Associate Scientist Jobs in Rockville, MD

DAP is looking to hire a Product Development Scientist in R&D Department. As a R&D Scientist, you will plan/Perform experiments and generate general test data and analytical data with minimal guidance from senior R&D personnel; perform basic data analysis. Participate in and help drive activities that improve the operation of the R&D function. Collaborate with other R&D personnel and participate in cross-functional teams to help drive innovation. Proven success in previous role. Responsibilities: Develop and carry out experimental plans for new product development, product modification and perform basic analysis of experimental results. Demonstrate competency in formulation practices, complex problem-solving, innovative solutions, and addressing scientific challenges. Demonstrate the ability to operate analytical and material characterization equipment, generate high quality data, and perform basic analysis of the data generated. Assist senior R&D Personnel to develop manufacturing procedures for new products and work collaboratively at plant trials with plant engineers and quality control managers. Demonstrate knowledge of basic process steps for plant trials. Adhere to Laboratory Quality Management System (QMS) practices and participate in QMS audits. Perform laboratory equipment calibration and maintenance. Assist in providing technical support for marketing, sales, and customer support including planning/conducting product demonstrations for customers, trade shows, Etc. Adhere to laboratory safety practices and participate in all safety and housekeeping initiatives. Demonstrate ability to independently assemble information for and generate highly effective written reports and oral presentations to communicate within R&D and with cross-functional teams. Requirements: Bachelor of Science degree in Chemistry, Polymer Science, Materials Science, or related field with 5 years' experience of relevant experience A passion for chemistry, science, problem solving, and creativity. Excellent interpersonal, written, and verbal communication and presentation skills. A breadth of technical knowledge and a keen interest in learning from others. Possess innovation skills evident as risk taking, result seeking, and idea integration. Hands-on bench experience with various chemistries (latex, moisture curing, reactive, etc.) in sealants, adhesives, coatings, repair or related field. Bench chemistry experience and familiarity with various analytical techniques: wet chemistry, titrations, microscopy, rheology, thermal analysis, tensile testing, etc. Experience operating lab scale mixing equipment as well as lab scale analytical and testing apparatus. Benefits: Medical, Dental and Vision Insurance Company Provided Life Insurance Paid Time Off (PTO) Company-paid short-term and long-term disability 401(k) plans Employer-funded pension plan Tuition Reimbursement Pay Range 75,000 to 100,000 per year. About DAP DAP is a market leading manufacturer, innovator and marketer of home repair and construction products including caulks, sealants, spray foam insulation, adhesives, and patch and repair products. DAP is part of RPM International Inc., a $7.3 billion, multinational company with subsidiaries that are world leaders in specialty coatings, sealants, building materials and related services. You will find DAP products in the hands of professional painters, remodelers, builders, and do-it-yourselfers, and in 60,000 retail outlets, ranging from home centers and mass merchandisers to your local hardware, pro contractor channels and paint stores. DAP's eight manufacturing and distribution facilities in the United States of America and Canada service North America and the world. At DAP, we hire the best people and give them a collaborative and rewarding work environment that empowers them to succeed! We support associates in continuous professional growth and collaborate on the steps it takes to get to the next level in their careers. Our associates enjoy a comprehensive benefits package including 401(k) with company match, pension, paid parental leave, competitive health insurance rates, employee stock purchase plan, tuition reimbursement, free wellness programs and more! Learn more about DAP's history, culture and benefits at ******************** DAP - On the job since 1865.

Job Category: Individual Contributor Apply now Full-Time Remote Salary Range: $113,000 USD to $156,000 USD Headquarters - Remote 100 International Dr Baltimore, MD 21202, USA Description About The Opportunity At Medifast, our team members are relentless in our mission of driving Lifelong Transformation, Making a Healthy Lifestyle Second Nature. When you join Medifast, you become part of a dynamic, fast-growing community of highly motivated, like-hearted people who share a passion for promoting health and wellness. Just as OPTAVIA Coaches inspire Clients to reach their personal wellness goals, at Medifast, we inspire each other to bring our best to work each day to further our shared mission. If you want to build a rewarding career that makes lives better on a daily basis, Medifast may be the perfect place for you. Overview Of Position The Principal Scientist, Health Care Data Sciences, will serve as subject matter expert in obesity and related co-morbidities clinical care, health outcomes research, data sciences, and health care policy. This role will help advance our medically supported weight loss programs by contributing to development of real-world evidence-based research programs, evidence-based clinical care protocols, programs, plans, and products. Responsibilities include driving education, training, communication, and benefit messaging to highlight the company's medical heritage, scientifically validate the Medifast and OPTAVIA brands, and support both Coaches and Clients effectively. This role will help evaluate existing scientific evidence, internal data, and contribute to data-driven decisions to support innovation of our Program, Plans and Products, and health and wellbeing of our Coaches and Clients. The successful candidate will also help create and substantiate company claims through in-house and third-party research and will guide the development of scientific initiatives that advance innovation of programs, plans, and products, and contributes to externalization of our science. The research work produced by this position will help support the company's marketing and public relations positioning, claims, product differentiation, and bolster the scientific credibility of OPTAVIA offerings. This will be a strategic role interfacing with key health care professionals, subject matter experts, and other external partners and will help define long-term focus areas for Medifast in the obesity and related co-morbidities clinical care and policy space. This role may also require the management of the Scientific Advisory Board, help develop research strategy and work cross-functionally to co-lead and deliver across the medically supported weight loss program and other future business initiatives. II. Job Responsibilities Subject matter expert in the obesity and related co-morbidities clinical care processes, including medical, pharmaceutical, nutrition, behavior, and lifestyle modification. Maintain robust knowledge of pharmaceutical interventions in obesity clinical care and identify opportunities for OPTAVIA. Subject matter expertise in data science, including scientific methods, biostatistics, machine learning, data systems, processing, and visualization with proficiency in R, Python, and SQL to enable the extraction of actionable insights from data. Develop relevant real-world evidence-based, health economics and clinical research programs and related data analytics to demonstrate efficacy of OPTAVIA programs, plans, and products in conjunction with medically supported weight loss programs. This includes contributing to the dissemination of findings through scientific publications, ensuring the research aligns with rigorous academic and industry standards to enhance credibility and support evidence-based practices. Contributes to the development of clinical care protocols, health care policy strategy for nutrition and lifestyle programs as part of medically supported weight loss programs. Develops and manages research partnerships with academia, thought leaders, health care, and other external partners to support medically supported weight loss. Provides input and support for Medifast's research, including the development of study design and protocol(s). Identifies and manages Key Opinion Leaders within academia, health care, and other external partners to support medically supported weight loss initiatives. Provides evidence-based recommendations for OPTAVIA programs, plans, and product innovation to support medically supported weight loss. This may entail reviewing new ingredients, technologies, developing and substantiating benefit messaging, identifying gaps in the evidence and opportunities to conduct research, communicating the science and benefits, while working cross-functionally with marketing, PR, R&D, legal, field operations, and other internal and external partners. Collaborates with nutrition support, nutrition and wellness, medical safety and surveillance, R&D (product development, regulatory, quality assurance), marketing, PR, legal, and other internal and/or external stakeholders to provide scientifically based reviews/recommendations for plans, products and/or programs and help ensure the messaging of these is evidence-based and consistent across Medifast OPTAVIA brands. Stays abreast of current medical advancements, scientific literature, nutrition, and wellness findings by investing a minimum of 10% of time on continuing education, attending related symposia, reviewing research publications and data reports; presentations on topic findings should be provided quarterly, as may be applicable. Obtain a minimum of 15 CEU's to maintain current health professional registration/licensure. Collaborate with the Vice President of Scientific and Clinical Affairs, Product Development, and Marketing to develop the company's strategic vision for products, programs, and research. III. Scope This is an individual contributor role supporting Scientific & Clinical Affairs projects across the organization. This position may also help manage the budget related to Medifast Sponsored Research, Investigator Initiated Studies, and Scientific Advisory Board. IV. Knowledge, Education, Skills & Abilities Required: Advanced Terminal Degree (PhD, DNP, PharmD, PA, other) in Health Sciences, Allied Healthcare or other biological or life science-related field (Nutrition Science, Exercise Science, Nursing, Pharmacy, Physician Associate, other). 5+ years scientific affairs and research experience, including biostatistics, data analytics, and machine learning, with programming skills in R, Python, and SQL for advanced data analysis and modeling. Maintain current professional credentials (RPh, RN, RDN, etc.), as applicable. 5+ years of experience in health care (clinical care, health care management, and related) or Pharmaceutical Industry. Experience of cross-functional evidence-based reviews, ingredient and technical reviews, clinical care processes, including data management, biostatistics, medical writing, and regulatory affairs. Strong interpersonal, verbal and written communication and presentation skills. Problem solving and decision-making skills; strategic thinking and leadership. Performs responsibilities with minimal supervision. Working knowledge of Microsoft Office, statistical, data collection, and analytical packages. At Medifast, Relationships Are At The Center Of What We Do! We thrive by elevating our connections with one another as well as with our Coaches & Clients. We believe that everyone has the potential to be OUTSTANDING . The Medifast culture is built on seven core values: integrity, courage, teaming, accountability, empowerment, partnership, and diversity. These values aren't just words on a page - they are celebrated as a core part of the company's philosophy. Mastering Relationships: We build trust, promote collaboration, and we are reliable. Being innovative: We strive to improve things in our areas of influence; test, refine and expand within the business strategy; and reach beyond real and perceived boundaries. Simplifying: We are committed to making things measurable, repeatable, and scalable; focusing on outcomes not activities; and eliminating complexity to increase focus. Anticipating: We predict long-term business and organizational needs; challenge assumptions; and expect and prepare for the unexpected. About Medifast Medifast (NYSE: MED) is the 40+ year old health and wellness company known for its habit-based and coach-guided lifestyle solution OPTAVIA, which provides people with a simple, yet comprehensive approach to address obesity and support a healthy life. OPTAVIA provides unparalleled coaching support along with community, tailored nutrition, and healthy habits, and empowers people to master their weight loss journey through each stage of life. Through the company's collaboration with national virtual primary care provider LifeMD (Nasdaq: LFMD) and its affiliated medical group, customers now have access to GLP-1 medications where clinically appropriate. Medifast remains committed to its mission of offering Lifelong Transformation, Making a Healthy Lifestyle Second Nature. Visit MedifastInc.com and OPTAVIA.com for more information and follow @Medifast on X and LinkedIn. #J-18808-Ljbffr

Core Responsibilities The Lead Upstream Scientist will have a broad range of responsibilities, often covering both technical and operational aspects. CDMO Collaboration Serve as the primary technical liaison between the company and the Upstream SMEs at the CDMO. Ensure smooth tech transfer and process optimization at the CDMO, including providing detailed protocols, strain information, and historical data. Review and approve development and manufacturing protocols, batch records, and reports from the CDMO. Attend CDMO-run fermentation campaigns (virtually or on-site) to oversee execution and address real-time challenges. Process Development, Scale Up, & Optimization Lead the development of E. coli fermentation processes for high-yield expression of biologics. Scale up fermentation processes from shake flasks to bioreactors and develop scale-up strategies considering mass transfer, oxygenation, and mixing constraints. Design and execute experiments to optimize media, feed strategies, induction conditions, and growth parameters. Troubleshoot fermentation-related challenges such as low expression, plasmid stability, oxygen transfer, and contamination issues. Data Analysis & Documentation Analyze process data using statistical tools and present findings in reports and meetings. Write technical documents, including standard operating procedures (SOPs), protocols, and batch records. Contribute to IND filing documentation by providing upstream process data. Qualifications Education & Experience PhD in Biochemistry, Chemistry, Chemical Engineering, Pharmaceutical Sciences with 0-3 years of relevant industry experience OR Master's degree in Biochemistry, Chemistry, Chemical Engineering, Pharmaceutical Sciences or life sciences and a minimum of 2 years of related industry experience OR Bachelor's degree in Biochemistry, Chemistry, Chemical Engineering, Pharmaceutical Sciences or life sciences and a minimum of 5 years of related industry experience Preference will be given to candidates with: Biologics product development from Pre-clinical to Phase 1 Experience working in CMC team and with authoring regulatory filings. Process optimization and characterization Knowledge in other CMC areas such as downstream and analytical sciences Knowledge in control strategy and establishing of established ranges for a process

Key Responsibilities: • Work collaboratively with cross-functional and multidisciplinary teams to develop si RNA delivery platforms with different types of ligands (small molecules, lipids, peptides, and antibodies), modification chemistry and formulation. • Design, synthesize, purify, and characterize nucleoside analogs/amidites with novel modifications. • Design, synthesize, purify, and characterize si RNA conjugates. • Develop analytical methods for si RNA conjugates. • Work with biologists evaluating the delivery effectiveness of si RNA conjugates. • Clearly document experimental details and results. • Manage and guide CRO for the synthesis work when necessary. • Communicate findings/results to the team and management when required. • Maintain a current appreciation of scientific literature and understanding of the state of the art in oligonucleotide therapeutics. Required Experience and Skills: • Ph.D. in synthetic organic chemistry, nucleotide/oligonucleotide chemistry, 1-3 years' experience for Scientist and >3 for Senior Scientist. • Strong background in nucleotide modification/synthesis, phosphoramidite chemistry, solid phase oligonucleotide synthesis, peptide/antibody conjugation chemistry and analytical chemistry. • Experience with analytical instrumentation (HPLC/LCMS) for oligonucleotides. • Ability to independently translate strategy into action in a timely manner. • Strong presentation skills. Effective communication and interpersonal skills.

Beacon Photonics is creating revolutionary optical microsystems to disrupt traditional laser markets. Founded by pioneers in the field of integrated photonics, we are a dynamic tech startup at the forefront of optical innovation. Our heterogeneous photonics technology enables high-performance products that provide unparalleled advantages in cost, size, and functionality for communications, sensing, and quantum systems. We are a dedicated group of world-class engineers and scientists devoted to realizing transformative capabilities and solving real-world problems. We are seeking an exceptional Laser Research Scientist to join our rapidly growing team. In this role, you will lead R&D efforts to create integrated lasers and advanced optical microsystems. The ideal candidate will have extensive expertise in the design, characterization, and control of lasers, with a proven ability to apply this knowledge in practice. As a key team member, you will refine and deliver products, propose and lead technical efforts, collaborate with cross-functional teams and state-of-the-art foundries, and report directly to senior leadership. To apply, send your resume to *************************** with the position in the subject line. Responsibilities: Design, develop, and prototype high-performance laser sources and systems based on heterogeneous integrated photonics Simulate laser components and devices to predict and optimize product performance Lead experimental testing efforts for lasers and optical microsystems at the wafer, die, and package level Conduct innovative R&D to deliver solutions to commercial and government customers and report key results to industry executives and government decision makers Collaborate with a team of integrated photonics designers and foundry partners Shape the company's future by building laboratory capabilities, proposing and leading new activities, and supporting ongoing research Work closely with senior leadership to inform technical decisions and company direction Requirements: Ph.D. degree in physics, electrical engineering, or similar field (or equivalent background) 3+ years of professional experience with advanced laser development Expertise in the design, simulation, and experimental characterization of optical hardware including semiconductor, solid-state, and fiber lasers and optoelectronic components Expertise in one or more applications of lasers, such as communications, sensing, industrial processing, defense, and quantum technology Demonstrated success in the preparation of technical proposals, publications, and patents Excellent written and verbal communication skills, strong work ethic, and attention to detail Desirable Skills and Experience: Design and characterization of ultrafast, pulsed, and high-power lasers Narrow linewidth lasers and stabilization techniques such as self-injection locking and PDH Nonlinear optics including optical down-conversion and frequency combs Design and fabrication of photonic integrated circuits and semiconductor optoelectronics Scripting and simulation tools such as Python, Simulink, VPI, Lumerical, and Matlab Advanced laser measurements including RIN, linewidth, feedback sensitivity, and lifetime Optomechanical and electrical packaging, prototyping, and product delivery Analog, digital, and RF electronics and laser instrumentation Beacon Photonics is based in vibrant Northern Virginia, consistently ranked as one of the most desirable places to live in the country. We value innovation, collaboration, open and honest communication, and a passion for technology. Come build your future with us. Our benefits include competitive compensation and employee stock ownership. We provide generous family medical, dental, and vision coverage and paid time off. Beacon is an equal-opportunity employer, committed to sustaining a diverse and inclusive workplace. We welcome applicants from all backgrounds regardless of race, color, religion, sex, national origin, age, marital status, sexual orientation, gender identity, veteran status, disability, or any other basis protected by law. This position involves access to technology that may be subject to U.S. export controls. Such access is granted to U.S. citizens (born or naturalized), lawful permanent residents, certain categories of refugees and asylees, and those who can obtain appropriate export control licenses from the U.S. Departments of State and Commerce.

Join Our Team as an Application Scientist - Scanning Electron Microscopy (SEM) Nanoscience Instruments Are you passionate about cutting-edge technology and materials science? Nanoscience Instruments is looking for an Application Scientist to help drive the future of Scanning Electron Microscopy (SEM). This is your chance to work with state-of-the-art instruments, collaborate with top researchers, and be part of a rapidly growing field. Who We Are At Nanoscience Instruments, we're pioneers in advanced microscopy, surface analysis, and nanomaterials synthesis. Our solutions empower researchers in academia, corporate R&D, and government labs to make breakthroughs in science and technology. What You'll Do Lead Demonstrations: Perform hands-on demonstrations of SEM systems both in our labs and at customer sites. Deliver Expertise: Provide top-tier technical training and support to ensure customers get the most from their SEM systems. Drive Results: Conduct in-depth sample analysis, showcasing the power of our instruments through detailed reports. Collaborate & Innovate: Work alongside sales, marketing, and R&D teams to craft strategies, develop outreach programs, and stay at the forefront of SEM advancements. Travel the World: Engage with customers and attend industry events, both domestically and internationally, to share your knowledge and expand your network. What You Bring A Master's or Ph.D. in Materials Science, Physics, Engineering, Chemistry, or a related field. Hands-on experience with Scanning Electron Microscopy (SEM) and a passion for advancing materials characterization. Excellent problem-solving skills and the ability to troubleshoot SEM systems. Strong communication skills to engage with scientists, engineers, and customers. A drive to work both independently and as part of a collaborative, customer-focused team. A willingness to travel to customer sites, conferences, and events to share your expertise. What Sets You Apart (Preferred Experience) 2-5 years of experience in surface science, microscopy, or analytical instrumentation. Experience in applications support or technical sales. Familiarity with vacuum technology, sample preparation, and imaging techniques. Why Nanoscience Instruments? Be at the cutting edge: Work with the latest in scientific instrumentation and be part of groundbreaking discoveries. Make an impact: Support researchers in academia, R&D, and industrial labs. Work with a collaborative team: Join a group of passionate experts who value innovation, creativity, and success. Ready to Join Us? If you're excited about SEM, materials science, and making a real impact, we want to hear from you! Send your resume and cover letter to ********************.

Data is at the center of everything we do. As a startup, we disrupted the credit card industry by individually personalizing every credit card offer using statistical modeling and the relational database, cutting-edge technology in 1988! Fast-forward a few years, and this little innovation and our passion for data has skyrocketed us to a Fortune 200 company and a leader in the world of data-driven decision-making. As a Data Scientist at Capital One, you'll be part of a team that's leading the next wave of disruption at a whole new scale, using the latest in computing and machine learning technologies and operating across billions of customer records to unlock the big opportunities that help everyday people save money, time, and agony in their financial lives. Team Description The US Card Acquisitions Data Science team builds industry-leading machine learning models to empower core underwriting decisions in the acquisitions of a new credit card customer. We collaborate closely with a wide range of cross-functional partner teams - data engineers, platforms engineers, product managers, credit and business analysts, to deliver the solutions from ideation to implementation. We are a team of model developers, who own the full life cycle of our models - development, deployment, monitoring, governance, and ongoing usage expansion and releases. We are also a team of creative problem solvers, who challenge the status quo on a continuous basis and are devoted to innovation to keep making our models more dynamic, adaptive, robust, and ultimately, smarter. Role Description In this role, you will: Partner with a cross-functional team of data scientists, software engineers, and product managers to deliver a product customers love. Leverage a broad stack of technologies - Python, Conda, AWS, H2O, Spark, and more - to reveal the insights hidden within huge volumes of numeric and textual data. Build machine learning models through all phases of development, from design through training, evaluation, validation, and implementation. Flex your interpersonal skills to translate the complexity of your work into tangible business goals. The Ideal Candidate is: Customer first. You love the process of analyzing and creating, but also share our passion to do the right thing. You know at the end of the day it's about making the right decision for our customers. Innovative. You continually research and evaluate emerging technologies. You stay current on published state-of-the-art methods, technologies, and applications and seek out opportunities to apply them. Technical. You're comfortable with open-source languages and are passionate about developing further. You have hands-on experience developing data science solutions using open-source tools and cloud computing platforms. Statistically-minded. You've built models, validated them, and backtested them. You know how to interpret a confusion matrix or a ROC curve. You have experience with clustering, classification, sentiment analysis, time series, and deep learning. A data guru. “Big data” doesn't faze you. You have the skills to retrieve, combine, and analyze data from a variety of sources and structures. You know understanding the data is often the key to great data science. Basic Qualifications: Currently has, or is in the process of obtaining one of the following with an expectation that the required degree will be obtained on or before the scheduled start date: A Bachelor's Degree in a quantitative field (Statistics, Economics, Operations Research, Analytics, Mathematics, Computer Science, or a related quantitative field) plus 5 years of experience performing data analytics. A Master's Degree in a quantitative field (Statistics, Economics, Operations Research, Analytics, Mathematics, Computer Science, or a related quantitative field) or an MBA with a quantitative concentration plus 3 years of experience performing data analytics. A PhD in a quantitative field (Statistics, Economics, Operations Research, Analytics, Mathematics, Computer Science, or a related quantitative field). Preferred Qualifications: Master's Degree in “STEM” field (Science, Technology, Engineering, or Mathematics) plus 3 years of experience in data analytics, or PhD in “STEM” field (Science, Technology, Engineering, or Mathematics). At least 1 year of experience working with AWS. At least 3 years' experience in Python, Scala, or R. At least 3 years' experience with machine learning. At least 3 years' experience with SQL. Capital One will consider sponsoring a new qualified applicant for employment authorization for this position. This role is expected to accept applications for a minimum of 5 business days. No agencies please. Capital One is an equal opportunity employer committed to diversity and inclusion in the workplace. All qualified applicants will receive consideration for employment without regard to sex (including pregnancy, childbirth or related medical conditions), race, color, age, national origin, religion, disability, genetic information, marital status, sexual orientation, gender identity, gender reassignment, citizenship, immigration status, protected veteran status, or any other basis prohibited under applicable federal, state or local law. Capital One promotes a drug-free workplace. #J-18808-Ljbffr

Our client, a mission-based nonprofit organization in Arlington, VA, has an immediate need for a long-term temporary Senior Research Associate to support their team for 6-12 months! About the Job: Instruct awardees on data collection processes and train on data collection systems. Create data dashboards. Serve as a subject matter on the database and respond to research and data questions. Serve as a liaison with the IRB, collaborate with external consultants, and work cross functionally with different departments. Support research, data generation, analysis, and other duties as assigned. About You: 3+ years of relevant non-profit or government research experience are required. Institutional Review Board experience is required. Proficiencies in statistical software or programming languages are required. A bachelor's degree is required; A master's degree is preferred. Strong analytical and critical thinking capabilities with advanced Excel skills. Effective and flexible teamwork approach with on the ground research experience. About the Position: $33/hr-$39/hr, depending on experience. Starting ASAP and lasting 6-12 months. Hours are 8:30am-5:00pm. Hybrid with 2days/week onsite in Arlington, VA. Metro accessible. Beacon Hill is an equal opportunity employer and individuals with disabilities and/or protected veterans are encouraged to apply. California residents: Qualified applications with arrest or conviction records will be considered for employment in accordance with the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act. If you would like to complete our voluntary self-identification form, please click here or copy and paste the following link into an open window in your browser: ***************************************** Completion of this form is voluntary and will not affect your opportunity for employment, or the terms or conditions of your employment. This form will be used for reporting purposes only and will be kept separate from all other records. Company Profile: Founded by industry leaders to set a new standard in search, career placement and flexible staffing, we deliver coordinated staffing solutions with unparalleled service, a commitment to project completion and success and a passion for innovation, creativity and continuous improvement. Our niche brands offer a complete suite of staffing services to emerging growth companies and the Fortune 500 across market sectors, career specialties/disciplines and industries. Over time, office locations, specialty practice areas and service offerings will be added to address ever changing constituent needs. Learn more about Beacon Hill and our specialty divisions, Beacon Hill Associates, Beacon Hill Financial, Beacon Hill HR, Beacon Hill Legal, Beacon Hill Life Sciences and Beacon Hill Technologies by visiting ************* Benefits Information: Beacon Hill offers a robust benefit package including, but not limited to, medical, dental, vision, and federal and state leave programs as required by applicable agency regulations to those that meet eligibility. Upon successfully being hired, details will be provided related to our benefit offerings. We look forward to working with you. Beacon Hill. Employing the Future (TM)

Employee Type: exempt full-time Division: Clinical Research Program Facility: Rockville: 9615 MedCtrDr The Frederick National Laboratory is a Federally Funded Research and Development Center (FFRDC) sponsored by the National Cancer Institute (NCI) and operated by Leidos Biomedical Research, Inc. The lab addresses some of the most urgent and intractable problems in the biomedical sciences in cancer and AIDS, drug development and first-in-human clinical trials, applications of nanotechnology in medicine, and rapid response to emerging threats of infectious diseases. Accountability, Compassion, Collaboration, Dedication, Integrity and Versatility; it's the FNL way. PROGRAM DESCRIPTION The Cancer Genomics Research Laboratory (CGR) investigates the contribution of germline and somatic genetic variation to cancer susceptibility and outcomes in support of the NCI's Division of Cancer Epidemiology and Genetics (DCEG), the world's most comprehensive cancer epidemiology research group. CGR is located at the NCI-Shady Grove campus in Rockville, MD and operated by Leidos Biomedical Research, Inc. We care deeply about discovering the genetic and environmental determinants of cancer, and new approaches to cancer prevention, through our contributions to the molecular, genetic, and epidemiologic research of the 70+ investigators in DCEG. Working in concert with epidemiologists, biostatisticians and basic research scientists in DCEG's intramural research program, CGR provides the capacity to conduct genome-wide discovery studies and targeted regional approaches to identify the heritable determinants of various forms of cancer. This includes the design and analysis of high throughput studies using various types of “-omics” technologies such as array- and sequence-based genome-wide association studies, studies of tumor characteristics using integrated genomic data analysis, and molecular epidemiologic studies based on novel assays focused on the metabolome and microbiome. We are seeking a highly motivated, independent scientist to join our Development, Optimization & Implementation team to establish and support new pipelines for extraction and downstream technologies required to support DCEG investigators in areas of human, bacterial, and viral nucleic acid research applications including metagenomics, targeted sequencing applications, and ct DNA and cf RNA sequencing. The successful incumbent will have extensive experience involving analytical characterization of nucleic acids using basic and advanced assays and will have responsibility for performing laboratory-based development and validation of applications across multiple areas of interest. KEY ROLES/RESPONSIBILITIES Work in close coordination with other CGR groups and DCEG investigators to develop, optimize and implement new protocols and applications into main CGR laboratories for molecular and digital pathology, sample extraction and characterization, genomics (germline and somatic), and proteomics analyses Utilize experience with extraction, isolation and handling of nucleic acids and available literature to design plans for new research approaches desired Conducting hands-on laboratory research activities involving assay development for nucleic acid testing Maintain thorough electronic documentation records of experimental plans, data, results, and next steps Preparation of results in report format and presentation in cross-functional meetings with senior CGR leadership and DCEG investigators Author documents supporting applications and convert newly developed protocols and procedures into SOPs Support automation method development and testing With DCEG and CGR senior staff, contribute to design of experiments for novel research applications within CGR BASIC QUALIFICATIONS To be considered for this position, you must minimally meet the knowledge, skills, and abilities listed below: Possession of a Bachelor's degree from an accredited college or university according to the Council for Higher Education Accreditation A minimum of eight (8) years related biomedical experience Must be able to obtain and maintain a clearance Demonstrated expertise with DNA/RNA extraction, RNA handling, nucleic acid quantitation and quality analysis and basic molecular biology techniques Proven experience of method qualification/development or validation for testing of DNA and RNA Prior experience working in a fast-paced development environment with GLPs and safe handling of biological material Strong technical and analytical skills for method/assay development and troubleshooting are required Excellent time and project management skills, with ability to work on several projects simultaneously Attention to detail and ability to independently identify critical variables Outstanding communication skills (verbal and written) Good interpersonal skills and ability to mentor and train junior staff Working knowledge of Windows-based computer operating systems and Microsoft office suite Ability to work in a fast-paced setting and effectively collaborate in a highly dynamic, cross-functional environment PREFERRED QUALIFICATIONS Candidates with these desired skills will be given preferential consideration: Substantial experience with a wide range of specimens and analytes used in genomics, transcriptomics, and proteomics. Expertise with a wide range of nucleic acid extraction methodologies used in both home-brew and commercially manufactured products. Substantial experience with advanced molecular biology techniques (including qPCR, primer design, and NGS library preparation). Experience with complex sequencing applications and assessment of pre-analytical variables. Experience using high-throughput laboratory equipment, such as automated liquid handlers is considered a strong plus including method development. Familiarity with eLN and/or LIMS systems Bioinformatics and statistics skills, including experience with Python or R Experience with reagent/buffer formulation, assay development, microbiology testing and/or HPV typing Job Hazards This position is subject to working with or have potential for exposure to infectious material, requiring medical clearance and immunizations. This position may require continuous or intermittent exposure to and exertion in environmental conditions such as working outdoors, temperature extremes, humidity extremes. etc. as part of the job. Commitment to Diversity All qualified applicants will receive consideration for employment without regard to sex, race, ethnicity, age, national origin, citizenship, religion, physical or mental disability, medical condition, genetic information, pregnancy, family structure, marital status, ancestry, domestic partner status, sexual orientation, gender identity or expression, veteran or military status, or any other basis prohibited by law. Leidos will also consider for employment qualified applicants with criminal histories consistent with relevant laws. #readytowork

onsite in Rockville, MD My client's Antibody Discovery team is expanding, and they seek a MS level (or BS level) candidate with phage display, antibody engineering, and/or molecular biology experience to contribute to their team's success. Key Responsibilities: 1. Perform hands-on lab work and apply molecular biology, phage display, and rational protein engineering techniques to generate novel multi-specific therapeutics. 2. Collaborate with team members to construct libraries and guide project development. 3. Provide technical expertise to design experiments and ensure deliverables. 4. Analyze and present data and recommend project advancements. Essential Qualifications: BS/MS degree and 2-15+ years of relevant experience. Preferred Experience: Phage display to discover and optimize antibodies from naïve, immune, and synthetic libraries. Strong problem-solving and analytical skills. Excellent communication, organizational, and time management skills. Additional Points: --This is a full time position and the title can be Associate Scientist, Sr Associate Scientist, or Scientist. --Title and salary (base plus annual bonus) are commensurate with experience, and relocation is provided. --This role is for BS and MS level only. If you're looking to work with the leaders in the antibody engineering field, apply now!

Who We Are Arcellx is a public, clinical-stage biotechnology company reimagining cell therapy by engineering innovative immunotherapies for patients with cancer and other incurable diseases. We believe that cell therapies are one of the forward pillars of medicine and our mission is to destroy cancer and advance humanity by developing cell therapies that are safer, more effective, and more broadly accessible. Our team members are made up of talented innovators and dreamers working from our offices in Rockville, Maryland, and Redwood City, California. At Arcellx, we hire exceptional people and create a fun, diverse, supportive, and informal environment that allows everyone to do their best work. What Matters to Us Living our core values is essential to maintaining a work environment that is high-performing, inclusive, and collaborative. We look for candidates who demonstrate strong values alignment and bring different backgrounds, viewpoints, and abilities to the team. Arcellx Core Values Character : Committed to always doing what's right. Audacity : Willing to challenge convention and share candid feedback with others. Determination : Curious and self-motivated. Always looking to improve and learn. Collaboration : "No job is too small" mentality. Humble and willing to help others. Originality : Will bring your unique perspective to the table and respect a diverse set of views and backgrounds. The “Fine Print” - What You'll Do Design, plan, and execute experiments independently to generate high quality data for ongoing clinical studies. Clinical trial sample processing. Immunostaining, sample acquisition and data analysis for flow cytometry assays. Support the development, optimization and validation of biomarker assays per ICH Q2 guidelines. Prepare data summaries, reports, and presentations for internal teams. Write and review SOPs and work instructions. Stay current with new technologies, methods, and trends in biomarker research contributing innovative ideas to improve processes and project outcomes. Skills and Experience We Look For Bachelor's or master's degree in a relevant scientific discipline. 2+ years of experience within the biotech or pharmaceutical industry. Proven experience with handling of immune cells and processing of whole blood and bone marrow samples. Experience with multi-parameter flow cytometry (>12 colors preferred), immunostaining and target engagement assays such as receptor occupancy. Experience with sample acquisition on instruments such as BD FACS Lyric and data analysis using FlowJo software. Demonstrated ability to design, plan, and independently conduct experiments. Ability to work effectively in a team-oriented environment and manage multiple tasks. Strong analytical and problem-solving skills. Rewards at Arcellx Our people are our greatest asset, and supporting their well-being is an essential part of delivering on our mission and impacting the lives of patients. Putting this belief into practice means offering strong compensation and benefits. The base salary range for this position is $77,000 - $83,000 per year. Where a candidate falls within that range is determined by factors such as years of experience. Our compensation package also includes an annual bonus based on company goals and an equity (RSU) grant. We do offer relocation assistance for roles if required. Our market-leading benefits package includes: 100% coverage for medical, dental and vision for team members and dependents, unlimited vacation, a 3-day weekend every month, fully-paid parental leave for up to 6 months, tuition reimbursement, 401k employer contribution and more. Join us in our quest to reimagine cell therapy and destroy cancer. For more on our technology, culture, and team, go to **************** #LI-Onsite

Overview Axle Informatics is a bioscience and information technology company that offers advancements in translational research, biomedical informatics, and data science applications to research centers and healthcare organizations around the globe. With experts in biomedical science, software engineering, and program management, we focus on developing and applying research tools and techniques to empower decision-making and accelerate research discoveries. We work with some of the top research organizations and facilities in the country including multiple institutes at the National Institutes of Health (NIH). Overview Axle is seeking a highly ambitious, adaptable, structured, and detail-oriented Flow Cytometry Immunology Scientist to join our vibrant team at the National Institutes of Health (NIH), National Institute of Allergy and Infectious Diseases (NIAID), Vaccine Research Center (VRC), Vaccine Production Program (VPP). Responsibilities Provide centralized support and service for all in vivo research, conducts collaborative research and animal model development, and operates a fully accredited laboratory animal facility. Develop assays to support development and/or QC testing as needed to support the flow cytometry core facilities and analytical programs. Perform a wide range of complex procedures and techniques to include cell culture, analytical flow cytometry, infectious cell sorting flow cytometry, monoclonal fluorescent conjugation and panel staining procedures. Draft standard operating procedures and update as needed. Plan and analyze data from animal and clinical studies evaluating immunogenicity of vaccine candidates entering product development. Provide guidance to flow cytometry manager regarding unusual and novel issues relating to broad policy matters and the potential impact on the VRC mission and strategic objectives for the intramural research. Review policies, standards, procedures, and guidelines and ensure dissemination to laboratory staffs for implementation. Provide basic research to clinical evaluation and potential licensure of vaccines by providing all aspects of oversight and programmatic assistance. This includes the support of teaching, training, and in vivo research for the VRC laboratories and researchers. Train research staff on the operation of flow cytometers and quality control practices. Interact with students, post-doctoral fellows and non-doctoral research technicians on experimental design and laboratory-based methodologies. Assist in the design of experimental approaches to provide evaluation of scientific data, interact with scientific staff and collaborate with other staff scientists; integrate and startup of new technologies within the laboratory. Experience Required / Requirements B.S. or M.S. in immunology or closely related field is required. Minimum two (2) years of specialized experience is required. Experience with flow cytometry technology and data analysis is required. Benefits 100% Medical, Dental & Vision premium coverage for Employees Paid Time Off (Including Holidays) Employee Referral Bonus 401K Match Tuition reimbursement and professional development opportunities Flexible Spending Accounts: Healthcare (FSA) Parking Reimbursement Account (PRK) Dependent Care Assistant Program (DCAP) Transportation Reimbursement Account (TRN) The diversity of Axle's employees is a tremendous asset. We are firmly committed to providing equal opportunity in all aspects of employment and will not tolerate any illegal discrimination or harassment-based age, race, gender, religion, national origin, disability, marital status, covered veteran status, sexual orientation, status with respect to public assistance, and other characteristics protected under state, federal, or local law and to deter those who aid, abet, or induce discrimination or coerce others to discriminate. Accessibility: If you need an accommodation as part of the employment process please contact: ******************** Disclaimer: The above description is meant to illustrate the general nature of work and level of effort being performed by individual's assigned to this position or . This is not restricted as a complete list of all skills, responsibilities, duties, and/or assignments required. Individuals may be required to perform duties outside of their position, job description or responsibilities as needed.

Who is USP? The U.S. Pharmacopeial Convention (USP) is an independent scientific organization that collaborates with the world's top authorities in health and science to develop quality standards for medicines, dietary supplements, and food ingredients. USP's fundamental belief that Equity = Excellence manifests in our core value of Passion for Quality through our more than 1,300 hard-working professionals across twenty global locations to deliver the mission to strengthen the supply of safe, quality medicines and supplements worldwide. At USP, we value inclusivity for all. We recognize the importance of building an organizational culture with meaningful opportunities for mentorship and professional growth. From the standards we create, the partnerships we build, and the conversations we foster, we affirm the value of Diversity, Equity, Inclusion, and Belonging in building a world where everyone can be confident of quality in health and healthcare. USP is proud to be an equal employment opportunity employer (EEOE) and affirmative action employer. We are committed to creating an inclusive environment in all aspects of our work-an environment where every employee feels fully empowered and valued irrespective of, but not limited to, race, ethnicity, physical and mental abilities, education, religion, gender identity, and expression, life experience, sexual orientation, country of origin, regional differences, work experience, and family status. We are committed to working with and providing reasonable accommodation to individuals with disabilities Brief Job Overview This is a hands-on, analyst position in USP's NMR Laboratory. The scientist will be an integral member of the nuclear Magnetic Resonance Spectroscopy (NMR) team and will assist in the execution of structural elucidation of reference materials by NMR and purity determination by quantitative NMR and Circular Dichroism (CD) instruments including designing and executing experiments supporting reference materials evaluations, product investigations and other relevant programs in the laboratory. This work includes development, execution and/or validation of complex analytical procedures supporting the identity, strength, and purity of the evaluated material. Reference materials encompass a diverse group including small molecules, biologics, excipients, oligosaccharides, vitamins, complex mixtures, peptides, and polymers, providing a broad range of experience for the scientist in this position. Scientist must have mastered many common NMR and CD techniques (preferably) with the laboratory and be able to contribute their own observations and input to difficult projects. The successful candidate can direct, troubleshoot, and share insights on complex projects, while drawing independent conclusions about the results and determining how to proceed with the project. The successful candidate demonstrates the ability to lead projects to completion with a high degree of scientific expertise How will YOU create impact here at USP? In this role at USP, you contribute to USP's public health mission of increasing equitable access to high-quality, safe medicine and improving global health through public standards and related programs. In addition, as part of our commitment to our employees, Global, People, and Culture, in partnership with the Equity Office, regularly invests in the professional development of all people managers. This includes training in inclusive management styles and other competencies necessary to ensure engaged and productive work environments. The Scientist III, NMR has the following responsibilities: About 70 % of the incumbent work is expected to be at the bench level. In this capacity the NMNR scientist: Actively performs testing at the bench, taking responsibility for interpreting, report writing, as well as ensuring the project is completed in a timely manner. Provides hands-on NMR sample preparation, multinuclear as well as 2D NMR data acquisition and processing using 600 MHz, 500 MHz, and 400 MHz spectrometers equipped with cryoprobes. Focuses on assessing data interpretation and analyzing the structures of small molecules, excipients, and polymers in support of the USP catalogue. Works independently and may help others to develop and validate methodologies for the analysis of drug substances, drug products, dietary substances, excipients, and other relevant products. Demonstrates solid scientific approach to analysis in the laboratory. Troubleshoots difficult/unusual lab problems independently; collaboratively assists others with troubleshooting. Conducts planning of research and development required for all projects; reviews literature; acts as a resource to others in the planning of projects and analysis of results. Works with the other team members collaboratively to develop effective testing plans and experimental designs. About 5% of the incumbent work would be related to the management of NMR instruments: cryogen filling and calibration, advising the metrology personnel, and/or assisting vendor technicians, etc. About 10% of the incumbent work may consist of training other instrument users, mentoring staff in the proper use of the NMR instruments, reviewing reports, and providing technical support within the organization when needed. About 10% of the incumbent work may be related to the experimental process and related documentation (review and revising of Standard Operating Procedures, proposing process improvements, etc.) and peer reviewed manuscripts submissions of scientific work. About 5% of the incumbent work may consist of adopting techniques particularly Circular Dichroism (CD) method development and training activities on work relating to reference materials and CRAFT software applications of NMR data Who is USP Looking For? The successful candidate will have a demonstrated understanding of our mission, commitment to excellence through inclusive and equitable behaviors and practices, ability to quickly build credibility with stakeholders, along with the following competencies and experience: Ph.D. in Polymer chemistry or Natural products isolation and structural elucidation or peptide related fields involved in NMR based thesis development with either graduate or postdoctoral research (0-2 years) exclusive experience polymer end group analysis, chain length and molecular weight determinations, excipient materials, and/or in natural products structural characterization and conformational analysis, peptide structure confirmation at natural abundance by testing primarily using solution NMR spectroscopy. Experience working in the pharmaceutical industry and/or academia strongly preferred. Working knowledge of methods and procedures, and expertise in calibrating and operating NMR equipment (Bruker/ JEOL) required. Quantitative NMR experience for determining purity. Must have demonstrated success in utilizing modern methods of NMR techniques for chemical structure characterizations. Relevant experience in preparation of organic samples for NMR data collection, as well as data interpretation as applied to structural verification and confirmation. Ability to maneuver and handle projects between two instrumental platforms (Bruker and JEOL) is essential. Takes personal responsibility to ensure work is delivered on time and is the highest possible quality with minimal supervision. Skill to anticipate, troubleshoot and solve technical problems. Ability to implement novel NMR methods from literature is highly desirable. Familiar with TopSpin and Delta JEOL software for data acquisition and processing. Strong communication and presentation skills, both verbal and written. Additional Desired Preferences Use additional software such as ACD and CRAFT for NMR data analyses. Experience with Circular Dichroism applications for small molecules. Supervisory Responsibilities None, this is an individual contributor role. Benefits USP provides the benefits to protect yourself and your family today and tomorrow. From company-paid time off and comprehensive healthcare options to retirement savings, you can have peace of mind that your personal and financial well-being is protected. Compensation Base Salary Range: USD $85,500.00 - $111,250.00 annually. Target Annual Bonus: % Varies based on level of role. Individual compensation packages are based on various factors unique to each candidate's skill set, experience, qualifications, equity, and other job-related reasons. Note: USP does not accept unsolicited resumes from 3rd party recruitment agencies and is not responsible for fees from recruiters or other agencies except under specific written agreement with USP.

Please, review and apply for this position through the QCI system following the link below (Copy and Paste): http://jobs.qcitech.com/jobseeker/Flow_Cytometry_Scientist_J02098387.aspx *You can apply through Indeed using mobile devices with this link. Additional Information

Data is at the center of everything we do. As a startup, we disrupted the credit card industry by individually personalizing every credit card offer using statistical modeling and the relational database, cutting edge technology in 1988! Fast-forward a few years, and this little innovation and our passion for data has skyrocketed us to a Fortune 200 company and a leader in the world of data-driven decision-making. As a Data Scientist at Capital One, you'll be part of a team that's leading the next wave of disruption at a whole new scale, using the latest in computing and machine learning technologies and operating across billions of customer records to unlock the big opportunities that help everyday people save money, time and agony in their financial lives. Team Description: In Capital One's Model Risk Office, we defend the company against model failures and find new ways of making better decisions with models. We use our statistics, software engineering, and business expertise to drive the best outcomes in both Risk Management and the Enterprise. We understand that we can't prepare for tomorrow by focusing on today, so we invest in the future: investing in new skills, building better tools, and maintaining a network of trusted partners. We learn from past mistakes, and develop increasingly powerful techniques to avoid their repetition. Role Description In this role, you will: Partner with cross-functional model development teams consisting of data scientists and software engineers to identify and quantify risks associated with machine learning, statistical, and financial models. Leverage expertise and interpersonal skills to accelerate the adoption of best practices related to the design and testing of model code. Evaluate the appropriateness of the design of model code with consideration to its business use to identify weaknesses and recommend improvements. Evaluate the effectiveness of the design and execution of code testing plans with consideration to the scope, complexity, and business impact of the underlying code. Perform independent code review and testing to validate model implementations are aligned with their design intent. Serve as a subject matter expert to support our code quality initiative and provide guidance to model development and validation teams. The Ideal Candidate is: Technical. You have hands-on experience developing and testing data science solutions using open-source tools and cloud computing platforms. Collaborative: You work well with leaders and fellow data scientists to balance code quality needs with existing project timelines. You are able to incorporate opinions from various stakeholders to come up with a plan that serves the most good. Detail Oriented. You believe the little things add up and you can show the value of paying attention to the finer points of coding. A Teacher. You know your way around a complex, collaborative code base, but you still remember what it was like writing your first script. You can articulate the why, the what, and the how of writing modular, unit-tested code so others can get on your level. Innovative. You continually research and evaluate emerging technologies. You stay current on published state-of-the-art methods, technologies, and applications and seek out opportunities to apply them. Basic Qualifications: Currently has, or is in the process of obtaining one of the following with an expectation that the required degree will be obtained on or before the scheduled start date: A Bachelor's Degree in a quantitative field (Statistics, Economics, Operations Research, Analytics, Mathematics, Computer Science, or a related quantitative field) plus 5 years of experience performing data analytics A Master's Degree in a quantitative field (Statistics, Economics, Operations Research, Analytics, Mathematics, Computer Science, or a related quantitative field) or an MBA with a quantitative concentration plus 3 years of experience performing data analytics A PhD in a quantitative field (Statistics, Economics, Operations Research, Analytics, Mathematics, Computer Science, or a related quantitative field) Preferred Qualifications: Master's Degree in “STEM” field (Science, Technology, Engineering, or Mathematics) plus 3 years of experience in data analytics, or PhD in “STEM” field (Science, Technology, Engineering, or Mathematics) At least 1 year of experience building or validating models for financial services At least 1 year of experience working with AWS At least 3 years' experience in Python, Scala, or R At least 3 years' experience with machine learning At least 3 years' experience with SQL Capital One will consider sponsoring a new qualified applicant for employment authorization for this position. This role is expected to accept applications for a minimum of 5 business days. No agencies please. Capital One is an equal opportunity employer committed to diversity and inclusion in the workplace. All qualified applicants will receive consideration for employment without regard to sex (including pregnancy, childbirth or related medical conditions), race, color, age, national origin, religion, disability, genetic information, marital status, sexual orientation, gender identity, gender reassignment, citizenship, immigration status, protected veteran status, or any other basis prohibited under applicable federal, state or local law. #J-18808-Ljbffr

Employee Type: exempt full-time Division: Clinical Research Program Facility: Rockville: 9615 MedCtrDr The Frederick National Laboratory is a Federally Funded Research and Development Center (FFRDC) sponsored by the National Cancer Institute (NCI) and operated by Leidos Biomedical Research, Inc. The lab addresses some of the most urgent and intractable problems in the biomedical sciences in cancer and AIDS, drug development and first-in-human clinical trials, applications of nanotechnology in medicine, and rapid response to emerging threats of infectious diseases. Accountability, Compassion, Collaboration, Dedication, Integrity and Versatility; it's the FNL way. PROGRAM DESCRIPTION The Cancer Genomics Research Laboratory (CGR) investigates the contribution of germline and somatic genetic variation to cancer susceptibility and outcomes in support of the NCI's Division of Cancer Epidemiology and Genetics (DCEG), the world's most comprehensive cancer epidemiology research group. CGR is located at the NCI-Shady Grove campus in Gaithersburg, MD and operated by Leidos Biomedical Research, Inc. We care deeply about discovering the genetic and environmental determinants of cancer, and new approaches to cancer prevention, through our contributions to the molecular, genetic, and epidemiologic research of the 70+ investigators in DCEG. Working in concert with epidemiologists, biostatisticians and basic research scientists in DCEG's intramural research program, CGR provides the capacity to conduct genome-wide discovery studies and targeted regional approaches to identify the heritable determinants of various forms of cancer. This includes the design and analysis of high throughput studies using various types of “-omics” technologies such as array- and sequence-based genome-wide association studies, studies of tumor characteristics using integrated genomic data analysis, and molecular epidemiologic studies based on novel assays focused on the metabolome and microbiome. KEY ROLES/RESPONSIBILITIES CGR is a fast-paced, high throughput organization that supports histology, molecular and digital pathology, nucleic acid extraction, sample QC, genotyping, sequencing, and analysis for genetic and epidemiologic studies for the investigators within DCEG. CGR is recruiting an Associate Scientist I/Team Lead position within the Extraction and Sample Preparation laboratory that supports sample quantitation, QC and normalization of extracted nucleic acid, high throughput aliquoting of biospecimens for downstream assays and extraction of HPV samples for sequencing and genotyping efforts. The Team Lead position will work within our high throughput, highly automated laboratory to support biospecimen, reagent and materials management activities. The successful candidate will be responsible for supervision and management of the day-to day execution of laboratory processes and applications including: Coordinate the preparation of sample collection kits for distribution to collaborators, receipt and organization of incoming sample shipments and reconciliation/organization for downstream activities. Organization of samples, including sorting by tube type and relabeling as needed for automation workflows. Support for sample inventory efforts, including freezer consolidation activities and preparation of samples for return to external collaborators and/or NCI Central Repository Responsible for QC practices including nucleic acid quantitation and qualification, normalization, volume checking, and residual creation. Preparation of standard curves and controls for sample QC on automated platforms Coordinate plating of DNA and RNA on automation platforms for downstream genomic assays Supervise the use of automated liquid handling robotics and/or manual methods in BSL-2+ controlled laboratory space to support biospecimen aliquoting tasks for both in house and outsourced assays. Ensure accurate use of LIMS for sample management and other laboratory activities. Draft, revise and ensure SOPs are reflective of best current practices. Responsible for documenting and reporting results and deviations for a variety of procedures in the laboratory, governed by SOPs. Ensure proper documentation of all laboratory processes are performed by lab personnel. React to any non-conformances or opportunities for improvement, by taking appropriate corrective actions in consultation with management, quality, development and automation teams and other relevant staff. Coordinate performance of routine maintenance of laboratory equipment, including scheduling repairs and performance of preventative maintenance activities in coordination with quality management and automation teams Work seamlessly and collaboratively with multiple teams across CGR including molecular and digital pathology, extraction, genomics, project management, technology development/optimization and quality management to successfully complete assigned projects and identify opportunities for continual improvement. Working with CGR senior staff, extraction experts and technology development personnel, contribute to the establishment of new QC assays (e.g., QC for ct/cf DNA and UHMW DNA) and other new protocols that may be needed to support the DCEG research portfolio. Responsible for mentorship, management and performance reviews for direct reports. Responsible for recruitment of laboratory staff. Model, practice and ensure safe work habits, including complying with all safety, health and environmental rules and regulations and maintain a clean and organized laboratory. Other duties as assigned and available BASIC QUALIFICATIONS To be considered for this position, you must minimally meet the knowledge, skills, and abilities listed below: Possession of a bachelor's degree from an accredited college or university according to the Council for Higher Education Accreditation in a field related to biomedical research. (Additional qualifying experience may be substituted for the required education). Foreign degrees must be evaluated for U.S. equivalency. In additional to educational requirement, a minimum of eight (8) years of experience Excellent laboratory skills and good knowledge of molecular biology with demonstrated ability to troubleshoot with minimal supervision. Experience with DNA and RNA extraction from a variety of biospecimen types Experience with DNA and RNA assessment for quantity and quality utilizing various instruments and methods Demonstrated experience in staff and laboratory management Experience with prioritization of workload in a high-pressure environment. Ability to multitask Ability to obtain and maintain a security clearance Strong written and oral communication skills Computer literacy (Microsoft Office products, general computer proficiency) PREFERRED QUALIFICATIONS Candidates with these desired skills will be given preferential consideration: Experience in development of user requirements and utilization of LIMS for sample and process tracking Familiarity with liquid handling robotics (use and maintenance, including but not limited to Tecan, Biomek platforms) Experience with data analysis and visualization tools such as Excel, Spotfire, Tableau Demonstrated attention to detail JOB HAZARDS This position is subject to working with or have potential for exposure to infectious material, requiring medical clearance and immunizations This position may require continuous or intermittent exposure to and exertion in environmental conditions such as working outdoors, temperature extremes, humidity extremes. etc. as part of the job Commitment to Diversity All qualified applicants will receive consideration for employment without regard to sex, race, ethnicity, age, national origin, citizenship, religion, physical or mental disability, medical condition, genetic information, pregnancy, family structure, marital status, ancestry, domestic partner status, sexual orientation, gender identity or expression, veteran or military status, or any other basis prohibited by law. Leidos will also consider for employment qualified applicants with criminal histories consistent with relevant laws. #readytowork

Arcellx (************************ is a clinical-stage biotech company headquartered in Gaithersburg, MD and Redwood City, CA. Arcellx is focused on the development of novel cell-based cancer therapies. A team of biotechnology professionals with expertise in biologics, discovery and tumor immunology incorporate proprietary technologies into genetically engineered human immune cells therapies. Arcellx's mission is to advance humanity by engineering cell therapies that are safer, more effective, and more broadly accessible. Primary Objective: Arcellx is seeking Scientists (levels Associate Scientist to Senior Scientist, depending on skill and experience) to collaborate in the innovation, discovery and development of protein and cell-based therapies. The successful candidate will work closely with a dedicated team of protein engineers and more broadly with scientists in other departmental groups (e.g. immunology, translation and manufacturing) to identify, produce, characterize and optimize recombinant proteins for use as therapeutic agents in a variety of oncology indications. The candidate will bring to the role expertise in protein engineering as well as a strong track record of innovation and creativity. Main Responsibilities: Responsibilities will depend, in part, on hiring level, but are likely to include some or all of the following: * Collaborate with other scientists to design, generate and characterize recombinant proteins, including biopharmaceutical products. * Develop and execute selection and screening strategies using phage, yeast and mammalian display. * Evaluate existing and emerging technologies, techniques and tools enhance products and streamline discovery workflows. * Independently plan, design, execute, record and analyze experiments. * Summarize and present data in internal meetings and discussions. * Write and review technical protocols and reports. Coauthor scientific abstracts, manuscripts and presentations. * Manage and drive the advancement of internal projects, products or technology initiatives. Preferred Qualifications: Preferred qualification will depend, in part, on hiring level, but are likely to include some or all of the following: * PhD in the life sciences (e.g. Biochemistry, Chemistry, Chemical Engineering, Biology, immuno-oncology), with minimum of 2 years post-degree experience in protein engineering. * Extensive experience in the design, construction, expression, characterization and optimization of recombinant proteins. * Experience with biopharmaceutical product design and lead optimization is ideal. * Experience in the design and execution of selection and screening strategies, utilizing phage display (or a related display method). * Proficiency with high throughput screening, sequencing and characterization of bacterial clones. * Experience with optimizing expression yield and quality. Experience with multiple protein expression systems (e.g. bacterial, yeast or mammalian systems) is preferred. * Experience utilizing and developing appropriate methods for assessment of protein-protein interactions (e.g. ELISA, Octet BLI, Biacore SPR, MSD) * Experience with sequence analysis software (e.g. SnapGene, Sequencher, Lasergene, BLAST, etc.), including construct and primer design and sequence confirmation. * Programming experience with Python and/or R (R Studio) is ideal. * Experience in oncology, immunology, and translational research is ideal. Submit cover letter and resume to: ************** Without exception, applicants must submit both a cover letter and resume to be considered for these positions and must have experience as described above.

~ Onsite in Rockville, MD ~ You will develop cutting-edge isothermal amplification techniques as the SME. Key Responsibilities: Spearhead the design, development, validation, and characterization of next-generation isothermal DNA amplification assays and devices for point-of-care applications. Innovate and optimize DNA extraction and sample preparation methods to enhance assay sensitivity and specificity. Develop sophisticated primers for advanced DNA amplification assays, leveraging deep understanding of molecular interactions. Experience: DNA biochemistry, advanced primer design, and state-of-the-art nucleic acid amplification technologies, with a particular focus on isothermal amplification techniques. DNA enzymology, especially working with DNA and RNA polymerases to optimize amplification reactions. Proven track record in developing molecular diagnostics, with emphasis on creating point-of-care nucleic acid tests using isothermal amplification methods. Strong background in research-oriented environments, either in academia or industry. Hands-on experience manipulating and optimizing enzymes for amplification reactions, demonstrating a deep understanding of enzyme kinetics and molecular interactions. Qualifications: PhD with a track record of research in molecular diagnostics, demonstrating innovative approaches to complex challenges. Expertise in molecular biology and biochemistry, with hands-on mastery of cutting-edge laboratory techniques and NGS. Outstanding publication record in peer-reviewed journals, showcasing contributions to the field of isothermal amplification and point-of-care diagnostics. Additional Points: -- This is a full-time position with the potential title of Scientist, Senior Scientist, or Principal Scientist and the title is commensurate with experience and expertise. -- This role is based in Maryland, with a comprehensive relocation package available.

Data is at the center of everything we do. As a startup, we disrupted the credit card industry by individually personalizing every credit card offer using statistical modeling and the relational database, cutting edge technology in 1988! Fast-forward a few years, and this little innovation and our passion for data has skyrocketed us to a Fortune 200 company and a leader in the world of data-driven decision-making. As a Data Scientist at Capital One, you'll be part of a team that's leading the next wave of disruption at a whole new scale, using the latest in computing and machine learning technologies and operating across billions of customer records to unlock the big opportunities that help everyday people save money, time and agony in their financial lives. In Capital One's Model Risk Office, we defend the company against model failures and find new ways of making better decisions with models. We use our statistics, software engineering, and business expertise to drive the best outcomes in both Risk Management and the Enterprise. We understand that we can't prepare for tomorrow by focusing on today, so we invest in the future: investing in new skills, building better tools, and maintaining a network of trusted partners. We learn from past mistakes, and develop increasingly powerful techniques to avoid their repetition. In this role, you will: Partner with a cross-functional team of data scientists, software engineers, and product managers to deliver a product customers love Leverage a broad stack of technologies (Python, Conda, AWS, H2O, Spark, and more) to reveal the insights hidden within huge volumes of numeric and textual data Build machine learning models through all phases of development, from design through training, evaluation, validation, and implementation Flex your interpersonal skills to translate the complexity of your work into tangible business goals The Ideal Candidate is: Customer first. You love the process of analyzing and creating, but also share our passion to do the right thing. You know at the end of the day it's about making the right decision for our customers. Innovative. You continually research and evaluate emerging technologies. You stay current on published state-of-the-art methods, technologies, and applications and seek out opportunities to apply them. Technical. You're comfortable with open-source languages and are passionate about developing further. You have hands-on experience developing data science solutions using open-source tools and cloud computing platforms. Statistically-minded. You've built models, validated them, and back tested them. You know how to interpret a confusion matrix or a ROC curve. You have experience with clustering, classification, sentiment analysis, time series, and deep learning. Basic Qualifications: Currently has, or is in the process of obtaining one of the following with an expectation that the required degree will be obtained on or before the scheduled start date: A Bachelor's Degree in a quantitative field (Statistics, Economics, Operations Research, Analytics, Mathematics, Computer Science, or a related quantitative field) plus 5 years of experience performing data analytics A Master's Degree in a quantitative field (Statistics, Economics, Operations Research, Analytics, Mathematics, Computer Science, or a related quantitative field) or an MBA with a quantitative concentration plus 3 years of experience performing data analytics A PhD in a quantitative field (Statistics, Economics, Operations Research, Analytics, Mathematics, Computer Science, or a related quantitative field) Preferred Qualifications: Master's Degree in “STEM” field (Science, Technology, Engineering, or Mathematics) plus 3 years of experience in data analytics, or PhD in “STEM” field (Science, Technology, Engineering, or Mathematics) At least 3 years of experience in Python, Scala, or R At least 3 years of experience with machine learning At least 3 years of experience with SQL At least 1 year of experience working with AWS #J-18808-Ljbffr