Scientist jobs in Delaware

Do you want to be part of an organization that is making a difference in the lives of millions of people worldwide? If so, we want to hear from you! QPS, LLC has an opening for an Associate Scientist I in our Bioanalytical department. In this role, you will play a pivotal part in QPS' continued expansion of our bioanalytical capabilities to support small molecule, antibody drug conjugate, protein, and gene therapy drug development. The LC-MS group's expertise lies in the quantitation of small molecules, oligonucleotides, peptides, proteins, and metabolite biomarkers by various mass spectrometric (LC-MS/MS, LC‑HRMS, hybrid/immunoaffinity mass spec), and hybridization-LC-fluorescence techniques. As an Associate Scientist I, you will be a fully-supervised trainee, responsible for sample preparation by various extraction methods; analysis of drug and metabolites in biological samples to support preclinical and clinical drug development programs under GLP regulations; and recording study results and observations. No visa sponsorship (e.g. H‑1B, L‑1, E) will be provided for this active position, now or in the future. Applicants must currently be authorized to work in the U.S. on a permanent or unrestricted basis. QPS' Story: Since its inception, QPS has been assisting pharmaceutical, biotechnology and medical device companies with their drug development efforts by providing a full range of DMPK, Toxicology, Bioanalysis, Translational Medicine, Early Phase Clinical and Phase II - IV Clinical Research services. To meet the needs of our clients, we strive to employ talented, caring and committed individuals who will work collaboratively towards achieving our mission of improving human health and the quality of life. Team members enjoy challenging and rewarding work, and are encouraged achieve their best. Underpinning the operation is a culture that values diversity, innovation, accountability, team work and a friendly atmosphere where performance is recognized and rewarded. We provide unique company benefits, training, and advancement opportunities. Most importantly, we value each of our team members as employees and as individuals. If this sounds like your ideal work environment, then we would love to speak with you, so apply today! Please visit our website (************ for more information and to see all current openings. The Job Perform routine lab operations, such as sample extraction, preparing reagents, operating automatic liquid handling equipment, pipetting, weighing, monitoring, and recording, in a neat/clean manner Assist Principal Investigator in performing quantitative analysis of drug and metabolites in biological samples utilizing validated liquid chromatography-tandem mass spectrometry (LC-MS/MS) methods under GLP regulations Document experiment details, calculations, results and observations in accordance with GLPs and SOPs Basic math skills to perform routine calculations Work Location This job will be 100% QPS-office/facility based Requirements The successful candidate will hold a degree in Analytical Chemistry, Biochemistry, Pharmacology, or related scientific discipline as follows: Bachelor's degree Why You Should Apply Great learning opportunities, especially for those new to the field. Our seasoned professionals are here to support and work with you to explore your learning potential and career goals. Structured Career Ladders that provide excellent growth based on your personal aspirations. Bonuses and merit increases are a part of the QPS total rewards approach and are linked to individual, team and company performance. Solid Benefits package, including Company-matched 401(k), and Company-sponsored Group Life/AD&D and Short and Long-term Disability Insurance Park-like setting in Newark, Delaware Internal committees designed with the needs and enjoyment of QPS employees in mind. QPS, LLC is an Equal Employment Opportunity/Affirmative Action Employer. In accordance with federal, state, and local laws, we recruit, hire, promote and evaluate all personnel without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, citizenship status, physical disability, protected veteran status, or any other characteristic protected by law. Job applicants and present employees are evaluated solely on ability, experience, and the requirements of the job. In addition, QPS, LLC is a federal contractor and desires priority referrals of protected veterans.

The Swank Autism Center at Nemours Children's Health is seeking a Research Scientist to join our team in Wilmington, Delaware. The Swank Autism Center provides comprehensive clinical services for children up to age 21 years and conducts research and community-based outreach and training. The Research Scientist will join a multidisciplinary team that includes faculty from psychology, developmental medicine, psychiatry, neurology, social work, nursing, and applied behavior analysis, as well as colleagues who are autistic and/or caregivers. The Research Scientist will also have a dual appointment in the Center for Healthcare Delivery Science (CHDS) - Delaware Valley ( ******************** ). The CHDS includes 20+ investigators across the enterprise that study ways to improve health care, health equity, and health and wellness beyond medicine for youth and their families. The Swank Autism Center has a dedicated Clinical Research Coordinator and CHDS has additional research coordination and data analysis resources. Teaching, training, and mentoring are core values in our division, and these efforts are also supported and encouraged. The Swank Autism Center is strongly affiliated with Delaware's Leadership Education in Neurodevelopmental Disabilities (LEND) program. Key Responsibilities: Develop a targeted research program in autism. This could include (but is not exclusive to) current areas of study: healthcare inequities, neuro-affirming care, supporting families who are newly diagnosed or awaiting evaluation, and other areas. Build and support research collaborations with other Nemours faculty and/or our external partners. Provide clinical services as a minor part of this role, which might include autism diagnostic services, individual/group therapy, and/or supervising trainees, e.g., externs, residents, and/or fellows who rotate through the center. What We Offer: Competitive salary Health, life, dental & vision benefits for Associates and their dependents Wellness program CME days and dollars 403(b) with employer match & a 457(b) plan Licensure and dues allowance after hire Tuition reimbursement & tuition discount programs with various Universities for Associates and their dependents Adoption assistance and 6 weeks of Paternity leave Qualifications: Candidates must hold a PhD in a health-related discipline Must be license-eligible Must demonstrate evidence of collaborative academic productivity and either success in obtaining funding for research or a strong potential to obtain funding for research The ideal candidate will have demonstrated training and experience conducting research in clinical and/or academic settings with autistic/neurodivergent children, adolescents, and/or young adults, and their families If you're looking for a position that will allow you to enjoy a work-life balance, have an opportunity for professional growth, and focus on pediatric care, this is the opportunity for you. #LI-KN1 About Us Nemours Children's Health is an internationally recognized children's health system. With more than 1.7 million patient encounters annually, we provide medical care in five states through two freestanding state-of-the-art children's hospitals - Nemours Children's Hospital, Delaware and Nemours Children's Hospital, Florida. Our pediatric network includes 80 primary-urgent-and specialty care practices and more than 40 hospitalists serving 19 affiliated hospitals. We generate annual revenues of more than $1.7 billion derived from patient services, contributions from the Alfred I. DuPont Trust, as well as other income. As one of the nation's premier pediatric health systems, we're on a journey to discover better ways of approaching children's health. Putting as much focus on prevention as cures and working hand in hand with the community to make every child's world a place to thrive. It's a journey that extends beyond our nationally recognized clinical treatment to an entire integrated spectrum of research, advocacy, education, and prevention, leading to the healthiest generations of children ever. Inclusion and belonging guide our growth and strategy. We are looking for individuals who are passionate about, and committed to, leading efforts to provide culturally relevant care, reducing health disparities, and helping build an inclusive and supportive environment. All of our associates are expected to ensure that these philosophies are embedded in their day-to-day work with colleagues, patients and families. To learn more about Nemours Children's and how we go well beyond medicine, visit us at *************** .

The Department of Neurology at Nemours Children's Health in Wilmington, Delaware seeks a motivated Research Scientist (tenure-track Assistant Professor equivalent) to be part of the highly collaborative and growing Neuroscience Center at Nemours. Applicants must hold a PhD or MD/PhD degree with significant postdoctoral research experience and demonstrated excellence in neuroscience. The Research Scientist will be responsible for the planning and execution of a wide range of research projects to develop and oversee an independent research program. Research activities include designing and fostering collaborative and independent research projects related to neuroscience and neurologic disease, supervision of postdoctoral associates, technicians and students, obtaining and coordinating external funding, and disseminating research in the form of manuscripts and conference presentations. Must hold academic rank (Assistant Professor) at one of Nemours' partner academic institutions at the time of accepting the position or immediately thereafter. The position includes a highly competitive salary, high-quality laboratory space, access to the Delaware network of cores and IDeA state funding, startup funding, and programmatic funding that renews yearly for the duration of employment. Applications should submit: * Cover letter (maximum of 2 pages) that includes: * Overview of the goals/vision of your research program in the context of our department and institution * A summary of significant scientific accomplishments as well as experiences and qualifications that position you to achieve your goals * Curriculum vitae * Detailed statement of research accomplishments and future plans (maximum of 3 pages) Essential functions: * Plan and oversee a wide range of projects in basic/translational research, including collaborations with our clinical and basic science researchers. * Prepare and submit grant applications to secure external funding support. * Publish high impact manuscripts in the field of neuroscience. * Supervise the maintenance, safety, and running of the laboratory and assure it is in regulatory compliance. * Supervise and train laboratory technicians, students, and postdoctoral fellows. * Involvement in a home department and graduate program at one of our academic affiliates, the University of Delaware or Thomas Jefferson University. * Participate in Nemours and Delaware service work, including involvement on regulatory and other committees. Qualifications: * PhD or MD/PhD degree with significant postdoctoral research experience and demonstrated excellence in neuroscience required

**Locations:** This role requires associates to be in-office **1-2** days per week, fostering collaboration and connectivity, while providing flexibility to support productivity and work-life balance. This approach combines structured office engagement with the autonomy of virtual work, promoting a dynamic and adaptable workplace. Alternate locations may be considered if candidates reside within a commuting distance from an office Please note that per our policy on hybrid/virtual work, candidates not within a reasonable commuting distance from the posting location(s) will not be considered for employment, unless an accommodation is granted as required by law. _PLEASE NOTE: This position is not eligible for current or future VISA sponsorship._ The **Research Scientist-Health Services Research** is responsible for Carelon Research research line of business; specific projects ranging from retrospective to large-scale, prospective studies in areas including population health, health economics, clinical effectiveness (drug, procedures, vaccine, and medical device), and implementation sciences. This role will conduct research studies for Elevance Health, Carelon, and external clients. **How you will make an Impact:** + Leads high quality research project proposal development from early conceptual stages for external and internal submissions. + Provides scientific rigorous input in the design and development of the research studies to fulfill study objectives. + Executes statistical analyses plans independently with effective problem solving and decision making as principal investigator across a broad program of studies related to a therapeutic area /healthcare intervention and/or external collaborator. + Collaborates with project team members to implement the study design and statistical analyses plans utilizing advanced statistical techniques such as propensity score modeling, GEE (generalized estimate equation) difference-in-difference, and graduate-level statistics in performing research study design and analysis. + Conducts review of administrative claims, electronic medical records, and survey and clinical data and statistical output and review of statistical output to ensure the superior quality of research activities and client deliverables. . + Summarizes key findings and generates value messages for incorporation into project deliverables, publications, and presentations. + Prepares study reports and manuscripts for submissions to peer-review journals demonstrating subject matter expertise. + Performs key project functions with minimal oversight. + Responsible for the final quality and accuracy of study deliverables, presentation of study deliverables and facilitation of the collaboration among project team members towards development. + Manage relationships with study champions/clients, communicates scientific decisions, and presents key study insights to the champions, including Elevance Health senior leadership team, internal decision makers, and other external stakeholders/clients. **Minimum Requirements:** Requires a MS in health sciences or related advanced degree, or clinical degree such as PharmD, or MD, combined with Master level degree and a minimum of 5 years of experience in health service research, biostatistics, epidemiology, health policy, economics or related field; or any combination of education and experience which would provide an equivalent background. **Preferred Skills, Experiences and Competencies:** + Ph.D. or MD strongly preferred. + Postgraduate or post-doctoral training or relevant experience in conducting observational and/or prospective research studies. + Understanding of the U.S. health care system, population health and implementation sciences strongly preferred. + Successful experience with research grants/funding applications is strongly preferred. + Proficient in statistical software, including SAS, STATA, R, and/or Python strongly preferred. + Proficient in data management tools, including SQL strongly preferred. Please be advised that Elevance Health only accepts resumes for compensation from agencies that have a signed agreement with Elevance Health. Any unsolicited resumes, including those submitted to hiring managers, are deemed to be the property of Elevance Health. Who We Are Elevance Health is a health company dedicated to improving lives and communities - and making healthcare simpler. We are a Fortune 25 company with a longstanding history in the healthcare industry, looking for leaders at all levels of the organization who are passionate about making an impact on our members and the communities we serve. How We Work At Elevance Health, we are creating a culture that is designed to advance our strategy but will also lead to personal and professional growth for our associates. Our values and behaviors are the root of our culture. They are how we achieve our strategy, power our business outcomes and drive our shared success - for our consumers, our associates, our communities and our business. We offer a range of market-competitive total rewards that include merit increases, paid holidays, Paid Time Off, and incentive bonus programs (unless covered by a collective bargaining agreement), medical, dental, vision, short and long term disability benefits, 401(k) +match, stock purchase plan, life insurance, wellness programs and financial education resources, to name a few. Elevance Health operates in a Hybrid Workforce Strategy. Unless specified as primarily virtual by the hiring manager, associates are required to work at an Elevance Health location at least once per week, and potentially several times per week. Specific requirements and expectations for time onsite will be discussed as part of the hiring process. The health of our associates and communities is a top priority for Elevance Health. We require all new candidates in certain patient/member-facing roles to become vaccinated against COVID-19 and Influenza. If you are not vaccinated, your offer will be rescinded unless you provide an acceptable explanation. Elevance Health will also follow all relevant federal, state and local laws. Elevance Health is an Equal Employment Opportunity employer and all qualified applicants will receive consideration for employment without regard to age, citizenship status, color, creed, disability, ethnicity, genetic information, gender (including gender identity and gender expression), marital status, national origin, race, religion, sex, sexual orientation, veteran status or any other status or condition protected by applicable federal, state, or local laws. Applicants who require accommodation to participate in the job application process may contact ******************************************** for assistance. Qualified applicants with arrest or conviction records will be considered for employment in accordance with all federal, state, and local laws, including, but not limited to, the Los Angeles County Fair Chance Ordinance and the California Fair Chance Act.

Sirius Staffing is seeking multiple Associate Scientists (Formulations Chemistry) for a contract position at a leading agricultural research site in Newark, DE. This is an exciting opportunity to join the formulation team and contribute to advancing a robust product pipeline while supporting existing products. Rate: up to $75K yearly + Benefits, PTO & Holiday Pay Schedule: Day shift, Mon-Fri Responsibilities: Work under the direction of a senior chemist with limited supervision. Prepare formulations for agricultural solutions using novel technologies. Perform physical tests on formulations to characterize products and simulate performance attributes. Conduct physical and chemical characterization of active ingredients. Support the evaluation of new technologies for the organization. Utilize wet and dry chemical techniques, including milling, extrusion, granulation, emulsification, suspensibility tests, and solution release tests. Operate physical-chemical instrumentation such as particle size analyzers and zeta potential analyzers. Use small-scale preparative equipment, including high-shear mixers and laboratory reactors. Interpret preliminary results and testing data. Manage small-scale or limited-scope projects as assigned. Key Responsibilities Preparation of laboratory-scale liquid and solid formulations. Planning and conducting experiments, troubleshooting issues, and suggesting improvements. Writing protocols and reports for assigned projects. Performing physical-chemical evaluations of formulations to ensure robust performance and shelf-life. Organizing and prioritizing activities within assignments. Analyzing and interpreting data and results. Communicating results and analyses promptly to chemists or management. Documenting experiments in a laboratory notebook. Ensuring compliance with all site, departmental, and group safety and GLP guidelines. Assisting in the training of new technical staff on laboratory procedures. Traveling to U.S. plant locations as needed (approximately 5% travel). Requirements Bachelor's degree in Chemistry, Biology, Physics, or a related field with 1-3 years of experience; or Associate degree in Chemistry or a related field with 5 years of laboratory research experience. Must be eligible to work for any U.S. employer without sponsorship now or in the future. Knowledge of computer systems and basic office applications (e.g., Excel, Word, PowerPoint, databases). Experience with laboratory equipment and apparatus. Experience conducting basic research in the field of chemistry. Proven ability to deliver high-quality results under tight timelines while managing competing priorities across multiple projects. Flexible and adaptable; able to adjust to changing demands and quickly learn new, unfamiliar materials and techniques, with a strong commitment to ongoing development. Strong commitment to safety, consistently following policies, procedures, and best practices in all work environments. Effective communicator with strong oral skills for presenting ideas, experiments, and results clearly. Strong written communication and interpersonal skills, including basic scientific writing, report preparation, and the ability to work well independently or as part of a team. Sirius Staffing is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to characteristics such as race, color, national origin, religion, gender, age, marital status, disability, veteran status, citizenship status, sexual orientation, gender identity, or any other status protected by law.

JobID: 210689616 JobSchedule: Full time JobShift: Day : The Workforce Planning (WFP) organization is a part of Consumer and Community (CCB) Operations division. The WFP Data Science organization is tasked with delivering quantitatively driven solutions to support the core WFP functions (demand forecasting, capacity planning, resource scheduling, and business analysis & support). The WFP organization supports Chase's call centers, back office, and ~5,200 retail branches. As a Data Scientist Lead - WFP Machine Learning Scientist, within JPMorganChase, you will engage in projects by the Artificial Intelligence(AI)/Machine Learning(ML) team that can be complex, data intensive, and of a high level of difficulty, each having significant impact on the business. You will typically encounter these problems which will be of an unstructured nature, whereby the employee will be expected to quickly assess and comprehend the situation then develop a practical problem solving strategy. You will be expected to analyze the topic in question, develop solution proposals and review their results and next steps with management for prioritization, timing, and delivery. The AI/ML team is tasked with building next-gen data science solutions that move us closer to real-time inference and decision making. Job Responsibilities * Design and development of Machine Learning, Artificial Intelligence and Statistical models. * Participate in the full model development lifecycle, from framing the problem to prepare documentation and passing independent model review (MRGR). * Lead AI/ML projects along with mentor and coach junior team members. * Collaborate with stakeholders to understand the business requirements and clearly define the objectives of any solution. * Identify and select the correct method to solve the problem while staying up to data on the latest AI/ML research * Ensure the robustness of any data science solution. * Develop and communicate recommendations and data science solutions in easy-to-understand-way leveraging data to tell a story. * Lead and persuade others while positively influencing the outcome of team efforts and help frame a business problem into a technical problem resulting in a feasible solution. Required Qualifications, Capabilities, and Skills * Master's Degree with 5+ years or Doctorate (PhD) with 3+ years of experience operating as an data science professional (e.g. data scientist, statistician, or related professions) in a quantitative field: Statistics, Analytics, Data Science, Engineering, Operations Research, Economics, Mathematics, Machine Learning, Artificial Intelligence, and related disciplines. * 2+ years of experience leading AI/ML projects with multiple team members * Hands-on experience developing statistical models, machine learning models, and/or artificial intelligence models. * Deep understanding of math and theory behind AI/ML algorithms. * Proficient in data science programming languages like Python, R or Scala. * Experience with big-data technologies such as Hadoop, Spark, SparkML, etc. & familiarity with basic data table operations (SQL, Hive, etc.). * Demonstrated relationship building skills, with a superior ability to make things happen through the use of positive influence. Preferred Qualifications, Capabilities, and Skills * Advanced expertise with Time Series and Operations Research techniques. * Natural Language Processing(NLP)/Natural Language Generation(NLG), Neural Nets, or other ML/AI skills. * Prior experience with public cloud technologies such as Amazon Web Services(AWS), Azure or Google Cloud Platform(GCP). * Previous experience leading highly complex cross-functional technical projects with multiple stakeholders This position is full time in office Monday - Friday. This position is not hybrid nor remote.

Welcome to Verdantas, where innovation meets sustainability, and your career finds purpose! At Verdantas, we're redefining environmental consulting and sustainable engineering through our use of cutting-edge modeling and digital technology and our genuine commitment to people. Our work spans high-growth sectors like water resources, resilient land use, energy transformation, and civil infrastructure. Our commitment to excellence, across more than 90 offices, is championed by a team of over 2,000 experts, scientists, engineers, geologists, and technical specialists, embedded in a people-focused culture, prioritizing the well-being of our employees, clients, and the communities we serve. We partner with clients to deliver smart, data-driven solutions to complex environmental and infrastructure challenges. We don't just solve problems; we help shape a more sustainable future. Join a people-first culture that values your well-being, empowers your growth, and amplifies your impact. At Verdantas, your career goes beyond the expected, and your work helps build a better world. Ready to shape the future of resilient communities? Verdantas is seeking a Staff Scientist I to join our Field Services Team in the Wilmington or Dover, Delaware offices. This is a unique opportunity to use your technical expertise to work on construction and engineering projects while also providing support to other disciplines across the organization. This position will support Verdantas' continued growth in Delaware, Pennsylvania, and Maryland. The ideal candidate brings enthusiasm for civil/environmental work and a desire to help create a more sustainable world. They're ready to build technical experience, thrive in a team setting, communicate openly, welcome feedback, and stay sharp with details, especially in the field. When joining our team, you will be welcomed into an environment that values what you bring to the table, supports continuous growth in your field, and celebrates the accomplishments you achieve. Ranked the #1 firm to work for in 2025 by Zweig Group and Verdantas employees, you won't be just joining a firm; you'll be investing in a strong foundation for your career. What You'll Do: Support our project managers on construction review and material testing projects, including assisting in the preparation of cost estimates and proposals Perform daily coordination with internal staff, clients, and construction personnel Review, understand, and interpret project plans and specifications, shop drawings, product data sheets, RFIs, and change orders Perform scheduled tests, observations, and inspections in accordance with applicable test procedures and project requirements Perform quality control review, field observation, testing, and sampling of construction materials, including soils, concrete, masonry, pavement, and steel construction Perform Certified Construction Review (CCR) services related to routine review of erosion and sediment controls, and during the construction of stormwater management facilities Perform Resident Project Representative review and oversight of contractors on a variety of municipal and civil engineering and construction projects, including stormwater, water, and wastewater systems, street, sidewalk, and drainage improvements Completion of field documentation and reports in a timely manner, including job safety analysis (JSA) forms, project field reports, field notes, soil/concrete/asphalt datasheets, soil boring logs, tables, chain-of-custody forms, and other illustrations to document and summarize project data Operation of various types of field equipment (e.g., GPS, data loggers, survey level, combustible gas meters, nuclear density gauge, etc.) Collect data through independent research and file review Perform basic computations and process data using computer software or other established methods Safely operate and maintain company vehicles What You Bring: Bachelor's degree in Construction Management, Environmental Science, Geology, or related discipline 0 to 4 years of experience with construction observation, reporting, and consultation Certifications for testing and field review (preferred), including American Concrete Institute (ACI), International Code Council (ICC), American Portage Nuclear Gauge Association (APNGA), and OSHA 40 Hour HAZWOPER. Must be able to carry up to 50 lbs. regularly and up to 80 lbs. occasionally with or without accommodation, sometimes over substantial distances Strong communication skills The ability to interpret work plans Must have and maintain a valid Driver's License Salary Range: 55,000 - 65,000 Benefits: Flexible Work Environment Paid Parental Leave Medical Dental Vision Life and AD&D Insurance Short-Term and Long-Term Disability 401(k) with Company Match Paid Time Off + Holidays Verdantas strives to develop new ways to increase diversity awareness within our organization. We recruit and reward our employees based on capability and performance - regardless of race, gender, sexual orientation, gender identity or expression, lifestyle, age, educational background, national origin, religion, or physical ability. For us, it is imperative to build balanced teams from all walks of life and we believe that a diverse workforce is a stronger workforce. Verdantas is an EOE race/color/religion/sex/sexual orientation/gender identity/national origin/disability/vet

Must be authorized to work in the United States - No Sponsorship Experience required - 2 to 10 years of solid dosage experience (capsule or tablet) Our client is looking for a highly dependent person with PhD or MS and a passion for great formulation science. Here are a few key points: - Modern spacious lab to run projects - Working on a 8 person departmental team (New Grad to 20+ years of experience) - Global 10,000 person company so room to grow. - This role you will present results to senior management and attend sales presentation so well spoken and professional demeanor is important. - Someone who is customer service focused. - Everyone can attend a conference and top performers can attend several a year. Keywords: Solid dispersion, fluid bed, Spray dryers, Twin Screw Extruders, Solid dosage form, roller compactors, Granulators, Tablet presses, Fluid bed, Coaters, pharmaceutical, CRO, Medical Device, Characterize powders, disintegration, flowability, DSC, compactibility, density, particle size distribution, TGA , USP dissolution, crushing force, XRPD, friability Additional Information Equal opportunity employer. D/V/M/F. Applicants will be considered without regard to age, race, creed, color, national origin, ancestry, marital status, sexual orientation, gender identity or expression, disability, nationality, sex, or veteran status.

As required by our governmental client, this position requires being a US Citizen, lawful resident alien, citizen of American Samoa or other territory owning permanent allegiance to the United States. As an Assistant Administrator and Forensic Toxicology Expert, I serve as a consultant and supervisor for the military drug testing community and the Armed Forces Medical Examiner. Responsibilities include directing laboratory operations, scheduling and supervising personnel, introducing method development ideas, and implementing research improvements. I review analytical data, make evidence-based decisions, and contribute as an analyst in research programs. My role extends to providing screening and confirmation data, quantitative analysis, and serving as the final tier data review authority. Compensation & Benefits: Pay commensurate with experience. Full time benefits include Medical, Dental, Vision, 401K and other possible benefits as provided. Benefits are subject to change with or without notice. Analytical Toxicologist IV Responsibilities Include: Serve as an assistant administrator, contractor supervisor, and/or analyst. Act as a consultant and assistant contractor supervisor/administrator to the military drug testing community and the Armed Forces Medical Examiner, providing expertise in Forensic Toxicology. Direct laboratory operations, including scheduling and supervision of analysts, technicians, and clerical/administrative support personnel. Introduce ideas for method development and improvement within the laboratory setting. Implement research and method development ideas post-completion, contributing to advancements in forensic science. Perform a review of analytical data, making analytical and administrative decisions based on scientific evidence and case history for final case review. Provide screening and confirmation data, quantitative data, and full scan mass spectra. Serve as the final tier data review authority, ensuring accuracy and reliability. Participate as an analyst in research programs, complete and implement research improvements. Perform any special testing as directed by laboratory management. Performs other job-related duties as assigned. Analytical Toxicologist IV Experience, Education, Skills, Abilities requested: A Ph.D. in Analytical Chemistry, Toxicology, Pharmacology, or a related field. Typically requires a minimum of 10 years or more of relevant experience in analytical toxicology. Advanced proficiency in a broad range of analytical techniques and instrumentation, including specialized expertise in complex analyses. Extensive experience in laboratory leadership roles, overseeing and managing analytical toxicology laboratories. In-depth understanding of and expertise in regulatory requirements and guidelines related to toxicology, with a focus on forensic and clinical toxicology procedures. Demonstrated leadership in implementing and maintaining quality assurance practices within a laboratory setting. Exceptional communication skills, both written and verbal, for reporting findings, leading teams, and providing expert testimony. A track record of substantial contributions to research projects, publications, or advancements in the field of toxicology. Proven supervisory experience, including overseeing and mentoring junior and senior staff, project management, and resource allocation. Experience serving as an expert witness in legal proceedings related to toxicology. Demonstrated expertise in method development, particularly in response to complex analytical challenges. Proven track record of successful management and leadership in complex analytical toxicology laboratories. Experience in making strategic decisions based on scientific evidence and case history for final case review. Leading innovative research initiatives, with the ability to implement research and method development ideas post-completion. Serving as the final authority in data review, ensuring the highest standards of accuracy and reliability. Proven ability to collaborate effectively with interdisciplinary teams, law enforcement, and other stakeholders. Must pass pre-employment qualifications of Cherokee Federal. Company Information: Cherokee Nation Integrated Health (CNIH) is a part of Cherokee Federal - the division of tribally owned federal contracting companies owned by Cherokee Nation Businesses. As a trusted partner for more than 60 federal clients, Cherokee Federal LLCs are focused on building a brighter future, solving complex challenges, and serving the government's mission with compassion and heart. To learn more about CNIH, visit cherokee-federal.com. #CherokeeFederal #LI Cherokee Federal is a military friendly employer. Veterans and active military transitioning to civilian status are encouraged to apply. Similar searchable job titles Senior Principal Toxicologist Chief Forensic Toxicologist Director of Analytical Sciences Toxicology Laboratory Director Principal Scientist in Analytical Toxicology Keywords 5 times Advanced toxicological analysis Forensic toxicology leadership Laboratory management expertise Regulatory compliance and expertise Complex method development Legal Disclaimer: All qualified applicants will receive consideration for employment without regard to protected veteran status, disability or any other status protected under applicable federal, state or local law. Many of our job openings require access to government buildings or military installations. Candidates must pass pre-employment qualifications of Cherokee Federal. Many of our job openings require access to government buildings or military installations. Candidates must pass pre-employment qualifications of Cherokee Federal. Please Note: This position is pending a contract award. If you are interested in a future with Cherokee Federal, APPLY TODAY! Although this is not an approved position, we are accepting applications for this future and anticipated need.

Job Description Signature Science, LLC is seeking highly motivated Forensic Scientists with specific expertise in human DNA analysis to contribute to our laboratory operations throughout the Mid-Atlantic region. These positions are contingent upon contract funding. The primary responsibility of this role is to perform DNA analysis on forensic casework samples, from initial sample processing to final report generation. This includes a range of tasks, such as DNA extraction, quantification, amplification, and genetic analysis. Additionally, the Forensic Scientist will contribute to research and validation efforts, ensuring the accuracy and reliability of our laboratory procedures. *This position can be located in Dover, DE* Essential Duties & Responsibilities: Laboratory Operations: Adhere to strict laboratory protocols and quality assurance standards. Utilize appropriate personal protective equipment (PPE) to maintain a safe working environment. Practice rigorous contamination control techniques to prevent sample cross-contamination. Handle and safeguard DNA samples and data in accordance with established procedures. Perform DNA analysis on diverse sample matrices, including touch DNA samples. Employ various DNA extraction methods, quantification techniques (e.g., Real-Time PCR), and amplification protocols. Utilize advanced genetic analyzer platforms to generate high-quality DNA profiles. Interpret complex DNA profiles, including single-source and mixture samples, using both manual and probabilistic genotyping methods. Prepare clear and concise forensic reports, summarizing findings and conclusions. Conduct technical reviews of casework to ensure accuracy and completeness. Collaborate with team members to efficiently process a high volume of casework. Adapt to changing priorities and deadlines to meet client needs. Maintain and troubleshoot laboratory equipment, such as Real-Time PCR instruments, thermocyclers, and genetic analyzers. Participate in validation studies of new DNA methodologies and established procedures. Required KSA's Strong understanding of forensic DNA analysis principles and techniques. Proficiency in using laboratory equipment and software (e.g., GeneMapper ID-X, STRmix). Excellent analytical and problem-solving skills. Attention to detail and ability to follow precise protocols. Strong written and verbal communication skills. Ability to work independently and as part of a team. Strong organizational and time management skills. Ability to obtain and maintain a security clearance. Education/Experience: Bachelor's degree in biological sciences, forensic science, or a related field. Minimum of 6 months of full-time laboratory experience, preferably in a forensic laboratory. Experience with DNA analysis techniques, including extraction, quantification, amplification, and genotyping. Adherence to FBI Quality Assurance Standards (QAS) for DNA analysis. Clearance: US Citizenship required; candidates will be subject to security screening. Working Conditions/Equipment/Travel: Laboratory environment requiring the use of PPE. Potential exposure to hazardous materials, including biological fluids. Ability to lift up to 20 pounds independently and 40 pounds with assistance. Limited ( Powered by ExactHire:160583

Join Agilent Technologies and contribute to the advancement of liquid chromatography products at our Newport manufacturing facility. As part of a high-impact team within our growing Consumables and Supplies Division, you'll play a key role in driving innovation, improving product quality, and enhancing customer satisfaction. This is a dynamic opportunity to apply your expertise in analytical chemistry while collaborating across disciplines in a Lean and Six Sigma-driven environment. Key Responsibilities Support and troubleshooting for quality testing lab for silica-based packing materials used in HPLC columns. Support investigations of customer issues related to LC column products. Analyze customer methods to generate insights and communicate product impact. Provide feedback to engineering and chemistry teams to reduce product variability. Run HPLC testing methods to support product and process improvements. Apply experimental design to deepen understanding of process chemistries. Collaborate on cross-functional projects, including capital and continuous improvement initiatives. Support new product introductions and represent manufacturing in cross-team efforts. Lead or participate in Lean, Six Sigma, and safety improvement initiatives. Qualifications Bachelor's or Master's degree in Chemistry or Chemical Engineering. 1+ years of hands-on experience with HPLC. Strong analytical and problem-solving skills. Effective written and verbal communication abilities. Demonstrated leadership and strategic thinking in technical environments. Proficiency in digital tools and data analysis. Additional Details This job has a full time weekly schedule. Applications for this job will be accepted until at least October 16, 2025 or until the job is no longer posted.The full-time equivalent pay range for this position is $79,200.00 - $123,750.00/yr plus eligibility for bonus, stock and benefits. Our pay ranges are determined by role, level, and location. Within the range, individual pay is determined by work location and additional factors, including job-related skills, experience, and relevant education or training. During the hiring process, a recruiter can share more about the specific pay range for a preferred location. Pay and benefit information by country are available at: ************************************* Agilent Technologies, Inc. is an Equal Employment Opportunity and merit-based employer that values individuals of all backgrounds at all levels. All individuals, regardless of personal characteristics, are encouraged to apply. All qualified applicants will receive consideration for employment without regard to sex, pregnancy, race, religion or religious creed, color, gender, gender identity, gender expression, national origin, ancestry, physical or mental disability, medical condition, genetic information, marital status, registered domestic partner status, age, sexual orientation, military or veteran status, protected veteran status, or any other basis protected by federal, state, local law, ordinance, or regulation and will not be discriminated against on these bases. Agilent Technologies, Inc., is committed to creating and maintaining an inclusive in the workplace where everyone is welcome, and strives to support candidates with disabilities. If you have a disability and need assistance with any part of the application or interview process or have questions about workplace accessibility, please email job_******************* or contact ***************. For more information about equal employment opportunity protections, please visit *************************************** Required: OccasionalShift: DayDuration: No End DateJob Function: Manufacturing

Description Job Description: Set up and make operationally ready a wide variety of laboratory instruments and equipment. Write, review, and edit experimental protocols, standard operating procedures, and operating instructions for projects of experimental programs, service casework procedures and general laboratory management operations. Assist in quality assurance activities such as standards maintenance, equipment preventive maintenance, reagent testing & validation, proficiency testing, and accreditation and certification. Conduct inspections and provide oversight to the adherence to established quality assurance activities including maintenance of standards and controls, preventive maintenance and equipment calibration, reagent testing and validation, and proficiency testing programs for accreditation or certification. Perform general laboratory housekeeping activities such as maintaining appropriate working-stock levels of expendable supplies and maintaining a clean environment within laboratory work areas. Perform investigative studies on tissue identification by DNA typing technologies. Maintain documentation of methods development and research activities in accordance with standard practice. Supervise/perform service casework involving routine nuclear and mt DNA typing and profiling procedures. Prepare formal written reports of service casework or research reports that contain professional interpretations and conclusions from the test data, and that are suitable for legal presentation in a court of law. Review casework and formal written reports. Assist in program maintenance and development at the direction of their designated supervisor. Supervise staff performing investigative studies on tissue identification by DNA typing technologies, carry out DNA typing casework. Testify as an expert witness as required; provide technical assistance in the area of bioinformatics, information technology and laboratory automation; and support logistical or resource management activities. Participate in the organization and presentation of educational activities. Serve as a Supervisory DNA Analyst. Qualifications: Bachelor's degree or an advanced degree in biology, chemistry, forensic science, or a related disciple required. Must have successfully completed a minimum of 9 cumulative semester hours or equivalent (graduate or undergraduate level) course work covering the following subject areas: biochemistry, genetics, molecular biology; and course work and/or training in statistics and/or population genetics as it applies to forensic DNA analysis. Must have six (6) months of forensic human DNA laboratory experience. Desired knowledge and experience in filing techniques; administrative typing; preparing and editing technical or general documentation using various software packages such as Microsoft Word, Microsoft PowerPoint, Microsoft Excel and Windows; transcription of documents, data entry, and preparing and editing management support documentation. Positions are contingent and will begin upon contract award. Why Join Us? At CICONIX, we are committed to providing high-quality services to support military families. By joining our team, you'll make a direct impact on the lives of children and families in crisis while working in a supportive, mission-driven environment. We offer flexible remote options, competitive pay, and the opportunity to work on meaningful programs that serve those who protect our country. About the Armed Forces Medical Examiner System (AFMES): The Armed Forces Medical Examiner System (AFMES) is a vital Department of Defense entity responsible for providing medical-legal investigations, including autopsies and forensic services, for deaths involving military personnel, their families, and authorized civilians. AFMES plays a key role in identifying remains, investigating causes of death, and offering expert testimony, while also managing the Armed Forces DNA Registry. In addition to its forensic casework, AFMES supports research and development to enhance forensic techniques and contributes to the education and readiness of military forensic professionals. CICONIX, LLC is an Equal Opportunity Employer, including disability/veterans. We participate in E-Verify.

The entry-level Forensic DNA Technician (Forensic Scientist I - FSI) will perform DNA analysis on a wide range of complex samples in support of the Armed Forces DNA Identification Laboratory (AFDIL) in Dover, DE. The FSI will be responsible for performing analysis of forensic evidence in accordance with laboratory accreditation and standard operating procedures. This role is essential for effective laboratory operations and requires collaboration and productivity with laboratory staff and management. It is crucial to prioritize job responsibilities in a fast-paced environment while ensuring excellent customer service. Responsibilities will include: * Assisting in program maintenance and development at the direction of their designated supervisor. * Supporting investigative studies on biological materials using DNA typing technologies. * Supporting the logistical or resource management activities of the DNA Registry * Participating in the organization and presentation of educational activities. * Accessioning forensic evidence in the Laboratory Information Management System (LISA). * Maintaining accurate and complete chain of custody for evidence. * Entering data into LISA and the Armed Forces Medical Examiners Tracking System (AFMETS). * Preparing correspondence/documents ensuring proper format, mathematical correctness, grammar, punctuation, and spelling, in preparation for or editing of recurring reports regarding case status and case tracking. * Preparing reagents and maintain documentation of reagent prep and Quality Control testing in accordance with SOPs. * Performing laboratory housekeeping activities such as preparing common laboratory reagents. * Maintaining appropriate stock levels of expendable supplies and maintaining a clean environment within laboratory work areas. * Assisting in casework involving nuc DNA and mt DNA typing and profiling procedures. * Supporting validation projects focusing on systems with increased sensitivity and discrimination power and advanced development of automated systems. * Supporting research projects focusing on various research projects to include population databasing and working to increase sensitivity, discrimination power, and automated systems for casework applications. Minimum Education and Experience Requirements: * BA/BS degree in forensic science or in physical or life sciences. * Successfully completed course work (graduate or undergraduate level) covering the following subject areas: biochemistry, genetics, molecular biology; and course work and/or training in statistics and/or population genetics as it applies to forensic DNA analysis. * Must successfully complete a National Agency Check with Inquiries (NAC-I) background investigation. The position does not require a security clearance, but the individual may be required to obtain a government security clearance at a future date if handling classified information or materials. (Please note: US citizenship is required to obtain a government security clearance) * General knowledge of forensic DNA analytical methods, especially nuc DNA and mt DNA profiling. * Ability to maintain minimum standards of technical proficiency as demonstrated by acceptable performance by internal and external proficiency testing programs * Must be self-motivated, detail oriented, and able to work well in a team laboratory environment. * Possess strong written and verbal communication skills. * Familiar with MS Word, PowerPoint, Excel, and Adobe Acrobat. * A resume and a copy of unofficial transcripts must be submitted. Amentum is proud to be an Equal Opportunity Employer. Our hiring practices provide equal opportunity for employment without regard to race, sex, sexual orientation, pregnancy (including pregnancy, childbirth, breastfeeding, or medical conditions related to pregnancy, childbirth, or breastfeeding), age, ancestry, United States military or veteran status, color, religion, creed, marital or domestic partner status, medical condition, genetic information, national origin, citizenship status, low-income status, or mental or physical disability so long as the essential functions of the job can be performed with or without reasonable accommodation, or any other protected category under federal, state, or local law. Learn more about your rights under Federal laws and supplemental language at Labor Laws Posters.

Introduction The Division of Waste and Hazardous Substances regulates the installation, operation, maintenance, and closure of underground and aboveground storage tank systems in order to prevent contamination of soils and groundwater. Click here for more information about Waste and Hazardous Substances Tanks Compliance. Summary Statement This position will be responsible for performing compliance assessments of regulated underground storage tanks (UST) and permitted Vapor Recovery facilities, in addition to oversight of the UST installations, removals, and retrofits. The person will be responsible for completing all required inspection reports, reviewing submitted compliance documentation and updating the Delaware Environmental Navigator UST module (DEN-UST). Career Ladder Upon satisfactory completion of department promotional standards and job requirements, employees may be eligible to be promoted to the next level. Essential Functions Essential functions are fundamental, core functions common to all positions in the class series and are not intended to be an exhaustive list of all job duties for any one position in the class. Since class specifications are descriptive and not restrictive, incumbents can complete job duties of similar kind not specifically listed here. Conducts field studies or inspections and evaluations for compliance with permit and regulatory requirements; observes, collects, analyzes, reviews and interprets data from standard field studies, compliance inspections, various regulatory submissions or literature and makes recommendations. Performs statistical analysis of data. Conducts technical reviews and makes recommendations on permit applications or other various regulatory submissions to ensure compliance with regulations. Prepares permits, technical reports and/or enforcement case documents. Responds to technical/regulatory inquiries from other state, local and federal agencies as well as public and private organizations or individuals. Job Requirements JOB REQUIREMENTS for Environmental Scientist I Applicants must have education, training and/or experience demonstrating competence in each of the following areas: Possession of a Bachelors degree or higher in Life, Physical, or Applied Science or related field. Knowledge of controlled sampling, monitoring and testing techniques. Knowledge of analyzing and evaluating data. Knowledge of technical report writing. Knowledge of using an automated information system to enter, update, modify, delete, retrieve/inquire and report on data. Conditions of Hire Applicants must be legally authorized to work in the United States. The State of Delaware Executive Branch participates in the Federal E-Verify system where the State will provide the federal government with each new hires Form I-9 information to confirm that you are authorized to work in the U.S. For more information refer to our job seeker resources. DNREC does not provide sponsorship for holders of H-1 B Visas. DNREC Medical Exam: To meet health and safety requirements, applicants for this position must successfully pass a baseline medical examination to demonstrate fitness for duty. As a condition of hire you must possess a valid driver's license (not suspended, revoked or cancelled, or disqualified from driving). Benefits To learn more about the comprehensive benefit package please visit our website at ********************************** Selection Process The application and supplemental questionnaire are evaluated based upon a rating of your education, training and experience as they relate to the job requirements of the position. It is essential that you provide complete and accurate information on your application and the supplemental questionnaire to include dates of employment, job title and job duties. For education and training, list name of educational provider, training course titles and summary of course content. Narrative information supplied in response to the questions must be supported by the information supplied on the application including your employment, education and training history as it relates to the job requirements. Once you have submitted your application on-line, all future correspondence related to your application will be sent via email. Please keep your contact information current. You may also view all correspondence sent to you by the State of Delaware in the “My Applications” tab at StateJobs.Delaware.gov. Accommodations Accommodations are available for applicants with disabilities in all phases of the application and employment process. TDD users may request an auxiliary aid or service by calling ************** or by visiting delawarerelay.com. You may also call ************** or email DHR_************************ for additional applicant services support. The State of Delaware is an Equal Opportunity employer and values a diverse workforce. We strongly encourage and seek out a workforce representative of Delaware including race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression.

Do you want to be part of an organization that is making a difference in the lives of millions of people worldwide? If so, we want to hear from you! The Translational Medicine (TLM) department of QPS is comprised of three laboratory operations units: Biomarker Analysis (BMA), Gene & Sequence Analysis (GSA), and Immunobioanalysis (IBA). An Associate Scientist in any of these units will be a fully-supervised trainee, responsible for gaining mastery of GCP and GDP, conducting assigned studies according to study protocols, and recording study results and observations. Our TLM department is continuing to expand, and has positions available in most of the above units. If you have a Bachelor's degree in Biology, Biochemistry, Immunology or other related disciplines, we would like to hear from you. No visa sponsorship (e.g. H‑1B, L‑1, E) will be provided for this active position, now or in the future. Applicants must currently be authorized to work in the U.S. on a permanent or unrestricted basis. QPS' Story: Since its inception, QPS has been assisting pharmaceutical, biotechnology and medical device companies with their drug development efforts by providing a full range of Neuropharmacology, DMPK, Toxicology, Bioanalysis, Translational Medicine, Early Phase Clinical and Phase II - IV Clinical Research services. To meet the needs of our clients, we strive to employ talented, caring and committed individuals who will work collaboratively towards achieving our mission of improving human health and the quality of life. Team members enjoy challenging and rewarding work, and are encouraged achieve their best. Underpinning the operation is a culture that values diversity, innovation, accountability, team work and a friendly atmosphere where performance is recognized and rewarded. We provide unique company benefits, training, and advancement opportunities. Most importantly, we value each of our team members as employees and as individuals. If this sounds like your ideal work environment, then we would love to speak with you, so apply today! Please visit our website (************ for more information and to see all current openings. The Job Perform routine lab operations, such as preparing reagents, pipetting, weighing, monitoring, recording, and replenishing supplies Assist supervisor in performing analysis of drug or other targets in complex biologic matrices Set-up, use and maintain complex instrumentation Document experiment details, calculations, results and observations in accordance with GLPs and SOPs Perform routine mathematical & chemical calculations Work Location This job will be 100% QPS-office/facility based Requirements The successful candidate will hold an undergraduate degree in Biology, Molecular Biology, Biochemistry, Immunology, Pharmacology, Medical Technology, or a related field as follows: Bachelor's Degree Associate's Degree plus 2 or more years relevant experience Desire to learn and grow professionally Why You Should Apply Great learning opportunities, especially for those new to the field. Our seasoned professionals are here to support and work with you to explore your learning potential and career goals. Structured Career Ladders that provide excellent growth based on your personal aspirations. Bonuses and merit increases are a part of the QPS total rewards approach and are linked to individual, team and company performance. Solid Benefits package, including Company-matched 401(k), and Company-sponsored Group Life/AD&D and Short and Long-term Disability Insurance Park-like setting in Newark, Delaware Internal committees designed with the needs and enjoyment of QPS employees in mind. QPS, LLC is an Equal Employment Opportunity/Affirmative Action Employer. In accordance with federal, state, and local laws, we recruit, hire, promote and evaluate all personnel without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, citizenship status, physical disability, protected veteran status, or any other characteristic protected by law. Job applicants and present employees are evaluated solely on ability, experience, and the requirements of the job. In addition, QPS, LLC is a federal contractor and desires priority referrals of protected veterans.

The Swank Autism Center at Nemours Children's Health is seeking a Research Scientist to join our team in Wilmington, Delaware. The Swank Autism Center provides comprehensive clinical services for children up to age 21 years and conducts research and community-based outreach and training. The Research Scientist will join a multidisciplinary team that includes faculty from psychology, developmental medicine, psychiatry, neurology, social work, nursing, and applied behavior analysis, as well as colleagues who are autistic and/or caregivers. The Research Scientist will also have a dual appointment in the Center for Healthcare Delivery Science (CHDS) - Delaware Valley (********************** The CHDS includes 20+ investigators across the enterprise that study ways to improve health care, health equity, and health and wellness beyond medicine for youth and their families. The Swank Autism Center has a dedicated Clinical Research Coordinator and CHDS has additional research coordination and data analysis resources. Teaching, training, and mentoring are core values in our division, and these efforts are also supported and encouraged. The Swank Autism Center is strongly affiliated with Delaware's Leadership Education in Neurodevelopmental Disabilities (LEND) program. Key Responsibilities: * Develop a targeted research program in autism. This could include (but is not exclusive to) current areas of study: healthcare inequities, neuro-affirming care, supporting families who are newly diagnosed or awaiting evaluation, and other areas. * Build and support research collaborations with other Nemours faculty and/or our external partners. * Provide clinical services as a minor part of this role, which might include autism diagnostic services, individual/group therapy, and/or supervising trainees, e.g., externs, residents, and/or fellows who rotate through the center. What We Offer: * Competitive salary * Health, life, dental & vision benefits for Associates and their dependents * Wellness program * CME days and dollars * 403(b) with employer match & a 457(b) plan * Licensure and dues allowance after hire * Tuition reimbursement & tuition discount programs with various Universities for Associates and their dependents * Adoption assistance and 6 weeks of Paternity leave Qualifications: * Candidates must hold a PhD in a health-related discipline * Must be license-eligible * Must demonstrate evidence of collaborative academic productivity and either success in obtaining funding for research or a strong potential to obtain funding for research * The ideal candidate will have demonstrated training and experience conducting research in clinical and/or academic settings with autistic/neurodivergent children, adolescents, and/or young adults, and their families If you're looking for a position that will allow you to enjoy a work-life balance, have an opportunity for professional growth, and focus on pediatric care, this is the opportunity for you. #LI-KN1

Must be authorized to work in the United States - No Sponsorship Experience required - 2 to 10 years of solid dosage experience (capsule or tablet) Our client is looking for a highly dependent person with PhD or MS and a passion for great formulation science. Here are a few key points: - Modern spacious lab to run projects - Working on a 8 person departmental team (New Grad to 20+ years of experience) - Global 10,000 person company so room to grow. - This role you will present results to senior management and attend sales presentation so well spoken and professional demeanor is important. - Someone who is customer service focused. - Everyone can attend a conference and top performers can attend several a year. Keywords: Solid dispersion, fluid bed, Spray dryers, Twin Screw Extruders, Solid dosage form, roller compactors, Granulators, Tablet presses, Fluid bed, Coaters, pharmaceutical, CRO, Medical Device, Characterize powders, disintegration, flowability, DSC, compactibility, density, particle size distribution, TGA , USP dissolution, crushing force, XRPD, friability Additional Information Equal opportunity employer. D/V/M/F. Applicants will be considered without regard to age, race, creed, color, national origin, ancestry, marital status, sexual orientation, gender identity or expression, disability, nationality, sex, or veteran status.

As required by our governmental client, this position requires being a US Citizen, lawful resident alien, citizen of American Samoa or other territory owning permanent allegiance to the United States. As a contractor administrator, director, and expert in Forensic Toxicology, provide oversight and consultancy to the military drug testing community and the Armed Forces Medical Examiner. Responsibilities encompass directing laboratory operations, supervising personnel, chairing research projects, and introducing method development ideas. Perform comprehensive analytical data reviews, make evidence-based decisions for final case review, and contribute to screening and confirmation data. Additionally, lead research teams, participate in programs, implement improvements, and assist in budget planning and contract development for optimal laboratory functionality. Compensation & Benefits: Pay commensurate with experience. Full time benefits include Medical, Dental, Vision, 401K and other possible benefits as provided. Benefits are subject to change with or without notice. Analytical Toxicologist V Responsibilities Include: Oversee and administer contractor activities related to Forensic Toxicology. Serve as the director, providing leadership and expertise in Forensic Toxicology. Offer expert consultation to the military drug testing community and the Armed Forces Medical Examiner. Direct day-to-day laboratory operations, ensuring efficiency and adherence to protocols. Supervise analysts, technicians, clerical, and administrative support personnel. Chair research projects, overseeing their planning, execution, and completion. Introduce ideas for method development and improvement within the laboratory. Perform comprehensive reviews of analytical data, making evidence-based decisions for final case review. Contribute to screening and confirmation data, providing critical insights into toxicological analyses. Lead research teams, participating as an analyst in research programs. Implement improvements identified through research initiatives. Assist in budget planning for the laboratory, ensuring optimal resource allocation. Participate in contract development to minimize risks of critical reagent shortages and instrument usage disruptions. Performs other job-related duties as assigned. Analytical Toxicologist V Experience, Education, Skills, Abilities requested: A Ph.D. in Analytical Chemistry, Toxicology, Pharmacology, or a closely related field. Minimum of 15 years or more of progressive experience in analytical toxicology. Expertise in a wide array of analytical techniques and instrumentation, with a focus on advanced and emerging technologies in toxicology. Extensive experience in leadership roles within analytical toxicology laboratories, including strategic planning and decision-making. In-depth understanding of and expertise in regulatory requirements, guidelines, and compliance in forensic and clinical toxicology. Proven leadership in implementing and maintaining rigorous quality assurance practices within a laboratory setting. Exceptional communication skills, both written and verbal, for reporting findings, leading teams, and providing expert testimony. A substantial track record of contributions to research projects, publications, or advancements in the field of toxicology. Extensive supervisory experience, overseeing and mentoring junior and senior staff, project management, and resource allocation. Demonstrated experience serving as an expert witness in legal proceedings related to toxicology. Proven success in managing and directing complex analytical toxicology laboratories. Experience in making strategic decisions based on scientific evidence and case history for final case review. Leadership in spearheading innovative research initiatives, with the ability to implement research and method development ideas post-completion. Serving as the final authority in data review, ensuring the highest standards of accuracy and reliability. Demonstrated ability to collaborate effectively with interdisciplinary teams, law enforcement, and other stakeholders. Must pass pre-employment qualifications of Cherokee Federal. Company Information: Cherokee Nation Integrated Health (CNIH) is a part of Cherokee Federal - the division of tribally owned federal contracting companies owned by Cherokee Nation Businesses. As a trusted partner for more than 60 federal clients, Cherokee Federal LLCs are focused on building a brighter future, solving complex challenges, and serving the government's mission with compassion and heart. To learn more about CNIH, visit cherokee-federal.com. #CherokeeFederal #LI Cherokee Federal is a military friendly employer. Veterans and active military transitioning to civilian status are encouraged to apply. Similar searchable job titles Chief Forensic Toxicologist Director of Analytical Sciences Senior Principal Toxicologist Chief Scientist in Toxicology Principal Investigator in Forensic Analytical Chemistry Keywords 5 times Advanced toxicological analysis Forensic toxicology leadership Cutting-edge analytical techniques Laboratory management expertise Regulatory compliance and strategy Legal Disclaimer: All qualified applicants will receive consideration for employment without regard to protected veteran status, disability or any other status protected under applicable federal, state or local law. Many of our job openings require access to government buildings or military installations. Candidates must pass pre-employment qualifications of Cherokee Federal. Many of our job openings require access to government buildings or military installations. Candidates must pass pre-employment qualifications of Cherokee Federal. Please Note: This position is pending a contract award. If you are interested in a future with Cherokee Federal, APPLY TODAY! Although this is not an approved position, we are accepting applications for this future and anticipated need.

Description Job Description: Accession of forensic evidence in the Laboratory Information System Analysis (LISA), maintain accurate and complete chain of custody for evidence, responsible for data entry into LISA and the Armed Forces Medical Examiners Tracking System (AFMETS), preparation of correspondence/documents ensuring proper format, mathematical correctness, grammar, punctuation, and spelling, and preparation & editing of recurring reports regarding case status and case tracking. Prepare reagents and maintain documentation of reagent prep and Quality Control testing in accordance with SOPs. Perform laboratory house-keeping activities such as preparing common laboratory reagents, maintaining appropriate stock levels of expendable supplies, and maintaining a clean environment within laboratory work areas. Perform service casework involving nuc DNA and mt DNA typing and profiling procedures. Support validation projects focusing on systems with increased sensitivity and discrimination power and advanced development of automated systems. Support research projects focusing on various research projects to include population data basing and working to increase sensitivity, discrimination power, and automated systems for casework applications. Perform as DNA Technicians and/or Evidence Custodian. Assist in program maintenance and development at the direction of their designated supervisor. Perform investigative studies on biological materials using DNA typing technologies; carry out DNA typing casework in support of routine casework and special projects; and support the logistical or resource management activities of the DNA Registry. Participate in the organization and presentation of educational activities. Qualifications: Bachelor's degree (or its equivalent) in biology, chemistry, DNA forensic science, physical science, or a related field required. Desired knowledge and experience in filing techniques; administrative typing; preparing and editing technical or general documentation using various software packages such as Microsoft Word, Microsoft PowerPoint, Microsoft Excel and Windows; transcription of documents, data entry, and preparing and editing management support documentation. Positions are contingent and will begin upon contract award. Why Join Us? At CICONIX, we are committed to providing high-quality services to support military families. By joining our team, you'll make a direct impact on the lives of children and families in crisis while working in a supportive, mission-driven environment. We offer flexible remote options, competitive pay, and the opportunity to work on meaningful programs that serve those who protect our country. About the Armed Forces Medical Examiner System (AFMES): The Armed Forces Medical Examiner System (AFMES) is a vital Department of Defense entity responsible for providing medical-legal investigations, including autopsies and forensic services, for deaths involving military personnel, their families, and authorized civilians. AFMES plays a key role in identifying remains, investigating causes of death, and offering expert testimony, while also managing the Armed Forces DNA Registry. In addition to its forensic casework, AFMES supports research and development to enhance forensic techniques and contributes to the education and readiness of military forensic professionals. CICONIX, LLC is an Equal Opportunity Employer, including disability/veterans. We participate in E-Verify.