using advanced instrumentation and laboratory experimentation requiring scientific operations support to execute routine and program management assistance for new domestic manufacturing initiatives.
OBP labs have generated valuable scientific findings and supported regulatory actions and policy, however there is opportunity for the OBP laboratory Advanced & Domestic Manufacturing (DM) program to further increase its impact and regulatory contributions.
Duties/Responsibilities: Enhance laboratory informatics and knowledge management (KM) using modern technology tools. Provide administrative support for DM acquisition activities such as purchase orders and requisition packages to
include tracking/reconciling orders, monitoring, and tracking milestones; follow-up with relevant stakeholders as necessary to meet deadlines. Provide administrative and technical support for lab maintenance activities to include upkeep inventory of supplies and laboratory equipment maintenance and repair coordination.
Provide administrative and technical support for DM research activities at White Oak campus and off-site facilities to include coordinating/tracking location and transportation of shared resources (such as equipment, supplies, consumables). Schedule and keep record of meetings, consultations, actions and work products associated with this task order; prepare summaries of
information/procedures and communicate to relevant stakeholders as needed.
Be able to generate and interpret charts, tables, and graphs for timelines, milestones, and other reports using common business/productivity applications; prepare Word summary report or Power Point presentation on analytical work when requested by program lead. Possess demonstrated organizational skills with achievements reflecting responsiveness with ability to anticipate, envision solutions, and maintain flexibility. Have regularly scheduled meetings with program lead for update briefing or issues. Provide status reports to the program lead according to the schedule provided above.
Support the development of relevant SOPs/Work Aids and coordinate the development of training resources. Complete all mandatory FDA training and maintain required credentials. Minimum Requirements: BA/BS degree with a preference for science and/or business degree major). At least 1 years' experience in office administration or health science, preferably as part of a biomedical or quality analytics or biotechnology research and development program. Apply online at our website: kikiktagruk. / Disclaimer: This is not to be an exclusive list of all responsibilities', duties, and skills required of the person in this job.
KIC is an Equal Opportunity Employer. KIC considers all applicants for employment without regard to race, color, interaction, national origin, religion, age, physical or mental disability, family responsibility, marital status, interactionual orientation, political affiliation, veteran's status or any other legal protected status. Pursuant to The Alaska Native Claims Settlement Act 43 U. S. C. Sec. 1601 et seq. and federal contractual requirements, Kikiktagruk Inupiat Corporation, may legally grant certain preference in employment opportunities to KIC Shareholders and their Descendants.
EOE/AA/M/F/D/V. Please view Equal Employment Opportunity Posters provided by OFCCP here. Successful candidate must pass, comply and adhere to KIC's Drug and Alcohol policy/testing requirements and pass a thorough background check including fingerprinting.
using advanced instrumentation and laboratory experimentation requiring scientific operations support to execute routine and program management assistance for new domestic manufacturing initiatives.
OBP labs have generated valuable scientific findings and supported regulatory actions and policy, however there is opportunity for the OBP laboratory Advanced & Domestic Manufacturing (DM) program to further increase its impact and regulatory contributions.
Duties/Responsibilities: Perform analytical laboratory testing for monoclonal antibodies, therapeutics proteins, and other protein products from multiple sources and compile sample information into multiple databases/data management
systems Culture mammalian (CHO) cells using aseptic techniques for suspension cell culture for shake flasks, spin flasks, and other industrial techniques; Perform microbial culture using aseptic techniques including preparation of appropriate liquid and solid media for detection, identification, enumeration, and inactivation procedures; Operate and maintain benchtop bioreactor systems, including 5L glass bioreactors, disposable wave rocker bioreactors, and disposable micro bioreactors; Operate and maintain additional laboratory instrumentation including: cell and biochemical analyzer systems, bio-layer interferometer, and protein purification systems; Assist with ongoing efforts for integration
of existing technologies with bioreactor and/or FPLC setups for online sampling; Assist with laboratory equipment maintenance and repair; Collect sample information and laboratory testing results from multiple sources and databases; Perform data processing and analysis of acquired data; Assist with the upkeep of inventory of lab supplies and laboratory equipment and instrumentation; Prepare Word summary report or Power Point presentation on cell culture work when requested by program lead; Have weekly meetings with program lead for update briefing or issues; Provide status reports to the program lead according to the schedule provided above; Write manuscripts and/or technique reports for publications or white papers on the project; Complete all mandatory FDA training and maintain required credentials.
Minimum Requirements: BA/BS (MS or advanced graduate degree highly preferred) degree in Biochemistry/Cell Biology/Biotechnology/Chemistry/Chemical or Bioengineering or related course of study 4 years experience (2 years for MS) in biomedical manufacturing or quality analytics or biotechnology research and development or other relevant field. Apply online at our website: kikiktagruk. / Disclaimer: This is not to be an exclusive list of all responsibilities', duties, and skills required of the person in this job.
KIC is an Equal Opportunity Employer. KIC considers all applicants for employment without regard to race, color, interaction, national origin, religion, age, physical or mental disability, family responsibility, marital status, interactionual orientation, political affiliation, veteran's status or any other legal protected status. Pursuant to The Alaska Native Claims Settlement Act 43 U. S. C. Sec. 1601 et seq. and federal contractual requirements, Kikiktagruk Inupiat Corporation, may legally grant certain preference in employment opportunities to KIC Shareholders and their Descendants.
EOE/AA/M/F/D/V. Please view Equal Employment Opportunity Posters provided by OFCCP here. Successful candidate must pass, comply and adhere to KIC's Drug and Alcohol policy/testing requirements and pass a thorough background check including fingerprinting.
advanced instrumentation and laboratory experimentation requiring scientific operations support to execute routine and program management assistance for new domestic manufacturing initiatives.
OBP labs have generated valuable scientific findings and supported regulatory actions and policy, however there is opportunity for the OBP laboratory Advanced & Domestic Manufacturing (DM) program to further increase its impact and regulatory contributions.
Duties/Responsibilities: Effectively communicate with regulatory backssors, laboratory staff, other contractors and management on developing and prioritizing software to advance knowledge-based tools and systems for oversight of biological
product quality; Translate a variety of inputs into the development and prioritizing of software to advance knowledge-based tools and systems for oversight of biological product quality; inputs may include conversations, diagrams, flow charts and other descriptions of needs for biological quality oversight; Be facile in the use of common software languages, as well as VBA and xml, and be familiar with data analysis tools (e.
g. Excel, Access, JMP, SAS); Support capture and entry of relevant information from a variety of information sources (people, documents and electronic systems) into office databases; Supporting linking of systems to reduce duplication and inconsistencies; Develop
and prioritize software to advance knowledge-based tools that organize integrate and analyze data to advance knowledge, tools and systems for oversight of biological product quality and systems for oversight of biological product quality; Be able to effectively communicate software prioritization and/or development specifications and requirements to programmers or managers; Assist with strategic planning for informatics software to support effective oversight of biological product quality; Assist in defining IT needs based on office requests and needs; Lead or support specific software development projects to deal with informatic needs; Develop user-friendly, searchable, efficient, meaningful software interfaces based on a thorough gathering and understanding of user needs; Prepare Word summary report or Power Point presentation on work when requested by program lead; Have weekly meetings with program lead for update briefing or issues; Provide status reports to the program lead according to the schedule provided below; Complete all mandatory FDA training and maintain required credentials.
Minimum Requirements: BA/BS degree and with 6 or more years of experience in bioinformatics or data science or an MS degree with two or more years of experience years of experience in bioinformatics or data science.
Coursework in biology or chemistry would be of value. Apply online at our website: kikiktagruk. / Disclaimer: This is not to be an exclusive list of all responsibilities', duties, and skills required of the person in this job. KIC is an Equal Opportunity Employer. KIC considers all applicants for employment without regard to race, color, interaction, national origin, religion, age, physical or mental disability, family responsibility, marital status, interactionual orientation, political affiliation, veteran's status or any other legal protected status.
Pursuant to The Alaska Native Claims Settlement Act 43 U. S. C. Sec. 1601 et seq. and federal contractual requirements, Kikiktagruk Inupiat Corporation, may legally grant certain preference in employment opportunities to KIC Shareholders and their Descendants. EOE/AA/M/F/D/V. Please view Equal Employment Opportunity Posters provided by OFCCP here. Successful candidate must pass, comply and adhere to KIC's Drug and Alcohol policy/testing requirements and pass a thorough background check including fingerprinting.
closed an oversubscribed Series A funding round in mid-2022 to enable the growth of the team and commercialization of the technology. We offer an inclusive environment with opportunities for growth and believe that a thriving workspace leads to a thriving company.
We hope you will contact us to learn more and to be a part of our diverse, collaborative team! We are looking to add a full-time Polymer Chemist to our team in Beltsville, MD. This position reports to the Ceramics R&D Manger and will lead development of polymer formulations for novel processes to manufacture the ceramic electrolyte in our solid-state battery. The Polymer Chemist will spearhead material and process innovation
focusing on material selection, processing, and characterization of curable polymers (thermal, UV, e-beam, 2-part, etc. ). The ideal candidate is energized by challenges and wants to be part of a fast-paced, cohesive team to make an impact.
Responsibilities: Apply polymer background to develop new formulations of ceramic polymer composite matrices and follow through to process feasibility Lead R&D projects directed towards achieving company goals - determining experimental approach, designing experiments, and efficiently communicating progress and critical findings Identify and implement new methods, analytical measurements, or equipment to achieve project goals Take the initiative to
anticipate and solve problems Look for opportunities to improve or invent products Maintain lab cleanliness and promote environmental health and safety in the daily work environment Required Experience: Ph.
D. in Chemistry, Polymer Chemistry, Chemical Engineering, or related field4+ years of experience (postdoctoral or industrial) in polymer research and development Experience with curable polymer formulation, processing, and characterization Experience with a variety of chemical and materials characterization tools, e. g. FTIR, NMR, GC/MS, LC/MS, TGA, DSC, etc. Required Skills: Ability to learn, adapt, and innovate in a dynamic R&D environment Ability to analyze and resolve highly complex technical challenges thoroughly and efficiently using an analytical approach Works well in a collaborative and team-focused setting Clear, effective, and efficient communication skillinteractioncellent organizational skills Department: R&D Location: Beltsville, MD This role is fully in-person.
Reports to: Ceramics R&D Manager Benefits: In addition to a competitive salary, we offer the following company benefits: Medical, dental, vision, disability, and life insurance Stock options in an early-stage company Company and floating holidays17 days of PTO to start, with increase upon tenure401k plan with a 4% company match beginning after first paycheck Wellness allowance of $1k annually Company Description Ion Storage Systems Inc.
located in Beltsville, MD, is a rapidly growing company commercializing its breakthrough lithium metal battery technology based on discoveries made at the University of Maryland. The company is committed to developing products that will impact everyday life on a global scale. Our technology improves product performance and safety in a variety of applications including, defense and aerospace, consumer electronics, electrified transportation, and renewable energy storage.
Our team is made up of innovative, driven & creative individuals who are passionate about their work. The company offers an inclusive environment, growth opportunities and encourages work/life balance. To all recruitment agencies: Ion Storage Systems, Inc. will not accept agency resumes for this role. Please do not forward resumes to our jobs email, or to any Ion Storage Systems employees or any other company email address. Ion Storage Systems is not responsible for any fees related to unsolicited resumes. Ion Storage Systems, Inc. is proud to be an Equal Opportunity/Affirmative Action Employer.
All qualified applicants will receive consideration for employment without regard to race, color, religion, interaction, ancestry, pregnancy, interactionual orientation, gender identity, national origin, age, citizenship, marital status, disability, or Veteran status. Eligibility to work in the United States as a U. S. Citizen or U. S. permanent resident is required for consideration. Proof of COVID-19 vaccination is required as well. Job Posted by Applicant Pro
instrumentation and laboratory experimentation requiring scientific operations support to execute routine and program management assistance for new domestic manufacturing initiatives.
OBP labs have generated valuable scientific findings and supported regulatory actions and policy, however there is opportunity for the OBP laboratory Advanced & Domestic Manufacturing (DM) program to further increase its impact and regulatory contributions.
Duties/Responsibilities: Perform analytical laboratory testing for monoclonal antibodies, therapeutic proteins, and other protein products from multiple sources and compile sample information into multiple databases. Operate and maintain advanced
analytical instrumentation such as liquid chromatography (U/HPLC) systems, rapid microbial detection and identification systems, and multimodal spectrophotomers for the analysis of protein products and for development of in-line/on-line measurement systems.
Operate and maintain additional preparative and analytical laboratory instrumentation including: protein purification systems, protein stability analyzers, microfluidic capillary systems, multi angle light scattering systems. Culture mammalian (CHO) and/or bacterial cells using aseptic techniques for suspension cell culture and analysis with shake flasks, spin flasks, and other industrial techniques; Assist with ongoing efforts for
integration of existing technologies with bioreactor and/or FPLC setups for online sampling.
Assist with laboratory equipment maintenance and repair. Collect sample information and laboratory testing results from multiple sources and databases. Perform data processing and analysis of acquired data. Assist with the upkeep of inventory of lab supplies and laboratory equipment and instrumentation. Prepare Word summary report or Power Point presentation on cell culture work when requested by program lead. Have weekly meetings with program lead for update briefing or issues. Provide status reports to the program lead according to the schedule provided above.
Write manuscripts and/or technique reports for publications or white papers on the project. Complete all mandatory FDA training and maintain required credentials. Minimum Requirements: BA/BS degree in Biochemistry/Cell Biology/Biotechnology/Chemistry/Chemical or Bioengineering or related course of study 1 year experience in biomedical manufacturing or quality analytics or biotechnology research and development or other relevant field. Apply online at our website: kikiktagruk. / Disclaimer: This is not to be an exclusive list of all responsibilities', duties, and skills required of the person in this job.
KIC is an Equal Opportunity Employer. KIC considers all applicants for employment without regard to race, color, interaction, national origin, religion, age, physical or mental disability, family responsibility, marital status, interactionual orientation, political affiliation, veteran's status or any other legal protected status. Pursuant to The Alaska Native Claims Settlement Act 43 U. S. C. Sec. 1601 et seq. and federal contractual requirements, Kikiktagruk Inupiat Corporation, may legally grant certain preference in employment opportunities to KIC Shareholders and their Descendants.
EOE/AA/M/F/D/V. Please view Equal Employment Opportunity Posters provided by OFCCP here. Successful candidate must pass, comply and adhere to KIC's Drug and Alcohol policy/testing requirements and pass a thorough background check including fingerprinting.
analysis. What The Job Entails: Participates in performance of lab-specific assay development, validation and sample analysis Prepares data tables and reports within Laboratory Information Management Systems (Watson™) Provides support in obtaining reference materials, control plasma and project-specific consumables to meet the objectives of the study Participates in data transfers, pre-clinical and clinical data management tasks Assists in training personnel in the operation, maintenance, and troubleshooting of laboratory equipment Contributes to department initiatives, e.
g. process improvements, as required Always complies with the Laboratory Safety Policy Always complies with company
Standard Operating Procedures unless specifically varied in the validation or sample analysis plan May perform study director/PI activities such as: Controls appropriate bioanalytical portion of studies by designing the experimental approach, overseeing the experimental execution, collating and interpreting scientific data and generating study reports, working in close co-operation with study Sponsors at all stages Carries out laboratory tasks, working with other laboratory staff to progress study-specific experimental work and, as necessary, to support non-study-specific laboratory duties Prepares or reviews standard operating procedures for use by the Company, as required Provides scientific
and technical support to colleagues in the Business Development group, as required This may involve participation in client visits, both inbound and outbound Contributes to the training, monitoring and mentoring of staff as necessary Assists with scientific investigations and efforts to troubleshoot/solve assay problems Attends and presents at Scientific Conferences Lead development and validation of Immunoassays, cell-based assays, q PCR, and/or flow cytometry as required, to detect/monitor biologics in clinical and preclinical analysis Highly experienced with performance of PK/PD, ADA and biomarker immunoassays Requirements: Bachelor's Degree or higher degree, in a scientific related discipline Minimum of 5 years relative work experience Exceptional analytical and problem-solving capabilities Full understanding of regulatory requirements of study types assigned Excellent written and verbal communication skills in a team environment
2016, the 21st Century Cures Act (Cures Act) was signed into law and codified CBHSQ. CBHSQ conducts national surveys tracking population-level behavioral health issues. CBHSQ also provides statistical and analytical expertise; both activities support the Assistant Secretary for Mental Health and Substance Use and the Secretary of HHS.
CBHSQ maintains several data collection systems and surveys on key topics in U. S. behavioral health. This position will support the Behavioral Health Services Information System (BHSIS), which collects information on the U. S. behavioral health treatment system and connects people with substance use and mental health treatment through the Behavioral Health
Treatment Services Locator. The Data Scientist will be collaborative and demonstrate focus and attention to detail. He / she receives, analyzes, and processes BHSIS substance abuse treatment services and mental health treatment services data.
Specifically: Analyze data files, produce error reports and work with stakeholders to resolve processing errors and creating automated anomaly detection Create, document, and implement quality control procedures that eliminate data errors Revise processing operations to incorporate new data elements and data quality control and timeliness procedures related to new elements Build, deploy, and maintain data management systems and back-end data infrastructure
Perform data mining, exploration, and analysis Create data visualizations, reports, dashboards, and data audits Design, train, and implement machine learning algorithms Leverage predictive models MINIMUM QUALIFICATIONS Exceptional technical writing skills Ability to communicate complex data in a simple, actionable way Ability to visualize data in the most effective way possible for a given project or study Analytical and problem-solving skills 3+ year experience using statistical computer languages (R, Python, SAS a must) to manipulate data and draw insights from large data sets 3+ Experience with ML/NLP/AI Familiarity with data management tools Ability to work independently and with team members from different background Excellent attention to detail Masters or Ph D in Informatics, Data Science, Statistics or related field, and 3+ years of work experience Hendall Inc.
is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, interaction, interactionual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability.
using advanced instrumentation and laboratory experimentation requiring scientific operations support to execute routine and program management assistance for new domestic manufacturing initiatives.
OBP labs have generated valuable scientific findings and supported regulatory actions and policy, however there is opportunity for the OBP laboratory Advanced & Domestic Manufacturing (DM) program to further increase its impact and regulatory contributions.
Duties/Responsibilities: Culture mammalian (CHO) cells using aseptic techniques for suspension cell culture for shake flasks, spin flasks, and other industrial techniques; Operate and maintain benchtop bioreactor systems, including
5L glass bioreactors, disposable wave rocker bioreactors, and disposable micro bioreactors; Operate and maintain additional laboratory instrumentation including: cell and biochemical analyzer systems, bio-layer interferometer, and protein purification systems.
Assist with ongoing efforts for integration of existing technologies with bioreactor setups for online sampling; Assist with laboratory equipment maintenance and repair; Collect sample information and laboratory testing results from multiple sources and databases; Perform data processing and analysis of acquired data; Assist with the upkeep of inventory of lab supplies and laboratory equipment and instrumentation; Prepare Word summary
report or Power Point presentation on cell culture work when requested by program lead; Have weekly meetings with program lead for update briefing or issues; Provide status reports to the program lead according to the schedule provided below; Write manuscripts and/or technique reports for publications or white papers on the project; Complete all mandatory FDA training and maintain required credentials.
Minimum Requirements: BA/BS (MS or advanced graduate degree highly preferred) degree in Biochemistry/Cell Biology/Biotechnology/Chemistry/Chemical or Bioengineering or related course of study 4 years-experience (2 years for MS) in biomedical manufacturing or quality analytics or biotechnology research and development or other relevant field.
Apply online at our website: kikiktagruk. / Disclaimer: This is not to be an exclusive list of all responsibilities', duties, and skills required of the person in this job. KIC is an Equal Opportunity Employer. KIC considers all applicants for employment without regard to race, color, interaction, national origin, religion, age, physical or mental disability, family responsibility, marital status, interactionual orientation, political affiliation, veteran's status or any other legal protected status. Pursuant to The Alaska Native Claims Settlement Act 43 U.
S. C. Sec. 1601 et seq. and federal contractual requirements, Kikiktagruk Inupiat Corporation, may legally grant certain preference in employment opportunities to KIC Shareholders and their Descendants. EOE/AA/M/F/D/V. Please view Equal Employment Opportunity Posters provided by OFCCP here. Successful candidate must pass, comply and adhere to KIC's Drug and Alcohol policy/testing requirements and pass a thorough background check including fingerprinting.
provides environmental and cultural resources consulting services. We are a value-driven, employee-first government small business contractor. Trust, expertise, and compassion drive our success, while gratitude, joy, and flexibility drive the team. You will conduct regulatory research, plan and manage technical projects, write reports, mentor junior staff, and collaborate with a team, while remaining flexible to prioritize clients' needs and deadlines.
Minimum Qualifications Bachelor's degree in Environmental Engineer/ Environmental Science , or a closely related field. Master's degree a plus Experience in SPCC, SWPPP, MS4, ASTs, and USTs compliance Working knowledge of Department of
Defense (Do D) Compliance programs and/or the state of Maryland is a plus Experience with estimating the level of effort for project tasks Excellent interpersonal communication and writing skills and attention to detail Ability to manage time efficiently, be responsive, and work independently Flexibility to serve in multiple roles and teams depending on the client and project Ability to work away from home, on-site, for 1-2 weeks at a time, including work outdoors Must be able to pass Do D security clearances and background checks US citizenship required Knowledge and Experience Familiar with federal and state environmental requirements related to Clean Water Act compliance; storm/wastewater
permitting, planning, and compliance; illicit discharge studies and inspections; outfall reconnaissance inventories and inspections; evaluation of structural and non-structural stormwater best management practices; oil pollution prevention; and evaluation of compliance with permit conditions.
Experience in preparing environmental compliance plans, permits, and reports and executing environmental compliance backssments/inspections to ensure compliance with federal, state, and local requirements. Experience in providing environmental compliance support to clients, including conducting site visits as needed. Work experience with the DOD, Maryland Department of the Environment, Virginia Department of Environmental Quality, and D.
C. Department Energy & Environment is preferred. Salary commensurate with experience and bonuses are offered for exceptional performance. The benefits package includes health insurance, paid holiday and vacation, fitness stipend, and a 401(k) plan with employer contribution regardless of employee contribution. Please send a CV and three references. Successful candidates should be prepared to submit a writing sample. ERG, LLC is an Equal Opportunity and Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, interaction, national origin, pregnancy, marital status, interactionual orientation, gender identity, age, physical or mental disability, or protected veteran status.
We participate in the E-Verify Employment Verification Program.
instrumentation and laboratory experimentation requiring scientific operations support to execute routine and program management assistance for new domestic manufacturing initiatives.
OBP labs have generated valuable scientific findings and supported regulatory actions and policy, however there is opportunity for the OBP laboratory Advanced & Domestic Manufacturing (DM) program to further increase its impact and regulatory contributions.
Duties/Responsibilities: Perform analytical laboratory testing for monoclonal antibodies, therapeutics proteins, and other protein products from multiple sources and compile sample information into multiple databases/data management systems; Interpret
and analyze large data sets from advanced chromatographic and/or spectroscopic instrumentation such as high-performance liquid chromatography (UHPLC) systems, Mass Spectrometry systems including QTo F's, Qda's, and QQQ, or Near Infrared detector systems for the analysis of protein products and for development of on-line measurement systems; Collect sample information and laboratory testing results from multiple sources and databases; verify laboratory testing results by performing actual calculations; Assist in operate and maintenance of benchtop bioreactor systems, including 5L glass bioreactors, disposable wave rocker bioreactors, and disposable micro bioreactors; Assist in operation and maintenance
of additional laboratory instrumentation including: cell and biochemical analyzer systems, and protein purification system, protein stability analyzers, microfluidic capillary systems s; Assist with ongoing efforts for integration of existing technologies with upstream and downstream unit processes for online sampling; Assist with laboratory equipment maintenance and repair; Assist with the upkeep of inventory of lab supplies and laboratory equipment and instrumentation; Prepare Word summary report or Power Point presentation on analytical work when requested by program lead; Have weekly meetings with program lead for update briefing or issues; Provide status reports to the program lead according to the schedule provided above; Write manuscripts and/or technique reports for publications or white papers on the project; Complete all mandatory FDA training and maintain required credentials.
Minimum Requirements: BA/BS (MS or advanced graduate degree highly preferred) degree in Biochemistry/Cell Biology/Biotechnology/Chemistry/Chemical or Bioengineering or related course of study 4 years experience (2 years for MS) in biomedical manufacturing or quality analytics or biotechnology research and development or other relevant field.
Apply online at our website: kikiktagruk. / Disclaimer: This is not to be an exclusive list of all responsibilities', duties, and skills required of the person in this job. KIC is an Equal Opportunity Employer. KIC considers all applicants for employment without regard to race, color, interaction, national origin, religion, age, physical or mental disability, family responsibility, marital status, interactionual orientation, political affiliation, veteran's status or any other legal protected status. Pursuant to The Alaska Native Claims Settlement Act 43 U. S. C. Sec. 1601 et seq. and federal contractual requirements, Kikiktagruk Inupiat Corporation, may legally grant certain preference in employment opportunities to KIC Shareholders and their Descendants.
EOE/AA/M/F/D/V. Please view Equal Employment Opportunity Posters provided by OFCCP here. Successful candidate must pass, comply and adhere to KIC's Drug and Alcohol policy/testing requirements and pass a thorough background check including fingerprinting.
instrumentation and laboratory experimentation requiring scientific operations support to execute routine and program management assistance for new domestic manufacturing initiatives.
OBP labs have generated valuable scientific findings and supported regulatory actions and policy, however there is opportunity for the OBP laboratory Advanced & Domestic Manufacturing (DM) program to further increase its impact and regulatory contributions.
Duties/Responsibilities: Effectively communicate with regulatory backssors, laboratory staff, other contractors and management on advancing knowledge, tools and systems for oversight of biological product quality; Translate organizational needs
into diagrams, flow charts and descriptions to allow development of approaches, tools and systems that increase the efficiency and effectiveness of biological product oversight; Be facile in the use of common data analysis tools (e.
g. Excel and Access with VBA, JMP, SAS); Collect relevant data from a variety of information sources (people, documents and electronic systems; Organize, integrate and analyze data to advance knowledge, tools and systems for oversight of biological product quality; Be able to effectively communicate software prioritization and/or development needs to programmers or managers; Assist with strategic planning for informatics to support effective oversight of biological
product quality; Assist in defining research needs based on data analysis; Lead or support specific projects to deal with regulatory challenges; Prepare user-friendly, searchable, meaningful data displays using common data analysis tools; Prepare Word summary report or Power Point presentation on work when requested by program lead; Have weekly meetings with program lead for update briefing or issues; Provide status reports to the program lead according to the schedule provided below; Complete all mandatory FDA training and maintain required credentials.
Minimum Requirements: BA/BS degree and with 6 or more years of experience in bioinformatics or data science or an MS degree with two or more years of experience years of experience in bioinformatics or data science.
Coursework in biology or chemistry would be of value. Apply online at our website: kikiktagruk. / Disclaimer: This is not to be an exclusive list of all responsibilities', duties, and skills required of the person in this job. KIC is an Equal Opportunity Employer. KIC considers all applicants for employment without regard to race, color, interaction, national origin, religion, age, physical or mental disability, family responsibility, marital status, interactionual orientation, political affiliation, veteran's status or any other legal protected status.
Pursuant to The Alaska Native Claims Settlement Act 43 U. S. C. Sec. 1601 et seq. and federal contractual requirements, Kikiktagruk Inupiat Corporation, may legally grant certain preference in employment opportunities to KIC Shareholders and their Descendants. EOE/AA/M/F/D/V. Please view Equal Employment Opportunity Posters provided by OFCCP here. Successful candidate must pass, comply and adhere to KIC's Drug and Alcohol policy/testing requirements and pass a thorough background check including fingerprinting.
relevant regulatory research using advanced instrumentation and laboratory experimentation requiring scientific operations support to execute routine and program management assistance for new domestic manufacturing initiatives.
OBP labs have generated valuable scientific findings and supported regulatory actions and policy, however there is opportunity for the OBP laboratory Advanced & Domestic Manufacturing (DM) program to further increase its impact and regulatory contributions.
Duties/Responsibilities: Establish, and fully-characterize genetically modified (engineered) cell lines; Purify the therapeutic proteins produced by engineered CHO cell lines; Analyze the glycans of
therapeutic proteins endogenous glycoproteins and other glycoconjugates with mass spectrometry (MS), such as MALDI-TOF, LC-MS, and Ion-mobility spectrometry-MS (IMS-MS or IMS), (U)HPLC and other state-of-the-art technologies; Establish new analytical methods to release and analyze O-glycans from glycoproteins; Establish new analytical methods and procedures for testing the quality of protein drugs; Summarize and prepare data reports using Microsoft Word or Power Point; Have weekly progress meetings to update the PI and report any pitfalls or shortcomings; Write manuscripts and/or technique reports for publications or white papers on the project; Complete all mandatory FDA training and maintain
required credentials.
Minimum Requirements: MS or Ph D in biochemistry, glycobiology, molecular biology, chemistry, pharmaceutics, or related field.
For a candidate possessing an MS, at least two years of relevant experience is required in biomedical manufacturing, quality analytics, biotechnology research and development or other relevant area. Apply online at our website: kikiktagruk. / Disclaimer: This is not to be an exclusive list of all responsibilities', duties, and skills required of the person in this job. KIC is an Equal Opportunity Employer. KIC considers all applicants for employment without regard to race, color, interaction, national origin, religion, age, physical or mental disability, family responsibility, marital status, interactionual orientation, political affiliation, veteran's status or any other legal protected status.
Pursuant to The Alaska Native Claims Settlement Act 43 U. S. C. Sec. 1601 et seq. and federal contractual requirements, Kikiktagruk Inupiat Corporation, may legally grant certain preference in employment opportunities to KIC Shareholders and their Descendants. EOE/AA/M/F/D/V. Please view Equal Employment Opportunity Posters provided by OFCCP here. Successful candidate must pass, comply and adhere to KIC's Drug and Alcohol policy/testing requirements and pass a thorough background check including fingerprinting.
of onsite and telework each week will likely be put in place in the coming months. Position Summary: The individual in this position will be a member of the satellite Sea-surface Salinity (SSS) Science Team, responsible for the development of SSS applications employing observations from ESA's SMOS mission and NASA's SMAP mission Primary Duties: Develop an approach for reconciling high-latitude satellite skin salinity observations with near-surface bulk salinity to enable assimilation of high-latitude satellite SSS observations Exploring/develop assimilation of satellite altimetry observations for improved model representation of thermohaline circulation and ocean heat content Characterize the
freeze/melt temperature for sea ice as a direct function of ocean surface water salinity; and supporting marine ecosystem backssments and modeling efforts through the exploitation of satellite SSS observations Required Education/Experience/Skills: Ph.
D. in a quantit ative field of research (Physics, Math , Stat istics, Remote Sensing , Oceanography, Meteorology) completed by date of hire Solid quantitative educational background (fundamental Physics, Math, Statistics ) Strong scientific analytical skills with detail-oriented working style Proficiency with computational programming (Fortran, MATLAB, IDL, Python, etc. ) and scripting (Unix/Linux) Proven list of deliverables (peer-reviewed
publications, derived products, etc. ) W illingness and ability to conduct independent research (from problem definition to technical solution to documentation in peer-reviewed literature ) while being a team player Desired Qualifications: Experience with SS S retrieval algorithms and SSS data sets ; Experience with backssing salinity impacts and dependencies in geophysical processes and ecological systems, as well as SSS utility as a predictor for Earth-system processes; Familiarity with Artificial Intelligence/Machine Learning techniques; Proficiency with global data handling and quality control procedures; Familiarity with radiative tran sfer modeling, particularly for the L band.
Selected applicants will be subject to a government background investigation. GST offers competitive salaries; vacation, sick, and holiday leave; major medical, dental, life, long-term and short-term disability insurance; 401K retirement plan; tuition assistance; and opportunities for employee career growth and development. All qualified applicants will receive consideration for employment without regard to age, race, color, religion, interaction, national origin, disability, veterans' status, interactionual orientation and gender identity. GST is an Equal Opportunity/Affirmative Action Employer.
Jim Coleman Automotive is a company that offers great team environment, great benefits and ongoing training and support for its employees. We don't have just salespeople, we have trained, certified, and motivated Automotive Product Specialists. If you are an energetic a motivated professional who loves to make clientele happy, please apply by uploading your resume.
Our dealership is rather progressive and has a highly energetic feel. We like to have a great time while providing even greater customer service. We also have one of the best pay plans in the area! The Right Candidate will be someone who is enthusiastic, outgoing, and full of positive energy. You will be someone who enjoys
working with people and possesses a passion for helping others. Responsibilities - Car Sales: Greet customers in a friendly manner and listen to their requirements in order to match their vehicle needs with one in current inventory.
Accompany customer on test drives and demonstrate vehicle features and technology. Follow guidelines and best practices for dealing with and handling internet inquires. Assist all customers who arrive in our showroom. Build rapport with customers to build a base of referrals to establish customer network. Work with sales managers and BDC staff to capitalize on all opportunities. Keep up with industry standards and best practices. Pass Cadillac's training classes
and e-modules to gain and maintain certifications. Most, importantly always take care of the customer and have fun while maintaining professionalism.
Benefits: · One of the most competitive pay plans in the area · Health, Dental and Vision insurance · 401k · Paid Vacations · Vehicles Assistance Bonuses · Paid Training · Opportunity to learn the business inside and out · Growth Potential Requirements: · Valid MD/DC/VA Driver's License · Ability to pass a background check and drug test Applicants have rights under Federal Employment Laws Family & Medical Leave Act (FMLA): www. dol. gov/agencies/whd/posters/fmla Equal Employment Opportunity (EEO): www. eeoc. gov/know-your-rights-workplace-discrimination-illegal-poster Employee Polygraph Protection Act (EPPA): eppac.
pdf (dol. gov)
will contribute to the strategic growth of the company, leading partnership development, marketing, and the production of winning proposals. The successful candidate will have the ability to lead initiatives from proposal-specific duties to overall team management, projection, and opportunity tracking in coordination with other proposal managers, coordinators, and the technical teams.
This position will report to the Chief Development Officer. Responsibilities: Leads and participates in all aspects of business development including facilitation of proposal design and writing; management of partner and staff identification, recruitment, selection, and negotiations; support to pricing;
preparation of graphics, and ongoing review and consolidation of proposal inputs. Leads the writing of management, personnel, and past performance sections of proposals as required.
Ensures proposal compliance and competitiveness. Supports marketing initiatives including drafting of qualifications statements and leading the team in discussions with potential partners, clients, and staff. Contributes to and leads business planning and capture activities including networking, research, and analysis to contribute to our ability to make strategic and informed decisions and backss viability of upcoming opportunities. Ensures the submission of complete, compliant, and competitive technical
and cost proposals. Formats, proofreads, designs basic graphics, and other functions associated with production and delivery.
Ensure proposal teams stay on track for draft reviews and proposal submission. Coordinates and facilitates critical meetings throughout the proposal process including kick-off meetings, design sessions, review discussions, post-submission debriefs, and after-action reviews; Contributes to the ME&A business development administrative processes, including managing tracking tools, providing proposal resourcing budget estimates, providing inputs to corporate BD presentations, and other related tasks. Leads capture teams in the field on strategic bids.
Works with senior leadership to develop, implement, and monitor corporate business strategies; Represents ME&A at conferences workshops and relevant industry gatherings. Performs other related duties as required. Qualifications: Bachelor's degree in international development, journalism, or another related field. Masters degree preferred. Minimum of four to five years of progressively responsible experience in managing proposal development processes for USAID and other donor solicitations. Strong working knowledge in MEL, water, environment, and other related fields. Ability to research local and international partners, develop trusting relationships, and facilitate partnership negotiations.
Strong expertise in writing proposal sections and ability to strengthen team members' capacity in proposal writing, particularly related to management, personnel, qualifications, and similar sections. Excellent conceptual and strategic thinking skills to guide teams, maintaining a strong grasp of the overall vision and process while ensuring attention to details. Ability to motivate teams and provide feedback on a timely basis to produce quality outputs within tight timeframes and while simultaneously managing several projects.
Ability to actively participate in and facilitate group meetings with diverse participants. Strong understanding of corporate BD processes and management, including proposal resourcing, budget and consultant tracking, and other tasks. Excellent organizational skills and ability to present information succinctly and professionally in support of senior management review and decision making. Proficiency with MS Office suite and an expert ability to format documents in Word, Power Point, and Visio. Demonstrated flexibility and interpersonal skills to interact with employees at all levels.
Ability to travel as required. All applications and CVs must be submitted in English. ME&A, Inc. is committed to hiring and retaining a diverse workforce. We are an Equal Opportunity Employer, making decisions without regard to race, color, religion, interaction, national origin, age, veteran status, disability, or any other protected class. ME&A will make reasonable accommodations in compliance with Title VII of the Civil Rights Act and the Americans with Disabilities Act of 1990. For our EEO Policy Statement and a copy of our EEO Policy Statement and information on your EEO rights under the law.
ME&A is committed to the principle of equal employment opportunity for all applicants