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.
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.
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.
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.
Oak (WO).
OPQ is an umbrella organization overseeing the activities of the Chemistry, Manufacturing, and Controls (CMC) review process and drug testing and scientific evaluation of drug products in support of the regulatory components of FDA. This includes backssment of product and process designed, evaluation of product quality in light of established standards and setting and maintaining new quality standards.
DPQR conducts regulatory research on continuous manufacturing as part of an interdisciplinary research approach to address emerging product quality issues. DPQR is doing research on continuous drug substance manufacturing to address regulatory challenges faced by the Agency
for this innovative technology. Duties/Responsibilities: Collaborates with DPQR staff to identify appropriate PAT equipment and methods based on expertise to advance product quality research goals including writing research proposals and protocols Collaborates with DPQR staff to identify prospective applications for PAT implementation, model development, and validation Develops and validates PAT models to predict manufacturing process performance and/or product quality attributes Documents and communicates research results generated from studies including writing technical reports and scientific papers, as well as delivering oral and poster presentations Works with DPQR management to coordinate
activities for the PAT group within DPQR Works with DPQR management to establish collaborations with other PAT groups within the FDA Works with DPQR management to establish collaborations with external stakeholders on advancing the utilization of PAT in medical development and manufacturing Develops training materials and courses on PAT applied to medical development and manufacturing Develops white papers on emerging topics in PAT for medical development and manufacturing Routinely updates management on the status and progress of the PAT-related research projects Minimum Requirements: Requires a bachelor's degree or higher in a science or engineering discipline (e.
g. chemical/mechanical engineering) Minimum four (4) years of experience in applying PAT to address scientific questions. Industrial or government experience applying PAT for processes and/or physical systems. Knowledge and hands-on experience with PAT instruments that can be applied to medical manufacturing including unit operations that involve particles, flowing powders, solutions, and suspensions (e. g. near infrared, Fourier transform infrared, and Raman spectroscopy, etc. ). Knowledge of chemometrics, multivariate modeling approaches, and data processing methods that can be applied to large data sets (e.
g. principal component analysis, partial least squares analysis, linear discriminant analysis, etc. ). Knowledge and hands-on experience with a range of software platforms used for multivariate analysis (e. g. Unscrambler, SIMCA, MATLAB, Eigenvector, Python, etc. ) and willingness to learn platforms as needed. Knowledge of PAT model development, verification, and validation practices. Attention to Detail - being thorough when planning, developing, and carrying out vital tasks in supporting research projects including PAT method documentation. Customer Service - assisting others in the resolution of issues when integrating PAT, developing models, or interpreting results.
Collaboration - willing to participate in interdisciplinary projects working with members and managers on product quality research projects and initiatives. Written Communication - expressing highly technical information (e. g. ideas or facts) to individuals or groups effectively, taking into account the audience and nature of the information, including scientific publications. Oral Communication - expressing highly technical information (e. g. ideas or facts) to individuals or groups effectively, taking into account the audience and nature of the information.
Problem Solving - conducting extensive investigation and analysis to determine the nature and scope of problems and devise solutions. Working knowledge of medical development and manufacturing is a plus. 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.
characterize drug induced changes in cell proteomics and immuno-proteomics. RESPONSIBILITIES: Develop and validate chromatographic and mass spectrometry-based assays for immuneproteomics of HLA presented peptides and small molecules. Produce reports for reliable, sensitive, and validated immunological methods of analyses (prepares, edit, and designate project reports) Perform analysis of mass spectrometry data in order to identify sequences of peptides and modifications using software including PEAKS.
Preparation of standard operating procedures (SOP) and protocols for method validation of immunological assays. Ensure that all work is in compliance with all pertinent SOPs and safe work
practices. Other duties as assigned. MINIMUM REQUIREMENTS: PD in Life Health and Medical Sciences, Biochemistry or any other related field with 2+ years of laboratory experience with immunology and biochemistry and the ability to work independently.
MS in Life Health and Medical Sciences, Biochemistry or any other related field with 5+ years of laboratory experience with immunology and biochemistry and the ability to work independently. Experience in developing and validating analyses of immune biologics and proteins by LCMS. Experience in isolating HLA molecules, affinity purifying peptides from HLA and then performing immune-proteomics using LCMS to characterize the peptides. Basic
office software skills (Word, Excel, Powerpoint, Sigmaplot, Access or File Maker Pro databases etc.
) are required and basic statistical data analysis skills are highly desired. Experience in Mass spectrometry software PEAKS for data analysis. If interested, please apply at 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
strains continue to emerge and spread rapidly worldwide. This poses challenges to diagnosing infected individuals and developing new vaccines and therapies. Therefore, it is imperative that the Food and Drug Administration (FDA) determine if newly developed tests for screening the blood supply can accurately detect all the existing and emerging HIV strains in blood samples.
One of our ongoing studies is that HIV virus panel study will help FDA in its global collaborations aimed at ensuring there are accurate HIV diagnostic tests and safe and effective vaccines available to respond to the changing population of AIDS viruses. HIV virus panel study will provide new insights and will support
development of improved diagnosis, disease monitoring, drug design, and vaccines. OBRR has also helped to produce a new FDA document that offers guidance to blood donor facilities in identifying donors at increased risk for being infected with the variety of HIV-1 called " group O.
" This will help to screen out donors who might be infected based on having spent time in certain parts of Africa or having received blood transfusions or engaged in interactionual activity with residents or former residents in those areas. Duties/Responsibilities: Extract and purify HIV RNA from cultured virus, perform reverse transcript HIV RNA to c DNA, use established primer pool and multiple
PCR methods to amplify the c DNA for Sanger or NGS Sequencing analysis.
Develop new methods and optimize the new systems to amplify highly diversify HIV-1 strains for whole genomic sequence. Sanger and NGS sequencing the PCR products from task 1 and 2. Initial the bioinformatics analysis to determine whole length HIV-1 genomic contigus, identify the genotype and HIV Circulating Recombinant Forms (CRFs). Prepare the aliquoted isolates to delivery to collaborators for Viral Load (VL) test and RNASeq studies. Minimum Requirements: A Ph D or Master degree in any branch of Life Science Research experience in virology or molecular biology area (HIV preferred). Training in the safe handling of human blood samples Experience in Biosafety Level 2 plus and Level 3 laboratories Experience with analysis of human genome data and HIV sequencing data preferred.
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.
human and animal health. We are a fast growing company and seek professional individuals to join our diverse and talented team of employees. We currently have a position for a Research Associate located at Walter Reed Army Institute of Research in Silver Spring, MD.
This position will be supporting Shigella vaccine development. KEY RESPONSIBILITIES Conducts bench research on Shigella (or other enteric pathogens) to include large scale production of purified proteins and LPS, immunogenicity, biochemistry and mechanisms of action of Shigella subunit vaccines. Assist in the evaluation of Shigella vaccines in clinical and pre-clinical studies to include immunizing small animals, collecting
blood, lymph nodes mucosal washes, and determining the immune response elicited after vaccination using cellular proliferation, antibody secreting cell (ASC), ELISA, and immunobead multiplexing assays.
Establishes and/or develops laboratory procedures and analyzes and/or evaluates research data; participates in a cooperative effort to accomplish goals of the laboratory; maintains proficiency and expertise in the field of research. Utilizes professional knowledge of: theories, principles, methods, and techniques of immunology, cell biology, and microbial pathogenesis, such as ELISA, ASC assays, cellular proliferation assays, western blotting, cell culture, small animal handling (such as
mice or guinea pigs), and aseptic technique. (NOTE: Work involving animals requires medical evaluation by a physician including animal allergy and immunization review.
) Duties shall be performed with daily interaction and technical oversight provided by the Principle Investigator. POSITION REQUIREMENTS Requires a Bachelor's degree in a scientific discipline. Must be able to pass background checks. Must be a U. S. Citizen or Green Card Holder with the right to work for any employer in the U. S. COMPENSATION/BENEFITS TMG offers comp. pay and benefits pkg. including health insurance; paid holidays, PTO; EAP; Education Assistance, 401(k) and College Savings Plan.
The Mc Connell Group is an equal opportunity employer EOE M/F/Disabled/Vet Job Posted by Applicant Pro
candidate will have a high school diploma or general education degree (GED. Three (3) or more years related experience in Criminal Justice, Security field and supervisory experience. Leisure World of Maryland Corporation (LWMC), the property management company for Leisure World of Maryland, is a private, age-restricted community comprised of 29 community associations representing over 5,600 homes and extensive Trust operations, located in Silver Spring, Maryland is seeking an experienced Special Police Officer (SPO) to work M onday-Friday, including weekends.
Must be available to work various shifts, 6:00 a. m. - 2:00 p. m. 2:00 p. m. - 10:00 p. m. and 10:00 p. m. - 6:00 a. m. The schedule
include weekends and it is subject to change based on operational needs. The Special Police Officer is responsible for the prevention and detection of crime, the enforcement of criminal and motor vehicle laws, and the enforcement of regulations designed to protect the life and property of the residents on the property of Leisure World of Maryland.
LICENSE/CERTIFICATION Special Police Officer Commission. Handgun (Wear and Carry) permit. Automatic Electronic Defibrillation (AED) Certification. CPR Certification. Current valid full driver's license with clean driving record (Note: Learners Permit/Provisional License is not sufficient). ESSENTIAL FUNCTIONS & BASIC DUTIES: Carries out the
policies and instructions of the Security Department, Mutuals, and LWMC.
Patrols the community/assigned on foot or using vehicle. Responsible for maintaining the peace and order, being observant of unauthorized persons, unauthorized situations, and emergencies. Takes appropriate action based on situation. Warn persons of rule infractions or violations. Enforce no trespass orders and apprehend or evict violators from premises using force only when necessary. Investigates and makes appropriate written reports on crimes, property damage, fires, sudden death, falls, and other incidents that meet the criteria of reportable as well as traffic and non-traffic accidents/incidents as well as reportable traffic accidents.
Gather and record evidence. Interview suspects, witnesses, and victims. Prepares a report of daily activities, any incidents/accidents occurring on the shift, maintains building/area security logs, documents irregularities, such as equipment or property damage, theft, presence of unauthorized individuals, disoriented individuals, falls, property damage, traffic accidents, and other unusual occurrences. Provide assistance to residents in both emergency and non-emergency circumstances. Request medical assistance when necessary. Perform CPR/AED actions based on backssment of the situation/as needed as prescribed by training.
Assists residents who are locked out. Performs welfare checks as requested. Responsible for pre and post duty inspection of vehicle, including but not limited to noting defects, maintaining cleanliness, fueling vehicle etc. Any defects are to be reported immediately to the Transportation Supervisor. Provides supplemental transportation as needed, including but not limited to ambulatory and non-ambulatory transportation services provided. Collects fees as they apply. Adheres to applicable regulations related to the Americans with Disability Act (ADA); correctly operating wheelchair lift with proper safety restraints as requested by passenger.
Secures the administration building, clubhouses, and other buildings as required. Responds to dispatched calls both emergent and non-emergent as needed. Interacts with residents and visitors in a courteous, professional, and helpful manner. Ability to obtain necessary licensing in compliance with state regulations, including but not limited to Special Police Officer Commission and qualify for a wear and carry permit, as well as maintain necessary certifications/licenses needed to operate and/or carry department mandated equipment i.
e. baton, handcuffs, OC spray. Maintains current licenses in good standing as required by state regulations, including but not limited to Special Police Officer commission and qualify for a wear and carry permit. Provides support, guidance, and direction to Gate Guards as needed. Assists with training of Gate Guards. Additional duties as assigned. SUPERVISORY RESPONSIBILITY: Supervises Security Guards on duty during his/her shift assignment. Is responsible for the daily direction, coordination, and evaluation of Security Guards during his/her shift assignment.
Fulfills supervisory responsibilities in accordance with the organization's policies and applicable laws. Responsibilities include interviewing, hiring, and training employees: planning, assigning, and directing work; appraising performance; rewarding and disciplining employees; addressing complaints and resolving problems. PRINCIPAL WORKING RELATIONSHIPS: In addition to the Leisure World of Maryland Corporation (LWMC) staff and contract personnel, the Special Police Officer's principal working relationships are Supervisory Special Police Officer, Operations Manager, Transportation Supervisor, community residents, their families and friends of family, employees of residents and vendors.
The physical requirements described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is regularly required to reach with hands and arms and talk or hear. The employee is frequently required to stand; walk; sit; use hands to finger, handle, or feel and stoop, kneel, crouch, or crawl.
The employee is occasionally required to climb or balance. The employee must regularly lift and /or move up to 10 pounds and occasionally lift and/or move up to 150 pounds. Specific vision abilities required by this job include close vision and ability to adjust focus. We can offer you a challenging and rewarding environment with many opportunities to learn, grow, and achieve great results. If you want to be part of our team, we'd love to hear from you. Competitive salary and excellent benefits. Job Posted by Applicant Pro
A hybrid mod el of onsite and telework each week will likely be put in place in the coming months. Position Summary: The Business Analyst I/Property Asset Inventory Specialist/Property Control will support the NOAA/NESDIS Office of Satellite Ground Services (OSGS) located in Silver Spring, MD and serves as the Property Contact for the Federal Property Custodian and is responsible for the physical custody of all personal property in all areas of the physical property control as well as the processes and procedures within their custodial area.
There may be one or more custodial areas within an accountability area. Primary Duties: Accountable for Federal Property with full life cycle inventory
documentation of the acquisition, utilization, care, rehabilitation and disposal of government property. Complete required Property Training courses and annual NOAA required training.
Provide policy adherence and oversight to ensure continued compliance with relevant Federal laws and regulations. Conduct routine (bi-monthly), quarterly and annual physical touch inventories of personal property. Maintain current custodial records for all accountable personal property within their assigned custodial area. Ensure that personal property is properly maintained and is used only for official purposes. Identify and report to the Property Accountability Officer any property excess to the needs
of the custodial area. Submit appropriate reports promptly for found, lost, missing, stolen, destroyed, damaged, or rendered unserviceable accountable personal property.
Affix property identification number (bar code) labels onto accountable personal property. Conduct physical inventories and reconciling inventory records. Participate in the employee separation clearance process by ensuring that all assigned property has been accounted for when personnel leave employment. Maintain a record of accountable personal property assigned to his/her custodial area that is removed for use or repair outside of the custodial area. Ensure that loaned accountable personal property is returned upon expiration of the loan.
Ensure that complete documentation (Contracts/Interagency Agreements, Accounting Codes, Invoices, Bank Statements and Shipping records) is received and provided to the Property Office for newly acquired property using the Sunflower Enterprise System. Surplus/Excess/ Retire equipment, in collaboration with IT Services to ensure equipment has been properly d-banned or wiped with ISSO approval. Required Education/Experience/Skills: Bachelor's degree - Job experience can be used in lieu of Education. MINIMUM REQUIRED KNOWLEDGE/EXPERIENCE 6-10 years of relevant Asset Inventory Control, Development of tracking spreadsheet/documentation for Records Management.
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.
team of scientists from remote locations. Duties: • Development of custom geoprocessing tools and data models to support high-end spatial analysis, data analytics, and visualization applications to support decision making • Perform geospatial and geostatistical analyses • Organize and input data into databases, maintain accurate detailed records of observations, measurements and results • Write reports and peer review journal articles • Set and meet deadlines for completion of work in timely manner • Work collaboratively in a team environment and contribute to other relevant projects as directed Qualifications: • BS degree in a relevant discipline and 1-2 years of relevant experience required•
Background in marine science is preferred and experience supporting NOAA or BOEM is highly desirable.
• Experience with data preparation, workflows and spatial processing• Proficient in the methods, practices and techniques of spatial modeling, including raster and vector analysis and cartography• Knowledge of Python is preferred• Proficient with Arc Map 10.
X, Arc GIS Pro, Arc GIS Online• Ability to maintain focus on routine and repetitive tasks• Effective verbal and written communication skills• Ability to be flexible in responding to changes in schedules and job priorities• Able to work in a team environment• Ability to work flexible hours, including some long days and infrequently
on weekends• A valid US driver's license• Experience with basic computer programs such as excel and word• Able to work in the US without sponsorship CSS is predominantly a Federal Contractor and is subject to following the terms of Executive Orders.
CSS requires all Employees (Direct, Indirect, government, state, and commercial), including employees working from home/remotely, to be fully vaccinated against COVID-19 or have an approved exemption. Exceptions to the COVID-19 vaccine requirements may be provided to individuals for religious beliefs or medical reasons. Requests for an exception must be submitted to the CSS HR Department. CSS is an Equal Opportunity/Affirmative Action Employer who provides equal employment opportunities to all employees and applicants for employment without regards to race, color, religion, interaction, gender identity, interactionual orientation, pregnancy, national origin, age, disability, veteran status or genetic information.
In addition to federal law requirements, CSS complies with applicable state and local laws governing nondiscrimination in employment in every location in which the company has facilities. 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.
in Silver Spring, MD, but is temporarily approved for telework due to Covid-19. A hybrid model of onsite and telework each week will likely be put in place in the coming months. Position Summary: Global Science & Technology, Inc. a fast-growing firm, is seeking an experienced Program Coordinator and Executive Resource Administrator with exceptional organizational skills to support a Work Force backssment, internal government standards, orientation/rotation programs in support of the Business Operations Support (BOS) Task Order for the Chief Administrative Office (CAO) located in Silver Spring, MD.
Primary Duties: Responsibilities include but are not limited to: Working directly with senior
government clients and closely with BOS support contractors as well as other support contractors. Developing implementation plans related to workforce backssment (including orientation and rotation).
Lead working groups and facilitate discussions on strategic goals, activities, and related tasks, including internal government standards, policies, and procedures. Support conference coordination, implementation, and reporting. Interpret data to understand the business implications of the research. Write detailed, professional reports/briefings and present them to the CAO client as well as other senior managers. Ability to think strategically, analytically, and proactively about diverse
business solutions. Ability to establish and maintain effective working relationships with executive management, peers, employees, clients, other agencies, and the public.
Required Education/Experience/Skills: Bachelor's degree in Business Administration or related field with a minimum of 4-8 years of experience. Years of experience/skill in lieu of education can be used to qualify. Experience in developing and implementing employee surveys. Experience in facilitating presentations and/or working groups in a client-facing environment, as well as experience in making appropriate research recommendations for business improvements. Excellent oral and written communication skills, including presentation skills (MS Visio, MS Power Point, MS Word, MS Excel).
Must be self-motivated, detail-oriented, and highly organized in a highly visible, and fast paced environment. 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.