Chemist Jobs in Largo, MD

Responsibilities - Perform cell-based assays, cell culture (iPSCs, ect) Prepare and submit samples, analyze and report the data, maintain safe and efficient lab operations Assist in design and execution of a variety of lab experiments per program needs Perform biochemical assays such as Western Blotting, Immunocytochemistry, ELISA In vivo based work Qualifications - Degree and lab research experience in cell and molecular biology, biochemistry, immunology, neurobiology or related field. Additional relevant experience for over two years with Bachelor's degree or one year with Master's degree Proficiency in basic laboratory techniques such as pipetting, centrifugation, and basic microscopy is required Experience with biochemical assays such as Western Blotting, Immunocytochemistry, ELISA, and cellular assays is required Experience working with in vivo research models is preferred A team player who also has resilience and is comfortable working in a fast-paced environment Effective communication skills (oral and written).

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.

We are seeking a Senior Analytical Scientist to support the Pilot Bioproduction Facility (PBF) at the Walter Reed Army Institute of Research (WRAIR) in Silver Spring, Maryland. PBF is a one-of-a-kind cGMP-compliant pharmaceutical manufacturing facility engaging in next-generation development for cutting-edge companies and government agencies. The professionals at PBF are engaging in trailblazing endeavors every day. Most exciting, the end products vary, so every year brings multiple opportunities for professional enrichment in original projects. CAMRIS International, LLC, is a dynamic medical research and development firm that achieves innovative solutions to health and development challenges through high-quality, cost-effective programs and research management services. We combine our proven systems with today's most effective, evidence-based best practices. Our core practice areas include vaccine research, development, and production; microbiology and infectious disease research; biodefense; clinical research; global health security; and HIV/AIDS programs. Our employees enjoy a collegial environment where individual contributions matter at all levels. At CAMRIS, you will notably improve the lives of people at home and abroad. Responsibilities Design, execute, and analyze experiments related to mRNA synthesis, purification, and formulation. Develop and optimize mRNA production processes, including IVT (in vito transcription) and downstream processing. Plan and conduct analytical tests for drug development and transfer the methods to CDMO. Collaborate with cross-functional teams, including formulation, analytical, and clinical development, to support the development of mRNA products. Analyze and interpret data and prepare technical reports. Perform IQ/OQ/PQ and maintain lab equipment. Follow safety procedures and good laboratory practice. Monitor and coordinate starting materials, drug substances, and drug product testing activities conducted at the PBF. Oversee method development for drug substances and drug products. Ensure methods are suitable, sufficient and development phase appropriate. Participate in method validation activities: review analytical methods, validation protocols, and reports at the PBF. Coordinate and manage analytical method transfers. Review analytical results and supporting documentation to ensure quality standards are met for release and stability testing of starting materials, drug substances, and drug products. Support analytical characterization activities (i.e., identification of new degradants). Draft and monitor project plans and timelines. Manage and coordinate reference standard supplies. Collaborate with the Quality Assurance department to ensure compliance. Reviews, as required, various technology transfer documentation with regulatory and other appropriate groups. Performs other related duties as assigned. Qualifications BS/MS with 10-12+ years of pharma industry analytical experience working within analytical development/validation. Excellent method development and validation skills and routine analysis. Ability to directly or indirectly manage small teams. Strong preference for an analytical scientist who has used a variety of analytical techniques/instrumentation. Strong preference for an analytical scientist who either has worked within a contract analytical lab working with external clients or has worked within a pharma company that outsourced some analytical work to external CDMOs. Ability to self-manage and take on new tasks. Ability to learn new analytical techniques by hands-on work and review published data. Ability to multi-task and hit project timelines. Excellent oral and written communication skills. Please submit your resume online at *************** CAMRIS is an Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, protected veteran status, disability status, or any other characteristic protected by any applicable federal, state, or local law. CAMRIS offers a comprehensive benefits package, including medical, dental, and vision insurance for individuals and families, FSAs, HSA, life and AD&D insurance, short- and long-term disability, legal services, voluntary hospital indemnity, critical illness and accident insurances, EAP, pet insurance, 401(k) with employer match and Roth option, tuition and professional reimbursement, public transportation support in the DMV area, a referral bonus program, vacation with tenure-based increases, PTO, 11 paid holidays, paid bonding leave, and paid supplemental short-term disability. Employment is contingent upon the successful completion of a Public Trust-level background check, a requirement for this position under an active federal contract. The background check process may include but is not limited to the following: (1) contacting your professional references; (2) verification of previous employment, education, and credentials; (3) a criminal background check; (4) use/abuse of federally controlled substances; and (5) a department of motor vehicle check. Candidates must be prepared to fully complete any required background check questionnaire during initial onboarding.

At our Cell Therapy Analytical Development team, we develop and deliver robust, technologically advanced biological assays to progress cell therapy products from research to commercial stages. Our team supports the end-to-end biological and bioanalytical characterization of cell therapy products, enabling manufacturing processes, formulation, drug product development, and regulatory filings from IND to BLA and beyond. We collaborate closely with analytical quality and several cross-functional teams, including clinical, regulatory, QA, and manufacturing. Accountabilities: • Perform basic lab experiments (e.g., ELISA, cell culture, cell co culture, cytotoxicity assay and/or flow cytometry-based assays). • Carry out sample testing to enable process and product development. • Participate in method development and optimization activities under the guidance of the supervisor. • Make detailed observations, analyze data with minimal supervision. • Maintain laboratory organization and comply with safety protocols. • Present and discuss experimental results at group/project team meetings. • Work in a team-based structure. • Maintain meticulous documentation (eLN, DLIMS). • Exhibit excellent written and oral communication skills. Education & Experience Requirements: Bachelor's degree in Immunology, Cell Biology, Biological Sciences, Biotechnology, or related field with 2-10 years of relevant experience. This role may not be the best fit for PhD-level candidates Proficient with basic immunology techniques is required and must have experience in cell culture and cell-based bioassays. Experience in ELISAs or similar technology platforms for cytokine production. Good time management and organizational skills. Skills Required: • Strong lab experience is required. • Experience in flow cytometry desirable but not required. • Cell Therapy industry experience is preferred. • Must have excellent documentation skills.

Consultant, Scientist Consultant (QC/AS) III, Pharmaceuticals Our growing, mid-sized pharmaceutical client has engaged GForce Life Sciences to provide a Scientist Consultant (QC/AS) to support the client studies of developmental, clinical, and commercial pharmaceutical and related products Duties / Expectations of Role Reviews analytical data, including raw data, of developmental, clinical, and commercial pharmaceutical and related products for accuracy and compliance with the clients GxP requirements. Initiate and monitor stability studies of developmental, clinical, and commercial pharmaceutical and related products tested by contract laboratories. Reviews, enters, and maintains stability data for developmental, clinical, and commercial pharmaceuticals and related products. Create studies in LIMS for multiple projects Enter or review sample test result data in LIMS Assists in technical investigations; enters deviations and investigations into Trackwise Maintain and manage analytical testing documentation, including protocols, reports, and data, in compliance with good documentation practices (GDP) and data integrity standards. Prepare stability reports and summaries for inclusion in INDs, NDAs, and regulatory submissions, ensuring accuracy, completeness, and adherence to regulatory requirements. Use descriptive statistical techniques to organize and summarize data Based on project needs, use statistical analysis techniques to identify patterns and trends Create graphs, profiles, and reports of testing and/or stability data and statistical analysis Required experience: Bachelor's degree in chemistry or related science + 5 years work experience in a GXP environment focused on analytical laboratory testing of pharmaceuticals and related materials Familiarity in GMP environment focused on analytical laboratory testing, including HPLC, Dissolution, etc. Experience with MS Office, especially MS Excel Experience in data review Nice to have • Experience with electronic document management systems - Veeva, CREDO, etc. • Experience with investigation software (Trackwise preferred) Term & Start • 12 month contract, open to 12+ month extension • 2 Video Interviews - Start 2 weeks from an offer • Full time, 40 hours/week • Remote with some travel to Rockville, MD • Benefits included (Medical, Dental, Vision, 401k)

Genex Systems is looking for Research Analytical Chemists to support the Chemistry Laboratory at the Federal Highway Administration (FHWA) Turner-Fairbank Highway Research Center (TFHRC) in McLean, VA. Research projects on highway-related materials, including designing and conducting experiments, analyzing results, and proposing future research goals. This work includes the investigation, analysis, and interpretation of the composition of pavement materials, mainly asphalt and concrete, using spectroscopic techniques (Raman, FTIR, and XRF) Assisting the Laboratory Contract Manager by providing timely feedback on the status of the projects. Helping to publish FHWA reports, peer-reviewed journal manuscripts and conference papers. Developing and presenting results at conferences and professional meetings. Required Qualifications Master of Science in chemistry, materials science, civil engineering or related field Preferred Qualifications Knowledge of pavement materials Experience with spectroscopic techniques, e.g., Raman, X-Ray Fluorescence (XRF) Analysis, Fourier Transform Infrared Spectroscopy (FTIR), and thermogravimetric analysis (TGA) of asphalt binders, as well as other techniques like XRD and ICP.

JRAD has an immediate opening for an Analytical Chemist in Washington DC. Analyzes environmental and/or air samples for Chemical contamination Operates and maintains laboratory equipment (e.g., Gas and Liquid Chromatography, Mass Spectrometers, and performs basic maintenance and checks on common laboratory systems Uses Laboratory Information Management System (LIMS) software for managing analytical data Participates in laboratory proficiency testing activities and maintains QAQC records to include performance charts, control limits, and detection and reporting limits for analytical methods governing use of laboratory instrumentation Maintains operator manuals and procedures, providing training to new staff in the operation and use of Lab equipment and LIMS Meticulously adheres to laboratory procedures, data management practices and safety protocols in accordance with Laboratory Quality Assurance Plans and safety policies/regulations Supports formal audits of laboratory quality control systems and practices, the inspection of safety practices and the review of Job Hazard Analyses Maintains inventory of lab supplies Required Skills and Education: Bachelor's Degree in Chemistry, Biochemistry, or similar, from an accredited college or university More than 3 year of experience with quantitative analysis of chemical compounds, and 2 years' experience with screening environmental samples for toxic industrial compounds (TICs) Must have demonstrated analytical laboratory skills as evidenced by participation in a Proficiency Test such as a Precision and Accuracy performance test or equivalent Must have experience with quality management standards (e.g., ISO 17025 or similar), sample preparation methods, techniques, regulations, protocols, safety measures, and the operation and maintenance of chemical laboratory instrumentation Working knowledge of Microsoft Office products including Excel, Project, Word, Access and Power Point Excellent written and oral communication skills Multiple experience level positions available for Journeyman to Senior level Chemists Minimum of 10 years of experience with a Bachelors Degree, or 6 years of experience with a Masters Degree Security Clearance Ability to obtain and maintain a secret security clearance When you work for JRAD you will never be just a number. We put people before profits! JRAD is committed to the health and well-being of its employees. We offer more paid time off than the average company upon hire, and the following benefits are available to all full-time employees: Health Insurance Dental Insurance Vision Insurance Life & Accidental Death and Dismemberment Insurance Section 125 Flexible Spending Accounts for unreimbursed Medical & Dependent Day Care Disability Insurance 401K Plan Tuition Reimbursement JRAD is an equal opportunity employer as to all protected groups, including protected veterans and individuals with disabilities. Please note this job description in no way states or implies that these are the only duties to be performed by this employee. The employee will be required to follow any other instructions and to perform any other duties requested by the supervisor. The JRAD salary range for this position is a general guideline only and not a guarantee of compensation or salary. There are many factors considered when determining the compensation provided in an offer. These factors include, but are not limited to position responsibilities, education, experience, knowledge, skills, and contract terms and conditions.

Full-time Description OriGene at a Glance: OriGene's greatest asset is our People! We know and understand that employees are the force that pushes our company forward. You might be wondering, then, how is it that our employees know they are valued? We start by respecting a work-life balance. Our leaders are aware and considerate that our employees perform at their best when energized. It is this respect for individuals' time that has contributed significantly to the happiness and innovative spirit of our employees. Every year, we host different events that allow our staff to unwind and get to know their colleagues rather than sitting behind a desk all the time. We do this because we want our company culture to be one of solid teamwork and tolerance for the diverse group that we have here at OriGene. In addition to this, our employees also receive abundant access to learning, development, and mentorship throughout their time and are recognized through annual merit increases and bonuses. Moving towards the future, OriGene has made many significant advancements in maintaining a green workspace. Because labs use four times the energy of a typical office environment, we made many changes to reduce our impact on the environment and ensure the longevity of our home. We hope that future individuals joining our team are not simply able to find a rewarding career but a positive experience to last them a lifetime. About us: OriGene Technologies Inc. is a thriving, reputable, and women-led life science company located in Rockville, MD, guided by a team with a combined 25+ years of experience in the industry. We have grown to have a national and global presence since our foundation in 1996. Although OriGene was created with the end goal of being “Your Gene Company,” we have added to our original initiatives to become the premier source for genomic and proteomic tools to accelerate scientific breakthroughs and novel diagnostics. We exist to serve customers by providing efficient, innovative, and comprehensive solutions for life science researchers. Our customers come to us because we provide high-quality products that contribute to their scientific advancements, and we are proud to be a part of such incredible achievements. Working with OriGene presents an opportunity to further your career aspirations, whether getting a professional certification or gaining tactical experience. Our leaders are committed to the professional growth of our employees because we know that this is the only way the company can continue to grow. We believe that nothing is more important than a diverse and engaged workforce, and we make every effort to display that through our recruitment practices. To learn more about OriGene, view our online presence: · Website · LinkedIn · Glassdoor · Indeed EEOC Statement: OriGene Technologies Inc. is an Equal Opportunity Employer and does not discriminate against any applicant due to any identification within a protected class. Mission: To provide a comprehensive genome, high-quality proteins, and antibodies built upon our proprietary cDNA clone collections through innovation and dedicated customer engagement, one target at a time. Benefits: OriGene provides a robust benefits package to its employees, including medical (prescription drug coverage and access to a comprehensive HealthJoy service), dental, and vision benefits. Our medical plans are supplemented with HSA/FSA (including dependent care) programs. Our Life/ADD, Short and Long-term Disability, and Employee Assistance Programs are fully covered by OriGene. OriGene matches employee contributions to their 401k up to 6%. In addition, OriGene offers a truly flexible working arrangement through 15 personal days every year, 11 holidays, two floating holidays. Requirements The ideal candidate will have an industrial background, with experience in IVD product development and a strong understanding of biotech research markets. A business- and marketing-oriented mindset is essential to align scientific innovation with customer needs and product positioning. In addition to technical responsibilities, this role may support technology transfer, regulatory submissions, and strategic planning in collaboration with other internal departments, including commercial and product management teams. Responsibilities and Job Duties · Contribute to rational protein engineering projects; analyze protein structures and properties to design antigens for antibody and diagnostic reagent development. · Perform recombinant protein expression, purification, formulation, and physical characterization using multiple systems (e.g., E. coli, insect, mammalian). · Support IVD-related product development and ensure compliance with quality and regulatory standards. · Collaborate cross-functionally with antibody, assay, clone, CRISPR, pathology reagent, lentiviral/AAV, and cell therapy R&D teams to drive innovation and expand the product pipeline. · Maintain a strong understanding of emerging science and technologies in the biomedical and diagnostic industries. · Engage in scientific discussions with collaborators and clients to evaluate current products, support ongoing projects, and identify new opportunities. · Develop and optimize SOPs and validation protocols; provide on-site technical guidance and training for research associates. · Communicate with customers to understand and fulfill custom protein and antibody project requirements. · Coordinate with sales, marketing, new product development and technical support teams to promote products, support order fulfillment, and resolve product-related issues. · Prepare and present technical reports, data summaries, and presentations for both internal teams and external stakeholders. · Prepare scientific posters, abstracts, and presentations; represent the company at relevant scientific conferences and industry meetings. · Perform routine maintenance and troubleshooting of lab equipment and instrumentation. Qualifications Education & Experience · Master's degree with 5-8 years of experience, or Ph.D. with 3-5 years of post-graduate experience in biology, biochemistry, molecular biology, or a related life science field. · Industrial experience required; experience with clinical diagnostic product development and regulatory awareness is strongly preferred. · Proven expertise in recombinant protein expression and purification from various heterologous systems (bacteria, yeast, insect, and mammalian). · Skilled in using liquid chromatography systems (e.g., AKTA) and a variety of separation matrices (e.g., SEC, IEX, HIC). · Proven ability to independently troubleshoot protein construct design in order to optimize protein expression and purification using various purification tags (His6, FLAG, MBP, GST, etc.) · Experience with protein formulation and analytical techniques (e.g., analytical SEC, BLI, DSF, ELISA). · Proficiency with structural modeling tools (e.g., PyMOL, Schrödinger, MOE, Rosetta) and structural-based protein engineering. · Familiarity with antibody or cell-based functional assays is a plus. · Practical experience with cell/molecular biology techniques such as PCR, mutagenesis, DNA/RNA extraction, western blotting, aseptic cell culture, and flow cytometry. Knowledge, Skills, and Abilities · Strong analytical and problem-solving skills with the ability to work independently and collaboratively. · Demonstrated success in cross-functional teamwork and project coordination across research, development, and business functions. · Understanding of the biotech market landscape with the ability to align product development with customer needs and business strategy. · Strong organizational and time management skills with the ability to handle multiple complex projects in a fast-paced environment. · Effective communicator with excellent written and oral communication skills; ability to convey technical information clearly to both scientific and non-scientific audiences. Proficient in Microsoft Office tools (Word, Excel, PowerPoint, Outlook) and scientific data analysis tools (e.g., GraphPad Prism, Photoshop, DNAStar). Salary Description $85,000 - $105,000

The company is looking for an amazingly talented Senior TTP Red Cyber Researcher to join our team! In this role you will get to research, identify and creatively think about novel TTPs that can be integrated into red cyber operations. What You'll Be Doing: Think creatively about potential new TTPs and how adversaries might deploy them against DoD targets Support active operations with real-time TTP development against unique targets or network defenses. Adversarial emulation or developing TTPs for offensive cyber operations. What Required Skills You'll Bring: 8+ years of experience total Active TS/SCI Clearance Knowledgeable about adversarial TTPs actively being utilized to ensure adversarial emulation capabilities remain current and relevant to the modern cyber landscape 4+ years' experience working with advanced cyber red teams which include adversarial emulation or developing TTPs for offensive cyber operations. Think creatively about potential new TTPs and how adversaries might deploy them against DoD targets. Additionally, they should be able to support active operations with real-time TTP development against unique targets or network defenses. Must be able to travel 15%- OCONUS and CONUS locations What Desired Skills You'll Bring: Strong industry experiences performing TTP research. Minimum Clearance Required to Start: Top Secret SCI This position is part of our Federal Solutions team. Our Federal Solutions segment delivers resources to our US government customers that ensure the success of missions around the globe. Our employees drive the state of the art as they provide services and solutions in the areas of defense, security, intelligence, infrastructure, and environmental. We promote a culture of excellence and close-knit teams that take pride in delivering, protecting, and sustaining our nation's most critical assets, from Earth to cyberspace. Throughout the company, our people are anticipating what's next to deliver the solutions our customers need now. We value our employees and want our employees to take care of their overall wellbeing, which is why we offer best-in-class benefits such as medical, dental, vision, paid time off, 401(k), life insurance, flexible work schedules, and holidays to fit your busy lifestyle! The company is an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, veteran status or any other protected status. We truly invest and care about our employee's wellbeing and provide endless growth opportunities as the sky is the limit, so aim for the stars! Imagine next and join the quest-APPLY TODAY!

Join Us in Making a Difference in the Lives of Those Defending Our Nation! Why SURVICE? Come join the SURVICE Engineering mission to protect, enhance, and enable those who defend the United States. Since 1981, we have supported the DoD community, as well as Homeland Security, advanced technologies, environmental, and commercial markets. Our employees have backgrounds in engineering, physics, mathematics, chemistry, computer science, acquisition, technical writing, training, and other technical and administrative fields. And many of our personnel have DoD and/or operational military experience. If you're looking for a challenging and rewarding career with a leading organization, come see what we can offer you! Position Forensic/Analytical Chemist * Location: Sterling, Virginia * Security Clearance: Must be able to pass CBP background investigation - U.S. citizenship required * Salary: $59,000 - $68,000 Depending on Experience and Education * Travel: 0% * Benefits: SURVICE Engineering offers a total rewards package to include competitive salaries, comprehensive insurance options, paid time off, 401k, profit sharing, flexible spending, tuition reimbursement. Position Summary SURVICE Engineering is currently seeking a Forensic/Analytical Chemist to support our Aberdeen Research Operation. You will accelerate your career and become an integral team member within the defense community. Primary Duties and Responsibilities * The successful candidate will perform analysis/adjudication of spectra of suspect substances in support of the Department of Homeland Security's (DHS) Customs and Border Protection (CBP) operational mission. * The primary mission is to provide officers/agents with the timely identification of suspect substances from spectra received from field systems. * Outputs may take the form of scientific analysis, reports, required government documents, information, alternatives and opinions. * Reach back analysis support is required 24 hours per day, 7 days per week, 365 days per year. Minimum Qualifications of Forensic/Analytical Chemist Bachelor's Degree in Physical Sciences from an accredited college or university in a physical science or an equivalent combination of education and work experience. Exceptional candidates with less experience will be considered. Candidates are not required to possess all qualifications; if you possess some of the desired qualifications, please apply. * Has successfully completed one semester of organic chemistry and one semester of analytical chemistry. * Familiar with both FTIR and Raman spectroscopy. * Has good written and oral communication skills. * Proficient in MS Word and Excel. * Has basic computer skills. About Us SURVICE Engineering is a nationally recognized, single-source engineering service provider for Government and Industry organizations involved in all phases of the systems engineering process. Our employees are our most valuable asset, and they are proud to have supported the development, testing, analysis, and modeling and simulation (M&S) of many of the major U.S. air, land, and sea combat systems in the field today. They have also contributed their expertise to other vital national defense programs and technologies that involve survivability, cybersecurity, information technology/management, software engineering, unmanned aerial systems (UASs), and metrology/reverse engineering. SURVICE Engineering is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law. VEVRAA Federal Contractor.

What Nuclear Manufacturing contributes to Cardinal Health Nuclear Manufacturing is responsible for the manufacturing of time sensitive radiopharmaceuticals in an integrity driven, highly regulated environment (i.e. FDA, NRC, DOT) to support patient treatment through disease diagnosis, staging, and monitoring. The Material Science and Technology Transfer Chemist, Nuclear Manufacturing position is part of a growing Technical Operations team within Cardinal Health's Nuclear and Precision Health Solutions organization tasked with the development and technology transfer of radiopharmaceutical products into and among our network of qualified manufacturing facilities. This position will be responsible for the adaptation, setup, transfer, training, and maintenance of drug products with strict adherence to cGMP, GDP, environmental health and safety and related guidelines, and internal policies and procedures. Job Summary Specific duties will at a minimum comprise technical evaluation, process and analytical equipment configuration, document creation and technical review, executing method validation, and process qualification, as well as production and testing activities typical for a cGMP pharmaceutical manufacturing operation including but not limited to the preparation of chemicals and components, the operation of production and laboratory equipment, and the execution of standard operating procedures for routine manufacture and testing of radiopharmaceutical products. The preferred individual will possess sufficient technical, functional, and administrative competence to work largely independently, in a team environment, to meet program timelines and occasional production demands. Responsibilities Primary focus in this role delivers on all operational timelines as it relates to the technical transfer project. Secondary focus is day to day support for the manufacturing site or NPHS projects. Executes of timelines, clear accurate communications, maintaining all required qualifications. Completes equipment qualification, computer system validation, and cleaning verification protocols developed in partnership with validations personnel. Leads investigations and document deviations and exceptions occurring during technology transfer. Trains facility personnel on new manufacturing and testing procedures and provide routine production support following completion of technology transfer. Facilitates day-to-day operation and maintenance of production equipment and testing instrumentation. Clean and maintain all production, testing, and related laboratory equipment during technology transfer. Collaborates and partners with cross functional teams. Communicates all issues related to safety, quality, and compliance to leadership. Travels as necessary based on business needs (around 35% travel). Qualifications Bachelor of Science degree or equivalent experience in analytical chemistry/engineering preferred. Strong written and verbal communication. Demonstrated experience in the operation, use, and maintenance of pharmaceutical production equipment and cleanroom facilities preferred. Experience in the manufacture of radiopharmaceutical products preferred. Foundational expertise in the setup, operation, and maintenance of conventional analytical instrumentation (HPLC/GC/TLC/etc.) and modern chromatography data systems preferred. Ability to work in a controlled environment requiring special attention to environmental, health, and safety regulations. Commitment to maintain data integrity through strict adherence to standardized procedures and relevant compliance requirements, including the ability to clearly document all work activities in a timely manner. Motivation to work effectively and cooperatively with others, and to establish and maintain good working relationships. Desire to create, develop, and mature manufacturing and testing processes, and facility and systems infrastructure, to streamline operational efficiency across a broad range of products. Flexibility to work periodic off-shift hours to accommodate routine production schedules among qualified facilities. Prior Authorized User certification is preferred. Nuclear Pharmacy Training can be provided. Ability to lift up to 55 pounds as needed. Travel as necessary based on business needs (around 35% travel). What is expected of you and others at this level Applies working knowledge in the application of concepts, principles and technical capabilities to perform varied tasks Works on projects of moderate scope and complexity Identifies possible solutions to a variety of technical problems and takes action to resolve Applies judgment within defined parameters Receives general guidance and may receive more detailed instruction on new projects Work reviewed for sound reasoning and accuracy Anticipated salary range: $75,600 - $108,000 Bonus eligible: No Benefits: Cardinal Health offers a wide variety of benefits and programs to support health and well-being. Medical, dental and vision coverage Paid time off plan Health savings account (HSA) 401k savings plan Access to wages before pay day with my FlexPay Flexible spending accounts (FSAs) Short- and long-term disability coverage Work-Life resources Paid parental leave Healthy lifestyle programs Application window anticipated to close: 04/12/2025 *if interested in opportunity, please submit application as soon as possible. The salary range listed is an estimate. Pay at Cardinal Health is determined by multiple factors including, but not limited to, a candidate's geographical location, relevant education, experience and skills and an evaluation of internal pay equity. Candidates who are back-to-work, people with disabilities, without a college degree, and Veterans are encouraged to apply. Cardinal Health supports an inclusive workplace that values diversity of thought, experience and background. We celebrate the power of our differences to create better solutions for our customers by ensuring employees can be their authentic selves each day. Cardinal Health is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, ancestry, age, physical or mental disability, sex, sexual orientation, gender identity/expression, pregnancy, veteran status, marital status, creed, status with regard to public assistance, genetic status or any other status protected by federal, state or local law. To read and review this privacy notice click here

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.

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

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.

This position is responsible for manufacturing product by vialing detection/capture antibodies, calibrators, or assembling antibody set products. DUTIES AND RESPONSIBILITIES Responsible for preparing manufacturing records, dilution and blending of anitbody/calibrator materials, assemble vial sets, and printing of labels as instructed by Standard Operating Procedures (SOP) in order to produce final goods products for MSD customers. Performs peer review of product labels prior to vialing as the first quality check in the production process. May operate automated vialing, bottling, labeling, or lyphilizing equipment. May handle BSL-2 reagents to produce calibrator products. Provides input to improve routine manufacturing processes that provide for better quality and quantity of products. Participates in 5S initiatives by maintaining and improving laboratory tidiness and efficiency. Completes appropriate documentation to support process and production procedures including data entry and batch records and daily maintenance and documentation of all production equipment Participates in general laboratory maintenance including maintaining laboratory cleanliness, supplies and equipment to include but not limited to: preparing, maintaining and reporting reagent inventories, maintain pipette calibration schedules, participating in year-end physical inventory, and defrosting freezers. Specific duties may vary depending upon departmental requirements. EXPERIENCE AND QUALIFICATIONS Associate's degree in Biology, Chemistry, Biotechnology, Engineering or related field field or equivalent work experience. Prior manufacturing experience a plus. KNOWLEDGE, SKILLS AND ABILITIES Demonstrates an aptitude for learning and adhering to standard laboratory techniques and safety precautions. Basic knowledge of scientific fundamentals. Basic knowledge of pipetting. Ability to follow laboratory safety instructions; ability to use protective equipment. Excellent oral, written communication and interpersonal skills. Effectively communicate issues/problems and results that impact timelines, accuracy and reliability of laboratory data. Proficiency in MS Office Suite. Ability to multi-task and work productively in a demanding manufacturing environment with changing priorities. Basic knowledge of cGMP and/or ISO certification highly preferred. Ability to utilize equipment necessary to perform the essential duties of the job. Ability to move/lift up to 25 pounds. PHYSICAL DEMANDS Utilize equipment necessary to perform the job, and lifting up to 25 lbs. Up to 80% of the day may be spent at a laboratory bench. WORK ENVIRONMENT Standard industrial laboratory environment COMPENSATION SUMMARY: The annual base salary for this position ranges from $44,300 to $64,300. This salary range represents a general guideline as MSD considers other factors when presenting an offer of employment, such as scope and responsibilities of the position, external market factors, and the candidate's knowledge, skills, abilities, education and experience. Employees may qualify for a discretionary or non-discretionary bonus in addition to their base salary. These annual bonuses are intended to recognize individual performance and enable employees to benefit from the Company's overall success. BENEFITS SUMMARY: At MSD, we offer a comprehensive benefits package to support our employees' well-being and financial security. In addition to competitive salaries, our benefits include medical, dental, and vision coverage, along with prescription benefits. We provide a 401(k) plan with company matching, flexible spending accounts, and company-paid short- and long-term disability insurance as well as group life and accidental death and dismemberment insurance. Our offerings also encompass paid vacation, paid sick leave, paid holidays, and paid parental leave, along with an employee assistance program. Additional voluntary perks include a fitness club membership contribution, pet insurance, identity theft protection, home and auto insurance discounts, and optional supplemental life insurance. EEO/AA STATEMENT: MSD is an Equal Opportunity/Affirmative Action Employer. We are committed to fostering a diverse and inclusive workplace where all individuals are treated with respect and dignity. We welcome applications from all qualified candidates, making employment decisions without regard to race, color, religion, creed, sex, sexual orientation, gender identity, genetic information, marital status, national origin, age, protected veteran status, pregnancy, disability status, or any other protected characteristic. For our full EEO/AA and Pay Transparency statement, please click on the following link: https://www.mesoscale.com/en/our_company/careers/equal_employment_opportunity_statement. Meso Scale Diagnostics uses E-Verify to validate the work eligibility of candidates.

**Who Are We?** Taking care of our customers, our communities and each other. That's the Travelers Promise. By honoring this commitment, we have maintained our reputation as one of the best property casualty insurers in the industry for over 160 years. Join us to discover a culture that is rooted in innovation and thrives on collaboration. Imagine loving what you do and where you do it. **Job Category** Product **Compensation Overview** The annual base salary range provided for this position is a nationwide market range and represents a broad range of salaries for this role across the country. The actual salary for this position will be determined by a number of factors, including the scope, complexity and location of the role; the skills, education, training, credentials and experience of the candidate; and other conditions of employment. As part of our comprehensive compensation and benefits program, employees are also eligible for performance-based cash incentive awards. **Salary Range** $79,400.00 - $130,900.00 **Target Openings** 1 **What Is the Opportunity?** Product Development teams play a critical role in the achievement of Travelers financial objectives (growth, profit & retention) for one or more insurance products through the development, implementation and monitoring of product strategies and corresponding actions. As a Sr Analyst, Product Development, you will assist and implement analysis and evaluation of existing market and new product opportunities that deliver product development and product enhancements to the marketplace. In this role you will implement existing and new product solutions including monitoring and evaluating product performance and action plans. **What Will You Do?** + Execute and enhance existing product strategies and actions by collaborating and communicating with business unit stakeholders and management to achieve financial objectives. + Conduct high level market, competitor, and consumer research analysis to identify and recommend new products, markets and services or enhance existing ones. + Identify potential opportunities through root cause analysis and propose solutions. + Understand and assist with developing and implementing system and process solutions that align with the product's strategy. + Execute product enhancement work including launch and rollout plans related to established product strategies and action plans. Ensure strategies and plans address compliance needs and regulatory requirements. + Perform analysis by accessing and utilizing data to update recommendations on new or existing products. When appropriate, partner with data analytic teams to build support for recommendations. + Develop communication, training, and marketing materials in support of new or enhanced products and initiatives and may deliver training to stakeholders when appropriate. + Support the post implementation monitoring and measurement mechanisms for product strategies and initiatives in support of outlined success criteria. + Perform other duties as assigned. **What Will Our Ideal Candidate Have?** + Bachelor's Degree. + Three years of product development experience preferably in the financial services industry. + General knowledge of underwriting, coverage, rules, compliance/regulatory environment, and insurance financials. + Ability to think strategically and use judgment to resolve issues as they arise. + Strong data analysis skills with the ability to interpret trends and provide insights and recommendations to business partners. + Excellent communication skills with the ability to consult and present information effectively. + Experience working on cross-functional teams. + Have strong innovation skills including thinking critically about multiple perspectives and approaches to solving problems. + Demonstrated ability to interact and across levels and organizations, including consensus and team building. **What is a Must Have?** + Bachelor's Degree or equivalent combination of education and experience. + Two years of relevant experience with understanding and knowledge of insurance products. **What Is in It for You?** + **Health Insurance** : Employees and their eligible family members - including spouses, domestic partners, and children - are eligible for coverage from the first day of employment. + **Retirement:** Travelers matches your 401(k) contributions dollar-for-dollar up to your first 5% of eligible pay, subject to an annual maximum. If you have student loan debt, you can enroll in the Paying it Forward Savings Program. When you make a payment toward your student loan, Travelers will make an annual contribution into your 401(k) account. You are also eligible for a Pension Plan that is 100% funded by Travelers. + **Paid Time Off:** Start your career at Travelers with a minimum of 20 days Paid Time Off annually, plus nine paid company Holidays. + **Wellness Program:** The Travelers wellness program is comprised of tools, discounts and resources that empower you to achieve your wellness goals and caregiving needs. In addition, our mental health program provides access to free professional counseling services, health coaching and other resources to support your daily life needs. + **Volunteer Encouragement:** We have a deep commitment to the communities we serve and encourage our employees to get involved. Travelers has a Matching Gift and Volunteer Rewards program that enables you to give back to the charity of your choice. **Employment Practices** Travelers is an equal opportunity employer. We value the unique abilities and talents each individual brings to our organization and recognize that we benefit in numerous ways from our differences. In accordance with local law, candidates seeking employment in Colorado are not required to disclose dates of attendance at or graduation from educational institutions. If you are a candidate and have specific questions regarding the physical requirements of this role, please send us an email (*******************) so we may assist you. Travelers reserves the right to fill this position at a level above or below the level included in this posting. To learn more about our comprehensive benefit programs please visit ******************************************************** .

Under minimal supervision of QC management, the QC Chemist performs physical and chemical testing on raw materials, in-process and finished products, as well as stability samples. Utilizes established methods and standard operating procedures and laboratory equipment to perform testing of materials. Prepares high quality written documentation, such as notebooks, logbooks, standard operating procedures (SOPs) and LIMS reports. Trouble shoots analytical equipment. Provides training on analytical methods and new technologies. Responsibilities: Performs analytical testing of raw materials, in-process materials, finished products and stability samples. Operates laboratory equipment such as balances, pH meters, hardness testers, particle size analysis, LOD, Karl Fischer, Melting Point, etc. in accordance with laboratory SOPs and test methods. Effectively performs routine testing using HPLCs, GCs, UV-VIS, FT-IR and ICP-MS equipment in accordance with SOPs and test methods. Performs data analysis and evaluation of test results. Prepares reports and reviews data. Maintains accurate records of test data, maintains laboratory notebooks and logbooks in accordance with company guidelines and GDPs. Assists in writing and revising SOPs and tests methods as needed. Follows documented procedures: SOPs, test methods, and transfer protocols. Performs routine maintenance, calibration, and performance verification on applicable instruments. Performs investigation activities and writes deviation and investigation reports. Suggests and writes CAPAs. Follows lab safety procedures. Perform other duties as assigned. Qualifications: Bachelors in chemistry or related physical/biological science, or equivalent combination of education, training and professional experience that provides the individual with the required knowledge, skills, and abilities. Minimum of 3 years' experience in Pharmaceutical Analysis Must understand analytical chemistry. Demonstrated knowledge of cGMP regulations and ICH guidelines Computer literacy and ability to use data acquisition and processing software, such as EMPOWER 3 Demonstrate the ability to read, analyze, and interpret USP/NF methods, SOPs and technical procedures manuals, and batch records. Demonstrate the ability to define problems, collect data, establish facts, and draw valid conclusions; interpret an extensive variety of technical instruction in mathematical or diagram form. Knowledge of basic laboratory practices, methods, and techniques Demonstrate the ability to carry out work assignments communicated orally or in writing. Demonstrate the ability to establish good working relationships with other departments, including vendors, colleagues, and subordinates. Demonstrate the appropriate technical knowledge necessary to make sound decisions on development issues with minimal supervision. Demonstrate the ability to analyze data and information and assess and resolve complex problems/issues as required. Must be able to comprehend and follow all applicable SOPs. Demonstrate knowledge and experience with electronic Quality Management Systems such as MasterControl and Trackwise. Demonstrate solid understanding of the current federal, local, and international regulations regarding the production, testing, and release of drug substances and products. Good understanding of cGMPs, industry, and regulatory standards and guidelines. Demonstrate familiarity with Microsoft programs like Word, Excel, PowerPoint, Project, Teams, Outlook, etc. Demonstrate the ability to portray the appropriate level of integrity and professionalism. Demonstrate the ability to communicate effectively with management, staff, regulators, and client representatives in written and verbal formats. Demonstrate the ability to complete tasks accurately and according to established and shifting timelines. Demonstrate the ability to make quality scheduling, resource allocation, and priorities decisions. Energetic, execution-focused, self-motivated, and organized individual who is accustomed to working in a deadline-focused, high-pressure entrepreneurial environment. Results-oriented and efficient. Creative and open-minded who fosters an environment in which sharing of ideas is encouraged. Demonstrate the ability to work closely with a diverse customer and employee base (internally and externally). Demonstrate the ability to work well in a cross-functional team environment. Must communicate fluently in English and have legible handwriting. Physical Demands: Ability to travel between and within facilities to visit staff, operations, and projects, as needed. Ability to sit, stand, climb stairs, and climb ladders to mezzanines (when necessary). Ability to lift up to 40 pounds on occasion. Ability to use PPE (safety shoes, goggles, respirators, gloves, etc. when necessary).

Cervello Global Corporation is looking for a Chemical, Biological, Radiological, and Nuclear (CBRN) Analyst specializing in tactical vehicle capabilities to support the US Marine Corps Capabilities Development Directorate (CDD) Technical and Operational Support Services (TOSS) Place of Performance is at the Marine Corps Base in Quantico Virginia. JOB DUTIES / EXPERTISE: CBRN Defense Branch General Support: Develop military-based concepts and capabilities. Conduct collaborative assessment and facilitation using decision support tools. Research and analyze to develop position papers on new and existing CBRN Defense guidance. Provide detailed trip reports for all CBRN-related travel. CBRN Acquisition Analysis: Provide comment resolution matrices and information papers. Contribute to Joint and service requirements documents (e.g., ICD, CDD, DOTMLPF&C Change Requests). Identify capability gaps and document implications on USMC CBRN tactics, techniques, procedures, doctrine, and logistics. CBRN Defense Force Development Support: Review and provide recommendations for the Marine Corps Force Development Process. Support Campaign of Learning activities, Capabilities Based Assessment process, and Programming Budgeting and Execution processes. CBRN Defense SharePoint Management: Update CBRN documentation and knowledge on the CBRN Branch SharePoint website. CBRN Defense TFSMS Support: Use the Total Force Structure Management System (TFSMS) to document and codify CBRN defense impacts to the force.

Job Code **4813** \# of Openings **1** Apply Now (**************************************************** Requisition?org=GATEWAYVENT&cws=55&rid=4813) **Eagle Harbor, LLC** , a subsidiary of Three Saints Bay, LLC, and a Federal Government Contractor industry leader is seeking an **Entry-level Chemists** to support our client in Dulles, VA. Position is on-site five days a week. **Responsibilities:** + Prepare routine solutions and reagents. + Perform reliability testing. + Prepare internal standard, calibration and quality control solutions. + Operate laboratory instrumentation for the collection of data in support of performance verification, method validation, and reference material verification. + Perform qualitative and quantitative method validations. + Conduct inventory of reference materials, stockpiles, chemical and stock solutions and laboratory equipment. + Conduct instrument performance checks and maintenance. + Verify reference materials. + Conduct stockroom supply inventory. + Restock the supply room. + Submit supply order requests. + Clean and level balances + Conduct balance calibration checks. + Daily cleaning and distribution of laboratory glassware **Requirements:** + Must be a US Citizen. + Must be able to pass Agency Clearance. + Must be able to pass pre-employment background check. + Prior work in a chemical laboratory setting working with quantitative/qualitative chemical analysis. **Minimum Educational Requirement** : + Successful completion of 2 years of study that included at least 12 semester hours in any combination of courses such as physical science, or any branch of mathematics, except financial and commercial mathematics. **OR** **Combination of Education and Experience:** + Equivalent combinations of education and experience may be combined to meet the total qualification requirements. + Recent college graduates are encouraged to apply. **PHYSICAL DEMANDS:** + The work requires some physical exertion, such as regular walking or bending. In many situations the duration of the activity (such as most of a workday) contributes to the arduous nature of the job. **TRAINING:** + Physical science technicians are required to attend 16 hours of training annually. + Travel may be anticipated to attend training. **Position is located in Dulles, VA** **Salary is $55,000.00** **Apply at:** ***************************************************** Requisition?org=GATEWAYVENT&cws=69&rid=4813** VEVRAA Federal Contractor Three Saints Bay, LLC and its subsidiaries offer a team-oriented working environment and the opportunity to work with exceptional, dedicated industry professionals. We offer our employees a comprehensive benefits package and the opportunity to take part in exciting projects with government and commercial clients, both domestic and international. We are an Equal Opportunity Employer. We invite resumes from all interested parties without regard to race, color, sex, sexual preference, religion, creed, national origin, age, genetic information, marital or veteran status, disability, or any other category protected by federal, state, or local law.