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Job Description Drive experimental strategy while remaining deeply hands-on at the forefront of fusion research. This senior scientist will both lead and contribute to several experimental physics projects to advance the physics basis for the high-field axisymmetric mirror. This work will include designing, building, and fielding new experimental diagnostics on the currently operating Wisconsin HTS Axisymmetric Mirror (WHAM) at the University of Wisconsin-Madison, proposing new experimental campaigns and plasma diagnostics needed to enhance physics understanding and validation efforts with computational tools, and helping design and diagnose of future axisymmetric mirror devices at Realta Fusion called Anvil and Hammir. This role will include leading and participating in collaborations with external research groups at both national laboratories and universities, publishing work in peer-reviewed journals and disseminating results at conferences. Realta Fusion is a rapidly growing start-up developing compact magneticmirror fusion energy systems to address the biggest challenge of our time –tackling global climate change while ensuring a sufficient energy supply for atleast ten billion people on (and off) earth. We are building a team withdiverse talents dedicated to making fusion energy a real solutionto humanity’s most pressing problem. Key Responsibilities • Develop complex research methodologies and procedures to identify solutions in a magnetic mirror fusion research device and optimize the design of Realta’s next fusion devices., • Design, build, and field new plasma diagnostic systems on WHAM at the University of Wisconsin-Madison and for our future fusion devices called Anvil and Hammir., • Collect and analyze highly complex research data, propose and conduct experiments, and document results according to established policies and procedures., • Interface with theory and modelling, engineering team and business leadership to deliver on technical milestones., • Conduct literature reviews, prepare reports and materials and disseminate information to appropriate entities., • Identify, write, or assist in developing grant opportunities, grant applications, proposals and other materials to secure funding in a startup-environment., • Serve as an institutional subject matter expert and liaison with key internal and external stakeholders providing expert level information and representing the interests of a specialized research area., • Contribute to the establishment of company safety standards and implement these standards within the R&D team. Foster a positive and inclusive work environment that aligns with the company's mission, values, and sustainability goals, promoting innovation, collaboration, and employee engagement. Qualifications • Education: PhD in Plasma Physics, or a related field + minimum of 5 years' experience in experimental plasma physics research., • Extensive experience with standard plasma diagnostics (e.g. bolometers, electrostatic ion energy analyzers, interferometers, magnetic probes, spectrometers, visible imagery, fusion neutron diagnostics, soft and hard x-ray detectors, Thomson scattering, etc…) and analysis techniques., • Extensive experience with standard plasma diagnostics (e.g. bolometers, electrostatic ion energy analyzers, interferometers, magnetic probes, spectrometers, visible imagery, fusion neutron diagnostics, soft and hard x-ray detectors, Thomson scattering, etc…) and analysis techniques., • Understanding of magnetically confined fusion plasma heating and current drive technologies, such as bias-induced rotation, electron cyclotron heating, neutral beam injection, and RF heating., • Collaboration: Exceptional interpersonal and communication skills (written and verbal) to collaborate effectively with colleagues, external partners, and stakeholders. Compensation & Benefits What we are working on is hard… and hugely important. Realta Fusion is assembling a talented team bound together by a passion to solve humanity’s biggest challenge with first-of-a-kind technology. Additionally, Realta offers: • Competitive compensation package, including equity stock options, • Comprehensive benefits including health, dental, and vision insurance, plus a 401(k), • Flexible paid time off (PTO) to support work-life balance

Job Description Arrowhead Pharmaceuticals, Inc. (Nasdaq: ARWR) is a clinical stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead therapies trigger the RNA interference mechanism to induce rapid, deep, and durable knockdown of target genes. RNA interference, or RNAi, is a mechanism present in living cells that inhibits the expression of a specific gene, thereby affecting the production of a specific protein. Arrowhead's RNAi-based therapeutics leverage this natural pathway of gene silencing. Arrowhead is focused on developing innovative drugs for diseases with a genetic basis, typically characterized by the overproduction of one or more proteins that are involved with disease. The depth and versatility of our RNAi technologies enables us to potentially address conditions in virtually any therapeutic area and pursue disease targets that are not otherwise addressable by small molecules and biologics. Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates. Arrowhead's corporate headquarters is in Pasadena, CA with research and development teams in Madison, WI & San Diego, CA, and a state of the art manufacturing facility in Verona, WI. Our employees are nimble, science-driven innovators who are collaborating to bring new therapies to patients in need. The Position This position is within the Quality Control structure, under the Quality Organization. A Senior Scientist I, Quality Control will support the analytical testing of Environmental monitoring samples, pharmaceutical raw materials, in process manufacturing samples, finished drug substances and drug product, and/or stability sample testing activities for new drug substances and drug products. The Senior Scientist I will also support testing required for GLP Toxicology and cGMP Clinical Trial material release, as well as stability studies. The Senior Scientist I is expected to be proficient in several analytical techniques and will be capable of making independent scientific decisions. The position also requires the ability to lead and mentor co-workers. This position reports to QC Laboratory Management. Responsibilities • Fully knowledgeable of cGMP requirements and ICH guidelines, • Works independently to meet project timelines and deliverables with minimal supervision to no supervision, • Collaborates routinely with Analytical Development on procedural method transfers and may participate in the execution of method validation protocols, • Performs routine analytical testing of pharmaceutical raw materials, in-process samples, finished products and stability samples using established test methods and procedures, • Proficient with various analytical instrumentation theory and practice, • Executes training requirements for assigned SOPs and participates in department specific training modules., • Independently completes complex instrumentation for testing according to written test methods and procedural documents to analyze samples, • Demonstrates proficiency with a variety of instrumentation (e.g., HPLC, GC, LC-MS, KF, FTIR, Endotoxin plate readers, and/or Raman spectroscopy) and will assist in training on instrumentation as, • Is a subject matter expert in technical aspects of both instrumentation and workflow management and prioritization, • Performs analyses in a timely and efficient manner to support ongoing prioritized studies, • Works closely with other department personnel for efficient project execution and timely/accurate deliverables while building a relationship with respect and communication, • Trains and mentors co-workers (analysts), • Shows initiative and interest in mastering new techniques and tests, • Ability to track/trend data and interpret degrative changes to the product on stability, • Uses stability tracking software as a repository generated results (data entry, review and approval)., • Owns and leads scientific technical discussions and brainstorming sessions, • Identifies and troubleshoots analytical method issues with instrumentation, general chemistry, test methodology and sample product, • Communicates laboratory testing issues or challenges to laboratory management, • Maintains a clear, concise, and accurate notebook, • Performs technical data review on data acquired by other QC analysts as applicable, • Drafts technical documents such as COAs, investigations, deviations, and CAPAs, • Possesses excellent written and verbal communication skills, • Embraces cGMP and ICH requirements for all associated work, • Works cooperatively in a team environment, • Demonstrates a high attention to detail, • Calibration, maintenance, and troubleshooting of analytical equipment with little to no guidance from management, • Routinely makes sound, scientific decisions independently and serves as a back-up to Laboratory Management, • M.S. in Chemistry (or related field) with 7+ years relevant laboratory experience, • B.S. in Chemistry (or related field) with 9+ years of relevant laboratory experience, • Fully knowledgeable of cGMP and ICH laboratory requirements and operations All applicants must have authorization to work in the US for a company. 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Job DescriptionCompany Description AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at . Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok. Job Description Purpose: We are seeking a highly motivated Peptide design and Machine Learning Scientist to join AbbVie’s Madison Peptide Therapeutics team. In this role, you will help drive our adoption and development of generative AI methods to accelerate peptide drug discovery. Our team uses a proprietary peptide synthesis platform capable of synthesizing bespoke peptide libraries consisting of millions of unique peptide sequences, that can incorporate a variety of amino acids including non-canonical amino acids. The platform enables rapid empirical evaluation of computationally designed peptide sequences, giving us a unique advantage in this field. The successful candidate will be responsible for identifying and developing novel algorithms and pipelines, as well as collaborating closely with both computational and experimental scientists to guide and optimize our AI-enabled hit generation strategies. Responsibilities: • Develop machine learning and computational chemistry methods to enable discovery of peptides and/or peptide-containing scaffolds that bind to target proteins, • Lead efforts to leverage various computational chemistry tools and machine learning architectures to accelerate design of peptide-based molecules, • Lead deployment of machine learning algorithms across various therapeutic areas, • Build data sets and develop novel strategies to quantify model performance, • Present results at internal and external scientific conferences, • Routinely demonstrate scientific initiative and creativity in research activities, • Formulate conclusions and design follow-on experiments based on multidisciplinary data, • May initiate new areas of investigation that are scientifically meaningful, reliable, and can be incorporated directly into a research or development program, • Author of publications, presentations, regulatory documents and/or primary inventor of patents, • Understand and adhere to corporate standards regarding code of conduct, safety, appropriate handling of materials, controlled drug and radioactive compounds, GxP compliance, and animal care where applicable, • Direct mentorship of othersQualifications, • Bachelor’s Degree or equivalent education and typically 10 years of experience, Master’s Degree or equivalent education and typically 8 years of experience, PhD and no experience necessary., • Proven experience developing deep learning approaches for peptide generation and peptide drug design, • Experience with protein structure modeling, design, or prediction algorithms, spanning physics-based to deep learning architectures, • Fluent in Linux command-line, python, and version control (git), • Demonstrated record of research excellence in machine learning as evidenced by conference presentations (e.g. NeurIPS) and journal publications, • Thorough theoretical and practical understanding of relevant scientific disciplines, • Applied experience in a quantitative science (e.g., Chemistry, Biology, Biochemistry, etc.), • Extensive experience working with large chemical and biological datasets, including graph, sequence, and structure-based data, • Hands-on experience building and training models, applying transfer learning, and/or fine-tuning models using deep learning frameworks (such as PyTorch), • Experience using cloud computing, high-performance computing, or GPU clusters, • Ability to work collaboratively on projects with multiple contributors, • Experience developing deep generative approaches for cyclic peptide drug design, • Experience developing deep generative approaches for peptides with non-canonical amino acids, • Experience developing novel strategies to quantify model performance, especially for diffusion, flow-matching, and transformer-based models, • Experience contributing to drug discovery efforts Additional Information Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law: * The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future. * We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees. * This job is eligible to participate in our short-term incentive programs. Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company’s sole and absolute discretion, consistent with applicable law. AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled. US & Puerto Rico only - to learn more, visit US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:

Job DescriptionEmpirico, a clinical-stage biotechnology company that combines unmatched expertise in human genetics-driven target discovery with world-class capabilities in siRNA medicines is seeking a chemist with an interest in solid-phase oligonucleotide synthesis and analytics. This is an excellent opportunity for a highly motivated, creative scientist to be a vital member of our team.Responsibilities: • You will be responsible for supporting the synthesis, purification, and characterization of oligonucleotides and their conjugates, and optimizing methodologies to support the development of siRNA medicines. The ideal candidate will have experience in organic and analytical chemistry and both upstream and downstream oligonucleotide manufacturing processes. A key focus of this role will be developing scalable processes suitable for technology transfer to CDMOs. You will be expected to –, • Perform solid-phase synthesis, purification, and characterization of oligonucleotides, • Develop and optimize scalable upstream (synthesis) and downstream (purification, formulation) manufacturing processes, • Support process development activities to enable successful technology transfer to CDMOs, • Analyze, interpret, and clearly communicate synthetic and analytical data, • Present findings to senior staff and cross-functional teams, • Troubleshoot and refine synthesis and purification protocols, • Manage multiple projects simultaneously in a fast paced environment, • Support GLP related activities and IND-enabling process development effortsRequirements:, • This position requires a BS in Chemistry with at least 12 years of relevant industry experience, or an MS in Organic Chemistry, Biochemistry, or Chemical Engineering with at least 7 years of relevant experience, or a PhD with at least 3 years of relevant experience., • Industry experience in solid-phase oligonucleotide synthesis is preferred, as well as familiarity with both upstream and downstream oligonucleotide manufacturing processes, • Minimum 1 year of experience working in a cGMP environment with demonstrated understanding of cGMP principles, • Hands-on proficiency with analytical instrumentation such as NMR, LC-MS, and RP-HPLC, • Demonstrated ability in analytical and purification method development using RPIP-HPLC, AEX-HPLC, UV, MALDI, and HRMS, • Background in process development and technology transfer to CDMOs, including development of scalable purification and formulation methodologies, • Working knowledge of tangential flow filtration (TFF) method development, • Experience supporting GLP studies and familiarity with regulatory expectations for IND-enabling work, • Experience with lyophilization and aseptic fill/finish operations

Job DescriptionCompany Description LGC is a leading, global life science tools company, providing mission-critical components and solutions into high-growth application areas across the human healthcare and applied market segments. Our high-quality product portfolio is comprised of mission-critical tools for genomic analysis and for quality assurance applications, which are typically embedded and recurring within our customers’ products and workflows and are valued for their performance, quality and range. Our tools play a key role in customer workflows from discovery applications through to commercial manufacture and enable its customers to: bring new diagnostics and therapies to market; progress research and development; optimize food production; and continuously monitor and enhance the quality of food, the environment and consumer products. Job Description The Associate Scientist II, Production is responsible for the manufacture of site product within one or more portfolios in a cost-effective manner and in compliance with appropriate quality and safety standards. This role supports departmental success by following approved operational protocols, using good documentation practices, escalating process variances, and helping to maintain a clean and safe work environment. This position is also expected to support or participate in process improvement activities, quality investigations, and operational excellence (OE) initiatives. To perform this job successfully, an individual must be able to capably perform each of the following essential duties: • Contribute to operations teams performing manufacturing, quality control, and production maintenance activities in a manner consistent with the company quality and safety standards, • Assist in the fermentation and purification of recombinant proteins from different expression systems, • In accordance with designated procedures and work instructions, prepare and operate chromatography systems, dialysis/TFF operations, and reagent preparation, • Support and follow production protocols geared towards robust and cost-effective supply of molecular biology product and NGS proteins, • Process, record, and analyze data following approved protocols and using good documentation practices, • Identify and escalate events that deviate from normal operations, • Support process improvements, nonconformance reporting, investigations, and corrective/preventative actions as assigned, • Effectively communicate results to immediate team, and other stakeholders as directed, • Maintain cleanliness and orderliness of operational area and work environment, • Conscientiously learn and diligently follow the requirements of the site’s quality management system, • Adhere to company Personal Protection Equipment (PPE) policy, • Perform other duties as required, or assigned by management, to meet business needs Qualifications, • Bachelor’s degree in relevant life sciences field (molecular biology, microbiology, biochemistry, etc.)—or applicable industry experience, • Prior experience operating standard laboratory equipment (e.g. pH meters, conductivity meters, pipettes), • Ability to follow standard operating procedures (SOP’s) and/or manufacturing protocols, • Familiarity with standard biological and analytical techniques, including PCR, SDS-PAGE, and western blotting, • Prior experience with manual or automated chromatography systems or processes (e.g., AKTA platform), • Proven ability to effectively communicate work results, including technical data, to colleagues, • Prior experience performing fermentation, protein production and purification in an industrial setting, • Prior experience performing operations on the AKTA platform and executing depth-filtration and Tangential Flow Filtration operations, • Experience with functional testing (PCR, LAMP, etc.), • Experience with bacteria fermentation Additional Information About LGC: LGC is a leading, global life science tools company, providing critically important components and solutions into high-growth application areas across the human healthcare and applied market segments. Its high-quality product portfolio is comprised of critical tools for genomic analysis and for quality assurance applications, which are typically embedded and recurring within our customers’ products and workflows and are valued for their performance, quality, and range. Our values • PASSION, • CURIOSITY, • INTEGRITY, • BRILLIANCE LGC strongly believes that every job applicant and employee should be valued for their individual talents regardless of age, disability, race, color, ethnic or national origin, sex, sexual orientation, gender reassignment, marital or civil partnership, pregnancy or parental status, religion, or belief. Short listing, interviewing and selection will always be carried out without regard these factors. For more information about LGC, please visit our website #scienceforasaferworld

Job Description AE Business Solutions is an IT powerhouse that helps clients implement, migrate, optimize, and support the cutting-edge technologies that drive their businesses forward. Our Talent Acquisition team plays a pivotal role in making that happen — not only by finding great people for our clients, but also by recruiting the engineers, architects, and specialists who deliver our own professional services and solutions. As a Technical Recruiter, you’ll do what you do best — connect top IT talent with rewarding opportunities — while enjoying the unique advantage of working for a true technology company. You’ll gain deeper insight into the roles you’re filling, collaborate with brilliant technologists, and help grow a business that’s thriving year after year. And because we believe that great work should be balanced with great experiences, you’ll join a team that values fun, family, and flexibility. From our hybrid-remote schedule to our employee and family events throughout the year, AE is a place where people love what they do — and who they do it with. A Day in the Life: • Manage full-cycle recruiting for a variety of technical roles — from internal engineers and architects to client-facing consultants and contractors., • Partner closely with hiring managers and internal hiring leaders to understand technical and cultural needs and deliver high-quality, well-matched candidates., • Use creative sourcing strategies across LinkedIn, social media, networking, referrals, and industry events to find top IT talent., • Screen and qualify candidates for both technical expertise and cultural alignment., • Guide candidates through every step of the hiring process — from first contact to onboarding., • Maintain accurate and up-to-date data in our ATS to ensure a smooth and organized recruiting process., • Continuously explore and implement new sourcing tools and methods to stay ahead in a competitive market., • Serve as a consultative partner to hiring managers and clients, promoting best practices in recruiting and hiring., • Represent AE’s values — teamwork, excellence, integrity, and fun — in everything you do. What You’ll Need: • 2+ years of experience in technical recruiting (agency or corporate) with proven success in full-cycle recruiting for IT or engineering roles., • Solid understanding of IT roles, technologies, and industry trends — you know your way around cloud, infrastructure, networking, and cybersecurity., • Familiarity with ATS platforms, LinkedIn Recruiter, and other modern recruiting tools., • Strong communication and relationship-building skills — you can connect with everyone from entry-level techs to senior IT leaders., • Excellent organizational skills and attention to detail; able to manage multiple requisitions in a fast-paced environment., • A self-starter who’s curious, resourceful, and motivated to exceed goals., • A team player who thrives in a collaborative, people-first culture., • Bachelor’s degree preferred, but we value experience, drive, and attitude just as much., • Ideal candidate will have experience recruiting on IT roles such as Infrastructure Engineer/Architect, Systems Administrator, Systems Engineer, Cloud/DevOps Engineer, Network Administrator/Engineer, Project Manager, Business Analyst, Database Administrator, Data Scientist, Server Engineer, etc. Life at AE Our culture is unique and defined by our 10 core values. This continued focus throughout our 75+ year history has enabled us to continue to achieve extraordinary growth year over year. These accomplishments have allowed us to be named among Top Workplaces in the Wisconsin area for the past several years. We’re looking for people driven by our values: • Put the client first. Always, • Care For Your Family, • Engage Locally, • Embrace Diversity, • Practice Honesty & Integrity, • Work Hard & Work Smart, • Laugh & Have Fun, • Propose Solutions, • Listen & Ask Questions, • Take Ownership & Show Respect Life at AE includes a bunch of incentives besides a comprehensive insurance package, including: Health, Dental, 401K… the standard basket of goodies. We also provide an ever-evolving employee experience that includes AE Cares Days, referral bonuses, remote work and flexible schedule options, lunch and learns, crumbl cookies, a collaborative work environment, and an environment where the intern’s ideas are given as much respect as the executive management. We believe that the experience a client has with our team should be an extension of our values. Interested? Let's talk! AE Business Solutions is an Equal Opportunity Employer

Job DescriptionLCMS Lead Scientist Job Description As a LC-MS Lead Scientist, you will play a pivotal role in overseeing bioanalytical studies, ensuring that all methods meet regulatory and client requirements. You will not be working directly in the lab but will be responsible for reviewing data, signing off on reports, and acting as the primary scientific point of contact. Your expertise will guide the bioanalytical study work, and you will coordinate with regulators and stakeholders, both internally and externally. Responsibilities • Oversee studies and ensure all methods are prepared, validated, executed, and documented to meet regulatory and client requirements., • Sign off on reports and approve raw data., • Act as the primary scientific point of contact for studies., • Coach and indirectly guide a team of up to 20 members., • Coordinate across internal and external stakeholders, including discussions with regulators for clinical or pre-clinical studies., • B.S. or Masters in Life Sciences (Chemistry, Biology, Biochemistry, etc.)., • 2-3 years of LCMS experience., • Experience as a Lead Scientist with 1-5 years (LS1) or 7-9 years (LS2) of experience., • Must have experience as a Lead Scientist/Responsible Scientist/Principle Investigator in the Bioanalytical sector (GLP or GCP regulations)., • Full responsibility over the study, with experience in BioA CRO regulated space., • Experience with Sciex Mass Spec and analysis software., • Familiarity with LIMS, Nautilus, and Analyst software. Medical Plan* No Charge Laboratory Testing Benefit and physical therapy Dental Plan Vision Plan Flexible Spending Accounts (FSAs) Health Care FSA Dependent Care FSA Disability Plan Short Term Disability (STD) Long Term Disability (LTD) Life and Accidental Death and Dismemberment (AD&D) Insurance Plans Basic Life Optional Life Dependent Life Optional AD&D Employee Stock Purchase Plan (ESPP) Workplace Type This is a hybrid position in Madison,WI. Application Deadline This position is anticipated to close on Feb 6, 2026. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email for other accommodation options.

Job Description Join Realta Fusion and help shape the future of fusion energy through advanced theory and computation. As a Theoretical and Computational Scientist, you’ll bridge simulation and experiment to drive groundbreaking progress on our next-generation magnetic mirror devices. Realta Fusion is a rapidly growing start-up developing compact magnetic mirror fusion energy systems to address the biggest challenge of our time – tackling global climate change while ensuring a sufficient energy supply for at least ten billion people on (and off) earth. We are building a team with diverse talents dedicated to making fusion energy a real solution to humanity’s most pressing problem. This Scientist will contribute to several theoretical and computational projects to advance the physics basis for the high-field axisymmetric magnetic mirror. This work will include validation of computational models with experimental data from the currently operating Wisconsin HTS Axisymmetric Mirror (WHAM) at the University of Wisconsin-Madison, proposing new experimental campaigns and plasma diagnostics to be fielded on WHAM to aid in validation efforts, and using computational modelling to guide the design of future axisymmetric mirror devices at Realta Fusion called Anvil and Hammir. This role will include participating in collaborations with external research groups at both national laboratories and universities, publishing work in peer-reviewed journals and disseminating results at conferences. Responsibilities • Develop complex research methodologies and procedures to identify solutions in a magnetic mirror fusion research device and optimize the design of Realta’s next fusion devices. Publish and present results to advance research and ensure credibility for our work in the field of plasma physics & fusion energy., • Lead and participate in theoretical and computational projects to advance the physics basis for the axisymmetric mirror, with a focus on validation and then extrapolative design to future devices., • Interface with the experimental physics, engineering team, and business leadership to deliver technical milestones., • Conduct literature reviews, prepare reports and materials and disseminate information to appropriate entities., • Identify, write, or assist in developing grant opportunities, grant applications, proposals and other materials to secure funding in a startup-environment., • Serve as an institutional subject matter expert and liaison with key internal and external stakeholders providing expert level information and representing the interests of a specialized research area., • Safety: Contribute to the establishment of company safety standards and implement these standards within the R&D team., • Education: PhD in Plasma Physics, or a related field + minimum of 3 years’ experience in theoretical and computational plasma physics research., • Experience with MHD equilibrium and linear stability calculations, and Extended-MHD / multi-fluid plasma simulations with codes such as NIMROD or JOREK., • Familiarity with Fokker-Planck, particle-in-cell (PIC) and RF heating simulation tools, such as WarpX, VPIC, Genray, AORSA, CQL3D., • Basic knowledge of standard plasma diagnostics (e.g. bolometers, electrostatic ion energy analyzers, interferometers, magnetic measurements) and analysis techniques., • Understanding of magnetically confined fusion plasma heating and technologies, such as bias-induced rotation, electron cyclotron heating, neutral beam injection, and RF heating., • Collaboration: Exceptional interpersonal and communication skills (written and verbal) to collaborate effectively with colleagues, external partners, and stakeholders. What we are working on is hard… and hugely important. Realta Fusion is assembling a talented team bound together by a passion to solve humanity’s biggest challenge with first-of-a-kind technology. Additionally, Realta offers: • Competitive compensation package, including equity stock options, • Comprehensive benefits including health, dental, and vision insurance, plus a retirement savings plan, • Flexible paid time off (PTO) to support work-life balance

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Join Meta as a Data Scientist and play a pivotal role in shaping innovative products across our family of applications, including Facebook, Instagram, Messenger, WhatsApp, and Oculus. Collaborating with cross-functional teams in Product, Engineering, Research, Data Engineering, Marketing, Sales, and

Implements appropriate data science techniques under the guidance of other data scientists, statisticians, and/or other researchers to find data patterns and answer research questions chosen by the lead researcher including data visualization, statistical analysis, machine learning, and data mining.

Join our dynamic team as a Senior Data Scientist and make a significant impact across multiple product areas. Engineering and cross-functional partners to guide data-informed product planning and strategy development. In this pivotal role, you will collaborate with diverse teams to tackle complex ch

Datavant is a data platform company and the leader in health data exchange. We support the development of your data analysis and coding skills to ensure you become proficient in analyzing large health-related datasets. Application of scientific methods to practical problems through experimental desi

The Research & Development Data Scientist Associate plays a crucial role in planning, developing, and executing data science analyses for research projects at the ETS Research Institute. This position emphasizes applying advanced data science techniques, machine learning, and AI to derive meaningful

You will focus on developing hypotheses and employ a varied toolkit of rigorous analytical approaches, different methodologies, frameworks, and technical approaches to test munication and influence: You won't simply present data, but tell data-driven stories. Data Scientist, Product Analytics Respon

Collaborate with fellow data scientists to exchange best practices, acquire new analytical methods, and support a culture where data-driven decision-making is paramount. Our skilled data scientists are focused on creating infrastructures, metrics, insights, and models that empower organizations glob

Join our innovative Shopbop/Zappos Catalog Tech team as a Senior Data Scientist, where you will spearhead groundbreaking approaches to enhance our product catalog data for an exceptional range of Shoes, Kids, and Active wear. In this pivotal role, you will collaborate with Zappos' Senior leadership

What roles can career switchers target? SynergisticIT typically supports candidates targeting roles like entry-level software programmer, Java full stack developer, Python/Java developer, DevOps engineer, data analyst, BI analyst, data engineer, data scientist, and machine learning/AI engineer—bas