Associate Scientist Jobs in Silver Spring, 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.

Precision for Medicine is the first global precision medicine clinical research services organization, purpose-built to improve the clinical research and development process for new therapeutics. Our novel approach integrates clinical operations excellence, with laboratory expertise, and advanced data sciences to inform every step. We apply our expertise to trials at all stages-from early development through approval-with embedded experience in oncology and rare disease. With over 2000 dedicated professionals and 35 offices worldwide, we stand ready to help accelerate life-changing treatments anywhere around the globe. Won't you join us today as a Principal Scientist, Bioanalytical? Position Summary: The Principal Scientist supervises laboratory staff to support bioanalytical activities. Lead Bioanalysis and Biomarker projects through assay design and development, validation, and execution in a timely manner. Perform assays according to SOPs and support technology development in Ligand Binding platform. Essential functions of the job include but are not limited to: Design and perform experiments, independently and accurately analyze and present data Provide high quality output with the ability to build efficiency into improving productivity metrics Serve as Technical Lead in Ligand Binding Platform Assist in establishing and improving all procedures and required SOP documentation Responsible for assay trouble shooting and correcting routine scientific issues/problems Identify, update and implement emerging laboratory techniques Maintain and support lab safety practices and environment Work collaboratively with other technical teams in resource sharing and providing technical expertise Support new equipment operational qualifications and performance checks Monitor Lab Service/R&D related project expenses Act as a scientific resource externally to clients and internally Assists with writing, reviewing and editing contract and grant applications/proposals as appropriate Assist with writing and publishing papers, abstracts, techniques/or chapters to maintain the scientific standard and image of the company. May present completed work at appropriate scientific meetings and in publications Supervision of assigned laboratory staff to ensure efficient organization, development and execution of project(s) Other duties as assigned Qualifications: Minimum Required: Must have a Ph.D. in life sciences or relevant field in life sciences At least 8 years of full-time post-doctoral laboratory experience Other Required: Strong background in various technology platforms such as Mesoscale Discovery, Quanterix, Luminex, ELISA. Ability to troubleshoot and refine bioanalysis and biomarkers assays such as ADA, PK, Potency Assay, Cytokine and PD biomarker measurement Experience in handling various sample matrix such as whole blood, plasma/serum, cell pellets/supernatant, urine and CSF Excellent communication, interpersonal, and organizational skills required. Must have the ability to organize and analyze data, as well as prepare technical reports. Must possess strong computational skills, preferably experienced with Softmax, MSD BenchWork, Word, Excel, Power Point, GraphPad Prism Excellent use of judgment and discretion required Extended work hours may be occasionally necessary in order to meet business demands Ability to lift and carry between 1-15 lbs.; Ability to lift up to 50 lbs. overhead with assistance; frequently required to sit, grasp, and use right/left finger dexterity; May be exposed to a cold freezer environment (Freezer temperatures range between -20ºC -196ºC) Must be able to read, write, speak fluently and comprehend the English language Preferred: A solid understanding of current bioanalytical method validation standards Experience supervising or mentoring scientists or technical personnel Previous work experience in GLP or GCLP or CLIA regulatory compliance Precision is required by law in some states or cities to include a reasonable estimate of the compensation range for this role. This compensation range takes into account the wide range of factors that are considered in making compensation decisions including but not limited to: skill sets, experience and training, licensure and certifications, and other business and organizational needs. The disclosed range estimate has not been adjusted for the applicable geographic differential associated with the location at which the position may be filled. At Precision, it is not typical for an individual to be hired at or near the top of the range for their role and compensation decisions are dependent on the facts and circumstances of each case. This role is also eligible for a discretionary annual bonus, health insurance, retirement savings benefits, life insurance and disability benefits, parental leave, and paid time off for sick leave and vacation, among other benefits. Reasonable estimate of the current range: $134,000 USD - $183,000 USD Any data provided as a part of this application will be stored in accordance with our Privacy Policy. For CA applicants, please also refer to our CA Privacy Notice. Precision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status or other characteristics protected by law. © 2020 Precision Medicine Group, LLC If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact Precision Medicine Group at **************************************. It has come to our attention that some individuals or organizations are reaching out to job seekers and posing as potential employers presenting enticing employment offers. We want to emphasize that these offers are not associated with our company and may be fraudulent in nature. Please note that our organization will not extend a job offer without prior communication with our recruiting team, hiring managers and a formal interview process.

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. 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

Responsibilities Peraton Labs delivers world-class cybersecurity, natural language processing, and machine learning research and engineering to government agencies, telecom carriers, utilities and commercial enterprises. Drawing on its Bell Labs heritage, Peraton Labs excels at creating innovative technologies and services to solve challenging and complex problems. We are looking for candidates that have a dual background in software engineering and Chinese language studies with research experience for full-time positions. Candidates will work as part of a team to research, conceive, and develop solutions by applying innovative approaches to solving problems. The Linguist Technical Research Scientist will be expected to: Work under the direction of project managers and senior scientists to design, develop and test software modules related to emerging cyber, data mining, or big data analytics topics. Design, test, and execute web scrapers to collect publicly available information (PAI) Collaborate with teams to ingest, process, and structure collected PAI data, ensuring that any Chinese character encoded data is normalized and searchable Explore, enrich and analyze Chinese data and/or source documents using commercial, academic, open source and custom software tools Develop technical reports, briefings, analytical findings, and other finished project deliverables. Participate in progress briefings and technical exchange meetings; present analytical findings to industry subject matter experts. Qualifications Skills and Experience You Should Possess: 5 years with BS/BA, 3 years with MS/MA, 0 years with PhD Additonal years of significant relevant experience will be considered in lieu of formal education. Ability to solve problems designing and implementing complex systems independently, as well as lead specific technical development efforts. Intermediate Chinese language reading ability Demonstrated software development ability in Python Experience with source control tools such as “git” Proficient at querying databases. SQL and Cypher are a plus Experience in one or more of the following: advanced software programs, natural language processing (NLP), machine learning (ML), querying, automated processes, integration, and evaluation of datasets, software or malware reverse engineering. Experience working with Chinese character encoded data US Citizenship Active Top Secret Clearance Desired Experience: IC Targeter background Peraton Overview Peraton is a next-generation national security company that drives missions of consequence spanning the globe and extending to the farthest reaches of the galaxy. As the world's leading mission capability integrator and transformative enterprise IT provider, we deliver trusted, highly differentiated solutions and technologies to protect our nation and allies. Peraton operates at the critical nexus between traditional and nontraditional threats across all domains: land, sea, space, air, and cyberspace. The company serves as a valued partner to essential government agencies and supports every branch of the U.S. armed forces. Each day, our employees do the can't be done by solving the most daunting challenges facing our customers. Visit peraton.com to learn how we're keeping people around the world safe and secure. Target Salary Range $112,000 - $179,000. This represents the typical salary range for this position based on experience and other factors. EEO EEO: Equal opportunity employer, including disability and protected veterans, or other characteristics protected by law.

BioIVT is a leading global provider of research models and value-added research services for drug discovery and development. We specialize in control and disease-state biospecimens, including human and animal tissues, cell products, blood and other biofluids. Our unmatched portfolio of clinical specimens directly supports precision medicine research, aiming to improve patient outcomes by coupling comprehensive clinical data with donor samples. As the premier supplier of hepatic products, including hepatocytes and subcellular fractions, BioIVT enables scientists to better understand the pharmacokinetics and drug metabolism of newly discovered compounds and their effects on disease processes. By combining our technical expertise, exceptional customer service and unparalleled access to biological specimens, BioIVT serves the research community as a trusted partner in elevating science. Summary Under general guidance the Associate Scientist I will perform manufacturing of products, troubleshoot product issues. Conducts routine functions and duties related to the production and/or characterization of products, as well as laboratory upkeep and drug metabolism-related biomedical research. Duties and Responsibilities · Prepares subcellular fractions from both human and animal tissues, including necropsy procedures, tissue processing and centrifugation. Dilutes and verifies protein concentration of bulk subcellular fractions. · Prepares fresh and/or cryopreserved hepatocytes from both human and animal livers, including necropsy procedures, tissue processing, isolation and plating of cells, maintenance of cultured cells, and cryopreservation of cells. · Manufacture products to meet internal specifications through strict adherence to SOPs. Escalate and assist in making changes to SOP's or work-flow processes. · Administers DEA approved Controlled Substances to humanely euthanize purpose bred laboratory animals. Performs small animal surgery, including organ harvesting. · Performs rodent hepatocyte isolations as a perfusionist. Can isolate rodent hepatocytes from at least 3 mice at a time, with minimal loss of cells. · Independently process intact human livers and tissues and performs all other types of animal hepatocyte isolations from intact animal livers. · Maintains laboratories and equipment, performs minor repairs and troubleshooting on equipment. Maintains laboratory supplies and solutions needed for production. · Completes Batch Record folders, maintains instruments, and equipment logbooks. Executes production related work orders. Requirements · Bachelor's degree (B.S./B.A.) from four-year college or university with 2 years' experience; combination of education and experience. Bachelor's degree in a biological or chemical science field preferred. · Literate and proficient in the use of personal computers and peripheral equipment. Proficient in software programs such as word processing, spreadsheet, and graphics. Ability to learn new software programs. · Ability to work in a team laboratory environment with knowledge or familiarity with scientific terminology. · Utilizes sterile technique. Safe handling of dry ice and liquid nitrogen. · A full-time Monday through Friday workweek with general business hours. This position serves on the On-Call Team and will work rotating weekends and occasionally work evening hours. We offer a comprehensive benefit package for eligible team members, including medical, dental, vision, short-term/long-term disability, life insurance, hospital indemnity and accident insurance. We also provide a generous retirement plan with a company match. Eligible employees enjoy competitive time-off policies and a collaborative environment that promotes growth from within. Enjoy company-sponsored events for the entire team! Join Us! We can't wait to work with you! At BioIVT, we believe that diversity and inclusion are key drivers of innovation and success. We are committed to creating a workplace where everyone feels valued, respected and empowered to bring their unique perspectives to the table. We seek to build a diverse team and encourage applications from people of all backgrounds, experiences and identities. To Learn more about our mission and team culture, click here! BioIVT is an equal opportunity employer. We celebrate diversity and are dedicated to creating an inclusive environment for all employees. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability status, protected veteran status, or any other characteristic protected by law.

Associate Bioanalytical Scientist Salary: $55,000 to $65,000 Are you ready to embark on an exhilarating journey with a team that's passionate about making a difference? Pharmaron is thrilled to invite you to join us as our newest Associate Scientist, Bioanalysis LC-MS! If you're craving a role that offers challenges, growth, and meaningful impact, then this is the opportunity you've been waiting for. Job Overview: Associate Scientist within our Bioanalysis team is a pivotal role which requires a dynamic professional with strong hands on experience working with Sciex LC-MS/MS and working knowledge of FDA and ICH bioanalytical method validation guidelines. You'll have the opportunity to collaborate with co-workers of all levels to maintain efficient day-to-day operations of the laboratory and play a crucial part of advancing our bioanalytical capabilities. Additional tasks: * Responsible for handling and processing of biological samples including competent handling and pipetting technique. * Ensure adequate levels of reference materials, control matrix, and project-specific consumables are available to meet the objectives of the study. * Prepare/review forms and SOPs. * Responsible for general solution preparation. * Sample preparation procedures using extraction techniques including but not limited to protein precipitation, solid phase extraction, and liquid-liquid extraction. * Basic operation and routine maintenance of LC-MS/MS instruments and other general laboratory equipment. * Review analytical run paperwork for completeness and address applicable QC review findings in timely manner. * Responsible for performing various monthly maintenance tasks for basic laboratory equipment. * Assist with laboratory cleaning, inventory of laboratory consumables and ordering activities. * Support experimental troubleshooting, method development, and validation experiments. What We're Looking For: * B.S or MSc in related field with at least 1-2 years experience. * Hands on experience working with Sciex LC-MS/MS * Working knowledge of basic functions of Watson LIMS * Working knowledge of FDA and ICH bioanalytical method validation guideline * GLP and GCP regulations * Solid scientific background, knowledge of chemical composition, structure and properties of substances and of the chemical processes and transformations that they undergo. Why Pharmaron? Pharmaron is a premier service provider for the life sciences industry. Founded in 2004, Pharmaron has invested in its people and facilities and established a broad spectrum of research, development, and manufacturing service capabilities throughout the entire drug discovery, preclinical, and clinical development process across multiple therapeutic modalities, including small molecules, biologics, and CGT products. With over 21,000 employees and operations in the U.S., the U.K. and China. Pharmaron has an excellent track record in delivering R&D solutions to its partners in North America, Europe, Japan, and China. Collaborative Culture: You'll thrive in our inclusive and collaborative environment, where teamwork and innovation go hand in hand. Here, your voice matters, and your contributions make a real impact. "Employees Number One" and "Clients Centered" are the core cultural values at Pharmaron. Our culture, which sets Pharmaron apart from other organizations, has evolved from our deep commitment to our employees, partners and collaborators. Comprehensive benefit package: As part of our commitment to your well-being, we offer a comprehensive benefits package: * Insurance including Medical, Dental & Vision with significant employer contributions * Employer-funded Health Reimbursement Account * Healthcare & Dependent Care Flexible Spending Accounts * 100% Employer-paid Employee Life and AD&D Insurance, Short and Long Term Disability Insurance * 401k plan with generous employer match * Access to an Employee Assistance Program How to Apply: Ready to seize this incredible opportunity? Join us at Pharmaron and be part of a dynamic team driving innovation and excellence in biopharmaceutical research and development. Apply online today! #LI-JB1

Fiber Laser Scientist Herndon, VA While working as a Fiber Laser Scientist at Fibertek, you will lead the design and development, integration, and test of advanced fiber laser systems typically with performance requirements beyond the state-of-the-art. Fibertek is a leader in the design, development, and delivery of advanced laser systems and technologies for military and aerospace applications. Your Job We are looking for and experienced and motivated fiber laser scientist or engineer to join a multi-disciplinary team and lead the design and demonstration of advanced laser systems. Example focus missions include space-based laser communications, lidar for tactical defense applications, earth-sensing lidar, and navigational lidars for planetary and docking missions. Fibertek's engineering teams simultaneously tackle laser optical performance beyond state-of-the-art while engineering systems for performance on challenging platforms with limited size, mass, and power and over stressing vibration, thermal, and/or radiation conditions. Delivered systems make a national impact to customers at NASA and throughout the defense community. The work-load will at times include multiple concurrent projects with a mix of short duration research programs and longer duration technology maturation programs resulting in a work culture that is team-oriented, intellectually stimulating, and consistently rewarding. Lead the engineering development of unique laser designs through modeling fiber laser performance, design analysis, component specification, and hardware assembly, integration, and test Coordinate and support the build, alignment, and performance characterization of fiber lasers including multi-stage amplifiers, phase & amplitude modulation implementation, spectral and coherent beam combining Coordinate and perform formal acceptance and qualification testing Participate in customer interactions including formal technical reviews Required Skills and Experience To exceed in this Fiber Laser Scientist role, you'll need the below expertise and experience: MS or PhD in Physics or Optical Engineering w/ a minimum of 5 years of direct hands-on fiber laser experience including designing, building, characterizing laser systems Knowledge of the laser theory and industry best practices associated with fiber laser systems including continuous wave lasers, pulsed, high peak power fiber, advanced fiber architectures, single-frequency injection locked lasers, low frequency noise lasers, electrical and thermal sub-systems. Expertise in laser physics of fiber lasers and amplifiers, including ytterbium, erbium, and/or thulium gain materials. Familiarity with relevant nonlinear processes and impacts to laser performance. Examples include Stimulated Brillouin Scattering, Four-Wave Mixing, Stimulated Raman Scattering, and Transverse Modulational Instability. Foundational understanding of fiber-optic components including types of fibers, pump lasers, couplers, modulators, isolators, mode-field adapters, polarization components, and others. Knowledge of tools for modeling fiber laser performance such as Matlab, RP Power Fiber or equivalent software Ability to design and execute experiments validating laser system performance and correlate the results with the expected performance Strong communication and documentation skills for efficient multidisciplinary communication US citizenship required Please apply today for this full-time Herndon-based Fiber Laser Scientist role and join the leader in the development of state-of-the-art laser and electro-optic solutions. Why Fibertek, Inc? At FIBERTEK, Inc. we pride ourselves in our innovation and customer success focused culture enabled by a creative and relaxed work environment with minimal bureaucracy. Fibertek fosters a progressive learning environment that values inspiration, promotes professional challenge and encourages personal growth. We offer a competitive and incentivized compensation package with excellent benefits. Fibertek, Inc. is an equal opportunity and affirmative action employer. Applicants are considered regardless of race, sex, gender identity, sexual orientation, religion, national origin, disability, protected Veteran status, age or any other protected characteristic in accordance with applicable law. If you need assistance or an accommodation for any part of the application process, please contact us by phone at ************ or via email at ***************.

US Tech Solutions is a global staff augmentation firm providing a wide-range of talent on-demand and total workforce solutions. To know more about US Tech Solutions, please visit our website ************************ We are constantly on the lookout for professionals to fulfill the staffing needs of our clients, sets the correct expectation and thus becomes an accelerator in the mutual growth of the individual and the organization as well. Keeping the same intent in mind, we would like you to consider the job opening with US Tech Solutions that fits your expertise and skillset. Job Description • BioProcess Engineering (BPE) department is responsible for scale up, tech transfer, and facility fit of clinical and commercial processes to manufacturing. BPE is also responsible for producing development drug substance material and data from pilot facilities. Members of Development Scale-up Center (DSC), within BPE, produce materials up to 500L scale for toxicology and process development studies, to confirm process performance and to troubleshoot issues in GMP facility, and work with cross functional team on technology evaluations. • This position is focused on upstream cell culture and fermentation processes supporting scalability and production of therapeutic proteins in DSC. Position is a hands-on laboratory and production-based role. Responsibilities include but are not limited to media preparations, routine sub-culturing of cells and fermentations. The candidate will assist in adaptation of transferred information for scale-up processes from late stage development to DSC as well as assisting in the production of various tox and development materials, troubleshooting and resolving technical issues with the production processes and/or equipment, identifying root causes for deviations, implementing corrective/preventative actions, assisting in implementing new technologies, and trending/analyzing data. • The candidate will assist in compiling data and expected to summarize and assist in interpreting results. The candidate will also maintain production and laboratory equipment. Qualifications Education: • Bachelor of Science (BS) or Master of Science (MS) in scientific, engineering or related field. Experience: • For the RA, we require a BS with 2 - 5 years or a MS with 0 - 2 years of relevant experience. • For the AS, we require a BS with a minimum of 5 years or MS with a minimum of 2 years of relevant experience. Additional Information Special Skills/ Abilities • Hands on proficiency in cell culture and/or fermentation and good aseptic techniques. Bioreactor/fermenter operation experience is preferred. • Good documentation, writing and communication skills in a team based setting are essential.

Type of Requisition: Regular Clearance Level Must Currently Possess: None Clearance Level Must Be Able to Obtain: None Public Trust/Other Required: NACLC (T3) Job Family: Scientists Job Qualifications: Skills: ADME, High-Performance Liquid Chromatography (HPLC), Mass Spectrometry (MS) Certifications: None Experience: 2 + years of related experience US Citizenship Required: Yes Job Description: GDIT is seeking a Bioanalytical Scientist to support the Walter Reed Army institute of Research's Experimental Therapeutics Branch. This position will support the research and any activities needed to most efficiently advance lead candidate drugs to the next level of testing and ultimately FDA approval.HOW YOU WILL MAKE AN IMPACT: Assist with the development and validation of analytical methods for the identification of candidate new drugs and putative metabolites using HPLC with UV/VIS, radioactive monitor analyses, and/or mass spectrometry as needed. Assist with the characterization of metabolites formation and metabolic profiles of candidate drugs using in vivo and in vitro techniques as needed. Prepare samples to be assayed using both manual and robotic/high-throughput means. Use in vitro techniques (liver microsomes, hepatocytes, slices) to assess for potential metabolism-based drug-drug interactions involving hepatic P450 enzymes. Assist with the design and implementation of cytotoxicity and permeability studies involving the use of cell cultures under aseptic techniques. Maintain and troubleshoot HPLC and mass spectrometry systems, a robotic liquid handling system, and basic pharmacology/toxicology laboratory equipment. Maintain appropriate data records and notebooks. Prepare biological samples for analysis using methods to include tissue homogenization, blood spot filter puncture, and solvent extraction. Conduct ELISA assays in support of pharmacokinetic and biomarker studies. Perform chemical derivatization reactions when required for analyte detection. Conduct in vitro assays using TECAN Liquid Handling systems. Assist in manual tasks including, but not limited to, filling liquid nitrogen dewars and tanks for use in laboratory operations, biohazard disposal, and acquisition/return of gas tanks from the logistics facility. Assist in chemical and supply inventories and laboratory organization as requested. Present novel laboratory findings at a nationally recognized scientific meeting and submit for publication in peer-reviewed journals. Assist with the initiation and tracking of purchase request, and service calls through Medical Maintenance Branch. Comply with all specified guidelines regarding safety, security, standard operating procedures, written protocols, technical manuals, and procurement of supplies/equipment as per WRAIR regulations WHAT YOU'LL NEED TO SUCCEED: BS in Chemistry, Biology, or related field with relevant bioanalytical coursework 2+ years of experience analytical chemistry Working knowledge of HPLC analysis and familiarity with the handling of biological samples. Experience to perform hands-on laboratory ADME assays, such as microsomal metabolic stability, water solubility and cell permeability. Experience with metabolism related studies, along with troubleshooting and basic maintenance of mass spectrometry equipment Experience with basic MS Office (or compatible) software for generating reports and summaries for presentations, managing data spreadsheets, requesting supplies and materiel as needed to perform general laboratory maintenance. Excellent organizational and interpersonal skills as well as good written and oral communication. Must be a US citizen with the ability to obtain a favorable NACI T1 security investigation. WHAT GDIT CAN OFFER YOU: 401K with company match Customizable health benefits packages Internal mobility team dedicated to helping you own your career Challenging work that makes a real impact on the world around you Full-flex work week #GDITHealth#GDITFedHealth#GDITLabScienceJobs#MilitaryHealthGDITJobsThe likely salary range for this position is $52,270 - $66,700. This is not, however, a guarantee of compensation or salary. Rather, salary will be set based on experience, geographic location and possibly contractual requirements and could fall outside of this range. Scheduled Weekly Hours: 40 Travel Required: Less than 10% Telecommuting Options: Onsite Work Location: USA MD Silver Spring Additional Work Locations: Total Rewards at GDIT: Our benefits package for all US-based employees includes a variety of medical plan options, some with Health Savings Accounts, dental plan options, a vision plan, and a 401(k) plan offering the ability to contribute both pre and post-tax dollars up to the IRS annual limits and receive a company match. To encourage work/life balance, GDIT offers employees full flex work weeks where possible and a variety of paid time off plans, including vacation, sick and personal time, holidays, paid parental, military, bereavement and jury duty leave. To ensure our employees are able to protect their income, other offerings such as short and long-term disability benefits, life, accidental death and dismemberment, personal accident, critical illness and business travel and accident insurance are provided or available. We regularly review our Total Rewards package to ensure our offerings are competitive and reflect what our employees have told us they value most.We are GDIT. A global technology and professional services company that delivers consulting, technology and mission services to every major agency across the U.S. government, defense and intelligence community. Our 30,000 experts extract the power of technology to create immediate value and deliver solutions at the edge of innovation. We operate across 30 countries worldwide, offering leading capabilities in digital modernization, AI/ML, Cloud, Cyber and application development. Together with our clients, we strive to create a safer, smarter world by harnessing the power of deep expertise and advanced technology.We connect people with the most impactful client missions, creating an unparalleled work experience that allows them to see their impact every day. We create opportunities for our people to lead and learn simultaneously. From securing our nation's most sensitive systems, to enabling digital transformation and cloud adoption, our people are the ones who make change real.Equal Opportunity Employer / Individuals with Disabilities / Protected Veterans

We are seeking an Associate Scientist II to join our R&D team. The ideal candidate will design experimental plans with guidance, execute experiments, analyze data, generate laboratory protocols, and contribute to technical reports and product summaries. This role involves direct support in cell culture maintenance, media preparation, and operation of bench-scale bioreactors. The candidate will work on problems of moderate scope, troubleshoot issues, and maintain accurate lab records. Additionally, the role requires interaction with internal departments and compliance with all safety and quality regulations. Responsibilities * Design experimental plans with guidance and execute experiments. * Analyze experimental data, generate laboratory protocols, and contribute to technical reports and product summaries. * Provide direct support in maintenance of adherent and suspension cell cultures, media/feed/supplement preparation, and operation of bench-scale bioreactors. * Troubleshoot and solve problems in the design and execution of development projects. * Exhibit creativity in selecting approaches and techniques for obtaining solutions. * Maintain accurate lab notebooks to support protection of intellectual property. * Present data internally and contribute to external publications when appropriate. * Interact with internal departments in the commercialization of new products. * Comply with all company safety, training, and quality regulations and procedures. Essential Skills * Bachelor's degree in Biology, Chemistry, Biochemistry, Biotechnology/Biomedical engineering, or a related field. * 0-2 years of experience in a manufacturing or lab environment. * Proficiency in small scale mammalian cell culture and aseptic technique. * Outstanding problem-solving skills and attention to detail. * Excellent communication and teamwork abilities. * Ability to excel in a fast-paced research environment and deliver detailed results. Additional Skills & Qualifications * Prior industrial experience, particularly in process development and/or cell culture media formulation. * Proficiency in microbiology and virus handling/infectivity techniques. * Knowledge or experience with biocontainment facilities and procedures, laboratory safety, and decontamination. * Experience with statistical experimental design and performance of DOE studies. * Familiarity with operation of bench-top stirred tank bioreactors or fermentation equipment. Work Environment This role is based in an R&D lab with a team of 8 people. You will work closely with the team and provide individual contributions. We are looking for someone who is not afraid to ask questions and actively engage with the team to solve problems. Pay and Benefits The pay range for this position is $35.00 - $35.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: * Medical, dental & vision * Critical Illness, Accident, and Hospital * 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available * Life Insurance (Voluntary Life & AD&D for the employee and dependents) * Short and long-term disability * Health Spending Account (HSA) * Transportation benefits * Employee Assistance Program * Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Hunt Valley,MD. Application Deadline This position is anticipated to close on Mar 31, 2025. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. Diversity, Equity & Inclusion At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through: * Hiring diverse talent * Maintaining an inclusive environment through persistent self-reflection * Building a culture of care, engagement, and recognition with clear outcomes * Ensuring growth opportunities for our people The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

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

Responsibilities Peraton Labs delivers world-class cybersecurity, natural language processing, and machine learning research and engineering to government agencies, telecom carriers, utilities and commercial enterprises. Drawing on its Bell Labs heritage, Peraton Labs excels at creating innovative technologies and services to solve challenging and complex problems. We are seeking a talented Network Security Research Scientist to join our high performing team. Must be able to work onsite five days a week. The Network Security Research Scientist will develop innovative solutions to solve hard, real-world networking problems. You'll take responsibility to accomplish deliverables within a small team setting of fellow engineers and conduct cutting edge network research. Qualifications Required: 2 years with BS/BA; 0 years with MS/MA; 6 years with no degree Python development Hands-on development experience in either cybersecurity, network protocols, and/or network engineering Must have knowledge and skills in the fundamentals of IP and routing technologies. Modern development practices and toolsets (Git, subversion, CI/CD toolchains) Experience running docker containers Experience with networking protocols (BGP, OSPF, etc.) Experience with Wireshark Experience with configuring L2/L3 network devices and their consoles (Cisco IOS, FRR etc.) A passion to learn something new every day and to stay up-to-date with developments in your field Adept at independent problem-solving and comfortable with a general approach of taking initiative to find and develop solutions U.S Citizenship Active Secret Clerance with the ability to obtain TS/SCI Desired: Expertise in one or more: C, C++, and/or Python Ability to grasp the “big picture” and see beyond specific problems Network emulation frameworks including CORE, EMANE, and/or MiniNet Experience with threat intelligence research Advanced network protocols understanding CCNA/CCNP Experience working with Ansible A current TS/SCI Clearance Peraton Overview Peraton is a next-generation national security company that drives missions of consequence spanning the globe and extending to the farthest reaches of the galaxy. As the world's leading mission capability integrator and transformative enterprise IT provider, we deliver trusted, highly differentiated solutions and technologies to protect our nation and allies. Peraton operates at the critical nexus between traditional and nontraditional threats across all domains: land, sea, space, air, and cyberspace. The company serves as a valued partner to essential government agencies and supports every branch of the U.S. armed forces. Each day, our employees do the can't be done by solving the most daunting challenges facing our customers. Visit peraton.com to learn how we're keeping people around the world safe and secure. Target Salary Range $86,000 - $138,000. This represents the typical salary range for this position based on experience and other factors. EEO EEO: Equal opportunity employer, including disability and protected veterans, or other characteristics protected by law.

US Tech Solutions is a global staff augmentation firm providing a wide-range of talent on-demand and total workforce solutions. To know more about US Tech Solutions, please visit our website ************************ We are constantly on the lookout for professionals to fulfill the staffing needs of our clients, sets the correct expectation and thus becomes an accelerator in the mutual growth of the individual and the organization as well. Keeping the same intent in mind, we would like you to consider the job opening with US Tech Solutions that fits your expertise and skillset. Job Description • BioProcess Engineering (BPE) department is responsible for scale up, tech transfer, and facility fit of clinical and commercial processes to manufacturing. BPE is also responsible for producing development drug substance material and data from pilot facilities. Members of Development Scale-up Center (DSC), within BPE, produce materials up to 500L scale for toxicology and process development studies, to confirm process performance and to troubleshoot issues in GMP facility, and work with cross functional team on technology evaluations. • This position is focused on upstream cell culture and fermentation processes supporting scalability and production of therapeutic proteins in DSC. Position is a hands-on laboratory and production-based role. Responsibilities include but are not limited to media preparations, routine sub-culturing of cells and fermentations. The candidate will assist in adaptation of transferred information for scale-up processes from late stage development to DSC as well as assisting in the production of various tox and development materials, troubleshooting and resolving technical issues with the production processes and/or equipment, identifying root causes for deviations, implementing corrective/preventative actions, assisting in implementing new technologies, and trending/analyzing data. • The candidate will assist in compiling data and expected to summarize and assist in interpreting results. The candidate will also maintain production and laboratory equipment. Qualifications Education: • Bachelor of Science (BS) or Master of Science (MS) in scientific, engineering or related field. Experience: • For the RA, we require a BS with 2 - 5 years or a MS with 0 - 2 years of relevant experience. • For the AS, we require a BS with a minimum of 5 years or MS with a minimum of 2 years of relevant experience. Additional Information Special Skills/ Abilities • Hands on proficiency in cell culture and/or fermentation and good aseptic techniques. Bioreactor/fermenter operation experience is preferred. • Good documentation, writing and communication skills in a team based setting are essential.

We are seeking a motivated and detail-oriented Associate Scientist II to join our dynamic R&D team. The ideal candidate will have strong experience in biology, chemistry, biochemistry, or a related field and will be responsible for designing and executing experiments, maintaining cell cultures, and contributing to the commercialization of new products. Responsibilities + Design experimental plans with guidance, execute experiments, analyze experimental data, generate laboratory protocols, and contribute to technical reports and product summaries. + Provide direct support in the maintenance of adherent and suspension cell cultures, media/feed/supplement preparation, and operation of bench scale bioreactors. + Work on problems of moderate scope, requiring evaluation of various factors. + Troubleshoot and solve problems in the design and execution of development projects. + Exhibit creativity in selecting approaches and techniques for obtaining solutions. + Maintain accurate lab notebooks to support protection of intellectual property in accordance with relevant required standards. + Present data internally and contribute to external publications when appropriate. + Interact with internal departments in the commercialization of new products. + Comply with all company safety, training, and quality regulations and procedures. Essential Skills + Bachelor's degree in Biology, Chemistry, Biochemistry, Biotechnology/Biomedical engineering, or a related field with 2 years of experience in a manufacturing/lab environment. + Demonstrated proficiency in small scale mammalian cell culture and aseptic technique. + Outstanding problem-solving skills and attention to detail. + Excellent communication and teamwork abilities. + Ability to excel in a fast-paced research environment and deliver detailed results. Additional Skills & Qualifications + Prior industrial experience, particularly in process development and/or cell culture media formulation. + Proficiency in microbiology and virus handling/infectivity techniques. + Knowledge or experience with biocontainment facilities and procedures, laboratory safety, and decontamination. + Experience with statistical experimental design and performance of DOE studies. + Familiarity with operation of bench-top stirred tank bioreactors or fermentation equipment. Pay and Benefits The pay range for this position is $35.00 - $35.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: - Medical, dental & vision- Critical Illness, Accident, and Hospital- 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available- Life Insurance (Voluntary Life & AD&D for the employee and dependents)- Short and long-term disability- Health Spending Account (HSA)- Transportation benefits- Employee Assistance Program- Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Hunt Valley,MD. Application Deadline This position is anticipated to close on Apr 2, 2025. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. Diversity, Equity & Inclusion At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through: + Hiring diverse talent + Maintaining an inclusive environment through persistent self-reflection + Building a culture of care, engagement, and recognition with clear outcomes + Ensuring growth opportunities for our people The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com (%20actalentaccommodation@actalentservices.com) for other accommodation options.