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American Family Insurance looking for a experienced and driven Lead Data Engineer to guide our Data Platform team. In this important role, you will oversee a team of engineers in advancing our service-oriented data platform. The Data Platform team influences multiple departments, including security and AI, at AmFam. You will create tools and infrastructure that empower other teams and departments within American Family Insurance. You will report to a Senior Manager, Data Engineering. In this flex office/home role, you will be expected to work a minimum of 10 days per month from the following office location: Madison, WI 53783. #LI-Hybrid Position Compensation Range: $131,000.00 - $220,000.00 Pay Rate Type: Salary Compensation may vary based on the job level and your geographic work location. Relocation support is offered for eligible candidates. • Partner with stakeholders to refine undefined use cases into clear requirements, translate those into technical specs, and implement working solutions., • Design and build platform capabilities that multiple teams consume, including feature stores, observability tooling, evaluation pipelines, and deployment patterns., • Define and implement reusable patterns and infrastructure: shared LLM serving, evaluation frameworks, CI/CD templates, internal SDKs., • Assess existing AI applications and establish standards for code quality, testing, deployment, and observability., • Mentor data scientist and data engineers, conduct meaningful code reviews, and provide architectural guidance across the platform., • Facilitate communication across project teams, architects, and business partners., • Document critical workflows, standards, and operational support aspects of the platform., • Demonstrated experience building AI/ML systems that run in production at scale - not notebooks or prototypes, but real software serving real users., • Proven ability to take ambiguous, undefined problems and deliver shipped products., • Strong system design skills with an emphasis on scalability, failure modes, and long-term maintainability., • Deep software engineering fundamentals: experience with large codebases, design patterns, testability, and enterprise SDLC., • Hands-on experience with LLMs in production: RAG, agents, evaluation, prompt engineering, or fine-tuning., • Expert-level Python programming in a software engineering context, not just scripting or pipelines., • Experience designing and building APIs for internal or external consumption., • Deep experience with GCP, specifically Vertex AI, Pub/Sub, BigQuery, and NoSQL databases (e.g., Firestore, Bigtable)., • Applied knowledge of Kubernetes for container orchestration and workload management., • Experience with infrastructure-as-code tools (e.g., Terraform, Docker) and CI/CD pipelines., • Up to 10%. Offer to selected candidate will be made contingent on the results of applicable background checks * Offer to selected candidate is contingent on signing a non-disclosure agreement for proprietary information, trade secrets, and inventions * Sponsorship will not be considered for this position unless specified in the posting • Your offer will be contingent on the results of applicable background checks and signing a non-disclosure agreement for proprietary information, trade secrets, and inventions., • We will not consider candidates who require sponsorship. We provide benefits that support your physical, emotional, and financial wellbeing. You will have access to comprehensive medical, dental, vision and wellbeing benefits that enable you to take care of your health. We also offer a competitive 401(k) contribution, a pension plan, an annual incentive, 9 paid holidays and a paid time off program (23 days accrued annually for full-time employees). In addition, our student loan repayment program and paid-family leave are available to support our employees and their families. Interns and contingent workers are not eligible for American Family Insurance Group benefits. We are an equal opportunity employer. It is our policy to comply with all applicable federal, state and local laws pertaining to non-discrimination, non-harassment and equal opportunity. We also consider qualified applicants with criminal histories, consistent with applicable federal, state and local law. American Family Insurance is committed to the full inclusion of all qualified individuals. If a reasonable accommodation is needed to participate in the job application or interview process, to perform essential job functions, and/or to receive other benefits and privileges of employment, please email ___ to request a reasonable accommodation. #LI-DB1

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 DescriptionJob Title: LCMS Lead ScientistJob Description As an LC-MS Lead Scientist, you will oversee studies, ensuring that methods are ready, validated, executed, and documented to meet regulatory requirements. You will not work in the lab but will review data, act as the primary scientific point of contact, and coach team members while coordinating with internal and external stakeholders. Responsibilities • Oversee bioanalytical study work of moderate complexity., • Sign off on reports and review/approve raw data., • Act as the primary scientific point of contact for studies., • Coordinate across internal and external stakeholders., • Provide scientific guidance and mentoring to team members., • Ensure methods meet regulatory requirements and are documented appropriately., • Engage with regulators for clinical or pre-clinical studies.Essential Skills, • B.S. or Masters in Life Sciences (Chemistry, Biology, Biochemistry, etc.)., • 2-5 years of experience working on LCMS., • Experience as a BioA Lead Scientist/Responsible Scientist/Principle Investigator in the Bioanalytical sector., • Proven data review/approval skills and method validation readiness., • Experience with Sciex Mass Spec and other analysis software., • Familiarity with GLP or GCP regulations.Additional Skills & Qualifications, • Experience with Nautilus and Analyst software., • Knowledge of ICH or 28BMV regulatory guidance protocols., • Familiarity with FDA internal standards. 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 Apr 1, 2026. Diversity, Equity & Inclusion At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I is embedded into our culture through: • Hiring diverse talent, • Maintaining an inclusive environment through persistent self-reflection, • Building a culture of care, engagement, and recognition with clear outcomes Our Bangalore, Hyderabad, Pune, and Chennai delivery centers are hubs of engineering expertise, with core capabilities in mechanical and electrical engineering, systems and software, and manufacturing engineering. Our teams deliver work across multiple industries including transportation, consumer and industrial products, and life sciences. We serve more than 4,500 clients, including many Fortune 500 brands. Learn more about how we can work together at actalentservices.com.

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. 2nd shift work hours are 1 pm – 11:30 pm, Monday - Thursday, and includes a 10% shift differential. 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 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 Arrowhead Pharmaceuticals is seeking a highly motivated Senior Scientist I to join our Discovery Analytical Chemistry team. In this role, you will play a critical part in advancing our protein and protein conjugate therapeutics by developing and implementing advanced LC-MS analytical strategies that support discovery and early process development activities. This is an opportunity to contribute at a high scientific level - designing innovative analytical solutions, influencing drug discovery direction, and collaborating cross-functionally to solve complex research challenges. The successful candidate will bring deep technical expertise in protein characterization and quantitation, along with the ability to translate analytical findings into meaningful insights that drive program decisions. You will serve as both a scientific leader and hands-on contributor, independently developing and optimizing analytical methods while mentoring junior scientists and helping shape analytical strategy within the team. Responsibilities • Develop project and technical strategy within area of expertise, • Apply advanced scientific principles, theories and concepts to a broad range of research problems and develop innovative solutions for analytical problems related to drug discovery and development, • Design and execute analytical studies to facilitate drug discovery and platform development in various disease areas, • Independently design and initiate development of analytical methods and improvement of existing ones, • Serve as a project coordinator for on-going and new analytical method development, • Work independently and collaboratively with teams to solve scientific /technical challenges, • Develop and validate analytical methods to quantify and characterize drugs and impurities, • Conduct sample analysis, analyze data/results, interpret the outcome of experiments and integrate scientific findings to gain further understanding of drug properties or synthetic/purification route, • Represent team to present research findings to cross-function teams, • Identify, propose and lead areas for initiatives /improvement, • Influence and support drug discovery/development directions with scientific findings, • Train and mentor junior scientists in the team, • PhD in analytical chemistry or close related fields with 2+ years relevant industry experience, • Strong hands-on experience of using LC-MS and HPLC for proteins/protein conjugates characterization and quantitation, • Expertise in sample preparation, peptide mapping, MS/MS peptide sequencing, glycosylation analysis, disulfide bond mapping, and post-translational modifications analysis, • In-depth understanding of protein chemistry and analytical chemistry, • Familiar with routine maintenance of mass spectrometers, • Strong troubleshooting and problem-solving skills, • Excellent ability for data interpretation and integration, • Excellent communication and presentation skills, • Ability and willingness to learn cutting edge technologies, • Open mind and willing to learn new technology, • Experience with a wide range of analytical techniques All applicants must have authorization to work in the US for a company. California Applicant Privacy Policy

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 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 Arrowhead is seeking a motivated process development scientist to join our Chemistry Manufacturing and Controls group focusing on formulation and drug product. The successful candidate will be tasked with managing external drug product manufacturing and developing drug product formulations. Responsibilities • Provide technical direction to Contract Development and Manufacturing Organizations (CDMO) for external Drug Product operations, • Develop formulations of oligonucleotide and oligonucleotide-conjugate drug products appropriate for the phase of pharmaceutical development, • Characterize drug product formulations to support clinical dosing and regulatory filings, • Review and approve batch records for use at CDMOs, • Author and execute formulation characterization protocols and author technical reports, • Draft and review technical documentation and leverage expertise to support regulatory filings, • Present data and technical information to intra- and inter-departmental colleagues and management, • Maintain a well-documented laboratory notebook., • Track project deliverables and provide updates on progress to team members, management, and cross-functional teams., • M.S. with at least 5+ years or B.S. with at least 7+ years of relevant industrial academic experience, • Experience with formulation development or drug product manufacturing., • Excellent analytical, critical thinking, and communication skills, • Proactive, solutions-oriented mindset to anticipate challenges and devise solutions, • Understanding of the drug development process and governing regulations., • Direct experience overseeing CDMOs and external partners, • Formulation development experience, • Experience authoring regulatory CMC sections for regulatory filings All applicants must have authorization to work in the US for a company. California Applicant Privacy Policy

Work Location: Madison, Wisconsin Shift: Department: LS-SC-UYWQFB QC Release, VOA Hiring Manager: Abel Madrigal This information is for internals only. Please do not share outside of the organization. Your Role: The Scientist, Quality position is responsible for the cGMP analytical laboratory analysis review in the Quality Control department of MilliporeSigma. Analysis may consist of all/some of the following: incoming raw material analysis, in-process testing, final product analysis, stability, reference standard requalification, method validation/qualification, cleaning, and environmental monitoring to support Quality Control activities at the Madison and Verona sites. Analysis includes techniques specific to, but not limited to: HPLC, GC, KF, DSC, TGA, IR, MS, NMR and LC-MS among other tests and instruments. Other responsibilities may include initiation and review of deviations, OOS/OOT's, change controls, and CAPA's. Additionally, participation in process improvement initiatives, working in a team environment, maintaining a clean and safe work area, and supporting the department in maintaining the laboratory in an audit ready state are other duties. \n • Analyze complex cGMP data using sound scientific rationale to identify root causes and implement effective CAPAs with minimal oversight.\n, • Perform in-depth analytical data review in support of QC, ensuring accuracy, integrity, and compliance with ALCOA+ principles.\n, • Prioritize and coordinate in-process testing reviews with manufacturing and laboratory teams to minimize downtime.\n, • Author and manage complex deviations, investigations, change controls, CAPAs, and OOS/OOT activities, communicating status to stakeholders.\n, • Review and support method development, validation, transfers, product changeovers, and ICP-MS testing for routine QC analysis.\n, • Maintain audit-ready laboratory operations, including safety, housekeeping, reagent management, waste disposal, and equipment qualification review (IQ/OQ/PV).\n, • Provide peer review, technical documentation, and training support for laboratory staff while upholding data integrity and "right first time" principles.\n, • Collaborate cross-functionally to manage projects and timelines while ensuring compliance with ICH Q7, 21 CFR Parts 11/210/211, and applicable regulatory standards.\n\n Physical Attributes: • Work in analytical testing lab with hazardous and toxic chemicals.\n Who You Are Minimum Qualifications: \n • Bachelors Degree in Chemistry, Biology, or other Life Science discipline.\n, • 5+ years experience in a GLP or cGMP analytical laboratory environment\n\n Preferred Qualifications: \n • Understanding of 21 CFR Part 11, 210 and 211, and ICH Q7.\n, • Excellent written and verbal communication skills, as well as good documentation practices and attention to detail.\n, • Knowledge and understanding of analytical chemistry techniques listed above in the 'your role'. (HPLC, GC, KF, DSC, TGA, IR, MS, NMR and LC-MS)\n, • Experience in reviewing GMP technical data from the analytical chemistry technique listed above in the 'your role'.\n, • Adequate technical writing skills to author reports, training memos and operating procedures.\n\n Pay Range for this position: $70,000-$109,200 The offer range represents the anticipated low and high end of the base pay compensation for this position. The actual compensation offered will be determined by factors such as location, level of experience, education, skills, and other job-related factors. Position may be eligible for sales or performance-based bonuses. Benefits offered by the Company include health insurance, paid time off (PTO), retirement contributions, and other perquisites. For more information click here. The Company is an Equal Employment Opportunity employer. No employee or applicant for employment will be discriminated against on the basis of race, color, religion, age, sex, sexual orientation, national origin, ancestry, disability, military or veteran status, genetic information, gender identity, transgender status, marital status, or any other classification protected by applicable federal, state, or local law. This policy of Equal Employment Opportunity applies to all policies and programs relating to recruitment and hiring, promotion, compensation, benefits, discipline, termination, and all other terms and conditions of employment. Any applicant or employee who believes they have been discriminated against by the Company or anyone acting on behalf of the Company must report any concerns to their Human Resources Business Partner, Legal, or Compliance immediately. The Company will not retaliate against any individual because they made a good faith report of discrimination.

OUR TEAM: The Nucleic Acids Technology group at Promega consists of highly experienced and dedicated scientists. The group focus is developing high quality products for amplification related workflows across multiple technologies and disciplines including Life Sciences and Diagnostics. YOUR ROLE: As Sr Research Scientist 1 you would be involved in the scientific leadership of the company, i.e. management, mentoring, consensus building and/or act as technical expert in multiple areas of specialization. Apply scientific leadership to individual R&D Projects. Demonstrate the ability to execute and champion innovative research. Formulate an overall project strategy for experimental design in the context of experimental results and scientific literature. CORE DUTIES: 1. Design, develop, and validate amplification assays and platform workflows for diverse applications including absolute quantification and rare target detection; troubleshoot complex amplification challenges., 2. Apply AI/ML tools, machine learning algorithms, and advanced data analytics to qPCR, dPCR, NGS and molecular biology datasets to extract biological insights, identify novel assay modalities, and develop predictive models for assay performance optimization., 3. Leverage NGS knowledge to support sequencing-related initiatives and integrate qPCR, dPCR and NGS capabilities within multi-omics workflows., 4. Work independently and collaboratively to create novel product concepts, experimental strategies, and applications for nucleic acid amplification technologies., 5. Collaborate across interdisciplinary teams-including bioinformatics scientists, data science groups, and commercial and product development teams-to accelerate assay innovation and computational integration., 6. Communicate findings effectively through scientific reports, presentations, and cross-functional discussions., 7. Provide scientific mentorship to junior scientists and contribute to building a collaborative, innovative team environment., 8. Demonstrates inclusion through their own words and actions and is accountable for a safe workspace. Acts with kindness, curiosity, and respect for others., 9. Embraces and is open to incorporating Promega's 6 Emotional & Social Intelligence (ESI) core principles in daily work., 10. Understands and complies with ethical, legal, and regulatory requirements applicable to our business. KEY QUALIFICATIONS: 1. PhD (or equivalent) in Molecular Biology, Biochemistry, Genomics, Computational Biology, Bioinformatics, Biostatistics, or a related discipline, with demonstrated ability to bridge experimental and analytical domains., 2. 2-5+ years of postdoctoral or industry experience applying experimental and/or computational approaches to nucleic acid technologies, assay development, or molecular biology research., 3. Demonstrated hands-on expertise in PCR-based technologies (PCR, qPCR, RT-qPCR) and assay design, including experience with multiparametric readouts., 4. Experience with NGS methodologies (DNA and/or RNA sequencing), with demonstrated application preferred., 5. Demonstrated ability to apply computational approaches-such as machine learning, statistical modeling, predictive simulations, or AI-driven analysis-to molecular biology or assay datasets., 6. Strong quantitative and problem-solving skills, with the ability to bridge computational and experimental domains., 7. Strong written and verbal communication skills, with the ability to collaborate effectively across scientific and commercial teams. PHYSICAL DEMANDS: 1. Ability to remain stationary at a laboratory bench or computer for extended periods., 2. Ability to operate and use laboratory equipment, prepare reagents, and assemble experimental systems., 3. Ability to position oneself in low positions (e.g., accessing freezers or lab equipment)., 4. Ability to move objects up to 20 pounds., 5. Ability to transport materials between laboratories and buildings. At Promega, we are committed to building a diverse workforce that reflects the communities we serve and creating a culture where everyone belongs. As an Equal Opportunity Employer, we welcome and encourage applications from all backgrounds, ensuring that employment decisions are made fairly and equitably.

Summary: As a Data Scientist at Meta, you will shape the future of people-facing and business-facing products we build across our entire family of applications (Facebook, Instagram, Messenger, WhatsApp, Oculus). By applying your technical skills, analytical mindset, and product intuition to one of the richest data sets in the world, you will help define the experiences we build for billions of people and hundreds of millions of businesses around the world. You will collaborate on a wide array of product and business problems with a wide-range of cross-functional partners across Product, Engineering, Research, Data Engineering, Marketing, Sales, Finance and others. You will use data and analysis to identify and solve product development's biggest challenges. You will influence product strategy and investment decisions with data, be focused on impact, and collaborate with other teams. By joining Meta, you will become part of a world-class analytics community dedicated to skill development and career growth in analytics and beyond.Product leadership: You will use data to shape product development, quantify new opportunities, identify upcoming challenges, and ensure the products we build bring value to people, businesses, and Meta. You will help your partner teams prioritize what to build, set goals, and understand their product's ecosystem.Analytics: You will guide teams using data and insights. You will focus on developing hypotheses and employ a varied toolkit of rigorous analytical approaches, different methodologies, frameworks, and technical approaches to test them.Communication and influence: You won't simply present data, but tell data-driven stories. You will convince and influence your partners using clear insights and recommendations. You will build credibility through structure and clarity, and be a trusted strategic partner. Required Skills: Data Scientist, Product Analytics Responsibilities: * Work with large and complex data sets to solve a wide array of challenging problems using different analytical and statistical approaches * Apply technical expertise with quantitative analysis, experimentation, data mining, and the presentation of data to develop strategies for our products that serve billions of people and hundreds of millions of businesses * Identify and measure success of product efforts through goal setting, forecasting, and monitoring of key product metrics to understand trends * Define, understand, and test opportunities and levers to improve the product, and drive roadmaps through your insights and recommendations * Partner with Product, Engineering, and cross-functional teams to inform, influence, support, and execute product strategy and investment decisions Minimum Qualifications: * Bachelor's degree in Computer Science, Computer Engineering, relevant technical field, or equivalent practical experience * Bachelor's degree in Mathematics, Statistics, a relevant technical field, or equivalent * 4+ years of work experience in analytics, data querying languages such as SQL, scripting languages such as Python, and/or statistical mathematical software such as R (minimum of 2 years with a Ph.D.) * 4+ years of experience solving analytical problems using quantitative approaches, understanding ecosystems, user behaviors & long-term product trends, and leading data-driven projects from definition to execution [including defining metrics, experiment, design, communicating actionable insights] Preferred Qualifications: * Master's or Ph.D. Degree in a quantitative field * Demonstrated ability to integrate AI tools to optimize/redesign workflows and drive measurable impact (e.g., efficiency gains, quality improvements) * Experience adhering to and implementing responsible, ethical AI practices (e.g., risk assessment, bias mitigation, quality and accuracy reviews) * Demonstrated ongoing AI skill development (e.g., prompt/context engineering, agent orchestration) and staying current with emerging AI technologies Public Compensation: $147,000/year to $208,000/year + bonus + equity + benefits Industry: Internet Equal Opportunity: Meta is proud to be an Equal Employment Opportunity and Affirmative Action employer. We do not discriminate based upon race, religion, color, national origin, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender, gender identity, gender expression, transgender status, sexual stereotypes, age, status as a protected veteran, status as an individual with a disability, or other applicable legally protected characteristics. We also consider qualified applicants with criminal histories, consistent with applicable federal, state and local law. Meta participates in the E-Verify program in certain locations, as required by law. Please note that Meta may leverage artificial intelligence and machine learning technologies in connection with applications for employment. Meta is committed to providing reasonable accommodations for candidates with disabilities in our recruiting process. If you need any assistance or accommodations due to a disability, please let us know at .

Target roles and stacks Current demand often includes entry-level software programmers, Java full stack developers, Python/Java developers, DevOps engineers, data analysts, data engineers, data scientists, and ML/AI engineers. The focus remains consistent: Java / Full Stack / DevOps plus Data Analyt

Work with Omnichannel Data Engineer to Integrate data from multiple sources (e. Build and maintain familiarity with Otsuka Machine Learning tech stack including AWS, Kubernetes, Snowflake, and Dataiku. Demonstrated experience with scripting and implementing data analytics algorithms and models.

Demonstrated experience working with large, complex datasets using big data technologies and script. Solid knowledge and understanding managing data to scale using data summarization, query and analysis software and tools. Creates business application and modeling framework, for new datasets, and di

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

Job Description Define the physics foundation powering the next generation of high-field magnetic mirror fusion. The Senior Theoretical & Computational Scientist will both lead and 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 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. 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., • Lead and participate in several 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 and business leadership teams 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., • 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 5 years’ experience in theoretical and computational plasma physics research., • Extensive 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 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. 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 We encourage applicants who don't meet all the criteria but believe they can thrive in this role to apply

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