Research scientist jobs in Modesto, CA

About the role: We're in search of an exceptional Research Associate to join our Spatial Team. You'll be an integral part of our highly collaborative R&D team, focused on demonstrating the value of 10x products. As a research associate, you will be responsible for performing the in situ analysis of biological tissue samples. This will involve supporting all aspects of the process, from library preparation, instrument operation, and initial analysis and QC of the data, ensuring the highest quality results are achieved throughout the entire process. The successful candidate in this position will work closely with expert scientists in spatial analysis and will have the opportunity to participate in the development of high profile cutting edge tools in spatial biology. You bring a strong background in the biological sciences and have acquired significant experience in conducting in situ and spatial genomic assays. You possess excellent communication skills, are detail oriented and can effectively collaborate with interdisciplinary teams, integrating their feedback into your experimental design. Your high motivation, proactiveness, and adaptability allow you to navigate changing priorities and methods with ease. Thriving in fast-paced environments, you excel at managing multiple priorities, communicating clearly, and consistently delivering results. What you will be doing: Performing in situ assays on tissue sections on microscope glass slides High throughput fluorescent microscopy imaging of the processed tissue samples, and image data pre-processing In-situ or NGS library preparation workflows Participate in troubleshooting of assays and microscope instruments Optimization studies of protocols for specific tissue samples Deliver processed image data to and work closely with computational biologists for image data analysis Maintain relevant documentation for record keeping related to the projects To be successful, you will need: MSc, or equivalent, in Biomedical Sciences, Molecular Biology, Biochemistry, or a related field Experience with molecular biology techniques, including immunostaining and/or in situ hybridization techniques (e.g. FISH, RNAscope, in situ hybridization) A proven track-record of using and optimizing and troubleshooting molecular biology protocols Additionally, we'd like to see: Tissue handling experience (fresh frozen, FFPE, cryosectioning, antigen retrieval, etc.) Strong organizational skills and ability to plan and structure your work Excellent interpersonal skills, including written and oral communication Ability to work in a fast-paced and quickly changing environment It would be advantageous if you had: Basic coding skills Experience with image analysis using relevant SW (e.g. CellProfiler, ImageJ) Familiarity with NGS library preparation workflows Light and fluorescent microscopy experience (confocal or standard epi-fluorescence) Knowledge and troubleshooting experience with liquid handling or automated systems (e.g. Tecan, Hamilton) Work experience from similar positions in academia, industry or a service provider/core facility Below is the base pay range for this full-time position. The actual base pay will depend on several factors unique to each candidate, including one's skills, qualifications, and experience. At 10x, base pay is also just one component of the Company's total compensation package. This role is also eligible for 10x's equity grants, its comprehensive health and retirement benefit programs, and its annual bonus program or sales incentive program. During the hiring process, your 10x recruiter can share more about the Company's total compensation package. Pay Range$90,600-$122,600 USD About 10x Genomics At 10x Genomics, accelerating our understanding of biology is more than a mission for us. It is a commitment. This is the century of biology, and the breakthroughs we make now have the potential to change the world. We enable scientists to advance their research, allowing them to address scientific questions they did not even know they could ask. Our tools have enabled fundamental discoveries across biology including cancer, immunology, and neuroscience. Our teams are empowered and encouraged to follow their passions, pursue new ideas, and perform at their best in an inclusive and dynamic environment. We know that behind every scientific breakthrough, there is a deep infrastructure of talented people driving the life sciences industry and making it possible for scientists and clinicians to make new strides. We are dedicated to finding the very best person for every aspect of our work because the innovations and discoveries that we enable together will lead to better technologies, better treatments, and a better future. Find out how you can make a 10x difference. Individuals seeking employment at 10x Genomics are considered without regards to race, color, religion, national origin, age, sex, marital status, ancestry, physical or mental disability, veteran status, gender identity, or sexual orientation, or any other characteristic protected by applicable law. 10x does not accept unsolicited applicants submitted by third-party recruiters or agencies. Any resume or application submitted to 10x without a vendor agreement in place will be considered unsolicited and property of 10x, and 10x will not pay a placement fee.

Our client, a world leader in diagnostics and life sciences, is looking for a "Scientist III” based out of Pleasanton, CA. Job Duration: Long term Contract (Possibility Of Further Extension) Pay Rate: $85/hr on W2 Company Benefits: Medical, Dental, Vision, Paid Sick leave, 401K Responsibilities: The role involves conducting and monitoring laboratory experiments under general supervision, ensuring accuracy, quality, and timeliness of results. Responsibilities include analyzing experimental data, documenting findings in electronic lab notebooks, preparing technical reports and presentations, and recommending process improvements. Analyzes experimental data using various data analysis software and/or applying quantitative methods. Forms conclusions, and provides/documents process improvements. Uses technical writing skills to produce reports and documents. May present findings at internal meeting. Qualifications: Ph.D./Master's/Bachelor's in life sciences, chemical sciences, or related scientific field with 0/2/5+ years relevant experience. If interested, please send us your updated resume at **********************/***************************

Pathology Biology & Integrated Analytics group is seeking a highly motivated Scientist for molecular cloning, cell culture, FPLC purification and antibody engineering and characterization. The qualified candidate will join a team of scientists focused on monoclonal antibody development for IVD and CDx assay. This position will be actively participating in antibody development, engineering, production and characterization. Job function requires the ability to evaluate, summarize and report study results, make independent decision and collaborate with teams at multiple sites. Responsibilities: Plans and/or manages smaller, less complex local projects (e.g. with moderate project management complexity, problem definition, and/or short to medium term implications). Participates in project teams across the R&D department and functional groups Can represent the Team Lead in project teams in his/her absence on instruction Ensures that quality standards are met and plans and coordinates the performance of tasks largely independently. Is aware of new developments in the field and refers to the possible use of these in diagnostics. Contributes to collaboration and close networking within the departments as part of R&D projects. Analyzes and interprets the R&D results largely independently and presents them to the relevant committees within their own function. Uses specified strategies to resolve problems and acts within defined guidelines.

About Us: How many companies can say they've been in business for over 177 years?! Here at ZEISS, we certainly can! As the pioneers of science, ZEISS handles the everchanging environments in a fast-paced world, meeting it with cutting edge of technologies and continuous advancements. ZEISS believes that innovation and technology are the key to a sustainable future and solutions for global change. We have a diverse range of portfolios throughout the ZEISS family in segments like, Industrial Quality & Research, Medical Technology, Consumer Markets and Semiconductor Manufacturing Technology. We are a global company with over 42,000 employees and have over 4,000 in the US and Canada alone! Make a difference, come join the team! What's the role? Position Summary: The senior systems scientist leads the research and investigation of new technologies for X-ray microscopy, pushing performance (resolution, contrast, speed, image quality, imaging modalities) beyond the state-of-the-art. This will involve contributing to and driving the organization's research agenda, and owning research projects in your area. The senior systems scientist's research is focused on the prototyping, investigation, and quantitative characterization of novel detector components, X-ray sources, X-ray source operation and modes, improved system designs, and novel system concepts. Sound Interesting? Here's what you'll do: Primary Duties and Responsibilities: * Actively drive innovation in your area through sound understanding of relevant challenges and a high level of creativity. * Collaborate with other scientists and engineers on subsystem and system research, characterization and development in the field of x-ray microscopy and CT. * Research, investigate, design, test, and optimize various subsystems of X-ray microscopes, as well as examining how individual system components interact and translate into final system performance. Works with all other Engineering functions, Manufacturing and Marketing on the successful system integration and implementation. * Support implementation & deployment of algorithmic solutions. * Manage the day-to-day activities of projects and communicate with project teams. * Identify and encourage areas for growth and improvement within the team. * Support visiting students and interns. Do you qualify? * Master's degree or PhD in Engineering, Physics, or Computer Sciences. * Significant experience in optical systems design, prototyping and quantitative characterization. * Experience in using or designing X-ray sources, Detectors, tomography systems preferred. * Fluency in English is required, including technical terms. Ability to work with and understand the work product of team members from all R&D-related departments, as well as Manufacturing and Marketing. Exceptional communication skills to resolve technical challenges between mechanical, electrical and software engineering, advanced development, manufacturing and marketing. The annual pay range for this position is $167,000 - $208,000 The pay offered for this role may be influenced by factors such as job location, scope of role, qualifications, education, experience, & complexity/specialization/scarcity of talent. This position is also eligible for a performance bonus or sales commissions. ZEISS also offers robust benefits, including medical plans, retirement savings plan and paid time off. We have amazing benefits to support you as an employee at ZEISS! * Medical * Vision * Dental * 401k Matching * Employee Assistance Programs * Vacation and sick pay * The list goes on! ZEISS is an EEO/AA/M/F/Disabled Veteran Employer Your ZEISS Recruiting Team: Clara Cresswell Zeiss provides Equal Employment Opportunity without unlawful regard to an Applicants race, color, religion, creed, sex, gender, marital status, age, national origin or ancestry, physical or mental disability, medical condition, military or veteran status, citizen status, sexual orientation, pregnancy (includes childbirth, breastfeeding or related medical condition), genetic predisposition, carrier status, gender expression or identity, including transgender identity, or any other class or characteristic protected by federal, state, or local law of the employee (or the people with whom the employee associates, including relatives and friends).

About Us: How many companies can say they've been in business for over 177 years?! Here at ZEISS, we certainly can! As the pioneers of science, ZEISS handles the everchanging environments in a fast-paced world, meeting it with cutting edge of technologies and continuous advancements. ZEISS believes that innovation and technology are the key to a sustainable future and solutions for global change. We have a diverse range of portfolios throughout the ZEISS family in segments like, Industrial Quality & Research, Medical Technology, Consumer Markets and Semiconductor Manufacturing Technology. We are a global company with over 42,000 employees and have over 4,000 in the US and Canada alone! Make a difference, come join the team! What's the role? Position Summary: The senior systems scientist leads the research and investigation of new technologies for X-ray microscopy, pushing performance (resolution, contrast, speed, image quality, imaging modalities) beyond the state-of-the-art. This will involve contributing to and driving the organization's research agenda, and owning research projects in your area. The senior systems scientist's research is focused on the prototyping, investigation, and quantitative characterization of novel detector components, X-ray sources, X-ray source operation and modes, improved system designs, and novel system concepts. Sound Interesting? Here's what you'll do: Primary Duties and Responsibilities: Actively drive innovation in your area through sound understanding of relevant challenges and a high level of creativity. Collaborate with other scientists and engineers on subsystem and system research, characterization and development in the field of x-ray microscopy and CT. Research, investigate, design, test, and optimize various subsystems of X-ray microscopes, as well as examining how individual system components interact and translate into final system performance. Works with all other Engineering functions, Manufacturing and Marketing on the successful system integration and implementation. Support implementation & deployment of algorithmic solutions. Manage the day-to-day activities of projects and communicate with project teams. Identify and encourage areas for growth and improvement within the team. Support visiting students and interns. Do you qualify? Master's degree or PhD in Engineering, Physics, or Computer Sciences. Significant experience in optical systems design, prototyping and quantitative characterization. Experience in using or designing X-ray sources, Detectors, tomography systems preferred. Fluency in English is required, including technical terms. Ability to work with and understand the work product of team members from all R&D-related departments, as well as Manufacturing and Marketing. Exceptional communication skills to resolve technical challenges between mechanical, electrical and software engineering, advanced development, manufacturing and marketing. The annual pay range for this position is $167,000 - $208,000The pay offered for this role may be influenced by factors such as job location, scope of role, qualifications, education, experience, & complexity/specialization/scarcity of talent.This position is also eligible for a performance bonus or sales commissions. ZEISS also offers robust benefits, including medical plans, retirement savings plan and paid time off. We have amazing benefits to support you as an employee at ZEISS! Medical Vision Dental 401k Matching Employee Assistance Programs Vacation and sick pay The list goes on! ZEISS is an EEO/AA/M/F/Disabled Veteran Employer Your ZEISS Recruiting Team: Clara Cresswell Zeiss provides Equal Employment Opportunity without unlawful regard to an Applicants race, color, religion, creed, sex, gender, marital status, age, national origin or ancestry, physical or mental disability, medical condition, military or veteran status, citizen status, sexual orientation, pregnancy (includes childbirth, breastfeeding or related medical condition), genetic predisposition, carrier status, gender expression or identity, including transgender identity, or any other class or characteristic protected by federal, state, or local law of the employee (or the people with whom the employee associates, including relatives and friends).

PromptBio, established in 2023 in Pleasanton, California, is a biotechnology company dedicated to developing AI-driven workflows that automate the discovery of novel biomarkers from multi-omics data, translating them into clinical diagnostic applications. Job Description We seek a motivated, hands-on AI Scientist to join our interdisciplinary team, focusing on integrating AI solutions within the life sciences domain. Key Responsibilities Design, prototype, and implement cutting-edge autonomous AI agents and multi-agent systems capable of dynamic planning, reasoning, memory management, and self-reflection. Develop and integrate core agent components, including planning modules (e.g., Tree-of-Thought, CoT-based planners), tool-use interfaces, and persistent long-term memory/retrieval mechanisms (RAG). Develop high-quality, production-ready code in Python/Go for integrating LLMs and other foundational models into functional agent architectures. Build and maintain scalable agent infrastructure using frameworks like LangChain ensuring seamless integration with cloud services (AWS preferred). Conduct rigorous testing, evaluation, and optimization of agent performance on complex, real-world tasks. Work closely with the engineering team to define agent use cases and translate research prototypes into deployable product features that deliver business value. Qualifications Minimum of 2-3 years of industry experience with demonstrated practical experience building and implementing LLM-based agents (e.g., using tool-calling, external memory, and multi-step reasoning). Strong understanding of key agentic concepts: Memory (Short-Term/Long-Term), Planning, Tool Use, and Self-Reflection/Evaluation. Hands-on experience with agentic automation/frameworks (e.g., LangChain, ReAct, etc), vector databases (e.g., Qdrant) and infrastructure services (e.g., Bedrock AgentCore). Fluency with software engineering best practices, including testing, code reviews, version control (e.g., Git), and containerization. Knowledge of AI ethics and safety principles, particularly as they apply to autonomous decision-making systems. Knowledge of bioinformatics data analysis will be a significant plus. Ph.D. in AI, Machine Learning, Statistics, Bioinformatics or a related field. Desired Attributes Entrepreneurial mindset with comfort in ambiguous, fast-paced environments. Proactive, results-oriented, and driven with a "get things done" mindset. Strong problem-solving skills and adaptability to evolving project requirements. Collaborative team player who thrives in dynamic environments. Additional Information Financial security through competitive compensation, incentives, and retirement plan Healthcare and well-being programs including competitive medical, dental, and vision benefits Generous paid time-off including vacation, sick time, holidays, and discretionary winter shutdown 401(k) retirement savings with a generous company match Other comprehensive voluntary benefits include but are not limited to pet insurance, life insurance, employee assistance program (EAP), discount programs, and many more We continue to optimize our benefits & wellness programs as we grow our organization to make sure they meet our diverse workforce needs Hybrid work opportunities.

PromptBio, established in 2023 in Pleasanton, California, is a biotechnology company dedicated to developing AI-driven workflows that automate the discovery of novel biomarkers from multi-omics data, translating them into clinical diagnostic applications. Job Description We seek a motivated, hands-on AI Scientist to join our interdisciplinary team, focusing on integrating AI solutions within the life sciences domain. Key Responsibilities Design, prototype, and implement cutting-edge autonomous AI agents and multi-agent systems capable of dynamic planning, reasoning, memory management, and self-reflection. Develop and integrate core agent components, including planning modules (e.g., Tree-of-Thought, CoT-based planners), tool-use interfaces, and persistent long-term memory/retrieval mechanisms (RAG). Develop high-quality, production-ready code in Python/Go for integrating LLMs and other foundational models into functional agent architectures. Build and maintain scalable agent infrastructure using frameworks like LangChain ensuring seamless integration with cloud services (AWS preferred). Conduct rigorous testing, evaluation, and optimization of agent performance on complex, real-world tasks. Work closely with the engineering team to define agent use cases and translate research prototypes into deployable product features that deliver business value. Qualifications Minimum of 2-3 years of industry experience with demonstrated practical experience building and implementing LLM-based agents (e.g., using tool-calling, external memory, and multi-step reasoning). Strong understanding of key agentic concepts: Memory (Short-Term/Long-Term), Planning, Tool Use, and Self-Reflection/Evaluation. Hands-on experience with agentic automation/frameworks (e.g., LangChain, ReAct, etc), vector databases (e.g., Qdrant) and infrastructure services (e.g., Bedrock AgentCore). Fluency with software engineering best practices, including testing, code reviews, version control (e.g., Git), and containerization. Knowledge of AI ethics and safety principles, particularly as they apply to autonomous decision-making systems. Knowledge of bioinformatics data analysis will be a significant plus. Ph.D. in AI, Machine Learning, Statistics, Bioinformatics or a related field. Desired Attributes Entrepreneurial mindset with comfort in ambiguous, fast-paced environments. Proactive, results-oriented, and driven with a "get things done" mindset. Strong problem-solving skills and adaptability to evolving project requirements. Collaborative team player who thrives in dynamic environments. Additional Information Financial security through competitive compensation, incentives, and retirement plan Healthcare and well-being programs including competitive medical, dental, and vision benefits Generous paid time-off including vacation, sick time, holidays, and discretionary winter shutdown 401(k) retirement savings with a generous company match Other comprehensive voluntary benefits include but are not limited to pet insurance, life insurance, employee assistance program (EAP), discount programs, and many more We continue to optimize our benefits & wellness programs as we grow our organization to make sure they meet our diverse workforce needs Hybrid work opportunities.

PromptBio, established in 2023 in Pleasanton, California, is a biotechnology company dedicated to developing AI-driven workflows that automate the discovery of novel biomarkers from multi-omics data, translating them into clinical diagnostic applications. Job Description We seek a motivated, hands-on AI Scientist to join our interdisciplinary team, focusing on integrating AI solutions within the life sciences domain. Key Responsibilities Design, prototype, and implement cutting-edge autonomous AI agents and multi-agent systems capable of dynamic planning, reasoning, memory management, and self-reflection. Develop and integrate core agent components, including planning modules (e.g., Tree-of-Thought, CoT-based planners), tool-use interfaces, and persistent long-term memory/retrieval mechanisms (RAG). Develop high-quality, production-ready code in Python/Go for integrating LLMs and other foundational models into functional agent architectures. Build and maintain scalable agent infrastructure using frameworks like LangChain ensuring seamless integration with cloud services (AWS preferred). Conduct rigorous testing, evaluation, and optimization of agent performance on complex, real-world tasks. Work closely with the engineering team to define agent use cases and translate research prototypes into deployable product features that deliver business value. Qualifications Minimum of 2-3 years of industry experience with demonstrated practical experience building and implementing LLM-based agents (e.g., using tool-calling, external memory, and multi-step reasoning). Strong understanding of key agentic concepts: Memory (Short-Term/Long-Term), Planning, Tool Use, and Self-Reflection/Evaluation. Hands-on experience with agentic automation/frameworks (e.g., LangChain, ReAct, etc), vector databases (e.g., Qdrant) and infrastructure services (e.g., Bedrock AgentCore). Fluency with software engineering best practices, including testing, code reviews, version control (e.g., Git), and containerization. Knowledge of AI ethics and safety principles, particularly as they apply to autonomous decision-making systems. Knowledge of bioinformatics data analysis will be a significant plus. Ph.D. in AI, Machine Learning, Statistics, Bioinformatics or a related field. Desired Attributes Entrepreneurial mindset with comfort in ambiguous, fast-paced environments. Proactive, results-oriented, and driven with a "get things done" mindset. Strong problem-solving skills and adaptability to evolving project requirements. Collaborative team player who thrives in dynamic environments. Additional Information Financial security through competitive compensation, incentives, and retirement plan Healthcare and well-being programs including competitive medical, dental, and vision benefits Generous paid time-off including vacation, sick time, holidays, and discretionary winter shutdown 401(k) retirement savings with a generous company match Other comprehensive voluntary benefits include but are not limited to pet insurance, life insurance, employee assistance program (EAP), discount programs, and many more We continue to optimize our benefits & wellness programs as we grow our organization to make sure they meet our diverse workforce needs Hybrid work opportunities.

Purpose Amador Bioscience (AmadorBio) is a Translational & Clinical Pharmacology CRO providing global-standard services in quantitative clinical pharmacology, GLP/GCLP bioanalysis, clinical research, and regulatory filing to leading biopharmaceutical companies. Our clients include multinational pharmaceuticals and mid- and small-size biotech companies. Amador Laboratory Services Division specializes in bioanalysis (PK/PD/ADA), biomarkers, assay development & validation, and sample analysis. The team has successfully supported multiple non-GLP, GLP (nonclinical) and GCLP (clinical) projects. To meet the needs of business growth, we are looking for a highly motivated, experienced scientist/senior scientist to join our passionate team to partner with our clients for success. The successful candidate will be responsible for providing bioanalytical supports for both pre-clinical and clinical projects and will report to the Laboratory Head. Role and Responsibilities Develop, validate, conduct, and troubleshoot UHPLC and LC-MS analytical methods to quantitate large molecules and metabolites in biological fluids Present/interpret data internally and/or externally as needed. Participate in interactions with clients and ensure overall customer satisfaction. Interacts with QA to ensure all audit findings are addressed in a timely fashion. Author and/or review key regulatory documents, laboratory data, and technical reports. Assist with the oversight of the laboratory and mentor junior staff. Assist in establishing and improving all policies, procedures and required SOP documentation. Understand and adhere to corporate standards regarding code of conduct, safety, and GLP/GCP/GDP compliance. Ensure and reviews lab maintenance activities and maintains a clean and safe lab environment Develop, write, and review protocols and SOPs. Participate in regulatory compliance activities Perform all other related duties as assigned Qualifications and Education Requirements Ph.D., Master's, or Bachelor's degree in biology, immunology, chemistry, pharmacology, or other related scientific fields required. Requires a minimum 0-9 years of relevant experience in a CRO or drug-development environment. Ability to work independently and have good attention to details. Good knowledge of regulated bioanalysis. GLP/GCLP experience preferred. Ability to achieve objectives/timelines through collaborative efforts with coworkers, managers, and clients. Must be goal-oriented, quality-conscientious, and client-focused. Effective written and verbal communication skills. Experienced with LCMS or tandem Mass-Spec method development and validation for PK and/or biomarker analysis. Preferred Skills Proficient in MS Office Watson LIMS Strong knowledge of GLP/GCLP regulations Salary range is from $105,000 to 120,000

Certified Group is a leading North American provider of laboratory testing and audit and certification services. The Certified Group of companies includes Food Safety Net Services (FSNS), Certified Laboratories, EAS Consulting Group, Labstat International Inc., Advanced Botanical Consulting & Testing (ABC Testing Inc.), Microconsult Inc. and Micro Quality Labs Inc. The Certified Group provides analytical testing and regulatory guidance services in the food & beverage, dietary supplements & NHP, cosmetics, OTC, personal care, tobacco, cannabis, nicotine and hemp industries. We are currently looking for a Contract Research Associate I to join our growing team! If you share our values - Ethical, Adaptable, Reliable, Accurate, Collaborative, Client Focused, Dedicated, Skilled, Innovative - and wish to develop in a dynamic environment focused on the future, then join us! Essential Functions: * Conducts all testing procedures in accordance with standard operating procedure and quality guidelines. * Accurately generates and transcribes pertinent data. * Interacts well with other department members to successfully accomplish department objectives. * Manages time and resources to maximize operational efficiency. * Proactively seeks ways to improve processes and better utilize departmental resources. * Accurately execute scheduled tasks and assignments. * Perform appropriate quality control tasks pertinent to the department including proper documentation and record keeping, in compliance with accrediting agencies. * Perform maintenance of laboratory equipment and instruments, including inspection, calibration, cleaning & sanitization, as directed. * Participate in special projects as assigned by the Department Manager/Supervisor. Requirements Requirements: * BS degree, preferably in Biology/Microbiology and appropriate industry specific experience. * Good conceptual basis in microbiology with proven ability to perform basic microbiology techniques. * 2 years relevant laboratory experience. * Critical thinking - use of logic and reasoning to trouble shoot issues and evaluate effectiveness of resolution. * Organization skills - ability to utilize time, energy, resources, etc. in an effective manner. * Training - complete all training as assigned and aid in the training of newer department members. * Communication skills - speaking, reading, writing, and listening, to effectively communicate pertinent information. * Experience with Microsoft Office Suite, and LIMs experience preferable. * Must have ability to distinguish colors and manual dexterity a * Ability to stand for prolonged periods. PHYSICAL DEMANDS * Dexterity of hands and fingers to operate a computer keyboard, mouse and to handle other communications/computer components * Potential exposure to odors, fumes, airborne particles, hazardous chemicals, and microbiological pathogens * Noise level varies from quiet to loud * Temperature varies from hot to cold * Interactive and fast-paced team-oriented tasks * Overnight Travel is required at the discretion of management * Occasionally lift and/or move up to 25 pounds. * Color vision and depth perception Benefits: * Progressive 401k Retirement Savings Plan * Employer Paid Short- Term and Long-Term Disability, and Life Insurance * Group Medical * Tuition Reimbursement * Flexible Spending Accounts * Dental * Paid Holidays and Time Off * Many positions which qualify for the company bonus program Certified Group values diversity in its workforce. The company is firmly committed to a policy of Equal Opportunity and will administer its policies in a manner that treats each employee and applicant for employment on the basis of merit. Certified Group will take affirmative action to seek out qualified applicants without regard to race, color, religion, sex, national origin, age, handicap, or veteran status. M-F 8-4:30pm Overtime and Weekends as needed 8 hours per day

Crystal Bio Solutions is a CRO providing global-standard services in GLP/GCLP bioanalysis and biomarker. Our clients include multinational pharmaceutical companies and biotech companies. The Bioanalysis & Biomarkers Department specializes in Method Development, Method Validation, GLP/GCLP Bioanalysis for PK, immunogenicity and biomarkers. The team has successfully supported non-GLP, GLP (non-clinical) and GCLP (clinical) projects. The role is responsible for providing bioanalytical support for both pre-clinical and clinical projects and partnering with our clients for project success. Key Responsibilities * Independently propose assay design and/or strategy, develop, validate, conduct, and troubleshoot bioanalytical methods, including PK, and Biomarker, for GLP/GCLP sample testing and data reporting. Present and interpret data internally and/or externally as needed. * Serve as the Principal Investigator responsible for interaction with the client from the study design to scheduling, conducting, reporting, and transferring data. Ensure responsiveness to the client, timely delivery, and overall customer satisfaction. * Serve as Subject Matter Expert (SME) for FLOW Cytometry * Author and/or review key regulatory documents, validation plans and reports, laboratory data, and technical reports. * Provide oversight of the laboratory, mentor junior staff, and collaborate to keep improving operational excellence. * Assist in establishing and improving policies, procedures, work instructions and SOPs. * Understand and adhere to corporate standards regarding code of conduct, Environment Health & Safety (EHS), and GLP/GCP/GDP compliance. * Perform other related duties as assigned. Qualifications & Educational Requirements * Ph.D., M.Sc., M.A., B.A., in Biology, Immunology, Chemistry, Pharmacology, or other related scientific fields required, including a minimum of 4+(Ph.D.), 9+(Master's) or 12+(Bachelor's) years of Pharma/Biotech/CRO experience. * Hands-on experience and strong knowledge of GLP/GCLP bioanalysis. * Experience in Flow Method Development, Validation for PK, and PD Biomarker assays. * Knowledge and hands on experience in one or more of the following assay platforms, Cell-Based Assays, qPCR, dPCR, ELISpot, are highly desirable * Supervisory experience in both project and talent (people) management is preferred. * Ability to work independently and pay good attention to details. * Ability to achieve objectives/timelines through collaborative efforts with co-workers, managers, and clients. * Must be goal-oriented, compliance-ensured, quality-conscientious, and client-focused. * Effective writing and communication skills. How to Apply CV can be e-mailed directly to: career_************************. Be sure to denote the Job Title of the position you are applying.

Job DescriptionSalary: Were seeking a PhD-level scientist to own the single cell-bead pairing phase of our single-cell assay, where cells and functionalized beads are brought together under tightly controlled physical and biochemical boundary conditions to enable one-to-one pairing. This role integrates surface chemistry, biophysics, and quantitative assay development to transform first-principles models into reproducible, manufacturable workflows. You will lead optimization of beadcell binding, applying rigorous experimental design to balance diffusion, shear, and binding kinetics. The position emphasizes hands-on assay execution, data analysis, and cross-functional collaboration with molecular biology, automation, and manufacturing teams. Key Responsibilities Design, perform, and interpret experiments to optimize beadcell pairing using defined physical and biochemical boundaries (bead-to-cell ratio, mixing conditions, surface density, coating fraction, geometry, etc.). Develop and characterize bead surfaces, including antibody or ligand conjugation, and orientation to control valency, maximize single bead binding, and minimize doublets. Quantify binding outcomes (1:1 yield, doublet rate, nonspecific binding) using microscopy, flow cytometry, and kinetic binding assays. Apply structured optimization frameworks (DoE, sequential sweeps) to identify parameter boundaries for yield and purity. Collaborate with downstream assay scientists to connect physical pairing parameters with molecular capture efficiency and sequencing performance. Document results and transfer optimized conditions into manufacturing and QC pipelines. Qualifications PhD in Chemical Engineering, Chemistry, Bioengineering, or related field with 3+ years of relevant postdoctoral or industry experience. Proven track record developing or optimizing surface-based biological assays (e.g., bead assays, immunoassays, biosensors). Expertise in surface functionalization and conjugation chemistry (e.g., antibodies, biotin-streptavidin, protein A/G, covalent coupling). Proficiency with plate-based systems (96/384-well formats), quantitative microscopy, and/or flow cytometry. Strong statistical and data-analysis skills, including use of DoE and curve fitting tools (JMP, R, Python, or equivalent). Excellent documentation, communication, and cross-disciplinary collaboration skills. Preferred Experience Working knowledge of binding kinetics, diffusion, or transport models sufficient to interpret or apply internal frameworks; experience performing modeling or simulation is advantageous but not required. Familiarity with orbital/pipette mixing dynamics and microscale hydrodynamics. Experience integrating physical assay parameters with downstream molecular outcomes. Comfort in a fast-paced, experimental development environment. What We Offer A chance to build something truly transformative from the ground up. High ownership and autonomy in a fast-moving environment. Opportunities to shape company direction and culture. Competitive salary, equity, and benefits.

： Lunar Biosciences is a cutting-edge biotech startup at the forefront of proteomics innovation. Headquartered in Pleasanton, California, our mission is to unlock the secrets of proteoforms through our revolutionary proteomics platform. Our technology is reshaping the landscape of drug discovery and biomarker development, driving the shift from traditional methods to precision, data-driven medicine. Job Description We are seeking a talented and passionate Senior Staff/Principal Scientist to join our growing team. You will lead chemistry efforts to develop multi-step chemical processes that will be implemented in our groundbreaking technology. As part of a fast-paced and collaborative startup environment, you will work closely with a multidisciplinary team to build core chemistry solutions for our sequencing technology. Key Responsibilities： Contribute as a full-time bench scientist and a leader of the chemistry team Design, implement, and adjust strategies & R&D plans in developing chemistries for a non-mass spec-based proprietary proteomics workflow Develop, verify, optimize protocols to accommodate cross-functional processes including automation Manage and prioritize multiple timelines across diverse projects/goals in coordination with other functional progress Communicate the overall chemistry strategy and rationale to external parties Proactively seek innovation - build and expand a technology pipeline & IP portfolio Actively identify, build, and secure internal and external resources to support R&D work Create and maintain a scientific advisory group to support R&D work Participate in multidisciplinary team activities, commit to rapid identification and resolution of problems, and advance projects through critical internal review processes Review research papers and intellectual property literature in support of ongoing research projects Qualifications Ph.D. in organic chemistry, biochemistry, medicinal chemistry, or chemical engineering with at least 10 years of professional experience in a biotech or pharma environment. A thought leader in protein and nucleic acid chemistry. Extensive experience in developing novel chemical methodologies for proximity ligation, surface/beads chemistry, assay development, protein (orthogonal) conjugation, proteomics sample preparation, post-translational modifications, solid-phase synthesis, and advanced purification techniques. Deep understanding of Edman degradation in protein sequencing chemistry. Good relationship with commercial resources providing services of analytical analysis of both small molecules and macromolecules. Strong problem-solving skills and the ability to work both independently and within a team. Excellent people skills and presentation skills. Willing and capable of being hands-on in the wet-lab Additional Information Why Join Us? At Lunar Biosciences, you'll be part of a mission-driven team working on the next wave of advancements in proteomics and precision medicine. We offer a dynamic and innovative startup environment where you'll have the opportunity to impact human health and well-being while working alongside passionate, dedicated professionals. Additional Information: Base salary: $175,000/year - $200,000/year. The final salary will be determined by the candidate's experience, qualifications, and skill set. Eligible employees may receive company equity as part of the total compensation package. Financial security through competitive compensation, incentives, and a retirement plan Health care and well-being programs, including competitive medical, dental, vision, life and long-term disability insurance. Generous paid time off including vacation, sick time, and holidays 401(k) retirement savings with a company match We continue to optimize our benefits & wellness programs as we grow our organization to make sure they meet our diverse workforce needs. How to Apply: If you're excited about joining a team that's driving revolutionary change in proteomics and precision medicine, we'd love to hear from you. Apply today!

Trans Ova Genetics is seeking a full-time IVF Embryologist to join their team in Turlock, CA! As an IVF Embryologist, you will become specialized in embryo evaluation, grading, and freezing, and other laboratory procedures within the IVF lab. Our ideal candidate would be passionate about laboratory procedures, client satisfaction, and, of course, embryos! Trans Ova Genetics provides in-depth training that provides a solid foundation prior to supporting client production and would require eight-twelve weeks at our training facility, which is critical to the success of this role. Responsibilities * Embryo evaluation, grading and freezing. * Fertilization and culture plate preparation. * Semen handling and preparation for IVF. * Recordkeeping/Data Entry. * Embryology training. * Quality Control. * Maintain good laboratory technique and follow lab protocols. * Follow Trans Ova's policies and procedures. Requirements * Education Requirements: * B.S. in Animal Science or a related field; or a Veterinary Technician degree. * Physical Requirements/Working Conditions: * Ability to sit for long periods of time behind a microscope, in a sterile lab setting. * Ability to work under a laminar flow hood. * Some travel may be required. * Other skills/experience: * Good hand to eye coordination. * Strong attention to detail and organization. Trans Ova Genetics, a member of the URUS Group, provides industry-leading reproductive technologies and expertise to cattle breeders through a unique professional services team that works closely with clients to understand their breeding goals and ultimately help clients advance and extend superior genetics. Trans Ova Genetics understands the process that will help multiply a herd's genetic success. Reproductive technologies such as embryo transfer, in-vitro fertilization (IVF), sexed-semen, genetic preservation, and cloning are considered the reproductive "tools" available for breeders looking to achieve specific breeding and reproductive goals. Internationally recognized as a source of superior animal husbandry and reproductive expertise, Trans Ova Genetics offers an integrated system of regional centers, satellite stations, and on-farm application of reproductive technologies. Trans Ova's headquarters are in Sioux Center, Iowa, but we have many offices and satellite centers across the country. On-going research and applied science allow Trans Ova Genetics to develop and implement new technologies to help move the science of bovine genetic improvement forward. Trans Ova is dedicated to meeting the requirements of their customers and to continual improvement. TOG has deep roots in the industry through its origin within the URUS family of companies. As a holding company with cooperative and private ownership, URUS is a family of businesses at the heart of the dairy and beef industry - Alta Genetics, GENEX, Genetics Australia, Leachman Cattle, Jetstream, PEAK, SCCL, Trans Ova Genetics and VAS. Each organization has its unique identity, products, and services. These companies work globally to provide cutting-edge dairy and beef genetics, customized reproductive services to maximize conceptions, dairy management information to take producers to the frontline of progressive dairy farming, and an array of products and services to help bovines reach their full genetic potential. URUS has 9 brands in 17 retail countries and employs nearly 2,800 people globally.

Trans Ova Genetics is seeking a full-time IVF Embryologist to join their team in Turlock, CA! As an IVF Embryologist, you will become specialized in embryo evaluation, grading, and freezing, and other laboratory procedures within the IVF lab. Our ideal candidate would be passionate about laboratory procedures, client satisfaction, and, of course, embryos! Trans Ova Genetics provides in-depth training that provides a solid foundation prior to supporting client production and would require eight-twelve weeks at our training facility, which is critical to the success of this role. Responsibilities Embryo evaluation, grading and freezing. Fertilization and culture plate preparation. Semen handling and preparation for IVF. Recordkeeping/Data Entry. Embryology training. Quality Control. Maintain good laboratory technique and follow lab protocols. Follow Trans Ova's policies and procedures. Requirements Education Requirements: B.S. in Animal Science or a related field; or a Veterinary Technician degree. Physical Requirements/Working Conditions: Ability to sit for long periods of time behind a microscope, in a sterile lab setting. Ability to work under a laminar flow hood. Some travel may be required. Other skills/experience: Good hand to eye coordination. Strong attention to detail and organization.

REQUIRED QUALIFICATIONS: * Undergraduate student must be registered/enrolled in a minimum of six (6) Fall/Spring units. * Must meet all other eligibility requirements per Unit 11-Academic Student Employee Hiring Policies (see *********************************** academic-student-employee-hiring-information) PREFERRED QUALIFICATIONS: * Must be currently accepted as an CSU-SPA participant. * Must submit a research proposal, with a faculty member, before hiring. * Must submit a current CITI Certificate before hiring (see **************** program.org) HOW TO APPLY & DEADLINE: A complete application must include a resume, available work schedule and class schedule indicating required enrollment as per the Student Employment Policies (See *********************************** academic-student-employee-hiringinformation), a research proposal with a faculty member. Compile all the required material in one single PDF document and include it as a Supporting Information in your application. If you have any questions regarding this recruitment, please contact: Dr. Elvin Aleman CSU-SPA Program Director California State University, Stanislaus One University Circle Turlock, CA 95382 ******************* CAMPUS & AREA: California State University, Stanislaus serves the San Joaquin Valley and is a critical educational resource for a six-county region of approximately 1.5 million people. The University is fully committed to creating a culture of diversity and inclusion - one in which every person in the University community feels safe to express their views without fear of reprisal. Widely recognized for its quality academic programs, the University has 10 nationally accredited programs and 662 faculty members. 94 percent of full-time faculty holds doctorates or terminal degrees in their fields. The University offers 43 undergraduate majors, 16 master's programs, 7 post-graduate credentials, a doctorate in education and serves more than 10,000 students. New instructional facilities have been built for the unique pedagogy of professional programs, laboratory sciences and performing arts. Stanislaus State continues to receive national recognition with its ranking as one of the best 384 colleges in the nation by The Princeton Review. The University was one of 12 public universities in the nation to be recognized by the American Association of State Colleges and Universities for demonstrating exceptional performance in retention and graduation rates. In addition, U.S. News and World Report ranks Stanislaus State in its top 10 among public universities in the West, while Washington Monthly honored Stanislaus State as the West's No. 1 university for the money. Stanislaus State also is recognized as a Hispanic-Serving Institution (HSI) by the U.S. Department of Education. CSU Stanislaus values shared governance: Handbook statement on shared governance EQUAL EMPLOYMENT OPPORTUNITY The university is an Equal Opportunity Employer and does not discriminate against persons on the basis of race, religion, color, ancestry, age, disability, genetic information, gender, gender identity, gender expression, marital status, medical condition, National origin, sex, sexual orientation, covered veteran status, or any other protected status. You can learn more about federal equal employment opportunity protections by accessing the Department of Labor's notices: **************************************************************** and **************************************************************************** Individuals with disabling conditions who require accommodation during the recruitment process may contact the ADA Coordinator at **************. In compliance with federal law, all persons hired will be required to verify identity and eligibility to work in the United States and to complete the required employment eligibility verification document form upon hire. The CSU is a state entity whose business operations reside within the State of California. The CSU prohibits hiring employees to perform CSU-related work outside California. CLERY ACT DISCLOSURE Pursuant to the Jeanne Clery Disclosure of Campus Security Policy and Campus Crime Statistics Act, the annual security report (ASR), is now available for viewing at ************************************************ The ASR contains the current security and safety-related policy statements, emergency preparedness and evacuation information, crime prevention and sexual assault prevention information, and drug and alcohol prevention programming. The ASR also contains statistics of Clery Act crimes for Stanislaus State for the previous three years. A paper copy of the ASR is available upon request by contacting the office of the Clery Director located at One University Circle, Turlock, CA 95382. CRIMINAL BACKGROUND CLEARANCE NOTICE The university requires a criminal and/or child abuse background check to be completed for many of its new employees, current employees seeking promotional or transfer opportunities, and current employees assigned new duties. Satisfactory completion of a background check (including a criminal records check) is required for employment. CSU will make a conditional offer of employment, which may be rescinded if the background check reveals disqualifying information, and/or it is discovered that the candidate knowingly withheld or falsified information. Failure to satisfactorily complete the background check may affect the continued employment of a current CSU employee who was conditionally offered the position. Failure to consent to any background check will disqualify an applicant from further consideration. Additionally, an applicant who fails to provide the necessary information or who provides false or misleading information may also be disqualified from further consideration. Later discovery of false or misleading information related to the background check may result in the offer of employment being withdrawn or subject the employee to disciplinary action, up to and including termination. Advertised: Aug 14 2025 Pacific Daylight Time Applications close:

GeneGenieDx is a biotech company founded in 2020 in the Bay Area, California. We aim to discover novel biomarkers and translate them into better clinical diagnostic products. Our current focus is to develop cutting-edge bioinformatics and machine learning algorithms to enable the discovery of diagnostic biomarkers and translate them into clinical products. EI Captian Biosciences is the subsidiary of GeneGenieDx. At El Capitan Biosciences, we are developing stool-based human RNA-seq technology for the discovery of novel biomarkers for different GI diseases and translating them into clinical diagnostic products. Job Description We are looking for an individual who is passionate about the technology of genomics sequencing and wants to make an impact in the field of personalized diagnostics; who has a deep understanding of the biochemistry involved in RNA-sequencing and methylation sequencing, who has insight on how to create novel techniques and make better assays; who is excited to work with a team of world experts on cutting-edge technology in genomic diagnosis. Qualifications Education Minimum Requirement: Ph.D. in Biological Sciences such as molecular biology, genomics, and biochemistry. Required Experience And Skills Experience in novel NGS method development Experience in RNA-seq, Methylation sequencing, and single-cell RNA-seq Deep knowledge of enzymes and molecular biology. Preferred Experience And Skills Experience in cancer biology Experience in working with challenging clinical specimens with low biomass such as stool and blood. Additional Information Base range: $120,000-$ 150,000. The final salary will be determined based on the candidate's experience, qualifications, and skill set. Financial security through competitive compensation, incentives, and retirement plan Health care and well-being programs including competitive medical, dental, vision & medical benefits. Generous paid time off including vacation, sick time, & holidays 401(k) retirement savings with a company match Other comprehensive voluntary benefits include but are not limited to pet insurance, life insurance, employee assistance program, discount programs, and many more. We continue to optimize our benefits & wellness programs as we grow our organization to make sure they meet our diverse workforce needs. The stability of a company with a record of strong financial performance year over year.

Join us and make YOUR mark on the World! Are you interested in joining some of the brightest talent in the world to strengthen the United States' security? Come join Lawrence Livermore National Laboratory (LLNL) where our employees apply their expertise to create solutions for BIG ideas that make our world a better place. We are dedicated to fostering a culture that values individuals, talents, partnerships, ideas, experiences, and different perspectives, recognizing their importance to the continued success of the Laboratory's mission. Pay Range $202,500 - $308,184 Annually $202,500 - $256,824 Annually for the SES.4 level $243,060 - $308,184 Annually for the SES.5 level This is the lowest to highest salary we in good faith believe we would pay for this role at the time of this posting; pay will not be below any applicable local minimum wage. An employee's position within the salary range will be based on several factors including, but not limited to, specific competencies, relevant education, qualifications, certifications, experience, skills, seniority, geographic location, performance, and business or organizational needs. Job Description We have an opening for an accomplished and innovative Senior Protein Design Scientist to advance our R&D initiatives as part of the Center for Predictive Bioresilience (CPB). CPB is an exciting and fast-paced engineering center combining predictive computational modeling, machine learning, and experimental biology to develop medical countermeasures. This position will be in the Computational Engineering Division (CED), within the Engineering Directorate, matrixed to the CPB. As a senior scientific leader, you will drive the next generation of our protein engineering platform, integrating advanced computational and experimental approaches to deliver impactful solutions for medical countermeasures and biotechnological innovation. You will collaborate with multidisciplinary teams of scientists, including biochemists, microbiologists, bioinformaticians, and analytical chemists, to execute ambitious enzyme engineering programs. A key focus will be the development and deployment of AI/ML pipelines for enzyme design and the integration of high-throughput automation throughout experimental validation processes. You will play a pivotal role in building and mentoring high-performing teams, cultivating strategic partnerships, and launching collaborative research programs with pharmaceutical, industrial, and government partners. Your passion for developing innovative technologies will help unlock new commercial and scientific opportunities, shaping the future direction of the CPB and the broader field of protein design. This position will be filled at either level based on knowledge and related experience as assessed by the responsibilities (outlined below) will be assigned if hired at the higher level. In this role you will * Provide technical leadership for protein design and engineering programs, setting strategy and direction for multidisciplinary teams. * Develop, implement, and provide highly advanced biotechnical analysis and solutions to resolve highly complex biotechnical and programmatic issues. * Architect and execute R&D strategies for protein engineering and biocatalysis platforms, integrating bioinformatics, analytics, and chemistry. * Develop and implement innovative AI/ML pipelines for enzyme engineering and high-throughput experimental validation. * Provide highly advanced guidance and mentorship to scientists across biochemistry, microbiology, bioinformatics, and analytical chemistry, fostering and supporting their technical growth and collaboration. * Oversee operational management, optimizing project workflows, reducing cycle times, and improving program efficiency. * Coordinate and interface directly with senior management and external sponsors to communicate technical milestones, solicit input from, and provide advice to leaders in the program. * Utilize technical expertise and analytical skills to communicate results through formal and complex technical reports, presentations, and peer-reviewed scientific journals as appropriate. * Lead the launch and execution of research programs and strategic partnerships with Contract Manufacturing Organizations (CMOs), pharmaceutical, industrial, and government partners, spanning diverse applications to expand capabilities and support commercialization. * Drive platform innovation, deploying new technologies in analytical chemistry, cell line development, and direct-to-biology screening. * Secure external funding by co-authoring grant proposals and leading strategic collaborations to advance core technologies. * Perform other duties as assigned. Additional job responsibilities, at the SES.5 level * Serve as a subject matter expert, providing scientific and technical direction for highly complex and sensitive protein design projects. * Champion the development and deployment of revolutionary methods and technologies, influencing the future direction of the organization and the field. * Advise senior management and external stakeholders on strategic technical decisions, representing the organization as the senior technical expert in high-impact collaborations and committees. Qualifications * PhD in Chemistry, Biochemistry, or a related scientific or technical field or the equivalent combination of education and related experience. * Expert-level knowledge and application of enzyme engineering, directed evolution, high-throughput screening, and biocatalysis. Significant experience with a broad range of bioengineering applications, such as biotherapeutics, biosensors, and vaccines. * Significant experience in developing and implementing R&D strategies for platform technologies. * Significant experience and background and demonstrated ability to successfully lead multidisciplinary scientific teams and manage complex research programs. * Demonstrated ability to integrate computational and experimental approaches, including AI/ML and bioinformatics. * Proven success in launching and managing collaborative research programs with external partners. * Expert-level strategic planning, organizational, and project management skills, with the ability to manage complex initiatives across multiple stakeholders. * Expert verbal and written communication skills and significant experience in preparing highly complex analyses and successfully delivering highly advanced technical presentations, as well as expert facilitation and collaboration skills to effectively influence and advise senior management and external sponsors. Additional qualifications at the SES.5 level * Recognized subject matter expertise in protein engineering and design, with significant impact acknowledged both internally and externally. * Extensive experience championing and leading innovative, high-impact scientific programs that advance the field. * Extensive experience and proven track record of successfully leveraging resources and partnerships to develop new project portfolios and drive innovation. Qualifications We Desire * Experience integrating AI/ML tools into protein engineering workflows. * Direct experience with grant writing, co-authoring proposals, and leading pre competitive collaborations. * Familiarity with Laboratory Information Management Systems (LIMS). Additional Information #LI-Hybrid Position Information This is a Flexible Term appointment, which is for a definite period not to exceed six years. If final candidate is a Career Indefinite employee, Career Indefinite status may be maintained (should funding allow). Why Lawrence Livermore National Laboratory? * Included in 2025 Best Places to Work by Glassdoor! * Flexible Benefits Package * 401(k) * Relocation Assistance * Education Reimbursement Program * Flexible schedules (*depending on project needs) * Our values - visit ***************************************** Security Clearance This position requires either no security clearance, or a Department of Energy (DOE) L-level or Q-level clearance depending on the particular assignment. If you are selected and a security clearance is required, we will initiate a Federal background investigation to determine if you meet eligibility requirements for access to classified information or matter. Also, all L or Q cleared employees are subject to random drug testing. L and Q-level clearances require U.S. citizenship. If no security clearance is required, but your assignment is longer than 179 days cumulatively within a calendar year, you must go through the Personal Identity Verification process. This process includes completing an online background investigation form and receiving approval of the background check. (This process does not apply to foreign nationals.) National Defense Authorization Act (NDAA) The 2025 National Defense Authorization Act (NDAA), Section 3112, generally prohibits citizens of China, Russia, Iran and North Korea without dual US citizenship or legal permanent residence from accessing specific non-public areas of national security or nuclear weapons facilities. The restrictions of NDAA Section 3112 apply to this position. To be qualified for this position, Candidates must be eligible to access the Laboratory in compliance with Section 3112. Pre-Employment Drug Test External applicant(s) selected for this position must pass a post-offer, pre-employment drug test. This includes testing for use of marijuana as Federal Law applies to us as a Federal Contractor. Wireless and Medical Devices Per the Department of Energy (DOE), Lawrence Livermore National Laboratory must meet certain restrictions with the use and/or possession of mobile devices in Limited Areas. Depending on your job duties, you may be required to work in a Limited Area where you are not permitted to have a personal and/or laboratory mobile device in your possession. This includes, but not limited to cell phones, tablets, fitness devices, wireless headphones, and other Bluetooth/wireless enabled devices. If you use a medical device, which pairs with a mobile device, you must still follow the rules concerning the mobile device in individual sections within Limited Areas. Sensitive Compartmented Information Facilities require separate approval. Hearing aids without wireless capabilities or wireless that has been disabled are allowed in Limited Areas, Secure Space and Transit/Buffer Space within buildings. How to identify fake job advertisements Please be aware of recruitment scams where people or entities are misusing the name of Lawrence Livermore National Laboratory (LLNL) to post fake job advertisements. LLNL never extends an offer without a personal interview and will never charge a fee for joining our company. All current job openings are displayed on the Career Page under "Find Your Job" of our website. If you have encountered a job posting or have been approached with a job offer that you suspect may be fraudulent, we strongly recommend you do not respond. To learn more about recruitment scams: ***************************************************************************************** Equal Employment Opportunity We are an equal opportunity employer that is committed to providing all with a work environment free of discrimination and harassment. All qualified applicants will receive consideration for employment without regard to race, color, religion, marital status, national origin, ancestry, sex, sexual orientation, gender identity, disability, medical condition, pregnancy, protected veteran status, age, citizenship, or any other characteristic protected by applicable laws. Reasonable Accommodation Our goal is to create an accessible and inclusive experience for all candidates applying and interviewing at the Laboratory. If you need a reasonable accommodation during the application or the recruiting process, please use our online form to submit a request. 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About Sandia Sandia National Laboratories is the nation's premier science and engineering lab for national security and technology innovation, with teams of specialists focused on cutting-edge work in a broad array of areas. Some of the main reasons we love our jobs: * Challenging work with amazing impact that contributes to security, peace, and freedom worldwide * Extraordinary co-workers * Some of the best tools, equipment, and research facilities in the world * Career advancement and enrichment opportunities * Flexible work arrangements for many positions include 9/80 (work 80 hours every two weeks, with every other Friday off) and 4/10 (work 4 ten-hour days each week) compressed workweeks, part-time work, and telecommuting (a mix of onsite work and working from home) * Generous vacation, strong medical and other benefits, competitive 401k, learning opportunities, relocation assistance and amenities aimed at creating a solid work/life balance* World-changing technologies. Life-changing careers. Learn more about Sandia at: ********************* * These benefits vary by job classification. What Your Job Will Be Like We are seeking a postdoctoral researcher to work on the development and applications of scanning electron microscopy techniques for functional characterization of electronic materials and devices. The department currently has two customized microscopes with unique capabilities that include electron beam induced current, cathodoluminescence, scanning ultrafast electron microscopy, and electron plume imaging. The candidate should be self-motivated, able to work independently, and contribute creatively to team efforts. The candidate will be expected to present results at national/international meetings and publish research in high profile peer-reviewed journals. On any given day, you may be called on to: * Conduct experiments using state-of-the-art characterization instrumentation.. * Analyze data using established and custom modeling tools. * Introduce new capabilities by integrating custom hardware. * Present research progress at group meetings, peer review events, and technical conferences. * Write and publish manuscripts in scientific journals Due to the nature of the work, the selected applicant must be able to work onsite. Qualifications We Require * PhD degree in physics, electrical engineering, materials science, chemistry, or a closely related field * Hands-on experience with electron sources and their application to semiconductor characterization. * A record of publications in peer-reviewed journals and presentations at scientific conferences, consisting of a minimum of three (3) first-author or co-authored scientific publications. * Highest degree received not more than five years prior to the date of application and all degree requirements completed before starting the appointment. * Ability to obtain and maintain a DOE Q-level security clearance. Qualifications We Desire * Experience with operando electronic device characterization. * Experience with data acquisition hardware and software * Experience with finite element modeling About Our Team The Materials Physics department performs fundamental research on the structure and properties of materials to support programs in energy research, device physics, materials reliability, and national security. Specific activities include experimental and modeling studies of surface electronic structure and surface atomic structure and dynamics of metals, oxides, low dimensional semiconductors, and adsorbates; atomic-scale structure and composition analysis of metals, semiconductors, and composites; electrical and optical properties of low-dimensional semiconductors and optoelectronic devices; and the structural and electrochemical characterization of solid-state ionic materials. The Department supports internal and external sponsors and government agencies that seek solutions to problems of fundamental scientific inquiry, energy sustainability, and national security Posting Duration This posting will be open for application submissions for a minimum of seven (7) calendar days, including the 'posting date'. Sandia reserves the right to extend the posting date at any time. Security Clearance Sandia is required by DOE to conduct a pre-employment drug test and background review that includes checks of personal references, credit, law enforcement records, and employment/education verifications. Applicants for employment need to be able to obtain and maintain a DOE Q-level security clearance, which requires U.S. citizenship. If you hold more than one citizenship (i.e., of the U.S. and another country), your ability to obtain a security clearance may be impacted. Applicants offered employment with Sandia are subject to a federal background investigation to meet the requirements for access to classified information or matter if the duties of the position require a DOE security clearance. Substance abuse or illegal drug use, falsification of information, criminal activity, serious misconduct or other indicators of untrustworthiness can cause a clearance to be denied or terminated by DOE, resulting in the inability to perform the duties assigned and subsequent termination of employment. EEO All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, or veteran status and any other protected class under state or federal law. NNSA Requirements for MedPEDs If you have a Medical Portable Electronic Device (MedPED), such as a pacemaker, defibrillator, drug-releasing pump, hearing aids, or diagnostic equipment and other equipment for measuring, monitoring, and recording body functions such as heartbeat and brain waves, if employed by Sandia National Laboratories you may be required to comply with NNSA security requirements for MedPEDs. If you have a MedPED and you are selected for an on-site interview at Sandia National Laboratories, there may be additional steps necessary to ensure compliance with NNSA security requirements prior to the interview date. Apply for Job * Careers * Sign In * New User