Lab Equipment Jobs Near Me - 83 Jobs

Successful applicant must be a U.S. Citizen with the ability to obtain a DoD Security Clearance Responsibilities Include Perceptive Innovations is seeking a self-starting and experienced individual to be a leader and primary contributor in FPGA signal processing development and implementation for radio frequency (RF) and optical/thermal imaging systems. Design and implementation of FPGA-based digital signal processing systems Development of self-checking unit/system-level test benches and simulations Troubleshooting and resolving design issues Preparation of detailed design documentation and required reports to the government pertaining to the FPGA designs and implementations Independent time management of responsibilities, to include work planning and assignment, communication of status and code reviews, with a startup spirit and work ethic to get the job done within constrained timelines and funding Qualifications The position requires RTL design, simulation, and implementation experience (VHDL primary, Verilog secondary) of challenging high performance FPGA embedded signal processing engines. The following skillsets are also required: Mastery of Xilinx FPGA design flows using Vivado (synthesis, place & route, etc) in both TCL scripted and GUI methodologies Experience with full development cycle of FPGA design and recent Xilinx experience with UltraScale+ devices, Zynq UltraScale+ MPSOC, and the latest Versal devices. Understanding of digital signal processing hardware architectures, and preferably experience with Xilinx/Avnet development boards, such as the VPK180, and FMC module interfacing. Experience with FPGA IP Core integration, preferably to include DDR memory interfaces, HDMI and Display Port Video interfaces, xGigabit Ethernet, SFP+, and USB3 designs. Familiarity with digital electronics hardware design Linux operating systems (including embedded) Strong understanding of software and hardware interaction, with experience in Xilinx SoC development with embedded multicore processors and FPGA hardware/software co-design Excellent verbal and written skills to interact with design teams, management and customers Other duties as assigned Minimum 5 years' (10+ desired) experience working with FPGAs The Following Skillsets Are Desired Experience with SIGINT, EW, Communications, Radar, Lidar, and Image processing Experience with PicoBlaze, MicroBlaze and ARM Cortex A9 Working knowledge of lab equipment such as oscilloscopes, spectrum analyzers, signal sources, power supplies Xilinx FPGAs and Vivado Tool Suite Altera FPGAs and Quartus Tool Suite Use of Subversion or similar tools for codebase control in team environment Experience with Hardware design, PCB design, fabrication, and testing Experience with OpenVPX hardware development, Vita49, and Digital Receivers/Transmitters MATLAB/Simulink modeling of signal processing systems, at a minimum able to understand a high level model and convert to an FPGA implementation High level language programming (C, C++), and ability to write simple embedded software modules for FPGA test purposes Experience with script languages (Tcl, Python, Perl, Ruby, etc.) A bachelor's degree in EE/CE/ECE is required; a master's degree is strongly preferred. Preference will be given to applicants with prior relevant experience. Perceptive Innovations offers competitive pay in a relaxed and independent work environment, with a growing benefits package and an early-stage startup incentive stock options plan for qualified applicants. Perceptive Innovations is an equal opportunity employer. Successful applicant must be a U.S. Citizen with the ability to obtain a DoD Security Clearance

We are seeking a Senior Analytical Scientist to support the Pilot Bioproduction Facility (PBF) at the Walter Reed Army Institute of Research (WRAIR) in Silver Spring, Maryland. PBF is a one-of-a-kind cGMP-compliant pharmaceutical manufacturing facility engaging in next-generation development for cutting-edge companies and government agencies. The professionals at PBF are engaging in trailblazing endeavors every day. Most exciting, the end products vary, so every year brings multiple opportunities for professional enrichment in original projects. CAMRIS International, LLC, is a dynamic medical research and development firm that achieves innovative solutions to health and development challenges through high-quality, cost-effective programs and research management services. We combine our proven systems with today's most effective, evidence-based best practices. Our core practice areas include vaccine research, development, and production; microbiology and infectious disease research; biodefense; clinical research; global health security; and HIV/AIDS programs. Our employees enjoy a collegial environment where individual contributions matter at all levels. At CAMRIS, you will notably improve the lives of people at home and abroad. Responsibilities Design, execute, and analyze experiments related to mRNA synthesis, purification, and formulation. Develop and optimize mRNA production processes, including IVT (in vito transcription) and downstream processing. Plan and conduct analytical tests for drug development and transfer the methods to CDMO. Collaborate with cross-functional teams, including formulation, analytical, and clinical development, to support the development of mRNA products. Analyze and interpret data and prepare technical reports. Perform IQ/OQ/PQ and maintain lab equipment. Follow safety procedures and good laboratory practice. Monitor and coordinate starting materials, drug substances, and drug product testing activities conducted at the PBF. Oversee method development for drug substances and drug products. Ensure methods are suitable, sufficient and development phase appropriate. Participate in method validation activities: review analytical methods, validation protocols, and reports at the PBF. Coordinate and manage analytical method transfers. Review analytical results and supporting documentation to ensure quality standards are met for release and stability testing of starting materials, drug substances, and drug products. Support analytical characterization activities (i.e., identification of new degradants). Draft and monitor project plans and timelines. Manage and coordinate reference standard supplies. Collaborate with the Quality Assurance department to ensure compliance. Reviews, as required, various technology transfer documentation with regulatory and other appropriate groups. Performs other related duties as assigned. Qualifications BS/MS with 10-12+ years of pharma industry analytical experience working within analytical development/validation. Excellent method development and validation skills and routine analysis. Ability to directly or indirectly manage small teams. Strong preference for an analytical scientist who has used a variety of analytical techniques/instrumentation. Strong preference for an analytical scientist who either has worked within a contract analytical lab working with external clients or has worked within a pharma company that outsourced some analytical work to external CDMOs. Ability to self-manage and take on new tasks. Ability to learn new analytical techniques by hands-on work and review published data. Ability to multi-task and hit project timelines. Excellent oral and written communication skills. Please submit your resume online at *************** CAMRIS is an Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, protected veteran status, disability status, or any other characteristic protected by any applicable federal, state, or local law. CAMRIS offers a comprehensive benefits package, including medical, dental, and vision insurance for individuals and families, FSAs, HSA, life and AD&D insurance, short- and long-term disability, legal services, voluntary hospital indemnity, critical illness and accident insurances, EAP, pet insurance, 401(k) with employer match and Roth option, tuition and professional reimbursement, public transportation support in the DMV area, a referral bonus program, vacation with tenure-based increases, PTO, 11 paid holidays, paid bonding leave, and paid supplemental short-term disability. Employment is contingent upon the successful completion of a Public Trust-level background check, a requirement for this position under an active federal contract. The background check process may include but is not limited to the following: (1) contacting your professional references; (2) verification of previous employment, education, and credentials; (3) a criminal background check; (4) use/abuse of federally controlled substances; and (5) a department of motor vehicle check. Candidates must be prepared to fully complete any required background check questionnaire during initial onboarding.

Lead, Cyber/EW/EMSO Convergence - Who We Are: Kudu Dynamics was forged out of a decade of experience in computer network operations and staffed with talent who have built, overseen, and enhanced capabilities through out the entire USG arsenal. Our team of hackers and engineers has experience spanning centuries of research, development, and operations missions across desktop, mobile, IoT, and embedded platforms. Hackers of more than just engineering domains, we have exploited IRS regulations to become an ESOP which is effectively a not-for-profit where we legally exist for the benefit of the Kudites instead of selling our souls to Private Equity. Kudu Dynamics is uniquely qualified to anticipate tomorrow's threats, to build the next generations of capabilities and be in it for the long game. Full Job Description: Cyber is the art of discovering and exploiting asymmetries in software systems that we call Cyberspace. Electronic Warfare and Electromagnetic Spectrum Operations are the art of discovering and exploiting asymmetries in physical devices that interact with the electromagnetic environment. Kudu specializes in developing capabilities for each area, so the Cyber, EW and EMSO Convergence Lead will converge Kudu's capabilities in these closely aligned domains. The lead will use this alignment to drive converged acquisitions, which are deployed to converged operations, resulting in a rejection of disjoint approaches at the oversight and policy levels. This role is expected to plan, bootstrap, and lead an experimentally iterative convergence over the FYDP and beyond drawing from and helping develop Kudu's engineering divisions to identify and exploit asymmetries at the intersection of the Cyber and Physical domains. Responsibilities: Devise a plan to converge Cyber and Physical domains built on Kudu's current and future capabilities. Work with the Engineering Divisions, their Directors, their principal investigators, and their engineers to: Understand the current and future programs. Help develop the existing portfolios in a way that they better support convergence. Shape future approaches. Work with Kudu's functional Divisions, their Directors, and their specialists to: Understand and plan for how the Kudu business model should evolve to exploit the converged domain. Help plan future Kudu facilities and CAPEX lab equipment to facilitate domain convergence based on the articulable expected return on the investment. Work with government Acquisition organizations to shape their understanding of the converged Cyber and Physical domains in a way that they fund Kudu's convergence. Work with government Operational organizations to both shape existing requirements/plans and evolve future requirements/plans based on opportunities inherent in converged domains. Work with government Oversight to build confidence in a maneuver approach to identifying/exploiting asymmetries in a converged approach where past brute-force attrition approaches have cost credibility. Work with government Policy to adapt doctrine to exploit opportunities at the speed and scale of modern warfare. This role and its responsibilities are expected to constantly self-evolve based on an iterative experimental approach to domain convergence as it interacts with the technical realities, the acquisition cycle, the operational realities, the oversight priorities, and the policy climate. This role is expected to be able to answer many of the natural clarifying questions by devising a technical or nontechnical experiment to evaluate the hypotheses, to find a way to fund and/or conduct those experiments, and to maneuver based on the results. Qualifications: A U.S. citizen with Top Secret, SAP, and SCI security clearance eligibility Have a B.S. or equivalent in an applicable field. 10 years of experience in Offensive Cyber. 10 years of experience in Electronic Warfare. A track record w/ Cyber and EW Acquisition offices, operational end-users, oversight, and policy. The ideal candidate will have an initial living plan to achieve convergence in a militarily relevant timeframe; that plan will be expected to naturally evolve as the individual better understands Kudu's portfolio and shapes said portfolio; and that plan will incorporate natural experimentation to maneuver with technical, acquisition, operations, oversight, and policy asymmetries are identified. Benefits: Equity at a company that is doing dynamic, fun, meaningful, and interesting work. A flexible work schedule, with the option to work remotely most days, if that's your style. Your own yearly discretionary budget to buy the things that make you happy. In addition to highly competitive salaries, we offer premium healthcare options, 401k matching, and an annual pass to a swim in the bonus pool. We also offer four weeks of paid time off and 11 federal holidays to utilize whenever you want throughout the year. Awesome, enthusiastic co-workers and a company culture that promotes a jerk- free environment. Rattle the windows with the company band, participate in board game or movie nights, and help balance out the scotch vs. bourbon ratio in the office. Kudu provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.

Looking to be a valuable member of the Facilities & Engineering department for a pharmaceutical manufacturer? We are looking to add an Inventory Specialist to support the physical inventory of spare parts for multiple groups within a fast-paced manufacturing environment. Here's a taste of what you'll be doing: * Verifying the accuracy of quantity and quality of incoming deliveries. * Labeling every product and placing them accordingly. * Identifying and locating the right products during the delivery process. * Keeping a well-maintained and updated account of stock and inventory. * Handling returns by completing technical documentation and other required communication. * Keeping all material handling equipment in the best condition by conducting regular maintenance. * Conveying purchasing requirements and keeping data on the availability of products in short supply. * Collaborating with internal departments to locate missing packages, fix incorrect deliveries and replace damaged products. * Operate a standup forklift. You'll be a perfect fit if you have: * High school diploma, technical school, or military training and experience in relevant field. * Three years of of experience preferably within GMP/lab equipment. * Good mechanical aptitude and administrative skills required. Compensation and benefits offering: * Pay: $22 - $32 an hour (based on experience). * Annual Profit Sharing Bonus (variable depending on firm's performance, employee performance, and tenure). * PTO and paid holidays. * Health benefits - Employee through family level coverage for medical, dental, and vision insurances. Company funded life and long-term disability insurances. Short Term Disability, FSA, HSA, EAP, and supplemental life insurances (employee - family) are also available! * 401k with employer match. If you're interested in learning more about TAI Engineering and what made us a top-20 partner to the manufacturing sector per Engineering News Record (ENR), please visit us at ***********************

Seeking a Technical Writer/ CSV Analyst - Experienced Technical Writer with a focus on system validation, specifically around validating IT systems, to support the large molecule group in documenting validation processes for their Electronic Lab Notebook (ELN) system. - This role emphasizes the importance of Computer System Validation (CSV) experience and requires the candidate to work independently while engaging with multiple stakeholders, including IT, R&D, Quality & Validation, and Product Owners. Key Responsibilities: - Develop and author validation documentation for the large molecule group, including: - User Requirements Specifications (URS) - Functional Specifications - Validation and Test Plans - IQ/OQ/PQ protocols - Standard Operating Procedures (SOPs) - Ensure validation documentation meets GxP and compliance standards. - Create and execute testing strategies and scripts to support system validation efforts. - Collaborate with IT, R&D, Quality & Validation, and Product Owners to gather requirements and document workflows. - Manage structured document control and version management within a Document Management System (DMS). Qualifications: - 3+ years of experience in technical writing within a regulated industry (Pharma, Biotech, Animal Health). - Strong CSV (Computer System Validation) experience, specifically in validating IT systems. - Experience with system validation, testing protocols, and technical documentation. - Prior experience with electronic Lab Notebooks (ELN) (Benchling preferred, but any ELN experience acceptable). - Strong knowledge of GxP, 21 CFR Part 11, and validation documentation processes. - Ability to work independently while engaging with multiple stakeholders. - Proficiency in MS Office, Visio, and Document Management Systems (DMS). This manager sits within the R&D group. He definitely wants someone who comes from CSV in a Life Sciences company. If they have work in R&D groups that would be the best scenario but not 100% needed. Someone who knows GxP and regulations would be great. This is true CSV work within IT systems (not lab equipment). Pay and Benefits The pay range for this position is $35.00 - $52.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: - Medical, dental & vision- Critical Illness, Accident, and Hospital- 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available- Life Insurance (Voluntary Life & AD&D for the employee and dependents)- Short and long-term disability- Health Spending Account (HSA)- Transportation benefits- Employee Assistance Program- Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully remote position. Application Deadline This position is anticipated to close on Apr 30, 2025. About TEKsystems: We're partners in transformation. We help clients activate ideas and solutions to take advantage of a new world of opportunity. We are a team of 80,000 strong, working with over 6,000 clients, including 80% of the Fortune 500, across North America, Europe and Asia. As an industry leader in Full-Stack Technology Services, Talent Services, and real-world application, we work with progressive leaders to drive change. That's the power of true partnership. TEKsystems is an Allegis Group company. The company is an equal opportunity employer and will consider all applications without regards to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

Enjoy what you do while contributing to a company that makes a difference in people's lives. Shady Grove Fertility, one of the premier fertility centers in the United States, continually seeks experienced, compassionate, and dynamic team players who are committed to delivering exceptional patient care to join our growing practice. The work we do building families offers stimulation, challenge, and personal reward. We are seeking a part-time/weekend Embryology Laboratory Assistant to work in our fast paced, high volume, Embryology Lab located at our Rockville, MD office. The schedule is working every other Saturday and Sunday from 6 am - 3 pm. Pay Range $21-$25 How You'll Contribute: We always do whatever it takes, even if it isn't specifically our “job.” In general, the Embryology Lab Assistant is responsible for: Assist with the preparation and cleaning of lab equipment and supplies Monitor and maintain lab cleanliness and organization Prepare media, solutions, and embryo culture dishes Perform basic data entry and maintain accurate lab records Processing semen samples for insemination Cryopreservation of semen samples Manage inventory and restock lab supplies Follow all safety, HIPAA, and lab protocol guidelines Assist with quality control checks and documentation What You'll Bring: The skills and education we need are: High school diploma or equivalent required; college coursework in biology, chemistry, or a related field preferred Prior experience in a laboratory or clinical environment is a plus Excellent attention to detail and organizational skills Ability to work efficiently and follow precise instructions Comfortable working in a highly regulated, sterile environment Basic computer skills for data entry and documentation Anticipate working every other weekend (flexible) More important than the best skills, however, is the right person. Employees who embrace our mission, vision, and core values are highly successful. What We Offer: Competitive pay + bonus Comprehensive training Retirement plan Ability to make an impact in the communities we serve At Shady Grove Fertility, we promote and develop individual strengths in order to help staff grow personally and professionally. Our core values - Empathy, Patient Focus, Integrity, Commitment, and Compassion (EPICC) - guide us daily to work hard and enjoy what we do. We're committed to growing our practice and are always looking to promote from within. This is an ideal time to join our team! To learn more about our company and culture, visit here.

Join TrustPoint and Build the World's First Commercial GPS System in Space GPS is a ubiquitous global utility in modern society; knowing one's location is critical for government, commercial, and personal applications. Still, today's solutions for determining location are inaccurate, slow, unencrypted, and susceptible to jamming and spoofing. These shortcomings make GPS insufficient for tomorrow's safety-critical and high-precision applications, a problem TrustPoint intends to solve. TrustPoint is developing a fully commercial next-generation GPS service to provide significant performance, security and reliability improvements for GPS users. This includes better accuracy, quicker Time to First Fix, and anti-spoof and anti-jam capabilities. The improvements will support US Government position and timing service resiliency as well as enable next-generation commercial applications like drone delivery, self-driving cars, urban air mobility, and augmented reality. The $260B annual GNSS Hardware, Software and Data Services market is ripe for disruption and TrustPoint intends to lead that revolution with our commercial infrastructure and services. The Position With locations outside Washington DC and in Silicon Valley, TrustPoint is currently seeking a Full-Time Government Projects Manager in our Herndon, Virginia office to lead execution of several Small Business Innovation Research (SBIR) projects. You will be responsible for managing resources across the company to deliver technology demonstrations, technical documentation, reports, and customer reviews as required by each contract. As an early leader in a rapidly growing company, this position offers significant upward mobility and an opportunity to shape the future of space-based Position, Navigation, and Timing (PNT) solutions. We'll Expect You To… Lead execution of several Small Business Innovation Research (SBIR) projects with the Department of Defense (DoD) focused on developing new technology related to fielding a commercial constellation in Low Earth Orbit (LEO) and associated ground support systems. Work collaboratively with engineering teams to balance resource scheduling (personnel and lab equipment/facilities) with the company's other technical work and commitments. Continuously identify and manage risks to successful execution, proactively solving issues and/or requesting support as needed. Regularly communicate project status and risks to government customers and stakeholders, as well as company leadership and other personnel. Engage with government customers and stakeholders to plan for post-contract activities, including transition to follow-on phases of work and/or integration into programs of record or commercial product offerings. Support contract milestones and budget planning in the context of the company's broader objectives. Manage subcontractors to ensure successful delivery of their scope of work. Contribute to proposal generation by providing appropriate scoping of work with feasible cost and schedule estimates. You'll Need to Have… Bachelor's degree in engineering or related field. Experience managing technical projects or programs with a track record of balancing cost, schedule, and scope appropriately to ensure successful delivery of technical capability on time and within budget. Demonstrated systems engineering skills across the development lifecycle - defining and fulfilling requirements, balancing system trades, and mitigating execution risk. Working knowledge of US federal government contracting regulations and general understanding of government acquisition and/or technology development practices. Excellent written and verbal communication skills to include presenting technical information and program briefs to high level government personnel as well as preparing written technical documentation. Creative problem-solving skills and attention to detail, able to manage both long term transition strategy and fine-grained technical execution. Ability to travel occasionally to customer sites or other networking opportunities as needed (approximately 1-2 times/quarter, depending on customer need). US citizenship required. We'd Like to See… Hands on experience developing technology in space-related, navigation and timing, or other defense-related fields. Leadership skills in team management, whether in a formal reporting structure or matrixed development teams. Advanced degree in engineering, business, or related field. Active security clearance. Cultural Fit Thrive in a start-up environment. Effective communication style that instills a culture of optimism and positivity. Sense of humor and ability to proactively problem solve. Encourages colleagues to think and plan strategically while executing well tactically. Works well with all company levels and disciplines (i.e. Legal, HR, etc.). Willing to “roll up sleeves” in a new venture, working closely with colleagues. Compensation and Benefits The selected candidate will be competitively compensated with salary, equity (stock options), and standard benefits.

A&M Technologies, Inc has an opening for Firewall engineers to support our government customers' global enterprise networks. Firewall engineering team provides next generation firewall solution for modernizing the firewall infrastructure, assists with migrating traffic from legacy firewall infrastructure to the new solution, and supports firewall service requests. The job duties of a firewall engineer under Core Services group: • Developing next generation firewall solution. • Performing lab equipment evaluation, integration, and testing. • Working with network engineering team to develop a migration plan and assisting migration effort. • Developing and maintaining relevant technical documentation. • On as-needed basis, the engineer will also be responsible for supporting Tier-4 production firewall troubleshooting and developing pro-active firewall data analysis. Requirements Required Clearance: TS/SCI with CI Poly Candidate must have 16 years of experience that can be a combination of work history and education. This equates to a Doctorate and 8 years, master's and 10 years, bachelor's and 12 years, associates and 14 years or HS diploma and 16 years. Additional required qualifications include: Compliance with Department of Defense (DoD) 8570 Information Assurance Technical (IAT) Level 2.

Ready to shape the future of science and global health? ATCC, a private nonprofit global biological resource center and standards organization, is excited to announce our 2025 Summer Internship Program. We are seeking local university students with a degree in biology or a related scientific field to join our incredible team in a paid full time 10-week summer internship program. Join us as we celebrate 100 years of supporting the global scientific community with reliable biomaterials, including cell lines, bacteria, viruses, and microorganisms from our extensive and diverse ATCC catalogue. Associate Biologist Intern - Molecular Biology Projects - Apply here to be considered for all 3 Molecular Biology Summer Internship Project Opportunities:MSAT Molecular Biology Project qualifications: Prior exposure to molecular biology techniques, understanding gene expression, sequencing technologies, and molecular cloning. Interest in bioinformatics, data authentication, and standardization is ideal. This project also focuses on AI and ML techniques. Ability to maintain accurate records. Project Involvement: Perform PCR-based assays. Conduct BLAST analysis. Routine Tasks: Understanding of molecular biology, including PCR and various DNA quantification techniques. MSAT Molecular Biology Project Involvement: Perform DNA extractions, PCR amplification, and post-PCR clean-up. Evaluate DNA quality and sequencing results. Gain experience in a real time production environment. Protocol Optimization: Refine DNA extraction and sequencing protocols based on pilot study findings. Training and Implementation: Participate in training sessions and help implement the new protocol. Data Collection and Reporting: Collect data on DNA extraction and sequencing quality. Assist in preparing reports and presenting findings. Bioproduction Molecular Biology Project qualifications: Knowledge of basic laboratory skills and safety procedures. Experience with standard molecular biology lab equipment. Preferred experience with bacterial cell and/or DNA samples, aseptic technique, and micropipettes. Project Involvement: Learn foundational molecular biology techniques and support DNA product manufacturing. Laboratory Work: Gain experience with DNA extraction methods, quality testing, and troubleshooting techniques. Safety and Documentation: Follow safety procedures while handling biological and chemical materials and meet training and documentation requirements. Responsibilities Manufacturing Operations: Manufacturing of biological products by following standard operating procedures (SOPs), work instructions, and other controlled documents. Maintain laboratory safety, operations, equipment, and supplies. Documentation: Maintain production batch records in compliance with good laboratory practices. Collect, analyze, and report data, ensuring meticulous documentation. Continuous Learning and Problem-Solving: Master aseptic technique, gain experience with various cell lines and organisms, and tackle routine challenges in alignment with organizational policies. Qualifications Program Qualifications: Must currently be enrolled as rising 3rd or 4th year undergraduate, or within 12 months of graduating from a BS or MS academic degree program at an accredited college or university, majoring in biology, cell biology, microbiology, molecular biology, biochemistry, bioengineering, biotechnology, bioinformatics, or a related science. Must be able to complete a 10-week consecutive full-time internship in Manassas, VA from June 2, 2025 - August 8, 2025. Deemed Export Control Notice: To comply with U.S. export control laws, candidates must be a U.S. citizen, lawful permanent resident, or have specific authorization under U.S. export control laws. Required Knowledge, Skills and Abilities: Prior experience in an undergraduate biological science lab, following safety procedures and properly handling biologicals and/or chemicals. Hands on laboratory experience and aseptic technique. Excellent interpersonal skills and ability to work effectively as part of a team. Ability to follow laboratory safety protocols and maintain a safe working environment. Excellent attention to detail, organization, and ability to follow strict protocols and corporate policies and procedures. Strong written and oral communication skills, computer skills, and the ability to critically analyze data sets. Benefits The expected compensation for this role is $28.00 per hour. Join ATCC, where we fuel your success, well-being, and development. We're a mission-focused non-profit Equal Opportunity Employer, celebrating a century of supporting global public health. All qualified applicants will receive consideration for employment without regard to sex, race, color, religion, national origin, disability, protected Veteran status, age, or any other characteristic protected by law. Shape the future of science with us.

The mission of the Allen Institute is to understand the principles that govern life and to advance health. Our creative and multi-dimensional teams focus on answering some of the biggest questions in bioscience. We accelerate foundational research, catalyze bold ideas, develop tools and models, and openly share our science to make a broad, transformational impact on the world. The mission of the Allen Institute for Neural Dynamics is focused on fundamental discoveries in systems neuroscience. We are interested in how the brain builds our understanding of the complex world to guide the flexible behaviors that address our biological needs. The answers will be in terms of defined neuron types and circuits interacting across the whole brain and body. We will develop next-generation methods and theories and employ a team-based approach to discovery neuroscience. Knowledge, data, models, and tools will be widely shared to support the development of therapies for brain disorders. We are seeking a Research Associate to contribute to a project to record the activity of thousands of neurons distributed across many brain regions in parallel. The ideal candidate will be team-oriented, have knowledge in neuroscience and behavior, and display a strong interest in studying brain-wide circuits during behavior. This position will leverage state-of-the-art electrophysiological methods, such as Neuropixels probes, as well as molecular and transgenic resources. The goal is to record simultaneously from many anatomically connected regions while mice are engaged in a variety of cognitive tasks. At the Allen Institute, we believe that science is for everyone and should be open to everyone. We are dedicated to combating biases and reducing barriers to STEM careers more broadly. We also believe that science is better when it includes different perspectives and voices. We strive to make the Allen Institute a place where everyone feels like they belong and are empowered to do their best work in a supportive environment. We are an equal-opportunity employer and strongly encourage people from all backgrounds to apply for our open positions. Essential Functions * Independently carry out experiments involving in vivo electrophysiology and optogenetics * Train mice to perform behavioral tasks * Collaborate with scientists and engineers to develop and evaluate methods for data collection, quantification, and analysis * Collaborate internally and externally to analyze physiology and behavior data * Note: Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. This description reflects managements assignment of essential functions; it does not proscribe or restrict the tasks that may be assigned.* Required Education and Experience * Bachelor's degree in Neuroscience, Biology, or related discipline Preferred Education and Experience * 2 years of experience in a laboratory setting * Practical experience in in vivo electrophysiology and/or mouse behavior * Ability to code in Python or Matlab Work Environment * Laboratory environment - possible chemical, biological, or other hazardous substances exposure * Possible exposure to BioSafety Level 2 organisms, such as recombinant viruses * This may include wearing personnel protective equipment (PPE) Animal Care Services * Exposure to and handling of laboratory animals required * Pre and post-operative care for mice * Administration of compounds to mice (iv, ip, sc, po, im, ro, icv) * Perform health assessments of mice * Perform euthanasia and tissue collections Physical Demands * Fine motor movements in fingers/hands to operate computers and other office equipment; repetitive motion with lab equipment * Stooping, bending, crouching * Reaching, or climbing ladders Position Type/Expected Hours of Work * Occasional evening and weekend hours may be required * This role is currently working onsite and is expected to work onsite for the majority of working hours. The primary work location for this role is 615 Westlake Ave N., with the flexibility to work remotely on a limited basis. Additional Eligibility Qualifications * All employees who work with live animals must complete an Occupational Health medical history form and/or consultation with an Occupational Health Provider and receive clearance to work with animals. Depending on your health history and job responsibilities, an annual respiratory health screening and clearance to use a respirator may also be required. Annualized Salary Range * $53,450 - $65,450* * Final salary depends on the required education for the role, experience, level of skills relevant to the role, and work location, where applicable. Benefits * Employees (and their families) are eligible to enroll in benefits per eligibility rules outlined in the Allen Institutes Benefits Guide. These benefits include medical, dental, vision, and basic life insurance. Employees are also eligible to enroll in the Allen Institutes 401k plan. Paid time off is also available as outlined in the Allen Institutes Benefits Guide. Details on the Allen Institutes benefits offering are located at the following link to the Benefits Guide:

Searching for a full time dental assistant. We are looking for a dental assistant who is willing to grow with us. If you are someone who takes initiative, cares about dental health/function and are looking to be a part of a great team. Skills required: - Have experience in four-handed dentistry. - iTero expertise and knowledge - Sustaining patient comfort, managing supplies, listening to patients' needs and educating them on dental procedures, working efficiently to maintain doctor's schedule. - Adhering to all OSHA and safety policies and procedures. Organizing and maintaining lab equipment, take and develop x-rays and provide comprehensive post-op dental procedures to patients. - Possessing exceptional written and verbal communication skills, a superior knowledge of dentistry and dental terminology, a friendly, outgoing demeanor and excellent organizational skills. Other Skills: X-ray certification & experience with digital x-rays Working knowledge of dental software including ability to chart and enter treatment Scheduling Appointments Answering phones Prepping patient about possible treatment options Job Type: Full-time Expected hours: 40 per week Experience: Dental assisting Organizational skills License/Certification: CPR Certification (Required) X-Ray Certification (Required) Pay: Variable depending on experience and trainability (Ranges from $23-$32) Hours: Monday-Thursday 8:15-5pm RequirementsDental Assistant Benefits Benefits: 40 PTO, Paid Holidays, dental benefits

Precigen is seeking a Manager / Senior Manager, Validation, to provide CQV leadership for our GMP manufacturing site in Germantown, Maryland. Key accountabilities include ensuring that the GMP facility and equipment comply with regulatory commissioning, qualification, and validation requirements for late stage clinical / commercial GMP manufacture of biopharmaceuticals. This role will also manage relationships with contract service providers while working cooperatively with internal stakeholders such as manufacturing, quality, QC, facilities, and metrology personnel. Estimated travel commitment for this role will be less than 10%. DUTIES AND RESPONSIBILITIES: Accountable for the ownership of the site Validation Master Plan (VMP) Coordinate writing, review, and execution of IQ, OQ, and PQ protocols for GMP facility and GXP equipment (manufacturing and lab equipment). Develop and maintain site commissioning, qualification, and validation (CQV) standard operating procedures (SOP). Accountable for execution of computer system validation, data integrity, and ALCOA++ principles on GXP qualified equipment and software applications while working closely with IT. Provide oversight and responsibility for the site shipping validation process. Responsible for cleanroom airflow visualization studies and associated validation documentation for ISO classified and CNC spaces. Author procedures, policies, and regulatory audit responses. Develop and provide leadership on system impact, system boundary, and component criticality assessment process. Author and/or review system risk assessments, factory/site acceptance protocols, validation plans, commissioning plans, design qualifications, functional specifications, system design documentation, and user requirement specifications. Lead periodic reviews and system re-qualification process for GXP equipment. Develop and report on key validation metrics that drive continuous improvement within the GMP facilities organization. Support regulatory and internal audits. Collaborate effectively with site quality on all aspects of GXP systems. Provide leadership with respect to the validated state of operation when investigating, troubleshooting, and resolving problems that occur during routine operations related to facilities, engineering, QC, and manufacturing. EDUCATION AND EXPERIENCE: Bachelor's Degree in Life Sciences or Engineering and at least five (5) years of validation experience in increasing levels of responsibility in GMP facilities, GXP equipment, and cleanroom operations within a /biotech/pharma organization or equivalent. Equivalent combination of education and experience may be substituted for the above, as applicable. Level of role will be determined based on experience. Understanding of cGMPs and operation of a biotech/pharma manufacturing facility. Experience with IQ/OQ/PQ documentation and validation lifecycle in a pharmaceutical or related environment. Knowledge and understanding of computer system validation and data integrity ALCOA++ principles. Hands on experience working with quality systems, including change/deviation management as well as implementation of CAPAs. Strong knowledge of Good Documentation Practices used within a pharmaceutical or equivalent environment. Ability to read and understand technical manuals and calibration reports for the setup and installation of GXP equipment. Hands on experience operating common equipment used for qualification of GXP equipment such as temperature loggers, smoke machines, biological indicators, etc Exceptional organizational skills and attention to detail required. Acumen for teaching/training and excellent communications and supervisory skills required. Advanced technical writing proficiency required. Experience using basic project management principles with respect to managing validation projects. Hands-on experience with statistical modeling and analysis, is a plus. DESIRED KEY COMPETENCIES: Highly organized with strong personal leadership and self-direction. Well-developed interpersonal skills and demonstrated ability to work with and coordinate demands from multiple customers, both internally and with partners. Experienced participation in a regulatory audit or inspections. Demonstrated attention to detail and ability to effectively manage own projects and priorities. Strong oral and written communication skills and an ability to communicate complex concepts in a concise, simplified manner. Ability to prioritize effectively and maintain adherence to project timelines and commitments with competing priorities Ability to understand and execute the company's mission and values. Clear communication in both oral and written form. Demonstrated ability to work and coordinate with multiple stakeholders. Exhibition of the highest degree of ethical standards and trustworthiness. Able to safely access difficult to reach mechanical spaces, ladder/steps to roof, and successfully obtain gowning qualification for cleanroom access. Ability to safely lift up to 30 pounds. WORK ENVIRONMENT: Frequent: Speaking; hearing; sitting; use of hands/fingers; handling or feeling objects, tools or controls; close vision; color vision; peripheral vision; ability to adjust focus. Occasional: Standing; walking indoors; reaching with hands and arms; stooping; kneeling; crouching; lifting and/or move up to 30 lbs. General: Moderate noise level, similar to typical office environment with computers, printers and light traffic EOE MFDV

HOW MIGHT YOU DEFY IMAGINATION? You've worked hard to become the professional you are today and are now ready to take the next step in your career. How will you put your skills, experience and passion to work toward your goals? At Amgen, our shared mission-to serve patients-drives all that we do. It is key to our becoming one of the world's leading biotechnology companies, reaching over 10 million patients worldwide. Come do your best work alongside other innovative, driven professionals in this meaningful role. Associate Manufacturing I - Nights Live What you will do Let's do this! Let's change the world! In this vital role you will perform operations in the Manufacturing area. Operations will be performed according to Standard Operating Procedures (SOPs), these can include bioreactor cleaning, steaming, inoculation, etc., operations. Perform and monitor critical processes, complete routine validation protocols, and regularly draft and revise documents such as Manufacturing Procedures, SOPs, and technical reports. Perform basic troubleshooting and assist in the review of documentation for assigned functions. Participate on cross-functional teams and represent the manufacturing teams. May also have the responsibility of owning deviations/CAPAs. Identify, recommend, and implement improvements related to routine functions. This position is for the AR5 A shift Upstream Cell Culture (Perfusion, Production, Harvest - PPH) team. The successful candidate will be expected to join a shift team working a 12-hour shift. The shift pattern will be 7PM-7AM with a two-week rotation covering 7 days per week. The rotating shift offers several benefits, with an average of 14 days on shift per month with every other weekend off. In addition, any Sundays worked receive Premium pay. Qualifications Win What we expect of you We are all different, yet we all use our unique contributions to serve patients. The dedicated professional we seek is an excellent teammate with these qualifications. Basic Qualifications: High school/GED + 2 years of manufacturing or operations work or military experience OR Associate's + 6 months of manufacturing or operations work or military experience Preferred Qualifications: Bachelor's degree in Science or Engineering Knowledge of large-scale biotechnology operations such as purification, cell culture, aseptic processing, etc. Knowledge of Single-use-Systems CFR and Regulatory knowledge Mechanical ability/expertise Basic statistical mathematical skills Ability to interpret and apply GMP knowledge Understanding of analytical methods for manufacturing area Demonstrated technical writing capability Able to demonstrate project management skills and presentation skills Ability to understand, apply and evaluate basic chemistry, biology and physical principles Basic troubleshooting skills on production equipment Experience with Delta V Experience with lab equipment/testing Additional Information Thrive What you can expect of us As we work to develop treatments that take care of others, we also work to care for our teammates' professional and personal growth and well-being. The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is posted. Actual salary will vary based on several factors including but not limited to, relevant skills, experience, and qualifications. Amgen offers a Total Rewards Plan comprising health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities including: Comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts. A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan Stock-based long-term incentives Award-winning time-off plans and bi-annual company-wide shutdowns Flexible work models, including remote work arrangements, where possible Apply now for a career that defies imagination Objects in your future are closer than they appear. Join us. careers.amgen.com Application deadline Amgen does not have an application deadline for this position; we will continue accepting applications until we receive a sufficient number or select a candidate for the position. Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation. All your information will be kept confidential according to EEO guidelines.

**Description:** **What We're Doing** At Lockheed Martin Rotary and Mission Systems, we're at the forefront of developing cutting\-edge technologies that make a real difference\. We are driven by a mission to deliver innovative solutions in areas like defense, cybersecurity, and aerospace\. As an Electromagnetic Interference Engineer, you will be a crucial part of our team working on high\-impact projects in Digital and RF programs, helping design hardware systems that meet the rigorous standards of the industry\. **The Work** Lead EMI Engineer for a variety of Digital and RF programs\. Provides EMI design/analysis, test planning and setup, debug support, and requirements definition\. Provides mentorship and timely problem resolution through root cause and corrective action analysis\. Reviews/builds/modifies procedures and control plans and seeks opportunities for improved efficiencies\. Performs simulation of lighting and ESD\. The individual will work alongside other Senior and Junior Engineers and across various programs to analyze circuit card designs to support system requirements\. Generate MIL\-STD\-461 test procedures and reports\. Also responsible for the reviewing supplier qualification data \(procedures and test reports\) for their equipment\. This role is based out of Owego, NY\. This role requires the ability to obtain and maintain a DoD government clearance at the Secret level\. **Who We Are** Lockheed Martin Rotary and Mission Systems is a global leader in technology and innovation\. We specialize in providing advanced solutions for aerospace, defense, and cybersecurity that make a difference in the world\. We are a team of individuals committed to integrity, excellence, and working collaboratively across programs to deliver superior results\. At Lockheed Martin, your contributions will help create a safer and more connected world\. **Who You Are** You are a highly skilled engineer with a background in EMI/E3 Engineering and hardware development\. You have experience working with circuit design, requirements definition, and qualification testing\. You bring attention to detail in your work, ensuring all procedures and reports adhere to rigorous standards\. Your expertise includes reviewing and verifying supplier qualifications and equipment\. You value teamwork and are ready to collaborate with both senior and junior engineers to achieve innovative solutions\. Above all, you have a passion for working on challenging projects that push the boundaries of technology\. **Why Join Us** Joining Lockheed Martin Rotary and Mission Systems means more than just a job - it's an opportunity to be part of something that makes a real difference in the world\. Our team members enjoy work\-life balance, with flexible schedules like the 4/10 Flex Schedule, allowing every Friday off\. We offer a competitive 401k match and bonus, comprehensive medical/dental/life insurance, and long\-term stability\. We are deeply committed to your career development, offering tuition assistance and mentoring opportunities\. Learn more about Lockheed Martin's Comprehensive benefits package here\! \(*********************************************************************************************** Location Located in Owego, New York, a charming town in the Southern Tier of New York State, you'll find a welcoming and vibrant community\. Owego is rich in history, surrounded by scenic rolling hills, riverside dining, and local festivals\. With proximity to major cities like New York City, Philadelphia, and Niagara Falls, you can enjoy both the peaceful rural landscape and easy access to larger urban centers\. Visit our Owego Site Virtually\! Click Here\! \#MSetech **Basic Qualifications:** \-Bachelor's degree from an accredited college in a related discipline, or equivalent experience/combined education, with 9 years of professional experience; or 7 years of professional experience with a related Master's degree\. \-Knowledge of circuits design and analysis\. \-Familiarity and knowledge of EMI design review/analysis\. \-Experience with Lab Equipment \- O\-Scopes, spectrum analyzers, EMI Receivers\. \- \-Ability to obtain and hold a DOD Security clearance will require US Citizenship\. **Desired Skills:** \- iNARTE Ceritification \- CE Mark experience \- Experience with RTCA DO\-160 \- Multiple years of background in leading EMI teams \- Knowledge of DevSecOps \-Earned value Management/Work Package Management\. **Security Clearance Statement:** This position requires a government security clearance, you must be a US Citizen for consideration\. **Clearance Level:** Secret **Other Important Information You Should Know** **Expression of Interest:** By applying to this job, you are expressing interest in this position and could be considered for other career opportunities where similar skills and requirements have been identified as a match\. Should this match be identified you may be contacted for this and future openings\. **Ability to Work Remotely:** Part\-time Remote Telework: The employee selected for this position will work part of their work schedule remotely and part of their work schedule at a designated Lockheed Martin facility\. The specific weekly schedule will be discussed during the hiring process\. **Work Schedules:** Lockheed Martin supports a variety of alternate work schedules that provide additional flexibility to our employees\. Schedules range from standard 40 hours over a five day work week while others may be condensed\. These condensed schedules provide employees with additional time away from the office and are in addition to our Paid Time off benefits\. **Schedule for this Position:** 4x10 hour day, 3 days off per week **Pay Rate:** The annual base salary range for this position in California and New York \(excluding most major metropolitan areas\), Colorado, Hawaii, Illinois, Maryland, Minnesota, Washington or Washington DC is $104,500 \- $184,115\. For states not referenced above, the salary range for this position will reflect the candidate's final work location\. Please note that the salary information is a general guideline only\. Lockheed Martin considers factors such as \(but not limited to\) scope and responsibilities of the position, candidate's work experience, education/ training, key skills as well as market and business considerations when extending an offer\. **Benefits offered:** Medical, Dental, Vision, Life Insurance, Short\-Term Disability, Long\-Term Disability, 401\(k\) match, Flexible Spending Accounts, EAP, Education Assistance, Parental Leave, Paid time off, and Holidays\. \(Washington state applicants only\) Non\-represented full\-time employees: accrue at least 10 hours per month of Paid Time Off \(PTO\) to be used for incidental absences and other reasons; receive at least 90 hours for holidays\. Represented full time employees accrue 6\.67 hours of Vacation per month; accrue up to 52 hours of sick leave annually; receive at least 96 hours for holidays\. PTO, Vacation, sick leave, and holiday hours are prorated based on start date during the calendar year\. This position is incentive plan eligible\. **Pay Rate:** The annual base salary range for this position in most major metropolitan areas in California and New York is $120,100 \- $208,150\. For states not referenced above, the salary range for this position will reflect the candidate's final work location\. Please note that the salary information is a general guideline only\. Lockheed Martin considers factors such as \(but not limited to\) scope and responsibilities of the position, candidate's work experience, education/ training, key skills as well as market and business considerations when extending an offer\. **Benefits offered:** Medical, Dental, Vision, Life Insurance, Short\-Term Disability, Long\-Term Disability, 401\(k\) match, Flexible Spending Accounts, EAP, Education Assistance, Parental Leave, Paid time off, and Holidays\. This position is incentive plan eligible\. **Lockheed Martin is an equal opportunity employer\. Qualified candidates will be considered without regard to legally protected characteristics\.** **The application window will close in 90 days; applicants are encouraged to apply within 5 \- 30 days of the requisition posting date in order to receive optimal consideration\.** Join us at Lockheed Martin, where your mission is ours\. Our customers tackle the hardest missions\. Those that demand extraordinary amounts of courage, resilience and precision\. They're dangerous\. Critical\. Sometimes they even provide an opportunity to change the world and save lives\. Those are the missions we care about\. As a leading technology innovation company, Lockheed Martin's vast team works with partners around the world to bring proven performance to our customers' toughest challenges\. Lockheed Martin has employees based in many states throughout the U\.S\., and Internationally, with business locations in many nations and territories\. **Experience Level:** Experienced Professional **Business Unit:** RMS **Relocation Available:** Possible **Career Area:** Electrical Engineering **Type:** Full\-Time **Shift:** First

This designer will be designing screens for software used in labs that use lab equipment. The applications are incredibly dense and are a part of complicated scientific processes. This means that on a day-to-day basis, this designer will need to be able to learn and navigate complex user journeys and needs, define the information architecture for complex needs, and design user interfaces that are dense but user friendly. This designer will utilize research & peer reviews to create their designs and work with developers to bring these applications to life. Enterprise Req Skills Ui design, Ux design, Information Architecture,Sketch, Miro, Mural, User Research, Adobe creative suite Job Title UX/UI Designer Top Skills Details 4-8 years of professional experience: - Designing dense user interfaces (think financial services, health care applications, feature and data-rich applications) - Utilizing and contributing to Design Systems - Working with developers in an agile environment Worksite Address 100% remote (Mexico based) Experience Level Entry Level - Mid Level External Communities Job Description Design applications that help scientists record their research with your expertise in user interfaces and your curiosity in the face of complexity. EVP This is a team that highly values talent and has been able to retain and convert several contract resources historically. They are having an impact on major scientific research (like COVID testing for example) and provides collaboration and support to develop people's skills. Work Environment 100% remote Additional Skills Tags Additional Skills & Qualifications Experience with tools like miro/mural. Communication and organization are critical.

Business Unit: Complaints Trending Employment Type: Contract Duration: 12 months with possible extensions or conversion to FTE Rate: $36-42 W2 with benefits Posting Date: 04/12/2025. Notes: Only qualified candidates need apply. Onsite 80% of time as needed (local candidates). 3 Key Consulting is hiring! We are recruiting an Engineer, Complaints Technical Investigator Medical Device for a consulting engagement with our direct client, a leading global biotechnology company. Ideal candidate: 5 years of experience performing complaints handling and failure analysis investigations within a medical device environment, specifically class II or class III devices. Proficient with ISO systems, risk analysis processes, and protocol or report writing. A bachelor's degree in engineering or sciences such as chemistry, physics, or biology is strongly preferred, though candidates with other educational backgrounds who possess robust laboratory experience will also be considered. Experience working in biohazard lab settings is a plus, but not mandatory. Excellent written and verbal communication skills, along with strong presentation abilities, are essential as the role involves regular presentations to internal teams. Candidates must have a background in medical devices, biotech, or biopharma industries and must be local, able to commute onsite 2-3 days per week (ideally residing within Los Angeles, Orange, or Ventura Counties). This role will begin as a one-year contract, with the potential for extension. Engineer - Complaints Technical Investigator: Requires a combination of working remote and going onsite 2 to 3 times per week (average) for complaint returns assessment and/or laboratory equipment setup, development and validation of test methods. Job Description: Our client is currently seeking an Engineer - Complaints Technical Investigator in our Complaints Trending and Investigation group. In support of Company's mission to serve patients, we are a diverse team working to continuously improve our clinical and commercial drug delivery devices in order to ensure supply and to optimize the patient experience. The Engineer - Complaints Technical Investigator conducts forensic evaluations of complaint units for Standard and Advanced complaint investigations associated with product design and/ or usability issues. This role understands customer/ patient use of Company's packaged and/or distributed products, as well as manufacturing processes for these products. Responsibilities also include helping with Root Cause Analysis, investigation lab infrastructure, equipment setup, and method development and validation. Top Must Have Skill Sets: 5+ years of experience in complaints or failure analysis investigation within a development or manufacturing environment, working with Medical Devices, ideally Class II and Class III Experience with risk management per ISO 14971 (System Risk Analysis, User Risk Analysis, DFMEA/FMEA and other Risk Management tools) Experience with protocol and report writing, process and test development and execution, and design of experiments Day to Day Responsibilities: Lead evaluation of returned product, product reserve sample inspections, batch records and review of complaint histories and trends Provide input to engineering for product improvements Partner with device engineering to develop structured failure analysis processes and tools for current and future device platforms Lead root cause analysis to identify the failure mode for Company's products and associated components due to product complaint Perform failure analysis to identify root cause using processes and tools such as fishbone diagrams, “5 Whys”, risk assessments such as FMEA's, Fault Tree Analysis, or tolerance analysis. Additional equipment such as CT scanners, Instron tensile test machines and SEM may be used. Lead cross functional ideation of design solutions to reduce complaints based on output of root cause analysis, determine feasibility of options through testing and analysis, develop business plans for implementation Generate final reports in accordance with established procedures, which may include data collection and statistical analysis of the data Help with investigations lab equipment setup, develop and provide equipment training to personnel, develop and validate test methods, and develop SOPs for equipment use. Basic Qualifications: Master degree OR Bachelor degree and 2 years of experience OR Associate degree and 6 years of experience OR High school diploma / GED and 8 years of experience Preferred Qualifications: Master's Degree in Science 5+ years of experience in complaints or failure analysis investigation within a development or manufacturing environment, working with Medical Devices, ideally Class II and Class III Understand customer / patient use of Company's packaged and/or distributed products Understand manufacturing processes for Company's packaged and/or distributed products Proven experience with medical devices Demonstrated Six Sigma proficiency specifically for root cause analysis methodology Experience with risk management per ISO 14971 (System Risk Analysis, User Risk Analysis, DFMEA/FMEA and other Risk Management tools) Experience with protocol and report writing, process and test development and execution, and design of experiments Experience in leading continuous improvement activities by driving the implementation of process and product quality improvement initiatives Strong technical writing and interpersonal skills Why is the Position Open? Supplement additional workload on team. Red Flags: Must be local to ATO or willing to relocate immediately. Must be willing to be on site 2-3 days per week. Must be familiar with good laboratory practices (GLP) Interview Process: Interview with Sr. Engineer, Lab Captain, and Associate Director of C&TI and others as necessary. We invite qualified candidates to send your resume to *****************************. If you decide that you're not interested in pursuing this particular position, please feel free to take a look at the other positions on our website ******************************* You are also welcome to share this opportunity with anyone you think might be interested in applying for this role. Regards, 3KC Talent Acquisition Team

Successful applicant must be a U.S. Citizen with the future ability to obtain a DoD Security Clearance Responsibilities Include Perceptive Innovations is seeking a self-starting and experienced individual to take the lead role as embedded software architect and developer for FPGA SoC and CPU SoC image processing and FPGA control development and implementation for a battery powered digital night vision goggle system, wideband RF signal processing, and synthetic aperture radar systems. Design and implementation of Embedded Software for FPGA or CPU SoC processing systems Embedded Linux and CUDA on NVIDIA Jetson GPU SoC processing systems Real time Software development with Linux and "Bare Metal" on Arm multicore processors Real time hardware control and interfacing with/within an FPGA, including shared memory, DMA, FIFOs, and I/O interfaces Development of self-checking unit/system-level tests, test benches, and simulations Troubleshooting and resolving design issues Preparation of detailed technical design documentation and required reports Independent time management of responsibilities, to include work planning and assignment, communication of status and code reviews, with a startup spirit and work ethic to get the job done within constrained timelines and funding Knowledge of Digital Signal Processing (DSP) is highly desired Bonus consideration for ability to Design and implement VHDL firmware in the FPGA Qualifications The position requires complete competence in embedded software development, and specifically experience with the real time considerations of a small embedded system with low-level hardware interfaces. Extra consideration given to candidates with experience with FPGA RTL design, simulation, and implementation experience (VHDL primary, Verilog secondary). The following skillsets are also required: Some familiarity with Xilinx FPGA design flows using Vivado (synthesis, place & route, etc.) in both TCL scripted and GUI methodologies Familiarity with full development cycle of FPGA design and recent Xilinx experience with UltraScale devices, preferably including the Zynq UltraScale+ MPSOC and Versal devices Understanding of digital signal processing hardware architectures, and ideally image processing Familiarity with digital electronics hardware design Linux and embedded operating systems Strong understanding of software and hardware interaction, and ideally experience in Xilinx SoC development with embedded multicore processors and FPGA hardware/software co-design Excellent verbal and written skills to interact with design teams, management and customers Other duties as assigned Bachelors degree in Computer Engineering or similar, Masters degree desired Minimum 1 years' (2-5 desired) experience working with embedded software development and FPGAs The Following Skillsets Are Desired Experience with digital signal processing, including video and RF signal processing Experience with PicoBlaze, MicroBlaze and ARM Cortex A9 Working knowledge of lab equipment such as oscilloscopes, spectrum analyzers, signal sources, power supplies Xilinx FPGAs and Vivado Tool Suite Altera FPGAs and Quartus Tool Suite NVIDIA JetPack and CUDA Toolkit Use of collaboration tools for codebase control in team environment MATLAB/Simulink modeling of signal processing systems, at a minimum able to understand a high level model and convert to an implementation At least a working knowledge of FPGA HDL languages (VHDL, Verilog) and understanding of PS/PL interactions and integration Experience with script languages (Tcl, Python, Perl, Ruby, etc.) A bachelor's degree in EE/CE/ECE is required; CS degree will be considered with relevant coursework and experience. A master's degree is strongly preferred. Preference will be given to applicants with prior relevant experience. Perceptive Innovations offers competitive pay in a relaxed and independent work environment, with a growing benefits package and an early-stage startup incentive stock options plan for qualified applicants. Perceptive Innovations is an equal opportunity employer. Successful applicant must be a U.S. Citizen with the future ability to obtain a DoD Security Clearance

A Medical Laboratory Technician performs laboratory tests to assist in diagnosing and treating diseases. Responsibilities include preparing samples, conducting tests, analyzing results, and maintaining lab equipment. Apply for specific facility details

We are seeking Firewall Engineers to join our team in supporting government customers' global enterprise networks. The Firewall Engineering team is dedicated to providing cutting-edge firewall solutions for the modernization of network infrastructure. This involves assisting in the migration of traffic from legacy firewall systems to the new solution and responding to firewall service requests. JOB DUTIES: Development of next-generation firewall solutions. Evaluation, integration, and testing of lab equipment. Collaboration with the network engineering team to devise migration plans and actively contribute to migration efforts. Creation and maintenance of relevant technical documentation. On an as-needed basis, the engineer will be responsible for Tier-4 production firewall troubleshooting and conducting proactive firewall data analysis. REQUIRED QUALIFICATIONS: A minimum of 16 years of experience, which may include a combination of work history and education. This equates to a Doctorate and 8 years of experience, a Masters and 10 years, a Bachelor's and 12 years, an Associates and 14 years, or a High School diploma and 16 years. Must meet Information Assurance Technical (IAT) Level 2 certification requirements. Required Clearance: Active TS/SCI with CI Poly. DESIRED QUALIFICATIONS: Familiarity with Alto, Forcepoint, and Cisco ASA.