Principal research scientist jobs in Newport News, VA

Novateur stands for Innovation. We value creativity, vision, collaboration, and above all, ambition to innovate. Novateur Research Solutions is an R&D firm located in Northern Virginia, developing intelligent systems that push the boundaries of computer vision, AI, and large-scale learning. We are hiring a Principal Research Scientist to lead cutting-edge programs in AI, computer vision, and intelligent systems. This role offers leadership opportunities to define new research directions and shape next-generation technologies. Responsibilities: • Serve as PI or co-PI on government-funded R&D programs. • Conceive, design, and oversee research in learning systems, spatiotemporal modeling, and geo-localization. • Publish, present, and contribute thought leadership to the AI community. • Mentor research staff and guide proposal development. Requirements: • PhD with 7+ years of research experience. • Demonstrated leadership in ML, vision, or scientific computing. • Record of funding, publications, and technical impact. • U.S. Citizen or Permanent Resident. Preferred: • Experience with multimodal learning, uncertainty quantification, or causal inference. Why Novateur? Join a team that values creativity and initiative. At Novateur, you'll lead transformative projects that redefine what's possible in intelligent systems. Company Benefits: Novateur offers competitive pay and benefits comparable to Fortune 500 companies that include a wide choice of healthcare options with generous company subsidy, 401(k) with generous employer match, paid holidays and paid time off increasing with tenure, and company paid short-term disability, long-term disability, and life insurance. We offer a work environment which fosters individual thinking along with collaboration opportunities within and beyond Novateur. In return, we expect a high level of performance and passion to deliver enduring results for our clients.

About the Company Our client is a well-established leader in the Bakery manufacturing industry. With decades of success and continuous growth, they are recognized for their innovative solutions and commitment to quality. They value collaboration, professional development, and take pride in delivering excellence to their customers. About the Role We are seeking a hands-on R&D Food Scientist to lead product innovation across our clean-label bakery and dough-based portfolio. This is a sole-contributor, highly technical role that collaborates directly with Sales and company leadership to design, test, and commercialize new baked goods and bread-style products. The ideal candidate has strong experience in bakery formulation-bread, rolls, dough products, tortillas, cookies, crackers, or similar-and the ability to translate customer needs into market-ready, scalable formulations. You will work closely with customers, owning the full development cycle from concept through commercialization. This role is perfect for someone who thrives in both hands-on bench development and customer-facing collaboration, converting ideas into innovative, high-quality bakery products. Responsibilities New Product Development & Innovation Collaborate with Sales/Marketing and Innovation Engineering to develop new bakery and dough-based products, from early concept to successful commercialization. Conceptualize, prototype, and refine formulations with a focus on bread, bakery items, dough systems, and clean-label ingredients. Conduct plant trials and support full-scale production start-ups for innovation and renovation projects. Customer Collaboration Act as a technical partner to customer R&D, Culinary, and QA teams. Present prototypes, discuss formulation strategies, and translate customer feedback into actionable development steps. Formulation & Documentation Maintain formulas, SOPs, and ingredient specifications in company systems. Generate Nutrition Facts Panels and ingredient statements. Drive change management for formulations, including issuing approved recipes and BOM updates. Ingredient Sourcing & Supplier Interaction Work with Procurement to identify, evaluate, and source bakery-appropriate ingredients that meet marketing, functionality, and quality requirements. Liaise with corporate teams to verify new suppliers, raw materials, and conduct feasibility assessments. Shelf-Life & Product Performance Coordinate and conduct internal and external shelf-life studies for bakery and dough-based products. Process Improvement & Cost Optimization Review formulas to identify cost-saving opportunities without compromising product quality or performance. Lead efforts to consolidate similar raw materials while maintaining product integrity. Evaluate new processing technologies and functional ingredients that align with emerging bakery trends. Cross-Functional Collaboration & Project Management Manage development timelines and communicate progress to internal partners. Work with Finance to build early-stage cost models. Participate in co-manufacturing or third-party development when needed. Serve as a key member of the NPD implementation team. Technical Expertise Reverse-engineer existing bakery or dough-based products for matching projects. Stay current with ingredient functionality, dough rheology, and bakery process technologies. Perform other R&D-related duties as assigned. Qualifications Bachelor's degree in Food Science, Microbiology, or related field; Master's preferred. Minimum 5 years in product development, preferably in bakery, bread, doughs, cookies, crackers, tortillas, or similar categories. Hands-on experience in bakery formulation, dough systems, fermentation (if applicable), ingredient functionality, and scale-up. Understanding of formula costing and financial feasibility. Knowledge of food safety programs (HACCP, GMP). Familiarity with process capability, quality control, and ISO 17025 standards. Understanding of SQF and food safety program design. Required Skills Strong communication skills (verbal and written). Ability to build collaborative relationships across teams. Effective at leading change and influencing stakeholders. Strong organizational skills with the ability to manage multiple projects. Expertise in food product design, ingredient interaction, scale-up, and commercialization. Proficiency with Microsoft Office. Action-oriented problem solver with ownership and accountability. Preferred Skills Previous experience in bread, bakery manufacturing, clean-label formulation, or dough-based operations. Experience in supply chain or operations is a plus. Strong analytical and documentation skills.

Kelly Government Solutions is seeking a Scientist - Downstream Process Development to work on-site with the Vaccine Production Program at the National Institute of Allergy and Infectious Diseases (NIAID)/National Institutes of Health (NIH) in Gaithersburg, MD. KEY TASKS/SERVICES (1) Support the Purification group of the Vaccine Production Program (VPP) Labs of the Vaccine Research Center (VRC). (2) Develop downstream (purification) processes, under the supervision of a project lead scientist, for recombinant proteins, virus vaccines, and virus-like particles (VLP) that may be used as clinical vaccine candidates. (3) Serve as a functional lead in chromatography process development unit operations. (4) Provide critical process step assessment and experimental design to define optimal process parameters for chromatography unit operations. (5) Train team members in large-scale unit operation such as AxiChrom column packing and Pilot-scale chromatography execution. (6) Work independently and collaboratively within the purification group to design, develop and optimize chromatography and filtration step unit operations to support process development of clinical trial vaccine candidates and mAb products. (7) Purify research-phase recombinant proteins, virus vaccines and/or virus-like particles in support of other groups at the VRC. (8) Work to prepare necessary materials (buffers, packed columns, etc.) in support of downstream process activities. (9) Perform protein/small molecule conjugation experiments to support method development or conjugate-based vaccine candidates. (10) Support technology transfer of processes to VRC Pilot Plant for manufacture of clinical products including authoring process descriptions, reports, and on-floor support. (11) Author training documents, process documents and summaries, instrument SOPs, technical reports, protocols, and other supporting documentation. KEY REQUIREMENTS (1) Ph.D. in a scientific field with at least 5 years of experience. MS with at least 10 years of specialized experience may also be considered. (2) Deep understanding of challenges and method development approaches of mAb, vaccine and mRNA scientific field. (3) Familiarity with monoclonal antibody and multi-specific antibodies, recombinant protein vaccine and nanoparticles; mRNA and mRNA/LNP vaccines. (4) Analytical skills and applications such as developing release and characterization methods using reversed phase HPLC/or UPLC -UV methods or HPLC/or UPLC - MS methods for pipeline project support. (5) Experience with other bio-separation techniques such as electrophoresis and lab-on-chip separation.

Hartmann Young is partnering with a leading innovator in the enzyme and life sciences sector to appoint a Senior Research Scientist & Clinical Trials Manager. This role will be based in Troy, Virginia (open to relocation support) and offers the opportunity to lead clinical programs and research projects that have global impact. The Role We are seeking an accomplished scientist with a strong background in clinical research, trial management, and manuscript development. This individual will oversee the start-up, execution, and close-out of clinical trials, while also contributing to product innovation, regulatory support, and publications. The position requires close collaboration with senior leadership to align research priorities with strategic growth initiatives. Key Responsibilities Lead and manage clinical trials from initiation through completion, ensuring compliance with regulatory and ethical standards. Identify, evaluate, and oversee trial sites, including site visits as needed. Manage trial budgets, timelines, and reporting to executive stakeholders. Contribute to research projects with high-quality data collection, analysis, and interpretation. Author and review manuscripts, patents, and technical publications. Collaborate with regulatory, compliance, and R&D teams on claims substantiation and documentation. Provide technical training to internal stakeholders and represent the company at conferences, client meetings, and industry events. Qualifications & Experience Advanced degree (PhD, MD, PharmD, or equivalent) in a relevant scientific discipline. 5+ years' experience in clinical research, trial execution, and manuscript preparation. Strong background in life sciences, ideally in enzymes, nutrition, or microbiome research. Proven project and budget management experience. Excellent written and verbal communication skills, including public speaking and technical writing. Knowledge of enzyme functions and applications desirable. Additional Details Full-time, on-site role. Full relocation support available. Requires willingness to travel for trial site visits, conferences, and client meetings.

Cydecor is a premier Federal Government solutions provider, delivering differentiated innovations in mission systems and business platforms. We leverage leading-edge secure systems and software development, backed by industry-leading subject matter expertise, and business intelligence to enable decision-support and remain ahead of ever-evolving national security challenges. Our success rests squarely on three bedrock principles: People, our center of gravity; Mission, what inspires us; and an unyielding commitment to Excellence, what separates us. Job Description: We are seeking a Senior Decision Scientist that can understand and improve the judgment and decision making of individuals, groups, and organizations. This individual will apply principles of psychology to business, analytic and other decision making processes to improve and / or empirically evaluate those processes. Activities include assisting in policy planning; workflow procedures testing and evaluation, analytic workflow redesign, training and development. Partner with management to prescribe workflow modifications that improve worker productivity and analytic judgment. Work locations vary throughout the National Capital Region (NCR), with Reston, VA and Washington, DC being primary locations. Responsibilities include: Managing end-to-end data science projects, analyzing user behavior, and building models. Requires a blend of strong analytical and technical skills, with qualifications including a background in statistics, programming languages and familiarity with cloud platforms and data visualization tools. Develop and implement solutions: Apply advanced analytics, machine learning, and AI to create systems that support strategic decision-making. Data analysis and interpretation: Analyze large datasets, identify trends, and present findings to both technical and non-technical stakeholders. Experimentation and evaluation: Design, build, and analyze experiments to evaluate product features and performance. Product support: Partner with product teams to influence decisions, provide recommendations, and report on the state of the business and experiment results. Data management: Work with data infrastructure, including tools like Hadoop, Hive, and SQL, and automate analysis and pipelines. Here's what you need: Minimum 12 years of overall experience with at least a portion of the experience within the last 2 years reflecting the above areas of responsibilities. Master's degree OR a Bachelor's degree and an additional 5 years of related experience, for a total of 17 years, as a substitute for the Master's degree. Proven ability to work independently and with minimal oversight. Technical skills: Strong knowledge of statistics, including hypothesis testing and regression. Experience with big data technologies. Familiarity with data visualization tools. Experience with generative AI and large language models is a plus. Analytical and soft skills: Strong quantitative and analytical mindset. Excellent communication and presentation skills to explain complex findings. Ability to manage projects from start to finish. Security Clearance: Active TS/SCI Education: Master's degree or Bachelor's with 5 additional years of relevant experience. Work Schedule: Monday - Friday, 8 hours each day. Benefits: Cydecor offers a comprehensive compensation package including Health and Dental Insurance, Vision and Life Insurance, Short-Term & Long-Term Disability, 401(K) + company match, Paid Time Off (PTO), Paid Company Holidays, Tuition and Professional Development Assistance and more. What We Believe We have an unwavering commitment to diversity with the aim that every one of our people has a full sense of belonging within our organization. As a business imperative, every person at Cydecor has the responsibility to create and sustain an inclusive environment. Equal Employment Opportunity Statement Cydecor is an Equal Employment Opportunity/Affirmative Action Employer (EEO/AA). All employment and hiring decisions are based on qualifications, merit, and business needs without regard to race, religion, color, sexual orientation, nationality, gender, ethnic origin, disability, age, sex, gender identity & expression, veteran status, marital status, or any other characteristic protected by applicable law. If you are a qualified individual with a disability and/or a disabled veteran, you may request a reasonable accommodation if you are unable or limited in your ability to access job openings or apply for a job on this site because of your disability. You can request assistance by contacting ************** or calling ************.

We are seeking a highly motivated and collaborative Research Scientist with skills and experience in natural products chemistry to join our dynamic research team. The ideal candidate will have research experience in chemical compounds derived from natural sources, such as sugars, polysaccharides, flavors and fragrances, focusing on their structure determination and their applications in new forms of tobacco products. Key Responsibilities: 1.Prepare and analyze samples of various formulation types, including natural polymer material complex, to determine the flow and deformation of materials. 2.Design and execute natural polymer crosslinking via reactive extrusion to improve material properties like shape stability and mechanical strength. 3.Perform instrumental analysis (GC-MS, HPLC, LC-MS) to study flavor chemistry and molecular mechanisms. 4.Evaluate flavor, create new flavor blends and make recommendations to satisfy project requirements. 5.Collaborate with cross-functional teams to innovate and improve flavor and fragrance formulations based on sensory feedback and market trends. 6.Maintain detailed records of formulations, tests, and evaluations to support product development and compliance with industry standards. 7.Stay updated on industry trends, emerging technologies, and regulatory changes in tobacco sector. 8.Adhere to laboratory protocols and safety programs of safe handling of chemicals and equipment. Qualifications: 1.Ph.D. degree in Organic Chemistry, Polymer Chemistry, Material Science, food Science or a related discipline with 0-2 years of relevant experience. 2.Proven experience in natural products chemistry, flavor chemistry and formulation design. 3.Knowledge of polymer material structure-property relationships and analytical characterization techniques (Rheometer, DSC, TGA, FTIR, NMR, particle size analyzer etc.). 4.Competence with the use of modern spectroscopic methods to determine structure of organic compounds, including HPLC, GC, HPLC-MS. Experience in maintaining related instruments is highly preferred. 5.Ability to work collaboratively in a team environment and contribute to a positive and productive work culture. Preferred Research Experience in the Following Areas: Flavor chemistry, natural flavor and fragrance Natural products, including sugar, starch, cellulose Extrusion, Polymer crosslinking via reactive extrusion Additional Skills: Bilingual: Fluent in English and Chinese is a plus Strong analytical and problem-solving abilities. Excellent communication and teamwork skills. Attention to detail and a commitment to quality.

CICONIX is seeking a Senior Human Subjects Protection Scientist with Human Subjects Research experience to support the Institutional Review Board (IRB) of the Headquarters of the Office of Human and Animal Research Oversight (OHARO), Office of Human Research Oversight (OHRO) at the US Army Medical Research and Development Command (MRDC) in Ft Detrick, Maryland. About the Role: A comprehensive pre-review of research protocols and supporting documents before review by a convened IRB or via expedited review procedure. Post-IRB approval lifecycle management of assigned research protocols, including pre-review of amendments, continuation reports, reports of unanticipated problems/serious adverse events/serious or continuing noncompliance/ research suspension or termination /protocol deviations, and final study reports. Support for site visits (monitoring, non-compliance) to include preparation and planning visits, assisting during visits, and preparing written reports. Assistance in the development and updating of the IRBs human subjects protection policies, procedures, guidelines, and process improvement initiatives. Assistance in developing human subjects protection education and training programs. Assistance in the IRB's internal quality control/assurance program. Support for the Human Research Protections Office, as needed, to include conducting DoD-required reviews for USAMRDC-supported research and DoD-conducted research. The individual will work on Ft. Detrick as a member of a team comprised of military, government civil service and contract employees. Qualifications: Education: Bachelor's Degree in Science, Public Health or related discipline Experience: 5+ years direct human subjects research experience supporting either an IRB office or regulatory office. Current training in humans subjects protection. Proficient in use of Microsoft Word, Outlook, and Excel. Ability to effectively communicate with researchers, research staff and IRB members on matters of research compliance and ethical human research practices. Ability to quickly become proficient in use of an on-line document management system and an Oracle-based protocol information management system. Security & Background Check: U.S. Citizenship and a successful background investigation are required. Ability to obtain and maintain a government security clearance. Additional Requirements: N/A Pay Range: $85k - $92k

We are seeking an experienced upstream/midstream scientist to support the development and scale-up of biological production processes used within the biopharmaceutical industry. This role involves working onsite in a modern facility and contributing to the production of biological materials that enable effective testing, optimization, and characterization of product performance. Responsibilities Produce and characterize non-GMP biological feed material from various mammalian cell lines Design, optimize, and scale upstream and midstream processes from small volumes to pilot-scale systems Transfer processes from bench-scale cultures to bioreactor systems Develop, refine, and document robust workflows and procedures Support testing and analytical evaluation of newly developed products Qualifications Bachelor's degree in Life Sciences, Biotechnology, or a related field At least 5 years of experience in upstream bioprocessing or related functions Hands-on experience with processes ranging from transfection through early-stage purification or clarification steps Analytical skills with techniques such as ELISA, HPLC, SEC, and flow cytometry Ability to work effectively in a fast-paced, growth-oriented environment Preferred PhD in Life Sciences, Biotechnology, or a related discipline Experience with downstream purification, including operation of FPLC systems Familiarity with Design of Experiments (DoE) and statistical analysis Working knowledge of relevant quality and regulatory standards (e.g., ISO9001, ICH, FDA guidelines)

ChromaGenix is an innovative start-up providing essential chromatography tools used globally to purify advanced biological therapeutics. As we expand, we are seeking an experienced Upstream/Midstream Scientist to support the development and commercialization of cutting edge purification media which are used globally in the biopharmaceutical industry. This is a unique opportunity to work onsite in our brand-new facility, where you'll help lead the production of biological material to enable the effective testing and understanding of key product performance attributes. Key Responsibilities · Production and characterization of non GMP feed material from both HEK and CHO lines · Design and upscale upstream and midstream processes from ml up to 25 liter scales · Transfer of processes from shake flasks to bioreactors · Generating robust processes and proceduralize them · Support product testing and analysis of new products developed at ChromaGenix Essential Criteria · Degree in Life Sciences, Biotechnology, or a related field · Minimum 5 years of experience in upstream roles · Process experience from transfection to depth filtration · Analytical experience in relevant techniques including but not limited to Elisa, HPLC, SEC and flow cytometry · Ability to thrive in a rapid-growth start-up environment Desirable Criteria · PhD in Life Sciences, Biotechnology, or a related field · Downstream purification techniques utilizing FPLCs · Experience with DoE and statistical analysis · Working knowledge of ISO9001, ICH and FDA standards and guidelines Be part of something impactful. Join ChromaGenix in shaping the future of biologics purification on the ground floor of our new manufacturing operation and in one of America's most exciting life sciences hubs.

Job Title: Research Chemist Reporting: Director of Innovation Ascent Industries Co. is seeking a Research Chemist to join our Research and Development team. This role will serve as the technical focal point for new custom and contract manufacturing projects and drive successful execution from proof of concept through commercial-scale production. This role will collaborate with cross-functional stakeholders in R&D, Sales, Marketing, Engineering, and Manufacturing to drive commercial success with a focus on speed to solution, commercial-scale viability, deep technical rigor, and a proactive safety mindset. The ideal candidate combines strong technical skills in experiment design, synthesis, process chemistry, commercial-scale unit operations, and scale up within the chemicals or materials industry. This role is expected to serve as the subject matter expert for all analytical testing related to the contract manufacturing projects, implementing customer specified tests and introducing new test methods that are critical for ensuring product quality. Duties and Responsibilities: Serve as the technical focal point for new contract manufacturing opportunities. Identify fastest and most efficient route to commercially viable solutions for new contract manufacturing and custom synthesis opportunities based on a deep understanding of process chemistry and plant unit operations. Establish R&D lab capabilities for synthesis, process development, sample preparation, and testing by evaluating current capabilities and additional needs to support project pipeline. Design experiments based on sound scientific principles and statistical methods to validate technical packages for proof of concept, optimize processes, and develop technical package for manufacturing to support First Time in Spec production. Rapidly produce samples for customer evaluation based on a thorough understanding of plant equipment capabilities and technical requirements Demonstrate expertise in a broad array of analytical instruments and drive new method development to align internal test methods and capabilities with customer methods and protocols. Leverage external labs for specialized test capabilities. Collaborate with key stakeholders in Sales, Engineering, Manufacturing, Procurement, and Product stewardship to drive successful commercialization. Engage with customers to gather process details, develop experimental plans, communicate project progress, present key findings, results, and support successful qualifications. Create Standard Operating Procedures and Work Instructions for core lab activities. Assure safe lab operations and compliance with site regulations while ensuring zero recordables. Skills, Qualifications, Experience, Special Physical Requirements: Bachelor's degree (advanced degree preferred) in Chemistry, Chemical Engineering, or Materials Science and Engineering Proven hands-on industrial scale-up and technical transfer experience (5+ years) in fine or specialty chemicals or materials industry with subject matter expertise in one or more product categories: Adhesives, Coatings, Surfactants, Dispersions, Specialty Additives, and Reactive Blends. Know-how of product requirements for one or more market segments: CASE, Oil and Gas Chemicals, Plastics/Engineered Polymers, Water Treatment Chemicals, Lubricants, and Personal Care. Strong lab scale synthesis skills, working knowledge of commercial-scale process equipment, and prior experience scaling a product from the laboratory scale through robust commercial scale production. Solid understanding of interplay between raw materials, formulations, manufacturing process variables, product specifications, and product performance. Prior experience with development of detailed technical packages for scale up. In depth analytical and method development experience with techniques such as GPC, GC, HPLC, FTIR, NMR, Rheology, Particle Size, and wet chemistry. Design of Experiments and Six Sigma Green Belt Experience Preferred. Ability to prioritize tasks, manage multiple projects simultaneously, and meet tight deadlines. Strong communication skills both written and verbal. US Citizenship or Green Card required Success Metrics On time execution of R&D work for new contract manufacturing projects per milestones established in NPD process Improve technology transfer from lab to plant with a focus on developing detailed technical packages for achieving target specifications in the first production run. Develop detailed understanding of customer technical protocols for testing and drive quick internal implementation Serve as a technical interface to provide outstanding customer engagement in all technical aspects and help position R&D as our unique value proposition to contract manufacturing customers

Must Haves: Ph.D. in Molecular Biology or Microbiology (recent graduates encouraged). Strong emphasis on molecular biology techniques; microbiology experience required. Ability to design and conduct independent research projects. Skilled in isolating strains within microbiota for probiotic applications. Proficient in data collection and statistical analysis using familiar software (e.g., R, Python, SPSS). Hands-on lab experience in molecular and microbiology methods. Dependable and capable of working independently with minimal supervision. Demonstrated interest in pollinators and sustainability, showing commitment beyond routine tasks. About the Role: We are seeking a Postdoctoral Researcher specializing in honey bee microbiology and molecular biology to lead an innovative research project focused on honey bee gut microbiomes and their impact on colony health and behavior. This full-time, 18-month position offers competitive pay and the potential for extension. The role combines cutting-edge research with an opportunity to contribute to the development of a novel honey bee health product. Work will take place at this university client's main campus. Occasional travel to scientific conferences may be required. Day-to-Day: Perform honey bee gut dissections and collect gut microbes. Prepare and maintain honey bee colonies at the apiary. Conduct experiments exposing caged bees to gut homogenates and monitor health and behavior. Run molecular assays such as 16S rRNA sequencing and qPCR to characterize microbiomes. Analyze collected data using statistical software (e.g., R, Python). Document findings, draft reports, and prepare figures for publications or presentations. Isolate microbes of interest for probiotic development. Mentor and train student researchers on lab and beekeeping techniques. Collaborate with the PI on experimental design and assist with related projects. Contribute to product development and commercialization efforts, including patent preparation.

This is a full-time remote role for a Research Associate in Signal Processing and Physiological Modeling, specializing in HD5y files extracted from hospital ICU machines. The incumbent will lead advanced research in signal processing and physical body flow modeling, with a focus on trauma patient data. Responsibilities include developing and implementing algorithms that link ECG and PPG signals to circulatory and systemic flow dynamics, particularly under acute stress conditions. This is a government-sponsored Research Associate role, offering the unique opportunity to contribute to federally backed trauma research. Unlike equivalent university posts, this position can also provide stock options as an incentive, aligning long-term rewards with the growth of MSAI LABS. Day-to-day tasks involve: Programming and algorithm development for physiological signal interpretation Applying pattern recognition and denoising techniques to trauma-linked biosignals Modeling circulatory flow and systemic responses using multi-modal data Collaborating with cross-functional teams to advance the lab's trauma-focused AI research objectives Qualifications Strong foundation in Python and/or R Experience modeling physical body flow dynamics using biosignals (ECG, PPG, BP, etc.) Familiarity with trauma physiology and acute care signal patterns Optimization skills for running models on cloud GPU/CPU instances Knowledge of autoencoders, STFFT, SSD architectures or other denoising methods Time series Transformers optimization Expertise in pattern recognition and physiological signal interpretation Proficient in programming languages relevant to signal processing and modeling Solid understanding of mathematics, especially as applied to dynamic systems and signal flow Strong analytical and problem-solving skills Ability to work independently and remotely Excellent written and verbal communication skills Experience in a research environment is a plus Master's or Ph.D. in a related field such as Biomedical Engineering, Computer Science, Electrical Engineering, or Applied Mathematics

Job Description & Requirements Adult Sickle Cell Director Virginia Commonwealth University Seeks a Sickle Cell Disease Director Leadership Opportunity at a Top Sickle Cell Disease Program Perform National Research Live and Work in Highly Desirable Richmond, Virginia Lead one of the top Sickle Cell programs in the United States in beautiful Richmond, Virginia, directing staff and advancing innovative clinical trials. Virginia Commonwealth University School of Medicine, Division of Hematology and Oncology, seeks a BC/BE Sickle Cell Disease Director. Leverage the NCI-designated Massey Cancer Center with more than 100 clinical trials and build extramural partnerships. Connect with us today to learn more. Opportunity Highlights Become Director of one of the top Sickle Cell programs in the United States Advance national research to develop new sickle cell treatments and potential cures Lead clinical trials for novel drugs, gene editing, and stem-cell therapies Richmond-based leadership role with autonomy to manage a nationally recognized Sickle Cell program Receive relocation and sign-on bonus when joining the VCU School of Medicine Train medical students, residents, and fellows in clinic and research environments Pursue funded research, clinical trials, and national presentations in sickle cell disease Obtain academic support for scholarly publications and extramural grant applications Access the institutional infrastructure of VCU Massey Cancer Center, an NCI-designated center Community Information Virginia's historic capital, Richmond is a thriving community rich in Southern charm and big-city amenities. Centrally located, the city has easy access to Washington, DC, the beach, and the mountains. There's something for everyone, with stunning scenery and a variety of events and activities for families and individuals alike. Richmond is a Best Place to Live and a Best Place to Retire (US News) CNN ranked Richmond the No. 1 Best Town to Visit in America in 2024 Exceptional Livability Score from Area Vibes, with A grades for Amenities, Commute, Housing, Health & Safety, and Schools Beautiful and friendly neighborhoods with a cost of living and housing prices lower than the national average Outstanding entertainment options and some of the top public and private schools in the state Thriving arts and culinary scene and excellent outdoor adventures Fantastic weather with mild climates throughout the year, allowing you to enjoy an abundance of outdoor recreation Convenient access to the mountains, the beach, and Washington, DC Facility Location Skyscrapers, antebellum homes and the State Capitol the old and the new stand together in graceful compatibility in modern-day Richmond. A thriving city with a strong sense of history and heritage, filled with tree-lined streets, quaint brick walkways and intriguing neighborhoods, Richmond offers a warm welcome any time of the year. Job Benefits About the Company At AMN Healthcare, we strive to be recognized as the most trusted, innovative, and influential force in helping healthcare organizations provide quality patient care that continually evolves to make healthcare more human, more effective, and more achievable. Internal Medicine, Hematology, Hematologist, Pathology, Internal Medicine, Pathologist, Pathology, Medical Pathologist, Laboratory, Physician, Mental Health, Medication, Md, General Practice Physician

Labcorp Genetics (formerly Invitae) is dedicated to bringing comprehensive genetic information into mainstream medicine to improve healthcare for billions of people. Our team is driven to make a difference for the patients we serve. We are leading the transformation of the genetics industry, by making clinical-grade genetic information affordable and accessible to guide health decisions across all stages of life. The genomics insights team leverages clinical genomic expertise, our massive genetics, laboratory and linked public/private datasets, and the latest AI/ML technologies to improve diagnosis, clinical care, and treatment options. We design and develop robust, quantitative, and scalable systems for variant interpretation and disease insights. Our research findings are broadly disseminated to improve testing guidelines, optimize reimbursement rates, and educate the healthcare ecosystem. We are seeking a Lead R&D Data Scientist to join our team and contribute to these initiatives. Responsibilities: Lead and deliver the translation of complex biological and clinical questions into actionable analysis plans. Architect and implement robust data pipelines that integrate large-scale genomic, phenotypic, laboratory, and real-world clinical datasets. Write clean, maintainable, and well-documented code following best practices for version control, testing, and scalability. Prepare technical reports, peer-reviewed publications, and conference presentations to share research outcomes with internal stakeholders and the broader scientific community. Collaborate closely with both internal and external stakeholders to drive impactful research and development initiatives. Ensure high standards of data privacy, security, and compliance are maintained in all projects. Minimum Qualifications: Ph.D., or equivalent industry experience in Computer Science, Statistics, Data Science, Computational Biology, or a related field. 5+ years of hands-on experience in data science and statistical methods, as applied to large biomedical datasets. Experience working within a collaborative technical team with strong software engineering practices. Proficiency in modern programming languages (Python and SQL), shell scripting, and version control (Git). Experience with data management, ETL, and business intelligence tools. Understanding of data privacy, security, and ethical considerations in clinical and biological research. Excellent communication skills for presenting research findings to diverse audiences. Preferred Qualifications: Experience with big data technologies (Snowflake, Databricks, etc.) and visualization/dashboarding (Looker, Dash, etc.). Experience with high performance computing (SGE etc.). Experience in the development and validation of complex computational models for biological data, in particular machine learning and bioinformatics techniques. Track record of impactful publications and presentations. Previous published work in genetics, functional genomics, or clinical research. This position is not eligible for visa sponsorship. Application window closes: 10/24/2025 Pay Range: $100,000.00 - $155,000.00 a year Schedule/Shift: M-F, 8-5 EST All job offers will be based on a candidate's skills and prior relevant experience, applicable degrees/certifications, as well as internal equity and market data. The position is also eligible for an annual bonus under the Labcorp Bonus Plan. Bonuses are payable based on corporate and/or business segment performance and are subject to individual performance modifiers. Compensation may also include discretionary short- and long-term incentive packages. Benefits: Employees regularly scheduled to work 20 or more hours per week are eligible for comprehensive benefits including: Medical, Dental, Vision, Life, STD/LTD, 401(k), Paid Time Off (PTO) or Flexible Time Off (FTO), Tuition Reimbursement and Employee Stock Purchase Plan. Casual, PRN & Part Time employees regularly scheduled to work less than 20 hours are eligible to participate in the 401(k) Plan only. For more detailed information, please click here. Labcorp is proud to be an Equal Opportunity Employer: Labcorp strives for inclusion and belonging in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications and merit of the individual. Qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex (including pregnancy, childbirth, or related medical conditions), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. Additionally, all qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable law. We encourage all to apply If you are an individual with a disability who needs assistance using our online tools to search and apply for jobs, or needs an accommodation, please visit our accessibility site or contact us at Labcorp Accessibility. For more information about how we collect and store your personal data, please see our Privacy Statement.

The Senior Research Associate in Antibody Discovery is responsible for advancing our antibody discovery programs by supporting and executing various laboratory-based activities, including phage display, antibody production, and downstream characterization. DUTIES AND RESPONSIBILITIES: Perform high-throughput screening of antibody libraries using techniques such as phage display. Conduct binding and functional assays (e.g., ELISA, flow cytometry, SPR, BLI) to characterize antibody-antigen interactions. Express, purify, and analyze antibodies using molecular biology, protein expression, and purification techniques (e.g., PCR, cloning, transient/stable transfection, chromatography). Analyze experimental data and present findings to the team. Maintain accurate and detailed laboratory records, including experimental procedures, results, and conclusions. Contribute to the preparation of technical reports, presentations, and scientific publications. Participate in project meetings and contribute to the design and planning of experiments. Communicate effectively with team members and external collaborators. EXPERIENCE AND QUALIFICATIONS: Bachelor's degree in Molecular Biology, Biochemistry, Immunology or related area is required. Master's degree is preferred. A minimum of two years of hands-on laboratory experience in antibody discovery or a related field. Industry experience is a plus. KNOWLEDGE, SKILLS AND ABILITIES: Proficiency in molecular biology techniques (e.g., cloning, PCR, site-directed mutagenesis). Experience with antibody screening and characterization assays (e.g., ELISA, flow cytometry, SPR, BLI). Familiarity with protein expression and purification methods (e.g., mammalian, bacterial, or yeast expression systems). Strong analytical and problem-solving skills. Demonstrated aptitude for learning of and adhering to standard laboratory techniques and safety precautions. Solid communication (written and verbal) skills regardless of the format (e.g., documents, public speaking situations, presentations, etc.). Excellent organizational, planning, and time management skills with the ability to manage multiple and often changing priorities and issues of varying complexity, while meeting time-sensitive deadlines and deliverables. Attention to detail with demonstrated commitment to excellence and performance. Demonstrated propensity to be creative, collaborative, proactive, and self-motivated in the execution and completion of assigned tasks. Ability to work both independently and as an effective team member. Ability to execute complex experiments with limited guidance. Ability to identify issues and troubleshoot solutions. Solid data analysis skills. Sound knowledge of MS Excel. Knowledge of GraphPad Prism and SharePoint a plus. Basic knowledge of statistics. PHYSICAL DEMANDS: While performing the duties of this job, the individual is frequently required to sit and stand for long periods. The individual is occasionally required to walk; use hands and fingers to operate, handle, or feel objects, tools, or controls; reach with hands and arms. Up to 75% of the day may be spent at a lab bench. There are aspects of the position's duties that require a person in this role to work at heights above four (4) feet on occasion and move/lift up to 25 pounds. WORK ENVIRONMENT: Laboratory environment working with chemical reagents and performing some Biosafety Level 2 work. May involve handling of BSL-2 materials and organisms including human blood and/or blood products.

Granules Pharmaceuticals, Inc., is seeking a detail-oriented and scientifically driven Sr. Scientist to join our team in the area of Analytical Method Development and Validation. The ideal candidate will possess strong expertise in developing and validating analytical methods for assay, related compounds, residual solvents, dissolution, and particle size analysis. Proficiency in Mass Spectroscopy and peptide testing is essential, with experience in bioassay methodologies considered a plus. This role requires a solid understanding of scientific principles to troubleshoot and solve analytical challenges, as well as experience in drafting and reviewing method validation protocols and reports in compliance with SOPs and regulatory guidelines. Strong communication skills and the ability to interpret technical procedures, FDA guidance documents, and scientific literature are essential for success in this role. JOB DUTIES & RESPONSIBILITIES include but not limited to: With minimal supervision, perform the analytical method development and method validation for dissolution, assay, and related compounds of raw material and finished products. Develops and validates methods to determine purity, potency, identity, residuals, and characterization of peptide products. Ability to individually work on development and validation for Reversed-Phase, Ion Exchange, and Size Exclusion chromatography using UPLC/HPLC/MS. Draft the analytical method validation protocols and reports Performs testing pharmaceutical raw materials, bulk and finished products, scale-up samples, process validation samples, cleaning verification/validation samples, and stability samples to support formulation development. Responsible for the timely and accurate execution of lab analysis. Independently compile the analytical data, make sound judgment of the data and interpret the data, and notify the results to manager/Director. Maintaining full compliance with all applicable US FDA - cGMP regulations and internal SOPs. Maintain laboratory notebooks and records of all the raw data as per Good Documentation Practices. Assists with training other junior members of the analytical development team as needed Maintain individual training records. Follow safety procedures and practices. Maintain a clean, orderly work environment. Works with computer-controlled equipment and processes. Performs other work-related duties as assigned Perform in-vitro dissolution testing for in-process, finished product and stability samples. Execute method transfer activities for raw materials and finished dosage forms. Ensures compliance with SOPs, policies and procedures required by the Company and regulatory agencies. Document experiments accurately and complete all associated documents (Instrument, Standard and Column usage logbooks) in compliance with internal SOPs and FDA guidelines. Evaluate test results against standards and timely reporting of any deviations, OOS, OOT and atypical results to the supervisor/department head. Other duties assigned by management based on requirements. Management Responsibility Assign daily work schedule in timely manner Provide Suggestions in method Development and validation. Interpret and review generated results Provide assistance in professional development. Reports to: Manager Analytical R&D Requirements Knowledge & Skills: Hands-on experience in Dissolution, HPLC, LC-MSGC, UV, FTIR, and other laboratory instruments. Experience with a wide variety of software and information systems (e.g. Empower, Microsoft word and Excel). Strong knowledge in analytical method development and validation under cGMP environment and experience in problem-solving skills and instrument troubleshooting. Good oral and written communication skills and the ability to write and review technical report Proven Knowledge of the major analytical techniques and operation of instruments such as HPLC, GC, dissolution, FT-IR, UV-VIS Spectrophotometer, Particle size analysis (Malvern Mastersizer, Sonic sifting and Sieve shaker), Karl Fisher Instrument, Potentiometric Titration, Density meter, pH meter, Melting point apparatus, Analytical Balances, Viscometer Proficient in documentation as per Good Documentation Practice Computer skills including Microsoft and Excel Excellent verbal and written communication and skills Experience & Education: Bachelor's degree in Analytical Chemistry or Chemistry or related field with 4+ years or MS/PhD with 2+ years of GMP and GLP-related pharmaceutical industry experience in Peptide and small molecule solid oral formulation analytical development. Knowledge of Good Manufacturing Practices (cGMP) Experience with software and information systems (e.g. Empower, Microsoft word and Excel) Physical Requirements/Working Environment Must be able to stand for long periods of time (up to 12-hour shifts), maneuver at least 40 pounds, wear a respirator and pass associated respirator tests and/or requirements, and be able to wear all required PPE. Vision - ability to see details at close range (within a few feet of the observer). Physical Requirements/Working Environment: Must be able to stand for long periods of time (up to 12-hour shifts), maneuver at least 40 pounds, wear a respirator and pass associated respirator tests and/or requirements, and be able to wear all required PPE. Vision - ability to see details at close range (within a few feet of the observer). Disclaimer: The above information on this description has been designed to indicate the general nature and level of work performed by employees within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities, and qualifications required of employees assigned to this job.

Apply now Back to search results Job no: 534650 Work type: Research Faculty Senior management: College of Science Department: Biological Sciences Job Description The Virginia Tech Center for Ecosystem Forecasting is recruiting a Research Scientist with a Ph.D. in Environmental Science, Quantitative Ecology, Ecological Statistics, Natural Resources, Environmental Engineering, or a related field. We are seeking to recruit an integral, long-term member of our team who will contribute to environmental modeling and forecasting research across multiple funded projects. Following the mission of the Virginia Tech Center for Ecosystem Forecasting, we seek a team member who is excited to both create and apply innovative environmental models and forecasts that provide actionable forecast insights to guide decision-making and management. We encourage applicants to visit our website (*********************************** to learn more about the Center, its mission and values, current projects, and our highly collaborative, interdisciplinary research team. Specific responsibilities for the on-site position include: 1) developing ecological forecasts (especially for lake and reservoir water quality) using a suite of models and datasets; 2) leading and co-authoring peer-reviewed publications, presentations, and data products; 3) providing guidance and mentorship to team members and supporting ongoing Center programs (including the Macrosystems EDDIE educational program); and 4) serving in a leadership role in the Center, which includes setting priorities, engaging partners, preparing reports, and collaborating with CEF co-directors and staff to apply for external funding. The review of applications will begin on Monday, 22 December, with anticipated Zoom interviews being scheduled in early January. Funding for this position is available for multiple years, pending satisfactory performance during an initial probationary period and subsequent annual performance reviews. We are unable to sponsor or take over sponsorship of an employment visa for this position at this time. Required Qualifications * Ph.D. in Environmental Science, Quantitative Ecology, Ecological Statistics, Natural Resources, Environmental/Civil Engineering, or a related field * Significant experience in publishing peer-reviewed journal articles, demonstrated by publication record * Significant quantitative research experience in ecosystem modeling, environmental forecasting, and/or computational ecology, demonstrated by publications and/or software development * Significant experience working in the R and/or Python programming language, demonstrated by GitHub (or other code repository) portfolio * Significant experience in environmental data analysis, demonstrated by publications and presentations * Experience with collaborative coding, demonstrated by GitHub (or other code repository) activity * Ability to work in interdisciplinary collaborative teams, demonstrated by previous team research experiences Preferred Qualifications * Postdoctoral research experience * Experience with water quality models, demonstrated by developing, calibrating, and applying water quality models, especially for lakes and reservoirs * Experience publishing data and code products, demonstrated by authorship of published data and code * Experience in data and forecast visualization, demonstrated by development and dissemination of data and forecast visualizations * Experience in mentoring and/or supervising * Experience working across computational platforms (e.g., command line, Docker, cloud computing and storage, RStudio, etc.) Overtime Status Exempt: Not eligible for overtime Appointment Type Restricted Salary Information Commensurate with experience Hours per week 40 hours - exempt position Review Date December 22, 2025 Additional Information The review of applications will begin on Monday, 22 December, with anticipated Zoom interviews being scheduled in early January. Funding for this position is available for multiple years, pending satisfactory performance during an initial probationary period and subsequent annual performance reviews. We are unable to sponsor or take over sponsorship of an employment visa for this position at this time. The successful candidate will be required to have a criminal conviction check. About Virginia Tech Dedicated to its motto, Ut Prosim (That I May Serve), Virginia Tech pushes the boundaries of knowledge by taking a hands-on, transdisciplinary approach to preparing scholars to be leaders and problem-solvers. A comprehensive land-grant institution that enhances the quality of life in Virginia and throughout the world, Virginia Tech is an inclusive community dedicated to knowledge, discovery, and creativity. The university offers more than 280 majors to a diverse enrollment of more than 36,000 undergraduate, graduate, and professional students in eight undergraduate colleges, a school of medicine, a veterinary medicine college, Graduate School, and Honors College. The university has a significant presence across Virginia, including Blacksburg, the greater Washington, D.C. area, the Health Sciences and Technology Campus in Roanoke, sites in Newport News and Richmond, and numerous Extension offices and research institutes. A leading global research institution, Virginia Tech conducts more than $650 million in research annually. Virginia Tech endorses and encourages participation in professional development opportunities and university shared governance. These valuable contributions to university shared governance provide important representation and perspective, along with opportunities for unique and impactful professional development. Virginia Tech does not discriminate against employees, students, or applicants on the basis of age, color, disability, sex (including pregnancy), gender, gender identity, gender expression, genetic information, ethnicity or national origin, political affiliation, race, religion, sexual orientation, or military status, or otherwise discriminate against employees or applicants who inquire about, discuss, or disclose their compensation or the compensation of other employees or applicants, or on any other basis protected by law. If you are an individual with a disability and desire an accommodation, please contact Dreama Price at ************* during regular business hours at least 10 business days prior to the event. Advertised: October 30, 2025 Applications close:

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We're looking for people who are determined to make life better for people around the world. Responsibilities: The Scientist - TSMS PAR will initially focus on the delivery of parenteral operations, specifically regarding technical transfer and process validation. TSMS PAR Scientists will support one of either formulation, filling, or visual inspection (VI), although may support multiple areas during start-up phase. Upon the start of commercial production, this role's objectives include maintaining the validated state of applicable processes, establishing and monitoring metrics/methods to ensure a state of capability and control, harmonization of control strategies across process teams, evaluate process improvement, and serving as an escalation point for day-to-day operations issues. The role will also author and execute protocols as well as conduct root cause investigations. The principal role is a position that develops and implements a technical agenda and is responsible for providing technical leadership for the Parenteral Process Team. The principal role expected to serve as a mentor within the TSMS team and engage in upstream and external to site activities related to parenteral manufacturing. Key Objectives/Deliverables: • Support the assigned Process Team (formulation, filling, or VI) as TSMS representative. • (Associate/Senior) Serve as floor-level support and technical interface for manufacturing components, equipment, and operations for the TSMS team. • Represent Concord TSMS team for internal and external communications on a regular basis • Lead risk management activities as it pertains to product/process • Provide technical support to non-routine (e.g., deviation, complaint) investigations, including consultation on quality and stability issues • Prepare and Review or approve, as required, relevant technical documents such as: Annual Product Reviews, Change Controls, Regulatory Submissions, Deviations, Validations, Procedures, PFDs, PFMEAs, etc. • Develop, monitor, and appropriately react to established statistically based metrics in real-time to assess process variability and capability • Identify opportunities and lead technical projects to improve process control and/or productivity • Serve as interface with upstream suppliers and parenteral product networks • Drive stability strategy for Concord products • Provide Audit support as needed • Identify opportunities and participate in projects to improve process control and/or productivity Basic Qualifications: • Bachelor's degree or higher an engineering, packaging science, or related field Additional Skills/Preferences: • Pharmaceutical and/or medical device manufacturing experience • Root Cause Investigation Experience • Proficiency with computer systems including Microsoft Office products, Veeva Vault, TrackWise, electronic batch records, and SAP • Demonstrated successful leadership of cross-functional teams • Strong interpersonal and teamwork skills • Strong self-management and organizational skills Additional Information: • Role is Monday through Friday. Must be flexible in providing support to accommodate other inputs (production schedules, shutdowns, etc.). Occasional extended hour and /or off-hour work may be required. Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form (******************************************************** for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response. Lilly is proud to be an EEO Employer and does not discriminate on the basis of age, race, color, religion, gender identity, sex, gender expression, sexual orientation, genetic information, ancestry, national origin, protected veteran status, disability, or any other legally protected status. Our employee resource groups (ERGs) offer strong support networks for their members and are open to all employees. Our current groups include: Africa, Middle East, Central Asia Network, Black Employees at Lilly, Chinese Culture Network, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinx at Lilly (OLA), PRIDE (LGBTQ+ Allies), Veterans Leadership Network (VLN), Women's Initiative for Leading at Lilly (WILL), en Able (for people with disabilities). Learn more about all of our groups. Actual compensation will depend on a candidate's education, experience, skills, and geographic location. The anticipated wage for this position is $66,000 - $171,600 Full-time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance). In addition, Lilly offers a comprehensive benefit program to eligible employees, including eligibility to participate in a company-sponsored 401(k); pension; vacation benefits; eligibility for medical, dental, vision and prescription drug benefits; flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts); life insurance and death benefits; certain time off and leave of absence benefits; and well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities).Lilly reserves the right to amend, modify, or terminate its compensation and benefit programs in its sole discretion and Lilly's compensation practices and guidelines will apply regarding the details of any promotion or transfer of Lilly employees. #WeAreLilly

Computational Biologist/Bioinformatician We are actively seeking a Computational Biologist/Bioinformatician to augment our R&D team. Our focus is on innovating advanced molecular diagnostics kits, devices, and methodologies for the analysis of biological data, reporting directly to the VP of Technology Development. Key Responsibilities: Pioneering the development of innovative software tools, algorithms, and analysis pipelines to expedite the transition from concept to practical testing. Leading the in-silico design and characterization of new molecular assays for infectious diseases, leveraging qPCR and related technologies. Supervising the conversion of extensive biological customer data into actionable insights through data mining, advanced visualizations, and machine learning. Assisting the R&D team in creating scripts for efficient calculations and project management. Directing the company's overarching initiatives in the digitization of biology. Requirements Hold a Master's or Ph.D. degree with a minimum of 3 years of relevant work experience. Possess extensive knowledge in computational biology or bioinformatics, mathematics, and computer programming. Capability to work independently on complex and challenging projects. Proficiency in and a passion for data visualization and effective communication of data science findings. Demonstrable experience with data science toolkits, machine learning, statistical modeling, and tool development. Solid understanding of developing ML and statistical models for real-world applications. Strong programming skills in Python and/or R; familiarity with Rust is a plus. Experience with Linux High Performance Computing (HPC) cluster is advantageous.