Chemist Jobs in Germantown, MD

The qualified individual should have experience in sample testing and product characterization using electrophoretic technologies such as SDS-PAGE, pH, total protein analysis including A280 and Western Blot. Experience or knowledge on other analytical technology such as PCR based assays is a plus. Responsibilities include but not limited to: Follow SOP to test in-process samples using SDS-PAGE densitometry, Western Blot, pH, and Total Protein via A280 to support process development and stability studies of nanoparticle vaccines. Analyze gel image data using Image Lab and document in-process testing data. Optimize and troubleshoot SDS-PAGE and Western Blot assays. Participate in qualification of in-process assays. Present sample testing data at internal meetings. Thoroughly analyze results and methods, solve analytical problems, troubleshoot assays and meet experimental expectations for analytics. Exercises judgment within generally defined practices and policies in selecting methods and techniques for obtaining solutions. Maintain effective communication within Analytical Development and cross-functional teams. Present scientific findings at internal and external meetings (if applicable). Minimal Requirements: MS in analytical science, chemistry, biochemistry, or related field with 4+ years of industry experience in biopharmaceutical and/or vaccine development. BS in analytical science, chemistry, biochemistry, or related field with 6+ years of industry experience in biopharmaceutical and/or vaccine development. Ability to critically analyze data using statistical tools and to compile and review technical reports. Ability to define priorities and process to get things done. Knowledge and expertise in principles and practice of current Good Manufacturing Practices (GMPs) is preferred. Excellent record keeping abilities to adequately record, analyze, and document analytical data generated in support of regulatory requirements. Good understanding of statistical tools and knowledge of DOE (Design of Experiments) and QbD (Quality by Design) principles is a plus. Strong communication, presentation, and writing skills.

TNT Environmental, Inc. (TNT) is a leading provider of Wetland and Natural Resource consulting services. Established in 2013, TNT offers cost-effective solutions for routine and complex projects for both public and private sector clients. With a focus on service, value, and results, TNT strives to be an active part of the solution to each project's individual demands. Our expertise includes wetlands and Waters of the U.S. delineation, stream assessments, regulatory permitting, and wetland and stream mitigation. Role Description This is a full-time, on-site role as a Wetland Scientist at TNT Environmental, Inc. located in Chantilly, VA. As a Wetland Scientist with 2-5+ years of relevant experience, you will be responsible for conducting wetland delineations, stream assessments, and regulatory permitting. You will also contribute to wetland and stream mitigation projects, providing expertise and guidance. Wetland Scientists work closely with clients and other team members to deliver high-quality and accurate results. Qualifications Experience in wetland delineation, stream assessments, and regulatory permitting Knowledge of wetland and stream mitigation Strong analytical and problem-solving skills Attention to detail and ability to accurately interpret data Excellent written and verbal communication skills Ability to work well in a team and collaborate with colleagues Experience with AutoCAD (CAD) is a plus Bachelor's degree in Environmental Science, Biology, Ecology, or related field

When you join Caring Cross, you will become part of a dynamic team determined to accelerate the development of advanced cell and gene therapies and to ensure their affordable access around the world. Your work will help to build research programs and create access to life-saving therapeutic opportunities for people living with HIV, cancer, and genetic diseases. We are seeking a highly efficient Quality Control Analyst/Scientist with hands-on laboratory experience, willing to work within a close-knit team by performing QC testing, analyzing, and delivering high-quality data while serving as lab coordinator for the entire group. How will you make an impact? You will: · Perform routine analytical testing methods such as qPCR/dPCR, ELISA, bioassays, and Cell Culture for product release and characterization in accordance with all protocols and procedures · Report out-of-specification results from testing and participate in laboratory investigations to determine the root cause and possible resolution. · Participate in projects related to problems encountered with testing and instruments, and make recommendations for solutions that will minimize future issues · Perform data analysis, maintain electronic lab notebook, report sample results, present data to team · Adhere to organizational and laboratory safety standards including the proper use of personal protective equipment to maintain a safe BSL-2 laboratory environment · Assist in analytical assay development and qualification as needed · Maintain cell culture readiness for analytical testing · Perform routine lab cleaning and equipment maintenance activities in accordance with SOPs as scheduled and escalate potential equipment issues Qualifications · BS or MS in a scientific discipline with a minimum of 2 or more years of relevant experience · Experience in two or more of the following areas required: ELISA, Bioassays, Cell Culture, Flow Cytometry, and qPCR/dPCR. · Ability to perform independently and as part of a team in a cooperative and respectful manner · Excellent pipetting skills · Attention to detail · Hands-on experience with cell culture is highly preferred

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

Piper Life Sciences is seeking a QC Analyst for a well-known biotech organization in the Gaithersburg, MD area. The QC Analyst will be supporting microbiology, environmental monitoring (EM) and utility testing programs for a GMP facility. Responsibilities for the QC Analyst:·Create and maintain materials and reagents needed to execute experiments·Perform environmental monitoring and utility testing of the GMP facility·Conduct routine testing including bioburden, endotoxin testing & TOC testing·Assist with training other QC Micro AnalystsQualifications for the QC Analyst:·Bachelor's Degree in Biology, Microbiology, Biotechnology, Chemistry, Biomedical Engineering or other life science related field·Experience performing environmental monitoring, endotoxin, bioburden & TOC testing Compensation for the QC Analyst:·Compensation: Between $30. 00 - $43. 00 hourly, commensurate with experience·Comprehensive Benefits: Medical, Dental, Vision Insurance (through Cigna), 401k, Sick leave as required by law This job opens for applications on 01/10/2025. Applications for this job will be accepted for at least 30 days from the posting date. Keywords:Research Associate, biotechnology, pharmaceutical, pharma, pharm, biotech, RA, research technician, laboratory technician, research assistant, researcher, ex vivo, cell culture, ELISA, cell maintenance, bioengineering, tissue engineering, biomaterials, cell characterization, mammalian cell lines, cho cells, 3D Printer, qPCR, PCR, tissue culture, materials science, bioink, cellularization, aseptic technique, immunostaining, qc, quality control, microbiology, microbiologist, EM, environmental monitoring, bioburden, endotoxinC#LI-BN1#LI-ONSITE

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

Description Are you motivated by conceiving creative solutions to tough problems? Are you searching for a role that leads to significant real-world impacts by applying your strengths in chemistry? Are you passionate about collaborating with outstanding scientists and engineers to develop your own skills while contributing to critical challenges? If so, we're looking for someone like you to join our team at APL. We are seeking a Research Chemist to help develop solutions to the diverse problems that we take on through chemistry and engineering. You will apply your strong background in chemistry to develop solutions for the government's challenging problems. We need a dedicated colleague who is enthusiastic about research. You will have the opportunity to work across a wide-range of research domains including synthetic chemistry, polymer science, catalysis, materials science, and more. In our group, your research will span fields, from synthesis of stimuli-responsive polymers to inorganic coatings for thermal management; from adhesive and ink technologies, to electrochemistry and catalysis. We enable our team members to generate their own research ideas and publish their findings. At APL, we are a hardworking, multidisciplinary team that is committed to solving diverse problems while embracing risk with the goal of realizing creative solutions. Our team is passionate about building advanced prototypes that will define the future of materials. We strive to foster a collaborative environment with world-class expertise that achieves game-changing impact. Our APL team values integrity and innovative ideas that will ensure our nation's preeminence in the 21st century. As a Research Chemist. . . Your primary responsibility will be to perform experiments at the direction of a project manager and assist with the development of new materials via chemical synthesis, material characterization, and performance testing, both in the lab and in the field. You will perform detailed data analyses and explain characterization results. You will document and present technical work internally and externally. You will get the chance to work on projects both independently and as part of a team. You will have the opportunity to publish your research and present at conferences. Qualifications You meet our minimum qualifications for the job if you. . . Possess a B. S. in chemistry, chemical engineering, or a related discipline. Have 1+ year of demonstrable research experience in a laboratory environment. Are experienced in organic synthesis, spectroscopy, or inorganic chemistry Have experience working as member of a diverse team in a collaborative manner. Are comfortable communicating research findings in various settings. Are willing and able to carry out laboratory research and travel for field testing, sponsor visits, conference attendance, and presentations. Are able to obtain a Secret level security clearance. If selected, you will be subject to a government security clearance investigation and must meet the requirements for access to classified information. You'll go above and beyond our minimum requirements if you. . . Have M. S. in any of the fields listed above. Have 4+ years of research experience. Have published research results in peer-reviewed journals. Are proficient in air-free chemical synthesis, catalysis, electrochemistry, and/or polymer synthesis and characterization. Are familiar with nuclear magnetic resonance spectroscopy, gas chromatography, liquid chromatography, and/or mass spectrometry. Why work at APL? The Johns Hopkins University Applied Physics Laboratory (APL) brings world-class expertise to our nation's most critical defense, security, space, and science challenges. With a wide selection of challenging, impactful work and a robust education assistance program, APL promotes a culture of life-long learning. Our employees enjoy generous benefits and healthy work/life balance. APL's campus is located in the Baltimore-Washington metro area. Learn more about our career opportunities at www. jhuapl. edu/careers. APL is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, gender identity, sexual orientation, national origin, disability status, veteran status, or any other characteristic protected by applicable law. About Us APL is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, creed, color, religion, sex, gender identity or expression, sexual orientation, national origin, age, physical or mental disability, genetic information, veteran status, occupation, marital or familial status, political opinion, personal appearance, or any other characteristic protected by applicable law. APL is committed to promoting an innovative environment that embraces diversity, encourages creativity, and supports inclusion of new ideas. In doing so, we are committed to providing reasonable accommodation to individuals of all abilities, including those with disabilities. If you require a reasonable accommodation to participate in any part of the hiring process, please contact Accommodations@jhuapl. edu. Only by ensuring that everyone's voice is heard are we empowered to be bold, do great things, and make the world a better place. The referenced pay range is based on JHU APL's good faith belief at the time of posting. Actual compensation may vary based on factors such as geographic location, work experience, market conditions, education/training and skill level with consideration for internal parity. For salaried employees scheduled to work less than 40 hours per week, annual salary will be prorated based on the number of hours worked. APL may offer bonuses or other forms of compensation per internal policy and/or contractual designation. Additional compensation may be provided in the form of a sign-on bonus, relocation benefits, locality allowance or discretionary payments for exceptional performance. APL provides eligible staff with a comprehensive benefits package including retirement plans, paid time off, medical, dental, vision, life insurance, short-term disability, long-term disability, flexible spending accounts, education assistance, and training and development. Applications are accepted on a rolling basis. Minimum Rate $85,000 Annually Maximum Rate $180,000 AnnuallyAre you motivated by conceiving creative solutions to tough problems? Are you searching for a role that leads to significant real-world impacts by applying your strengths in chemistry? Are you passionate about collaborating with outstanding scientists and engineers to develop your own skills while contributing to critical challenges? If so, we're looking for someone like you to join our team at APL. We are seeking a Research Chemist to help develop solutions to the diverse problems that we take on through chemistry and engineering. You will apply your strong background in chemistry to develop solutions for the government's challenging problems. We need a dedicated colleague who is enthusiastic about research. You will have the opportunity to work across a wide-range of research domains including synthetic chemistry, polymer science, catalysis, materials science, and more. In our group, your research will span fields, from synthesis of stimuli-responsive polymers to inorganic coatings for thermal management; from adhesive and ink technologies, to electrochemistry and catalysis. We enable our team members to generate their own research ideas and publish their findings. At APL, we are a hardworking, multidisciplinary team that is committed to solving diverse problems while embracing risk with the goal of realizing creative solutions. Our team is passionate about building advanced prototypes that will define the future of materials. We strive to foster a collaborative environment with world-class expertise that achieves game-changing impact. Our APL team values integrity and innovative ideas that will ensure our nation's preeminence in the 21st century. As a Research Chemist. . . Your primary responsibility will be to perform experiments at the direction of a project manager and assist with the development of new materials via chemical synthesis, material characterization, and performance testing, both in the lab and in the field. You will perform detailed data analyses and explain characterization results. You will document and present technical work internally and externally. You will get the chance to work on projects both independently and as part of a team. You will have the opportunity to publish your research and present at conferences.

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

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

- **Quality Control Chemist i** Contract: Frederick, Maryland, US Salary: $31.00 Per Hour Days Left: 24 days, 15 hours left **To discuss more about this job opportunity, please reach out to Chitrank Rastogi (LinkedIn URL - ********************************************************* email your updated resume at Email - ****************************** or give me a call at **************. Thank you!** **Pay Range - $28 to $31/hr. (negotiable)** **Job Description:** **Job Roles & Responsibilities:** * Perform testing of raw materials, intermediates and final products by following analytical methods: Cell-based bioassays, Flow Cytometry, ELISA and qPCR assays. * Work with internal and external resources to maintain lab in an optimal state. * Assist with monitoring and trending data, complete routine record review of test data and related documents for in-process testing, drug substance and drug product release. * Supply information to support generation of CoAs for product release. * Maintains laboratory instruments for calibration and routine maintenance * Author or revise SOPs, qualification/validation protocols and reports. * Asist with lab investigations regarding out of specifications (OOS) results. Participate in determination of root cause for deviations related to analytical procedures. * Provide updates at daily and weekly meetings. * Monitor the GMP systems currently in place to ensure compliance with documented policies. * Review proposed changes to systems, procedures, methods, and submissions to regulatory agencies, as appropriate. * Gather metric information for use in continuous improvement of areas of responsibility. * Perform other duties as required. **Basic Qualifications:** * Bachelor's Degree OR * AA Degree and 2+ years' experience in biotechnology or related field and Quality Control experience OR * High School Degree and 3+ years' experience in biotechnology or related field and Quality Control experience **Preferred Qualifications:** * Strong knowledge of GMP, SOPs and quality control processes. * Identifying, writing, evaluating, and closing OOS's and investigations. * Proficient in MS Word, Excel, PowerPoint and other applications. * Strong written and verbal communication skills. * Ability to communicate and work independently with scientific/technical personnel. * Well versed in various analytical techniques such as Flow Cytometry, ELISAs, PCR, and cell bioassays and other applicable methods to the testing of biopharmaceuticals. * Working knowledge of quality systems and regulatory requirements (21 CRF Part 11/210/211). * Preferred: Experience in the biotech and/or pharmaceutical industry. * Quality Control Chemist * raw materials * Cell-based bioassays * Flow Cytometry * ELISA * PCR * qPCR * biotechnology * GMP * GLP * SOPs * ELISA * pharmaceutical * Biology * Biological Sciences * Molecular Biology * Cellular Biology * Biochemistry **Privacy Overview** CookieDurationDescription

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

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

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

IEH Laboratories, a Leader in Food Safety, is now accepting applications for a Laboratory Analyst - 12hr Rotating Night Shift position at its facility in Laurel, MD. Ideal candidates will possess the following: - A BS or BA in the biological sciences or related field (required) - Proficiency with data entry and computer applications - Strong attention to detail - Ability to multitask and work in a fast-paced environment - Strong written and verbal communication skills - Strong understanding of aseptic technique in the laboratory Laboratory Analyst duties include: analysis of food samples for pathogens via PCR and immunoassay, various microbe enumerations, data entry, laboratory reporting, quality control, media preparation, and other duties as assigned. The pay range for this position is $21.24 - $23.24 hourly. This is a full-time position and is eligible for the following benefits after a brief waiting period: medical, dental, vision, life/AD&D insurance, long- and short-term disability insurance, 401(k), health and dependent care FSA plans, employee assistance program, 15 days of paid time off per year for sick leave and/or vacation, 3 days paid bereavement leave, and 6 paid holidays per year. The laboratory operates weekends, so candidates must be willing to work occasional weekends. Due to exposure to various food allergens in the laboratory environment, applicants with moderate-to-severe food allergies are discouraged from

Posted 28 November by Easy Apply Our client, a UKAS Accredited Laboratory within the manufacturing sector, is currently looking for a Laboratory Analyst to join their team in Winchester, Hampshire. This contract position is an excellent opportunity for someone aiming to gain or expand their lab-based experience in a dynamic and supportive environment. **Key Responsibilities:** * Analysing samples according to precise UKAS methods * Producing accurate and timely reports * Ensuring compliance with laboratory standards and protocols * Participating in quality control and quality assurance processes * Working collaboratively within a team **Job Requirements:** * Understanding of laboratory techniques and procedures * Degree in Chemistry or a relevant Science-based subject * Analytical thinking and attention to detail * Good communication and teamwork skills * Ability to work under minimal supervision **Benefits:** Our client offers a competitive package including: * Full training provided * Free parking * NEST Auto-enrolment pension scheme * 20 days holiday plus bank holidays * Staff kitchen area * Friendly, family-run company environment * On-site parking **Schedule:** * Monday to Thursday: 8:30 am - 5:15 pm * Friday: 8:30 am - 4:00 pm * No weekends If you are enthusiastic, with a background in Chemistry or a relevant Science-based subject, and are looking to start a new laboratory role ASAP, we would love to hear from you. Apply now to join our client's dedicated team. **Required skills** * laboratory * production * technician **Laboratory Analyst** Matchtech

Senior QC Analyst page is loaded **Senior QC Analyst** **Senior QC Analyst** locations Germantown, MD time type Full time posted on Posted Yesterday job requisition id JR100720 If you find science, speed, and helping address serious infectious diseases exhilarating, you have come to the right place. Individually, we're skilled, driven, and confident risk-takers. Collectively we're collaborative and accomplished. We're SuperNovas! Together we use our unique experiences, cultures, and learnings to turn innovation into reality while maintaining the highest standards. We value balance, encourage growth, and recognize that you are our most important asset. Build your future with us while bringing innovative vaccines to the world. We have a place for you! Novavax, Inc (Nasdaq:NVAX) is a biotechnology committed to helping address serious infectious diseases globally through the discovery, development and delivery of innovative vaccines to patients around the world. We have more than a decade of experience contending with some of the world's most devastating diseases, and we are here to make a difference. Hard-won lessons and significant advances illustrate that our proven technology based on solid science tested by decades of research, has tremendous potential to make a substantial contribution to public health worldwide. The Quality Control Senior Analyst is responsible for day to day operations related to release and stability testing, maintaining QC cell culture lines, and writing SOPs, deviations, change controls and CAPAs as part of typical QC operations. **Responsibilities include but are not limited to**: * Performs GMP release and stability testing in Quality Control * Write technical reports and supporting documentation such as deviation, reports, testing protocols, and trend analyses * Review of laboratory notebooks, protocols and reports * Perform day to day activities for cell propagation used for QC release and stability assays. * Participate in technology transfer, method qualification and validation * Perform validations or transfers of analytical methods in accordance with applicable policies or guidelines * Participate in internal assessments and regulatory audits as required * Ensure that written records and work undertaken are performed in accordance with cGMP and company procedures * Leading the lab in 5S and routine housekeeping activities * Maintain effective communication with other relevant groups, including but not limited to Quality Assurance, Manufacturing and Analytical Development * Other duties as assigned **Minimum requirements**: * Minimum of a Bachelor's degree or equivalent in a scientific discipline * Minimum 8 years of industry experience in a cGMP laboratory, preferably related to biopharmaceutical industry operations * Hands on experience performing ELISA in a cGMP environment * Hands on experience performing SDS-PAGE in a cGMP environment * Working knowledge of Sf9 Insect Cell Culture Procedures and cell-based assays e.g. HS plaque and Rapid Titer assay * GxP (regulatory relevant skills and knowledge) GLP/GCP/GMP required * Excellent analytical skills and knowledge * Strong troubleshooting skills for equipment and software * Solid ability to work independently (minimum supervision) * Ability to lead others, as needed * Ability to effectively collaborate with others * Excellent communications skills and be conversant in computer systems * Excellent multi-tasking and organizational skills. * Excels in time management * Strong attention to detail * Job holder should be a good understanding of relevant regulatory/industry standards and requirements The annual base salary (or hourly wage) for this position falls within the range of kr33,555.00 - kr41,950.00. However, the actual base pay offered may vary based on several individualized factors, such as market location, job-related knowledge, skills, and experience. Novavax offers a base salary, annual bonus, equity grants, professional career development/growth opportunities, and a comprehensive benefits package including medical, dental, vision, Rx, STD, LTD, Life, Optional Life, 401(k) plan.Equal Opportunity Employer/Veterans/Disabled Novavax is an equal employment opportunity employer. Employment and advancement opportunities are available to all individuals on an at-will basis, regardless of their race, color, national origin, religion, ancestry, citizenship status, military or veteran status, sex, sexual orientation, gender identity or expression, age, marital status, family responsibilities, pregnancy, disability, genetic information, protective hairstyle, or any other characteristic protected by applicable federal, state, or local law. If you find science, speed, and success exhilarating, you have come to the right place. Novavax, Inc (Nasdaq:NVAX) is a biotechnology company that creates transformational vaccines that address some of the world's most pressing infectious diseases. We have more than a decade of experience contending with some of the world's most devastating diseases, including COVID-19, seasonal influenza, RSV, Ebola, MERS, and SARS. Hard-won lessons and significant advances illustrate that our proven technology has tremendous potential to make a substantial contribution to public health worldwide. Our scientists are committed to developing vaccine candidates for some of the world's toughest viral threats by utilizing the power of our innovative recombinant nanoparticle vaccine platform. Our vaccine technology combines the power and speed of genetic engineering with the immunogenicity enhancing properties of our Matrix-M™ adjuvant to efficiently produce highly immunogenic particles targeting some of the most pressing viral infectious diseases. Novavax, Inc. is headquartered in Gaithersburg, Maryland with additional facilities in Uppsala, Sweden and Bohumil, Czech Republic.

**9510 Harmony Rd** Myersville, MD 21773 $420,000 For information about this home for sale 9510 Harmony Rd in Myersville MD 21773 with MLS# MDFR2048162. Located in Myersville in Frederick. View larger photos, pricing, information and more, **Status:** Under Contract **Property Type:**Detached **MLS #:**MDFR2048162 **Sq. Feet:**2,617 **On Site:**28 Days **Lot Size:**1.33 Acres **County:**Frederick **Listing Office** **Office:**Lpt Realty, LLC Step into this updated 5-bedroom, 2-bath all-brick farmhouse set on a tranquil 1.33-acre lot. Combining historic charm with modern updates, this property offers the best of both worlds in a beautiful country setting. Recent improvements include a foundation and brick wall in 2017, a heat pump in 2018, and a roof replacement around 2015, ensuring peace of mind for years to come. The remodeled bathroom (2018) and stainless steel appliances (2017) further enhance the home's blend of classic style and modern convenience. A finished walk-up attic adds additional **Address:**9510 Harmony Rd, Myersville, MD 21773 LevelSizeDescription**Lot Description:** Backs to Trees GO SEE THIS LISTING 9510 Harmony Rd Myersville, MD 21773 ASAP Tue 4 Jun Wed 5 Jun Thu 6 Jun Fri 7 Jun Sat 8 Jun Sun 9 Jun Mon 10 Jun Choose Your Date -- It's Free, Cancel Anytime 9510 Harmony Rd Myersville, MD 21773 $420,000

Epic Travel Staffing is hiring a Travel - Cath Lab Tech Shift: Days, 7a-5:30p, 10x4, 40hrs per week, EOWLength: 13 Weeks Call: 2-3 call shifts per week with 1-2 call weekends in a 6 weeks Requirements: VA License 1 Year of experience Must have experience in LHC, LHC PCI, RHC, Peripherals, IMPELLA, Balloon Pump, Rota General Skills Required: Scrub, Monitor, EKG Cardiac Cath Lab Procedure Experience Required: Balloon Angioplasty, PCI, Stents, Thrombectomy, Impella insertion, Left heart catheterization, Right heart catheterization, Rotablader Electrophysiology Procedure Experience Required: Cardioversion BLS Must have either RCIS or ARRT Other Details: Circulate, IV Start, Phlebotomy, Watchman Procedures, Septal Closure, Ablations, Pacemaker/defib device placement, Pacemakers, Sinus Node Rhythms, Pacemaker Insertion, EPIC COVID-19 Vaccine (Facility Guideline): Required - Medical/Religious Exemptions Only Flu Vaccine (Facility Guideline): Required - Medical Exemptions Only Profession: Cath Lab Tech (Tech must have either RCIS or ARRT. If ARRT, traveler MUST have state license as well. They do allow the VA Temp procees!) Start date: As listed in the job posting. VHC needs the start date listed in the job order. To be considered, please update both the submission packet and the candidate's Lotus Connect profile to match this date.Duration: 13-weeks Schedule: 4x10-Hour (07:00 - 17:30) Call: 2-3 call shifts per week with 1-2 call weekends in a 6 weeks **Must have experience in LHC, LHC PCI, RHC, Peripherals, IMPELLA, Balloon Pump, Rota** DEPARTMENT DETAILS:• Our cath lab consists of 4 labs. We run Monday through Friday 7am-530pm. We perform an array of procedures including coronary angios/PCIs, CTOs, Peripherals, EPS with possible ablations, Pacmakers, BIVs, TAVRs, Mitraclips, Watchman/Amulet, Mitral valves.• Daily Caseload: 25-30 cases• Rooms: 4 Labs• Scrubs: provided REQUIRED:• Must have experience in LHC, LHC PCI, RHC, Peripherals, IMPELLA, Balloon Pump, Rota.• General Skills Required: Scrub, Monitor, EKG• Cardiac Cath Lab Procedure Experience Required: Balloon Angioplasty, PCI, Stents, Thrombectomy, Impella insertion, Left heart catheterization, Right heart catheterization, Rotablader• EKG Settings and Experience Required: Obtaining vitals, Outpatient, 12 Leads EKG, Rhythm Interpretation• Electrophysiology Procedure Experience Required: Cardioversion• Certs/Licenses Required: BLS, ACLS. Techs must have either RCIS or ARRT. If ARRT, traveler MUST have state license as well. The temp process is accepted here! ADDITIONAL PREFERENCES:• Circulate, IV Start, Phlebotomy, Watchman Procedures, Septal Closure, Ablations, Pacemaker/defib device placement, Pacemakers, Sinus Node Rhythms, Pacemaker Insertion, EPIC VACCINE INFO:- The Flu vaccine is required during flu season. (Oct 1st - Mar 31st).- If your traveler is requesting a religious or medical Flu exemption, it will be the responsibility of the agency to ensure the traveler's request complies with CMS guidelines. Qualivis will review/approve each request with supporting documentation. Unit: Cath Lab Tech, 7460 Epic Travel Staffing: Day 1 health insurance coverage and comprehensive benefits options 401(k) matching program Weekly direct deposit Concierge state licensing program for RN and other healthcare modalities in multiple states, including CA Industry leading allowances and reimbursements Referral program with cash bonuses and additional perks Exclusive job openings - Only at Epic Epic Elite Program - Priority status at top facilities and exclusive loyalty bonuses Epic Staffing Group provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, sex, national origin, housing, age, disability, or genetics. We will consider all qualified applicants for employment, including those with criminal histories, in a manner consistent with the requirements of applicable federal, state, and local laws. By applying for this position, you agree that any calls from Epic Staffing Group and its subsidiaries may be monitored or recorded for training and quality assurance purposes. Pay rate is estimated based on weekly gross income. Weekly gross pay based on qualifications and experience. Rate applies to travel positions only (50+ miles from permanent address). Estimated Weekly Rate: $2808 per week Job ID: 925442

Piper Health Sciences is seeking a Quality Control Associate to join a biotech company located in Elkridge, MD. The Quality Control Associate will participate in the manufacture of LI under GMP and in process development and facilities operations and maintenance. Responsibilities of the Quality Control Associate include:Ensure accurate filing of raw material records Receive QC materials and organize samples as needed Process rooms and maintain inventory Monitor, clean, and sanitize equipment Complete the required calibration and logbook forms Qualifications for the Quality Control Associate include:1+ year of experience Understand Good Manufacturing Processes (cGMP) High School Diploma, Associate, or Bachelor's degree Compensation for the Quality Control Associate includes:Rate Range: $17 - $18 Per Hour **depending on experience**Comprehensive Benefits: Cigna Medical/Dental/Vision, 401k, Sick Leave as required by law Keywords: QC, quality control, Manufacturing Technician, Manufacturing process technician, process technician, batch record, cell culture, upstream, downstream, all stream, fill finish, central services, GMP, aseptic, harvest prep, harvest, vpro, sanitation, purification, equipment, calibration, buffers, solutes, media prep, mixing chemicals, pH, LI, clinical LI, manufacturing, raw materials, good manufacturing processes, sample shipment, raw material testing, quarantined materials, manufacturing production This job opens for applications on December 20, 2024. Applications for this job will be accepted for at least 30 days from the posting date. #LI-ONSITE #LI-JA2