Associate scientist jobs in Fremont, CA

The Enigma Project (enigmaproject.ai) is a research organization based in the Department of Ophthalmology at Stanford University School of Medicine dedicated to understanding the computational principles of natural intelligence using the tools of artificial intelligence. Leveraging recent advances in neurotechnology and machine learning, this project aims to create a foundation model of the brain, capturing the relationship between perception, cognition, behavior, and the activity dynamics of the brain. This ambitious initiative promises to offer unprecedented insights into the algorithms of the brain while serving as a key resource for aligning artificial intelligence models with human-like neural representations. As part of this project, we seek exceptional individuals with extensive experience building, using, and fine-tuning large-scale multimodal foundation models. The team will be responsible for training frontier multi-modal models on large-scale data of neuronal recordings that relate sensory input to neuronal correlates of perception, action, cognition, and intelligence. We expect the candidate to have expertise in modern deep learning libraries (preferably PyTorch) and recent developments in multimodal foundation models. This position promises a vibrant atmosphere at Stanford University in a collaborative community renowned for expertise in computational neuroscience and deep learning. Role & Responsibilities: Design and implement large-scale multimodal deep learning architectures that relate sensory inputs to neuronal correlates of perception, action, and cognition Develop novel computational approaches for training and optimizing frontier models on unprecedented amounts of neural data Provide technical leadership in distributed training systems and model optimization techniques Guide cross-functional teams in establishing technical frameworks and evaluation metrics for brain foundation models Communicate research findings through publications, presentations, workshops and research blogs Stay ahead of the latest developments in machine learning and neuroscience, and propose innovative solutions to advance the project's goals * - Other duties may also be assigned What we offer: A rich environment in which to pursue fundamental research questions in AI and neuroscience A dynamic team of engineers and scientists in a project dedicated to one mission, rooted in academia but inspired by science in industry. Access to unique datasets spanning artificial and biological neural networks State-of-the-art computing infrastructure Competitive salary and benefits package Collaborative environment at the intersection of multiple disciplines Location at Stanford University with access to its world-class research community Strong mentoring in career development Application: In addition to applying to the position, please send your CV and one page interest statement to: *************************** **The job duties listed are typical examples of work performed by positions in this job classification and are not designed to contain or be interpreted as a comprehensive inventory for all duties, tasks, and responsibilities. Specific duties and responsibilities may vary depending on department or program needs without changing the general nature and scope of the job or level of responsibility. Employees may also perform other duties as assigned. Desired Qualifications: Ph.D. in Computer Science, Machine Learning, Computational Neuroscience, or related field plus 2+ years post-Ph.D. research experience At least 2+ years of practical experience in training, fine-tuning, and using multi-modal deep learning models Strong publication record in top-tier machine learning conferences and journals, particularly in areas related to multi-modal modeling Strong programming skills in Python and deep learning frameworks Demonstrated ability to lead research projects and mentor others Ability to work effectively in a collaborative, multidisciplinary environment Preferred Qualifications: Background in theoretical neuroscience or computational neuroscience Experience in processing and analyzing large-scale, high-dimensional data of different sources Experience with cloud computing platforms (e.g., AWS, GCP, Azure) and their machine learning services Familiarity with big data and MLOps platforms (e.g. MLflow, Weights & Biases) Familiarity with training, fine tuning, and quantization of LLMs or multimodal models using common techniques and frameworks (LoRA, PEFT, AWQ, GPTQ, or similar) Experience with large-scale distributed model training frameworks (e.g. Ray, DeepSpeed, HF Accelerate, FSDP) EDUCATION & EXPERIENCE (REQUIRED): Bachelor's degree and five years of relevant experience, or combination of education and relevant experience. KNOWLEDGE, SKILLS AND ABILITIES (REQUIRED): Expert knowledge of the principles of engineering and related natural sciences. Demonstrated project leadership experience. Demonstrated experience leading and/or managing technical professionals. CERTIFICATIONS & LICENSES: None PHYSICAL REQUIREMENTS*: Frequently grasp lightly/fine manipulation, perform desk-based computer tasks, lift/carry/push/pull objects that weigh up to 10 pounds. Occasionally stand/walk, sit, twist/bend/stoop/squat, grasp forcefully. Rarely kneel/crawl, climb (ladders, scaffolds, or other), reach/work above shoulders, use a telephone, writing by hand, sort/file paperwork or parts, operate foot and/or hand controls, lift/carry/push/pull objects that weigh >40 pounds. * - Consistent with its obligations under the law, the University will provide reasonable accommodation to any employee with a disability who requires accommodation to perform the essential functions of his or her job. WORKING CONDITIONS: May be exposed to high voltage electricity, radiation or electromagnetic fields, lasers, noise > 80dB TWA, Allergens/Biohazards/Chemicals /Asbestos, confined spaces, working at heights 10 feet, temperature extremes, heavy metals, unusual work hours or routine overtime and/or inclement weather. May require travel. The expected pay range for this position is $156,560 to $180,039 annually. Stanford University provides pay ranges representing its good faith estimate of what the university reasonably expects to pay for a position. The pay offered to a selected candidate will be determined based on factors such as (but not limited to) the scope and responsibilities of the position, the qualifications of the selected candidate, departmental budget availability, internal equity, geographic location and external market pay for comparable jobs. At Stanford University, base pay represents only one aspect of the comprehensive rewards package. The Cardinal at Work website (***************************************************** provides detailed information on Stanford's extensive range of benefits and rewards offered to employees. Specifics about the rewards package for this position may be discussed during the hiring process. Consistent with its obligations under the law, the University will provide reasonable accommodations to applicants and employees with disabilities. Applicants requiring reasonable accommodation for any part of the application or hiring process should contact Stanford University Human Resources by submitting a contact form. Stanford is an equal employment opportunity and affirmative action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or any other characteristic protected by law.

SUMMARY/JOB PURPOSE: The Scientist III, Biologics Downstream Process Development will independently conduct laboratory experiments with limited supervision to develop purification processes and support technology transfer and manufacturing of biological drug candidates. The incumbent will utilize their technical expertise in downstream/purification process development of biologics (therapeutic proteins, antibodies, bispecifics, ADCs, etc) to advance CMC development and manufacturing for pre-IND and in-clinic therapeutic proteins.? A strong technical focus is critical to ensure the speed, cost effectiveness, and technical quality of our CMC activities. The incumbent should have excellent hands-on technical abilities and a strong theoretical grasp of purification unit operations such as affinity chromatography, ion exchange chromatography (IEX), ultrafiltration/diafiltration (UF/DF), viral filtration, etc. The incumbent is expected to work in the laboratory full time, including operating state-of-art downstream equipment (FPLC, TFF, depth filtration systems, etc), performing routine instrument maintenance, and providing training to peers. The incumbent is also expected to effectively document lab results and draft test methods/SOPs in accordance with company, departmental, and regulatory guidelines. The individual should have familiarity with upstream process development, analytics, and formulation development, as they will be working closely with these groups, in addition to a general working knowledge of Biologics CMC. ESSENTIAL DUTIES AND RESPONSIBILITIES: Under minimial supervision, develop and execute laboratory studies in downstream process development (chromatography purification, viral filtration, TFF, etc) to support unit operation scale up and technology transfers to enable clinical production. Undertake production campaigns from Lab - Pilot Scale Collaborate with internal and external partners in upstream process development, analytical development, and formulation development groups to advance CMC biologics programs Maintain complete and accurate records of laboratory work in conformance with company standard operating procedures (SOPs) and training. Provide detailed reviews of peer generated data as well as that generated from contracted service providers. Maintain the inventory of laboratory consumables and clean glassware. Coordinate vendors service calls for repair and maintenance of laboratory instruments, perform routine maintenance of laboratory instrumentation, and maintain complete and accurate records of instrument service and repairs in conformance with company SOPs and policies. Work to establish, maintain, and lead internal downstream process development and scale up lab capabilities in CMC Biologics SUPERVISORY RESPONSIBILITIES: None EDUCATION/EXPERIENCE/KNOWLEDGE & SKILLS: Education/Experience: Bachelor's degree in chemistry, biochemistry, biochemical engineering, chemical engineering or related field and a minimum of three (3) years of relevant drug discovery/development experience; or, Master's degree in chemistry, biochemistry, biochemical engineering, chemical engineering or related field and a minimum of one (1) year of relevant drug discovery/development experience; or, Equivalent combination of education and experience. Experience/The Ideal for Successful Entry into Job: Experience applying their technical knowledge to drive critical objectives for CMC biologics across the product life cycle Hands-on experience in recombinant protein purification and downstream process development Familiarity with harvest and clarification unit operations Hands-on experience with Fast Protein Liquid Chromatography (FPLC) systems (e.g. Akta Avant, Akta Pilot, Akta Ready, etc) for chromatography-based purification development. Experience developing scalable chromatography purification unit operations (Affinity, IEX, HIC, SEC, mixed mode, etc). Experience developing scalable viral filtration and TFF unit operations. Working knowledge of CMC upstream process development, analytical development, formulation development, bioconjugation process development, technology transfer, and GMP quality requirements Ability to run basic analytical purity assays (SEC-HPLC) and in-process impurity clearance assays (HCP, res DNA, res ProA) independently Demonstrated capability to work independently on complex technical problems, effectively in cross-functional teams, and with external CDMOs and partners Experience planning, generating, analyzing, and linking experimental capabilities and results to critical CMC objectives Knowledge/Skills: Expertise in downstream (purification) process development Broad and deep knowledge of CMC biologics downstream processes Working knowledge of upstream process development, analytics, formulation development, and bioconjugation process development. Ability to apply technical knowledge to CMC development and manufacturing for biologics across the product life cycle Ability to multi-task in a fast-paced dynamic environment while delivering high quality work Strong understanding of cGMP quality and regulatory requirements for CMC biologics Sets goals with understanding of priority and impact to the program, department, and organization Excellent interpersonal, presentation, and written communication skills Excellent organizational and documentation skills and habits Creative thinker and complex problem solver WORKING CONDITIONS: Environment: primarily working in laboratories Exposures encountered, such as hazardous materials, and extreme cold. Limited travel requirement

I am building a strategic talent pipeline for future opportunities in the biotech space. If you're a senior-level professional with a strong background in commercial operations, sales leadership, or business development, I'd love to connect. Our clients include innovative biotech startups and established industry leaders focused on diagnostics, molecular platforms, and interventional technologies. While this is not a live role, I am actively networking with top talent for upcoming leadership searches. Key Focus Areas Commercial strategy and execution Sales team leadership and scaling Business development and strategic partnerships Market expansion and go-to-market planning Operational excellence and cross-functional collaboration CRM and analytics-driven decision-making (e.g., Salesforce, Tableau, Power BI) Ideal Background 10+ years of experience in biotech, diagnostics, or medical devices Proven track record of revenue growth, team building, or market development Experience with scaling commercial teams or launching new technologies Strong analytical and strategic thinking skills Comfortable in fast-paced, growth-oriented environments

We are seeking an AI EM Application Scientist with a strong conviction and experience in AI electron microscopy, EM-imaging, material science research and failure analysis. The position will support a full sales cycle activity, including but not limited to product AI demonstrations, customer sample preparation recommendation, customer AI workflow optimization, and customer training on Borries Optimus 100 AI EM platform. Key Responsibilities: • Conduct Borries product AI demos, AI workshops, and AI training for customers in materials analysis and research etc. • Help customers design AI workflows on Borries AI EM. • Develop product application notes and co-author scientific publications with our strategic partners. • Gather customer feedback to guide R&D and product roadmap improvements. • Collaborate closely with marketing and engineering teams to deliver customer centric AI solutions. Qualifications: • Master's degree or PhD in materials science, materials engineering, or physics. • 3-8 years of hands-on experience with EM sample preparation, EM imaging and analysis. • Familiarity with AI EM workflows in material science research and failure analysis is a plus. • Excellent communication and presentation skills. • Self-driven, adaptable, and able to thrive in a startup environment.

Amber Bio is a biotechnology company pioneering new gene editing modalities using multi-kilobase edits to reach previously undruggable patient populations. Founded by pioneers in the CRISPR field from leading institutions for gene editing research, the company is developing a first-of-its-kind RNA editing platform that can correct thousands of bases at once, thereby correcting genetic mutations safely and reversibly. If you are interested in building a new frontier in genetic medicine, we welcome you to apply. Job Description: Research Associate III/ Senior Research Associate (Biodesigner), Assay Development / Bioanalytical Development Position Overview: The Research Associate III/ Senior Research Associate in Assay Development and Bioanalytical Development will play a critical role in the development, qualification, and validation of bioanalytical methods to support our RNA editing programs. The successful candidate will work under the guidance of an assay development scientist to develop custom assays for the analysis of samples, including AAVs, cells, and tissues. This role also involves drafting key documents such as Standard Operating Procedures (SOPs) and method development reports. Key Responsibilities: Method Development, Qualification, and Validation: Support the development, qualification, and validation of bioanalytical methods in accordance with regulatory guidelines. Develop, optimize, and execute robust bioanalytical methods for the characterization, release, and stability testing of Amber's gene therapy. Sample Analysis: Support drug absorption, distribution, metabolism, and excretion studies. Perform analysis of AAVs, cells, and tissues to support various stages of research and development. Lead efforts to streamline and optimize sample storage and processing, as well as establishing and maintaining critical reagent stocks and cell banks. Documentation Reporting: Draft and review key documents such as SOPs, method development, and sample analysis reports. Maintain accurate and detailed records of all experiments and analyses. Collaboration & Communication Collaborate with manufacturing and preclinical teams to support pipeline needs. Communicate and present findings clearly to internal stakeholders. Qualifications: B.A./B.S. or M.S. in Molecular Biology, Biochemistry, Analytical Chemistry, or a related field. 3+ years of experience in bioanalytical and assay development in the biotechnology or pharmaceutical industry. Demonstrated strong proficiency in a wide range of molecular biology techniques such as molecular cloning, DNA/RNA extractions, RT-qPCR, dd PCR, and ELISA. Experience with cell-based assays and detection methods such as fluorescence, luminescence, and ECL. Hands-on experience using laboratory automated systems (e.g., liquid handlers, extraction robotics, etc.). Background in RNA-based therapies is highly desirable. Experience writing SOPs and reports supporting IND filings (e.g. development, qualification sample analysis reports, etc.) Knowledge of FDA and ICH guidelines for method development, qualification, and validation. Prior history in compiling and analyzing data and generating reports that are routinely presented to project teams. Ability to work effectively in a collaborative, fast-paced environment. Preference will be given to those who display: High motivation, with a strong work ethic and dedication to generating impact. Attention to detail, with the ability to extract deep insights from data. Ability to go from ideation to data in an independent fashion. Long-term personal vision with defined career goals. Team-oriented thinking. Demonstrated excellence in small team environments, including a “no task is too small” attitude. If you have a passion for advancing gene editing technologies and desire to be part of a pioneering biotech company, we encourage you to apply and join our ambitious team. Please apply directly through LinkedIn. Amber Bio is an equal-opportunity employer and encourages applications from candidates of diverse backgrounds. We value diversity and are committed to creating an inclusive and supportive work environment for all employees.

⚡ Research Scientists/Engineers (all levels) 🔍 Focus on Vision Data Infrastructure 🤖 Fundamental AI Research Institute 🌎 San Francisco Bay Area, USA 💸 $250,000 - $600,000 salary + annual bonus Come join one of the only research institutions globally with resources to compete with top AI companies =>10s of 1000s of GPUs to explore state-of-the-art research in LLMs, Multimodal and Agentic AI. Currently seeking AI talent with expertise in building scalable pipelines for vision data to support both image/video generative training and multi-modal alignment. You'll design high-performance pipelines for large-scale image and video datasets, enabling efficient pretraining, alignment, and simulation-based data generation. Responsibilities: Vision Data Sourcing & Curation Collect and organize image and video data from open datasets and the web. Handle data cleaning, filtering, deduplication, and metadata generation. Ensure ethical and compliant data collection at scale. Processing & Augmentation Build high-throughput pipelines for vision data preprocessing (frame extraction, resolution normalization, format conversion, latent caching). Implement GPU-accelerated augmentation and distributed data loading (WebDataset, TFRecords, Parquet). Synthetic & Simulation-Based Data Generation Use simulation tools (e.g., Unreal Engine 5, Isaac Sim, Unity) to generate high-quality synthetic vision data. Create specialized datasets for VLM training, visual reasoning, and agent interaction. Requirements: Strong experience with data engineering, computer vision, or machine learning infrastructure. Expertise in building and scaling ETL/data pipelines for large unstructured datasets. Proficiency with Python, PyTorch, and distributed data frameworks (e.g., Ray, Spark, Dask). Experience with WebDataset, TFRecords, Parquet, or similar high-throughput data formats. Familiarity with GPU-accelerated preprocessing, NVIDIA DALI, or equivalent systems. Understanding of image/video codecs, data compression, and cloud storage optimization. Preferred Experience: Prior work with simulation-based or synthetic data generation using Unreal Engine, Isaac Sim, or Unity. Experience curating datasets for multimodal or vision-language model training. Knowledge of data ethics, privacy, and compliance frameworks for large-scale AI datasets. Experience contributing to open datasets or data-centric AI research. Why apply: Opportunity to join a fast-growing core team that are already pushing AI breakthroughs Highly competitive salary package Work alongside ambitious and bright superstars from tech and academia Medical, Dental and Vision Insurance Relocation package available 🌎 San Francisco Bay Area, USA 📧 Interested in applying? Please click on the ‘Easy Apply' button or alternatively email me your resume at ************************

Job Title: Scientist I - Chemistry Duration: 12 months The Scientist I, Manufacturing Sciences, will be responsible for the synthesis of functionalized resins used in columns. Use manufacturing protocols to accurately synthesize raw and functionalized resins for column production Address and report problems in daily manufacturing and propose effective countermeasures Communicate effectively with other production staff regarding delays, issues in production, etc Draft and revise SOPs to the ISO9001 standard and collaborate with senior chemists in their revisions Interact efficiently in a cross-functional setting across several departments Collaborate in PPI initiatives to improve overall quality and yields of various synthesized resins Participate in 5S, JDI, and Safety initiatives Required: Requires a Bachelor's degree or higher in Chemistry. 0-1 years of experience in a manufacturing environment Direct experience with polymer chemistry Experience with chromatography software, H/UPLC, and interpretation of chromatograms Knowledge of analytical chemistry ideology and principles is a plus Ability to perform routine analysis on the size distribution and surface area of resins Solid understanding of manufacturing environments and standard chemistry techniques and principles Familiarity working with standard software programs such as Microsoft Word, Excel, and PowerPoint.

We are a group of people united by a strong purpose. We want you to get to know us, and Giuseppe, our very own artificial intelligence. We love good food, but above all, we love the planet, and that's why, to protect it, we reinvent the food industry, one delicious bite at a time, elevating what we eat, through our technology and based on plants. Our recipe has three mega-important components: science, technology, and of course, disruptive talents who work daily to create a better future. At NotCo we are not and do not seek to be the perfect company, but rather the right one. We are here to produce changes, and that is why we dare, fail, and sometimes achieve incredible successes. We are currently looking for a Product Development Scientist for our NotCo B2B Research & Development located in San Francisco, California, requiring an active on-site presence. This position will report to our R&D Sr. Team Lead and the incumbent will work cross-functionally to ensure R&D activities are successfully deployed locally. Responsible for the: Independently conducts day-to-day product development activities as directed by the manager across multiple projects. This includes supporting activities related to the full product lifecycle process (from product concept to successful commercial launch as needed)and supporting process development, scale-up and technology transfer Supports the design and execution of bench-top tests, pilot-plant trials and full-scale formulations to deliver high-quality food products that meet and exceed the sensory, cost, and other performance targets Proactively proposes and uses sensory and analytical analysis to guide and validate the development process Maintains detailed documentation, experiment tracking and outcomes, and documents finished goods and ingredient specifications Provides feedback to project lead regarding relevant technical and process information Communicates proactively and effectively with cross-functional teams, clearly articulating perspectives and trade-offs related to new product development goals Utilizes NotCo's proprietary AI technology to develop and improve food products Supports formula validation activities as well as process development, scale-up and technology transfer Engages in client communications and workshops, bringing technical Maintains detailed documentation across all R&D activities in a timely manner Qualifications / Requirements: Bachelor's degree in Food Engineering, Food Science, Engineering in Biotechnology or a similar discipline. 2 + years of Food R&D experience is desired, preferably across both food and beverage categories. Be agile, adaptable, and thrive in a dynamic and changing culture; works relentlessly to overachieve, anticipate obstacles, and create plans to overcome them. Adapts easily to changing priorities and direction based on new project learnings and team priorities. Demonstrated competency to effectively communicate (oral & written) cross-functionally with solid collaboration skills. Comfortable in client-facing situations and able to communicate complex topics clearly and simply. Excel in a startup environment, is excited to create new procedures and processes from scratch and has a strong entrepreneurial mindset. Be a problem solver, have a general manager mindset, and take the initiative to get the job done Possess strong planning, project management, and execution skills, and the ability to articulate where and how you have used them. Rigorous data-driven/analytical capability and ability and presence to present data effectively to a leadership team Work well in teams and cross-functional groups in a matrixed environment, both regionally and globally Possesses strong computer skills, including a high level of proficiency in MS Office, specifically Excel Authorization to work in the U.S. is required Ability to travel up to 50% of the time, including international travel and extended trips. NotCo is committed to fair and equitable compensation practices. The pay range for this role is $65,000 - $75,000. Actual compensation packages are based on several factors that are unique to each candidate, including but not limited to skill set, depth of experience, certifications, and specific work location. This may be different in other locations due to differences in the cost of labor. We are an equal opportunity employer. All applicants will be considered for employment without attention to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status.

Yoh is looking for a skilled and driven Senior Research Scientist, Biophysics with hands-on experience in small molecule drug discovery to join our collaborative Lead Discovery team. This is a lab-based role focused on the biophysical and mechanistic characterization of small molecule-protein interactions to support our drug discovery pipeline. Industry: Discovery and Development Location: South San Francisco, CA Key Responsibilities: Design and execute binding characterization studies using SPR (Biacore S200 and 8K+). Conduct routine compound screening and mechanistic studies using biophysical assays (e.g., nano DSF, DLS, Spectral Shift). Manage and coordinate outsourced biophysical studies with CROs. Analyze and interpret data to support SAR and lead optimization across multiple projects. Maintain detailed experimental records and present findings in internal meetings and reports. Qualifications: PhD in Biophysics, Biochemistry, or a related field. Minimum 3 years of relevant experience in small molecule drug discovery biophysics (industry or academic). Proven expertise in SPR assay development and data interpretation. Demonstrated expertise in designing, developing, and interpreting biophysical characterization of small molecule-protein interactions by SPR. Strong familiarity with additional biophysical techniques (TSA, DLS, Spectral Shift, NMR, ITC, etc.). Proficiency with data analysis and graphing tools is a plus. Ideal Candidate Attributes: Critical thinker with the ability to integrate complex data and communicate insights clearly. Thrives in a fast-paced, collaborative environment. Proactive in identifying challenges and implementing solutions. Passionate about science and making a meaningful impact. Contributes positively to team culture and company values. #IND-SPG Estimated Min Rate: $70.00 Estimated Max Rate: $80.00 What's In It for You? We welcome you to be a part of the largest and legendary global staffing companies to meet your career aspirations. Yoh's network of client companies has been employing professionals like you for over 65 years in the U.S., UK and Canada. Join Yoh's extensive talent community that will provide you with access to Yoh's vast network of opportunities and gain access to this exclusive opportunity available to you. Benefit eligibility is in accordance with applicable laws and client requirements. Benefits include: Medical, Prescription, Dental & Vision Benefits (for employees working 20+ hours per week) Health Savings Account (HSA) (for employees working 20+ hours per week) Life & Disability Insurance (for employees working 20+ hours per week) MetLife Voluntary Benefits Employee Assistance Program (EAP) 401K Retirement Savings Plan Direct Deposit & weekly epayroll Referral Bonus Programs Certification and training opportunities Note: Any pay ranges displayed are estimations. Actual pay is determined by an applicant's experience, technical expertise, and other qualifications as listed in the job description. All qualified applicants are welcome to apply. Yoh, a Day & Zimmermann company, is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran. Visit ************************************************ to contact us if you are an individual with a disability and require accommodation in the application process. For California applicants, qualified applicants with arrest or conviction records will be considered for employment in accordance with the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act. All of the material job duties described in this posting are job duties for which a criminal history may have a direct, adverse, and negative relationship potentially resulting in the withdrawal of a conditional offer of employment.

Clorox is the place that's committed to growth - for our people and our brands. Guided by our purpose and values, and with people at the center of everything we do, we believe every one of us can make a positive impact on consumers, communities, and teammates. Join our team. #CloroxIsThePlace Your role at Clorox: The Research and Development organization is embedded within each of our Clorox businesses, taking new generations of consumer products from concept to reality. With such diverse roles as engineers, scientists, packaging experts, and technicians R&D is a community of technical leaders and managers actively involved in virtually every step in the lifecycle of our products, from initial concept to raw materials to final goods on store shelves. R&D is committed to leveraging the latest technology to bring consumers the high-quality, innovative products they expect and deserve. In this role, you will: As an R&D Product Development Scientist 2 at Clorox you will play a pivotal role in driving technical excellence and ensure superior product innovation across our Consumer Products and Professional Products portfolios. You'll apply your PhD-level expertise to develop and optimize product formulations that meet the needs of diverse end users from everyday consumers to hospital disinfection. Collaborating cross-functionally with teams in Marketing, Sales, Insights, Microbiology, Analytical Chemistry, and Digital Data, you'll translate scientific insights into impactful product solutions. You'll make a difference from day one, contributing to products used by millions of people while growing your technical and leadership skills working on some of the most trusted brands in the consumer goods industry. In this role you will: Drive Innovation: Develop and refine novel product formulations that deliver a superior product experience, while also creating consumer and customer facing claims and demos Execute with Excellence: Troubleshoot formulation challenges and make relevant measurements to generate data that supports technical solutions and translates them into business impact, while maintaining product specifications, formulation standards, and technical documentation to ensure consistency and compliance. Own the Technical Details: Identify and document novel technical solutions and formulation approaches that may be eligible for intellectual property protection and ensure Clorox's competitive advantage. Support Commercialization: Develop and apply SOPs, test methods, and best practices while leading product and consumer testing, and continuously research ways to evolve and improve R&D tools and approaches to ensure consumer delight and successful product launches. Collaborate Across Functions Work closely with Marketing, Sales, Digital Data, Insights, and cross-functional R&D teams to analyze problems from multiple points of view and connect disparate ideas to create innovative solutions, proposals, and concepts. Grow your Career: Be part of a team that values playing to win, technical curiosity, and raising the bar where your contributions help shape the future of Product Innovation at Clorox. What we look for: Ph.D. Chemistry, Chemical Engineering, or a related field Candidates must have education and expertise in at least one of the following areas: Aqueous oxidants, kinetics, and equilibria for cleaning, bleaching and antimicrobials Organic chemistry, aqueous surfactants, colloids, and interfacial science for household product formulation. Water soluble polymers for household product formulation. Experience in evaluation, characterization, and measurement of technology in their area of expertise Confident self-starter, critical thinker, capable of working independently and cross-functionally with minimal supervision and direction in a fast-paced environment. Workplace type: Our values-based culture connects to our purpose and empowers people to be their best, professionally and personally. We serve a diverse consumer base which is why we believe teams that reflect our consumers bring fresh perspectives, drive innovation, and help us stay attuned to the world around us. That's why we foster an inclusive culture where every person can feel respected, valued, and fully able to participate, and ultimately able to thrive. Learn more. [U.S.]Additional Information: At Clorox, we champion people to be well and thrive, starting with our own people. To help make this possible, we offer comprehensive, competitive benefits that prioritize all aspects of wellbeing and provide flexibility for our teammates' unique needs. This includes robust health plans, a market-leading 401(k) program with a company match, flexible time off benefits (including half-day summer Fridays depending on location), inclusive fertility/adoption benefits, and more. We are committed to fair and equitable pay and are transparent with current and future teammates about our full salary ranges. We use broad salary ranges that reflect the competitive market for similar jobs, provide sufficient opportunity for growth as you gain experience and expand responsibilities, while also allowing for differentiation based on performance. Based on the breadth of our ranges, most new hires will start at Clorox in the first half of the applicable range. Your starting pay will depend on job-related factors, including relevant skills, knowledge, experience and location. The applicable salary range for every role in the U.S. is based on your work location and is aligned to one of three zones according to the cost of labor in your area. -Zone A: $88,700 - $165,900 -Zone B: $81,300 - $152,100 -Zone C: $73,900 - $138,300 All ranges are subject to change in the future. Your recruiter can share more about the specific salary range for your location during the hiring process. This job is also eligible for participation in Clorox's incentive plans, subject to the terms of the applicable plan documents and policies. Please apply directly to our job postings and do not submit your resume to any person via text message. Clorox does not conduct text-based interviews and encourages you to be cautious of anyone posing as a Clorox recruiter via unsolicited texts during these uncertain times. To all recruitment agencies: Clorox (and its brand families) does not accept agency resumes. Please do not forward resumes to Clorox employees, including any members of our leadership team. Clorox is not responsible for any fees related to unsolicited resumes.

NVIDIA is looking for a dedicated Deep Learning Scientist specializing in LLM training datasets engineering. This is a highly technical role requiring deep expertise in machine learning, data science and data engineering to develop innovative solutions that address the unique challenges of training foundation models. This role involves addressing innovative machine learning challenges through building and improving our data ecosystem. What you'll be doing: Develop datasets for LLM pre-training and post training (fine-tuning and reinforcement learning), optimize models and evaluate performance. Design and implement data strategies for model training and evaluation that includes data collection, cleaning, labeling, augmentation, RL verifier datasets to improve model performance. Actively identify and manage data issues such as outliers, noise, and biases. Generate high-quality synthetic data to augment existing datasets, especially for domain-specific or safety-critical use cases and multi-modal use cases (text, image, video, etc) Define data annotation guidelines and curate high-quality labeled datasets for model alignment, including reinforcement learning with human feedback (RLHF). Conduct experiments to optimize Large Language Models with SFT and RL techniques. Design and develop systems for reasoning, tool calling, multi-modal processing, RL verifiers. Implement post-training tasks for LLMs, including fine-tuning, RL, distillation, and performance evaluation, and adjust hyperparameters to improve model quality. Partner with ML researchers, data scientists, and infrastructure teams to understand data needs, integrate datasets, and deploy efficient ML workflows. What we need to see: You have a Master's or PhD in Computer Science, Electrical Engineering or related field - or equivalent experience. 3+ years of work experience in developing datasets and training large language models or other generative AI models. Hands-on programming expertise in python. Solid understanding of machine learning concepts and algorithms for managing data and experiments, including multi-modal datasets. Experience with synthetic data generation techniques, and evaluation strategies. Background with high-performance data processing libraries and machine learning frameworks like PyTorch, Data Loader, TensorFlow Data. Experience with alignment/fine-tuning of LLMs, VLMs (img-to-text, vid-to-text)or any-to-text large models. Familiarity with distributed training paradigms and optimization techniques. Good at problem solving and analytical ability as well as excellent collaboration and communication skills. Demonstrates behaviors that build trust: humility, transparency, respect, intellectual integrity. Ways to stand out from the crowd: Strong track record of contributions to open-source data tools or research publications. Experience with cloud platforms (e.g., AWS, GCP, Azure) and data storage systems (e.g., S3, Google Cloud Storage). Stay ahead of research: Continuously evaluate new tools, techniques, and methodologies in data engineering and generative AI to improve training data infrastructure. Passion for AI and a demonstrated commitment to advancing the field through innovative research, prior scientific research and publication experience. With highly competitive salaries and a comprehensive benefits package, NVIDIA is widely considered to be one of the technology industry's most desirable employers. We have some of the most forward-thinking and hardworking people in the world working with us and our engineering teams are growing fast in some of the hottest state of the art fields: Deep Learning, Artificial Intelligence, and Large Language Models. If you're a creative engineer with a real passion for robust and enjoyable user experiences, we want to hear from you. Your base salary will be determined based on your location, experience, and the pay of employees in similar positions. The base salary range is 148,000 USD - 235,750 USD for Level 3, and 184,000 USD - 287,500 USD for Level 4. You will also be eligible for equity and benefits. Applications for this job will be accepted at least until October 21, 2025.NVIDIA is committed to fostering a diverse work environment and proud to be an equal opportunity employer. As we highly value diversity in our current and future employees, we do not discriminate (including in our hiring and promotion practices) on the basis of race, religion, color, national origin, gender, gender expression, sexual orientation, age, marital status, veteran status, disability status or any other characteristic protected by law.

Artech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients' immediate skill-sets availability, deliver emerging technology skill-sets, refresh existing skill base, allow for flexibility in project planning and execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost. Job Description • Plan and execute scientific experiments in collaboration with a multi-functional project team coordinated by a Project Leader, in support of pharmaceutical product developm ent. • Experienced individual contributor in a relevant scientific field. • Has a broad range of basic technical skills and laboratory skills to support inhalation drug products that can be applied to routine and non-routine scientific studies. • Proficient with laboratory and/or technical tools used to support inhalation drug products . • Awareness/proven experience for safe handling of chemicals, potentially dangerous materials and equipment. • Characterize physicochemical and aerosol performance of formulations and drug products. • Plan, organize, perform, and document complex scientific experiments requiring evaluation of various factors. • Maintain accurate and well organized laboratory records, worksheets and notebooks. • Make detailed observations, document and analyze raw data and contribute to the interpretation of results. Propose and provide input for the design of subsequent experiments. • May act as test method owner capable of training new hires • May act as study lead for test protocols • Write lab procedures, reports, and/or SOPs. • Work according to appropriate SOPs, GMP, GLP, QM, HSE, ISEC, and company Guidelines. • Maintain current training requirements • Adhere to Quality culture and ensure a safe working environment • Contribute to the continuous improvement of existing Quality, Compliance and Safety processes and systems. • Contribute to maintenance of infrastructure/equipment. • Evaluate new lab equipment and/or instruments. • Schedule and perform routine maintenance of lab instruments/equipment. Conduct routine lab inspections. • May serve as a laboratory owner (e.g., safety inspections, chemical inventory, etc.) • Proactive in identifying and solving problems of a semi-routine nature, with generally defined solution strategy and new assignments. • Optimize existing methods and develop more efficient ones. • Communicate and address problems, perform safety and literature searches under moderate guidance from more experienced team members. • Leadership • Normally receives general instructions on new assignments. May determine methods and procedures on new assignments • Others seek advice on simple tasks. Trains others how to execute simple tasks. • Executes complex tasks. Analyzes simple data and makes simple conclusions, e.g., identify obvious trends • Basic oral presentation skills and scientific/technical writing skills. • Working knowledge of MS word, Excel, and PowerPoint is required. Qualifications Education: B.S. and minimum of >5 years of related experience in pharmaceutical industries or MS (or equivalent) and >3 years of related experience. Equivalent experience may be accepted. Additional Information For more information, Please contact Sneha Shrivastava ************

Help define the next generation of mass profiling data analysis software! Agilent is developing a unified profiling software program to provide customers with an integrated workspace with feature finding, statistical analysis, identification and reporting capabilities. As a part of this effort, we are seeking a talented R&D Product Owner to guide this new vision into reality. You will work with an Agile software development team to produce innovative solutions for our customers that will improve profiling data analysis experience. The primary responsibility of this role is defining the requirements needed to meet Agilent's goals for the next generation software application. This requires a detailed understanding of customer needs and workflows as well as fluency in Agile software development methods and processes. The ideal candidate must be able to break down the requirements into clear tasks that software development teams can take and build into the product features and provide detailed acceptance criteria to enable both the correct implementation and quality assurance. Other responsibilities include helping to provide collateral for outbound marketing and visiting customers to get clarity on their workflows and pain points. Translate product roadmap features into well-defined product requirements including features, user stories, and acceptance test criteria. Prioritizes and maintains the sprint backlog for assigned products, balancing the requirements of stakeholders. Leads the product functional design process based on an intimate knowledge of the users and technology. Works with cross-functional teams and various stakeholders, including analytics, design/user experience, engineering, and user enablement. Maintain subject matter expertise with a deep understanding of the technical details within your focus area. Help in discussing (and negotiating) priority decisions with product marketing. Qualifications Bachelor's or master's degree in chemistry, biochemistry, or related field. Candidate with Ph.D. or Post Doctorate studies or application in Chemistry and Analytical Chemistry with expertise in Mass Spectrometry is a plus! 8+ years of working of relevant work experience is required with 3 or more years of direct Mass Spectrometry and software data analysis experience is required. Candidates with both small molecule and biopharma large molecular analysis highly desired. #LI-SM1 Additional Details This job has a full time weekly schedule. Applications for this job will be accepted until at least November 6, 2025 or until the job is no longer posted.The full-time equivalent pay range for this position is $167,328.00 - $261,450.00/yr plus eligibility for bonus, stock and benefits. Our pay ranges are determined by role, level, and location. Within the range, individual pay is determined by work location and additional factors, including job-related skills, experience, and relevant education or training. During the hiring process, a recruiter can share more about the specific pay range for a preferred location. Pay and benefit information by country are available at: ************************************* Agilent Technologies, Inc. is an Equal Employment Opportunity and merit-based employer that values individuals of all backgrounds at all levels. All individuals, regardless of personal characteristics, are encouraged to apply. All qualified applicants will receive consideration for employment without regard to sex, pregnancy, race, religion or religious creed, color, gender, gender identity, gender expression, national origin, ancestry, physical or mental disability, medical condition, genetic information, marital status, registered domestic partner status, age, sexual orientation, military or veteran status, protected veteran status, or any other basis protected by federal, state, local law, ordinance, or regulation and will not be discriminated against on these bases. Agilent Technologies, Inc., is committed to creating and maintaining an inclusive in the workplace where everyone is welcome, and strives to support candidates with disabilities. If you have a disability and need assistance with any part of the application or interview process or have questions about workplace accessibility, please email job_******************* or contact ***************. For more information about equal employment opportunity protections, please visit *************************************** Required: OccasionalShift: DayDuration: No End DateJob Function: R&D

CEPTON (A Koito Group Company, Automotive Tier1), a leading intelligent lidar solution provider, is seeking a seasoned R&D Sensor System Algo Scientist who is passionate about solving challenges related to advanced sensor technology to join us. Working as part of our brilliant R&D HW & system teams and closely interfacing with our professional and highly capable SW development team, you will work in a dynamic, cross-functional, collaborative work environment for the advanced LiDAR product driven by the robust embedded system for automotive and non-automotive customers. Here at CEPTON, we use technology to make some difficult problems become easy and some impossible tasks become feasible. We value one's ability to learn higher than the knowledge one has acquired in the past. We enjoy solving hard problems together. As we are at the cutting edge of technological advancement, join us if you are willing to work with like-minded people to face the challenges posed by the new era of technology, together with opportunities to work with strong industry leaders in the fields of automotive OEM, ADAS, and Imaging based AI application. What You Will Do Collaborate with the R&D Systems team to design, integrate, and validate high-speed embedded platforms spanning commercial CPUs, FPGAs, MCUs, and Cepton ASIC chipsets. Prototype LiDAR-enabling algorithms in Python, build reference datasets/tools, and port/optimize implementations in C/C++ for embedded targets. Develop and maintain C-level firmware, device drivers, and board-support code (e.g., SPI/I²C/UART, Ethernet/PCIe, DMA, timers/interrupts) for real-time operation on heterogeneous SoC/FPGA systems. Define and implement hardware/software interfaces; support module-level bring-up, and perform system-level co-simulation and integration with algorithm models. Deliver production-quality embedded C/C++ (and Rust where appropriate) from prototype through pre-production, including code reviews, unit/integration tests, and CI. Diagnose and resolve issues across algorithm / firmware / software / hardware boundaries; drive root-cause analysis, fixes, and regressions. Analyze and quantify end-to-end system performance and margins (e.g., latency, cycle time, compute/memory bandwidth, power) and implement targeted optimizations. Create Python tooling for automation, data capture/analysis, and testbenches to accelerate development and verification Who You Are PhD/Postdoc in CE/EE/CS/Physics, or MS + 5 years (or BS + 8 years) in embedded systems development. Strong proficiency in C for embedded systems (bare-metal or RTOS): drivers, BSP, interrupts/ISRs, timers, DMA, memory-mapped I/O. Working knowledge of Python for algorithm prototyping, data/fixture tooling, and test automation; ability to translate Python reference code into efficient C implementations. Solid grasp of real-time/concurrency concepts: interrupt-driven design, multi-threading (RTOS), memory management (static allocation, ring buffers), latency/jitter budgeting. Experience with ARM-based MCUs/SoCs and heterogeneous SoC/FPGA systems; comfortable reading schematics and working with HW teams. Hands-on with common interfaces: SPI, I²C, UART, CAN (nice), Ethernet/PCIe, GPIO; familiarity with boot/bring-up flows (bootloaders, secure boot basics). Strong debugging skills with JTAG/SWD, gdb, logic analyzer/oscilloscope; methodical root-cause analysis across HW/FW/SW boundaries. Good engineering hygiene: version control (Git), unit/integration testing, and build systems (e.g., CMake). Preferred Qualifications Proficiency in C++ (embedded-safe subset) or Rust for selected components; comfort disabling exceptions/RTTI or using no_std where appropriate. Exposure to Linux on ARM (user-space HALs or kernel drivers for PCIe/Ethernet/DMA). Collaboration with FPGA teams: AXI/AXI-Lite register interfaces, timing/throughput considerations; Xilinx/AMD toolchains (Vivado, IP Integrator) a plus. Background in signal processing / LiDAR algorithms (fixed-point, SIMD/NEON, profiling / optimization). Familiarity with electrical design fundamentals for embedded devices (power, clocks, signal integrity) and bench validation. What We Will Offer Opportunities to work with strong industry leaders and opportunities to relocate to Silicon Valley. Competitive compensation package. Comprehensive employee benefits program, including medical, dental, vision, life, disability, and more. Paid time off and paid holidays Bonus Program eligibility. 401k, FSA and/or HSA. Location: Cepton Headquarters - San Jose, CA (fully on-site). Some local on-site visits to key customers. Travel to regional customer sites and support trade shows and conferences, if needed. Cepton is committed to fair and equitable compensation practices. The pay range for this role is $160,000 to $220,000. Actual compensation packages are based on several factors that are unique to each candidate, including but not limited to skill set, depth of experience, certifications, and specific work location. This may be different in other locations due to differences in the cost of labor. The total compensation package for this position may also include an annual performance bonus, benefits and/or other applicable incentive compensation plans. Cepton Technologies is an Equal Opportunity Employer We are an Equal Opportunity Employer and do not discriminate against applicants due to race, ethnicity, gender, veteran status, or on the basis of disability or any other federal, state, or local protected class. About Cepton, Inc. Cepton, Inc. provides state-of-the-art, intelligent, lidar-based solutions for a range of markets such as automotive (ADAS/AV), smart cities, smart spaces and smart industrial applications. Cepton's patented MMT -based lidar technology enables reliable, scalable and cost-effective solutions that deliver long range, high resolution 3D perception for smart applications. Founded in 2016 and led by industry veterans with over two decades of collective experience across a wide range of advanced lidar and imaging technologies, Cepton is focused on the mass market commercialization of high performance, high quality lidar solutions. Cepton is headquartered in San Jose, California, USA, with a presence in Germany, Canada, Japan and India, to serve a fast-growing global customer base. Salary range$160,000-$220,000 USD

Neurodegenerative diseases are one of the largest medical challenges of our time. Denali Therapeutics is a biotechnology company dedicated to developing breakthrough therapies for neurodegenerative diseases through our deep commitment to degeneration biology and principles of translational medicine. Denali is founded on the collaboration of leading scientists, industry experts, and investors who share the vision that scientific discovery energetically applied to translational medicine is the key to delivering effective therapies to patients. We invite you to consider an opportunity with Denali to help achieve our goal of delivering meaningful therapeutics to patients. We are seeking a highly motivated and collaborative Associate Scientist to join our Bioprocess Development team. This is a lab-based position focused on executing and optimizing mammalian cell culture processes to support clinical manufacturing. The successful candidate will be responsible for setting up and running bioreactor experiments, analyzing cell culture performance, and supporting process improvements. The candidate will also collaborate with the cell line development team to support the generation and evaluation of commercially viable cell lines for novel and complex therapeutic molecules. Key Accountabilities/Core Job Responsibilities: * Independently execute and analyze lab-scale fed-batch bioreactor experiments to support upstream process development and optimization efforts. * Support hands-on cell line development workflows, including transfection, selection, single cell cloning, clone screening, and banking. * Operate, maintain, and troubleshoot key laboratory equipment such as Vi-CELL, Nova Flex2, Octet, and bench-scale bioreactors. * Maintain accurate and timely lab notebooks and author clear, well-structured technical development reports. * Actively contribute to platform process improvements and evaluate emerging technologies through practical lab testing. * Consistently follow established experimental protocols and lab workflows and provide input for their refinement and improvement. Qualifications/Skills: * BA/BS or MS degree in biology, biochemistry, chemical engineering, or related scientific discipline with 3+ years mammalian cell culture experience in the biotech/biopharma industry * Good understanding of mammalian/CHO cell culture and upstream process development concepts * Hands on experience with AMBR bioreactor systems is a plus * Excellent critical thinking, scientific problem-solving, communication skills and strong attention to detail * Experience in executing projects with ambitious timelines with the ability to adapt to rapid changes in project priorities Salary Range: $107,000.00 to $131,000.00 . Compensation for the role will depend on a number of factors, including a candidate's qualifications, skills, competencies, and experience. Denali offers a competitive total rewards package, which includes a 401k, healthcare coverage, ESPP and a broad range of other benefits. Learn more at ****************************************** This compensation and benefits information is based on Denali's good faith estimate as of the date of publication and may be modified in the future.This compensation and benefits information is based on Denali's good faith estimate as of the date of publication and may be modified in the future. Denali is committed to its core company value of unity by creating a diverse and inclusive environment. We are proud to be an equal opportunity employer and do not discriminate against any employee or applicant for employment because of race, color, sex, age, national origin, religion, sexual orientation, gender identity and/or expression, status as a veteran, basis of disability, or any other federal, state, or local protected class.

Scientist II Do you want to be part of an inclusive team that works to develop innovative therapies for patients? Every day, we are driven to develop and deliver innovative and effective new medicines to patients and physicians. If you want to be part of this exciting work, you belong at Astellas! Astellas Pharma Inc. is a pharmaceutical company conducting business in more than 70 countries around the world. We are committed to turning innovative science into medical solutions that bring value and hope to patients and their families. Keeping our focus on addressing unmet medical needs and conducting our business with ethics and integrity enables us to improve the health of people throughout the world. For more information on Astellas, please visit our website at ***************** Purpose and Scope: The primary purposes of the Scientist II, in Formulation & Analytical Development, are to design, evaluate and develop suitable formulations and manufacturing processes for rAAV drug product under development, supporting the growing and diversifying portfolio of programs within AGT's pipeline. This position will be based onsite in our South San Francisco, CA location. Responsibilities * Evaluate and understand the properties of new rAAV and propose formulations with sufficient stability during storage and suitability for clinical use. * Conduct in-use stability and delivery device compatibility studies to ensure the quality of drug products during administration at clinical sites. * Author regulatory documents such as IND and briefing documents for meetings with healthcare agencies.; prepare responses to Information Requests from agencies. * For preparing PPQ of drug product manufacturing process and BLA, organize necessary activities, plan studies and obtain sufficient data. * Evaluate new medical devices or container-closures for local injection products * Lead the technical discussion cross-functional/divisional to align and enable efficient drug development work * Evaluate and understand analytical tools and methods to develop rAAV formulation appropriately * Participate the program meetings to achieve key milestones in a timely manner * Regularly present data and conclusions in sub-team meetings * Occasionally presents technology summaries to management and program teams

At Weston Solutions, Inc. you will do meaningful work and make valuable contributions. Employee-ownership at Weston is a path to professional growth and access to diverse opportunities in a highly connected community that works together across key service areas to make a difference in the environment. Weston continues to evolve and adapt to our changing world as a premier provider of environmental and infrastructure services for over sixty years. In both the public and private sectors our teams help identify, solve, mitigate, and manage critical environmental issues to help clients achieve a more sustainable future. This EHS Associate Scientist role supports Environmental Health & Safety (EHS) initiatives as a hands-on technical contributor, working either as part of a consulting team or embedded with client staff. You'll help design and implement EHS programs, conduct assessments, and provide regulatory guidance, while also beginning to support business development and client relationship management. The position involves solving routine EHS challenges, preparing reports, coordinating logistics, and may include mentoring junior staff-all with a strong focus on delivering high-quality service and building client trust. Location: Bay Area, CA; Dallas, TX Expected Outcomes: * Conduct facility inspections, sampling, and assessments to identify hazards and ensure regulatory compliance. * Develop, implement, and maintain EHS programs, procedures, and documentation. * Investigate incidents and recommend corrective actions. * Provide regulatory guidance, technical support, and onsite safety services. * Deliver EHS training and support ergonomic evaluations. * Independently plan and prioritize work; coordinate with teams and manage logistics. * Analyze data to support decision-making and regulatory interpretation. * Prepare accurate reports and proposals aligned with quality standards. * Communicate professionally with clients, regulators, and internal teams. * Support business development through client engagement and proposal contributions. * May supervise or assist junior staff. * Adhere to company policies and ensure high-quality deliverables. * May require travel, use of PPE, and work in physically demanding or hazardous environments. Knowledge, Skills & Abilities: * Bachelor's degree in science/engineering or equivalent experience. * 1-5 years of relevant EHS experience; advanced degrees may substitute. * Should hold or be actively working toward: ASP, CHMM, CBCA, EIT. * Strong knowledge of EHS regulations, environmental issues, and permitting. * Familiarity with health & safety programs, industrial hygiene (IH), ergonomics, and emergency response. * Experience with regulatory agencies (OSHA, EPA) and ISO standards. * Skilled in environmental sampling, data analysis, and technical reporting. * Strong communication, presentation, and teamwork skills. * Proficient in Microsoft Office and relevant tools. We fully invest in our people: Weston provides a generous, comprehensive benefits package program that offers employees high value options with solid financial protection, meeting the personal needs of its people and their families. * Medical, Dental, Vision, 401K with base and matching employer stock contributions. * Paid time off including personal, holiday, and parental leave. * Life and disability plans. * Critical illness and accident plans. * Work/Life flexibility. * Professional development opportunities. Compensation will vary based upon experience, education, skill level, and other compensable factors.

At Veracyte, we offer exciting career opportunities for those interested in joining a pioneering team that is committed to transforming cancer care for patients across the globe. Working at Veracyte enables our employees to not only make a meaningful impact on the lives of patients, but to also learn and grow within a purpose driven environment. This is what we call the Veracyte way - it's about how we work together, guided by our values, to give clinicians the insights they need to help patients make life-changing decisions. Our Values: * We Seek A Better Way: We innovate boldly, learn from our setbacks, and are resilient in our pursuit to transform cancer care * We Make It Happen: We act with urgency, commit to quality, and bring fun to our hard work * We Are Stronger Together: We collaborate openly, seek to understand, and celebrate our wins * We Care Deeply: We embrace our differences, do the right thing, and encourage each other The Position: We are looking for a highly motivated individual to join the Veracyte R&D Team as a Scientist III. This position requires planning and executing technical studies aimed at evaluating the performance of molecular in vitro diagnostic tests in the field of oncology. To be a successful candidate, we would like you to share our commitment to teamwork and collaboration and be excited by the challenges of applying your scientific expertise to develop genomic tests that improve patient diagnosis and treatment. Location: This is an onsite position based in our South San Francisco office. Contract length: 12 months Responsibilities: * Participate in diagnostic test development, inclusive of development and verification testing, to ensure that IVD products conform to product specifications * Participate in writing study protocols and technical reports related to development and verification studies testing diagnostic products that become part of the Design History File and regulatory filings. * Collaborate with technical team members to conduct laboratory experiments and document testing. * Interact with multi-disciplinary teams such as the data analysis team to coordinate data transfer. Who You Are: * PhD in chemistry, biochemistry, molecular biology, or a related field with 5+ years of relevant industry experience, or a BS/MS in the same fields with 8+ years of experience. * Prior experience in developing and/or verifying molecular IVD assays, genomics assays, or laboratory developed tests is required. * Experience with molecular platforms (e.g. next-generation sequencing, microarrays and/or qPCR) in the context of assay development and testing clinical specimens. Experience with NGS protocols is strongly preferred. * Prior experience with IVD assay Verification and/or Validation study design, planning, lab execution and documentation is strongly preferred. * Hands-on knowledge of the biochemistry underlying multi-component molecular biology methods at the sample preparation and assay level. * Strong organizational, communication, and interpersonal skills; including demonstrated ability to work well with others in team environment. * Ability to translate experimental results into technical reports and presentations. * Familiarity with IVD regulations (FDA 21 CFR Parts 820 and ISO 13485:2016) or CLIA regulations is desired. The final salary offered to a successful candidate will be dependent on several factors that may include but are not limited to the type and length of experience within the job, type and length of experience within the industry, education, etc. Base pay is one part of the Total Package that is provided to compensate and recognize employees for their work, and this role may be eligible for additional discretionary bonuses/incentives, and restricted stock units. Veracyte is a multi-state employer, and this salary range may not reflect positions that work in other states. Pay range $68-$75 USD What We Can Offer You Veracyte is a growing company that offers significant career opportunities if you are curious, driven, patient-oriented and aspire to help us build a great company. We offer competitive compensation and benefits, and are committed to fostering an inclusive workforce, where diverse backgrounds are represented, engaged, and empowered to drive innovative ideas and decisions. We are thrilled to be recognized as a 2024 Certified Great Place to Work in both the US and Israel - a testament to our dynamic, inclusive, and inspiring workplace where passion meets purpose. About Veracyte Veracyte (Nasdaq: VCYT) is a global diagnostics company whose vision is to transform cancer care for patients all over the world. We empower clinicians with the high-value insights they need to guide and assure patients at pivotal moments in the race to diagnose and treat cancer. Our Veracyte Diagnostics Platform delivers high-performing cancer tests that are fueled by broad genomic and clinical data, deep bioinformatic and AI capabilities, and a powerful evidence-generation engine, which ultimately drives durable reimbursement and guideline inclusion for our tests, along with new insights to support continued innovation and pipeline development. For more information, please visit **************** or follow us on LinkedIn or X (Twitter). Veracyte, Inc. is 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. Veracyte participates in E-Verify in the United States. View our CCPA Disclosure Notice. If you receive any suspicious alerts or communications through LinkedIn or other online job sites for any position at Veracyte, please exercise caution and promptly report any concerns to ********************

This role is 100% on-site at our South San Francisco Headquarters. The R&D team at Twist is searching for a curious, thoughtful, and driven molecular biologist with excellent lab hands to help us develop new products and applications in the Synthetic Biology (SynBio) space. You will use molecular biology to improve existing methods for gene synthesis as well as create entirely new ones. Leveraging our silicon-based, massively-parallel DNA synthesis platform, you will perform experiments for synthesis, assembly, cloning, scale-up, sequencing, and characterization of DNA. We are looking for people who have: Deep technical knowledge. You know exactly what's going on in the tube Fire in the belly. You want to move fast and see your work turn into real products that people use. The Pareto principle is in your blood. Common sense. Your scientific intuition is usually correct. Occam's razor is your friend. Your work will be mainly at the bench; however, you will have the opportunity to use high-throughput robotic instruments and coding and bioinformatics tools to expand your expertise. You will work alongside and learn from some of the best scientists and bioinformaticians in the business. Key Responsibilities: Lead molecular biology research projects in DNA synthesis, assembly, cloning, scale up, sequencing, and characterization. Independently design and execute experiments and analyze experimental data. Move projects forward efficiently / manage time and resources effectively / prioritize tasks in accordance with the company's goals. Document and communicate results clearly and succinctly Discuss experimental results with other team members and stakeholders Work collaboratively with a diverse group of scientists and bioinformaticians Coordinate with internal Twist teams, including product management, manufacturing, and QC/QA, on cross-functional projects Solicit technical input from others/participate in scientific discussions / come up with new ideas Be helpful/collaborative / proactive Stay up to date with new developments, companies, and technologies Be the ultimate subject matter expert, and understand all aspects of your work as profoundly as possible, including details that are adjacent (as opposed to directly related) to your project/experiment. What You'll Bring to the Team: Deep technical knowledge in molecular biology methods, with a focus on nucleic acids. Extensive experience in DNA synthesis, assembly, and manipulation methods is a must Broad experience with DNA cloning and the different methods for DNA amplification using cells or enzymes A track record of successful and creative method development Broad experience in bacterial cell culture and plasmid biology Strong background in NGS library preparation methods, sequencing technologies, and data analysis Proficient in bioinformatics and bioinformatics tools, including genome alignment, mapping, variant calling, and annotation, with the ability to conduct analyses and effectively communicate requirements to bioinformaticians. Excellent communication and interpersonal skills and a demonstrated ability to collaborate effectively within a team. Independent, driven, and creative Qualifications: PhD in molecular biology or related field, or master's degree with 3-5 years of experience, or equivalent experience Extensive experience in molecular biology of nucleic acids Familiarity with Python, R, or equivalent programming languages Experience with liquid-handling systems and automation is a plus About Twist Bioscience Twist Bioscience synthesizes genes from scratch, known as “writing” DNA. Just as children learn to both read and write, the next phase of development for the genomics revolution is the ability to write DNA. At Twist Bioscience, we work in service of people who are changing the world for the better. In fields such as health care, agriculture, industrial chemicals and data storage, our unique silicon-based DNA Synthesis Platform provides precision at a scale that is otherwise unavailable to our customers. Twist Bioscience Corporation is an Equal Opportunity Employer. Twist Bioscience Corporation provides equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, genetic characteristics, or any other category protected by law. The base cash compensation for this California-based role is below. In addition to base salary, this role is eligible for bonus, equity, and a generous benefits package. Final compensation amounts are determined by multiple factors, including candidate skill, experience, expertise, and location and may vary from the amount listed above. Compensation may be different in other locations.San Francisco Bay Area Pay Range$114,660-$154,097 USD