Chemist jobs in Dundalk, MD - 95 jobs

The Field Chemist facilitates Lab Pack Program, Household Hazardous Waste (HHW), and other field activities by providing field services for customers on their site, including the characterization, packaging, handling, and transportation of wastes. Incumbent maintains safety, meticulous attention to detail, profitability and efficiency. Principle Responsibilities Provides Lab Packing services at customer sites maintaining compliance with applicable regulations and with established company procedures. Samples and characterizes hazardous and non-hazardous waste. Generates waste profiles into end-user facility. Performs price quotes for customer. Provides customer with detailed inventory of waste on site. Transports wastes from customer sites to end user or transfer facility. Generates required internal paperwork in order to provide accurate and timely customer service and invoicing. Help to off load waste at end user facility. De-packs and consolidates waste. Provides technical support. We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to ********************.To learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy: **************************************************** Skills and Requirements 2+ years experience in field chemist role OSHA 40 HAZWOPER Separation ion of hazardous waste Science Degree (chemistry, biology or environmental science)

JRAD has an immediate opening for an Analytical Chemist in Washington DC. J 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.

Job DescriptionDescription: The Analytical Chemist plays a fundamental role in Sterilex R&D by enabling New Product Development and Product Stewardship initiatives. This role is responsible for developing and validating new analytical methods to support new product development and manufacturing quality control processes. The ideal candidate has experience with basic wet chemistry quality control methods, analytical chemistry instrumentation, method development, statistics, and validation of those methods under Good Laboratory Practices. The candidate works closely with R&D Formulation Chemists and key contacts in Operations. This position is regularly scheduled to be staffed Monday through Friday, 8:30 a.m. to 5:00 p.m. with occasional overtime as needed to support department and company business needs. KEY RESPONSIBILITIES 1. Analytical Chemistry Method Development & Validation Improve existing analytical methods and develop new methods to support new product development and product stewardship initiatives. Validate and maintain the portfolio of current analytical methods utilized in Sterilex chemistry labs. 2. R&D Product Stewardship & Technical Support Lead initiatives to support existing products, such as qualification of new and equivalent raw materials or locally sourced raw materials in new geographies. Identify key raw material characteristics, contaminants, unreacted byproducts, etc. using sound analytical techniques. Conduct and/or oversee GLP chemical characterization studies of current or in-development products Serve as GLP study director or sponsor as needed in studies supporting regulatory approval. Respond to field / customer technical support inquiries as needed. 3. Quality Control Method Transfer & Support Lead or co-lead the qualification of manufacturing QC procedures, specifications and processes. Provide on-going support of manufacturing QC methods & quality control troubleshooting, working jointly with Sterilex Operations. Identify cost effective and relatively simple analytical methods for co-packers, especially for critical chemical components in raw materials and finished goods. 4. Analytical Chemistry Laboratory Quality Management & Operations Work jointly with QA to maintain the analytical chemistry lab quality program in full compliance with Sterilex QMS practices Develop, implement, and maintain laboratory safety protocols, ensuring compliance with all laboratory safety rules and regulations. Oversee regular maintenance as well as scheduling and execution of annual preventative maintenance/calibrations of Sterilex analytical instruments within chemistry and analytical labs Identify analytical equipment gaps for the Sterilex laboratory with the ability to propose cost effective equipment solutions. Identify and cooperatively manage third-party analytical lab relationships when outsourcing is required. 5. Uphold R&D Process Rigor & Foster Talent Development Conduct and oversee essential training of new technician hires Use experience to propose improvements to R&D processes and contribute innovative ideas for product improvements and new product concepts. Prepare and present written and oral reports on research findings, project status, literature reviews, and technical issues that affect the business. Survey scientific literature to remain current with developments and stay abreast of current trends, practices, regulatory changes that would impact Sterilex products. Interface effectively with Sterilex scientific, business development, and management staff to understand Sterilex markets, innovation and product development goals. Document and protect intellectual property by maintaining laboratory notebooks and timely completion of other patent-related documentation. Adhere to Sterilex's Stage Gate and Quality Management processes, use of associated tools, and documentation of research, project status, recommendations, and decisions made. Requirements:QUALIFICATIONS · Education: B.S. or M.S. degree in Chemistry or related degree from an accredited college or university. Ideally a degree is in Analytical Chemistry and/or with an emphasis on Analytical Chemistry. · Experience: 5+ years of independent research or development experience in an academic or industrial analytical chemistry or QC laboratory setting Moderate+ experience with chromatographic (HPLC, GC) and spectroscopic (MS, UV/Vis) analytical techniques and basic wet chemistry methods (titrations, pH, surface tension measurements, foam tests, etc.) In-depth working knowledge of analytical method development, method transfer, and method validation. Experience working in a Good Laboratory Program (GLP) environment and validation of methods under GLPs. · Skills: Ability to draw scientifically supportable conclusions and recommendations, and develop follow-up experiments as appropriate. Demonstratable organizational skills and ability to maintain a clean and orderly working environment Demonstrate ability to understand chemical interactions and reactions and propose analytical methods to confirm. Utilize industry standard statistical software and methods when reporting results. Ability to execute written procedures and experiments with minimal supervision. · Key Competencies: Ability to recognize inconsistencies in data and execute corrective actions in consultation with R&D management to mitigate issues Understanding of industrial laboratory processes and procedures including proper maintenance of laboratory notebooks and general laboratory safety procedures Ability to read, comprehend and follow documents, including standard operating procedures, test methods, safety rules and regulations, and instrument operating and maintenance instructions. Motivated to take full ownership of assigned tasks Competent to prepare and carefully review figures, computations, tests, reports, etc., and ensure internal consistency. Good written and oral communication skills and effective interpersonal skills Computer literate: MS Office, statistical software, programs to operate equipment, other related software, email etc. Ability to work independently, multi-task and balance priorities

Full-time Description The Analytical Chemist plays a fundamental role in Sterilex R&D by enabling New Product Development and Product Stewardship initiatives. This role is responsible for developing and validating new analytical methods to support new product development and manufacturing quality control processes. The ideal candidate has experience with basic wet chemistry quality control methods, analytical chemistry instrumentation, method development, statistics, and validation of those methods under Good Laboratory Practices. The candidate works closely with R&D Formulation Chemists and key contacts in Operations. This position is regularly scheduled to be staffed Monday through Friday, 8:30 a.m. to 5:00 p.m. with occasional overtime as needed to support department and company business needs. KEY RESPONSIBILITIES 1. Analytical Chemistry Method Development & Validation Improve existing analytical methods and develop new methods to support new product development and product stewardship initiatives. Validate and maintain the portfolio of current analytical methods utilized in Sterilex chemistry labs. 2. R&D Product Stewardship & Technical Support Lead initiatives to support existing products, such as qualification of new and equivalent raw materials or locally sourced raw materials in new geographies. Identify key raw material characteristics, contaminants, unreacted byproducts, etc. using sound analytical techniques. Conduct and/or oversee GLP chemical characterization studies of current or in-development products Serve as GLP study director or sponsor as needed in studies supporting regulatory approval. Respond to field / customer technical support inquiries as needed. 3. Quality Control Method Transfer & Support Lead or co-lead the qualification of manufacturing QC procedures, specifications and processes. Provide on-going support of manufacturing QC methods & quality control troubleshooting, working jointly with Sterilex Operations. Identify cost effective and relatively simple analytical methods for co-packers, especially for critical chemical components in raw materials and finished goods. 4. Analytical Chemistry Laboratory Quality Management & Operations Work jointly with QA to maintain the analytical chemistry lab quality program in full compliance with Sterilex QMS practices Develop, implement, and maintain laboratory safety protocols, ensuring compliance with all laboratory safety rules and regulations. Oversee regular maintenance as well as scheduling and execution of annual preventative maintenance/calibrations of Sterilex analytical instruments within chemistry and analytical labs Identify analytical equipment gaps for the Sterilex laboratory with the ability to propose cost effective equipment solutions. Identify and cooperatively manage third-party analytical lab relationships when outsourcing is required. 5. Uphold R&D Process Rigor & Foster Talent Development Conduct and oversee essential training of new technician hires Use experience to propose improvements to R&D processes and contribute innovative ideas for product improvements and new product concepts. Prepare and present written and oral reports on research findings, project status, literature reviews, and technical issues that affect the business. Survey scientific literature to remain current with developments and stay abreast of current trends, practices, regulatory changes that would impact Sterilex products. Interface effectively with Sterilex scientific, business development, and management staff to understand Sterilex markets, innovation and product development goals. Document and protect intellectual property by maintaining laboratory notebooks and timely completion of other patent-related documentation. Adhere to Sterilex's Stage Gate and Quality Management processes, use of associated tools, and documentation of research, project status, recommendations, and decisions made. Requirements QUALIFICATIONS · Education: B.S. or M.S. degree in Chemistry or related degree from an accredited college or university. Ideally a degree is in Analytical Chemistry and/or with an emphasis on Analytical Chemistry. · Experience: 5+ years of independent research or development experience in an academic or industrial analytical chemistry or QC laboratory setting Moderate+ experience with chromatographic (HPLC, GC) and spectroscopic (MS, UV/Vis) analytical techniques and basic wet chemistry methods (titrations, pH, surface tension measurements, foam tests, etc.) In-depth working knowledge of analytical method development, method transfer, and method validation. Experience working in a Good Laboratory Program (GLP) environment and validation of methods under GLPs. · Skills: Ability to draw scientifically supportable conclusions and recommendations, and develop follow-up experiments as appropriate. Demonstratable organizational skills and ability to maintain a clean and orderly working environment Demonstrate ability to understand chemical interactions and reactions and propose analytical methods to confirm. Utilize industry standard statistical software and methods when reporting results. Ability to execute written procedures and experiments with minimal supervision. · Key Competencies: Ability to recognize inconsistencies in data and execute corrective actions in consultation with R&D management to mitigate issues Understanding of industrial laboratory processes and procedures including proper maintenance of laboratory notebooks and general laboratory safety procedures Ability to read, comprehend and follow documents, including standard operating procedures, test methods, safety rules and regulations, and instrument operating and maintenance instructions. Motivated to take full ownership of assigned tasks Competent to prepare and carefully review figures, computations, tests, reports, etc., and ensure internal consistency. Good written and oral communication skills and effective interpersonal skills Computer literate: MS Office, statistical software, programs to operate equipment, other related software, email etc. Ability to work independently, multi-task and balance priorities

Analytical Chemist I Duration: 12+ Months Contract Total Hours/week: 40.00 1st Shift: Work days/hours: M - F 8:30am -- 5pm Client: Medical Device Company Employment Type: Contract on W2 (Need US Citizens Or GC Holders Only) No H1B's Onsite daily Description: Work within a team to provide Analytical Chemistry support to our customers using various analytical instruments and techniques. Develop and follow protocols for analytical testing and reporting results following current good laboratory practices. Duties And Responsibilities: 1. Develop, follow protocols and perform analytical testing using wet chemistry analysis, UV/VIS Spectroscopy, UPLC/MS, FTIR, ICP-MS and other techniques as required. 2. Use office and instrumentation specific computer software. 3. Perform tasks according to existing protocols, applying basic scientific principles to assigned tasks, developing experiments and documenting the performed work as required. 4. Identify and troubleshoot problems, collect and record data, report data. 5. Participate in technical meetings and data reviews. 6. Make sure Lab supplies are properly ordered, labeled, and stored. 7. Make sure required safety and other training is completed and training records are maintained according to department policies. 8. Perform laboratory work and documentation in accordance with GLP and company guidelines. 9. Perform tasks under general supervision. Qualifications: Knowledge And Skills: • Basic understanding in the use of liquid chromatography systems. • Basic understanding of chromatography theory and hands-on experience with HPLC or UPLC. • Excellent verbal and written communication skills are necessary together with the ability to interact effectively in team and cross-functional environments. • Understanding of GLP laboratory guidelines. • Optional experience includes the use of UPLC/MS using Empower software, FTIR and ICP-MS. • Experience in method development. Education And Experience • Minimum of a Bachelor's degree in Chemistry, Biochemistry, Biology or related discipline. • Prefer a minimum of 1 year of industrial or academic experience in Analytical Chemistry testing.

Exploit Developer/Vulnerability Researcher Key Requirements: Deep experience in Linux kernel development and reverse engineering Strong background in C/C++, Assembly, and Python Expertise with tools like IDA Pro, Ghidra, and Binary Ninja Solid understanding of SELinux, AppArmor, and modern exploit mitigations (ASLR, DEP, etc.) Prior OCO/CMF support preferred 10+ years of experience

MacroGenics is a leader in the discovery and development of innovative medicines that utilize our next generation antibody-based technologies.  Our team of 350+ dedicated individuals is advancing a pipeline of product candidates to treat patients with cancer. Our products and platforms have attracted multiple partnerships with leading pharmaceutical and biotechnology companies around the globe. The Company considers its employees to be its most valuable asset and we are committed to providing opportunities for individuals to learn and grow as a means to further their professional development. MacroGenics' corporate culture promotes an atmosphere of innovation, open communication and teamwork where employees can see firsthand how they contribute to the success of the organization. Summary of Position As a member of the Protein Science team, this individual will set up transfections to express proteins in mammalian cells followed by their purification and characterization to support the Biologics discovery pipeline. Job duties Culture of mammalian cells in suspension following aseptic techniques and cell-line specific protocols. Transient transfection of cell lines or expansion of stable cell pools, from 3 ml - 10 L scale, to express proteins of interest. Monitor and optimize culture conditions to maximize protein quality and expression. Protein purification from milligram to gram scale using semi-automated FPLC systems. Analytical characterization of purified proteins to support research projects for drug discovery. Collect, analyze, and summarize experimental data in electronic lab notebook for archiving and sharing. Maintain lab and lab equipment in optimal functioning condition. Report any problems to supervisor. Qualifications: Education/Experience Associate Scientist II Bachelor's degree in Biology or Biochemistry or a related field of study with a minimum of 2 years of bench-related experience Scientist I Bachelor's degree in Biology or Biochemistry or a related field of study with a minimum of 3 years of bench-related experience or Master's degree in Biology or Biochemistry or a related field of study. Laboratory experience gained through undergraduate coursework, graduate research, or an internship is required. A minimum of 1 year of bench-related experience, strongly preferred. Knowledge, Skills and Abilities Experience with mammalian cell culture, transfections, maintaining cell lines, etc. with meticulous sterile technique and lab practices. Experience with recombinant protein purification and analytical characterization (CE or SDS-PAGE, SEC). Experience with experimental design and execution with minimal supervision. Experience with standard lab software for data analysis (MS Excel, Prism, etc.). Good organizational skills and ability to multi-task. Good verbal and written communication skills. Demonstrated ability to work in a collaborative environment with other team members. Willingness to work on occasional weekends. Preferred Experience Experience with antibody purification using automated FPLC system. Experience with quantitative assays (BLI Octet, ELISA, etc.). Supervisory Responsibilities: None Additional Information The annual rate of pay for the Associate Scientist II position ranges from $67,200 - $102,500. The annual rate of pay for the Scientist I position ranges from $84,400 - $128,800. For non-exempt roles, and according to applicable regulations, there may be the possibility for overtime pay. This role is eligible for the Company's discretionary bonus and discretionary equity incentives. Eligible employees may participate in the Company's benefits programs, including medical / dental / vision / prescription coverage, employee wellness resources, 401(k) plan with employer match, access to an Employee Stock Purchase Plan, (ESPP), paid time off & paid parental leave benefits, and disability benefits. The annual pay rate range is described in good faith, and the Company believes is the range of possible compensation for this role at the time of this posting depending on the candidate's experience, qualifications, geographic location, and other factors permitted by law. The Company may ultimately pay more or less than the posted range, and this range may be modified in the future. No amount is considered to be wages or compensation until such amount is earned, vested, and determinable under the terms and conditions of the applicable policies and plans. The amount and availability of any bonus, commission, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole discretion unless and until paid and may be modified at the Company's sole discretion, consistent with the law. Statement MacroGenics is proud to be an equal opportunity employer. Employment selection and related decisions are made without regard to race, color, national origin, sex, gender identity, sexual orientation, religion, age, disability, protected veteran status, or any other characteristic protected by federal, state or local law. We are committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the employment process, please email ******************** or call ************** and/or 711 for TTD/TTY service. Equal Opportunity Employer/Veterans/Disabled We do not accept non-solicited resumes or candidate submittals from search/recruiting agencies.

Work Your Magic with us! Start your next chapter and join MilliporeSigma. Ready to explore, break barriers, and discover more? We know you've got big plans - so do we! Our colleagues across the globe love innovating with science and technology to enrich people's lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us. This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US. Your Role: At MilliporeSigma, as a Scientist 2 - Analytical Development, you will be the primary scientific resource for a given study with the Product Characterization Laboratory in our Biologics department. The Scientist will act as subject matter expert in analytical method development/validation and feasibility/transfer for testing required to manufacture clinical and commercial products. * Understand GMP requirements for validation/transfer and documentation * Act as subject matter expert (SME) in analytical methods and provide guidance to analysts and study managers. * Apply laboratory techniques and skills to complete experiments designed to address a variety of specific problems. * Lead development/validation and feasibility/transfer of analytical methods and ensure timely initiation and completion of studies. * Prepare/ review protocols, reports, SOPs, laboratory records, tech specifications, and other related documents. * Execute analytical methods in the lab for assay development/validation, feasibility/transfer. * Perform testing in accordance with SOPs and regulations (cGMP) * Transfer GMP assays to the routine team and provide training to the analysts, study managers, report writers and QA. * Operates, maintains lab equipment as required by SOPs and testing procedures. * Utilize applicable computer programs during testing and routine tasks (i.e. Word, Excel, Oracle, LIMS, BRIQS, etc) * Lead general change control and resolve deviations by completing event records * Contribute ideas and suggestions to improve standard laboratory techniques, protocols, processes, and equipment * Ensure current regulatory requirements and technical needs of internal and external clients are appropriately met. * Maintain strong communication skills to effectively interact with internally and externally stakeholders. * Engage directly with clients. * Performs other duties as assigned. Who You Are Minimum Qualifications: * Ph.D. in a scientific discipline (e.g., Analytical Chemistry, Chemistry, Biology, etc.), with 3+ years relevant experience -OR- * Master's Degree in a scientific discipline (e.g., Analytical Chemistry, Chemistry, Biology, etc.), with 5+ years relevant experience -OR- * Bachelor's Degree in a scientific discipline (e.g., Analytical Chemistry, Chemistry, Biology, etc.), with 7+ years industry experience Preferred Qualifications: * Experience with some or all of the following technical disciplines: * Liquid Chromatography (SEC, RP, IEX, etc.), * Mass Spectrometry (Intact Molecular weight, Peptide mapping, Disulfide mapping, Glycan Profiling, N-/C-Terminal Sequencing) * Capillary Electrophoresis Methods (CE-SDS, cIEF) * Compendial assays, etc. * Broad working knowledge of filed and experience with relevant laboratory practices, techniques, equipment, materials and mathematical calculations. * Intermediate skills in applicable computer programs. * Experience of method development in a pharmaceutical laboratory or similar field. * Excellent verbal and written communication skills that have been demonstrated through presentations/seminars, oversight of projects, implementation of new services, etc. * Excellent time management skills. * Demonstrates a high level of initiative and leadership capabilities. * Effective coaching and training skills for complex and highly technical work. Pay Range for this position - $75,400 - $131,400 The offer range represents the anticipated low and high end of the base pay compensation for this position. The actual compensation offered will be determined by factors such as location, level of experience, education, skills, and other job-related factors. Position may be eligible for sales or performance-based bonuses. Benefits offered by the Company include health insurance, paid time off (PTO), retirement contributions, and other perquisites. For more information click here. What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We believe that this variety drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress! Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Lab Pack Chemist with Class A&B Commercial Driver's License (At a minimum, a valid Class B CDL with a current Hazmat Endorsement AND Lab Pack experience is required) About Us: Ace Environmental Holdings, LLC is a locally owned full-service Environmental and Industrial Services company that provides a full range of services: 24-hour Spill Response Soil Remediation Oil Water Separator Cleaning Material Storage Tank Cleaning (both aboveground and underground) Bulk Liquid Transportation Pipeline Jetting Stormwater Facility Cleaning Industrial Cleaning Confined Space Entry services Residential Aboveground & Underground Oil Tank Removal We are looking for a Lab Pack Chemist with a Class A &B CDL Driver's License with a Hazmat Endorsement. At Ace Environmental Holdings, LLC , our CDL Lab Pack Chemists work in the field teaming up with our Hazardous Waste Project Manager and our Business Development Manager, conducting chemical and waste management, packaging, transportation, and disposal of both non-hazardous and hazardous materials. Duties & Responsibilities: Follow company safety guidelines and provide clients with high quality and professional customer service. At our customers' facilities, handle, classify, segregate, package, and label hazardous and non- hazardous materials according to Federal and State regulations. Prepare shipping documents and coordinate transportation of chemical products and hazardous materials from customer sites. Perform consolidation of hazardous materials and/or waste according to the Federal and State regulations (i.e. bulking and/or repackaging). Provide expert knowledge on government regulations, health and safety practices, and proper disposal methods to customers. Respond to emergency chemical spills and perform cleanup duties. Maintain good attendance and punctuality. When on call, participate in quick and immediate response. Secure coverage for shifts when necessary. Maintain Ace standards and reputation in the industry. Requirements: Must be able to pass pre-employment drug screen and DOT physical. Prior experience operating tankers, roll-off and/or vacuum trucks, box trucks (preferred). Must be able to perform lab packs, sort chemicals, properly placard the truck and fill out manifests. Hazmat endorsement required. Compensation: $30.00-$35.00 per hour (commensurate with experience) Monthly bonus potential based on attendance, punctuality and quality of work. Paid training and certifications Competitive Benefit Package with paid holidays and vacation. Salary Description $30-35 PER HOUR

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 familiarity with Lean Six Sigma Methodologies and proven analytical/ problem solving capabilities. Demonstrates the ability to establish good working relationships with other departments, including vendors, colleagues, and subordinates. Demonstrates 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 ability to acquire the appropriate knowledge from resources on with electronic Quality Management Systems such as MasterControl and Trackwise. Demonstrate 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).

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.

Job Description The R&D Technician I performs a wide variety of tasks in support of the Global Engineering team's technology and innovation initiatives under the direction of the R&D lab lead. The role works in a team environment to support the operation and maintenance of all aspects of the R&D Lab including the test facility, equipment, tools and instrumentation. Responsible for safely assembling and modifying evaporative heat transfer equipment and components under the direction of R&D Lab Lead. Conducts all aspects of the evaporative thermal test process. PRINCIPAL ACCOUNTABILITIES Piping and instrumentation of evaporative heat transfer equipment for thermal, sound and vibration testing Installation and monitoring of sensors and various measurement devices associated with product tests Generation of accurate and detailed test reports to communicate test results to various internal customers Assist with the preventive maintenance and upkeep of the R&D laboratory facilities and equipment Safely assemble and disassemble evaporative heat transfer equipment and components Demonstrate thermal testing concepts and develop the essential mechanical, electrical and computer skills necessary for successful completion of Global Engineering test projects NATURE AND SCOPE The R&D Tech I reports to the R&D Lab Supervisor. This role interfaces with multiple engineering teams and the production environment. KNOWLEDGE & SKILLS High School Diploma or GED required. Technical trade schools highly desired. 2 years+ of experience in the mechanical, electrical, or plumbing trades preferred Demonstrated efficiency in use of hand tools, power tools, powered lift trucks and platform scissor-lifts preferred Knowledge of electrical and mechanical concepts Good written and oral communication skills; strong team player Good computer skills with working knowledge of Microsoft products and data collection spreadsheets Self Directed and ability to work with minimal supervision. WORKING CONDITIONS: The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is regularly required to stand and walk up to 80% of the time. Frequent use of hands to perform mechanical tasks including turning, torquing, lifting, pushing, pulling is required. Working conditions include inside a lab area and occasionally outside exposed to weather. Ability to work on ladders and lifts is required. This position requires occasional lifting of up to 50 lbs. to shoulder height. Weekend and shift work may be necessary depending upon workload Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities The contractor will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the contractor's legal duty to furnish information. 41 CFR 60-1.35(c) BAC Hiring Compensation Range $21.75-$32.63 BAC offers a comprehensive benefits package to include medical, dental, vision, paid time off, 401k, employee stock ownership plan, and more. Please see additional details on the BAC website at************************* BAC Employees are eligible to participate in an annual bonus incentive program.

Join our dynamic antibody engineering group as an Associate Scientist, contributing to the design, construction, and evaluation of monoclonal and bispecific antibodies. Utilize modern molecular techniques to engineer antibodies and conduct immunoassays to assess their function, stability, and serum clearance. Responsibilities * Contribute to the engineering and evaluation of monoclonal and bispecific antibodies. * Utilize molecular techniques and computational tools to enhance antibody affinity, stability, and developability. * Conduct immunoassays such as ELISA to evaluate antibody function, stability, and serum clearance. * Employ analytical instruments like flow cytometry to assess antibody functions. * Design and engineer various antibody formats using molecular techniques. Essential Skills * Experience with monoclonal antibodies, ELISA, and immunoassay techniques. * Proficiency in molecular cloning, RNA isolation, and sequencing analysis. * Hands-on experience in immune-binding assays such as ELISA. * Strong experience in molecular biology techniques including mutagenesis and Quikchange. * Competence in using software for plasmid map generation and nucleotide sequence analysis, such as Snapgene. Additional Skills & Qualifications * Bachelor's Degree in a scientific discipline with a minimum of two years of related experience or a Master's Degree in a scientific discipline. * Industry experience preferred, with 4-5 years being ideal for Scientist level. * Basic experience with programming languages such as Python, VBA, or R is advantageous. * Exceptional attention to detail and rigorous experimental practices. * Excellent time-management skills. Work Environment The role is based in a lab environment, requiring full onsite presence. Expect to spend 15-20% of your time at your desk. As part of a mid-sized company, you will have the opportunity to engage with many exciting products in the pipeline. Job Type & Location This is a Contract position based out of Rockville, MD. Pay and Benefits The pay range for this position is $30.00 - $40.00/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 Rockville,MD. Application Deadline This position is anticipated to close on Jan 21, 2026. 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. 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 due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Job Code **5484** \# of Openings **1** Apply Now (**************************************************** Requisition?org=GATEWAYVENT&cws=55&rid=5484) Bennett Aerospace, Inc., a subsidiary of Three Saints Bay, LLC, is seeking an experienced Weapon Systems Innovative Materials and Novel Manufacturing Scientist specializing in innovative materials processing and manufacturing sciences for weapon systems manufacturing. Aberdeen, MD **Position Requirements:** + Must have minimum of twenty (20) years of hands-on experience and knowledge in weapon systems materials and manufacturing research. **Security Requirements:** + Successful completion of Bennett Aerospace Background Investigation, Drug Screening, and Credit Check. + Must be a U.S. Citizen with the ability to obtain a Government background investigation and meet suitability requirements. **This position is located in Aberdeen, MD.** **Apply online here at:** 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.

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 $45,500 to $66,000. 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.

Job DescriptionAbout Us: uBriGene is a leading Contract Development and Manufacturing Organization (CDMO) specializing in cell and gene therapy manufacturing. We are committed to providing comprehensive solutions delivering high-quality products, testing and filing, to support drug developers at every stage of their journey and to accelerate the development, manufacturing and commercialization of life-changing therapies. We are looking for a motivated QC Scientist to join our team and play a critical role in the release testing of cell and gene therapy products in a GMP environment. If you are passionate about cutting-edge biotechnology and thrive in a fast-paced environment, this could be the perfect role for you. Key Responsibilities: Perform QC release testing for cell and gene therapy products, including flow cytometry, qPCR, endotoxin, viability assays and functional potency assays. Must be able to properly operate flow cytometers, run and analyze multi-color biomarkers flow panels. Perform stem cell product-related assays, including cell differentiation culture, defining cell surface/nuclear markers by flow cytometry, immunofluorescence staining, and imaging. Draft, review, and maintain Standard Operating Procedures (SOPs), worksheets, and QC release reports. Collaborate with Analytical Development (AD), Process Development (PD), and MSAT teams to perform method suitability and qualification studies. Set up, calibrate, and maintain QC instruments (e.g., drafting SOPs, performing Preventive Maintenance (PM), and conducting IQ/OQ/PQ). Ensure compliance with GMP guidelines and regulatory requirements for product release. Work effectively with cross-functional teams to ensure timely release and keep compliance of cell and gene therapy products requirement. Maintain QC data and records using Microsoft Office software and other relevant systems. Given the GMP nature of the role, some weekend work is expected, and compensatory time off will be granted. Qualifications: PHD's degree in Biology, Biochemistry, immunology or a related field. 3-5 years of GMP QC testing experience, or assay development experience is plus Experience in GMP product release is highly preferred. Hands-on experience with flow cytometry, qPCR, dd PCR, ELISA.endotoxin, and viability assays. Knowledge of QC instrument maintenance and qualification (PM, calibration, IQ/OQ/PQ). Proficiency with Microsoft Office (Excel, Word, etc.). Self-motivated and able to adapt to a fast-paced work environment. Strong communication skills and the ability to work as a collaborative team player. Experience with designing and setting up multicolor flow assays. Bilingual is preferred (English & Mandarin). Desired Skills: Smoothly operate multi-color flow cytometer, perform and analyze multi-color biomarker flow panel. Perform qPCR, dd PCR, ELISA. Prior experience in a CDMO setting is a plus. Experience in immune and stem cell culture, as well as cell product potency assays, is a plus. Why uBriGene? At uBriGene, we offer an innovative and collaborative work environment where you will contribute to the development of cutting-edge cell and gene therapies. We are passionate about fostering professional growth and delivering impactful solutions for our clients. Powered by JazzHR 4Gmkg3Eyw7

Chimera Enterprises International is seeking a Chemical and Nuclear Surety Analyst to support the Army Treaty Compliance and Surety Division (DAMO-SSD), Deputy Assistant Secretary of the Army for Environment Safety & Occupational Health (DASA(ESOH)), and U.S. Army Nuclear and Countering Weapons of Mass Destruction Agency (USANCA) Description The ideal candidate will have substantial experience in chemical and nuclear surety, as well as familiarity with Department of Defense (DoD) guidelines and regulations. The Chemical and Nuclear Surety Analyst will support DAMO-SSD by ensuring compliance with U.S. laws and DoD directives related to chemical and nuclear surety, providing technical and policy support, participating in related meetings, and maintaining oversight of surety-related activities. Mission To ensure the Army's adherence to chemical and nuclear surety requirements by providing expert analysis, strategic guidance, and comprehensive support. This role involves implementing surety programs and policies in alignment with DoD and Army guidelines to ensure the safety, security, and accountability of chemical agents and special nuclear materials (SNM). Clearance Level Required: SECRET JOB DESCRIPTION AND RESPONSIBILITIES: Provide continuous support to DAMO-SSD, including the study and assessment of USG, DoD, Joint, and Army surety guidance issues. Determine the impact of chemical and nuclear surety and accident and incident response on Army operations, plans, force structure, training, and resources. Provide operations, program oversight, and staff support to DAMO-SSD to assist in the execution of its responsibilities for developing, implementing, and overseeing compliance with surety guidance measures. Utilize database management systems to collect, analyze, present, communicate, and file information related to surety guidance and surety I&C planning. Attend and participate in meetings, conferences, briefings, seminars, training courses, and guidance meetings. Support and accompany the Department of the Army Inspector General (DAIG) on surety-related inspections. Monitor available information sources for surety-related matters and provide regular updates and reports. Prepare synopses, after-action reports (AAR), trip reports, significant activity reports (SIGACT), information memorandums, and information papers as required. Recommend special studies and research and analysis topics pertaining to surety issues for approval and assignment by the Government. Review and comment on U.S. government, DoD, and Army documents and publications related to chemical and nuclear surety. Support the revision of formal Army surety-related guidance documents such as AR 50-5, AR 50-6, AR 190-17, and DA Pam 50-5. Assist with implementation of chemical and surety-related guidance, including reviewing requests for exceptions and surety status termination. Knowledge, Skills, and Abilities: Minimum of two (2) years of experience interacting with Service Staff, Joint Staff, and Office of the Secretary of Defense (OSD) organizations. Strong knowledge of chemical and nuclear surety operations and compliance measures. Proficiency in database management and the ability to utilize them for surety analysis. Excellent analytical skills with the capability to develop and implement compliance measures. Strong communication and interpersonal skills for effective collaboration with various stakeholders. Ability to draft, review, and update technical and policy documents related to surety. Minimum Qualifications: Education: Bachelor's Degree in engineering, scientific, technical, management, or a related discipline relevant to this PWS. Experience: 2 to 5 years' experience in managing and overseeing chemical and nuclear surety programs and interacting with high-level DoD personnel. Clearance: SECRET Location: Primarily on-site in the National Capital Region (NCR), with occasional travel as required. Chimera Enterprises International is committed to equal opportunity and affirmative action in hiring and retaining a diverse workforce, including protected veterans and individuals with disabilities. Powered by JazzHR B2tWE3MSCy

Mahalo for your interest in this role! Please see the full position description below and click Start Your Application when ready. For more information about DAWSON, please visit dawsonohana.com. This position is intended to support the Naval Treaty Implementation Program (NTIP) in its role for implementation and compliance of the specific arms control treaties and agreements under NTIP s purview. The work for this position will be located at the Washington Naval Yard, Washington District of Columbia (D.C.) Job Description Work with the Government to identify and assign qualified personnel to critical functions in support of the assistance team Accompany Department of the Navy (DON) personnel to the DON facility designated for inspection Store, periodically test, maintain, and rapidly deploy inspection support equipment to the Point of Entry at Dulles International Airport and to the DON installation designated for a Challenge Inspection s (CI) or CI exercise Provide day-to-day support to the NTIP staff in the conduct of routine business Attend meetings, draft Memoranda for Record, prepare presentations, and reports Monitor the arms control treaty community for movement toward any type of new or altered framework or arms control agreements Provide research and analytical support to program and resource management decision making Assess impacts to the Department of the Navy, as required Prepare and deliver all technical studies, analysis, research, documentation Qualifications Secret Security Clearance Bachelor s degree from an accredited institution Seven (7) plus years of experience in arms control, international relations, national security, or a related field Available to deploy to an affected DON installation as directed *Position is Contingent Upon Award DAWSON is an Equal Opportunity/Affirmative Action/VEVRAA federal contractor. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, national origin, disability status, protected veteran status, or any other characteristic protected by law. DAWSON offers a best-in-class benefits program including medical, dental, and vision insurance; a 401(k) program with employer match; paid vacation and sick leave; employer-paid basic life and AD&D insurance; an Employee Assistance Program; and a flexible work environment. Additionally, employees can choose from several voluntary benefits including critical illness coverage; accident insurance; identity theft coverage; pet insurance, and more. DAWSON gives preference to internal candidates. If no internal candidate meets our qualifications, external candidates will be given consideration.

IEH Laboratories, a Leader in Food Safety, is now accepting applications for a Laboratory Analyst - Night Shift position at its facility in Laurel, MD. Ideal candidates will possess the following: - A BS or BA in the biological sciences or related field (required) - Proficiency with data entry and computer applications - Strong attention to detail - Ability to multitask and work in a fast-paced environment - Strong written and verbal communication skills - Strong understanding of aseptic technique in the laboratory Laboratory Analyst duties include: analysis of food samples for pathogens via PCR and immunoassay, various microbe enumerations, data entry, laboratory reporting, quality control, media preparation, and other duties as assigned. The pay rate for this position is $21.24 - $23.24 hourly. The shift for this position is full-time (40 hours/week), with a fixed schedule (operating hours are Tuesday through Saturday, between the hours of 8:00 pm - 4:00 am). This position is eligible for the following benefits after a brief waiting period: medical, dental, vision, life/AD&D insurance, long- and short-term disability insurance, health and dependent care FSA plans, employee assistance program, 15 days of paid time off per year for sick leave and/or vacation, 6 paid holidays per year, 3 days paid bereavement leave, and 401(k) (with up to 3% employer match after eligibility criteria are met). Due to exposure to various food allergens in the laboratory environment, applicants with moderate-to-severe food allergies are discouraged from