal Employment Opportunity employer.

Job Description Our client is an innovative, fast-growing biotechnology company delivering rapid, affordable DNA and RNA sequencing services to scientists worldwide. They are seeking a hands-on Lab Technician to support high-throughput DNA sequencing operations. You'll work with automated laboratory systems, prepare sequencing libraries, monitor quality, troubleshoot issues, and help improve laboratory workflows. Why You Should Join • Competitive salary of $70K–$85K plus equity., • Contribute to sequencing services used by over 70,000 scientists worldwide., • Work alongside R&D, product, and engineering teams on emerging technologies., • Make a real impact by improving protocols and laboratory processes., • Join a growing, financially stable company with opportunities for career development. What You'll Be Doing • Receive and log samples in the in-house LIMS and organize them into 96-well plates., • Perform sequencing library preparation using automated liquid-handling systems., • Load prepared libraries onto sequencers and monitor sequencing runs., • Perform quality control, investigate failed samples, and repeat preparations when needed., • Troubleshoot instrument and protocol issues independently., • Maintain laboratory supplies and reagents, and suggest protocol improvements. Qualifications • Bachelor's degree in Biology or a related scientific field., • 2–10 years of experience in a commercial or production laboratory; academic or research-only experience does not qualify., • Practical experience with DNA extraction, PCR, NGS library preparation, and DNA sequencing., • Familiarity with liquid-handling automation, 96-well plate workflows, and laboratory quality control., • Ability to troubleshoot independently in a fast-paced, high-volume environment., • Availability to work the evening shift, Monday–Friday, from 4:00 PM to 12:00 AM PT., • Authorization to work in the United States without visa sponsorship.

Job DescriptionAbout Nosis Bio: Nosis Bio is a well-funded biotech startup exclusively focused on cell-specific delivery of RNA therapeutics. We are an all-scientist team of biologists, chemists, and machine learning experts who believe targeted extrahepatic delivery is the key to making RNA therapies the standard of care for a wide range of chronic diseases. We combine deep expertise in receptor biology, generative AI, and high-throughput in vivo data generation to accelerate the development of RNA therapeutics for new tissues. We are addressing a major unmet need across the industry and actively partner with pharmaceutical companies, research institutions, and biotech companies. About the Role: We are seeking a Technical Specialist / Research Associate to conduct in-vivo experiments to evaluate the pharmacokinetic (PK), pharmacodynamic (PD), and efficacious properties of therapeutic candidates. The successful candidate will have hands-on experience with in-vivo animal studies and will work closely with multidisciplinary teams to support various drug discovery projects. This is an on-site, in person position. Responsibilities Perform in-vivo PK/PD and efficacy studies in animal models, including intravenous (IV) and subcutaneous dose administration, blood sampling, tissue collection, and necropsy. Adopt new techniques and develop disease models for in house use. Ensure proper animal handling and dosing techniques, following established protocols and ethical guidelines. Collect, organize, and document experimental data accurately and maintain laboratory records in compliance with company protocols and regulatory standards. Stock/maintain consumables and reagents necessary for experiments. Collaborate with cross-functional teams, including biology, chemistry, and translational science, to support project goals and timelines. What we’re looking for: Ability to work on site in our lab spaces located in the California Bay Area – Research park at Marina Village (Alameda, CA) Motivated and proactive with strong problem-solving skills. Team-oriented and open to collaboration across scientific disciplines. Title and track is dependent on academic and professional experience – we recruit diverse backgrounds including those with academic, non-profit, and industry experiences! General Requirement: AS or BS degree with 3+ years in vivo experience (industry or academia) and 1+ years experience in an industry (or similar) environment

Job DescriptionDescription: We are seeking an enthusiastic, goal-oriented scientist to join our Analytical Development team and develop, optimize, and implement analytical methods for novel therapeutic products, including monoclonal antibodies, bispecific antibodies, fusion proteins, and other biologics. This exciting opening offers the candidate the opportunity to be a part of a professional, customer-focused, pharmaceutical company with a competitive salary and full benefits package. The role focuses on ELISA and cell-based bioassays supporting programs from early development through commercialization and product lifecycle management. The successful candidate will contribute to multiple projects supporting process development, formulation development, release testing, stability studies, and product characterization. The position may be filled at the Associate Scientist or Scientist level, depending on relevant experience, technical expertise, and demonstrated independence. Zylidac Bio LLC is a leading Contract Development and Manufacturing Organization specializing in the development and manufacturing of biologics, particularly antibodies. We are committed to delivering high-quality products and services that meet the evolving needs of our clients in the biopharmaceutical industry. RESPONSIBILITIES: • Develop, optimize, and perform ELISA and cell-based bioassays to characterize biologic therapeutics., • Perform analytical testing to support process development, formulation development, release testing, stability studies, and product characterization., • Support assay qualification, validation, and method transfer activities as needed., • Analyze data, interpret results, identify trends, and troubleshoot assay performance., • Maintain accurate documentation of experimental procedures, results, and conclusions in laboratory notebooks and analytical records., • Present experimental results and scientific findings in team meetings and technical discussions., • Collaborate across multidisciplinary teams to complete assigned work and meet project timelines., • Contribute to the evaluation and implementation of new technologies, methods, and laboratory processes., • Follow laboratory safety requirements and applicable quality systems, procedures, and regulatory requirements., • Support laboratory operations, including instrument maintenance, reagent and sample management, and supply ordering., • Contribute to technical documentation supporting quality and regulatory activities., • Design and execute experiments, develop and troubleshoot assays, and own technical deliverables with increasing independence.Requirements: QUALIFICATIONS – SKILLS & REQUIREMENTS: • Relevant laboratory experience in bioassay development, analytical development, or cell and molecular biology., • Hands-on experience with ELISA, qPCR, cell-based assays, mammalian cell culture, and aseptic techniques, with preference for experience in host cell protein, leached Protein A, host cell DNA, and other bioassay/analytical methods., • Experience working in accordance with GMP requirements, quality systems, and data integrity principles, with strong attention to data quality, accurate documentation, and compliance., • Ability to execute experiments, analyze data, troubleshoot assays, and communicate findings, with independence appropriate to the position level., • Strong organizational, time-management, verbal, and written communication skills., • Ability to learn new technologies and adapt to changing project priorities. PREFERRED QUALIFICATIONS: • Experience with assay qualification, validation, or method transfer., • Experience working in a biopharmaceutical development or regulated laboratory environment., • Experience with surface plasmon resonance (SPR). EDUCATION & EXPERIENCE: • Associate Scientist: Bachelor's degree with 4+ years, or Master's degree with 2+ years of relevant laboratory experience., • Scientist: Bachelor's degree with 6+ years, Master's degree with 4+ years, or PhD with 0–2 years of relevant experience., • Degree in Biochemistry, Molecular Biology, Cell Biology, Immunology, Biotechnology, or a related scientific discipline.

Job DescriptionAbout Rezo Therapeutics Rezo is a different kind of biopharma company. Our mission is to dramatically increase the success rate of drug development by building a disease-agnostic, fully-integrated, network biology platform that will redefine our understanding of human disease and ability to treat it. We are leveraging a unique integrated approach, combining capabilities in genetics, proteomics, structural biology and AI to generate deep biological insights and novel therapeutic approaches. Located in San Francisco’s vibrant Mission Bay neighborhood, Rezo is in close proximity to UCSF, numerous urban amenities, and outdoor recreational opportunities. We recognize that realizing our mission depends as much on our people as it does on our science and are building a workplace that fosters collaboration, respect, and diversity where contributing to your team’s success is valued as highly as individual achievements. If you’re passionate about team science and breaking down barriers to progress in drug development, please consider joining us! The Opportunity We are seeking a highly organized, detail-oriented, and proactive Contracts Associate to join our growing biotechnology company. Reporting to the VP of Strategy and Business Development, this individual will be responsible for coordinating and administering the company’s contracting activities, ensuring contracts move efficiently through review, approval, execution, and ongoing management. The Contracts Associate will serve as the central point of contact for contract-related activities across the organization. This individual will also maintain our Contract Management System, coordinate purchase orders, monitor contractual obligations and deadlines, and ensure leadership has visibility into contract status and priorities. This position will initially be part-time at approximately 20 hours per week, with the potential to expand as the company grows.What You'll Do: • Contract Administration & Management, • Manage and coordinate the contracting process, including contract requests, preparation, review, approvals, execution, and filing of completed agreements, • Serve as the primary point of contact for contract-related activities, working closely with internal stakeholders, outside legal counsel, and external partners, • Maintain and continuously improve the company’s Contract Management System, ensuring all agreements and associated information are accurate, complete, and up to date, • Help establish and maintain efficient contracting workflows, standardized templates, and clear approval processes to streamline contract execution and minimize administrative burden on internal teams, • Proactively monitor contract obligations and deadlines, including payment milestones, renewals, termination notice periods, and deliverables, communicating upcoming commitments and required actions to appropriate stakeholders, • Contract Review, Negotiation & Legal Coordination, • Coordinate with outside legal counsel to facilitate timely review, negotiation, and execution of agreements, • Conduct initial administrative and business reviews of standard agreements to identify missing information, clarify business terms, and flag items requiring legal review, • Partner with functional leaders to understand business requirements and coordinate contract negotiations and revisions with internal stakeholders, vendors, consultants, and other external partners, • Support the preparation and processing of agreements, including confidentiality agreements (CDAs/NDAs), consulting agreements, master service agreements (MSAs), statements of work (SOWs), research agreements, and vendor contracts, • Purchase Order & Financial Coordination, • Coordinate with Finance to ensure purchase orders are appropriately linked to executed agreements, approved budgets, and spending commitments, • Track outstanding contractual obligations, following up on discrepancies, missing information, or required approvals, • Help maintain visibility into financial commitments associated with contracts and purchase ordersAbout You:, • Bachelor’s degree or equivalent combination of education and relevant professional experience, • Approximately 3–5 years of relevant experience in contract administration, contract management, legal operations, purchasing, or a related field, • Experience managing contract workflows, coordinating reviews and approvals, and maintaining contract databases or tracking systems, • Familiarity with common business agreements, including NDAs/CDAs, consulting agreements, MSAs, SOWs, and vendor contracts, • Strong organizational and project management skills, with exceptional attention to detail and follow-through, • Excellent written and verbal communication skills, including the ability to work effectively with senior leaders, scientists, and external partners, • Ability to manage multiple priorities, work independently, and maintain momentum on projects with minimal oversight, • Demonstrated ability to handle confidential and sensitive business information with sound judgment and discretion, • Prior experience in biotechnology, pharmaceuticals, or life sciences is strongly preferredCompensation at Rezo The expected hourly rate for this part-time position based in San Francisco, California is $40-$47 per hour. Actual starting pay will be determined based on multiple job-related factors including a candidate’s skills, education, and experience, the level at which they are hired, market demand, business needs, and internal parity. EEOC At Rezo we value a diverse, equitable, inclusive workplace and provide equal employment opportunity to all persons without regard to race, color, sex, gender identity, gender expression, religion, age, national origin, ancestry, citizenship, physical or mental disability, medical condition, family care status, marital status, domestic partner status, sexual orientation, genetic information, military or veteran status, or any other basis protected by federal, state or local laws. This statement covers all facets of employment and is especially important when it comes to growing our team. If you are wondering if you’ll belong at Rezo, or are worried that you don’t meet 100% of the qualifications for this role, take a chance on us and yourself — please apply! SF Fair Chance Ordinance Pursuant to the San Francisco Fair Chance Ordinance, Rezo considers qualified applicants with arrest and conviction records for employment. 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 Direct Counsel is representing a prestigious AmLaw firm seeking a midlevel Intellectual Property Associate (1–5 years) to join its highly regarded Life Sciences Patent Prosecution practice. Locations: • Boston, • Chicago, • Houston, • Orange County (Costa Mesa), • Philadelphia, • San Francisco, • Seattle, • Silicon Valley, • Washington, D.C. This is an exciting opportunity for an attorney or patent agent with a strong scientific background and biotechnology patent prosecution experience to work with cutting-edge life sciences and emerging growth companies. Responsibilities • Handle sophisticated patent prosecution and IP counseling matters for innovative life sciences companies, • Advise clients in areas including:, • Antibodies, • DNA & RNA therapeutics, • Gene-editing technologies, • Chemical biology, • Molecular and cellular therapeutics, • Collaborate closely with emerging companies and scientific innovators on strategic intellectual property protectionQualifications, • 1–5 years of biotechnology patent prosecution experience, • Advanced degree required, preferably a Ph.D., in a life sciences discipline such as:, • Molecular Biology, • Immunology, • Biochemistry, • Cell Biology, • Related scientific fields, • USPTO Registration Number / Patent Bar membership required, • Strong academic credentials and excellent analytical, writing, and communication skillsCompensation Expected salary range in Massachusetts: $225,000 – $435,000, depending on experience, qualifications, and market factors. Comprehensive benefits package includes medical, financial, retirement, and paid leave benefits. If you are interested in this opportunity, please apply through directcounsel.net with your resume, law school transcripts, and cover letter.

Job DescriptionThe Fountain Group is currently seeking an AI/ML Engineer / Data Scientist (Predictive Modeling Contractor) for a prominent client of ours. Open for 100% Remote Candidates. Prefer someone who can work Hybrid or go onsite occasionally at South San Francisco, CA office. Details for the position are as follows: Pay Rate - $60 – 71.07/hr on W2 14 months Contract Role (HIGH Possibility for further extension) Position Summary We are seeking a contractor with a background combining AI rapid prototyping and Predictive Modeling to support the platform and predictive analytics subteams within the program. This role focuses on co-developing shared data and technical foundations (e.g. Ontologies, Knowledge Graphs), prototyping agentic AI capabilities, and advancing predictive models for drug safety risk prediction across the product lifecycle. Key Responsibilities AI Prototyping & MCP Tool Development: Rapidly explore, evaluate, and prototype emerging AI tools and agentic capabilities, specifically developing MCP tools and AI agent integrations for DAISAE. Predictive Modeling: Build and refine predictive models using multi-modal datasets (including in vitro, in vivo, omics, clinical trial data, real-world data (RWD), and spontaneous safety reports) to enable risk prediction from early molecule-level evaluation to late-stage and post-marketing patient safety. Architecture & Platform Design: Translate feasibility findings and prototype evaluations into concrete architectural design and platform requirements for shared data and technical foundations. Co-Development & Governance Collaboration: Work in an agile way to prototype reusable technical capabilities before transitioning components to RDT for formal validation, compliance, and production rollout. Cross-Functional Alignment: Collaborate with data scientists, safety scientists, and RDT technical partners to ensure technical execution aligns with business priorities. Qualifications & Experience Education: MSc or PhD in Data Science, Computer Science, Computational Biology, Bioinformatics, Biostatistics, Epidemiology, or a related quantitative field. Minimum of a Masters Degree required. Expertise in predictive modeling, machine learning, and AI prototyping. Hands-on experience developing agentic AI systems, LLM tools, and MCP tools. Proficiency in handling biomedical datasets (omics, clinical trials, RWD, or in vitro/in vivo data). Agile prototyping mindset with software engineering skills tailored for data science. If you are interested in hearing more about the position, please respond to this posting with your resume attached. Please forward this posting to any friends or colleagues as we do offer a Referral Bonus for any candidate hired. By applying for this job, you agree to receive calls, AI-generated calls, text messages, or emails from and its affiliates, and contracted partners. Frequency varies for text messages. Message and data rates may apply. Carriers are not liable for delayed or undelivered messages. You can reply STOP to cancel and HELP for help. You can access our privacy policy at Privacy Policy #LI-SP1

Job Description Lab Robotics Research Associate Full-Time | On-site (5 days/week) SF Bay Area, CA $90,000 – $120,000 + Competitive Equity Company Overview We are a high‑growth genomics technology company revolutionizing DNA and RNA sequencing through a fully automated, overnight sequencing engine. Our proprietary platform—bootstrapped to $80M ARR—supports more than 70,000 scientists worldwide, including Nobel laureates and leaders across Fortune 100 pharmaceutical organizations. By combining robotics, automation, and advanced molecular biology workflows, we deliver rapid sequencing results at a fraction of traditional industry costs. Role Summary We are seeking a Lab Robotics Research Associate to help scale and optimize the world's largest high‑throughput automated liquid handling fleet. In this role, you will translate wet‑lab protocols into automated workflows, validate robotic performance, troubleshoot hardware issues, and prototype custom lab tools that enhance our automation capabilities. Key Responsibilities • Protocol Automation: Convert wet‑lab R&D protocols into automated, step‑by‑step liquid handler scripts using Python, AI‑assisted coding tools, and robotics frameworks., • System Validation: Run manual vs. robotic experiments side‑by‑side to ensure automated workflows meet scientific quality benchmarks., • Hardware Troubleshooting: Diagnose and resolve robotic failure modes, including low‑volume pickup, viscous liquid handling, and other mechanical issues., • Custom Prototyping: Design and 3D‑print custom adapters, fixtures, and lab tools to expand the capabilities of our liquid handling fleet.Technical Environment, • 200+ high‑throughput robotic workstations (Opentrons, Hamilton), • Python for device control, automation, and data parsing, • AI‑assisted coding frameworks, • 3D printing & CAD (Fusion 360), • Molecular biology assay instrumentationQualifications/Requirements, • 1–3 years of wet‑lab Research Associate experience (biotech or academic), ideally ~2 years, • Hands‑on experience with liquid handling robotics (Opentrons, Hamilton), • BS degree in Biology, Biochemistry, Biomedical Engineering, or related field (BS preferred over MS), • Self‑taught or practical Python skills for automation and data parsing, • Strong problem‑solving skills and comfort working in a fast‑paced automation environment, • Work authorization: US Citizen or Green Card holder; no visa sponsorship, • Fully on‑site in the SF Bay Area (no relocation support)

Job Description About us Pain & Rehabilitative Consultants Medical Group “We have built a system that’s dedicated to help providers focus on what they do best: Provide Excellent Care.” Pain and Rehabilitative Consultants Medical Group is an industry leader in both Acute and Chronic Pain Management and has been serving Northern California for more than 25 years. The providers at PRCMG have dedicated their professional careers to providing cost-effective medical care of the highest quality, with a commitment to exceptional service. Our providers are constantly furthering their education on the techniques and approaches to promote the most advanced, comfortable, and personalized pain management care. Our professional team includes board certified providers in the fields of Pain Management, Anesthesiology, Neurology, Physical Medicine & Rehabilitation, Medical Acupuncture, Behavioral Medicine and Psychology, Physical Therapy and more. Using our proven collaborative team and multi-modality approach to pain management, we are able to extend exceptional service and provide the best treatment plan to our patients. Our ultimate goal is to relieve suffering, help patients effectively manage their pain, and improve their quality of life by educating them, increasing their functional capacity and optimizing their use of medical resources. PRCMG recruits the highest quality providers in the industry. Our board-certified & experienced pain professionals manage everything from acute to chronic conditions. Our services include medical management, functional restoration program, brain injury program, psychological services, acupuncture, neuro-diagnostics, and interventional pain procedures. For more information please visit: www.PRCMG.com and www.NCFRP.com POSITION SUMMARY The Clinic Support Specialist II is responsible for greeting and checking in patients, verifying demographics, updating insurance information, collecting copayments, and managing check-out procedures. This role also includes scheduling appointments, verifying insurance eligibility and authorizations, answering and routing calls professionally, and maintaining a clean and welcoming reception area. plays a key role in supporting clinical operations and ensuring a seamless patient experience. This position provides both administrative and clinical assistance, helping to maintain efficient clinic workflow, support patient care, and ensure the smooth functioning of clinic services across multiple locations. ESSENTIAL DUTIES AND RESPONSIBILITIES • Greet patients and visitors in a professional, courteous, and welcoming manner., • Check patients in and out; verify demographics; collect copayments; and update insurance and registration information., • Answer, screen, and route incoming telephone calls, responding to routine inquiries and escalating complex issues as appropriate., • Schedule, audit, and maintain accurate appointments to support continuity of care and proper documentation., • Verify commercial insurance eligibility and benefits and process authorizations for HMO and Medicare office visits., • Maintain a clean, organized, and patient-friendly waiting area., • Perform clerical and administrative support duties, including filing, data entry, scanning, and document management., • Provide Front Office coverage as needed., • Travel to Castro Valley and Walnut Creek office locations as required., • Room patients and support efficient clinic flow., • Accurately enter Review of Systems (ROS) information into the electronic medical record., • Assist patients with Microsoft Teams access for virtual appointments., • Oversee assigned medical equipment and ensure proper operation, including EMG machines and pump refill equipment., • Support acupuncture clinic operations by preparing supplies and sanitizing rooms after each patient., • Provide coverage for Back Office staff as needed., • Retrieve and complete required forms, including FCA documentation., • Assist with patient education related to treatment options, including ESI, FRP, and CBI., • Collect urine specimens, perform preliminary urine drug screens, and process specimens for laboratory testing., • Bill for preliminary and confirmatory urine drug screenings (UDS)., • Perform other related duties as assigned. QUALIFICATIONS REQUIRED (EDUCATION, EXPERIENCE, AND SKILLS) • High school diploma or General Education Degree (GED) required., • Knowledge of medical terminology and clinical and laboratory procedures., • Valid driver’s license and current auto insurance coverage., • Proficiency with office equipment and software, including electronic medical record (EMR) systems., • Strong data entry, documentation, and recordkeeping skills with high attention to detail., • Ability to monitor workflow and perform quality control checks., • Effective verbal and written communication skills with patients, staff, and providers., • Strong customer service skills and professionalism when handling sensitive or difficult situations., • Detail-oriented, organized, and able to work well under pressure in a fast-paced environment., • Team-oriented with the ability to collaborate across departments., • Sound judgment and critical-thinking skills to evaluate situations and make decisions., • Ability to manage multiple tasks, meet deadlines, and adapt to changing priorities., • Ability to meet the physical and environmental demands of a clinical office setting., • Ability to travel as needed to other clinic locations. PREFERRED • Bilingual (English/Spanish) strongly preferred, with the ability to communicate effectively with patients, staff, and providers, • Previous Workers’ Compensation experience, • Certified Medical Assistant with 2 years of previous experience or bachelor’s degree in biology or a closely related field, • Current CPR/BLS certification PHYSICAL DEMANDS AND WORK ENVIRONMENT The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this position. Reasonable accommodations may be made to enable qualified individuals with disabilities to perform these functions. • While performing the duties of this position, the employee is regularly required to communicate clearly and effectively, both verbally and in writing, with patients, staff, and vendors., • The employee is frequently required to use hands and fingers to handle, feel, type, and operate computers, telephones, and other standard office and medical administrative equipment., • The employee is primarily required to sit for extended periods; occasional standing, walking, and reaching with hands and arms may be necessary., • The employee may occasionally be required to stoop, kneel, or bend to retrieve files, supplies, or office equipment., • The employee must occasionally lift and/or move up to 20–25 pounds (e.g., files, supply boxes, or office equipment)., • Specific vision abilities required include close vision, distance vision, color vision, and the ability to adjust focus for computer work and reviewing documents., • The noise level in the work environment is generally moderate, consistent with a standard office or clinic setting, and tasks are often performed in close proximity to other staff. We offer a competitive benefits package (eligible 90 days after date of hire) including: • PTO, • 8 paid holidays annually, • Medical, dental, and vision plan options, • Qualified retirement plan (eligible 1 year after date of hire), • Hourly rates will be finalized based on equivalent experience Job Type: Full-time Benefits: • 401(k), • 401(k) matching, • Dental insurance, • Health insurance, • Paid time off, • Vision insurance Work Location: In person \nCompany Description Pain & Rehabilitative Consultants Medical Group (PRCMG) is a leading Northern and Central California practice providing comprehensive, evidence-based pain management and rehabilitative care through a multidisciplinary team dedicated to improving function and quality of life. Pain & Rehabilitative Consultants Medical Group (PRCMG) is a leading Northern and Central California practice providing comprehensive, evidence-based pain management and rehabilitative care through a multidisciplinary team dedicated to improving function and quality of life.

Job DescriptionCompany Description At Sobi, we believe diversity drives innovation and inclusion creates stronger teams. We are committed to building a workplace where everyone feels valued and empowered to contribute. If this role excites you but you’re unsure if you meet every requirement, we encourage you to apply. Your unique perspective and experiences could be exactly what we need. We look forward to hearing from you! At Sobi, each person brings their unique talents to work as a team and make a difference. We are dedicated to developing and delivering innovative therapies to improve the lives of people who live with a rare disease. Our edge comes from our team of people and our commitment to patients. Our mission and culture at Sobi North America get us excited to come to work every day, but here are a few more reasons to join our team: • Competitive compensation for your work, • Generous time off policy, • Opportunity to broaden your horizons by attending popular conferences, • Emphasis on work/life balance, • Collaborative and team-oriented environment, • Making a positive impact to help ultra-rare disease patients who are in need of life saving treatmentsJob Description Sobi is hiring for 3 Sr MSL, Lymphoma (Lacutamab) openings. Candidates can work remotely anywhere in the continental U.S., with a strong preference that they're located within 30-40 minutes of a major airport. As the Senior Medical Science Liaison (MSL), Lymphoma (Lacutamab), you will serve as a field-based scientific expert on cutaneous T-cell lymphoma (CTCL) and lacutamab, a humanized monoclonal antibody immunotherapy targeting KIR3DL2. You will build trusted scientific relationships, exchange balanced medical information, and generate actionable insights that inform US Medical Affairs strategy and launch readiness. You will support Sobi's rare disease portfolio in the hematology franchise and serve as a trusted scientific resource across the hematology-oncology, dermatology, and dermato-oncology communities. You will collaborate with academic, community, and multidisciplinary care teams, always in accordance with regulatory, legal, and compliance requirements. This is a field execution role within Hematology Medical Affairs. You will contribute insights and a field perspective to the CTCL medical strategy, which is led by Medical Affairs leadership. What You Will Do Scientific Engagement and External Relationships • Serve as a primary field-based scientific point of contact for Sobi Medical Affairs within your assigned geography., • Develop and maintain meaningful, two-way relationships with opinion leaders, healthcare professionals, medical organizations, investigators, and other stakeholders involved in CTCL care., • Exchange accurate, fair, balanced, and scientifically rigorous information on CTCL, lacutamab, relevant clinical data, disease biology, treatment approaches, and the evolving care landscape., • Engage across academic, community, and multidisciplinary settings, including hematology-oncology, dermatology, and dermato-oncology practices., • Respond appropriately to unsolicited scientific inquiries and connect stakeholders with Sobi resources in line with applicable policies and procedures. Medical Insights and Strategy Execution • Identify, document, and share high-quality field insights on unmet needs, clinical practice, patient pathways, evidence gaps, stakeholder perspectives, competitive developments, and the treatment landscape., • Partner with Medical Affairs leadership and cross-functional colleagues to interpret insights and inform adjustments to medical strategy, tactics, educational priorities, and engagement plans., • Execute territory-level medical plans aligned with the US CTCL and lacutamab medical strategy, adapting engagement to local and regional stakeholder needs., • Support key institution and stakeholder engagement planning, helping establish Sobi as a trusted scientific partner in CTCL. Launch Readiness, Education, and Congress Support • Contribute to lacutamab launch preparedness through disease-state education, articulation of unmet need, scientific exchange, stakeholder mapping, and field execution of approved medical tactics., • Provide internal and external scientific training on CTCL disease biology, preclinical science, clinical data, evidence gaps, and relevant outcomes., • Participate in or support advisory boards, medical roundtables, webinars, symposia, and other educational activities at local, regional, and national levels., • Represent Sobi Medical Affairs at scientific and medical congresses, and synthesize and communicate key updates and implications to internal stakeholders., • Collaborate to identify and develop field resources and scientific materials specific to CTCL and lacutamab. Evidence Generation and Clinical Development Support • Provide field-based support to Clinical Development and Clinical Operations, including site identification and recommendations, investigator engagement, communication facilitation, site initiation support, and patient accrual support., • Identify evidence gaps and potential research opportunities, and communicate them to appropriate internal partners., • Contribute scientific and field perspectives to evidence generation activities, real-world evidence initiatives, publications, and medical education programs, as appropriate., • Support investigator-sponsored research and other research collaborations in accordance with company processes and governance. Cross-Functional Collaboration and Territory Leadership • Partner with colleagues in Medical Affairs, Medical Information, Clinical Development, Market Access, Patient Advocacy, Commercial, Legal, Compliance, and other functions, while maintaining the independence and integrity of the Medical Affairs role., • Serve as a scientific resource to internal stakeholders and contribute to cross-functional initiatives consistent with Medical Affairs objectives and company guidelines., • Demonstrate excellence in territory planning, stakeholder prioritization, documentation, follow-through, and management of multiple projects and competing priorities., • Contribute to the broader Field Medical organization's success by sharing best practices, supporting colleagues, and fostering a collaborative, respectful, patient-focused culture. What Success Looks Like Success in this role is marked by: • Scientific credibility and curiosity, • Strategic territory leadership, • Insight generation and synthesis, • Trusted stakeholder partnership, • Cross-functional collaboration, • Clear, balanced communication, • Agility and a solution-oriented approach, • Operational excellence, • A patient-centered mindsetQualifications Required and Preferred Qualifications • Education: Accredited doctorate degree in a life-science, health-science, or basic-science discipline, such as PharmD, PhD, DNP, DSc, MD, or DO., • Candidates with another advanced health degree and extensive relevant industry or clinical experience may be considered., • Experience: At least 5 years of MSL experience in hematology/oncology, heme-onc, or a closely related therapeutic area is required., • Further experience in the following is highly valued:, • Clinical practice, Cutaneous T-cell lymphoma (CTCL), Peripheral T-cell lymphoma (PTCL), lymphoma, dermatology, dermato-oncology., • Rare disease and/or product launch., • Scientific acumen: Strong ability to understand, critically evaluate, and clearly communicate complex scientific and clinical information., • Clinical hematology-oncology background is highly preferred., • Knowledge of CTCL and/or PTCL and the multidisciplinary care environment is an advantage., • Patient focus: Strong commitment to patient needs and advancing scientific understanding within the CTCL community. Location, Travel, and Work Environment • Remote, field-based position supporting an assigned US geography., • Frequent domestic travel by ground and/or air is required (60% or more), depending on territory size, stakeholder needs, congress participation, and business requirements., • Ability to attend local, regional, and national meetings, including occasional evening or weekend programs, as business needs require., • Ability to work effectively from a remote office and manage a geographically dispersed territory. Additional Information Compensation and Total Rewards at Sobi At Sobi, we are dedicated to providing our employees with a comprehensive and industry-competitive total rewards package. Our compensation philosophy is designed to recognize and reward talent, ensuring that your contributions are valued and reflected in your overall rewards. Your total compensation at Sobi goes beyond just your base salary and annual bonus. It also includes a robust suite of benefits, such as: • A competitive 401(k) match to support your financial future., • Tuition and wellness reimbursements to invest in your personal and professional growth., • A comprehensive medical, dental, and vision package to prioritize your health and well-being., • Additional recognition awards to celebrate your achievements. The base salary range for this role is $215,000 - $230,000. Each individual offer will be determined based on several factors, including your experience, qualifications, and location. Additionally, this role is eligible for both short-term and long-term bonuses, as outlined in the plan details. All Sobi employees need to demonstrate behaviors in line with Sobi's core values: Care, Ambition, Urgency, Ownership and Partnership. Are you ready to be on the Sobi team? Come join a culture that empowers every person to be the person that makes a difference for rare disease. Why Join Us? We are a global company with over 1,900 employees in more than 30 countries and are committed to the societies where we operate. With a deeply skilled management team directing our day-to-day wins, and a Board with a stellar track record, we’re ready to take on the world’s diseases, ailments and adversity. Our people believe they have the power to make a positive impact in others’ lives because that’s exactly what we do here. If you’re seeking a career that taps into your talents in a way that makes the world a better, healthier place, we just may have a job for you. We know our employees are our most valuable asset, and our culture conveys that. We offer a competitive benefits package, to support the health and happiness of our staff. Sobi Culture At Sobi, we refuse to accept the status quo. This is because we have witnessed first-hand the challenges facing those affected by rare diseases, and have used this knowledge to shape our business to find new ways of helping them. As a specialized biopharmaceutical company, we are dedicated to rare diseases. And we see this focus as a strength. By effectively turning our research into ground-breaking treatments, we help make medicine more accessible and open up more possibilities for patients and more opportunities for those caring for them. This has been our approach since day one, but we know we can’t change the world of rare diseases on our own. Accomplishing this requires strong partnerships with patients, partners and stakeholders across the entire value chain. Together, we define how our business can create solutions that serve the needs of those affected by rare diseases while facilitating sustainable growth. An Equal Opportunity Employer Sobi is an Equal Opportunity Employer and prohibits discrimination and harassment of any kind. All employment decisions at Sobi are based on business needs, job requirements and individual qualifications, without regard to race, color, religion or belief, national, social or ethnic origin, sex (including pregnancy), age, physical, mental or sensory disability, HIV Status, sexual orientation, gender identity, protected veterans and/or expression, marital, civil union or domestic partnership status, past or present military service, family medical history or genetic information, family or parental status, or any other status or protected groups by the laws or regulations in the locations where we operate. If you are a qualified individual with a disability or a disabled veteran, you may request a reasonable accommodation if you are unable or limited in your ability to use or access this website to apply for a vacancy as a result of your disability. You can request reasonable accommodations by sending an email to jennifer.partyka@sobi.com. Know Your Rights

Job Description Technical Sales Specialist – Chromatography & Laboratory Automation Location: Remote – United States (San Francisco Bay Area Preferred) Travel: 60–80% About the Opportunity: We are partnering with a leading provider of laboratory automation and analytical instrumentation solutions to identify a Technical Sales Specialist to support business growth across the United States. This opportunity is ideal for a technically knowledgeable sales professional with a strong background in chromatography systems, automated sample preparation, and laboratory instrumentation. The ideal candidate will bring hands-on familiarity with chromatography technologies and PAL automation systems, along with the ability to develop customer relationships, identify new business opportunities, and deliver technical solutions to scientific and laboratory customers. Key Responsibilities • Drive new business development and revenue growth within the assigned territory., • Build and maintain relationships with laboratories, research organizations, and scientific customers., • Identify customer needs and recommend chromatography, automated sample preparation, and laboratory automation solutions., • Deliver technical product presentations, demonstrations, and consultative sales support., • Collaborate with application scientists, service engineers, and internal technical teams to support customer requirements., • Help customers optimize laboratory workflows through automation and instrumentation solutions., • Develop and execute territory sales strategies, manage pipelines, and maintain accurate forecasts., • Represent the organization at industry conferences, trade shows, and customer meetings., • Maintain strong customer relationships and identify opportunities for account expansion. Qualifications: Required Qualifications: • Bachelor's degree in Chemistry, Biochemistry, Biology, or a related scientific discipline., • 5–8 years of relevant sales experience in analytical instrumentation, laboratory automation, or scientific markets; alternatively, equivalent hands-on laboratory experience in chromatography or automated sample preparation., • Strong technical understanding of chromatography systems, including GC, GC-MS, HPLC, or LC-MS technologies., • Experience with or strong working knowledge of PAL systems, autosamplers, or related automated sample preparation technologies., • Ability to communicate complex scientific and technical concepts to laboratory professionals and decision-makers., • Strong relationship-building, presentation, and consultative selling skills., • Ability to independently manage a territory and travel 60–80%. Preferred Qualifications: • Direct experience with PAL automation systems or CTC Analytics technologies., • Background selling chromatography instrumentation, laboratory automation, or analytical chemistry solutions., • Experience working with pharmaceutical, biotechnology, environmental, chemical, or research laboratories., • Experience delivering technical product demonstrations or supporting laboratory applications., • Proficiency with Salesforce or a comparable CRM platform. Why Consider This Opportunity? • Join a growing organization specializing in innovative laboratory automation technologies., • Work directly with scientific customers to solve complex laboratory workflow challenges., • Represent advanced chromatography and automated sample preparation solutions., • Collaborate with experienced scientists, engineers, and technical professionals., • Make a meaningful impact on business growth and customer success. Apply Today If you have a strong technical background in chromatography, laboratory automation, or analytical instrumentation and enjoy building customer relationships, we'd welcome the opportunity to connect. Apply today to learn more about this opportunity. #LI-MM1

Job DescriptionThe Position The Drug Discovery team is looking for a Senior Research Associate I, Compound Management to join our group. In this role, you will help power the discovery of new medicines by ensuring scientists across the organization have access to the high-quality compounds and samples needed to advance research programs. Your work will directly enable scientists to advance programs aimed at translating novel genetic insights into lifesaving medicines. You will partner closely with colleagues across Drug Discovery, including Chemistry, Biology, and other cross-functional teams, to manage compound inventory, support sample management workflows, and help maintain the efficient operation of our compound management capabilities. As a key member of a collaborative and growing organization, you will contribute to the infrastructure and processes that drive our research and drug discovery goals. This role offers a unique opportunity to expand your technical expertise, develop strong cross-functional relationships, and grow your career within a dynamic biotech environment. If you are detail-oriented, analytical, and motivated to make an impact, you will find meaningful opportunities to learn and contribute as the company continues to grow. This position reports to the Director of Chemistry. The Impact You'll Have • Manage the weighing, storage, maintenance, and distribution of compound inventories., • Responsible for the operation of automated laboratory equipment to support the processing of samples., • Proactively monitor the compound request queue and fulfill the requests in a timely manner., • Partner with Facilities Department for the shipping and tracking of compounds both locally and internationally to our collaborating CROs., • Routinely perform sample QC checks and analysis., • Coordinate with R&D operations, vendors, and CROs to procure, track, and process samples to support internal and external studies., • Assist in the development and implementation of workflows to support error-free high throughput compound processing., • Coordinate cross-departmentally for routine or ad hoc compound plating., • Maintain lab consumable inventory. What We're Looking For, • Minimum of a BS degree in Biological or Chemical Sciences with 3+ years of experience in small molecule compound handling and processing., • Experience with laboratory automation, specifically liquid handling platforms like Tecan EVO, Labcyte ECHO or similar., • Experience with troubleshooting and maintenance of instrumentation platforms and automated integrated systems., • Experience with optimizing compound processing workflows including knowledge and use of Mosaic is desired., • Innate attention to detail, organization skills, ability to multi-task and work across initiatives simultaneously under tight deadlines, • Effective communication skills and strong interpersonal skills to engage in cross-functional collaboration and teamwork. About Maze Therapeutics Maze Therapeutics is a clinical-stage biopharmaceutical company harnessing human genetics to develop precision medicines for patients with kidney and metabolic diseases. Our clinical pipeline is anchored by two small molecule programs: MZE829, an APOL1 inhibitor for patients with APOL1‑mediated kidney disease, and MZE782, which targets genetic drivers of disease in phenylketonuria (PKU) and chronic kidney disease. We are also advancing a preclinical pipeline through our Compass platform, which links human genetic variants to the biological pathways that drive disease. Our People Maze is comprised of a team of passionate and creative professionals committed to discovering and delivering transformative medicines to patients suffering from both rare and common genetic diseases. We are fostering a culture that encourages vision, initiative and the development of talent. Our supportive work environment inspires creative thinking and freedom of expression, resulting in a stimulating atmosphere where people enjoy coming to work. While we have a passion for advanced science and pride ourselves on excellence in execution, ultimately, everything we do is about patients. Our Core Values Further Together – Our path is paved with challenges, but with resilience and a team-first mentality, we'll achieve our mission. Impact Obsessed – We embrace the bold, take calculated risks, and learn from our mistakes to improve the lives of others. Stand True – Our integrity is foundational; it guides us no matter the obstacle. The expected annual salary range for employees located in the San Francisco Bay Area is $105,000 - $128,000. Additionally, this position is eligible for an annual performance bonus. Maze performs position-based compensation benchmarking to industry market data to ensure we pay competitive wages. Determination of starting salary will depend upon a variety of job-related factors, which may include professional experience, skills, and job location. The expected salary range for this role may be modified in the future. Maze offers a robust benefits package to our eligible employees including competitive medical, dental, and vision insurance, mental health offerings, equity incentive plan, 401(k) program with employer match and a generous holiday and PTO policy. #LI-Hybrid

Job Description Septerna is a biotechnology company based in South San Francisco, CA on a mission to develop life-changing medicines for patients with the vision to become the industry-leading G protein-coupled receptor (GPCR)-focused drug discovery company. The company's Native Complex Platform™ recapitulates GPCRs with their native structure, function, and dynamics outside of the cellular context. This approach enables novel access to modern structural and screening technologies used in industrial-scale drug discovery for the entire class of GPCRs. Septerna has an emerging pipeline of GPCR-targeted small molecule programs, many in the Endocrinology space, with potential for growth to target many GPCRs that have been undruggable and unexploited to date. We are excited to expand our multidisciplinary team of individuals focused on creating revolutionary medicines to address the unmet needs of patients. At Septerna we strive to embrace diversity of thought, expertise, and background through collaboration. To join our ambitious team, be prepared to bring your real self to work every day; grow and learn from a talented team of drug hunters, scientists, and business professionals; and contribute your passion, creativity, and energy to accomplish our mission. We share a fearless pursuit of ground-breaking innovations and cultivate an environment where our employees succeed by learning from each other and working as a team. We are committed to the development of meaningful therapeutics for patients with indications of high unmet need. This is a tremendous opportunity to work with talented individuals on the frontlines of therapeutic discovery and development. You will directly help move therapies through preclinical research, positioning them for success in the clinic. The successful candidate will add their passion, unique talents, and expertise to a dynamic team motivated to discover new disease-modifying therapeutics for patients in a fast-paced environment. For more information see: www.septerna.com. The Role: Septerna is seeking an experienced scientific leader with expertise in AI/ML to lead our Data Science function. The successful candidate will implement advanced machine learning and statistical approaches to leverage Septerna's proprietary GPCR structural and assay data in advancing our small-molecule drug discovery programs. This is a visionary, hands-on leadership role that requires a strong understanding of our internal data assets, modern drug discovery practices, and advanced computational methods. This leader will create and execute a strategy for fully leveraging Septerna's proprietary data, while collaborating closely with Computational Chemistry, Structural Biology, and other cross-functional research teams to accelerate hypothesis generation and advance scientific discovery. The ideal candidate brings technical depth in machine learning, practical expertise in statistics, a strong scientific foundation in drug discovery, and the leadership capability to build a high-impact function in a fast-moving environment. Key Responsibilities • Lead Septerna's Data Science team, providing technical direction, developing team capabilities, and integrating and prioritizing projects, with a primary focus on machine-learning applications., • Develop and execute a roadmap for implementing state-of-the-art AI/ML approaches that use Septerna's GPCR structural data to discover and refine novel chemical matter., • Identify productive emerging technologies; lead their integration into Septerna's computational stack through internal development, strategic partnerships, or a combination of both., • Oversee and extend analysis pipelines, including DNA-encoded library (DEL), high-throughput screening (HTS), and assay-data workflows, and identify opportunities to advance Data Science as part of the broader Platform development team., • Advance and support ML-QSAR models leveraging internal and external assay and ADMET data to impact the efficiency of DMTA cycles and as a basis for generative chemistry workflows., • Refine data-engineering and cloud-infrastructure requirements while establishing best practices for data curation and model validation. Required Qualifications • PhD in computational biology, computational chemistry, or a degree in computer science, applied mathematics or statistics that was focused on modeling biological systems., • Minimum of 10+ years of relevant industry experience including application of machine learning to diverse scientific problems., • Demonstrated leadership in machine learning for drug discovery, with a track record of building and applying predictive models to real-world, noisy, and multimodal scientific datasets., • Experience applying co-folding or hybrid models to enable productive ligand pose prediction ideally on membrane proteins and flexible protein classes., • Previous work transfer learning or fine-tuning foundation models and using appropriate metrics to demonstrate model performance improvements and characterize applicability domain., • Experience leading teams and serving as the senior technical lead of cross functional initiatives with track record of applying technical insight and scientific judgement to guide research strategy. Technical and Platform Requirements • Expertise in scientific machine-learning and drug discovery dependencies such as PyTorch, scikit-learn, numpy, pandas, pyarrow, and RDKit., • Deep knowledge of modern machine-learning and statistical methods, including gradient boosting decision trees (XGBoost, LGBM), graph neural networks (GNN/D-MPNN), transformers, generative modeling, active learning, and Bayesian optimization., • Extensive experience with cloud and distributed computing environments, including AWS, GCP, or Azure, as well as building and maintaining containerized machine-learning workflows., • A strong track record in MLOps and in partnering with software and platform engineering teams to define fit-for-purpose infrastructure for scientific applications. Preferred Qualifications • Experience with molecular property prediction, generative chemistry, graph neural networks, protein–ligand modeling, sequence modeling, or physics-informed machine learning., • Hands on structure-based drug discovery and experience collaborating closely with Computational Chemistry teams., • Publications, patents, or open-source contributions in relevant scientific or machine-learning domains. The anticipated salary range for candidates who will work in South San Francisco, CA is $240,000 - $300,000. Individual pay may vary based on additional factors, including, and without limitation, job-related skills, experience, work location and relevant education or training. Septerna's compensation package also includes benefits, stock options, and annual target bonus for full-time positions. We are an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status. Note to Employment Agencies: Please do not forward any agency resumes. The company will not be responsible for any fees related to resumes that are unsolicited. Note to Employment Agencies: Please do not forward any agency resumes. The company will not be responsible for any fees related to resumes that are unsolicited. We are an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status. Septerna participates in the E-Verify program. California Consumer Privacy Act Privacy Notice For Job Applicants. If you are a California resident, click here for our CCPA Notice.

Job DescriptionThe Opportunity We're looking for a Director of Field Medical to serve as the regional scientific lead during a pivotal stage of our growth. This senior, full-scope Medical Science Liaison role rests on two pillars: leading high-level scientific exchange and key opinion leader relationships across your region and serving as the field-facing scientific partner to Maze's clinical development programs. It's a genuine scientific leadership position, not site support with a scientific veneer. With MZE829 entering its pivotal program in 2027 and MZE782 advancing through Phase 2, your immediate priority is enabling the clinical programs, so trial and investigator support carries real weight from day one. Because Maze is genetics-first, you'll need credibility across two distinct communities: nephrology (AMKD, FSGS, CKD) and metabolic disease (PKU). Initially, an individual contributor, you'll build the region's scientific relationships and support trial execution, then help recruit, mentor, and eventually lead a regional MSL team as we grow The Impact You'll Have Scientific Exchange & KOL Engagement You'll be a recognized scientific expert and the trusted face of Maze in your regions. • Lead compliant, peer-to-peer scientific exchange with thought leaders, physicians, renal pathologists, and PKU specialists, and build a durable regional KOL map, including in a metabolic community where Maze isn't yet known., • Provide accurate scientific education on AMKD, FSGS, CKD, and PKU, including APOL1 biology and SLC6A19 substrate reduction, and respond to unsolicited medical inquires., • Represent Maze at major congresses (ASN, NKF, and metabolic/PKU societies) and support advisory boards, scientific meetings, and patient advocacy partnerships. Clinical Development & Investigator Partnerships The immediate priority. You'll be the field-facing scientific partner accountable for site engagement and scientific barriers affecting enrollment across your region. • Serve as the regional scientific partner to Maze's trials, including HORIZON and the MZE829, and MZE782, and the single point of contact for investigators and sites., • Shape site selection through feasibility input, and support site identification, investigator meetings, and start-up., • Own the field-side response to enrollment and retention barriers, driving compliant scientific solutions with Clinical Operations. Genetic Testing & Patient Identification • Support adoption of APOL1 genotyping and advance genotype-driven patient identification pathways, the mechanism by which eligible patients reach the trials., • Address the trust and access barriers facing an AMKD population disproportionately of African ancestry, a concrete enrollment lever, not a peripheral consideration. Medical Insights & Strategic Input • Capture field insight (treatment patterns, unmet need, evidence gaps, competitive intelligence) on a consistent cadence, and translate it into recommendations that shape medical strategy, evidence generation, and launch readiness. Because Maze is small, these insights land directly with the people who set direction. Building the Field Medical Organization • Carry your assigned territory personally as the senior regional scientific leader, and help recruit, mentor, and develop MSLs as we scale, growing into regional team leadership over the next 1–2 years. As a Director, we also expect you to demonstrate the following Leadership Competencies: • Communication and Influence, • Builds communication channels across Maze for sharing information, • Influences Senior Management decisions through persuasive arguments, • Respectfully addresses differing opinions leading to support of decision, • Teamwork and Collaboration, • Champions partnerships and connections across Maze, • Proactively addresses issues that could result in breakdown of team relationships, • Spotlights team and individual contributions in public forums, • Execution and Results, • Addresses gaps and leverages strengths to get best results, • Maintains a steadying presence and clarifies priorities during change, • Anticipates and removes barriers that put functional/corporate goals at risk, • Develop Others and Self, • Removes barriers to staff development and empowers them to make their own decisions, • Stays current on industry trends and keeps direct-reports prepared and responsive What We're Looking For What you'll need • An advanced scientific degree (PharmD, PhD, MD, DO, or equivalent)., • a minimum of 7 years of Medical Affairs, Field Medical, Clinical Development, or related biopharmaceutical experience., • A demonstrated track record building KOL relationships and leading peer-to-peer scientific exchange. This is a core requirement, not a nice-to-have; if you're strong on trial logistics but light on scientific engagement and KOL relationships, this role isn't the right fit., • Demonstrated accountability for site engagement and clinical trial enrollment, not solely data presentation at sites., • Deep scientific fluency and the credibility to hold a peer-level conversation with an academic specialist., • Willingness to travel approximately 60–70% within the assigned region. What would be great to have • Nephrology depth with existing relationships in the kidney community, and genuine willingness to build metabolic and PKU fluency., • Pre-commercial or first-launch biotechnology experience, built without an established field infrastructure., • Experience with genotype-driven patient identification and diagnostic testing pathways., • Experience mentoring MSLs or leading congress and or scientific-platform initiatives. About Maze Therapeutics Maze Therapeutics is a clinical-stage biopharmaceutical company harnessing human genetics to develop precision medicines for patients with kidney and metabolic diseases. Our clinical pipeline is anchored by two small molecule programs: MZE829, an APOL1 inhibitor for patients with APOL1‑mediated kidney disease, and MZE782, which targets genetic drivers of disease in phenylketonuria (PKU) and chronic kidney disease. We are also advancing a preclinical pipeline through our Compass platform, which links human genetic variants to the biological pathways that drive disease. Our People Maze is comprised of a team of passionate and creative professionals committed to discovering and delivering transformative medicines to patients suffering from both rare and common genetic diseases. We are fostering a culture that encourages vision, initiative and the development of talent. Our supportive work environment inspires creative thinking and freedom of expression, resulting in a stimulating atmosphere where people enjoy coming to work. While we have a passion for advanced science and pride ourselves on excellence in execution, ultimately, everything we do is about patients. Our Core Values Further Together – Our path is paved with challenges, but with resilience and a team-first mentality, we'll achieve our mission. Impact Obsessed – We embrace the bold, take calculated risks, and learn from our mistakes to improve the lives of others. Stand True – Our integrity is foundational; it guides us no matter the obstacle. The expected annual salary range for employees located in the San Francisco Bay Area is $205,000 - $295,000. Additionally, this position is eligible for an annual performance bonus. Maze performs position-based compensation benchmarking to industry market data to ensure we pay competitive wages. Determination of starting salary will depend upon a variety of job-related factors, which may include professional experience, skills, and job location. The expected salary range for this role may be modified in the future. Maze offers a robust benefits package to our eligible employees including competitive medical, dental, and vision insurance, mental health offerings, equity incentive plan, 401(k) program with employer match and a generous holiday and PTO policy. #LI-Remote

Job DescriptionEducation Minimum Requirement: • Bachelor's degree in Engineering, Automated Sciences, Computer Science, Biology, Chemistry or equivalent with scientific expertise with laboratory equipment in the development and execution of bioanalytical assays Required Experience and Skills: Hands-on experience with Hamilton, Echo (Labcyte), and GBG platforms, including method development, troubleshooting, and day-to-day operation of automated workflows. Experience programming and operating automated laboratory equipment such as liquid handlers, dispensers, washers, centrifuges, and related instrumentation. Strong problem-solving skills and the ability to independently identify and resolve technical issues. Ability to generate, analyze, and interpret scientific data produced on automated platforms. Strong communication and collaboration skills, with experience working effectively across scientific, engineering, software-focused teams. Must be self-sufficient and able to hit the ground running Preferred Experience and Skills: • Integrating robotic system schedulers (e.g. High Resolution BioSolution, Biosero, Thermo Momentum), • Working in pharmaceutical or biotech company and/or laboratory experience, • Implementing Client automation workflows and authoring operations SOPs, • Microsoft programming languages (VB, C#, labview or equivalent), • Electro-Mechanical design/assembly skills, • Use of electronic laboratory notebooks Responsibilities: The automation scientist in DMPK at South San Francisco will be responsible for driving the implementation of automated workflows to support pre-clinical studies. The Scientist will work collaboratively with other team members in a fast-paced environment to operate automated laboratory equipment and systems to support various DMPK assays. This specific position is a 6-month contract, and the individual should possess knowledge of the principles and concepts of various biological assays as they pertain to method development and sample testing using various liquid handlers and laboratory equipment. They should have a propensity towards technology. The successful candidate will play a crucial role in laboratory automation and modernization, providing input into the optimization of experimental methods with laboratory equipment and automation using state-of-the-art robotic systems. • Support the design, planning, and execution of robust automation strategies to support the DMPK group in SSF, • Work jointly with department members, IT, and across functional teams to implement automation workflows, support lab instrumentation and robotic platforms, and develop Client data handling and analysis workflows, • Contribute to the development of automated workflows to support assays such as immunoassay (IA), peptide stability, protein binding, automated sample preparation for plasma and tissue drug concentration analysis, cell culture maintenance & cell-based assays, • Map and integrate all the workflows for efficient use of automation and space, • Develop/update operations SOPs, • Troubleshoot errors, maintain, and update instruments, • Train and support scientists in automation workflows & platforms Manage data integrity through automated processes, • Collaborate to identify, evaluate, and recommend Client and cutting-edge automation and assay strategies to drive our discovery programs, including machine learning and artificial intelligence Nesco Resource offers a comprehensive benefits package for our associates, which includes a MEC (Minimum Essential Coverage) plan that encompasses Medical, Vision, Dental, 401K, and EAP (Employee Assistance Program) services. Nesco Resource provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.