Senior scientist jobs in New Hampshire - 60 jobs

Reality Labs at Meta is seeking Research Scientists with experience in product-focused machine learning and signal processing research to advance our pioneering work in neuromotor interfaces, which has grown out of the acquisition of CTRL-labs. We're building a practical interface drawing on the rich neuromotor signals that can be measured non-invasively via surface electromyography (EMG) with single motor neuron resolution. This technology could become one of the main pillars for interaction with virtual and augmented worlds.We are a multi-disciplinary team of researchers investigating the nature of human neuromotor signals, developing novel signal processing and machine learning methods to infer a user's intent, and creating novel interaction techniques and user experiences. Help us unleash human potential by removing the bottlenecks between user intent and action. **Required Skills:** Research Scientist - CTRL Labs Responsibilities: 1. Research and develop Deep Learning or other computational models 2. Design methods, tools and infrastructure to analyze and leverage rich multimodal data sets 3. Set technical direction for a project of 2-3 researchers and engineers 4. Help transition and deliver our work from research into product 5. Adapt standard machine learning methods to best leverage modern parallel environments (e.g. distributed clusters, multicore SMP, and GPU) **Minimum Qualifications:** Minimum Qualifications: 6. Bachelor's degree in Computer Science, Computer Engineering, relevant technical field, or equivalent practical experience 7. Ph.D. degree in Computer Science and Engineering, Electrical Engineering, Statistics/Mathematics 8. Experience with developing machine learning models at scale from inception to business impact 9. Programming experience in Python and hands-on experience with frameworks such as PyTorch 10. Exposure to architectural patterns of large scale software applications 11. Must obtain work authorization in the country of employment at the time of hire, and maintain ongoing work authorization during employment **Preferred Qualifications:** Preferred Qualifications: 12. Proven track record of achieving significant results as demonstrated by grants, fellowships, patents, as well as first-authored publications at peer-reviewed AI conferences (e.g. NeurIPS, CVPR, ICML, ICLR, ICCV, ACL, and ICASSP) 13. Demonstrated software engineer experience via an internship, work experience, coding competitions, or widely used contributions in open source repositories (e.g. GitHub) 14. Experience bringing machine learning-based products from research to production **Public Compensation:** $184,000/year to $257,000/year + 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 accommodations-ext@meta.com.

About iCAD: iCAD, a global leader on a mission to create a world where cancer can't hide by providing clinically proven AI-powered solutions that enable medical providers to accurately and reliably detect cancer earlier and improve patient outcomes. iCAD's industry-leading ProFound Breast Health Suite provides AI-powered mammography analysis for breast cancer detection, density assessment and risk evaluation. The ProFound Breast Health Suite is cleared by the U.S. Food & Drug Administration (FDA) and has received CE mark and Health Canada licensing. Used by thousands of providers serving millions of patients, ProFound is available in over 50 countries. POSITION DESCRIPTION: iCAD is seeking a talented and motivated Senior AI Researcher to join our dynamic and innovative team. As a critical contributor to our research and development efforts, you will play a pivotal role in designing, developing, and improving AI-based medical devices that will drive the next generation of solutions in medical imaging and healthcare, particularly in breast cancer detection and diagnosis. This position offers the opportunity to work in a fast-paced environment with cutting-edge technology while directly contributing to saving lives through improved healthcare solutions. RESPONSIBILITIES: AI Model Development: Design, develop, and optimize AI/ML models, specifically deep learning algorithms, to advance our breast cancer detection and imaging tools. Algorithm Research: Conduct research to identify new methodologies, techniques, and technologies in artificial intelligence and machine learning that can be applied to medical image analysis. Collaboration with Product Management: Work closely with Product Management to identify key innovation areas where AI can drive meaningful product functionality and market differentiation improvements. Contribute to strategic roadmaps by providing insights on AI trends and potential research breakthroughs that align with customer needs and business goals. Data Analysis: Work with large medical datasets, performing data preprocessing, annotation, and enhancement tasks to improve the accuracy and efficiency of AI models. Collaborate Across Teams: Partner with software engineers, radiologists, clinical teams, and other stakeholders to integrate AI solutions into production environments and evaluate their real-world performance. Validation and Testing: Lead the testing and validation of AI models to ensure they meet regulatory standards, including FDA clearance, and are robust for clinical use. Research Publications and Product Marketing Support: Provide write-ups, white papers, and technical documentation that clearly describe the functionality, benefits, and impact of AI models and innovations. Collaborate with Product Management and Marketing teams to highlight the key benefits of research deliverables for external audiences, including customers, investors, and healthcare professionals. Mentorship: Provide mentorship and guidance to junior researchers and collaborate with cross-functional teams to accelerate research and development efforts. Regulatory Compliance: Ensure all AI development activities comply with healthcare industry regulations and are accompanied by supporting documentation for submissions to regulatory bodies. REQUIREMENTS: Ph.D. in Computer Science, Artificial Intelligence, Data Science, or a related field. 5+ years of R&D experience in medical imaging, computer vision, or machine learning, with a proven track record of developing AI solutions. Expertise in deep learning frameworks such as TensorFlow, Keras, or PyTorch. Advanced knowledge of Python and C++ for implementing AI solutions. Demonstrated experience with large-scale data processing and managing complex datasets. Experience with medical imaging datasets (e.g., DICOM, mammography, CT, MRI) is highly preferred. Solid understanding of AI model validation techniques, regulatory requirements (e.g., FDA 510(k)), and experience working in a healthcare environment. Strong publication history in top-tier conferences and journals, showcasing original research. Strong communication skills, with the ability to present complex research results to technical and non-technical stakeholders. Excellent analytical, organizational, and communication skills with the ability to present complex ideas clearly. A proactive team player, capable of working independently while contributing to cross-functional teams. Ability to generate patentable ideas and contribute to intellectual property development. Preferred Qualifications: Experience with explainable AI (XAI) and model interpretability in medical applications. Familiarity with cloud platforms (Google Cloud, AWS) and deploying AI solutions in cloud environments. Knowledge of biostatistics, healthcare regulations, and clinical workflows. Experience working in cross-functional teams and fast-paced R&D environments. LOCATION: Full Remote.

Sumitomo Pharma Co., Ltd., is a global pharmaceutical company based in Japan with operations in the U.S. (Sumitomo Pharma America, Inc.), focused on addressing patient needs in oncology, urology, women's health, rare diseases, cell & gene therapies and CNS. With several marketed products and a diverse pipeline of early- to late-stage investigational assets, we aim to accelerate discovery, research, and development to bring novel therapies to patients sooner. For more information on SMPA, visit our website ********************************** or follow us on LinkedIn. **Job Overview** We are currently seeking a dynamic, highly motivated, and experienced individual for the position of Scientist II. This position will be part of the Translational Research and Medicine-Oncology team, with a primary focus on advancing translational research to support oncology programs in clinical trial stages. This individual will be responsible for designing, oversighting, and interpretating translational studies to understand mechanism of action, resistance pathways, and potential new indications. The candidate may also be involved in biomarker analysis to support these translational objectives. **Job Duties and Responsibilities** + Develop hypotheses by integrating insights from scientific literature, preclinical and clinical data + Design experiments to support identification of mechanism of action, resistance mechanisms, and potential indications + Manage translational research and biomarker studies conducted with CROs and academic investigators to ensure high-quality, timely delivery of data + Maintain organized, detailed logs of studies and data to ensure accuracy, reproducibility, and compliance with regulatory standards + Present data and insights in internal meetings and cross-functional program team discussions **Key Core Competencies** + Scientific curiosity with ability to generate and test hypotheses that inform drug development + Excellent problem-solving and critical-thinking skills to interpret complex data + Strong organizational skills and attention to detail in managing studies, data, and documentation + Strong project management and vendor oversight skills + Adaptability and resilience in a fast-paced, evolving research environment **Education and Experience** + PhD degree in a related field of science (Biology, Biochemistry, Molecular & Cellular biology, Cancer Biology, Immunology) + 1-3 years of postdoctoral or industry research experience + Familiarity with oncology research preferred + Experience with common biomarker platforms (e.g. NGS, flow cytometry, IHC) preferred The base salary range for this role is $102,000 to $127,000. Base salary is part of our total rewards package which also includes the opportunity for merit-based salary increases, short incentive plan participation, eligibility for our 401(k) plan, medical, dental, vision, life and disability insurances and leaves provided in line with your work state. Our robust time-off policy includes flexible paid time off, 11 paid holidays plus additional time off for a shut-down period during the last week of December, 80 hours of paid sick time upon hire and each year thereafter. Total compensation, including base salary to be offered, will depend on elements unique to each candidate, including candidate experience, skills, education and other factors permitted by law. Disclaimer: The above statements are intended to describe the general nature and level of work being performed by people assigned to this classification. They are not to be construed as an exhaustive list of all responsibilities, duties, and skills required of personnel so classified. All personnel may be required to perform duties outside of their normal responsibilities from time to time, as needed. **Confidential Data** : All information (written, verbal, electronic, etc.) that an employee encounters is considered confidential. **Compliance** : Achieve and maintain Compliance with all applicable regulatory, legal and operational rules and procedures, by ensuring that all plans and activities for and on behalf of Sumitomo Pharma America (SMPA) and affiliates are carried out with the "best" industry practices and the highest ethical standards. It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability. **Mental/Physical Requirements** : Fast paced environment handling multiple demands. Must be able to exercise appropriate judgment as necessary. Requires a high level of initiative and independence. Excellent written and oral communication skills required. Requires ability to use a personal computer for extended periods of time. **Sumitomo Pharma America (SMPA)** **is an Equal Employment Opportunity (EEO) employer** Qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; marital, domestic partnership or civil union status; sex, gender; affectional or sexual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law. Sumitomo Pharma Co., Ltd., is a global pharmaceutical company based in Japan with operations in the U.S. (Sumitomo Pharma America, Inc.), focused on addressing patient needs in oncology, urology, women's health, rare diseases, cell & gene therapies and CNS. With several marketed products and a diverse pipeline of early- to late-stage investigational assets, we aim to accelerate discovery, research, and development to bring novel therapies to patients sooner. For more information on SMPA, visit our website ********************************** or follow us on LinkedIn. Sumitomo Pharma America (SMPA) endeavors to make its application process accessible to all. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process, please contact SMPA at ********************************************** This contact information is for accommodation requests only and cannot be used to inquire about the status of applications. At Sumitomo Pharma America, our work is guided by the Sumitomo Pharma mission, vision and values, which tie closely to our company's cultural pillars. **Our** **Mission** _To broadly contribute to society through value creation based on innovative research and development activities for the betterment of healthcare and fuller lives of people_ _worldwide_ **Our** **Vision** _For Longer and Healthier Lives, we unlock the future with cutting edge technology and_ _ideas_

Invent, implement and deploy state-of-the-art machine learning and/or specific domain industry algorithms and systems. Build prototypes and explore conceptually new solutions. Work collaboratively with science, engineering, and product teams to identify customer needs in order to create and implement solutions, promote innovation and drive model implementations. Applies data science capabilities and research findings to create and implement solutions to scale. Responsible for developing new intelligence around core products and services through applied research on behalf of our customers. Develops models, prototypes, and experiments that pave the way for innovative products and services. Build cloud services that work out of the box for enterprises, e.g. decision support, anomaly detection, forecasting and recommendations), natural language processing (NLP), Natural Language Understanding (NLU),Time Series, Automatic Speech Recognition (ASR), Machine Learning (ML), and Computer Vision (CV). Design and run experiments, research new algorithms, and find new ways of optimizing risk, profitability, and customer experience. Conversant on ethical problems in consideration of sciences. **Responsibilities** Leading contributor providing guidance and mentorship to define, design and deliver product quality improvements from ideation stage to shipping to the customer. Write high quality code to power experiments and build models. Contributes to writing production model code. Work closely with product management and engineering to deliver products which solves the needs of our customers by building relevant, innovative results which strategically differentiates Oracle in the market. Set up environment needed to run experiments for all projects. Set up distributed environments. Engage with customers and help solve complex problems with the customer/partner. Directly impact our customers via innovation in products and services that make use of ML/AI technology. Clearly articulate technical work to audiences of all levels and across multiple functional areas. Keep track of the progress and ensure the team is following the best practices. Works on training data collection, feature engineering, model training, offline and online experimentation. Drives independent research and development. Advance the state-of-the-art machine learning and algorithms for real-world large-scale applications. Ensure solutions are designed with fairness and explainability in mind. May perform other duties as assigned. Disclaimer: **Certain US customer or client-facing roles may be required to comply with applicable requirements, such as immunization and occupational health mandates.** **Range and benefit information provided in this posting are specific to the stated locations only** US: Hiring Range in USD from: $120,100 to $251,600 per annum. May be eligible for bonus, equity, and compensation deferral. Oracle maintains broad salary ranges for its roles in order to account for variations in knowledge, skills, experience, market conditions and locations, as well as reflect Oracle's differing products, industries and lines of business. Candidates are typically placed into the range based on the preceding factors as well as internal peer equity. Oracle US offers a comprehensive benefits package which includes the following: 1. Medical, dental, and vision insurance, including expert medical opinion 2. Short term disability and long term disability 3. Life insurance and AD&D 4. Supplemental life insurance (Employee/Spouse/Child) 5. Health care and dependent care Flexible Spending Accounts 6. Pre-tax commuter and parking benefits 7. 401(k) Savings and Investment Plan with company match 8. Paid time off: Flexible Vacation is provided to all eligible employees assigned to a salaried (non-overtime eligible) position. Accrued Vacation is provided to all other employees eligible for vacation benefits. For employees working at least 35 hours per week, the vacation accrual rate is 13 days annually for the first three years of employment and 18 days annually for subsequent years of employment. Vacation accrual is prorated for employees working between 20 and 34 hours per week. Employees working fewer than 20 hours per week are not eligible for vacation. 9. 11 paid holidays 10. Paid sick leave: 72 hours of paid sick leave upon date of hire. Refreshes each calendar year. Unused balance will carry over each year up to a maximum cap of 112 hours. 11. Paid parental leave 12. Adoption assistance 13. Employee Stock Purchase Plan 14. Financial planning and group legal 15. Voluntary benefits including auto, homeowner and pet insurance The role will generally accept applications for at least three calendar days from the posting date or as long as the job remains posted. Career Level - IC4 **About Us** As a world leader in cloud solutions, Oracle uses tomorrow's technology to tackle today's challenges. We've partnered with industry-leaders in almost every sector-and continue to thrive after 40+ years of change by operating with integrity. We know that true innovation starts when everyone is empowered to contribute. That's why we're committed to growing an inclusive workforce that promotes opportunities for all. Oracle careers open the door to global opportunities where work-life balance flourishes. We offer competitive benefits based on parity and consistency and support our people with flexible medical, life insurance, and retirement options. We also encourage employees to give back to their communities through our volunteer programs. We're committed to including people with disabilities at all stages of the employment process. If you require accessibility assistance or accommodation for a disability at any point, let us know by emailing accommodation-request_************* or by calling *************** in the United States. Oracle is an Equal Employment Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, sexual orientation, gender identity, disability and protected veterans' status, or any other characteristic protected by law. Oracle will consider for employment qualified applicants with arrest and conviction records pursuant to applicable law.

The research scientist will play an integral role in the organic growth strategy focused on the development of new materials for the organization. The primary responsibilities of this position include advancing the growth processes of novel single crystalline materials such as Ga2O3, ultimately contributing to new product sales. Additional responsibilities encompass identifying, testing, and managing raw material inventories for the research and development team; designing experiments and conducting growth trials for crystalline materials; modifying furnace designs to facilitate crystal growth and enhance performance; monitoring the performance characteristics of the produced crystals; and supporting the transition of research and development initiatives to the production team. The ideal candidate should possess knowledge of semiconducting materials and general crystallography, along with experience or familiarity with various high-temperature oxides such as sapphire and garnets, as well as several growth methods, including Czochralski, EFG, HEM, and Bridgman, among others. Key Responsibilities Assist in the development of Ga2O3 single crystal growth processes, including the planning and carrying out of growth trials, and reporting on overall developments. Provide support for characterization of Ga2O3 crystals, either those grown internally or sourced from external vendors or collaborators. This includes characterization of material in house, and management of material sent for analysis externally. Assist in defect identification, analysis, material improvement and scale up of EFG grown oxides. Stay abreast of and provide information to others at Luxium Solutions on technical advances in the field of functional materials with a focus on materials for power electronics. Requirements Bachelor of Science in Materials Science, Physics, or Chemistry Ph.D. preferred Minimum of 5 years of experience in the development of ceramic materials, including but not limited to crystal growth, processing, and characterization. A minimum of 5 years of experience in crystal growth technologies. Comprehensive understanding of solid-state physics and/or materials science. Effective written and oral communication skills are necessary for interface with internal team members, other operations within Luxium Solutions, and outside experts. Advises manufacturing, engineering and sales on technical specifics. Proficient in utilizing computer software relevant to an industrial research and development environment. Demonstrated experience in defect engineering of ceramic materials and devices. Strong organizational, analytical, and problem solving skills using root cause analysis methods Experience with crystal growth techniques, such as Czochralski and EFG, is highly desirable. Familiarity with semiconducting materials and their applications in electronics, along with experience in modular instrumentation for materials testing and characterization, is preferred.. As an employer, we operate as an ITAR-regulated site and must comply with U.S. export control laws, which may limit employment to U.S. Citizen as defined under ITAR regulations Benefits Luxium Solutions offers a goal-oriented team dedicated to Safety, Excellence, Agility and Respect. Come pursue your career within a niche business and learn something that you can't find anywhere else! We have a great benefits package with: ANNUAL BONUS Salary: $90,000-$117,000 Paid Time Off available on day one (pro-rated for new hires) Medical/Dental/Vision/Prescriptions available on day one Employer Paid Life Insurance and AD&D Short/Long Term Disability HSA/FSA EAP 401(k) & company match Generous Tuition Reimbursement 6 week Paid Parental Leave & many more!

We are looking to fill a **Scientist III - (HPLC) Chromatography - Separations & Molecular Biology - Immunoassay Experience** position working as **a full-time employee of Parexel FSP on long-term assignment** onsite at one of our clients located in **Rahway, NJ.** This position offers full benefits, sick time, 401K, paid holidays, and paid time off. **This position does not offer any sponsorship.** **Description** Support of routine bioanalytical testing of samples from cell-line development, in-process, process development/characterization, forced degradation, release & stability, and pre-formulation. Other potential opportunities include method development/optimization, workflow optimization, and template development. **Responsibilities** + Support of high-throughput, pre-formulation, pre-qualification, robustness, or admixture testing + Results processing and documentation by following appropriate methods / protocols / procedures + Sample management and monitoring of controlled temperature units. + Following all appropriate laboratory safety and hygiene procedures **Qualifications** + BA/BS (3-5 yrs.) of relevant experience in analytical chemistry or biologics testing lab + MS (1-2 yrs.) of relevant experience in analytical chemistry or biologics testing lab **Required Skills and Experience** + Must have separations experience for large molecules or plate-based assay experience. + Experience in analyzing biologics including monoclonal antibodies and/or other therapeutic proteins using at least one of the following techniques: + Liquid Chromatography (HPLC / UPLC) + Protein A Titer, Size Exclusion Chromatography (SEC), Ion Exchange Chromatography (IEX, AEX, CEX), Reverse Phase (RP), or Hydrophobic interaction chromatography (HIC) + Electrophoretic methods such as capillary electrophoresis sodium dodecyl sulfate (CE-SDS) and/or capillary isoelectric focusing (cIEF) + ELISA (HCP, proA) and binding potency assay + qPCR and basic molecular biology techniques (gel electrophoresis, etc.) + High-throughput liquid handling system, e.g., Tecan, Bravo, etc. + Basic instrumentation troubleshooting + **Ability and willingness to train in molecular biology and immunoassay testing** + **Familiarity with Microsoft Office Applications (Outlook, Excel, Word, PowerPoint, OneNote, Teams, etc.)** **Desired Skills and Experience** + Familiarity with compendial testing such as UV 280, pH, and Physical Observations + **Ability to follow complicated scientific protocols / procedures** + Making accurate reagent preparations (dilutions / solutions / buffers / mobile phases) + Good documentation practices & utilization in electronic lab notebooks (ELN) + Analytical software such as Empower. + Knowledge of Laboratory Information Management Systems (LIMS) + Sample submission & sample management + Monitoring of controlled temperature units + Experience with BSL2 (Biosafety Level 2) **About Parexel** Parexel FSP includes the CMC Operations group. We provide pharmaceutical and biopharmaceutical companies with qualified and talented technical professionals to support the development and delivery of new therapies. For results-driven and caring individuals who want to make a meaningful difference in the world, Parexel is trusted by life sciences companies to meet their long-term staffing needs for scientists and engineers and related professionals in discovery and development of novel therapies, keeping patients at the center of everything we do, and where an inclusive community helps you be your best, transforming any career into a life-changing achievement. **Come join us!** \#LI-DK1 EEO Disclaimer Parexel is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to legally protected status, which in the US includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.

**What does Clinical Affairs contribute to Cardinal Health** The Clinical Affairs function manages the clinical education, medical writing and communications, research, health care economics and patient safety while ensuring compliance with applicable regulatory and governing requirements for Cardinal Health products and services. Medical Writing is a specialized role that creates clear, accurate, and compliant documents to communicate complex clinical and scientific data. It supports regulatory submissions, clinical research, and scientific communications by interpreting data and producing protocols, reports, regulatory dossiers, presentations, congress abstracts, and peer-reviewed publications, all in alignment with industry and regulatory standards. **Responsibilities:** The Senior Medical Writer will plan and develop high quality clinical documents to support Cardinal Health devices. Primary responsibilities include preparing Clinical Evaluation Reports (CERs), Post Market Plans & Reports (PMS and PMCF) as required by EU regulations. Additional responsibilities include providing input for product development and post-market sustaining core teams. Additional responsibilities may be assigned. The Senior Medical Writer has medical writing and project management experience, a thorough understanding of research methodology and the ability to develop high-quality clinical documents. Extensive knowledge of the European medical device guidelines/regulations such as MEDDEV and MDD/MDR is required, as well as other global requirements for clinical evaluation and PMS/PMCF. The Senior Medical Writer has the ability to lead cross-functional project teams. **Qualifications** + 8-12 years of experience, preferred + Bachelors in life science discipline; master's degree or PhD preferred or equivalent work experience. **Additional skills:** + Proven experience performing literature reviews, analyzing data and communicating outputs. + Ability to provide thorough peer reviews of team members' documents for completeness and correctness of data analysis & regulatory requirements. + Experience working within a medical device or pharmaceutical organization in a Research & Development, Scientific and Medical Affairs, Clinical or Regulatory role. + Experience writing scientific documents for regulatory or journal submissions + Experience presenting scientific/clinical evidence in a written and oral manner to cross-functional teams. + Demonstrated ability to build positive constructive relationships with cross-functional team members + Demonstrated high level of personal integrity, emotional intelligence, flexibility + Extensive knowledge of MDD, MDR and MEDDEV requirements, along with other applicable global requirements for clinical evaluation and PMS/PMCF + Experience creating and performing literature searches in Embase, PubMed and Google Scholar + Excellent working knowledge of Microsoft Word, Excel, PowerPoint. + Proficient in using EndNote or other reference manager software + Strong data extraction and analysis skills + Proactive with a sense of urgency in managing job responsibilities + Recommends new practices, processes, metrics or models **What is expected of you and others at this level** + Applies advanced knowledge and an understanding of concepts, principles and technical capabilities to manage a wide variety of projects + Participates in the development of policies and procedures to achieve specific goals + Recommends new practices, processes, metrics or models + Works on or may lead complex projects of large scope + Projects may have significant and long-term impact + Provides solutions that may set precedent + Independently determines method for completion of new projects + Receives guidance on overall project objectives + Acts as a mentor to less experienced colleagues **Anticipated salary range** : $123,400 - $149,855 **Bonus eligible** : Yes **Benefits** : Cardinal Health offers a wide variety of benefits and programs to support health and well-being. + Medical, dental and vision coverage + Paid time off plan + Health savings account (HSA) + 401k savings plan + Access to wages before pay day with my FlexPay + Flexible spending accounts (FSAs) + Short- and long-term disability coverage + Work-Life resources + Paid parental leave + Healthy lifestyle programs Application window anticipated to close: 2/6/2026*if interested in opportunity, please submit application as soon as possible. The salary range listed is an estimate. Pay at Cardinal Health is determined by multiple factors including, but not limited to, a candidate's geographical location, relevant education, experience and skills and an evaluation of internal pay equity. \#LI-MP1 \#LI-remote _Candidates who are back-to-work, people with disabilities, without a college degree, and Veterans are encouraged to apply._ _Cardinal Health supports an inclusive workplace that values diversity of thought, experience and background. We celebrate the power of our differences to create better solutions for our customers by ensuring employees can be their authentic selves each day. Cardinal Health is an Equal_ _Opportunity/Affirmative_ _Action employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, ancestry, age, physical or mental disability, sex, sexual orientation, gender identity/expression, pregnancy, veteran status, marital status, creed, status with regard to public assistance, genetic status or any other status protected by federal, state or local law._ _To read and review this privacy notice click_ here (***************************************************************************************************************************

**About ETS:** ETS is a global education and talent solutions organization enabling lifelong learners worldwide to be future-ready. For more than 75 years, we've been advancing the science of measurement to build benchmarks for fair and valid skill assessment across cultures and borders. Our worldwide impact extends through our renowned assessments including TOEFL , TOEIC , GRE and Praxis tests, serving millions of learners in more than 200 countries and territories. Through strategic acquisitions, we've expanded our global capabilities: PSI strengthens our workforce assessment solutions, while Edusoft, Kira Talent, Pipplet, Vericant, and Wheebox enhance our educational technology and assessment platforms across critical markets worldwide. Through ETS Research Institute and ETS Solutions, we're partnering with educational institutions, governments, and organizations globally to promote skill proficiency, empower upward mobility, and unlock opportunities for everyone, everywhere. With offices and partners across Asia, Europe, the Middle East, Africa, and the Americas, we deliver nearly 50 million tests annually. Join us in our journey of measuring progress to power human progress worldwide. The Associate R&D Data Scientist contributes to the planning, development, and execution of data science analyses for research and development projects within the ETS Research Institute. This role focuses on applying advanced data science, statistics, machine learning, and AI to make inferences and/or predictions from data. The position requires expertise in modern frameworks and cloud computing environments to support innovative research in educational measurement and assessment. **Primary Responsibilities** _Technical Responsibilties:_ Data Management and Analysis + Collect, preprocess, and manage structured and unstructured data from diverse sources, ensuring data quality and integrity. + Perform exploratory data analysis to identify trends, patterns, and actionable insights. Model Development and Evaluation + Design, implement, and validate predictive models and machine-learning algorithms using frameworks such as PyTorch/TensorFlow, and scikit-learn. + Experiment with large language models and generative AI techniques (e.g., working with large language model APIs, prompt engineering) to support innovative research. Deployment and Scalability + Develop and maintain pipelines for model deployment in cloud computing environments (e.g., AWS, Azure) to ensure scalability and reproducibility. _Research and Collaboration_ + Collaborate with scientists and cross-functional research teams to align data science efforts with program objectives + Contribute to technical reports, presentations, and publications that disseminate research findings. + Communicate complex technical concepts clearly to both technical and non-technical stakeholders. \#LI-MM1 \#Remote + Demonstrable proficiency and experience in Python and/or R for data analysis and modeling. + Hands-on experience with PyTorch/TensorFlow, Scikit-learn, and other machine learning frameworks. + Familiarity with generative AI methods and their practical applications. + Strong understanding of statistical methods, experimental design, and data visualization. + Ability to work in cloud computing environments (e.g., AWS) for model deployment and data processing. + Excellent problem-solving skills and adaptability to evolving research priorities. + Effective written and verbal communication skills for collaborative research environments. + Exceptional attention to detail, ensuring accuracy and reliability in data analysis, modeling, and reporting. **Education:** Master's degree in Data Science, Computer Science, Statistics, or a related quantitative field; or equivalent combination of education and experience. **ETS is mission driven and action oriented** + We are passionate about hiring innovative thinkers who believe in the promise of education and lifelong learning. + We are energized by cultivating growth, innovation, and continuous transformation for the next generation of rising professionals as leaders. In support of this ETS offers multiple Business Resource Groups (BRG) for you to learn and advance your career growth! + As a not-for-profit organization we will encourage you to lean in to your passion for volunteering. At ETS you may qualify for up to an additional 8 hours of PTO for volunteer work on causes that are important to you! + The base salary range advertised represents the low and high end of the anticipated salary range for this position. The base pay actually offered will take into account internal equity and also may vary depending on the candidate's geographic region, job-related knowledge, skills, and experience among other factors. The base pay is only one aspect of the Total Rewards Package that will be offered to the successful candidate. **ETS is an Equal Opportunity Employer. We are committed to providing equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, sex, national origin, age, disability, marital status, veteran status, sexual orientation, gender identity, or any other characteristic protected by law. We believe in creating a work environment where all individuals are treated with respect and dignity.**

Are you looking to build your career in environmental fieldwork and permitting with a company that values collaboration, professional growth, and work-life balance? Join Haley Ward, a 100% employee-owned, multidisciplinary firm named one of the Best Places to Work in Maine and one of the Best Firms to Work For in the country! AND, as an added benefit, we will offer you a $2,500 signing bonus. About Haley Ward At Haley Ward, our 300+ employee-owners provide environmental, engineering, and architectural services across the Northeast. We believe in teamwork, mentoring, and professional development, and we take pride in delivering high-quality, practical solutions for our clients. What We Offer $2,500 Signing Bonus Employee Stock Ownership Plan (ESOP) you ll be an owner! Competitive salary and benefits package, including health, dental, and vision insurance 401(k) with company match and Roth option Paid time off and 11 holidays Company-paid life and disability insurance Flexible Spending Accounts (FSA), Health Savings Accounts (HSA), and Health Reimbursement Arrangement (HRA) options Culture that values mentorship, flexibility, and volunteerism What You ll Do We are seeking a motivated Natural Resources Scientist to join our Environmental Team. This position will support senior permitting specialists and project managers with field investigations, data collection, and environmental documentation for permitting and compliance projects. Typical Responsibilities Conduct wetland delineations, vernal pool surveys, and wildlife and habitat assessments. Assist with soil evaluations, vegetation inventories, and hydrology observations. Collect and organize field data using GPS and mobile data collection tools. Prepare field forms, maps, and technical figures to support environmental reports and permit applications. Support preparation of Maine Department of Environmental Protection (MDEP), Maine Land Use Planning Commission (LUPC), Natural Resources Protection Act (NRPA), and U.S. Army Corps of Engineers (USACE) permit applications. Collaborate with multidisciplinary teams on environmental and infrastructure projects. Maintain accurate field records and contribute to project documentation. Note: Approximately 50% of work is conducted in the field, varying with project requirements, with the balance of time in an office setting. What You ll Bring Bachelor s degree in Environmental Science, Ecology, Natural Resources, Biology, or related field. 5+ years of field experience in wetlands, wildlife, or environmental science. Familiarity with state and federal environmental permitting preferred. Strong field identification skills for vegetation, soils, and hydrology indicators. Proficiency with GPS data collection and Microsoft Office; GIS or AutoCAD skills a plus. Excellent written and verbal communication. Ability to work independently outdoors and as part of a team. Valid driver s license and satisfactory driving record. Location: Saco, ME reliable commute or relocation required Haley Ward is proud to be an Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, marital status, age, national origin, disability, or veteran status.

The Scientist will contribute to Extractables & Leachables studies performed in the E&L laboratory at Boston Analytical to support client submissions. The ideal candidate will have experience operating LC-MS and GC-MS systems for analysis of volatile, semi-volatile, and nonvolatile organic extractables and leachables samples. PRIMARY DUTIES AND RESPONSIBILITIES • Prepares extractions for analysis. • Analysis of sample extract solutions by GC-MS and LC-MS to adequately resolve and identify all compounds. • Coordinate findings with the team to generate conclusions. • Author detailed cGMP report sections for work performed outlining study findings. • Develop analysis methods for drug product leachables testing. • Performs system maintenance and calibrations to ensure equipment is operating with specified requirements. Ensures all work performed strictly adheres to Company, client and Pharmacopial requirements. • Proper handling of hazardous waste in compliance with the Company and DES hazardous waste rules. REQUIREMENTS & QUALIFICATIONS Qualification includes a Ph.D. in Analytical Chemistry with 2+ years' experience or a Master's degree and 4+ years' experience or a Bachelor's with 6+ years' of experience performing and interpreting MS analysis. Knowledge of current Extractable & Leachables guidance (USP, ISO 10993) and best practices preferred. Experience working in a cGMP environment required. MINIMUM SKILLS REQUIREMENTS • Must have the ability and skill to perform the detailed job requirements noted above competently, safely and proficiently. • A self-starter, motivated person who possesses good interpersonal skills capable of effectively interacting with all departments and client personnel. • Must have excellent organizational, verbal communication and technical writing skills. • Must be a team player with integrity and concern for the quality of Company products, services and staff members. • Demonstrated LC-MS and/or GC-MS operation and data interpretation capability. • Ability to develop and optimize HPLC, UPLC, and GC methods. • Documented success managing complex projects to completion within customer expectations for deadline, cost, and overall deliverable

GZA GeoEnvironmental, Inc. (GZA) is seeking a Building Scientist to support our Construction Management and Building Sciences practices in our Hooksett, New Hampshire office. GZA is looking for candidates with educational and/or professional experience in building systems, hazardous building materials, and construction. Our close-knit culture here at GZA will allow you to grow professionally. You will be mentored by seasoned professionals, who will in turn look to you to share technical knowledge and ideas. Our success relies on this collaborative environment. Between on-site assignments, you will work in a professional office setting, preparing detailed and accurate project documentation, data analysis and reporting. GZA emphasizes a One Company environment, and as a member of our team, you may be asked to assist on projects and tasks outside of your primary practice group. Key Responsibilities Work with Construction Managers to evaluate buildings for the presence of potentially hazardous building materials. Conduct asbestos, lead paint, and hazardous material building assessments in accordance with federal and State regulations. Plan, execute, and report on asbestos, lead, and hazardous building material inspections, monitoring, and abatement projects. Perform abatement monitoring in accordance with federal and State regulations. Conduct oversight and on-site management (as applicable) of asbestos, lead, hazardous materials, environmental remediation, and demolition projects. Execute field tasks independently, such as material assessments, sample logging, site sketches, sample labeling, etc. Gather data and other information to be used in the preparation of reports; compile and organize environmental data collected by others. Conduct analytical data review, data interpretation, and report preparation. What You Will Bring Candidate should have an interest in and have a minimum basic knowledge of building systems, construction, and management of regulated materials. Experience related to construction, demolition, building sciences, asbestos, and lead-containing paint is a plus. Bachelor's Degree in Civil Engineering, Environmental Science, Environmental Engineering, Construction Management or similar relevant degree. 2+ years of experience in building science, hazardous building material, environmental, or civil engineering preferred. Candidate must possess a valid driver's license in good standing and ability to rent a vehicle. Strong verbal and written communication skills. Demonstrated reliability and ability to follow direction, work independently, and within a team. Experience in preparing field documentation, project specifications, and reports a plus. Availability to work Monday through Friday and occasionally evenings and weekends as warranted by project demands. Ability to travel overnight as warranted by project demands. Candidates should have the capacity to work outdoors in all seasons through various kinds of weather. Strong attention to detail with analytical and judgment capabilities. Ideal candidate will possess the following professional traits: ability to multi-task, take initiative and be highly motivated, work within a team of diverse engineers, technicians, clients, and contractors, adhere to project deadlines, and demonstrate a good work ethic. What You Will Be Getting Exciting and friendly work environment Convenient location Professional development and enrichment Leadership and technical training Professional society involvement and sponsorship Commitment to technical excellence and client relationships Collaborative and cooperative work community Advancement and ownership opportunities Generous benefits package, including medical, dental, vision and 401K retirement plan About GZA GZA is an employee-owned multidisciplinary engineering consulting firm with a history of more than 50 years of providing innovative engineering solutions to improve the natural and built environment. We are an ENR Top 500 Design firm focused on geotechnical, environmental, water, ecological, and construction management services. With a staff of interrelated professionals dedicated to providing high-level expertise on complex projects above, below and at ground-level, GZA's experts provide seamless integration across practice areas, client type, and location. GZA GeoEnvironmental, Inc. is an Affirmative/Equal Opportunity Employer and does not discriminate on the basis of race, color, religion, national origin, ancestry, sex, sexual orientation, physical or mental disability, citizenship status, marital or veteran status, age or other protected status. Note to Staffing Agencies: GZA GeoEnvironmental, Inc. and its subsidiaries do not accept unsolicited resumes from staffing agencies, recruiting firms, or other third parties. All unsolicited resumes will be considered a gift, and GZA will not be obligated to pay a referral fee. GZA explicitly reserves the right to hire those candidate(s) without any financial obligation to the recruiter or agency. This policy is in place to ensure we respect the relationships with our preferred vendors and avoid any potential misunderstandings.

Are you looking to build your career in environmental fieldwork and permitting with a company that values collaboration, professional growth, and work-life balance? Join Haley Ward, a 100% employee-owned, multidisciplinary firm named one of the Best Places to Work in Maine and one of the Best Firms to Work For in the country! AND, as an added benefit, we will offer you a $2,500 signing bonus. About Haley Ward At Haley Ward, our 300+ employee-owners provide environmental, engineering, and architectural services across the Northeast. We believe in teamwork, mentoring, and professional development, and we take pride in delivering high-quality, practical solutions for our clients. What We Offer * $2,500 Signing Bonus * Employee Stock Ownership Plan (ESOP) youll be an owner! * Competitive salary and benefits package, including health, dental, and vision insurance * 401(k) with company match and Roth option * Paid time off and 11 holidays * Company-paid life and disability insurance * Flexible Spending Accounts (FSA), Health Savings Accounts (HSA), and Health Reimbursement Arrangement (HRA) options * Culture that values mentorship, flexibility, and volunteerism What Youll Do We are seeking a motivated Natural Resources Scientist to join our Environmental Team. This position will support senior permitting specialists and project managers with field investigations, data collection, and environmental documentation for permitting and compliance projects. Typical Responsibilities * Conduct wetland delineations, vernal pool surveys, and wildlife and habitat assessments. * Assist with soil evaluations, vegetation inventories, and hydrology observations. * Collect and organize field data using GPS and mobile data collection tools. * Prepare field forms, maps, and technical figures to support environmental reports and permit applications. * Support preparation of Maine Department of Environmental Protection (MDEP), Maine Land Use Planning Commission (LUPC), Natural Resources Protection Act (NRPA), and U.S. Army Corps of Engineers (USACE) permit applications. * Collaborate with multidisciplinary teams on environmental and infrastructure projects. * Maintain accurate field records and contribute to project documentation. Note: Approximately 50% of work is conducted in the field, varying with project requirements, with the balance of time in an office setting. What Youll Bring * Bachelors degree in Environmental Science, Ecology, Natural Resources, Biology, or related field. * 5+ years of field experience in wetlands, wildlife, or environmental science. * Familiarity with state and federal environmental permitting preferred. * Strong field identification skills for vegetation, soils, and hydrology indicators. * Proficiency with GPS data collection and Microsoft Office; GIS or AutoCAD skills a plus. * Excellent written and verbal communication. * Ability to work independently outdoors and as part of a team. * Valid drivers license and satisfactory driving record. Location: Saco, ME reliable commute or relocation required Haley Ward is proud to be an Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, marital status, age, national origin, disability, or veteran status.

The Senior Food Scientist is a leading member of the Product Development and a cross- functional team responsible for delivering the initiatives, business plan, and objectives of High Liner Foods Inc. The Senior Food Scientist applies scientific, culinary and engineering principles in research & development, production technology, quality control, processing and utilization of ingredients to design, develop and produce new and/or improved products. The Senior Food Scientist is a Research & Development Subject Matter Expert for the organization and acts as a mentorship/coaching/training role within the PD Department. This position plays a major role in leading the creation of new products and therefore plays an important part in supporting HLF's overall strategic goals. Essential Duties and responsibilities Product Development Leads the development of new products and/or product optimization through HLF project management system including: Gold standard development Formulation development Bench top preparation and testing Sensory evaluation/product cuttings with internal cross functional team members Sample preparation for various activities Customer presentation Specification development Cooking Instruction Development Organoleptic Shelf-Life Studies Collaborates with Sales and/or Marketing to define project parameters based on customer input/request. Leverages vendor relationships to deliver new products and products optimized products on time, within cost and quality Leads the coordination, design and execution of line test and first production processes. Provides technical expertise for all internal and external customers Leads the development and training of SOPs for the PD team and cross functional team members where applicable Acts as a mentor/coach for R&D team members. Continuous Improvement: Leads problem solving with Purchasing and Procurement teams regarding ingredient and raw material substitutions and cost saving initiatives. Lead and collaborates with Quality Assurance, Production, Purchasing, Procurement and Engineering to identify root causes and solutions when quality issues are clearly identified. Provides approval for modifications to existing product formulas and/or processes to improve productivity, quality and/or cost. Operational Excellence: Educates and ensures accurate laboratory and project work documentation. Leads R&D meetings to update and report project status and issues to broader team and leads corporate training sessions as needed. Leads and collaborates with the Commercialization Team through the stage gate process. Recommends and influences processes improvements within R&D and cross functional team members in order to drive efficiency and profitability through the organization. Acts as a SME on ingredients and researches and recommends new ingredient opportunities. Collaborates with Process Engineer and other SME's to be a leader in the knowledge of food manufacturing processes and equipment as they apply to the seafood industry and the food industry. Qualifications Minimum 5 years of experience and a B.S. in Food Science or related degree Seafood and Value-Added Coating Knowledge is a plus. Culinary training is a plus. Knowledge of Sensory testing an asset. Experience in coaching and mentoring team members Leadership in various environments includes but not exclusive to manufacturing and processing. Able to handle multiple projects in a fast-paced environment. Excellent time management skills. Excellent interpersonal and communication skills Self- Motivated; Able to work with little supervision, eagerness to learn and grow. Proficient in MS Office Working conditions This position is located at High Liner Headquarters. The position involves daily or frequent contact with satellite R&D groups, operations, business channel managers, sales, procurement, purchasing, regulatory, and quality assurance managers. It also involves external contact with suppliers. The position requires frequent and occasional travel, domestically and internationally. Physical requirements/Allergens The physical demands described are representative of those that must be met by an employee to successfully perform the essential functions of the job. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is frequently required to walk, sit, talk, listen, and reach with hands and arms. The employee is required to use hands to handle, operate, and feel objects, tools, or controls. The employee is occasionally required to operate a motor vehicle to travel to off-site meetings. The employee must have visual acuity sufficient to operate a motor vehicle and digital camera, as well as other office and position equipment. Specific vision abilities required by the job include close vision and the ability to adjust focus. Employees must be able to hear and speak clearly in order to communicate with clients, coworkers, employees and vendors. Must be able to lift up to 25lbs Must be able to stand for extended periods of time. Allergens found inside the plant include fish, shellfish, nuts, eggs, wheat, soy, milk and coconut. Travel North American Travel to visit suppliers and manufacturing locations required. (Travel 20% to 30%) What's in it for you? Join High Liner Foods for a career where you shape your path, backed by great benefits, flexible work, and a culture of diversity, innovation, and sustainability. Immerse yourself in opportunities to make a real impact and grow with us in our mission to nourish lives. Start your adventure where endless possibilities to thrive together await. Competitive Salary Heath, dental & vision coverage Pay for performance incentives Employee & Family assistance programs Wellness Programs Retirement Planning Supplemental Parental Leaves Disability Support Family friendly Flex policies Volunteer hours Learning and mentorship opportunities Safety focused work environment #HLSJ

The Research Scientist II will collaborate with project director B. Chandran and other members of his research group to carry out scientific research on turbulence and kinetic plasma physics in the solar wind.

SENIOR AI RESEARCH SCIENTIST About iCAD: iCAD, a global leader on a mission to create a world where cancer can't hide by providing clinically proven AI-powered solutions that enable medical providers to accurately and reliably detect cancer earlier and improve patient outcomes. iCAD's industry-leading ProFound Breast Health Suite provides AI-powered mammography analysis for breast cancer detection, density assessment and risk evaluation. The ProFound Breast Health Suite is cleared by the U.S. Food & Drug Administration (FDA) and has received CE mark and Health Canada licensing. Used by thousands of providers serving millions of patients, ProFound is available in over 50 countries. POSITION DESCRIPTION: iCAD is seeking a talented and motivated Senior AI Researcher to join our dynamic and innovative team. As a critical contributor to our research and development efforts, you will play a pivotal role in designing, developing, and improving AI-based medical devices that will drive the next generation of solutions in medical imaging and healthcare, particularly in breast cancer detection and diagnosis. This position offers the opportunity to work in a fast-paced environment with cutting-edge technology while directly contributing to saving lives through improved healthcare solutions. RESPONSIBILITIES: AI Model Development: Design, develop, and optimize AI/ML models, specifically deep learning algorithms, to advance our breast cancer detection and imaging tools. Algorithm Research: Conduct research to identify new methodologies, techniques, and technologies in artificial intelligence and machine learning that can be applied to medical image analysis. Collaboration with Product Management: Work closely with Product Management to identify key innovation areas where AI can drive meaningful product functionality and market differentiation improvements. Contribute to strategic roadmaps by providing insights on AI trends and potential research breakthroughs that align with customer needs and business goals. Data Analysis: Work with large medical datasets, performing data preprocessing, annotation, and enhancement tasks to improve the accuracy and efficiency of AI models. Collaborate Across Teams: Partner with software engineers, radiologists, clinical teams, and other stakeholders to integrate AI solutions into production environments and evaluate their real-world performance. Validation and Testing: Lead the testing and validation of AI models to ensure they meet regulatory standards, including FDA clearance, and are robust for clinical use. Research Publications and Product Marketing Support: Provide write-ups, white papers, and technical documentation that clearly describe the functionality, benefits, and impact of AI models and innovations. Collaborate with Product Management and Marketing teams to highlight the key benefits of research deliverables for external audiences, including customers, investors, and healthcare professionals. Mentorship: Provide mentorship and guidance to junior researchers and collaborate with cross-functional teams to accelerate research and development efforts. Regulatory Compliance: Ensure all AI development activities comply with healthcare industry regulations and are accompanied by supporting documentation for submissions to regulatory bodies. REQUIREMENTS: Ph.D. in Computer Science, Artificial Intelligence, Data Science, or a related field. 5+ years of R&D experience in medical imaging, computer vision, or machine learning, with a proven track record of developing AI solutions. Expertise in deep learning frameworks such as TensorFlow, Keras, or PyTorch. Advanced knowledge of Python and C++ for implementing AI solutions. Demonstrated experience with large-scale data processing and managing complex datasets. Experience with medical imaging datasets (e.g., DICOM, mammography, CT, MRI) is highly preferred. Solid understanding of AI model validation techniques, regulatory requirements (e.g., FDA 510(k)), and experience working in a healthcare environment. Strong publication history in top-tier conferences and journals, showcasing original research. Strong communication skills, with the ability to present complex research results to technical and non-technical stakeholders. Excellent analytical, organizational, and communication skills with the ability to present complex ideas clearly. A proactive team player, capable of working independently while contributing to cross-functional teams. Ability to generate patentable ideas and contribute to intellectual property development. Preferred Qualifications: Experience with explainable AI (XAI) and model interpretability in medical applications. Familiarity with cloud platforms (Google Cloud, AWS) and deploying AI solutions in cloud environments. Knowledge of biostatistics, healthcare regulations, and clinical workflows. Experience working in cross-functional teams and fast-paced R&D environments. LOCATION: Full Remote.

Job Description The research scientist will play an integral role in the organic growth strategy focused on the development of new materials for the organization. The primary responsibilities of this position include advancing the growth processes of novel single crystalline materials such as Ga2O3, ultimately contributing to new product sales. Additional responsibilities encompass identifying, testing, and managing raw material inventories for the research and development team; designing experiments and conducting growth trials for crystalline materials; modifying furnace designs to facilitate crystal growth and enhance performance; monitoring the performance characteristics of the produced crystals; and supporting the transition of research and development initiatives to the production team. The ideal candidate should possess knowledge of semiconducting materials and general crystallography, along with experience or familiarity with various high-temperature oxides such as sapphire and garnets, as well as several growth methods, including Czochralski, EFG, HEM, and Bridgman, among others. Key Responsibilities Assist in the development of Ga2O3 single crystal growth processes, including the planning and carrying out of growth trials, and reporting on overall developments. Provide support for characterization of Ga2O3 crystals, either those grown internally or sourced from external vendors or collaborators. This includes characterization of material in house, and management of material sent for analysis externally. Assist in defect identification, analysis, material improvement and scale up of EFG grown oxides. Stay abreast of and provide information to others at Luxium Solutions on technical advances in the field of functional materials with a focus on materials for power electronics. Requirements Bachelor of Science in Materials Science, Physics, or Chemistry Ph.D. preferred Minimum of 5 years of experience in the development of ceramic materials, including but not limited to crystal growth, processing, and characterization. A minimum of 5 years of experience in crystal growth technologies. Comprehensive understanding of solid-state physics and/or materials science. Effective written and oral communication skills are necessary for interface with internal team members, other operations within Luxium Solutions, and outside experts. Advises manufacturing, engineering and sales on technical specifics. Proficient in utilizing computer software relevant to an industrial research and development environment. Demonstrated experience in defect engineering of ceramic materials and devices. Strong organizational, analytical, and problem solving skills using root cause analysis methods Experience with crystal growth techniques, such as Czochralski and EFG, is highly desirable. Familiarity with semiconducting materials and their applications in electronics, along with experience in modular instrumentation for materials testing and characterization, is preferred.. As an employer, we operate as an ITAR-regulated site and must comply with U.S. export control laws, which may limit employment to U.S. Citizen as defined under ITAR regulations Benefits Luxium Solutions offers a goal-oriented team dedicated to Safety, Excellence, Agility and Respect. Come pursue your career within a niche business and learn something that you can't find anywhere else! We have a great benefits package with: ANNUAL BONUS Salary: $90,000-$117,000 Paid Time Off available on day one (pro-rated for new hires) Medical/Dental/Vision/Prescriptions available on day one Employer Paid Life Insurance and AD&D Short/Long Term Disability HSA/FSA EAP 401(k) & company match Generous Tuition Reimbursement 6 week Paid Parental Leave & many more!

Job DescriptionSalary: The Scientist will contribute to Extractables & Leachables studies performed in the E&L laboratory at Boston Analytical to support client submissions. The ideal candidate will have experience operating LC-MS and GC-MS systems for analysis of volatile, semi-volatile, and nonvolatile organic extractables and leachables samples. PRIMARY DUTIES AND RESPONSIBILITIES Prepares extractions for analysis. Analysis of sample extract solutions by GC-MS and LC-MS to adequately resolve and identify all compounds. Coordinate findings with the team to generate conclusions. Author detailed cGMP report sections for work performed outlining study findings. Develop analysis methods for drug product leachables testing. Performs system maintenance and calibrations to ensure equipment is operating with specified requirements. Ensures all work performed strictly adheres to Company, client and Pharmacopial requirements. Proper handling of hazardous waste in compliance with the Company and DES hazardous waste rules. REQUIREMENTS & QUALIFICATIONS Qualification includes a Ph.D. in Analytical Chemistry with 2+ years experience or a Masters degree and 4+ years experience or a Bachelors with 6+ years of experience performing and interpreting MS analysis. Knowledge of current Extractable & Leachables guidance (USP, ISO 10993) and best practices preferred. Experience working in a cGMP environment required. MINIMUM SKILLS REQUIREMENTS Must have the ability and skill to perform the detailed job requirements noted above competently, safely and proficiently. A self-starter, motivated person who possesses good interpersonal skills capable of effectively interacting with all departments and client personnel. Must have excellent organizational, verbal communication and technical writing skills. Must be a team player with integrity and concern for the quality of Company products, services and staff members. Demonstrated LC-MS and/or GC-MS operation and data interpretation capability. Ability to develop and optimize HPLC, UPLC, and GC methods. Documented success managing complex projects to completion within customer expectations for deadline, cost, and overall deliverable

**What Real World Evidence and Clinical Research contributes to Cardinal Health** The **Scientist, Real World Evidence (Clinical Research)** , will have responsibility to support the design and implementation of innovative Real-World Evidence (RWE)/Health Economics & Outcomes Research (HEOR) strategies and activities to produce scientific evidence and publications for our pharmaceutical clients, with guidance from Lead/Senior Scientists. Ideally, this individual will have experience conducting observational research studies from various data sources including administrative claims, electronic health records (EHR), or through primary data collection. This Scientist will collaborate with cross-functional teams in developing study proposals, research protocols, interpreting data, and reporting results. A majority of the work this team is involved with is focused in oncology. **_Responsibilities_** + Support the generation of high-quality real-world research studies using administrative claims, EHR, and primary data collection. + Conduct background product/disease area literature reviews. + Draft portions of research proposals, research protocols, table shells, statistical analysis plans, and study reports. + Proactively address research design and analytical issues. + Will work in a fast-paced environment engaging on multiple projects with multiple manufacturers at the same time. + Support the development of research study concepts, protocol, and reports. + Utilize appropriate research methods and data sources to deliver high-value and quality real-world research to pharmaceutical manufacturers. + Prepare proposal requests for RWE/HEOR work projects and manages selection process. + Prepare technical presentations and actively engage with the external environment in improving the state of the discipline. + Prepare HEOR data as background materials for discussion with pharmaceutical customers. + Communicate effectively and professionally with pharmaceutical HEOR customers. + Ability to provide excellent customer service when delivering work on projects. + Develop expertise in RWE/HEOR through publications and presentations of scientific research. + Collaborate with HEOR team, as required, to compile evidence required to execute projects for pharmaceutical clients. + Generate communication materials, publications, and reports. + Interact with HEOR personnel to assist with background materials for reports and publications. + Interact with HEOR staff to identify research activities and/or evidence to advance health care efficiencies for pharmaceutical clients. **_Qualifications_** + Experience with research protocol development and conducting observational research, highly preferred. + Experience (in education or through work experience) in a clinical setting, a plus. + Experience in Statistics or an individual with a degree in Public Health or Epidemiology, a plus. + Experience in Oncology, a plus but not required. + Problem-solving capability with well-developed conceptual and integrative thinking required. + Demonstrated success implementing projects, including engagement with key stakeholders, with high degree of autonomy, preferred + Excellent written and verbal communication skills, required. **_What is expected of you and others at this level_** + Applies comprehensive knowledge and a thorough understanding of concepts, principles, and technical capabilities to perform varied tasks and projects + May contribute to the development of policies and procedures + Works on complex projects of large scope + Develops technical solutions to a wide range of difficult problems. Solutions are innovative and consistent with organization objectives + Completes work independently; receives general guidance on new projects + Work reviewed for purpose of meeting objectives + May act as a mentor to less experienced colleagues **Anticipated Pay Range:** $94,900 - $122,000 **Bonus Eligible:** No **Benefits** : Cardinal Health offers a wide variety of benefits and programs to support health and well-being. + Medical, dental and vision coverage + Paid time off plan + Health savings account (HSA) + 401k savings plan + Access to wages before pay day with my FlexPay + Flexible spending accounts (FSAs) + Short- and long-term disability coverage + Work-Life resources + Paid parental leave + Healthy lifestyle programs **Application window anticipated to close** : 2/13/2025 * if interested in opportunity, please submit application as soon as possible. _** The salary range listed is an estimate. Pay at Cardinal Health is determined by multiple factors including, but not limited to, a candidate's geographical location, relevant education, experience and skills and an evaluation of internal pay equity._ _Candidates who are back-to-work, people with disabilities, without a college degree, and Veterans are encouraged to apply._ _Cardinal Health supports an inclusive workplace that values diversity of thought, experience and background. We celebrate the power of our differences to create better solutions for our customers by ensuring employees can be their authentic selves each day. Cardinal Health is an Equal_ _Opportunity/Affirmative_ _Action employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, ancestry, age, physical or mental disability, sex, sexual orientation, gender identity/expression, pregnancy, veteran status, marital status, creed, status with regard to public assistance, genetic status or any other status protected by federal, state or local law._ _To read and review this privacy notice click_ here (***************************************************************************************************************************

Job Description Are you looking to build your career in environmental fieldwork and permitting with a company that values collaboration, professional growth, and work-life balance? Join Haley Ward, a 100% employee-owned, multidisciplinary firm named one of the Best Places to Work in Maine™ and one of the Best Firms to Work For™ in the country! AND, as an added benefit, we will offer you a $2,500 signing bonus. About Haley Ward At Haley Ward, our 300+ employee-owners provide environmental, engineering, and architectural services across the Northeast. We believe in teamwork, mentoring, and professional development, and we take pride in delivering high-quality, practical solutions for our clients. What We Offer $2,500 Signing Bonus Employee Stock Ownership Plan (ESOP) - you'll be an owner! Competitive salary and benefits package, including health, dental, and vision insurance 401(k) with company match and Roth option Paid time off and 11 holidays Company-paid life and disability insurance Flexible Spending Accounts (FSA), Health Savings Accounts (HSA), and Health Reimbursement Arrangement (HRA) options Culture that values mentorship, flexibility, and volunteerism What You'll Do We are seeking a motivated Natural Resources Scientist to join our Environmental Team. This position will support senior permitting specialists and project managers with field investigations, data collection, and environmental documentation for permitting and compliance projects. Typical Responsibilities Conduct wetland delineations, vernal pool surveys, and wildlife and habitat assessments. Assist with soil evaluations, vegetation inventories, and hydrology observations. Collect and organize field data using GPS and mobile data collection tools. Prepare field forms, maps, and technical figures to support environmental reports and permit applications. Support preparation of Maine Department of Environmental Protection (MDEP), Maine Land Use Planning Commission (LUPC), Natural Resources Protection Act (NRPA), and U.S. Army Corps of Engineers (USACE) permit applications. Collaborate with multidisciplinary teams on environmental and infrastructure projects. Maintain accurate field records and contribute to project documentation. Note: Approximately 50% of work is conducted in the field, varying with project requirements, with the balance of time in an office setting. What You'll Bring Bachelor's degree in Environmental Science, Ecology, Natural Resources, Biology, or related field. 5+ years of field experience in wetlands, wildlife, or environmental science. Familiarity with state and federal environmental permitting preferred. Strong field identification skills for vegetation, soils, and hydrology indicators. Proficiency with GPS data collection and Microsoft Office; GIS or AutoCAD skills a plus. Excellent written and verbal communication. Ability to work independently outdoors and as part of a team. Valid driver's license and satisfactory driving record. Location: Saco, ME - reliable commute or relocation required Haley Ward is proud to be an Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, marital status, age, national origin, disability, or veteran status.