Research Scientist Jobs in Indian Trail, NC

Element is currently seeking an experienced Analytical Scientist for an amazing client in the nutraceuticals industry! This role requires a strong background in FDA-regulated cGMP laboratories. This is a permanent full-time salaried position with annual performance-based bonus and a robust benefits package. Summary of the Position: The Analytical Scientist will be expected to develop and validate new analytical methods with minimum to no supervision as well as to provide technical support to other corporate groups including Quality Control, Quality Assurance, and International Business. Roles and Responsibilities: Analytical Scientist reports to Analytical Chemistry (AC) Management. Performs Quality Control testing and data review to support timely release of product in weekly basis. Effective development, optimization, and validation of scientifically sound analytical methods to ensure analysis and prompt release of raw materials, finished products, and stability studies. Proficient in Empower Software and other laboratory software use in QC environment for chromatographic, spectroscopic methods as well as wet chemistry. Assess testing methodologies and their application to different sample matrix, instrumentation and will include evaluation of testing results from contract laboratories to be sure that the agreed methods and testing parameters were properly followed. Maintains current knowledge of latest technological and scientific trends and serves as an analytical science resource for the rest of the group. Mentor and train chemists in the proper execution, including interpretation of validation studies. Responsible for producing hazardous waste from it point of generation. Managing all produced in accordance with RCRA and SCDHEC regulations to include: proper containers, accumulation, labeling, marking, and storage. Perform other assigned duties and follow verbal and written instructions issued by supervisor or designee related to meeting company goals and objectives. Communicate effectively with other departments within the organization and function within a team environment. Regular attendance is required. Minimum Requirements: Able to develop analytical methods for chromatographic, spectroscopic, titrimetric, and wet chemistry analyses. Must be proficient on laboratory instrument trouble shooting. In-depth knowledge of strategies of analytical method development and specification setting for raw materials and finished products. Knowledge in most of laboratory instrumentation such as FTIR, HPLC, ICP, GC, UV-Vis, LC-MS, GC-MS, ICP-MS, HPTLC and test methods. Knowledge in the characterization and elucidation of botanical compound structures by study of the compound structure, spectroscopic methods, and Mass spectrometry. Proficient in the selection of analytical columns for chromatographic analyses, proper techniques or technologies and the selection for proper reagents to design effective analytical methods in timely manner. Experience in effective sample preparation techniques to support high number of samples for testing such as liquid-liquid extraction, derivatization, chemical manipulation, and mechanical manipulation. Knowledge of statistical techniques, such as data trend analysis and design of experiments, is highly desirable. Proficiency in reviewing and interpretation of laboratory data. Detailed knowledge of principles of routine laboratory operations. Thorough working knowledge of industry regulations, FDA and ICH guidelines; experience implementing and maintaining adherence to pharmaceutical and/or nutritional supplement GLP/GMP is strongly desired. Demonstrated aptitude to function in a dynamic fast-paced environment. Education and Experience A Bachelor's degree with 10 years of experience in validation and development of analytical methods for nutraceuticals and/or pharmaceutical samples in a GMP environment. A Master's degree and a minimum of 5 years of technical experience is preferred. Extensive experience may be accepted in lieu of an advanced degree. A degree in analytical chemistry, biochemistry, chemical engineering, or related fields is strongly preferred. A need to work on the bench to accomplish tasks along with the Analytical Chemistry team.

(Pharmaceutical Manufacturing Industry) Previous work experience in formulation development department with good experience in formulation development, process development. Previous work experience in formulation technology and development in dietary supplements, nutraceuticals, or medical foods. Are you looking to make a career change to a stable company? This exciting opportunity offers a competitive salary plus an excellent benefits package including medical insurance, dental insurance, vision insurance and paid PTO.Does this position match your future career goals? Then this opportunity could be the right fit for you. Compensation: Competitive Salary , Full Benefits Job Duties and Requirements: Bachelor's degree in Chemistry ,Biochemistry, Biotechnology or related field. Previous 3 plus years of in a pharmaceutical manufacturing industry. Formulation/process development Formulation/process development, commercial support, and/or technology transfer. Comply with GMP's, SOP's and all regulatory documentation. Understanding of pharmaceutical manufacturing concepts. Knowledge of pharmaceutical GMPs and regulatory requirements. Perform root cause analysis to troubleshoot formulation issues and ensure compliance with FDA regulations and GMP standards. Collaborate with cross-functional teams in drug discovery and manufacturing processes. Follow applicable cGMP processes. Provide training to manufacturing associates on new processes and process modifications/improvements. Assist in developing new formulations for new active raw materials. Compile and provide summaries of stability data. Possesses applied knowledge of root cause analysis and troubleshooting techniques. Able to apply statistical analyses and experimental design techniques. Must have knowledge of cGMPs, Quality Concepts, and Microsoft Office. Excellent written and verbal communication skills. Proficiency in MS Office. Strong attention to detail. Jasleen Kaur ********************************* Ajulia Executive Search is a search firm specializing in Manufacturing, Finance, IT, Legal and Pharmaceutical positions. This is a confidential search for one of our preferred clients. It is a direct hire position that includes competitive compensation and full comprehensive benefit package #ZR

If its possible, you will find it at Atrium Healththe leading community-focused academic healthcare system serving North Carolina and South Carolina. We invite experienced Hematology/Oncology APPs to discover all that we can do when we bring healing hearts, inquisitive minds, and progressive visionaries together at Levine Cancer Institute - Pineville Heme/Onc Consult Service. With more than 25 cancer care locations, we provide access to top-ranked physician expertise, groundbreaking clinical trials and the latest cancer treatments across the Carolinas. Position Details: Inpatient Weekender APP role Perform medical history, physical exam, document findings and plan of care in timely manner Order and interpret laboratory and radiographic testing Support inpatients receiving chemotherapy Determine treatment plans with supervision of Attending Physician Attend, participate in and contribute to group/practice meetings, development of policies and procedures, quality improvement initiatives Schedule consists of 4 days/10-hour shift Friday-Monday Eligible for PTO and Performance Incentive bonuses; $2500/1 week of CME This APP functions in the inpatient weekender Heme/Onc Consult Service and demonstrates appropriate critical thinking and interpersonal skills when working in a fast paced, high acuity work environment. Works well with multidisciplinary team. Qualified candidates will be able to perform thorough history and physical assessment. Ideal Candidate: 1 year of experience in hematology/oncology working as an APP preferred, New grads considered Effective communication (written and verbal) Willingness to collaborate closely with clinical team Current on best practice and standards of care Displays self-initiative to learn Position Qualifications: Graduation from an accredited NP or PA program. Current license to practice as an NP or PA in North Carolina. Current prescriptive privileges and DEA license required. BLS for healthcare provided from a required. Nurse practitioners required to have Master's degree or Doctorate in nursing practice. Physician Assistants with certification from the National Commission on Certification of Physician Assistants preferred. Current or pending CAQ certification preferred. When you join Atrium Health, you will be welcomed into an inclusive culture that celebrates and respects the contributions a diverse team can make together. Practice where your voice is valued, your passion for advancing medicine is rewarded, and you get the resources and support you need to thrive personally and professionally. In our nationally-renowned integrated health system, you can work alongside the most advanced minds in medicine to improve medicine, elevate hope and advance healingfor all.

Corvid Technologies is seeking a highly talented Research Scientist. This person will be responsible for research and development of weapons systems and related applications, drawing on an understanding of fundamental physics. Innovative and independent thinking is an absolute must, but must be achieved in the context of collaborative team efforts. Projects will require the ability to start with a problem, create concept solutions, and mature that concept into a prototype that can be tested. Problems will be diverse and multifaceted, ranging from the purely mechanical to the purely computational. General Requirements: Ability to obtain a U.S. Security Clearance is required Must be willing to travel up to 20% of the time 0-5 Years of previous experience Required Education: Master's or Doctorate Desired Backgrounds: Mechatronics, Embedded Systems, Flight Vehicles, RF Design, AI/ML Desired Skills and Experience Experience in both experimental work and computational tools. Simulation and design skills. Innovative and independent thinking. Knowledge of how to build prototypes. Possess the ability to evaluate systems and solutions by creating or adapting mathematical models (Models might be either analytical or numerical). Efficiency in prototyping in Python or other open interpreted language required. Fluency in C or FORTRAN is desirable. Why Corvid? Founded in 2004, we are a group of over 300 engineers and scientists, about 3/4 with master' degrees or Ph.D.'s, that provide end-to-end solutions including concept development, design and optimization, prototype build, test and manufacture. We leverage the predictive capability of our high-fidelity computational physics solvers, indigenous massively parallel supercomputer system, prototyping plant, and ballistics and mechanics lab to investigate a variety of high-rate physics phenomena. The results are complex engineering solutions for a variety of applications; aircraft, ballistic missile defense, cybersecurity, motorsports, armor development, biological systems, and missile and warhead design and development. These results are achieved with optimal design and cost efficiency due to the predictive capability of Corvid's tools and our in-house, end-to-end integrated approach, which differentiates Corvid from the market. We value our people and offer employees a broad range of benefits. Benefits for full-time employees include: Paid gym membership Flexible schedules Blue Cross Blue Shield insurance including Medical, Dental and Vision 401k match up to 6% Three weeks starting PTO; increasing with tenure Continued education and training opportunities Uncapped incentive opportunities All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability or protected veteran status, or any other legally protected basis, in accordance with applicable law.

**Our Mission** As the world's number 1 job site*, our mission is to help people get jobs. We strive to cultivate an inclusive and accessible workplace where all people feel comfortable being themselves. We're looking to grow our teams with more people who share our enthusiasm for innovation and creating the best experience for job seekers. **Day to Day** The Business Technology & Trust Analytics Science team's mission is to provide analytics services to drive Indeed's business priorities. We are a team of data scientists, product scientists, and data engineers with years of experience helping Indeed's business leaders use statistical and Machine Learning (ML) model outputs to make data-driven recommendations. We leverage internal data and advanced ML techniques to innovate and push the boundaries of Artificial Intelligence (AI) at Indeed. On a daily basis, you will explore data, formulate problem statements, deploy and monitor models, and communicate progress and insights with business partners. **Responsibilities** + Become adept in our core data sets and systems + Collaborate closely with cross-functional teams, including Finance, Product, Engineers, and other Data Scientists, to ensure cohesive strategy and execution + Research and experiment with proof of concept ML model improvements, scale them to production, and run iterative A/B experiments to improve our forecasting models and methods + Autonomously decompose larger business initiatives into pieces that leverage the right technologies and ML platforms to deliver incremental business value + Extract and communicate actionable insights from our models to influence business growth and strategic decision-making + Partner closely with senior leaders across Indeed as they look to measure and improve how our products and processes help people get jobs + Share your thoughts, guidance, and enthusiasm for problem-solving with your team of experienced scientists and engineers **Skills/Competencies** + Bachelor's degree in Data Science, Mathematics, Computer Science, or related fields + 3+ years of industry experience as a Data Scientist, Machine Learning Engineer, Economist, Quantitative Model Developer, or Software Engineer. Preferably with exposure to financial and forecasting models + Knowledge and direct experience with statistical modeling and time series analysis + Programming experience in Python (preferred) or R + Proficiency using SQL in large-scale relational databases (i.e. Snowflake, Trino, AWS Athena, etc.) + Prior success in deploying impactful Machine Learning solutions to large-scale production systems. Preferably using SageMaker. + Excellent written and verbal communication in English, effective with both technical and non-technical audiences **Salary Range Transparency** US Remote 122,000 - 178,000 USD per year **Salary Range Disclaimer** The base salary range represents the low and high end of the Indeed salary range for this position in the given work location. Actual salaries will vary depending on factors including but not limited to location, experience, and performance. The range(s) listed is just one component of Indeed's total compensation package for employees. Other rewards may include quarterly bonuses, Restricted Stock Units (RSUs), a Paid Time Off policy, and many region-specific benefits. **Benefits - Health, Work/Life Harmony, & Wellbeing** We care about what you care about. We have a multitude of benefits to support Indeedians, as well as their pets, kids, and partners including medical, dental, vision, disability and life insurance. Indeedians are able to enroll in our company's 401k plan, as well as an equity-based incentive program. Indeedians will also receive open paid time off, 12 paid holidays a year and up to 26 weeks of paid parental leave. For more information, select your country and learn more about our employee benefits, program, & perks at ***************************** **Equal Opportunities and Accommodations Statement** Indeed is deeply committed to building a workplace and global community where inclusion is not only valued, but prioritized. We're proud to be an Equal Employment and Affirmative Action employer seeking to create a welcoming and diverse environment. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, gender identity or expression, family status, marital status, sexual orientation, religious creed, national origin, genetics, neuro-diversity, disability, age, status as a protected veteran, or any other non-merit based or legally protected grounds. Indeed is dedicated to providing reasonable accommodations to qualified individuals with known disabilities to participate in the employment application process. To request an accommodation, an applicant should contact Talent Attraction Accommodations at **************, or by email at accommodations@indeed.com. In the request for an accommodation, please inform us of the nature of your request and your contact information. If you are requesting accommodation for an interview, please reach out at least one week in advance of your interview. **Inclusion & Belonging** Inclusion and belonging are fundamental to our hiring practices and company culture, forming an integral part of our vision for a better world of work. At Indeed, we're committed to the wellbeing of our employees and on a mission to make this the best place to work and thrive. We believe that fostering a diverse and inclusive environment where every employee feels respected and accepted benefits everyone, fueling innovation and creativity. We value diverse experiences, including those who have had prior contact with the criminal legal system. We are committed to providing individuals with criminal records, including formerly incarcerated individuals, a fair chance at employment. Those with military experience are encouraged to apply. Equivalent expertise demonstrated through a combination of work experience, training, military experience, or education is welcome. **Indeed's Employee Recruiting Privacy Policy** Like other employers Indeed uses our own technologies to help us find and attract top talent from around the world. In addition to our site's user and privacy policy found at **************************** , we also want to make you aware of our recruitment specific privacy policy found at ****************************/indeed-jobs . **_Reference ID:_** **44818** **_U.S. Remote Only - Posting Duration:_** **The deadline to apply to this position is January 10th, 2025. Job postings may be extended at the hiring team's discretion based on applicant volume.** Reference ID: 44818

360 IT Professionals is a Software Development Company based in Fremont, California that offers complete technology services in Mobile development, Web development, Cloud computing and IT staffing. Merging Information Technology skills in all its services and operations, the company caters to its globally positioned clients by providing dynamic feasible IT solutions. 360 IT Professionals work along with its clients to deliver high-performance results, based exclusively on the one of a kind requirement. Our services are vast and we produce software and web products. We specialize in Mobile development, i.e. iPhone and Android apps. We use Objective C and Swift programming languages to create native applications for iPhone, whereas we use Android Code to develop native applications for Android devices. To create applications that work on cross-platforms, we use a number of frameworks such as Titanium, PhoneGap and JQuery mobile. Furthermore, we build web products and offer services such as web designing, layouts, responsive designing, graphic designing, web application development using frameworks based on model view controller architecture and content management system. Our services also extend to the domain of Cloud Computing, where we provide Salesforce CRM to effectively manage one's business and ease out all the operations by giving an easy platform. Apart from this, we also provide IT Staffing services that can help your organization to a great extent as you can hire highly skilled personnel's through us. We make sure that we deliver performance driven products that are optimally developed as per your organization's needs. Take a shot at us for your IT requirements and experience a radical change. Job Description This position requires a senior-level usability specialist. Candidates should possess a deep understanding of both qualitative and quantitative user experience research methods. Experience in the design and usability of financial services web products is preferred. • As part of the Digital Design team, the successful candidate will lead usability studies, and provide usability consultation. Responsibilities • Develop research plans, conduct usability tests and cognitive walkthroughs, and report outcomes. • Manage project with designers, UX Lead, IA, Content, and/or Prototyping directly, to improve the user experience. • Craft documentation to help communicate the experience to the project team, UX team, and prototyping team. Qualifications Experience & Skills Requirements • 7+ years of experience in a senior usability engineer or analyst role. • Evaluate project requirements to generate research and user-testing plans and estimates. • Vast experience with usability improvements and design efforts. • Mastery-level user experience research and analysis skills with ability to quickly synthesize reports of findings. • Create and lead the passion for being the voice of the user and experience building user centric solutions. • Strong verbal and visual communication, written communication, interpersonal and presentation skills. • Collaborate with designers, developers, stakeholders and UX leaders to identify and address barriers to making platforms accessible to individuals with disabilities • Experience leading usability improvements and design efforts. • Experience guiding and mentoring senior software engineers and test engineers. • Proven ability to document requirements, designs, and project status. Additional Information Thanks and Regards, Karan Sharma 510-254-3300 ext. 150

Clinical Research Investigator (MD/DO) DM Clinical Research, the largest privately-owned research management organization in the Houston area and one of the top 50 in the country, is looking for an Investigator for our site in Charlotte, NC. This individual will conduct all clinical trials (studies) according to ICH, GCP, local regulations, study protocols, and company processes. Responsibilities Ensures the medical well-being and safety of the participants through the safe performance and execution of the studies. Assists in maintaining clinical oversight and quality on the studies registered on and delivers on study targets, thereby contributing to the commercial success of the site. Reviews enrollment progress, pre-screening and screening success rates, screen failure rates, safety, and retention of participants. Interprets protocols and IB and participates in initiatives to strategize for patient recruitment. Carries out clinical evaluation and assessment of participants to ensure eligibility to enroll in studies. Ensures and protects the welfare and safety of participants through ethical conduct. Fulfills and complies with all medical duties as per protocol, SOP/COP and ICH GCP and local regulations. Exercises meticulous attention to detail in documentation and patient care. Requirements Medical license (MD, DO) - Charlotte, NC 2 years experience as a Clinical Research Investigator (Principal Investigator or Sub-Investigator) Bilingual Spanish a plus Flexible hours - schedule can be tailored as required.

Full-time Description Job Purpose Design, develop, and maintain detection and identification algorithms for CSES technologies through multivariate data analysis, chemometrics, predictive modeling, artificial intelligence, and machine learning. Key Accountabilities - Performs data analytics, specifically data clean-up, data processing, predictive modeling, chemometric statistical modeling and analysis, multivariate data analysis, artificial intelligence, machine learning, and/or data mining, as related to scientific data - Plan and execute work related to data pre-processing routines, data clean-up scripts, predictive analytics, data summarizations, data visualizations and plotting, development and application of machine learning and artificial intelligence models, and development of detection algorithms - Develop and maintain operational integrity of computational assets - Prepare and maintain documentation related to computer code / scripts, including end user guides and instructions Requirements Knowledge - Skills - Abilities - Minimum Master's degree in Chemistry, Biology, Physics or related field, Ph.D. Preferred - Must be eligible to obtain and/or maintain a U.S. Government Security Clearance commensurate with the level of facility clearance - Proficiency in performing data analytics, specifically chemometrics, predictive analytics, machine learning, multivariate data analysis, predictive analytics, and/or data mining as it related to chemical, biological, biochemical, or other scientific data - Working to expert level knowledge of one or more analytical/physical analysis methods including: chromatography, mass spectrometry, optical spectroscopy, proteomics, genomics, or other biochemical analysis methods - Software programming/scripting proficiency in R, Python, Java, and/or MATLAB - Ability to plan sequence of experiments to answer complicated technical questions - Previous research and development experience related to chemical, biological, radiological, nuclear, and/or explosive (CBRNE) threats - Experience in developing instrumentation based on vibrational spectroscopy - Working knowledge of software development practices such as version control systems (e.g., Git) and Agile development - Working knowledge of statistics, experimental error, and quantification as it applies to scientific data - Excellent written and verbal communication skills - Ability to communicate technical information to non-technical audiences - Ability to work independently and to interact effectively with individuals on multi-disciplinary teams Additional Preferred Capabilities - Development of detailed optical specifications for spectroscopic instrumentation - Development of interface software required to command and control excitation and imaging subsystems - Capable of defining, assembling, and testing optical component breadboards for spectroscopic applications #zr

Job Purpose Design, develop, and maintain detection and identification algorithms for CSES technologies through multivariate data analysis, chemometrics, predictive modeling, artificial intelligence, and machine learning. Key Accountabilities * Performs data analytics, specifically data clean-up, data processing, predictive modeling, chemometric statistical modeling and analysis, multivariate data analysis, artificial intelligence, machine learning, and/or data mining, as related to scientific data * Plan and execute work related to data pre-processing routines, data clean-up scripts, predictive analytics, data summarizations, data visualizations and plotting, development and application of machine learning and artificial intelligence models, and development of detection algorithms * Develop and maintain operational integrity of computational assets * Prepare and maintain documentation related to computer code / scripts, including end user guides and instructions Requirements Knowledge - Skills - Abilities * Minimum Master's degree in Chemistry, Biology, Physics or related field, Ph.D. Preferred * Must be eligible to obtain and/or maintain a U.S. Government Security Clearance commensurate with the level of facility clearance * Proficiency in performing data analytics, specifically chemometrics, predictive analytics, machine learning, multivariate data analysis, predictive analytics, and/or data mining as it related to chemical, biological, biochemical, or other scientific data * Working to expert level knowledge of one or more analytical/physical analysis methods including: chromatography, mass spectrometry, optical spectroscopy, proteomics, genomics, or other biochemical analysis methods * Software programming/scripting proficiency in R, Python, Java, and/or MATLAB * Ability to plan sequence of experiments to answer complicated technical questions * Previous research and development experience related to chemical, biological, radiological, nuclear, and/or explosive (CBRNE) threats * Experience in developing instrumentation based on vibrational spectroscopy * Working knowledge of software development practices such as version control systems (e.g., Git) and Agile development * Working knowledge of statistics, experimental error, and quantification as it applies to scientific data * Excellent written and verbal communication skills * Ability to communicate technical information to non-technical audiences * Ability to work independently and to interact effectively with individuals on multi-disciplinary teams Additional Preferred Capabilities * Development of detailed optical specifications for spectroscopic instrumentation * Development of interface software required to command and control excitation and imaging subsystems * Capable of defining, assembling, and testing optical component breadboards for spectroscopic applications #zr

Work Your Magic with us! Start your next chapter and join EMD Electronics. Ready to explore, break barriers, and discover more? We know you've got big plans - so do we! Our colleagues across the globe love innovating with science and technology to enrich people's lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us. Everything we do in EMD Electronics is to help us deliver on our purpose of being the company behind the companies, advancing digital living. We are dedicated to being the trusted supplier of high-tech materials, services and specialty chemicals for the electronics, automotive and cosmetics industries. We foster a global collaborative organization made up of individuals who have the passion to win, obsess about the customer, are relentlessly curious and act with urgency. Together, we push the boundaries of science to make more possible for our customers. Location: The Senior R&D Scientist Silica Materials is an on-site position based in Charlotte, NC with occasional domestic and internal travel to meet business needs. Your Role: This role is a product development scientist for the global silica business. Scientist must work well in a multi-disciplinary team environment and develop good working relationships both internally and externally. This role is part of a team that works to create novel customer focused solutions. Creating solutions involves ideation, design, testing, scaling, and introduction. Solutions span from new materials and technologies to improvement of existing products. Essential Duties and Responsibilities: * Create new products through the support of current customers and the development of solutions for application specific targets. * Use design tools, data management, and statistical techniques to advance solution development and improve results at customers faster. * Develop novel solutions for existing and new market applications with a focus on creating value by improving product efficiency and quality. * Collaborate with development partners and stakeholders to solve problems and enhance product development cycle and capabilities. Who You Are Minimum Qualifications: * Bachelor degree in chemical engineering, chemistry, material science, or related colloidal, nanoparticle, or particle science field, or related degree area plus 5+ years' experience in colloidal silica, related silica chemistry or related industrial chemical industry OR * Master degree in chemical engineering, chemistry, material science, or related colloidal, nanoparticle, or particle science field, or related degree area plus 3+ years experience in colloidal silica, related silica chemistry or related industrial chemical industry * Knowledge and experience working in the Semiconductor industry or similar industrial, chemical, or manufacturing industry. Preferred Qualifications: * Knowledge of colloids, nanoparticles, and/or polymers * Experience with: * Colloidal silica production methods including synthesis, filtration, and characterization. * Colloidal material fundamentals including stability and interactions. * Chemical mechanical planarization applications and requirements. * Knowledge of statistical techniques for advanced design and development * Experience with project management and stage gate processes. * Ability to perform laboratory work and interface with engineering concepts and personnel. * Computer skills using statistical analysis and data management / analysis software. * Well organized and self-motivated. Able to work independently with minimal supervision. * Able to read and/or speak French (not required but a positive for the role) What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We celebrate all dimensions of diversity and believe that it drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress! Apply now and become a part of our diverse team! If you would like to know more about what diversity, equity, and inclusion means to us, please visit ********************************************************

Preferred Qualifications Experience in extraction and analysis of biochemicals from foods Experience with the characterization of plant-based proteins Knowledge in plant science, biochemistry, food science and technology, and/or human nutrition Experience in membrane filtration is desired Working experience in twin screw extrusion is also desirable. Work Schedule Monday-Friday, 8AM-5PM

Title: Quantitative Research Associate Duration: 18 months Work Engagement: W2 Benefits on offer for this contract position: Health Insurance, Life insurance, 401K and Voluntary Benefits In this contingent resource assignment, you may: Participate in low to moderately complex initiatives and identify opportunity for process improvements within Business Execution. Review and analyze basic or tactical Business Execution assignments or challenges that require research, evaluation, and selection of alternatives, related to low-to-medium risk deliverables. Present recommendations for resolving low to moderately complex situations and exercise some independent judgment while developing understanding of function, policies, procedures, and compliance requirements. Provide information to client personnel in Business Execution. Responsibilities: * Leverage mathematical and statistical methods to analyze data, develop models and inform Quantitative team * Reviewing processes and researching what data needs to be pulled in and how trade is booked and valued Qualifications: * Applicants must be authorized to work for ANY employer in the U.S. This position is not eligible for visa sponsorship. * 2+ years of Business Execution, Implementation, or Strategic Planning experience * Master's in Mathematics or Quantitative Research * Investment Banking * Python * GitHub

******2-year work commitment required.****** The position involves almost daily, direct interaction with patients and their families, and exposure to almost every part of the CMC hospital system (ED, OR, ICUs, hospital floor units, labs, etc). Our Sr Research Associates are vital members of our clinical research team that work alongside the Research Director, our Research Coordinators, the Trauma and Acute Care Surgeons and countless other clinicians. Our focus is mainly in the critically ill and injured patient populations. We generally have about 15 different clinical trials open at a given time, ranging from new investigational drugs, medical devices, or changes in patient care practices in pediatric and adult populations. Some of our clinical trials enroll patients at our Atrium Health Cabarrus, University, and Pineville hospitals, with potential to expand further. Travel to facilities outside Carolinas Medical Center is sometimes required, but travel expenses beyond normal daily commute are reimbursable. Sr RAs must be self-motivated, detail-driven, and willing to work the described schedule (nights). This position is ideal for candidates seeking clinical research experience to develop a career in clinical research, or apply for Medical School or PA School. Job Summary Collects, enters and analyzes research data. Provides reports using computerized databases and information systems. Prepares reports from requests from the director, faculty, study sponsor, and outside collaborators. Designs, implements, and evaluates request using databases as information source. Essential Functions Maintains designated applications in research department databases. Creates new databases, prepares and runs data analysis queries, and uploads local database to the national database center. Uses existing database to create reports as requested. Performs data manipulation and migration. Reviews data quality reports for data submissions and errors. Ensures data requests are received, have authorizations, are evaluated, and reported. Prepares specifications and summary reports for data queries and requests. Performs chart abstraction. Provides administrative support when needed. Physical Requirements Work consistently requires sitting for 5-6 hours. Intact senses of sight, hearing, smell, touch, and manual dexterity. Each employee has the responsibility to work in a safe manner. Education, Experience and Certifications Bachelor's Degree in Computer Science or health-related field required but Associates Degree and equivalent work experience will be considered. Training in information systems technologies, desktop application, and databases required. Experience with analytical software and database analysis and reports preferred.

WFUSM Biochemistry/Cell Biology Discipline Director The Wake Forest University School of Medicine Office of Undergraduate Medical Education is seeking a Biochemistry/Cell Biology Discipline Director and Medical Educator to join in the creation of a new 4-year medical school campus in Charlotte, North Carolina. In collaboration with Atrium Health educators and clinicians, the Biochemistry/Cell Biology Discipline Director and Medical Educator will be part of a Charlotte-based team responsible for the design and delivery of curriculum for the new Wake Forest University School of Medicine in Charlotte. The foundational science faculty will be appointed on a non-tenure track with academic rank commensurate based on experience. Committed to creating a welcoming and inclusive environment for all, the Wake Forest University School of Medicine MD program is seeking innovative, creative educators for the MD program curriculum who demonstrate evidence of a commitment to promoting a culture that respects and advances diversity and inclusion of all people. Ideal candidates will demonstrate strong interpersonal and communications skills, effective critical thinking, and the ability to set priorities and manage multiple tasks. The new 4-year medical campus in Charlotte will matriculate the inaugural class in July 2025 and will feature a highly innovative curriculum. The 18-month foundational phase will be delivered primarily through a problem-based learning (PBL) approach, comparable by LCME standards to that of the Winston-Salem campus. As such, we are seeking a highly motivated Biochemistry/Cell Biology Discipline Director and Medical Educator to serve as content expert and small group PBL facilitator during this exciting time of development, growth, and implementation of the active learning approach. Ideal candidates will have experience in curricular design and interactive instructional methods, including PBL and TBL. Additionally, ideal candidates will have the ability to collaborate within multidisciplinary teams on a foundational science curriculum that is grounded in integrating biomedical science and clinical concepts and is delivered through interactive and inquiry-based methodologies, with multi-modal techniques and small group learning. Faculty responsibilities will primarily be within the domain of medical education. These responsibilities will include refinement of cases to be delivered in a problem-based learning curriculum in coordination with Winston-Salem campus curriculum, to ensure comparability of assessments and equivalency of learning objectives are achieved. Responsibilities will also include development and oversight of discipline-related content and assessments. Upon matriculation of the inaugural class in 2025, faculty will also participate as a Course Director and small group facilitator within the curriculum. While medical education will be the priority for each faculty member, allocation of time and effort for research and scholarship, student scholarly mentoring, and institutional service will be required. Opportunities exist for scholarly collaborations with teammates in Charlotte and Winston-Salem campuses providing faculty the opportunity to participate in the broader academic community. Qualifications: M.D. D.O., or Ph.D. in foundational/biomedical sciences, or equivalent. Minimum of two years of experience with medical education or related fields, including, but not limited to, small group learning facilitation and curriculum oversight. Five or more years preferred. Experience in applying the principles of adult learning theory, development of competency-based education, and assessment of student learning (skills, knowledge, and attitudes) through course, module, or new content development. Candidates with experience in problem-based learning curriculum will be given priority for consideration. To be considered for this opportunity, please submit a CV and teaching philosophy via the online application system.

: Resolution Economics is a leading economic consulting firm focused on providing economic, statistical, and financial analysis, litigation and consulting support, and expert testimony to the world's leading companies and law firms. Resolution Economics is headquartered in Los Angeles with offices in Washington, D.C., Chicago, New York City, Charlotte, and Austin. Working at Resolution Economics is a rewarding experience where teamwork, creativity, and academic rigor translate into real-world results. We regularly apply advanced economic concepts to create narratives that are digestible to a non-technical audience. Our work has the potential to influence case law, and directly impact the outcomes of future litigations. In addition, the analyses that we perform often inform settlement agreements and payments made to classes that may consist of hundreds of thousands of individuals. Our clients rely on our ability to maintain an extremely high degree of reliability in our work product. The Labor and Employment Practice typically engages in matters relating to Wage and Hour or Discrimination litigation as well as other employment-related business consulting. We frequently provide analysis and support related to minimum wage/overtime claims, meal and rest break claims, employee misclassification claims, and discrimination matters in hiring, pay, promotion, and/or wrongful termination at all stages of the litigation process. The work product we provide to clients is often in the form of complex exposure models, expert reports, and expert testimony. Job Description: The Research Assistant position is a paid part-time position at Resolution Economics, primarily for college students in their sophomore, junior, or senior year. No work experience or specific majors are required to apply, but an interest in economics or litigation is certainly a plus. Research Assistants typically assist with the data management portion of a project. This includes data entry, researching publicly available data sources, and document and video review. Research Assistants also assist with clerical duties such as preparing binders, answering the telephone, stocking supplies, and assisting with the general upkeep of the office. Research Assistants will gain an understanding of the consulting environment and will learn how the field of economics is used within the legal system. Though it is not a requirement for the position, Research Assistants have the option to learn how to perform statistical analysis in SAS through training modules and mentorship from full-time staff members if they are interested. We have an immediate opportunity for a Research Assistant - Intern to join our team onsite in our Charlotte, NC office! Wage Scale: Research Assistants are paid at a base hourly rate of $23.00 for non-overtime work hours, subject to all required deductions and withholdings, and not including the value of benefits under any Resolution Economics-maintained benefit plan. Research Assistants are eligible for overtime pay to the extent provided by applicable federal and state law. Responsibilities of this position may include: Database creation Data entry Video observations Creating charts and graphs in Excel Internet research Clerical work such as filing and answering the front desk telephone Assisting with general upkeep of office and stocking supplies Job Qualifications: Skills and Abilities Experience with Microsoft Office (Word, Excel, Outlook) Comfortable around PC computers Attention to detail Ability to work in a team environment Problem solving skills Good work ethic Resolution Economics, LLC is an Equal Opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, protected Veteran Status, or any other characteristic protected by applicable federal, state, or local law.

Full-time Description Summary of the Position: The Formulation Scientist will provide product development, product reformulation and process improvement support to a wide range of growth/quality/cost savings projects from ideation through commercialization under direction of the Manager, Technical Operations. Additionally, this position will work with operations, quality, business teams, and other functional partners; acting as product and process development/improvement support on cross-functional new product development and quality improvement/cost savings teams. Roles and Responsibilities: Capable of supporting and leading moderately complex formula development, reformulation and process improvement for powders, tablets, capsules, soft chews, pellets, and liquids. Cooperate with PD staff in preparation/execution of pilot batches and product scale up batches and gather data to support in-process parameters and finished product specifications. Perform bench trials, physical evaluations, and collect data to support alternate materials approval process. Able to direct product development technicians in data collection and processing. Provide training to manufacturing associates on new processes and process modifications/improvements. Assist in developing new formulations for new active raw materials. Work with new equipment/develop studies with equipment that could improve soft chew manufacturing process and/or formulation. Prepare and approve Master Batch Records, Change Control Requests for all scale up or production batches. Follow applicable cGMP processes. Compile and provide summaries of stability data. Provide Technical support to Manufacturing and Operations teams, monitor initial production batches for new and reformulated products. Continue education by attending expos and conferences and applying knowledge gained Communicate effectively with other departments within the organization and function within a team environment Regular attendance is required Perform other assigned duties as may be required in meeting company objectives Minimum Requirements: · Experience working with soft chew (or similar) dosage forms · Excellent interpersonal, communication, and organizational skills · Basic ability to define problems, collect data, establish facts, draw valid conclusions, and offer solutions. Education and Experience · BS/BA in chemistry, food science, life sciences, engineering, or a related discipline, or equivalent experience. · Must have >5 years of hands-on experience in product development of food, dietary supplements or related products, including dough, confectionery, or pet treats (animal feed/animal health a plus). · Experience in a cGMP environment with understanding of cGMP principles and requirements. · Experience working as part of a cross functional team. · Knowledge of animal feed regulations a plus Supervisory Responsibilities: None

Summary of the Position: The Formulation Scientist will provide product development, product reformulation and process improvement support to a wide range of growth/quality/cost savings projects from ideation through commercialization under direction of the Manager, Technical Operations. Additionally, this position will work with operations, quality, business teams, and other functional partners; acting as product and process development/improvement support on cross-functional new product development and quality improvement/cost savings teams. Roles and Responsibilities: * Capable of supporting and leading moderately complex formula development, reformulation and process improvement for powders, tablets, capsules, soft chews, pellets, and liquids. * Cooperate with PD staff in preparation/execution of pilot batches and product scale up batches and gather data to support in-process parameters and finished product specifications. * Perform bench trials, physical evaluations, and collect data to support alternate materials approval process. * Able to direct product development technicians in data collection and processing. * Provide training to manufacturing associates on new processes and process modifications/improvements. * Assist in developing new formulations for new active raw materials. * Work with new equipment/develop studies with equipment that could improve soft chew manufacturing process and/or formulation. * Prepare and approve Master Batch Records, Change Control Requests for all scale up or production batches. * Follow applicable cGMP processes. * Compile and provide summaries of stability data. * Provide Technical support to Manufacturing and Operations teams, monitor initial production batches for new and reformulated products. * Continue education by attending expos and conferences and applying knowledge gained * Communicate effectively with other departments within the organization and function within a team environment * Regular attendance is required * Perform other assigned duties as may be required in meeting company objectives Minimum Requirements: * Experience working with soft chew (or similar) dosage forms * Excellent interpersonal, communication, and organizational skills * Basic ability to define problems, collect data, establish facts, draw valid conclusions, and offer solutions. Education and Experience * BS/BA in chemistry, food science, life sciences, engineering, or a related discipline, or equivalent experience. * Must have >5 years of hands-on experience in product development of food, dietary supplements or related products, including dough, confectionery, or pet treats (animal feed/animal health a plus). * Experience in a cGMP environment with understanding of cGMP principles and requirements. * Experience working as part of a cross functional team. * Knowledge of animal feed regulations a plus Supervisory Responsibilities: None

Covia is a leading supplier of minerals and material solutions to the industrial and energy markets. Covia's rich legacy includes many achievements across industries and capital success through partnership. Our ability to deliver the right product, to the right place, at the right time, is unmatched. Just as strong is our commitment to building partnerships that help our customers succeed. Quality and innovation are at the foundation of Covia; but our real strength is our people. Covia employs a diverse and highly skilled team of professionals to convert natural minerals into engineered solutions for our customers. Every member of our team has a valuable opportunity to help shape our future and make a positive impact on the world around us through our commitment to the locations where we live and work. COVIA IS COMMITTED TO EMBRACING AND PROMOTING DIVERSITY AND INCLUSION (D&I) WHERE WE WORK, WITH WHOM WE DO BUSINESS, AND WHERE WE LIVE. We strive to create an inclusive culture where diversity is valued and respected and where all feel included and engaged. We are intentional in our efforts to bring Team Members together and create opportunities to contribute their unique skills, experiences, and perspectives in the pursuit of Covia's business growth objectives. Enabling all Team Members to perform at their best while being themselves is fundamental to the Clearly Covia Values and Culture. Covia is looking for a dynamic Coatings Application Scientist who will have a positive impact on the Applications Development Team in Charlotte, NC. As a Coatings Application Scientist, you will support the innovation in the Paint, Coatings, Adhesives, & Sealants markets through formulation design, evaluation, and engagement with paint and coatings customers. The successful candidate will have the following Key Accountabilities: Lead the design, installation, commissioning, and on-going maintenance of the coatings laboratory to support coatings formulation applications Conduct the coatings laboratory projects supporting new product development and commercial growth. Develop technical value propositions. Translate voice of customers (VOC) into key performance attributes. Design and conduct experiments to demonstrate and quantify functional and performance benefits using customer language. Interface with the technology platform, corporate analytical laboratory, and pilot staff to ensure seamless technology transfer and scale-up. Support coatings technical product commercialization, assisting in the creation of technical data sheets, brochures, and new product launch packages Support within a cross-functional team to develop IP strategy in the coatings space. Conduct annual coatings IP landscape study, stay up to date to competitive IP. Coordinate comparative testing & evaluation of competitive products in the coatings markets. Supervise lab technicians. Provide training and technical assistance to Sales, Operations, Marketing and other Covia affiliated employees involved in supplying and servicing the coatings markets. Serve as a resource for customer problem resolving and technical support. Represent the organization in forums and conferences within specific area of application expertise. The successful incumbent will have the following Minimum Qualifications: Bachelor's degree in chemistry or chemical engineering with 10 years' experience in the relevant industry, or Master /Ph. D degree with 5 years of industrial experience Experience in resin systems and formulations with pigments, fillers, curing agents, activators Experience in various paint and coating systems, including architectural interior, exterior coatings, industrial coatings, and specialty applications such as solar reflection coatings. Laboratory experience with chemicals, MSDS, ventilation and safety training Hands-on ability to execute analytical / laboratory procedures and maintain applicable equipment / systems Deep knowledge of coating formulations with a structured methodology for building, optimizing, and testing coating formulations is preferred Experience with Critical to Quality (CTQ) process is preferred Benefits: Excellent Healthcare Benefits - medical, vision, dental 401K with company matching Vacation + Paid Holidays Disability, Life / AD&D, and Long-Term Care Insurances Employee Assistance Program At Covia, we strive for and support a diverse workforce as we firmly believe this lays the foundation of our success. Our compelling culture supports inclusion, individuality and respect within the workplace. We are committed to providing employment opportunities to the most qualified candidate based on work-related factors and without regard to non-work-related factors including race, color, religion, national origin, gender, sexual orientation, gender identity, age, disability, or veteran status. The organization offers competitive salaries, advancement opportunities, and a full range of benefits. An Equal Opportunity Employer IND2

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 Sterility Assurance Scientist is a technical role that assists in development and implementation of the site's sterility assurance programs and provides technical guidance and expertise in environmental monitoring, contamination control, aseptic process simulations, gowning/aseptic techniques, and cleaning/sanitization strategies, including disinfectant efficacy. Key Objectives/Deliverables: Ensure and provide oversight and technical guidance for sterility assurance programs at the manufacturing floor level. Lead or provide technical oversight for Provide technical support for activities related to sterility assurance programs including but not limited to; Airflow Pattern Testing, Environmental Monitoring Performance Qualifications, Aseptic Process Simulations, Cleaning, Sanitization, and Disinfection, Gowning within GMP Classified Areas, Aseptic Processing Techniques, Contamination Control Assist in the development and implementation of processes and facility monitoring to ensure effective contamination control strategies are established. Lead or assist in the development and implementation of processes and facility monitoring to ensure effective contamination control strategies are established. Lead/assist with support and/or provide technical expertise for developing the site's contamination control strategy and cleaning and sanitization program/strategy, and disinfectant efficacy strategies. Lead/assist with support and/or provide technical expertise for the facility's cleanroom gowning and aseptic technique strategy/program. Apply sterility assurance risk management to evaluate manufacturing processes and associated controls with respect to potential introduction of microbial, endotoxin, and particulate contamination. Analyze microbial and manufacturing data to identify trends, process discrepancies, and opportunities for continuous improvements. Lead or provide technical support for root cause investigations associated with sterility assurance programs. Participate and/or provide technical sterility assurance support during internal and external audits. Create, execute, review, and/or approve technical documents and change controls related to sterility assurance programs. Work within cross-functional teams to implement TS/MS objective and deliver on business and quality objectives. Basic Qualifications: Bachelor's or Master's Degree in Microbiology, Biology, Biochemistry, Biochemical Engineering, Chemical Engineering, or other related scientific discipline. Demonstrated understanding and relevant experience of scientific principles required for manufacturing of parenteral drug products within operations, microbiology, environmental monitoring, sterility assurance, validation, technical services, and/or quality assurance associated cGMP pharmaceutical manufacturing. 2+ years in pharmaceutical manufacturing (Microbiology, TSMS, Sterility Assurance, or related dept). Additional Skills/Preferences: Possess strong interpersonal skills to work cross-functionally within a team. Possess strong self-management and organizational skills. Possess strong oral and written communication skills for communicating to colleagues, management, and other departments. Experience with data analysis and trending. Ability to wear appropriate PPE and other safety related equipment or considerations in manufacturing, warehouse, or laboratory areas. Ability to gown into facility dedicated cleanroom attire, as required to perform job responsibilities. Additional Information: Role is Monday through Friday based and will be phased from a project support role to a routine support role as the development facility and processes progress. 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. Tasks may require repetitive motion and standing or walking for long periods of time. Travel may be required during the project phase for training and implementation of sterility assurance programs 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 an EEO/Affirmative Action Employer and does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, 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 help our company develop talented individuals for future leadership roles. Our current groups include: Africa, Middle East, Central Asia Network, African American Network, Chinese Culture Network, Early Career Professionals, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinos at Lilly, PRIDE (LGBTQ + Allies), Veterans Leadership Network, Women's Network, Working and Living with Disabilities. Learn more about all of our groups. #WeAreLilly