Chemist Jobs in Alexandria, VA

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 Hybrid - Rockville, MD Benefits included (Medical, Dental, Vision, 401k)

Cell Culture (~25%): Culturing primary human fibroblasts from patients with retinal degenerative diseases. Catalog and freeze early passages of these fibroblasts. Reprogram these fibroblasts into induced pluripotent stem cells (iPSCs) using standard available techniques. Maintain iPSC colonies and freeze their early passages. Differentiation of patient iPSCs into retinal pigment epithelium (RPE) and endothelial cells and maintenance of those RPE and endothelial cultures. This work will include: Preparing media, supplements, and reagents needed cell culture work. Maintaining the cell culture room biosafety level 2 standards and maintaining aseptic conditions in cell culture flow hoods, incubators, and prepare sterile tools needed for work with cell cultures. The cell culture maintenance work will require working for short periods of times on the weekends and some holidays. Work to characterize the iPSC colonies for their pluripotency. This will require: Immunostaining of iPSCs, preparing RNA and cDNA from iPSCs, and performing qRT-PCR assays. Additionally, will perform three germ layer assay based functional characterization of iPSCs. This work will also include any cell types that act as control for their iPSC work. Other experiments needed to perform these assays utilize one or several of following techniques: immunoblot analysis, immunohistochemistry, immunofluorescence staining, PCR, real time-PCR, RNA and proteins extraction, F ACS, and total tissue resistance measurements. Perform experiments in the lab involving techniques like immunoblot, qRT-PCR, immunostaining, ELISA, FACS. Document their results, and compile them for presentations and publications. Participate in lab meetings and discussions, present their work and the relevant literature, and help in the lab organization. Help with the other ongoing projects in the lab with the expertise developed on iPSC projects. Cell Therapy Manufacturing for a CRADA (~10%) Optimize and develop allo-iPSC-RPE product for comparability studies with auto-iPSC-RPE product Perform comparability between allo and auto iPSC-RPE using the following assays - flow cytometry, ReShape, SEM, phagocytosis, gene expression, and TER Manufacture GLP-grade allo-iPSC-RPE for preclinical tox studies Assist in completing IND-write up for allo-iPSC-RPE Coordinate tech transfer of allo-iPSC-RPE to the clinical center for use in a phase I clinical trial GLP/GMP manufacturing of cells (~25%) Provide conceptual and technical assistance to staff in understanding and implementing the FDA GMP guidelines. Ensure compliance with GMP; provide guidance to staff. Lab Management: ordering and supply inventory (~20%) Oversee lab organization, supplies and reagent inventory, and maintenance of cell culture room. Oversee repairs, replacement, etc. of laboratory equipment, interacting appropriately with procurement, secretarial, and other staff with related responsibilities Develop Standard Operating Procedures (SOPs) with the Contract Research Organization (CRO). Serve on committees/work groups; serve as a conduit of information between these workgroups. Coordinate meetings between all parties working on the cell therapy project so they can brief us about the progress they have made for their respective parts of the project. Organize internal and external meetings by setting up meeting agenda, taking meeting notes and sending out meeting minutes. DESIRED BACKGROUND BS degree in relevant field is required; MS degree is desirable Knowledge of stem cells, cell therapy, cell culture techniques Knowledge of the eye is highly desirable Familiarity with Good Manufacturing Practices (GMP) guidelines in preferred LOCATION The world famous NIH's main campus in Bethesda Maryland

We are seeking a Scientist to support the National Institutes of Health's (NIH), world renowned National Institute of Allergy and Infectious Diseases (NIAID) in Bethesda, MD. Our NIAID professional, technical, and scientific support personnel are part of a preeminent team focused on positively impacting millions of lives around the world with groundbreaking research. Candidates will work at a prominent, diverse and vibrant NIAID worksite to directly support exciting ongoing research activities as a contractor team member. Accelerate your career and apply below to help us make a difference. CAMRIS International is a dynamic clinical research and international 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: clinical research; vaccine research, microbiology and infectious disease research, development and production; biodefense; global health security; and HIV/AIDS programs. Our employees enjoy a diverse, collegial environment where individual contributions matter at all levels. At CAMRIS, you will notably improve the lives of people at home and abroad. Responsibilities Perform maintenance for multiple cell culture lines used in laboratory experiments. Perform routine flow cytometry to test cell surface and intracellular proteins. Conduct protein/antibody production, purification and analysis (SDS-PAGE, Western blot, ELISA etc.). Perform RT-PCR, cloning, plasmid purification and analysis. Isolate/identify monoclonal antibodies from convalescent donors and vaccine immunized animals. Produce pseudotyped lentiviruses for multiple viruses including influenza and coronaviruses (SARS-CoV, MERS-CoV, SARS-CoV-2 and others). Perform neutralization assays to evaluate monoclonal antibodies and vaccinated sera against multiple viruses including influenza and coronaviruses (SARS-CoV, MERS-CoV, SARS-CoV-2 and others). Maintain special knock-in mice colonies for use in critical experiments exploring HIV-1 and influenza vaccines. Conduct animal studies to evaluate the immunogenicity of vaccines (including intramuscular, subcutaneous, intraperitoneal, and intravenous injection, sample collection and processing). Interact/collaborate with scientists from internal and external organizations. Conduct research independently including planning experiments, data analysis and peer-reviewed publication of data. Manage ordering and maintenance of supplies for large, complex laboratory, to include record keeping, inventory, restocking, and training of personnel for inventory assistance. Perform inventories of laboratory specimens, manage tracking logs, reconcile discrepancies to ensure accurate records in accordance with biospecimen policies and regulations. Catalog, record, and handle a variety of laboratory/biological samples. Manage input of laboratory/biologic sample information in centralized database; responsible for maintenance and input of plasmid information into lab-wide database. Serve as primary point of contact to facilitate and monitor biological materials shipments across the lab, to include training of laboratory staff. Qualifications Ph.D. degree in Biology, Life Sciences or a related discipline. Three (3) years of specialized experience plus a Master's degree is equivalent to a Ph.D. degree. BS degree with a minimum of ten (10) years of experience in virology research, experience on virus neutralization assay preferred. Demonstrated experience working in a laboratory environment. Demonstrated knowledge of maintaining accurate and detailed records. Demonstrated knowledge of proper laboratory disposal methods and safety procedures. 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 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.

M-F 8AM-5PM Shift Duties and Responsibilities: RT-PCR and qPCR Will be responsible for sample accession, sample testing, and sample analysis. Will be responsible for performing routine proficiency testing. Required to perform operational qualification on the instruments. Must follow all lab policies and procedures. Minimum Qualifications and Requirements: Bachelor level degree in a scientific discipline (preferable in Biology or Molecular Biology) from an accredited institution. Legally eligible to work in the U.S. without sponsorship. Real-Time PCR or qPCR Experience. Ability to compose effective and efficient reports and correspondence. Self-starter, motivated and takes initiative; strong interpersonal and problem-solving skills; able to work collaboratively with all levels of staff to resolve problems to maximize performance, creativity, problem solving and results. Seek, learn, and apply new skills/knowledge to perform job responsibilities. Attentive to detail with a high level of accuracy; exercise sound judgment. Resourceful, diplomatic and professional; deliver outstanding customer service; a can-do attitude and work style that supports teamwork, collaboration and positive relationships. Excellent written and verbal communication skills, including excellent listening skills to communicate clearly, concisely and effectively. Position-relevant computer experience including Microsoft Office. Follow all safety regulations as outlined in the SOPs, including maintenance of contamination-free laboratory. Preferred Qualifications: One (1) to three (3) years' experience. CLIA Laboratory Experience. Graduated from a Clinical Laboratory Training Program.

The Ford Agency is spearheading a search for a Scientist to join a DC based consulting firm. The Scientist will draft submissions to regulatory agencies, prepare content for peer reviewed publications, and provide scientific support to clients regarding risk assessment and regulatory issues as they relate to product safety. The successful candidate will have a strong toxicology and/or chemistry background, including both lab and risk assessment experience. This is a terrific opportunity for a toxicologist or a chemist looking to make a transition from a laboratory or academic environment into a consulting culture. Responsibilities Include: Lead scientific projects for multi-stakeholder groups Respond to scientific and technical inquiries from clients Research and develop data submissions for regulatory entities Produce safety and risk assessments evaluations for regulatory agencies Write and edit articles for peer-reviewed publications Evaluate protocol and oversee studies and reporting Qualifications Include: MS degree in Toxicology, Chemistry, or Public Health and 5+ year's experience PhD highly preferred Experience with risk assessment and regulatory issues Strong knowledge of organic chemistry and biochemistry Professional writing, communication, and interpersonal skills Excellent attention to detail and organization skills Candidates for this position must be based in DC, MD, or VA area or have independent plans for relocation. The Ford Agency is a recruiting firm based in Washington, DC. We represent a broad range of organizations including: non-profits, associations, legal, consulting, and government relations firms. This position is an opening with one of our clients. To see more positions available through The Ford Agency, please check out our website at ********************

When you join Caring Cross, you become part of a dynamic team determined to accelerate the development of advanced cell and gene therapies and to ensure their affordable access around the world. Your work will be helping to build research programs and create access to life saving therapeutic opportunities for people living with HIV, cancer, and genetic diseases. We are seeking a serious Quality Control Scientist with knowledge and strong hands-on experience in cell culture and various PCR (qPCR, dPCR) methods, who is willing to work within a small and dynamic team. How will you make an impact? Working on multiple assay development projects: experiment design, execution, data analysis. Writing: lab notebooks, SOPs, assist in report generation. Performing quality control testing: cell culture, flow cytometry, DNA extraction, qPCR/dPCR, ELISA. Communicating analyzed data via power point presentation slides to a larger team. Maintaining testing databases. Performing routine laboratory equipment maintenance. Maintaining a safe BSL-2+ laboratory environment. How will you get here? Qualification: • BS/MS/PhD with 1-2+ years of relevant experience. • Must be skilled in basic molecular biology techniques. • Hands-on experience with cell culture, flow cytometry, qPCR, plate-based assays. • Experience with CAR T is a plus. • Assay development experience is a plus. • Great attention to detail. • Ability to perform independently and as part of a team. If interested, please send your cover letter, and resume to ******************* for consideration.

Piper Health Sciences is seeking a Laboratory Technician to join a biotech company located in Elkridge, MD. The Laboratory Technician will perform quality control of raw materials, and assist with manufacturing. Responsibilities of the Laboratory Technician include:Ensure accurate filing of raw material records Receive QC materials and organize samples as needed Process rooms and maintain inventory Monitor, clean, and sanitize equipment Complete the required calibration and logbook forms Qualifications for the Laboratory Technician include:1+ year of experience Understand Good Manufacturing Processes (cGMP) High School Diploma, Associate, or Bachelor's degree Compensation for the Laboratory Technician includes:Rate Range: $17 - $18 Per Hour **depending on experience**Comprehensive Benefits: Cigna Medical/Dental/Vision, 401k, Sick Leave as required by law Keywords: QC, quality control, Manufacturing Technician, Manufacturing process technician, process technician, batch record, cell culture, upstream, downstream, all stream, fill finish, central services, GMP, aseptic, harvest prep, harvest, vpro, sanitation, purification, equipment, calibration, buffers, solutes, media prep, mixing chemicals, pH, LI, clinical LI, manufacturing, raw materials, good manufacturing processes, sample shipment, raw material testing, quarantined materials, manufacturing production This job opens for applications on January 24, 2025. Applications for this job will be accepted for at least 30 days from the posting date. #LI-ONSITE #LI-JA2

Division of Chemistry The National Science Foundation is seeking qualified candidates for a Chemist (Program Director) position within the Directorate for Mathematical and Physical Sciences (MPS), Division of Chemistry (CHE), Alexandria, VA. For more information on MPS please click . For more information on CHE please click . **Location** + ** Clarification from the agency** Applications will be accepted from all US citizens who meet citizenship and eligibility requirements. Please see the "Other Information" section for further information. **Duties** NSF Program Directors bear the primary responsibility for carrying out the agency's overall mission to support innovative and merit-reviewed activities in basic research and education that contribute to the nation's technical strength, security, and welfare. To fulfill this responsibility requires not only knowledge in the appropriate disciplines, but also a commitment to high standards, a considerable breadth of interest and receptivity to new ideas, a strong sense of fairness, good judgment, and a high degree of personal integrity. The responsibilities of the NSF Program Director include, for example, long-range planning and budget development for the Program, the administration of the merit review process and proposal recommendations, the preparation of press releases, feature articles and material describing advances in the research supported, and coordination and liaison with other programs in NSF, other Federal agencies and organizations. Additional duties and responsibilities include: PROGRAM PLANNING AND MANAGEMENT * Maintains a healthy balance of support for all the needs of the research and education enterprise through program, division, directorate, Foundation, or interagency activities. * Manages program resources to provide optimal appropriate scientific judgment to insure integrity and consistency in the grant/declination process without conflict of interests, and with balance among appropriate sub-fields and institutions, and participation of all qualified scientists. * Incorporates cross-directorate responsibilities into program administration. * Manages an effective, timely merit review process, with attention to increasing the size and quality of the reviewer pools and insuring participation by women, minorities and disabled scientists. * Provides scientific expertise, evaluation and advice for other programs in NSF, including international programs, and other research programs, and cross-directorate programs. * Advises and assists in the development of short-and-long range plans, establishing goals and objectives for support of research programs. * Plans the budget for the program/programs considering past, present and future fiscal years, allocates resources within the budget by distributing scarce resources among major competitive programs, and manages post-award evaluation. * Controls waste, fraud and abuse. REPRESENTATION, COMMUNICATION AND LEADERSHIP * Represents the Program, Division and the Foundation within the scientific community, with other NSF Divisions, with other appropriate agencies and organizations, and with the public, accurately reflecting NSF policy and positions. * Creates and maintains linkages to other NSF units and other Federal agencies in pursuit of the overall NSF mission. * Participates in staff, panel, committee and other meetings, providing input relevant to program area and/or Division. * Pursues affirmative action and Equal Employment Opportunity (EEO) goals. * Pursues and/or is responsive to assignment on special projects and temporary function teams across the Foundation to solve problems, improve staff communication, and effect coordination for special programs. * Contributes ideas and effort to improving the quality of policies and NSF's performance of the overall mission. * Develops policies and plans for strengthening support of research and education programs. * Provides information to the community on how NSF is pursuing its mission and gathers data and impressions from the community on the effectiveness of NSF's performance of its mission. * Prepares and disseminates a variety of informational documents which may include data on progress being made toward NSF goals, trends and opportunities, and budget plans. PROFESSIONAL DEVELOPMENT * Establishes contacts and maintains active involvement in Program and related areas through participation in professional activities. * Maintains familiarity with salient current research developments. * Pursues individual research as workload and travel funds permit. * Expands administrative capabilities through training courses or assumption of new management. **Requirements** ** Conditions of Employment** **This position is outside the competitive civil service.** You must meet eligibility and qualification requirements by the closing date of the announcement. All online applicants must provide a valid email address. If your email address is inaccurate or your mailbox is full/blocked, you may not receive important communication that could affect your consideration for this position. This position is in the bargaining unit represented by AFGE Local 3403. The Selected Candidate(s) may be subject to a background investigation. ** Qualifications** Candidates must have a Ph.D. in Chemistry plus after award of the Ph.D., six or more years of successful research, research administration, and/or managerial experience pertinent to the position. The applicant will fill a leadership position in our Research Experience for Undergraduates (REU) or Broadening Participation (BP) Programs, and provide technical expertise to at least one of our core disciplinary research programs. Applicants should demonstrate breath of knowledge regarding how REU or BP Programs are managed to be successful, and must demonstrate expert knowledge in a chemistry disciplinary research program. The ability to effectively lead individuals and teams within a collaborative environment is a must, as is the commitment to high scientific standards, high ethical standards, and problem solving skills. Experience in managing budgets and working with NSF electronic and financial systems is desirable. **Education** Please refer to the Qualifications section. If your degree was obtained from a foreign institution, please also submit the certification from the Association for International Credential Evaluation Professionals, or certification equivalency. **Additional information** Relocation expenses MAY be paid contingent upon the availability of funds. It is NSF policy that NSF personnel employed at or IPAs detailed to NSF are not permitted to participate in foreign government talent recruitment programs. Failure to comply with this NSF policy could result in disciplinary action up to & including removal from Federal Service or termination of an IPA assignment & referral to the Office of Inspector General. This announcement is open to All US Citizens who meet citizenship and eligibility requirements. Federal Appropriations Law requires that Non-Citizens meet certain eligibility criteria to be considered. Therefore, Non-Citizens must certify eligibility by signing and attaching this to their application. Non-citizens who do not provide the affidavit at the time of application will not be considered. This announcement may be used to fill like positions in other organizations within the National Science Foundation. NSF has determined that all of its positions are eligible for telework. Work suitable for telework depends on job duties; therefore, employees must receive approval from their supervisor for telework and have a telework agreement in place. Entering into a telework agreement is voluntary. * A career with the U.S. government provides employees with a comprehensive benefits package. As a federal employee, you and your family will have

* Cookie cookielawinfo-checkbox-others * Duration 11 months * Description * Cookie cookielawinfo-checkbox-necessary * Duration 11 months * Description * Cookie cookielawinfo-checkbox-functional * Duration 11 months * Description * Cookie viewed\_cookie\_policy * Duration 11 months * Description **Cyber Researcher & Developer** by in Reading Time: 3 mins read A A **Job title:** Cyber Researcher & Developer **Company:** Leidos **Job description**: The evolving Cyber landscape requires research and development of emerging technologies to imagine the future state of the art of CNO capabilities that advance the Cyber mission. The Leidos Office of Technology supporting the Cyber & Analytics Business Area (CABA) is seeking an enthusiastic Cyber Researcher & Developer to join a diverse team of researchers contributing to an internal research and development portfolio focused on CNO. The successful candidate will be a subject matter expert in one or more key areas of 5G technology, including the 5G Core, 5G RAN, and/or 5G User Equipment. The successful candidate will have hands on experience in one or more areas described below. 5G Core Experience: * Operating a multi-site 5G system and supporting Vulnerability Research and Operations * Experience setting up, configuring, and administrating 5G Core virtual network functions * Experience with OpenRAN architectures, implementations, functions, and interfaces * Understanding of the O-RAN specifications * Experience setting up, configuring, and administering xApps 5G RAN Experience: * Experience setting up, configuring, and administering RICs. * (Desired) Expertise in LTE/5G Baseband Implementation, Digital Signal Processing, Algorithm Development, debugging, and troubleshooting. * Experience performing capture, analysis, debugging, and troubleshooting the above 5G UE Experience: * Experience setting up, configuring, Android phones * (Desired) Experience deploying custom Android ROMs RF Equipment Experience: * Experience working within an RF lab environment including lab safety and security processes * Experience setting up and maintaining RF equipment like software defined radios, precision clocks, spectrum analyzers, and signal analyzers This role will support the growth of Cyber for Leidos and CABA and requires an individual who can effectively contribute to various projects, develop proof of concepts, and contribute to/lead demonstrations, provide technical guidance and direction to other engineers, work collaboratively across the sector. Primary Responsibilities (supporting two or more of the following): * Lead 5G mobile core configuration * Support configuration of network equipment such as routers, managed switches, and firewalls * Researching 5G network slicing implementation and vulnerability research * Utilization of RF Testing, Debugging and Analysis tools like software defined radios, precision clocks, spectrum analyzers, and signal analyzers * Applying knowledge of security concepts and networks * Exploring systems to devise new features, vulnerabilities, and techniques **Minimum Qualifications:** * Bachelor's in Computer Engineering, Computer Science, or Electrical Engineering (or other technical degree) with 8 years of relevant work experience * 4 years experience related to mobile networking and telecommunication technologies * Experience configuring and administrating 5G Core virtual network functions * Understanding of 5G network slicing * Understanding of network vulnerabilities * Ability to work collaboratively, document work, and contribute to or present demonstrations * US Citizen with a willingness and ability to obtain a TS clearance **Preferred Qualifications:** * TS/SCI with Poly Security Clearance * Experience in CU C-Plane and writing features in RRC * Understanding of DU C-Plane * Understanding of RRC procedures, expected behavior, and typical performance trade-offs, especially as they relate to RRC and overall system performance * Experience with reverse engineering, vulnerability research, exploit development * DevSecOps and/or System Administration experience such as setup, administration and troubleshooting Docker and Kubernetes containers; orchestration tool experience (e.g. Ansible); OpenStack and hypervisor experience * Experience using RF Testing, Debugging and Analysis tools like software defined radios, precision clocks, spectrum analyzers, and signal analyzers Original Posting Date: 2024-08-05 While subject to change based on business needs, Leidos reasonably anticipates that this job requisition will remain open for at least 3 days with an anticipated close date of no earlier than 3 days after the original posting date as listed above. Pay Range: Pay Range $101,400.00 - $183,300.00 The Leidos pay range for this job level is a general guideline only and not a guarantee of compensation or salary. Additional factors considered in extending an offer include (but are not limited to) responsibilities of the job, education, experience, knowledge, skills, and abilities, as well as internal equity, alignment with market data, applicable bargaining agreement (if any), or other law. **Expected salary**: $101400 - 183300 per year **Location**: Columbia, MD **Job date**: Wed, 07 Aug 2024 00:55:10 GMT Tags:

Job Details Alexandria, VA Full Time 4 Year Degree Up to 25% Day Chemist, Technical and Scientific Analyst supporting the Defense Threat Reduction Agency (DTRA). This position supports high level DTRA Chemical Biological Directorate stakeholders encompassing a full range of Advisory and Assistance Services (A&AS). Must be a U.S. Citizen. Clearance Required: SECRET w/ Ability to obtain TS Responsibilities: Applies a graduate level understanding of Chemistry in support of furthering the client's Science & Technology (S&T) objectives across the chemical threat spectrum (traditional, non-traditional, emerging and Pharmaceutical Based Agents) providing R&D analysis to the Joint Science and Technology Office Chemical & Biological Technologies Department Advanced & Emerging Threats Division (RD-CBS), with emphasis on supporting the development of prophylactic and therapeutic medical countermeasures against known and emerging chemical threats. Provide cross-functional expertise in applying basic and advanced scientific principles, with a focus on acetylcholinesterase (AChE) reactivator chemistry, Organophosphate (OP) agents including Fourth Generation Agents (FGAs), Pharmaceutical Based Agents (PBAs), decontamination of wounds and other emerging chemical threat agents. Assess capability gaps and assist in setting project- and product-level strategy and priorities, ensuring portfolios are responsive and mapped to program goals (Joint Science and Technology Office Science and Technology Plan) Coordinate and consolidate complex, technical, programmatic, and strategic responses to support division initiatives to a variety of internal and external audiences and tasker execution Liaise with industry, start-ups, government, and academia performers (includes working knowledge of University-affiliated Research Centers (UARCs) and Federally Funded Research and Development Centers (FFRDCs)); utilize scientific knowledge to evaluate and analyze novel technologies, research proposals, published and unpublished research, and data to ensure accurate and reliable information and provide recommendations to the government. Establish and maintain relationships with relevant internal and external stakeholders in the CBDP community Prepare a variety of objective analytical studies and descriptive background reports, memoranda and other written materials on subjects or public policy issues of national significance for biosecurity and biodefense Provide technical evaluation and recommendations for proposals, whitepapers, and Broad Agency Announcement (BAA) responses, monthly reports, and quad charts Familiarity in reviewing and coordinating paperwork associated with Research Oversight Board (ROB) approval and IACUC (The Institutional Animal Care and Use Committee) approval for human cell lines and animal research projects Brief both technical and senior leader audiences; formulating presentations for Joint Science Reviews (JSRs), Transitions Quarterly Reviews (TQRs), as well as miscellaneous formal and informal requests for information (RFIs) Qualifications: Master's degree in chemistry (Physical Chemistry, Pharmaceutical Science, Biochemistry, Chemical Engineering, Organic Chemistry, Medicinal Chemistry, Synthetic Chemistry, or related science field.) Minimum of 2 years experience in U.S. Government/national security, public or private scientific research organization consulting, project or contract management related to evaluation of chemical hazards and/or drug development, pre-clinical or clinical research Knowledge of technical proposals and reports, experimental or theoretical techniques, scientific studies and statements of work to ensure technical validity Ability to evaluate current and emerging chemical defense technologies. Ability to evaluate project aspects, including design, implementation and execution of Chemical Medical Countermeasure development. Demonstrated understanding of scientific principles involved in basic and applied research Preferred Qualifications: CBDP Experience (research, policy, project management) Experience in preparing senior-level briefings and reports Experience providing subject matter expertise to DoD clients Specialization in organic chemistry, toxicology or microphysiological systems Top Secret Clearance Prior Military experience About Mayvin: Mayvin offers our employees an innovative culture, excellent benefits and amenities, an inclusive work environment, ongoing career development, and recognition and rewards to honor hard work. Most importantly, our employees have a voice and are heard; we treat our employees with unwavering dignity and respect. Mayvin is dedicated to protecting the interests of the United States. We made a commitment to deliver unparalleled service to serve the interests of national security. Come join us in tackling our nation's hardest problems in a place where #PeopleMatter #ReimagineYourMission.

Applied Research Associates, Inc. is currently seeking an experienced Chemist for a growing list of projects involving modernization of explosives & energetic materials production facilities, munitions production, and novel production system design. These projects will require knowledge of and close coordination with explosives and munitions SMEs, federal stakeholders, research and development capabilities and ongoing production operations. A strong technical background is necessary to provide creative technical solutions while participating in and leading small teams. An ideal candidate has experience in analytical techniques, small molecule synthesis or scaling from beaker to batch, creative design, and prior exposure to pyrotechnics, propellants, combustion reactions, or other high hazard chemical environments. **Responsibilities** Working and partnering with the client organizations, provide leadership and vision for safe and cost-effective execution of production capabilities for energetic materials and related applications (munitions, rockets, warheads, etc.). Candidates for this position must be a US citizen residing within the US. + Develop and maintain strong working relationships with client representatives and key decision makers and achieve client satisfaction in all areas of performance. + Quick to learn synthetic pathways for producing energetic materials and their precursors + Familiarity with traditional analytical techniques (TGA, GC-MS, various spectroscopies) + Basic understanding of mass and heat transport in chemical process systems. + Continuous learning to ensure technical competence. + Ensure proper execution of the project including planning, scheduling, procurements, per the customer's requirements. + In conjunction with the project managers develop, plan, and execute goals and objectives which support the client's objectives. + Responsible for the implementation of safety and quality programs by all project staff. Assure business practices align with Contract terms (scope of work). **Qualifications** + Bachelor's in Chemistry (or equivalent), with 2-4 years of experience, or a Masters with 0-2 years of experience. + Experience in a wide variety of analytical technical for monitoring solvated and crystalized synthetic small molecule production. + Demonstrated experience in planning and prioritization. + Demonstrated ability to provide clear written and oral briefings including the ability to adopt content for specific audiences. + Support development of test plans, reports, presentations, laboratory safety assessment plans, standard operating procedures, and other support documentation. + Maintain qualification in chemical, radiation, and laser safety, and explosive handling as mandated by facility procedures and training. **Desired Qualifications** + Experience with the production, handling, processing, and design of energetic materials related to defense applications. + Process engineering and integration knowledge is preferred. + Knowledge of quality requirements and system qualification. + Experience managing production modernization projects, including new capabilities design and development. + Active DOD or DOE security clearance is preferred. **Who is ARA?** Do you want to work for a purpose? Applied Research Associates, Inc. (aka ARA) is an employee-owned international research and engineering company. We have been providing technically superior solutions to complex and challenging problems in the physical sciences since 1979. ARA has over 1,700 employee-owners and continues to grow rapidly. Together, our offices throughout the U.S. and Canada provide a broad range of technical expertise in defense, civil, and health technologies, computer software and simulation, systems analysis, environmental technologies, and testing and measurement. ARA also prides itself, on having a challenging culture where innovation & experimentation are the norm. The motto, "Engineering and Science for Fun and Profit" sums up the ARA experience. Employee ownership ensures you have a voice with what happens in the company. We are also very proud of our Women's Initiative Network (WIN), whose purpose is to motivate, support, and encourage professional career development for women to maximize career and professional accomplishments. To find out more about what the Algorithms, Modeling & Assessments Division has to offer, visit our website at: ***************************** 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)

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 Disabled/Veterans 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.

For more than two decades, FoodChain ID has been at the forefront of the New Food industry, providing expertise worldwide to navigate the requirements of an ever-growing demand for higher levels of transparency, accountability, safety, and sustainability. Our technical and business services include serving clean labels, food safety, and sustainability claims through offerings of the non-GMO Project standard and verification, USDA Organic certification, BRC and SQF food safety certification, DNA and Contaminant testing and more. Today, more than 30,000 companies in over 100 countries rely on our industry-leading solutions. The FoodChain ID vision encompasses nothing less than assuring the safety, transparency, and integrity of the global food chain, one client and product at a time. Summary An Analytical Chemist I will execute all aspects of daily business operations in the Instrumentation Laboratory and assist with technical and non-technical activities. An ideal candidate will collaborate effectively with all team members to ensure that our customers receive on-time and accurate delivery of test results and services in alignment with our quality system requirements. Responsibilities Understanding of testing requirements and concepts Analytical testing according to Standard Operating Procedures (SOP) using specific and universal analytical instrumentation Operate and do basic maintenance on analytical instruments (GC-ECD, GC-NPD, LC-DAD, GC-MSMS, ICPMS) Identify and assist in resolving anomalous events Maintain accurate records for traceability through all department procedures Responsible for calibration standards preparation and verification of specific equipment and their accompanying records Will learn quality control procedures and method development Document QC data from analytical sequences to be able to calculate control limits Requirements 1-2 years of work experience working with equipment used in the chromatography or ICPMS laboratory Interpersonal/Communication Skills Excellent verbal and written communication skills; clear, organized, meticulous Offers and receives useful and constructive feedback Able to establish and maintain effective work relationships in a team-based environment Personal Skills Highly organized with exceptional diligence Able to work efficiently under deadlines Dependable and punctual work schedule Takes responsibility for all work activities and personal actions Technology Literacy Proficiency with operation of desktop computers LIMS, MS Excel, Outlook, Chemstation, MassHunter Competencies Pass at least 1 of the following test batches for at least 2 analytical methods in at least 2 laboratory matrices: 1 PT (External or Internal) IDOC - Blank and 4 laboratory control samples (blank spikes) Basic Instrument Maintenance Replace septa, liners, clipping analytical GC capillary columns Review Sample Preparation and Analytical Documentation Have been trained by a Analyst III, Lead Analyst, Supervisor, Manager, or Director reviewing at least 50 sample preparation records - all training records retained in the employee training record folder (hardcopy or electronic retention) Language Skills Read and interpret documents such as safety rules, operating and maintenance instructions, and procedure manuals. Mathematical Skills Perform everyday math to complete job-related tasks. Reasoning Ability Interpret a variety of instructions furnished in written, oral, diagram, or schedule form. Physical Demands 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. While performing the duties of this job, the employee is regularly required to stand; use hands to finger, handle, or feel objects, tools, or controls; talk or hear; and taste and smell. The employee frequently is required to walk, reach with hands and arms with repetitive motions of the hands and wrist related to the standard operating procedures; and rarely required to stoop, kneel, crouch, or crawl. The employee is required to sit with repetitive motions of the hands and wrist related to writing and typing at a desktop or mobile keyboard. Specific vision conditions include close vision reading. It requires the ability to operate a computer and phone. Employees must have reliable transportation. Work Environment The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. This job operates in a professional office and laboratory environment. While performing the duties of this job, the employee occasionally is occasionally exposed to hazardous material, fumes, or airborne particles, and toxic or caustic chemicals. Work is performed primarily indoors in an office and/or laboratory setting. The noise level in the work environment is low to moderate. The employee will be required to wear all appropriate safety equipment including lab coat and gloves. The employee will operate equipment properly as described in the owner's manual and according to SOP specifications. Position Type and Expected Working Hours Some flexibility in hours is allowed, but the employee must be available during the “core” work hours of 9:00 a.m. to 5:00 p.m. Travel The employee may be required to travel. Additional Duties Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job. Duties, responsibilities, and activities may change at any time with or without notice. EEO Statement FoodChain ID, Inc. provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation, and training.

STR is hiring a Senior Vulnerability Researcher who has a passion for research and analysis of vulnerabilities in cyber physical systems. Work must be performed onsite What you'll do: Reverse engineering complex software or firmware targets, ranging from typical Windows/Linux binaries to embedded firmware running non-traditional computer architectures and operating systems Developing and applying automated reverse engineering and binary analysis tools to characterize protocols, interfaces, and functionality of target systems Developing innovative cybersecurity solutions Working in multi-discipline teams to tackle challenging problems from a wide variety of technologies to develop innovative cybersecurity solutions Performing vulnerability weaponization, exploit development, payload development, and exploit mitigation on a variety of challenging targets Developing custom emulation solutions to enable dynamic analysis Documenting, demonstrating, and presenting research Solving real world problems that have an impact on national security Who you are: This position requires an Active Top Secret (TS) security clearance, for which U.S. citizenship is needed by the U.S. Government BS, MS or PhD in Computer Science, Computer Engineering, Cybersecurity or related field (or equivalent work experience) 5+ years of relevant professional experience Experience with binary analysis of software/firmware Experience with disassembly tools, such as IDA Pro, Binary Ninja, or Ghidra Experience with DSP architectures, such as Texas Instruments, STMicroelectronics, NXP, or Analog Devices. Proficiency in one or more programming languages: C/C++, Python, etc. Proficiency in one or more Assembly Languages: x86, ARM, etc. General understanding of reverse engineering fundamentals: memory layout, calling conventions, etc. Nice to haves: Vulnerability research and analysis Knowledge of weaponizing discovered vulnerabilities into exploits Implant or software patch development Familiarity with binary emulation or vulnerability research, including tools such as QEMU or AFL++ Operating system internals including memory/process/thread management Embedded systems or firmware analysis Knowledge of anti-reverse engineering techniques Analyzing protocols or message structures Knowledge of binary file structures and formats Developing automated reverse engineering or software analysis tools Developing disassembler/decompiler modules Debugging software without source code Analyzing and reconstructing code/data flow Knowledge of intrusion detection and anti-malware systems and techniques STR is a growing technology company with locations near Boston, MA, Arlington, VA, near Dayton, OH, Melbourne, FL, and Carlsbad, CA. We specialize in advanced research and development for defense, intelligence, and national security in: cyber; next generation sensors, radar, sonar, communications, and electronic warfare; and artificial intelligence algorithms and analytics to make sense of the complexity that is exploding around us. STR is committed to creating a collaborative learning environment that supports deep technical understanding and recognizes the contributions and achievements of all team members. Our work is challenging, and we go home at night knowing that we pushed the envelope of technology and made the world safer. STR is not just any company. Our people, culture, and attitude along with their unique set of skills, experiences, and perspectives put us on a trajectory to change the world. We can't do it alone, though - we need fellow trailblazers. If you are one, join our team and help to keep our society safe! Visit us at ********** for more info. STR is an equal opportunity employer. We are fully dedicated to hiring the most qualified candidate regardless of race, color, religion, sex (including gender identity, sexual orientation and pregnancy), marital status, national origin, age, veteran status, disability, genetic information or any other characteristic protected by federal, state or local laws. If you need a reasonable accommodation for any portion of the employment process, email us at **************** and provide your contact info. Pursuant to applicable federal law and regulations, positions at STR require employees to obtain national security clearances and satisfy the requirements for compliance with export control and other applicable laws.

Overview: Addx Corporation is seeking a highly skilled and experienced Decision Scientist to provide comprehensive testing support for established Test and Evaluation (T&E) processes. The successful candidate will support IS Product Owners by conducting comprehensive reviews, analysis, evaluations, and tests of the project's technical capabilities in various operational environments (NIPR, SIPR, JWICS). This role involves facilitating early detection and correction of cost and schedule variances, enhancing management insight into process and product risk, and ensuring compliance with regulatory, performance, schedule, and budget requirements. Responsibilities: Provide T&E support to IS Product Owners, including conducting comprehensive reviews, analysis, evaluations, and tests of the project's technical capabilities (e.g., system behaviors, processes and interfaces, operational use, feasibility, or practicality of the technology) in each operational environment (NIPR, SIPR, JWICS) to confirm that requirements are correctly implemented. Facilitate early detection and correction of cost and schedule variances. Enhance management insight into process and product risk. Support project cycle processes to ensure compliance with regulatory, performance, schedule, and budget requirements. Validate the project's product and processes to ensure compliance with defined requirements. Ensure appropriate coordination with Government verification and validation POC, as applicable through iterative User Acceptance Testing (UAT) as a feedback mechanism. Develop Comprehensive Test (CT) and UAT plans. Assist with coordination and scheduling of CT/UAT events. Document and consolidate test results. Review test event associated artifacts to ensure accuracy (pre and post-release announcements). Ensure each test includes the operational environment (as close as possible), consisting of any hardware, software, interfacing applications and systems, documentation, operators, and user experience to ensure that the product is well-engineered and able to be deployed and developed in accordance with DoD requirements per industry best practices. Provide testing support to established T&E processes, including collaboration with government entities. Conduct reviews, analysis, evaluations, inspections, and tests of the project's technical capabilities, system behaviors, processes and interfaces, operational use, feasibility, or practicality of the technology in each operational environment, and durability of the system. Qualifications: Bachelor's degree in Data Science, Computer Science, Information Technology, or a related field. A Master's degree is preferred. Minimum of 5 years of experience in testing support, T&E processes, or decision science, preferably within a DoD or federal government environment. Strong knowledge and functional capability to operate testing tools, data analysis tools, and task management systems. Excellent communication, collaboration, and documentation skills. Experience in developing CT/UAT plans and coordinating and scheduling CT/UAT events. Strong understanding of data security protocols and compliance with federal regulations. Experience with operational environment testing and ensuring compliance with DoD requirements.

+ **Friendly and welcoming work environment** + **On-going training and development** + **Part-Time opportunity** **About Us:** United Chemists are a group of independently owned pharmacies that have united to serve our local communities better. Our vision is to build a healthy and happy local community where customers see United Chemists as their first choice provider of healthcare products and services at an affordable price. It's all about delivering prices and advice to make you smile! **About the role:** United Chemists Southgate is recruiting for a Part-Time Dispensary Technician looking for an innovative, challenging and highly rewarding position in a supportive and collaborative work environment where everyone can thrive. The Dispensary Technician role will include: - Assisting the pharmacist in the dispensary; - Stock Ordering & unpacking of dispensary lines; - Providing appropriate information and advice to customers on OTC medicines; - Maintaining order and cleanliness of the dispensary; - Providing exceptional customer service in the dispensary as well as the front of the shop when needed; - Webster packing as required. **About You:** To be successful in applying for this opportunity, you will ideally possess the following: - Previous experience working as a Dispensary Technician; - Strong Pharmacy product knowledge - Excellent computer skills; - Exceptional customer service skills- you will surprise and delight our customers - every day; - Reliable and enthusiastic work ethic; - Adaptability and willingness to work as part of a team; - Excellent communication skills. **We offer:** * A friendly and supportive team environment * Opportunity to be a part of a progressive, growing company * Supportive leadership team and ongoing head office support **How To Apply:** If you are a passionate, aspiring, motivated individual looking for an opportunity to make your mark we want to hear from you. **Apply Now!** 4.2 39,183 Applicants have voted on the ease, speed and acceptability of making an application here Apply Now Dispensary Technician United Chemists Southgate ** Part Time** ** View Further information.** A map showing this Job's location is not available

Toowoomba 4350, Gold Coast, Queensland **Description** USA - Maryland - Rockville The Associate QC Chemist is responsible for performing quality sampling, testing and data review for raw materials under cGMP conditions. The role will support the manufacturing campaigns by ensuring raw materials testing completion within established timelines. The role will also support operation and maintenance of QC laboratory equipment/instrument to comply with cGMP regulations. KEY RESPONSIBILITIES: Conducts and documents routine compendial (NF/USP/BP/EP/JP/ACS) and non-compendial raw material testing, in cGMP environment to support manufacturing. Able to seek additional tasks or non-routine functions and accomplish them according to written procedures in compliance with cGMP with general supervision. Overcomes minor conflicts with priorities. Consults supervisor with major conflicts of priorities. Work with manager to conduct laboratory investigations related to raw material testing. Able to use SAP to manage notifications on-site (DE/LI/MC/CAPA) by adhering to timelines. Able to work effectively as part of a team and exhibit effective interpersonal skills within group as well as with other groups within the department. Trained as an L1 Auditor and participate in (25% of department's L1 Inspections. Maintain laboratory according to EHS requirements. Participate in continuous improvement programs such as GPS, ZAPs, ZIPs. Participates in the on-call response team for chamber maintenance or ADHOC raw material testing. Trained as a Self-Inspector Auditor and participates in department Self Inspections, as assigned. Basic Qualifications: We are looking for professionals with these required skills to achieve our goals: BS/BS in scientific field Experiences in a pharmaceutical development or quality control environment. Preferred Qualifications: If you have the following characteristics, it would be a plus: Writing, communication skills and experience using analytical equipment. Technologies include those in the disciplines of Chemistry or other Biological Sciences Ability to be follow established procedures. Ability to be flexible, understand risk, and using analytical mindset to troubleshoot. Ability to continuous improvement Strong organizational and communication skills and attention to detail. We make and supply medicines and vaccines all around the globe and our teams own every production stage, from creating quality products at our manufacturing sites to designing effective supply forecasting and regulatory inspections; all powered by digital, data and analytics. We operate at impressive scale, producing over 1.7 billion packs of medicine and 767 vaccine doses in 2021. We continue to modernize, so we can launch even more new products at speed whilst turbo-charging delivery across our entire portfolio through our relentless focus on quality, safety, and . The way we work will change. For some, the shift in technology and products will be revolutionary. Our R&D pipeline demands a new kind of supply chain, and we need the very best minds and capability to help us on our journey to make more complex products, harnessing the power of automation and robotics so we can work smarter together. *LI-GSK GSK is a global biopharma company with a special purpose - to unite science, technology and talent to get ahead of disease together - so we can positively impact the health of billions of people and deliver stronger, more sustainable shareholder returns - as an organisation where people can thrive. Getting ahead means preventing disease as well as treating it, and we aim to impact the health of 2.5 billion people around the world in the next 10 years. Our success absolutely depends on our people. While getting ahead of disease together is about our ambition for patients and shareholders, it's also about making GSK a place where people can thrive. We want GSK to be a workplace where everyone can feel a sense of belonging and thrive as set out in our Equal and Inclusive Treatment of Employees policy. We're committed to being more proactive at all levels so that our workforce reflects the communities we work and hire in, and our GSK leadership reflects our GSK workforce. If you require an accommodation or other assistance to apply for a job at GSK, please contact the GSK Service Centre at ************** (US Toll Free) or *************** (outside US). GSK is an Equal Opportunity Employer and, in the US, we adhere to Affirmative Action principles. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, national origin, religion, sex, pregnancy, marital status, sexual orientation, gender identity/expression, age, disability, genetic information, military service, covered/protected veteran status or any other federal, state or local protected class. At GSK, the health and safety of our employees are of paramount importance. As a science-led healthcare company on a mission to get ahead of disease together, we believe that supporting vaccination against COVID-19 is the single best thing we can do in the US to ensure the health and safety of our employees, complementary workers, workplaces, customers, consumers, communities, and the patients we serve. GSK has made the decision to require all US employees to be fully vaccinated against COVID-19, where allowed by state or local law and where vaccine supply is readily available. The only exceptions to this requirement are employees who are approved for an accommodation for religious, medical or disability-related reasons. Important notice to Employment businesses/ Agencies GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site. Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK's compliance to all federal and state US Transparency requirements. For more information, please visit GSK's Transparency Reporting For the Record site. no -- Principals only. Recruiters, please don't contact this job advertiser. no -- Please, no phone calls about this job! no -- Reposting this message elsewhere is NOT OK. * Placed or Updated: 08 Dec 2024 * Category: * ID: 21398 * 7,723views **Location:** Toowoomba 4350,Gold Coast, Queensland **View on map:** Toowoomba 4350, Gold Coast, Queensland **To:**

Status: Full Time Type: Faculty School: Whiting School of Engineering Department/Program: Commercial and Government Programs Office Salary: $86.00/HR-$124.00/HR Closing Date: Open until filled To apply: **General Description** **Climate & Community Resilience Planning PREP Research Associate** This position is part of the National Institute of Standards (NIST) Professional Research Experience (PREP) program. NIST recognizes that its research staff may wish to collaborate with researchers on specific projects of mutual interest and thus requires that they be the recipients of a PREP award. The PREP program enables staff from a wide range of backgrounds to work on scientific research in many areas. Researchers become employees of universities identified as part of the PREP Program. In this position, the researcher will perform technical work that supports the scientific research of the collaboration. A senior researcher or faculty member is sought with expertise in community resilience planning and applied climate science to support the development of a new addendum to the NIST Community Resilience Planning Guide and Playbook (). The new addition will focus on aiding community practitioners with incorporating leading practices and methods to identify relevant climate data, scenarios, and natural hazard information to enhance the resilience of buildings, infrastructure, and communities when subjected to climate-affected hazards. The work will be informed by a series of workshops NIST organized in 2023 that focused on sea level rise (SLR) and coastal flooding, precipitation and inland flooding, and wildfires (). Other climate-related hazards may also be addressed. Future climate effects may include both acute shocks and persistent stressors - some examples include air and water temperature rise, non-hurricane wind events, changes in precipitation, sea level rise, and their associated storm surge and coastal flooding. There is an urgent need for climate projections to be incorporated into community planning so that designers, planners, and engineers can address future climate impacts on community systems and services. Currently, communities are beginning to address this issue in varying ways with available tools and knowledge, but significant advances are still needed to develop guidance on how to characterize localized future climate and natural hazard conditions, how to account for these conditions in infrastructure design, and how to improve construction practices for future climate conditions. NIST has long-standing expertise in reducing natural hazard risks and enhancing the resilience of the built environment. Through this PREP research associate appointment, NIST is continuing to develop technical capacity in applied climate sciences and natural hazard risk reduction and seeks to advance community-scale resilience through climate-informed planning with a focus on advancing the design of buildings and infrastructure systems. The PREP researcher will work with NIST researchers to develop a new addition to the NIST Community Resilience Planning Guide and Playbook to inform communities about leading practices for incorporating future climate conditions into community resilience planning for the built environment. The researcher will identify leading practices for incorporating climate considerations in community resilience planning, which will be informed by , as well as identifying other sources and methods for determining appropriate sources of climate projections and their application to community planning. The primary focus of the PREP researcher will be to identify actionable methods for incorporating climate information in community resilience planning, which are supported by the best available science and case studies, and integrate them into the NIST Community Resilience Planning Guide and Playbook. **Key responsibilities will include, but are not limited to:** - In collaboration with NIST researchers, develop a new addendum to the NIST Community Resilience Planning Guide and Playbook to inform communities about leading practices for incorporating future climate conditions into resilience planning for sea level rise, precipitation, and wildfire, and associated hazard impacts, such as flooding. - Identify other climate-affected natural hazards that may affect future infrastructure performance, and associated climate science and community case studies. - Develop materials for the addendum that describe actionable methods for community resilience planning that are supported by best available science and case studies. **Qualifications** **Qualifications** § A master's or PhD degree in engineering, atmospheric science, or another discipline related to applied climate sciences for the built environment. § An excellent record of research, publications, and documented strong communication skills related to climate and community resilience planning. § A strong background in community decision-making, climate change, and risk assessment. § The ability to work both independently and as part of a larger, multi-disciplinary team to achieve project objectives, meet project deadlines and reporting requirements, and help mentor other team members. Preferred Qualifications - Experience working with communities and municipal governments - Experience developing climate science guidance for use at a local to regional scale **Application Instructions** Please upload the following (preferably in a single PDF) with your application: § 1-2 pg statement of interest that highlights experience and capabilities § Curriculum vitae **Privacy Act Statement** **Authority:** 15 U.S.C. § 278g-1(e)(1) and (e)(3) and 15 U.S.C. § 272(b) and (c) **Purpose:** The National Institute for Standards and Technology (NIST) hosts the which is designed to provide valuable laboratory experience and financial assistance to undergraduates, post-bachelor degree holders, graduate students, master degree holders, postdocs, and faculty. PREP is a 5-year cooperative agreement between NIST laboratories and participating PREP Universities to establish a collaborative research relationship between NIST and U.S. institutions of higher education in the following disciplines including (but may not be limited to) biochemistry, biological sciences, chemistry, computer science, engineering, electronics, materials science, mathematics, nanoscale science, neutron science, physical science, physics, and statistics. This collection of information is needed to facilitate the administrative functions of the PREP Program. **Routine Uses:** NIST will use the information collected to perform the requisite reviews of the applications to determine eligibility, and to meet programmatic requirements. Disclosure of this information is also subject to all the published routine uses as identified in the Privacy Act System of Records Notices: NIST-1: NIST Associates. **Disclosure:** Furnishing this information is voluntary. When you submit the form, you are indicating your voluntary consent for NIST to use the information you submit for the stated purpose. To apply for this position, visit: **Salary Range** The referenced salary range represents the minimum and maximum salaries for this position and is based on Johns Hopkins University's good faith belief at the time of posting. Not all candidates will be eligible for the upper end of the salary range. The actual compensation offered to the selected candidate may vary and will ultimately depend on multiple factors, which may include the successful candidate's geographic location, skills, work experience, internal equity, market conditions, education/training and other factors, as reasonably determined by the University. **Total Rewards** Johns Hopkins offers a total rewards

Full-Time Flexible Schedule Earning Potential of $65,000 - $95,000 Are you ready to embark on a dynamic career path with abundant opportunities for growth? Join our team as a Water Purification Sales Professional and experience a fulfilling role that combines autonomy, potential for advancement, and the chance to positively impact people's lives. Why Choose Us: Pre-Qualified Leads: Benefit from a steady stream of pre-qualified leads, streamlining your workflow and allowing you to focus on building relationships. Comprehensive Paid Training: Receive in-depth training designed to equip you with the skills and knowledge necessary for success, regardless of your previous experience. Flexible Work Hours: Enjoy a flexible work schedule that accommodates your lifestyle, promoting a healthy work-life balance. Lucrative Compensation: Take advantage of a commission-based structure with unlimited earning potential. Your income will reflect your dedication and achievements, with annual earnings expected to range from $65,000 to $95,000, plus opportunities for further growth. Key Responsibilities: Negotiate and finalize sales agreements with clients, ensuring mutually beneficial terms. Clearly explain contract details to clients, providing comprehensive information and addressing any questions. Conduct water testing procedures for potential customers, identifying their specific needs and recommending appropriate solutions. Guide clients through the installation process, ensuring a seamless and satisfactory experience. Qualifications: Previous in-home sales experience is preferred but not required. Willingness and ability to travel within your territory, with appointments provided. A valid driver's license and personal transportation are required for client visits and product demonstrations. Ready to embark on a rewarding career journey with us? We look forward to your application!