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Job Description Electrical Engineer – Own Power and Control Systems for Advanced Space Platforms! El Segundo, CA | On-site Opportunity Summary A venture-backed space technology startup with active government programs is building next-generation propulsion and spacecraft power systems designed to support high-performance missions in low orbital environments. The company is growing quickly and expanding its technical team to support rapid hardware development, flight readiness, and system integration. As the Electrical Engineer, you will be the primary owner of spacecraft electrical hardware across the stack, developing power electronics, high-voltage systems, and embedded control boards that support advanced propulsion architectures. This is a highly visible role within a small engineering team where you will design, prototype, and qualify electronics that operate in demanding orbital conditions. If you enjoy taking real hardware from concept through laboratory testing and into flight applications, this position offers both technical challenge and meaningful ownership. About Us We are an early-stage space engineering startup focused on propulsion, spacecraft power systems, and advanced electrical control hardware for both government and commercial missions. Our team works across plasma systems, embedded electronics, power conversion, and space systems integration, moving quickly from design into hands-on testing and validation. Engineers here work across disciplines and have a direct role in shaping the technology as we scale our flight hardware programs. Job Duties • Design power electronics and control systems supporting spacecraft propulsion and related subsystems, • Develop high-voltage converters, switching units, and power distribution architectures, • Build embedded control boards and sensor interfaces to support system behavior and monitoring, • Prototype circuitry, perform bring-up testing, analyze performance data, and iterate designs, • Write embedded control software or automation scripts in C, C++, or Python, • Conduct reliability analyses for launch and on-orbit environments, • Collaborate closely with propulsion, avionics, and mechanical engineering teams, • Support qualification testing including vibration, thermal vacuum, cycling, and EMI or EMC evaluations, • Prepare documentation, design packages, and review material for internal and external stakeholders, • Assist with manufacturing readiness including fixtures, vendor engagement, and production test procedures Qualifications • Bachelor’s or Master’s degree in electrical engineering or a closely related field, • 3+ years of experience in power electronics, high-voltage systems, or embedded control hardware, • Hands-on experience developing analog and digital circuits for demanding applications, • Proficiency with Python or C++ for embedded or automation development, • Experience working with microcontrollers, instrumentation, and hardware interfaces, • Strong troubleshooting, diagnostics, and lab testing ability, • Comfortable operating in a fast-paced and collaborative startup environment Preferred Experience • Exposure to propulsion systems, high-energy electrical hardware, or plasma technologies, • Experience supporting ruggedized or flight-intent electrical hardware, • Familiarity with PCB layout tools such as Altium, KiCad, or OrCAD, • Understanding of spacecraft power architecture or avionics integration, • Prior work in small engineering teams with end-to-end hardware responsibility Why Join Us • Direct ownership designing the electrical backbone of new spacecraft systems, • High-impact role as the dedicated Electrical Engineer on a small and growing team, • Opportunity to work across propulsion, avionics, and spacecraft integration, • Fast-moving environment with real visibility into mission outcomes, • Equity participation and growth potential as programs expand, • Strong medical, dental, and vision benefits Compensation Details $115,000 - $170,000 #LI-AV

Job DescriptionPlease Note: To conform with the United States Government Space Technology Export Regulations, the applicant must be a U.S. citizen, lawful permanent resident of the U.S., conditional resident, asylee or refugee (protected individuals as defined by 8 U.S.C. 1324b(a)(3)), or eligible to obtain the required authorizations from the U.S. Department of State. At CesiumAstro, we are developers and pioneers of out-of-the-box communication systems for satellites, UAVs, launch vehicles, and other space and airborne platforms. We take pride in our dynamic and cross-functional work environment, which allows us to learn, develop, and engage across our organization. If you are looking for hands-on, interactive, and autonomous work, CesiumAstro is the place for you. We are actively seeking passionate, collaborative, energetic, and forward-thinking individuals to join our team. We are seeking a Principal Power Electronics Engineer I to join our growing satellite communication (SATCOM) terminal development team. In this position, you will contribute across the entire development lifecycle of next-generation power electronics hardware for military and commercial power systems—from leading the definition of power system architectures and trade studies to detailed circuit design, simulation, printed circuit board (PCB) layout, verification and integration testing, production transition, and manufacturing support. JOB DUTIES AND RESPONSIBILITIES • Lead the development of power system architectures and derive power subsystem requirements, • Design DC-DC power converters, power supplies, and power distribution systems ranging from a few watts to more than 20 kW of power in the 0.8 V to 400 V range, • Design single-phase and three-phase AC-DC power supplies and power distribution systems ranging from a few kilowatts to more than 20 kW, • Perform comprehensive analysis of AC-DC and DC-DC power supplies including worst-case circuit analysis (WCA), stress analysis, small signal modeling analysis, failure modes and effects analysis (FMEA), reliability analysis, and power integrity analysis, • Develop design verification test plans, requirement compliance matrices, system integration and qualification test plans, and production acceptance test plans for power converters and power supplies, • Lead board bring-up and design verification testing of analog and power electronics circuits, • Lead system integration, qualification campaigns, and production release of power supply modules and power systems, • Mentor younger engineers and foster knowledge sharing, • Lead a small team of power electronics engineers to drive project execution JOB REQUIREMENTS AND MINIMUM QUALIFICATIONS, • Bachelor of Science (BS) degree or higher in Electrical Engineering from an accredited university., • Minimum of 9 years of experience designing analog and power electronics, • Experience working with electrical power systems and subsystems, including developing power architecture and power requirements, performing trade studies for size, weight, power, and cost optimization (SWAP-C), selecting power converter topologies, and defining power management and control blocks, • Experience designing, testing and qualifying single-phase and three-phase off-line AC-DC power supplies, and DC-DC power supplies for industrial, airborne, or military systems, • Knowledge of control theory and stability of power electronics, including experience characterizing control loops and impedances in the laboratory, • Experience designing power filters for low noise outputs and for power line electromagnetic compatibility (EMC), • Experience developing design verification test plans, requirement compliance matrices, system integration and qualification test plans, and production acceptance test plans, • Experience performing worst-case circuit analysis (WCA), stress analysis, failure modes and effects analysis (FMEA), and reliability analysis for power supplies, • Extensive hands-on experience with testing and troubleshooting electronics and power converters using laboratory instruments such as oscilloscopes, impedance analyzers, spectrum analyzers, electronic loads, and signal generators, • Experience with analysis and simulation tools such as SPICE, LTSPICE, SIMetrix/SIMPLIS, PLECS, Simulink, MATLAB, MathCAD, ANSYS Q3D and SiWave, or HyperLynx, • Experience with isolation and grounding, failure mode effects analysis and fault tolerant design, and thermal management of power electronics, • Experience designing and testing power electronics units to meet industry standards and requirements in the automotive, industrial, aircraft, or military markets (e.g., FCC, CISPR, UL safety standards, ECSS, NASA, MIL standards), • Excellent written and verbal communication skills PREFERRED EXPERIENCE, • Experience designing and testing isolated and non-isolated DC-DC power converters (e.g. discrete linear regulators, Buck, Boost, Buck-boost, Flyback, Forward), • Experience designing or specifying custom power magnetics for power supplies and power line filters, • Knowledge of power stage design and control methods for power factor correction (PFC) converters and active rectifiers, • Experience generating statements of work and requirements for external vendors, vendor selection, and vendor management for power supply and power system rack developments, • Experience with electronics schematic capture and printed circuit board (PCB) layout tools such as Altium, OrCAD, Allegro or Xpedition, • Experience running board-level power integrity simulation using tools such as Ansys SiWave, or HyperLynx, • Knowledge of soft switching and resonant power converter topologies (e.g. LLC, CLLC, series resonant, phase shifted full bridge, dual active bridge, etc.)

Job DescriptionPlease Note: To conform with the United States Government Space Technology Export Regulations, the applicant must be a U.S. citizen, lawful permanent resident of the U.S., conditional resident, asylee or refugee (protected individuals as defined by 8 U.S.C. 1324b(a)(3)), or eligible to obtain the required authorizations from the U.S. Department of State. At CesiumAstro, we are developers and pioneers of out-of-the-box communication systems for satellites, UAVs, launch vehicles, and other space and airborne platforms. We take pride in our dynamic and cross-functional work environment, which allows us to learn, develop, and engage across our organization. If you are looking for hands-on, interactive, and autonomous work, CesiumAstro is the place for you. We are actively seeking passionate, collaborative, energetic, and forward-thinking individuals to join our team. We are looking to add a Senior Power Electronics Engineer II to our team. If you enjoy working in a startup environment and are passionate about developing leading-edge power electronics for satellites, spacecraft, and aerospace systems, we would like to hear from you. At the Senior level, you will be tasked with full-stack power electronics development. You will have the opportunity to start at concept development and progress through detailed design, analysis, board layout, testing, and delivery, doing hands-on work at each phase. At a small company and a startup, your work will make direct contributions to the success of the business. The work is challenging and impactful, requiring both breadth and depth of technical knowledge. Our products are made for high-reliability space and airborne applications, so designs require high levels of technical rigor while maintaining the agility of a startup environment. The successful candidate will also present engineering design review materials to our customers and executive team. As such, excellent written and verbal communication skills are required.JOB DUTIES AND RESPONSIBILITIES • Own end-to-end design of power converters, and power management and control circuits, from concept and architecture definition to schematic, printed circuit board (PCB) design, testing, qualification, production transition and production support., • Perform detailed and complete schematic design for low to high complexity power electronics designs , ranging from single power converters to mukti-output power supply modules and power management circuitry., • Perform detailed PCB layout in Altium Designer independently or in collaboration with a PCB Drafter., • Perform modeling and analysis of analog and power electronics designs including worst-case circuit analysis, stress analysis, small signal and stability analysis, power loss and efficiency optimization analysis, and power integrity analysis., • Develop design verification test plans, requirement compliance matrices, system integration and qualification test plans, and production acceptance test plans for power converters and power supply designs., • Perform bring-up and design verification testing of power electronics circuits and modules, often working with a technician or junior engineer to complete design verification., • Collaborate with multi-discipline engineering team and lead system integration and qualification campaigns, and release analog and power electronics designs to production., • Mentor junior engineers to build technical understanding and foster professional development of team., • Perform research and keep up with new power electronics technology and industry trends to drive innovation and generation of intellectual property.JOB REQUIREMENTS AND MINIMUM QUALIFICATIONS, • Bachelor of Science (BS) degree or higher in Electrical Engineering from an accredited university., • Minimum of 6 years of industry or university research experience in board-level power electronics design, analysis, and test., • Experience owning the design phase of power electronics or power subsystems, including power architecture and requirements definition, trade studies, power converter and analog electronics design, component selection, and detailed design., • Experience performing or guiding complex PCB layout for analog and power electronics., • Experience with analysis and simulation tools such as SPICE, LTSPICE, SIMetrix/SIMPLIS, PLECS, Simulink, MATLAB, or MathCAD, • Strong laboratory testing and troubleshooting experience for prototyping, design verification testing and qualification of analog and power electronics hardware., • Direct experience designing high-reliability electronics for automotive, space or defense applications, including part derating, worst-case analysis, and thermal constraints., • Excellent written and verbal communication skills.PREFERRED EXPERIENCE, • Experience delivering subcircuit or board designs to production and deployment., • Proficiency in printed circuit board design tools such as Altium, OrCAD/Allegro, PADS/Xpedition, or similar., • Experience running board-level power integrity simulation tools such as Ansys SiWave, ADS SIPro, or HyperLynx.

Job Description GKY is a small business-owned dental laboratory that places an emphasis on providing thorough and highly personalized dental services and products to clinicians. The products and services we offer are crowns, bridges, metal-free restorations, removables, implants, guided surgeries, and shade matching. We are dedicated to helping smaller dental practices have their needs met through creating and perfecting these products and providing these services. Job Overview: We are seeking a highly organized and detail-oriented Dispatcher to join our team. The Dispatcher will be responsible for coordinating and managing the schedules and movements of personnel, vehicles, and products. This role is crucial in ensuring timely, safe, and efficient delivery of services. The ideal candidate is a problem-solver who can thrive in a fast-paced environment and maintain effective communication under pressure. Key Responsibilities: • Schedule and dispatch drivers, vehicles, and/or service teams based on customer needs, service calls, or predetermined routes., • Monitor and track the location of drivers in real-time using GPS or other tracking software., • Maintain detailed records of service calls, route changes, and other dispatch-related data in the system., • Communicate with drivers, field staff, and customers to ensure accurate delivery and/or service completion., • Respond to doctor inquiries, providing updates on the status of services., • Troubleshoot and resolve any operational issues that arise during the dispatching process., • Ensure compliance with all safety regulations and company policies., • High School Diploma or equivalent; additional education or certifications in logistics or transportation management is a plus., • Proven experience as a Dispatcher or in a similar role., • Strong communication skills, both verbal and written., • Proficiency in using Microsoft Excel., • Ability to multitask, prioritize, and manage time effectively in a high-pressure environment., • Strong problem-solving skills and attention to detail., • Ability to work Monday to Fridays from 8am to 5pm., • Bilingual in Spanish is a plus.

Job Description California Skin Institute (CSI) now partnered with Schweiger Dermatology Group is the largest and fastest growing private dermatology practice in California offering an unwavering commitment to excellence in medical, surgical, and cosmetic dermatology and plastic surgery. We have one of the most state-of-the-art and comprehensive skin-based service lines including laser, light, radio-frequency, reconstructive and cosmetic surgery techniques, Medicare-approved surgery centers and a full-service dermatopathology laboratory. Come join our team as we innovate both in the clinical setting and in practice operations! As our mission is safe patient care, we require all our employees to be vaccinated as such vaccinations are available, and subject to the narrow exceptions provided by applicable law. Job Responsibilities • Promote a professional and welcoming atmosphere that enhances the quality of service and care offered to patients, respective providers, and fellow colleagues. Lead by example, maintains office presence and highest level of professionalism., • Dress & present appropriately from head to toe at all times; business casual attire required. Professional body language and communication with colleagues & patients must be always adhered to. This includes keeping cell phone usage to a minimum while at the front desk., • Responsible for accurately completing beginning and end of day checklists daily., • Assist in ensuring that all scheduling, cancellations, and confirmations are being done appropriately., • Execute working knowledge of HIPAA privacy laws by protecting patient information during phone calls, discussing information quietly with patients at front desk or defer to a GM to discuss matters with patient in an exam room, and shredding sensitive materials. Maintain confidentiality of all patient and employee information., • Assist in ensuring the creation of new medical records for each patient. Obtain all necessary copies of insurance cards, referrals, and demographic information., • Responsible for completing Daily Activity Report and proper financial duties such as entering charges and payments throughout the day., • Responsible for accurate cash handling with Petty Cash & collected payments. Scan all cash & credit card receipts into respective folder. Verify proper cash is collected and accounted for during your shift and at close each day; sign off on Cash logs and deposit cash in office safe/lock boxes before closing., • Responsible for answer incoming phone calls within three rings, confirming ZocDoc appointments as well as making outgoing calls for patient retention purposes., • Maintain a neat and orderly work area throughout the front desk, keeping sensitive patient information out of view and shred once uploaded to EMR or server., • Maintain a clean and neat waiting area; slideshow and music is always appropriately playing, trash left behind is removed immediately, as well as maintaining neat product display areas at all times., • Constantly check your email inbox, respective scan inbox, handling time sensitive emails immediately or communicated need for support to GM/teammates., • Assist as needed office supply inventory count. Notify GM when inventory needs to be adjusted for any reason., • Have thorough knowledge of ALL procedures performed at offices., • Notify the General Manager of all personnel and patient complaints or issues., • Experience using EMR software and patient scheduling systems preferred., • Must be computer savvy and familiar with Microsoft Word, Excel, and Outlook., • Strong communication, interpersonal, and organizational skills., • Excellent patient relations and customer services skills., • Must be professional, reliable, and dedicated employee., • Prefer prior experience working in a dermatology / medical environment., • Open availability to work during office and/or scheduled hours. From time to time, operational business needs (e.g. training sessions, emergency coverage issues, etc.) may require employee travel to alternate locations within a reasonable distance based upon GM or RM discretion. Work Environment • This job description indicates in general the nature and levels of work, knowledge, skills, abilities, and other essential functions (as covered under the Americans with Disabilities Act) expected of an employee., • This job operates in a professional work environment, • This role routinely uses standard office equipment such as computers, telephones, photocopiers, filing cabinets, and fax machines. We value our employees' time and efforts. Our commitment to your success is enhanced by our competitive pay in addition to a benefits package including: • Medical Health Insurance, • Vision & dental plan, • Flexible Spending Account, • Life Insurance, • 401 (K), • Generous paid time off, • Growth and development opportunities, • Recognition Program

Job Description About Castelion Castelion is bringing a new approach to defense development and production: one that focuses on short, iterative design cycles, rapid testing in development, and modern commercial manufacturing strategies for production at scale. We're designing, building, and testing next generation long range strike weapons systems to give America and its Allies a definitive edge and deter future conflicts. EHS Specialist The Environmental, Health & Safety (EHS) Specialist supports manufacturing, R&D, and test operations by executing and maintaining EHS programs that ensure safe, compliant day to day operations. This role provides hands on field support across the site, including conducting inspections, supporting training, managing hazardous materials and waste, and maintaining required records and permits. The EHS Specialist works closely with operations, engineering, and leadership teams to identify hazards, verify controls, and reinforce safe work practices in a fast paced, high hazard environment. This role plays a critical part in keeping people safe, maintaining regulatory compliance, and enabling the organization to operate efficiently as it scales. Responsibilities • Conduct routine safety and compliance inspections of manufacturing, R&D, and test areas to verify that approved controls, procedures, and permits are being followed and escalate higher risk conditions to the Senior EHS Engineer, • Perform task walkdowns and document Job Hazard Analyses (JHAs) using approved formats, ensuring job steps, hazards, and controls are accurately captured and kept current, • Verify proper use and condition of PPE, guarding, lockout devices, ventilation, gas monitors, and other safety controls during daily operations, • Support PPE programs by assisting with PPE assessments, coordinating fittings and issuance, delivering PPE training, and verifying proper use and condition, • Support implementation and maintenance of EHS programs, plans, and procedures by maintaining required records, permits, postings, and inspection logs, • Support industrial hygiene activities by deploying sampling equipment, collecting exposure data, coordinating laboratory analysis, and maintaining monitoring records, • Support incident, near miss, and injury investigations by gathering facts, documenting events, and tracking assigned corrective actions to closure, • Schedule, deliver, and document EHS training including onboarding, refresher, and task specific training, • Manage hazardous waste accumulation areas including container labeling, inspections, inventory tracking, and coordination of waste shipments, • Maintain chemical inventories, Safety Data Sheets, and container labeling to support hazard communication and chemical management, • Support environmental reporting and permit compliance by maintaining required records, conducting routine inspections, and coordinating submittals and renewals as directed, • Associates or Bachelors degree in occupational health and safety, environmental science, or a related field, • 2+ years of experience supporting EHS programs in manufacturing, laboratory, or industrial environments, • Working knowledge of OSHA or Cal-OSHA requirements, • Strong organizational and communication skills, • Willingness and ability to travel periodically to support operations at other locations as needed, • Experience in aerospace, defense, or other high hazard industries, • OSHA 30, HAZWOPER, or similar safety training Leadership Qualities Bias to Action and Creative Problem Solving. Desire and experience questioning assumptions in ways that lead to break through ideas that are ultimately implemented. Successfully bring in applicable processes/concepts/materials from other industries to achieve efficiency gains. Ability to personally resolve minor issues in development without requiring significant support. High Commitment, High Initiative. A successful candidate will have a genuine passion for Castelion's mission and consistently look for ways to contribute to the company's technical goals and prevent hardware blockers. Ability to work in a fast paced, autonomously driven, and demanding atmosphere. Strong sense of accountability and integrity. Clear Communicator. Proactively communicates blockers. Trusted in previous roles to be voice of company with regulators, suppliers, gate keepers and customers. Capable of tactfully managing relationships with stakeholders to achieve company-desired outcomes without compromising relationships. Emails, IMs and verbal interactions are logical, drive clarity, and detailed enough to eliminate ambiguity. ITAR Requirements:

Job DescriptionSalary: $65,001 - $112,613 Based on Education & Experience DA VINCI SCHOOLS TEACHER - HIGH SCHOOL PHYSICS DEFINITION Teach and facilitate instruction in grades 9 through 12 in secondary academic subject matter, social, behavioral, and other educational skill areas with an emphasis on diversity, equity, and inclusion; plan, develop, organize, and conduct a comprehensive educational program for secondary level pupils in Physics instruction. Da Vinci Schools are project-based, college preparatory schools, each with a distinct focus which drives the curriculum students take in addition to their A-G college preparatory requirements. As a project-based school, class curricula are centered around projects, which teach students the essential skills and knowledge of a course. Da Vinci teachers use Mastery Based Grading and work with industry partners to provide real-world connections to their projects. Da Vinci Schools is looking for candidates who desire to: • Work closely with a grade level team to plan interdisciplinary projects and units, • Create and facilitate inquiry-based project-based curriculum, • Connect academic subject matter to the world outside the classroom, • Actively create space for diverse voices and points of view that reinforce each students identity, • Act as an advisor to a group of students, • Engage in self-reflection and a diversity of thinking, particularly related to the schools mission to support diversity, equity inclusion and anti-racism EXAMPLES OF DUTIES • Provide instruction based on Next Generation Science Standards and other state frameworks and standards., • Collaborate on a course of study, instructional program guidelines, and other materials in planning and developing lesson plans and teaching outlines., • Pursue a variety of methodology in teaching and instructing pupils, including mini-lessons, demonstrations, discussions, laboratory experiences, and other instructional methods., • Conduct teaching and instructional activities, using educational equipment, materials, books, and other learning aids., • Plan, develop, and utilize a variety of instructional materials and aids appropriate to the intellectual and instructional level of pupils from varied socio-economic and cultural backgrounds, and who possess a range of mental and emotional maturity., • Review, analyze, and evaluate the history, background, and identity of pupils in designing instructional programs to meet individual educational needs., • Individualize and adapt educational processes and procedures to enhance pupil educational opportunities., • Provide group and individual instruction to motivate pupils, and effectively utilize the time available for instructional activities., • Maintain appropriate standards of pupil behavior, using behavioral management strategies and techniques, including positive reinforcement and behavior shaping procedures., • Review, analyze, evaluate, and report pupil academic, social, and emotional growth., • Select and requisition appropriate educational supplies, materials, books, equipment, and learning aids., • Perform a variety of non-instructional duties, including curriculum and instructional development activities, student supervision, and consultation activities. KNOWLEDGE OF: • A wide-range of effective teaching strategies (e.g., Universal Design and Learning - UDL), along with a willingness to learn to ensure student learning., • Working knowledge of technology and computer software applications relative to instruction, assessment and teacher recordkeeping., • Demonstrated appreciation and support for diversity in student backgrounds, • California Standards for the Teaching Profession current version, • Current assessment methodologies, their use and efficacy,, • Federal, state and local laws, policies and procedures related to duties as a teacher, • Correct English usage, grammar and spelling, punctuation and vocabulary, • Oral and written communication Interpersonal skills using tact, patience, diligence and courtesy ABILITY TO: • Work independently with appropriate direction., • Manage and prioritize multiple activities and work with frequent interruptions Communicate orally, in writing and through technology to express ideas, thoughts, lesson materials, and instructions to students, community, and staff., • Champion the success of students from culturally and linguistically diverse backgrounds, • Perform problem-solving tasks requiring independent judgment, • Maintain accurate records and prepare reports, • Work confidentially with discretion, • Integrate technology into instruction, • Establish and maintain effective working relationships with others, • Meet personal and student schedules and timelines, • Understand and interpret rules and written directions and apply to specific situations, • Ability to operate office and classroom technology including, but not limited to: computer, webcam, LCD projector, copy machine, white board, document camera and use of related instructional software and hardware, • Work effectively as part of a school team. QUALIFICATIONS: • Hold a Bachelors Degree from an accredited university and a California Single Subject credential with authorization to teach Physics, including English Learner Authorization;, • Successful completion of interview, screen process and hiring requirements;, • Commitment to the goals and philosophy of Da Vinci Schools

Job Description About Epirus Epirus is a high-growth technology company dedicated to overcoming the asymmetric challenges inherent to the future of national security. Epirus' flagship product, Leonidas, is a software-defined system built using intelligent power management techniques which allow power-hungry systems to do more with less. Job Summary: this is an exciting role in a growing company. The ideal candidate for the position is someone who has experience in product development, manufacturing, electronics, and mechanical assembly. The role is critical to success of Epirus hardware and will be responsible for RF circuit board testing. This position will also be flexible and support electro-mechanical assembly and harness building as required. Responsibilities: • Understands, plans, and executes testing and troubleshooting activities to produce a prototype, MIL-STD understanding desired, • Assembles LRU and element array with direction from Engineers, • Utilizes standard laboratory test equipment including: oscilloscopes, logic analyzers, spectrum analyzers, network analyzers, voltmeters, and other measurement equipment to perform engineering support functions, • Troubleshoots equipment using standard documentation packages including assembly drawings and schematics, • Works with various levels of the system (from the board and component level to the LRU, to the system level) to identify and resolve performance problems, • Mentors less experienced peers and provides feedback on assembly work, • Capable of completing assembly and harness building work in addition to test tasks. Basic Qualifications:, • Experience with electro-mechanical assembly, • Minimum of 2 years RF test experience, • Testing and troubleshooting skills with the capability of defining and configuring standard and special test equipment to perform tests at the circuit card, LRU or system level, • Ability to work with standard laboratory test equipment, • Knowledge of Environmental, Health and Safety elements, especially related to RF testing, • Good written and oral communication skills, • Computer skills to use MES system, JIRA, etc., • Collaborative; capable of working across all levels of the organization, • US Citizen and/or Permanent Resident (future security clearance may be required) Preferred Skills and Experience:, • Associates Degree in technical field or equivalent trade school or military training., • 2-4 years of related experience, • Soldering certification and experience soldering cables and harnesses (circuit boards come pre-assembled), • Aerospace/Defense experience and/or military experience, • Knowledge of Production Systems and Lean Manufacturing elements, • Experience with ISO9001/AS9100 quality management systems elements ITAR REQUIREMENTS: • To conform to U.S. Government space technology export regulations, including the International Traffic in Arms Regulations (ITAR) you must be a U.S. citizen, lawful permanent resident of the U.S., protected individual as defined by 8 U.S.C. 1324b(a)(3), or eligible to obtain the required authorizations from the U.S. Department of State. Learn more about the ITAR here. At Epirus, you'll work with technical peers and great people—and get first crack at some of the defining technology challenges of our time. Here, "impossible" is just a challenge. We're a diverse, fast-growing team of change-makers fueling the future of energy with revolutionary solutions. Join us and rewrite the rules. As required by the Equal Pay Transparency Act, Epirus provides a reasonable range of minimum compensation for roles that may be hired. Actual compensation is influenced by a wide array of factors including but not limited to skill set, level of experience, and specific office location. For the state of California only, the range of starting pay for this role is: $32.84—$40.43 USD

Job Description About This Role Varda Space Industries is seeking a motivated Temporary Laboratory Scientist to provide critical laboratory support for our biologics formulation team. This role will focus on preparation of stock solutions, maintenance of laboratory equipment and chemical inventory, and execution of analytical testing to support ongoing protein formulation development activities. The ideal candidate will have hands-on experience in biopharmaceutical laboratory operations and familiarity with protein characterization techniques. Key Responsibilities Laboratory Operations & Supply Chain Support • Prepare and maintain stock solutions for formulation development activities, • Manage laboratory chemical inventory and coordinate with supply chain to ensure uninterrupted operations, • Monitor equipment status and maintain laboratory instruments in working order, • Execute solution preparation according to established Standard Operating Procedures (SOPs), • Perform basic analytical characterization of protein formulations, • Prepare reagents, buffers, and sample systems in advance of scheduled experiments, • Conduct routine instrument calibration and qualification activities, • Work closely with formulation scientists to anticipate laboratory needs, • Communicate inventory requirements and potential supply issues proactively, • Bachelor's degree in Biochemistry, Pharmaceutical Sciences, Biotechnology, or related field, • 1-3 years of experience in biopharmaceutical or academic research laboratory settings, • Hands-on experience with protein preparation and handling, • Knowledge of basic analytical techniques for protein characterization, • Strong attention to detail and ability to follow SOPs precisely, • Excellent organizational skills and ability to manage multiple priorities, • Effective written and verbal communication skills, • Master's degree in Biochemistry, Pharmaceutical Sciences, Biotechnology, or related field, • Experience in formulation development or protein drug product development, • Familiarity with biophysical characterization instruments (DLS, viscometry, capillary electrophoresis), • Previous experience working in GLP-compliant environments, • Knowledge of monoclonal antibodies or therapeutic proteins Pay Range * • Hourly Rate: $28 to $40 Per hour, • This role is on-site in El Segundo, CA, • Leveling and base salary is determined by job-related skills, education level, experience level, and job performance, • You will be eligible for long-term incentives in the form of stock options and/or long-term cash awards ITAR Requirements From life-saving pharmaceuticals to more powerful fiber optics, there is a world of products used on Earth today that can only be manufactured in space. Varda is accelerating innovation in the orbital economy by creating both the products and infrastructure needed so space can directly benefit life on Earth. Our mission is to expand the economic bounds of humankind. Our team is uniquely suited to accomplishing this goal, with leadership and staff comprised of veterans from SpaceX, Blue Origin, major pharmaceutical companies and Silicon Valley. Varda was founded in January 2021 by Will Bruey and Delian Asparouhov with significant backing from world class investors including Khosla Ventures, Lux Capital, Founders Fund, Caffeinated Capital, General Catalyst, and Also Capital. Varda is headquartered in El Segundo, California, where we have offices and a production facility where our vehicles, equipment, and materials are built, integrated, and tested. Join Varda, and work to create a bustling in-space ecosystem.Low Earth orbit is open for business. Varda is accelerating the development of commercial space infrastructure, from in-orbit pharmaceutical processing to reliable and economical reentry capsules. \r\n\r\nFrom life-saving pharmaceuticals to more powerful fiber optics, there is a world of products used on Earth today that can only be manufactured in space. Varda is accelerating innovation in the orbital economy by creating both the products and infrastructure needed so space can directly benefit life on Earth. Our mission is to expand the economic bounds of humankind. \r\n\r\nOur team is uniquely suited to accomplishing this goal, with leadership and staff comprised of veterans from SpaceX, Blue Origin, major pharmaceutical companies and Silicon Valley. Varda was founded in January 2021 by Will Bruey and Delian Asparouhov with significant backing from world class investors including Khosla Ventures, Lux Capital, Founders Fund, Caffeinated Capital, General Catalyst, and Also Capital. \r\n\r\nVarda is headquartered in El Segundo, California, where we have offices and a production facility where our vehicles, equipment, and materials are built, integrated, and tested.\r\n\r\nJoin Varda, and work to create a bustling in-space ecosystem.

Encode INC is seeking a travel nurse RN Cardiac Cath Lab for a travel nursing job in Torrance, California. Job Description & Requirements • Specialty: Cardiac Cath Lab, • Discipline: RN, • Start Date: 03/16/2026, • Duration: 52 weeks, • 36 hours per week, • Shift: 12 hours, days, • Employment Type: Travel Registered Nurse (RN) – Cardiac Catheterization Laboratory (Cath Lab) Facility: Torrance Memorial Medical Center Location: Torrance, CA (3330 Lomita Blvd, Torrance, CA 90505) Region: Southern California Community Hospital Engagement Type: Contract – Long Term Assignment Schedule: 3 × 12-hour day shifts Shift Timing: Typically 07:00 AM – 07:30 PM Call: As required by assignment About Torrance Memorial Medical Center Torrance Memorial Medical Center is a 401-bed community hospital serving the South Bay region of Los Angeles County. It offers a broad range of inpatient and procedural care, including a busy Cardiac Catheterization Laboratory where RNs deliver critical support for diagnostic and interventional cardiac procedures. Position Summary The Registered Nurse (RN) – Cardiac Cath Lab provides expert peri-procedural nursing care to patients undergoing cardiovascular diagnostic and interventional procedures. The Cath Lab RN partners with cardiologists and the interdisciplinary team to promote patient safety, maintain sterile technique, and support optimal patient outcomes throughout the procedure continuum. This role includes pre-procedure preparation, intra-procedure monitoring, and post-procedure recovery care for adult patients in a high-acuity cardiovascular environment. Key Responsibilities • Provide comprehensive nursing care to patients before, during, and after cath lab procedures, • Prepare the procedural area with appropriate sterile supplies and equipment, • Monitor patient vital signs, hemodynamic parameters, and ECG continuously during procedures, • Assist with interventional procedures such as angioplasty, stent placement, pacemaker insertion, and other cardiac interventions based on scope of practice, • Apply and maintain aseptic technique and safety protocols throughout the procedure, • Administer medications, contrast agents, and emergency drugs safely per physician orders and nursing scope, • Educate patients and families on procedural expectations, post-procedure care, and discharge instructions, • Document all assessments, interventions, and outcomes in the electronic health record (EHR) accurately and timely, • Collaborate with cardiologists, anesthesiologists, and support staff to ensure coordinated patient careRequired Qualifications, • Active California RN license, • Basic Life Support (BLS) certification required, • ACLS certification preferred (common in cardiac procedural settings), • Minimum 1–2 years of RN experience, preferably in:, • Cardiac cath lab, interventional cardiology, ICU, PCU, telemetry, or cardiac step-down units, • Experience with cardiac monitoring and hemodynamic assessments is strongly preferred, • Demonstrates knowledge of cardiac anatomy, physiology, and pathophysiology, • Proficient in cardiac rhythm interpretation and emergency response (e.g., ACLS protocols), • Able to troubleshoot equipment and respond to acute procedural changes, • Excellent communication with patients, families, and interdisciplinary teams, • Ability to function effectively in a fast-paced procedure areaAbout Encode INCAt Encode, we empower organizations and individuals through innovative, human-centric workforce and technology solutions. With decades of experience and a proven track record, we deliver more than just healthcare staffing, we provide integrated, strategic support across industries, with particular strength in federal and government contracts.Benefits, • 401k retirement plan, • Vision benefits, • Dental benefits, • Referral bonus, • Life insurance, • Medical benefits

Encode INC is seeking a local contract nurse RN Cardiac Cath Lab for a local contract nursing job in Torrance, California. Job Description & Requirements • Specialty: Cardiac Cath Lab, • Discipline: RN, • Start Date: 03/16/2026, • Duration: 52 weeks, • 36 hours per week, • Shift: 12 hours, days, • Employment Type: Local Contract Registered Nurse (RN) – Cardiac Catheterization Laboratory (Cath Lab) Facility: Torrance Memorial Medical Center Location: Torrance, CA (3330 Lomita Blvd, Torrance, CA 90505) Region: Southern California Community Hospital Engagement Type: Contract – Long Term Assignment Start Date: As agreed Schedule: 3 × 12-hour day shifts Shift Timing: Typically 07:00 AM – 07:30 PM Call: As required by assignment About Torrance Memorial Medical Center Torrance Memorial Medical Center is a 401-bed community hospital serving the South Bay region of Los Angeles County. It offers a broad range of inpatient and procedural care, including a busy Cardiac Catheterization Laboratory where RNs deliver critical support for diagnostic and interventional cardiac procedures. Position Summary The Registered Nurse (RN) – Cardiac Cath Lab provides expert peri-procedural nursing care to patients undergoing cardiovascular diagnostic and interventional procedures. The Cath Lab RN partners with cardiologists and the interdisciplinary team to promote patient safety, maintain sterile technique, and support optimal patient outcomes throughout the procedure continuum. This role includes pre-procedure preparation, intra-procedure monitoring, and post-procedure recovery care for adult patients in a high-acuity cardiovascular environment. Key Responsibilities • Provide comprehensive nursing care to patients before, during, and after cath lab procedures, • Prepare the procedural area with appropriate sterile supplies and equipment, • Monitor patient vital signs, hemodynamic parameters, and ECG continuously during procedures, • Assist with interventional procedures such as angioplasty, stent placement, pacemaker insertion, and other cardiac interventions based on scope of practice, • Apply and maintain aseptic technique and safety protocols throughout the procedure, • Administer medications, contrast agents, and emergency drugs safely per physician orders and nursing scope, • Educate patients and families on procedural expectations, post-procedure care, and discharge instructions, • Document all assessments, interventions, and outcomes in the electronic health record (EHR) accurately and timely, • Collaborate with cardiologists, anesthesiologists, and support staff to ensure coordinated patient careRequired Qualifications, • Active California RN license, • Basic Life Support (BLS) certification required, • ACLS certification preferred (common in cardiac procedural settings), • Minimum 1–2 years of RN experience, preferably in:, • Cardiac cath lab, interventional cardiology, ICU, PCU, telemetry, or cardiac step-down units, • Experience with cardiac monitoring and hemodynamic assessments is strongly preferred, • Demonstrates knowledge of cardiac anatomy, physiology, and pathophysiology, • Proficient in cardiac rhythm interpretation and emergency response (e.g., ACLS protocols), • Able to troubleshoot equipment and respond to acute procedural changes, • Excellent communication with patients, families, and interdisciplinary teams, • Ability to function effectively in a fast-paced procedure areaAbout Encode INCAt Encode, we empower organizations and individuals through innovative, human-centric workforce and technology solutions. With decades of experience and a proven track record, we deliver more than just healthcare staffing, we provide integrated, strategic support across industries, with particular strength in federal and government contracts.Benefits, • 401k retirement plan, • Vision benefits, • Dental benefits, • Referral bonus, • Life insurance, • Medical benefits

SkyBridge Healthcare Therapy is seeking a travel Speech Language Pathologist for a travel job in Inglewood, California. • Specialty: Speech Language Pathologist, • Discipline: Therapy, • Start Date: 02/23/2026, • Duration: 13 weeks, • 40 hours per week, • Shift: 8 hours, days DEDICATED RECRUITER: You’ll have a personal recruiter who genuinely cares about your goals—we’re here to guide and support you every step of the way. COMPREHENSIVE BENEFITS: Including health insurance, PTO, and sick time. PAID COMPLIANCE AND LICENSING: We cover the cost of onboarding requirements and offer license reimbursement. CONTINUED EDUCATION: CEU reimbursements to help you grow professionally. REQUIREMENTS: Please note: All positions require an active therapy state license and corresponding education credentials. To be considered, your license information must be included in your application or profile. A recruiter will reach out once this information is provided. EXPERIENCE New grads are welcome to apply! However, candidates with 2+ years of relevant experience are preferred. SkyBridge Healthcare Therapy Job ID #311911. Pay package is based on 8 hour shifts and 40 hours per week (subject to confirmation) with tax-free stipend amount to be determined. It is our mission at SkyBridge Healthcare to connect professionals within the healthcare community through both genuine relationships and quality work. We understand the demands of healthcare positions which is why we want to give back to Healthcare Professionals who give so much to their communities. We’re partnered with some of the greatest facilities in the nation, therefore we ensure our Healthcare Professionals will receive top-notch treatment every step of the way. Our specialties include Nursing, Allied Health, Laboratory, Therapy, Healthcare Information Technology, and Revenue Cycle. Follow us on social media to stay in the know of our latest company updates and job postings. • Mileage reimbursement, • Medical benefits, • Dental benefits, • Employee assistance programs, • Vision benefits, • Holiday Pay, • Guaranteed Hours, • License and certification reimbursement, • Life insurance, • 401k retirement plan, • Referral bonus, • Weekly pay

Job Description General Position Summary Under general supervision, performs a wide variety of electromechanical or mechanical production sub-assembly and assembly operations to build up and assemble difficult and complex instruments. Duties may include following techniques to wire, prepare cable harnesses and install cable harnesses. Perform coating, mixing and cooking of raw materials to create finished products. Essential Job Functions Assembly Activities • Under general supervision, performs various tasks requiring knowledge of assembly techniques, tools, materials, machines and equipment., • Assembles electromechanical instruments or fabricated parts to make subassemblies or complete instruments using hand tools, power tools and special tools and/or calibration equipment., • Determines methods and sequence of assembly operations where complete information is not readily available or follows assembly shop and production operations sheets, wire lists, samples, blue prints, schematics and verbal instructions to perform a wide variety of assembly operations., • Fits, aligns, calibrates and adjusts parts and mechanisms to meet tolerances and product operating and quality requirements., • Works from engineering drawings, rough sketches, and manuals, verbal or written instructions from Lead Assembler or Supervisor., • Performs in-process and final quality inspection of assembled products., • Examines drawings and work orders to determine the work that needs to be performed., • Utilizes appropriate machines and tools to install, mount, fasten, align and adjust parts, components, wiring and harnesses., • Evaluates assembly procedures and manuals and recommends revisions when required., • Performs such tasks as replacing components and wiring circuits., • Trains new hires and co-workers as necessary to enhance skill level and knowledge base., • Examines and tests assembly at various stages of production to identify errors., • Maintains a record of the assembly process, progress and problems., • Provides feedback to supervisor when a deviation from accepted practice or safety issues are recognized., • Utilizes small hand tools such as wire strippers, crimpers, wrenches, screwdrivers, pliers, and hammers., • Identifies and selects components to be integrated into sub-assembly and assembly units., • Makes own set-ups, alignments and adjustments maintaining tolerance in accordance with instructions., • Disassembles, modifies, reworks, refurbishes, reassembles, and tests instruments as required., • Clean and coat molds for fixtures and product used., • Perform mixing and cooking of gels in a laboratory environment. Other Activities • Evaluates and recommends changes in methods and procedures in assigned area of responsibility., • Performs data entry on work-in-process transaction and parts ordering., • Recommends and implements methods to promote teamwork and maintains a pleasant work environment within department and with other departments., • Trains new team members on how to fill out DHR such as batch record and traveler during the production run., • Seeks constant improvement in work processes and techniques., • Assures that laboratory and assembly areas are in an orderly and functional condition., • Suggests improvement in departmental work processes and procedures., • Maintains good communications with peers, Lead Assembler and Supervisor., • Attends and participates in group meetings, task force groups, etc., as needed., • Works with Support Engineering to develop and maintain time standards., • Aids Support Engineering with design of assemblies and units for manufacturing capability., • Performs other duties and projects as assigned by Supervisor and/or Lead Assembler. Essential Job Requirements Education High school diploma, GED or equivalent education and experience. Experience & Minimum Qualifications • 4-6 years of assembly experience in a fast-paced manufacturing environment, • Ability to follow schematics and assemble wire harnesses is a must., • Ability to read and interpret documents such as safety rules, operating and maintenance instructions, and procedure manuals, engineering prints and schematics., • Ability to add, subtract, multiply and divide in all units of measure, using whole numbers, common fractions, and decimals using a calculator., • Ability to compute rate, ratio and percent, and to draw and interpret bar graphs., • Ability to solve practical problems and deal with a variety of concrete variables in situations where only limited standardization exists., • Ability to interpret a variety of instructions furnished in written, oral, diagram, or schedule form., • Ability to use standard power hand tools and custom tools, gauges, and other calibration equipment and assembly fixtures., • Ability to lift 25 to 50 pounds is an asset, • Strong organizational skills through demonstrated ability to multi-task and manage time, • Established collaboration skills and the ability to communicate with openness and transparency., • Ability to comply with FDA Good Manufacturing Practices (GMP)., • Ability to meet production schedules and project deadlines., • Exposure and training to Six Sigma and/or lean manufacturing preferred. Physical Requirements & Working Environment • Ability to work safely and according to departmental procedures when working at high temperatures with hazardous equipment and materials such as oven, mixers, hot plates, ultrasonic cleaner, pressure cooker, fume hood, power tools, wire strippers, heat guns, heated cutting blades and others., • Ability to work safely and according to departmental procedures when handling volatile chemicals which may or may not be hazardous., • Ability to work safely in a chemical laboratory environment., • Ability to occasionally lift and/or move up to 50 lbs., • Ability to successfully respond to multiple work pressures., • Ability to communicate verbally to individuals and groups., • Ability to communicate verbally in person and using a phone., • Ability to listen for understanding and assisting in problem solving., • Ability to regularly use hands to utilize maximum dexterity., • Ability to frequently to walk, stand, sit, and reach with hands and arms., • Ability to occasionally to stoop, kneel, crouch, or crawl and hear., • Specific vision abilities required include close vision, color vision, and ability to adjust focus. "Sakura Finetek USA, Inc. is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex including sexual orientation and gender identity, national origin, disability, protected Veteran Status, or any other characteristic protected by applicable federal, state, or local law.” The above description identifies the essential job functions and skills needed by the person or persons assigned to this position. These job functions and skills are not intended to be a complete and exhaustive list of all responsibilities, duties and skills required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential job functions. The information contained herein is subject to change at the company's discretion.

Location: Carson, Ca (Los Angeles) Company Size: 250/ Team Size: 15 Industry: Manufacturing Duties & Responsibilities • Perform preventive maintenance of instruments or equipment., • Follow SOP, Safety and GMP, • Monthly, weekly, and daily lab equipment calibration., • Generate IQ PQ OQ for new equipment., • Determine daily system suitability., • Preparation of sample solution, standards, and reagents, • Preparation of lab batches at various concentrations for method validation., • Conduct placebo batch and perform of validation on new product formula., • Daily maintenance and troubleshooting when the system error., • Update/Maintain System Database., • Maintain accurate laboratory notebook for traceability., • Disposal of solvent waste follow safety protocols and procedures., • Approve and release internal assay results, • Investigate & Report OOS to appropriated HPLC Department., • Degree in chemistry and any science-related field or work experience in HPLC Lab setting., • Instrumental analysis using HPLC., • Operating, troubleshooting, process validation, and development of the HPLC system.

Job Title: Business Analyst/Label Designer Contract Duration: 12 months (extensions possible) Locations: El Segundo or Santa Monica, California Essential Duties and Job Functions: Label Design & Development • Design, develop, configure, and optimize labels using Bartender, including advanced templates, dynamic data handling, automation, and printing logic., • Utilize Visual Basic scripting to support conditional logic, formatting, and integration with upstream systems., • Implement standardized label formats across systems and sites to support harmonization and reduce deviations. Label Lifecycle Management • Drive the full label lifecycle: requirement gathering, design, configuration, testing, validation, production deployment, and support., • Troubleshoot label-related issues across interconnected systems (e.g., MES, Robar, ERP/EBS, Bartender)., • Maintain documentation, SOP updates, and knowledge transfer materials. System & Process Integration • Collaborate with Supply Chain, Regulatory, Quality, Manufacturing, and IT teams to ensure alignment of label workflows with end‑to‑end business processes., • Participate in cross‑functional workshops to define future‑state process flows, roles, responsibilities, and support models., • Ensure solutions comply with cGMP, data integrity requirements, and regulatory standards. Testing, Validation & Compliance • Develop and execute test plans for label functionality, integrations, and printing performance., • Support validation deliverables and change control processes for regulated systems., • Ensure accuracy, security, and compliance throughout the label lifecycle. Support & Continuous Improvement • Provide hands-on support during transitions, system upgrades, and site enablement projects., • Assist with troubleshooting high‑priority incidents and participating in cross-team triage., • Identify opportunities to improve labeling processes, tooling, and documentation. Required Qualifications • Expert-level proficiency with Bartender, including design, automation, and server components., • Strong Visual Basic / VBScript skills applied to label automation and dynamic behavior., • Strong troubleshooting skills in complex labeling ecosystems involving MES, ERP, and printing hardware., • Experience in biotech, pharma, or cell therapy supply chain, with familiarity in materials management, batch/lot control, serialization, and regulated operations., • Ability to collaborate with global cross-functional teams and translate requirements into technical label specifications., • Experience supporting systems and processes within a GMP-regulated environment. Highly Desirable Qualifications • Experience implementing or supporting laboratory instruments in QC labs or research environments (e.g., , label printers, scanners, nucleocounters, cytometry instruments, and similar)., • Experience working in IT site support, particularly in environments managing lab, manufacturing, or supply chain systems., • Experience working with Robar labeling software (configuration, troubleshooting, integration)., • Experience with EBS (Oracle E‑Business Suite) for label data sourcing or workflow integration. Preferred Qualifications • Prior involvement in labeling system standardization, migration, or transformation initiatives., • Familiarity with validation documentation (URS, FRS, IQ/OQ/PQ)., • Experience supporting enterprise label architecture involving MES (e.g., PAS-X), ERP, or middleware integrations. Engagement Details

Yoh is hiring a QC Analytical Chemist for our El Segundo, CA client. In this role, you will be a hands-on technical contributor responsible for executing, troubleshooting, and overseeing HPLC-based analytical testing in support of OTC drug and cosmetic product release, stability, and validation activities. This position serves as the primary HPLC subject matter expert within Quality Control, ensuring data integrity, GMP compliance, and timely batch disposition while actively working at the bench. The QC Analytical Chemist works under the general direction of the Quality Control Director. Industry: Cosmetics Location: El Segundo, CA Compensation: $85,000 - 100,000 Annually DOE Type: Direct Hire Job Functions: • Independently perform HPLC testing of raw materials, in-process samples, finished OTC drug products, stability samples, investigational samples, validations, and studies., • Prepare standards, samples, mobile phases, and reagents according to approved analytical methods., • Execute system suitability testing, injections, and data processing with minimal supervision., • Actively perform bench work while meeting QC turnaround times and release deadlines., • Perform first- and second-level review of chromatographic data and calculations., • Lead and support OOS, OOT, deviation, and laboratory investigation activities., • Conduct root cause analysis and implement corrective and preventive actions (CAPAs)., • Defend analytical results during internal and external audits., • Write, execute, and support method validation, verification, and transfer protocols and reports for OTC drug products., • Write, execute, and support bulk hold studies, cleaning validation, and recovery study protocols and reports as required., • Evaluate and implement USP and compendial methods applicable to OTC monographs., • Troubleshoot analytical methods and instrument issues to minimize downtime., • Operate, maintain, and troubleshoot HPLC systems., • Perform routine instrument maintenance, column performance evaluations, and readiness checks., • Maintain instrument logs, usage records, and calibration documentation., • Interface with vendors and service providers for instrument service and qualification support., • Ensure all QC activities comply with 21 CFR Parts 210/211, OTC monographs, USP/NF, and internal SOPs., • Maintain accurate, contemporaneous laboratory documentation in compliance with ALCOA+ principles., • Author and revise SOPs, analytical test methods, and protocols., • Support FDA inspections and third-party audits for OTC drug and cosmetic operations., • Provide technical guidance and on-the-job training to junior QC analysts., • Support analyst qualification and method proficiency assessments., • Serve as the QC analytical point of contact for Manufacturing and Quality Assurance. Education, Licensure and/or Experience: • Bachelor’s degree in Chemistry, Pharmacy, Biology, or a related scientific discipline, or equivalent work experience., • Minimum of 5 years of hands-on analytical chemistry experience in a GMP-regulated QC laboratory., • Strong experience supporting OTC drug and/or cosmetic product testing., • Demonstrated success in a high-throughput, release-driven QC environment., • Experience with method validation, OOS investigations, and audit preparation and response., • Experience supporting regulatory inspections, cGMP audits, and method or process validation., • Strong working knowledge of FDA OTC regulations, USP/NF methods, and ICH stability guidelines., • Demonstrated discretion in handling confidential and sensitive information. #IND-SPG Estimated Min Rate: $85000.00 Estimated Max Rate: $100000.00 What’s In It for You? We welcome you to be a part of the largest and legendary global staffing companies to meet your career aspirations. Yoh’s network of client companies has been employing professionals like you for over 65 years in the U.S., UK and Canada. Join Yoh’s extensive talent community that will provide you with access to Yoh’s vast network of opportunities and gain access to this exclusive opportunity available to you. Benefit eligibility is in accordance with applicable laws and client requirements. Benefits include: • Medical, Prescription, Dental & Vision Benefits (for employees working 20+ hours per week), • Health Savings Account (HSA) (for employees working 20+ hours per week), • Life & Disability Insurance (for employees working 20+ hours per week), • MetLife Voluntary Benefits, • Employee Assistance Program (EAP), • 401K Retirement Savings Plan, • Direct Deposit & weekly epayroll, • Referral Bonus Programs Yoh, a Day & Zimmermann company, is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran. Visit to contact us if you are an individual with a disability and require accommodation in the application process. For California applicants, qualified applicants with arrest or conviction records will be considered for employment in accordance with the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act. All of the material job duties described in this posting are job duties for which a criminal history may have a direct, adverse, and negative relationship potentially resulting in the withdrawal of a conditional offer of employment. It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability. By applying and submitting your resume, you authorize Yoh to review and reformat your resume to meet Yoh’s hiring clients’ preferences. To learn more about Yoh’s privacy practices, please see our Candidate Privacy Notice:

Job Title: QC Lab Technician Pay Rate: $23/Hr. Duration: 12 Months Location: Compton, CA Shift: 4 AM to 12:30 PM Our client is a global industrial and consumer products manufacturer. We are looking for a QC Lab Technician • Perform standard quality control testing on incoming raw materials, semi-finished goods, and finished goods according to specifications., • Accurately calculate and report test results., • Able to locate needed test methods, SOPs, and work instructions in the document management system., • Record test data into the SAP database., • File and maintain the retain samples; dispose of old retain samples per retention protocols., • Maintain a clean working environment, including lab benches, the retain sample room, ovens, and the hood., • Participate in Quality Lab 5S activities., • Actively participate in daily Quality Lab/department (MOS) meetings., • Complete, maintain, and control the required Quality records and/or documents as directed by the department's standard operating procedures., • Use proper Good Documentation Practices (GDPs) when recording information., • Perform and support validation and calibration of lab equipment, including documenting and reporting equipment issues within the lab., • Assist Quality Engineers with complaint investigations and testing samples/reports., • Comply with all Health, Safety, and Environmental rules, procedures, and regulations., • Support training efforts within the lab and maintain status for all learned test methods and requirements., • Proficient in SAP in regard to Quality Lab transactions., • Also including all responsibilities entailing the upkeep of the Quality Department and any assigned projects determined by the departmental Manager, Supervisor, and Leads. Qualifications: • Associate degree in chemistry or equivalent college credit, or 3 years minimum technical/lab experience., • The Quality Control Technician plays a critical role in ensuring product integrity and compliance by conducting standardized testing and analysis on raw materials, in-process items, and finished goods., • This position supports the broader Quality Department by maintaining accurate records, calibrating lab equipment, and contributing to continuous improvement initiatives., • The role requires strong attention to detail, proficiency in SAP, and adherence to safety and documentation protocols, while also collaborating with cross-functional teams to uphold quality standards throughout the production process., • Experience in Quality Control preferred., • Background in materials testing - viscosity testing, melting point testing, and general lab testing., • Knowledgeable in the use of laboratory equipment and instruments., • Good communication skills - verbal and written., • Able to work well in a team environment., • Computer literate – MS Office

Job Description GKY Dental Arts Inc., a leader in dental technology and innovation, is excited to announce the opening of an E-Max Dental Technician. This role is integral to our mission of delivering superior dental restorations and services to our clientele. As an E-Max Dental Technician, you will be involved in the design and fabricate high-quality dental prosthetics with a special focus on E-max ceramics—an esteemed material known for its strength and esthetics. This is an in-house position based at our state-of-the-art facility and requires the presence of a technician on-site, highlighting that this employment opportunity is not a remote job. Joining our team means becoming part of a dynamic environment committed to professional growth and excellence in the dental arts. We foresee our E-Max Dental Technician playing a crucial role in maintaining the standards of quality and innovation that GKY Dental Arts Inc. is known for. Duties and Responsibilities • Design and fabricate dental prosthetic appliances using E-max ceramics., • Analyze dental prescriptions and specifications received from dentists., • Prepare and manage materials and tools required for the creation of dental prosthetics., • Utilize advanced technical skills to construct aesthetically pleasing and functional dental items., • Test prosthetics for quality, precision, and fit to ensure alignment with client specifications., • Collaborate with other technicians and dental professionals to ensure optimal outcomes for patients., • Stay updated with the latest trends, techniques, and technologies in E-max ceramic dentistry., • Maintain accurate records of laboratory tasks and client orders to ensure compliance with regulations., • Must be authorized to work in the United States., • Proven experience as an E-max technician in a dental lab setting., • Prior experience in a dental lab required., • Deep understanding of dental anatomy and morphology., • Anterior experience required, showcasing ability to handle complex dental aesthetics., • High precision manual dexterity and attention to detail., • Proficient in using digital and traditional equipment essential for crafting E-max prosthetics., • Ability to interpret and follow the details contained within dental prescriptions., • Excellent teamwork skills, with a proven ability to work under supervision and collaboratively., • Strong communication skills required for effective interaction with colleagues and clients., • Commitment to ongoing professional development and learning in dental technologies. California Consumer Privacy Act Notice (CCPA/CPRA) for Job Applicants • If you are a California resident applying for a position with us, we are required by the California Consumer Privacy Act (CCPA), as amended by the California Privacy Rights Act (CPRA), to provide you with this notice regarding the collection and use of your personal information., • We may collect and use the personal information you provide in your application (such as your resume, cover letter, name, phone number, employment history, education, qualifications, references, and any other information you choose to provide) for purposes related to evaluating your candidacy for employment, conducting interviews, verifying information, complying with legal obligations, and, if applicable, preparing for your potential employment with us., • We do not sell or share your personal information as defined under the CCPA/CPRA. For more information about how we use and retain personal information, and your rights under California law, please contact the Human Resources Department at 310-802-4560.

Job DescriptionSalary: up to 90,000 non negotiable Position Title: Sr Chemist Reports to: Vice President of R&D Department: R&D (Research and Development) Local Candidates Only Key Responsibilities: Develop new formulas and reverse engineered formula based on customers briefs and price target. Be very careful about customers no-no lists. Reformulate and improve existing formulas. Follow new trends closely with new products launches, ingredients and new concept such as free from claims. Be familiar with the formulation restrictions using these claims. Be familiar with cosmetic ingredient especially their function, delivery system, interaction depending of media/base. Meet with suppliers and keep product files (clinical and regulatory). Work on Innovation, create new textures, concepts, actives to keep our R&D with cutting edge formulation. Help creating marketing sheet to present to our customers in innovation seminars. Request raw material pricing and input in our pricing matrix. Evaluation/Selection/Advice regarding testing; Claims, Safety, Microbiology. Assist Regulatory department requesting all the necessary ingredient information. Be flexible with project priorities as they vary from time to time and manage a large workload under tight timeline. Be able to make decisions to troubleshoot production or compounding. Improve and/or revise manufacturing/filling process if needed. Work closely with our chemists to help on challenging projects or when needed. Work closely with our Quality department to improve knowledge about new formulas, establishing standards. Represent Cosmetix West during cosmetics events such as suppliers seminars, SCC events, CEW, ICMAD, or other conferences or shows. Networking is a big part of our business model. Be able to understand Cosmetix West business model and new directions taken to insure easy transition, and success. Maintain the laboratory clean and organized, respecting GLPs. Qualifications: BS or more in chemistry or related field.

Job DescriptionPlease Note: To conform with the United States Government Space Technology Export Regulations, the applicant must be a U.S. citizen, lawful permanent resident of the U.S., conditional resident, asylee or refugee (protected individuals as defined by 8 U.S.C. 1324b(a)(3)), or eligible to obtain the required authorizations from the U.S. Department of State. At CesiumAstro, we are developers and pioneers of out-of-the-box communication systems for satellites, UAVs, launch vehicles, and other space and airborne platforms. We take pride in our dynamic and cross-functional work environment, which allows us to learn, develop, and engage across our organization. If you are looking for hands-on, interactive, and autonomous work, CesiumAstro is the place for you. We are actively seeking passionate, collaborative, energetic, and forward-thinking individuals to join our team. We are seeking a Power Electronics Engineer II to join our growing spacecraft payload development team. In this position, you will contribute across the entire development lifecycle of next-generation power electronics hardware for satellites and space power systems payloads—from helping define power system architectures and trade studies to detailed circuit design, simulation, printed circuit board (PCB) layout, verification and integration testing, and manufacturing support. JOB REQUIREMENTS AND MINIMUM QUALIFICATIONS • Bachelor of Science (BS) degree or higher in Electrical Engineering from an accredited university, • Minimum of 2 years of experience designing analog and power electronics, • Experience with power stage design of basic DC-DC power converter topologies (e.g. discrete linear regulators, Buck, Boost, Buck-boost), • Knowledge of voltage mode control and peak current mode control theory for DC-DC converters, • Experience with electronics schematic capture and printed circuit board (PCB) layout tools such as Altium, OrCAD, Allegro or Xpedition, • Hands-on experience with testing and troubleshooting electronics and power converters using laboratory instruments such as oscilloscopes, spectrum analyzers, electronic loads, and signal generators, • Experience with analysis and simulation tools such as SPICE, LTSPICE, SIMetrix/SIMPLIS, PLECS, Simulink, MATLAB, MathCAD, ANSYS Q3D and SiWave, or HyperLynx, • Excellent written and verbal communication skills PREFERRED EXPERIENCE, • Master of Science or PhD in Electrical Engineering with research focus in power electronics, • Experience running board-level power integrity simulation using tools such as Ansys SiWave, or HyperLynx, • Experience with power magnetics modeling, design and laboratory characterization, • Experience with control loop modeling and laboratory characterization, • Knowledge of power electronics applications utilizing GaN or SiC wide bandgap power semiconductor devices, • Experience with laboratory characterization of power magnetics

Job Description About Castelion Castelion is bringing a new approach to defense development and production: one that focuses on short, iterative design cycles, rapid testing in development, and modern commercial manufacturing strategies for production at scale. We're designing, building, and testing next generation long range strike weapons systems to give America and its Allies a definitive edge and deter future conflicts. Avionics Technician II Castelion is looking for an Avionics Technician II—reporting to the manufacturing organization—to directly support the development and manufacturing of avionics, harnessing, and test equipment for long-range hypersonic strike vehicles. This will be an hourly, non-exempt position located in our Torrance facility. As an Avionics Technician II, you will work closely with engineering to build and integrate a wide variety of hardware such as avionics assemblies, test racks, and interface boxes at the highest level of quality. RESPONSIBILITIES: • Work with avionics engineering by rapidly iterating electronic components and cables, • Construct superior wire cables according to engineering drawings, • Assemble, test, calibrate, and operate test racks, electro-mechanical units, engineering enclosures, and other test equipment, • Collaborate closely with engineering to transform concepts into reality, • Monitor one's own work progress against established standards and deliver all work on schedule, • Examine, interpret, and implement builds according to drawings and procedures, • Understand intricate cable harnesses, wiring diagrams, and mechanical drawings, • Verify flight hardware and thoroughly document outcomes, • Aid in developing manufacturing processes for initial production runs, • 3+ years of avionics technician experience, • Experience reading wiring harness drawings to build and troubleshoot laboratory and flight articles, • Knowledge of and adherence to industry standards, such as IPC-610 and IPC-620, • Proficient with test equipment such as multimeters, oscilloscopes, and signal generators., • Experience in a research and development environment, • Previous involvement in a high-speed production environment, handling flight hardware, • Prior involvement in a high-output environment, involving hands-on experience in constructing cables, electro-mechanical devices, or building prototypes, • Ability to acclimate to frequently changing assignments and a fast-paced working environment, • Excellent communication skills, both written and oral, along with effective teamwork abilities, • Superb focus and attention to detail, with remarkable work efficiency and accuracy, • Expertise in manufacturing and repairing intricate testing systems, • Familiarity with Atlassian tools such as SVN, Confluence, and JIRA, • Basic comprehension of electronic principles and theory, • Skills in project management, • Bias to Action and Creative Problem Solving. Desire and experience questioning assumptions in ways that lead to break through ideas that are ultimately implemented. Successfully bring in applicable processes/concepts/materials from other industries to achieve efficiency gains. Ability to personally resolve minor issues in development without requiring significant support., • High Commitment, High Initiative. A successful candidate will have a genuine passion for Castelion's mission and consistently look for ways to contribute to the company's technical goals and prevent hardware blockers. Ability to work in a fast paced, autonomously driven, and demanding atmosphere. Strong sense of accountability and integrity. All employees are granted long-term stock incentives as part of their employment at Castelion. All employees receive access to comprehensive medical, vision, and dental insurance, and the company offers four weeks of paid time off per year.

Job Description DropletPharma is developing two microscale devices to vastly accelerate radiopharmaceutical discovery and production and execute our vision to drastically improve health outcomes. As an Integration Engineering Intern on our team, you will be tasked with taking ownership and implementing core improvements to the mechanical and fluidic systems for our two flagship systems. This will be a fully in-person position in West Los Angeles, CA (near LAX), given involved and hands-on engineering work. Requirements What you will have ownership over: • Work with the engineering team to test and characterize mechanical, pneumatic, and fluidic subsystems for our radiopharmaceutical production and discovery systems., • Build and test assemblies and prototyping systems., • Create DOEs/experimental plans and perform experiments to evaluate new concepts and designs., • Perform data analysis on experimental data., • Assist with the development and maintenance of testing documentation as well as manuals and SOPs for operation of prototype systems., • Troubleshoot and improve designs. What we hope to see on your resume: • Pursuing B.S. degree or higher in Mechanical Engineering, Biomedical Engineering or similar., • Working knowledge of design of experiments., • Experience with statistical analysis tools such as ANOVA, significance analysis, etc., • Assembly of complex systems (mechanical, electromechanical, fluidic, pneumatic)., • Experience with metrology and measurement devices such as pressure transducers, flow sensors, thermocouples, etc., • Ability to work in both laboratory and machine shop environments., • 3D Printing & Rapid prototyping experience., • Microsoft Office (Excel, PowerPoint, Word). Experience that would be great, but not required: • Data analysis using various python libraries (NumPy, pandas, matplotlib)., • GD&T (ASME Y14.5) What we hope to observe about you during our conversation about your work (even one great project/experience can cover all these!): • Meticulous, logical, fundamental approach across all your work., • Ability to communicate key messages of your work succinctly across written, oral and slide presentations, and have mastery over your work such that you can elaborate deeply when needed., • A demonstrated deep curiosity., • Examples of how you tackled roadblocks and cleared them., • Experience in collaborating across engineering disciplines (e.g., interacting with electrical engineers, software teams, etc. on large projects)., • Demonstrated ability to work in a dynamic environment, adapt to changes and deliver on milestones on tight timelines., • Comfortable working as part of a startup team, taking on outsized responsibility of assigned projects and tasks and demonstrating ability to suggest key improvements - including ones that shape the company’s future. DropletPharma aims to provide competitive compensation. We expect this position to be a regular, full-time position, with an hourly rate of $25-40/hour, depending on your experience and education. Please note that we are unable to sponsor a visa for this position and therefore can only consider applications from individuals already authorized to work in the United States. Although our primary location is in Los Angeles, CA, we welcome applications from candidates residing anywhere. Ensuring purpose and belonging at our company: Cancers don’t discriminate, and neither do we. We prohibit discrimination and harassment of any kind based on race, color, sex, religion, sexual orientation, national origin, disability, genetic information, pregnancy, or any other protected characteristic as outlined by federal, state, or local laws. DropletPharma is committed to providing the best possible environment to ensure that our team members feel valued and have purpose in the work they do.

Job Description General Position Summary The Senior Scientist has an overall responsibility for reagent and product development following design control guidelines to meet Food and Drug Administration (FDA) and the in-vitro medical devices Regulation (IVDR) regulatory requirements. The incumbent is responsible for developing and improving reagents and assays for automated and manual immunohistochemistry (IHC) and in situ hybridization (ISH) staining and in other areas as assigned. Essential Job Functions Research and Development Activities • Develop quality reagents and IHC or ISH staining protocols to meet the demands of Sakura's global IHC and ISH market., • Develop new antibodies, probes, and IHC/ISH detection reagents to expand the reagent lines, documenting appropriate specificity/sensitivity, precision, robustness, and stability as required., • Continually monitor productivity and quality and make improvements., • Facilitate technology and reagent development process transfers., • Support program directives from senior management., • Perform microscopic interpretation of stained slides., • Work with the project manager and team to develop and launch new products., • Ensure compliance with all applicable environmental, health, and safety regulations., • Develop, plan, and implement product and process development for new products and technologies from the laboratory through manufacturing scale-up., • Provide technical expertise for all Reagent Product/Process Development activities., • Participate as needed in project teams, task forces, and business or technical meetings., • Provide technical advice to internal and external customers., • Support products from early development, finalization, manufacturing, and launch., • Write and file patent applications as warranted., • Capable of working with external collaborators on complex scientific projects., • Present scientific research findings or new technology in scientific meetings and workshops., • Ensure that Sakura's Quality System is deployed and actively seek continuous improvement opportunities., • Adhere to Good Laboratory Practice (GLP) and support any activity that is needed for FDA and IVDR compliance and/or ISO certification., • Follow up on R&D action items addressed by different teams and assist in resolving quality issues., • Implement preventive action based on improvement opportunities or trends identified during Leadership Review meetings., • Initiate action items and assign responsibilities. Education • Ph.D. or master’s degree or equivalent in a relevant scientific discipline., • Experience in tissue histology or pathology., • Minimum of five years of laboratory experience, including independent experimental design, data collection, interpretation, and report writing., • Must have demonstrated expertise with histology and anatomic pathology methods, including IHC/ISH staining and microscopic interpretation of stained slides., • Must possess essential knowledge of immunochemistry, histology, and molecular biology methods., • Must be proficient in immunohistochemistry and in-situ hybridization methodologies on formalin-fixed, paraffin-embedded human tissues such as antibody development/characteristic/production, immunohistochemistry detection system, and antibody conjugations., • Must be able to troubleshoot assay performance issues independently., • Practical experience with light and fluorescence microscopy, ideally including proficiency in whole slide scanning. Requires clear and concise verbal and written communication skills, strong technical writing abilities, and the capacity to present complex technical information in an easily understandable manner. Proficient computer skills, including Excel Spreadsheets, and PowerPoint., • Excellent analytical, organizational, and problem-solving abilities. Required skills include interpreting data, performing mathematical calculations, drawing informed conclusions, and creating and executing strategies and processes to achieve objectives. Proven capability to lead and coordinate teams to reach targets and assess the success of various programs and projects., • Track record of assay development and optimization, preferably in tissue- and slide-based settings., • Track record of establishing and maintaining collaborations with other departments and external organizations., • Laboratory work experience should include a thorough understanding of principles, theories, and practices of immunohistochemistry assay and cell/molecular biology., • Experience in DNA/RNA isolation from cells and tissues, sequencing, and designing nucleic acid probes and primers is a plus., • Hands-on experience with mammalian cell culture and bacterial culture, preferably including cytogenetic specimen preparation, is a plus., • Excellent interpersonal skills with the ability to analyze and weigh the opinions of experts in the field of biomarker detection., • Interact in a professional and proactive manner with internal and external customers., • Must be able to generate, interpret, and present technical data to meet customer requirements., • Must orchestrate the technical expertise of all team members in answering customer requirements., • This position requires the employee to sit and work in a laboratory setting frequently. In addition, the employee is occasionally required to stand, walk, use hands and fingers, and reach with hands and arms., • Must be able to lift, push and/or pullup to 50 pounds occasionally with assistance., • Ability to successfully respond to multiple work pressures. The above description identifies the essential job functions and skills needed by the person or persons assigned to this position. These job functions and skills are not intended to be a complete and exhaustive list of all responsibilities, duties and skills required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential job functions. The information contained herein is subject to change at the company's discretion.

Job Description Overview $22.00-$30.75/Hourly Registered Dental Assistants perform a variety of patient care, office, and laboratory duties. The primary role of the Registered Dental Assistant (RDA) is to assist the dentist in gaining the patient’s commitment to the best possible treatment, with urgency. Key duties associated with assisting the dentist in starting treatment include: utilizing x-ray time to promote the good qualities of the dentist, learning the patient’s expectations while educating them with intra-oral pictures, using effective and anticipatory chair-side skills, and effectively supporting the dentist’s diagnosis after the examination when the patient asks questions. The RDA should abide by procedures needed for compliance with state and federal safety regulation, infection control, and permitted duties. Responsibilities • The primary role of the Registered Dental Assistant (RDA) is to assist the dentist as necessary to gain the patient’s commitment for the best possible treatment with urgency, • Actively participate in the Perfect Patient ExperienceÔ by striving to keep your patients focused on optimal treatment while attending to their individual needs and concerns, • Maintain a clean, sterile, and cheerful environment where your patients feel comfortable; prepare patients for treatment, and assist the doctors - thereby enabling them to provide efficient, quality dental treatment, • At the direction of the dentist, complete x-rays and intra-oral pictures of patients as appropriate, • At the direction of the dentist, instruct patients on postoperative and general oral health care., • Sterilize and disinfect instruments, equipment, and operatories in accordance with the American Dental Association guidelines, • Maintain strict compliance with State, Federal, and other regulations, (e.g., OSHA, WC, Dental Board, HIPAA, ADA, DOL, HR policies and practices) Qualifications • Equivalent to high school diploma or general education degree (GED), and specified training courses as mandated by state for certification, licensure, or registration, • Certifications/licenses/registrations as mandated by applicable state (e.g. coronal polish, radiograph exposure, ultrasonic scaling for orthodontic procedures, pit and fissure sealant application, etc), • Associate degree or one-year certificate from an accredited college or technical school; or equivalent combination of education and experience preferred Benefits • Medical, dental and vision insurance, • Paid time off, • Tuition Reimbursement, • Child care assistance, • 401K, • Paid time to volunteer in your local community, • Shift premium pay for eligible roles who work weekends Responsibilities PDS Health is an Equal Opportunity Employer. We celebrate diversity and are united in our mission to create healthier and happier team members.

Job Description Who We Are Dermalogica stands tall as a beacon in the professional skincare realm, winning the trust of skin therapists across the globe. As a shining gem in the crown of the Unilever Prestige family, our commitment isn't just to nurture skin, but also to redefine industry standards with revolutionary skincare innovations. With a commitment to innovation, sustainability, and excellence, Dermalogica has been at the forefront of the skincare industry for over three decades. Bolstered by our International Dermal Institute – the apex of post-graduate skin and body therapy training – we are on an exhilarating journey of expansion. And you could be a part of this adventure! We are currently seeking a curious, meticulous Regulatory Intern to join our Research & Development team during an exciting period of growth and innovation. This internship offers firsthand exposure to cosmetic and OTC regulatory processes while supporting new product launches and our existing product portfolio. This is an excellent opportunity for a science-focused student who is eager to learn, contribute, and gain real-world experience within a fast-paced, collaborative R&D environment. What You’ll Do As a Regulatory Intern, you will support the Regulatory and R&D teams by helping ensure raw materials and products meet regulatory and documentation requirements. Your responsibilities will include: • Partnering with external suppliers to collect and organize raw material data, escalating requests when needed., • Maintaining and updating the raw material database to ensure accuracy and compliance, • Supporting R&D with sample initiation, scheduling, preparation, packing, and coordination of product testing and clinical trials, • Assisting with regulatory documentation related to product development, validation, and registration, • Supporting the International Regulatory documentation process within the Product Information Management (PIM) system, • Tracking and logging international requests to ensure proper communication and queries are addressed in a timely manner, • Manage safety testing spreadsheet logs, • Maintaining validation documentation within R&D and International folders, • Coordinate with chemists to support in samples submission for testing What You’ll Bring • Familiarity with or interest in a laboratory environment, • Strong interest in cosmetic and/or OTC regulations, • Ability to manage multiple tasks, prioritize effectively, and meet deadlines., • Strong attention to detail with the ability to multitask efficiently., • Excellent organizational, written, and verbal communication skills Education/Experience: • Currently enrolled in and pursuing a bachelor’s degree, preferably in a science-related field, • 0–1 years of experience; prior exposure to cosmetic, pharmaceutical, food, or science-based environments is a plus, but not required The expected base hourly pay rate is $18.50/hr. The exact base hourly rate is determined by various factors including experience, skills, education, geographic location, and budget. This role is eligible for participation in our company bonus plan, rewarding personal performance and company results. Why Join Us? • A Legacy of Success: Dermalogica is the preferred choice of Skin Therapists worldwide, renowned for our exceptional skincare line and industry-leading postgraduate education. We have a record of achievement and are committed to building upon our brand's legacy., • Entrepreneurial Spirit and Innovation: At Dermalogica, we foster an entrepreneurial spirit and encourage our employees to bring their best ideas to the table. You'll have the opportunity to make a difference and contribute to our success by implementing innovative solutions that reach skincare professionals and consumers., • Backed by Unilever: In 2015, Dermalogica became part of the Unilever family, one of the world's largest and most successful consumer goods companies. While operating as an independent business, we now have access to cutting-edge capabilities and resources, empowering us to win in our markets. Ready to make a meaningful impact and advance your career with a global brand revolutionizing the skincare industry? Apply now and complete your online application. Rest assured, all applications will be thoughtfully reviewed, and our HR team will contact you if your skills align with the position. Dermalogica is an equal opportunity employer committed to fostering an inclusive culture where all employees are valued, supported, and empowered to succeed.

Job Description Medical Assistant We offer competitive salary, full benefits package, Paid Time Off, and opportunities for professional growth. Aegis / Pinnacle Treatment Centers is a growing leader in addiction treatment services. We provide care across the nation touching the lives of more than 30,000 patients daily. Our mission is to remove all barriers to recovery and transform individuals, families, and communities with treatment that works. Our employees believe we are creating a better world where lives and communities are made whole again through comprehensive treatment. As a Medical Assistant, you will be the face of the front office. You will register patients, create appointments, collect payments, and escort patients throughout their visit to your clinic. You will also help provide a positive experience for every patient during their visit. Pay Range: $18 to $22 per hour Benefits: • 18 days PTO (Paid Time Off), • 401k with company match, • Company sponsored ongoing training and certification opportunities., • Full comprehensive benefits package including medical, dental, vision, short term disability, long term disability and accident insurance., • Substance Use Disorder Treatment and Recovery Loan Repayment Program (STAR LRP) High School Diploma or GED (General Equivalency Diploma) * Must possess a current medical assistant certificate or emergency medical technician certificate from an accredited teaching school and/or provide transcripts. * Experience as a medical assistant. * Must maintain continuing education credits as required by the state employed * Ability to administer medications. * CPR (Cardiopulmonary resuscitation), First Aid, and BLS (Basic Life Support) certification. Preferred • Graduation of a post-secondary medical assisting education program accredited by an agency recognized by the U.S. Department of Education. Current certification from the Certifying Board of the American Association of Medical Assistants (AAMA), or registration from the American Medical Technologists (AMT), or the National Center for Competency Training (NCCT), or any recognized certifying body approved by the Board., • CNA (Certified Nursing Assistant), RMA (Registered Medical Assistant). Works as part of the intake team to ensure patients are seen promptly. * Observe urine samples for urine drug screens, test onsite and package for laboratory for confirmation testing. * Obtain vital signs and report findings to nurse when needed. * Makes appointments for patients to see physician, provide lab work and referrals for additional follow up care. * Maintain and keep updated all medical records and documentation pertaining to the patients. * Assist with Purchasing and ordering of medical supplies * Assists in education with pregnant patients about prenatal care and assists primary counselor in coordinating outside services as needed. * Attend team meetings and complete all training courses timely as required. * Other duties as assigned Join our team. Join our mission.

Radiant is an El Segundo, CA-based startup building the world’s first mass-produced, portable nuclear microreactors. The company’s first reactor, Kaleidos, is a 1-megawatt failsafe microreactor that can be transported anywhere power is needed and run for up to five years without the need to refuel. Portable nuclear power with rapid deploy capability can replace similar-sized diesel generators, and provide critical asset support for hospitals, data centers, remote sites, and military bases. Radiant’s unique, practical approach to nuclear development utilizes modern software engineering to rapidly achieve safe, factory-built microreactors that leverage existing, well-qualified materials. Founded in 2020, Radiant is on track to test its first reactor next year at the Idaho National Laboratory, with initial customer deliveries beginning in 2028. Software Software Engineer Radiant is seeking a driven Senior Software Engineer to work on a variety of internal tools and platforms. In this role, you will design, build, maintain, and scale the internal systems and platforms that support simulation, hardware testing, data processing, and analysis. You will have an opportunity to work in an interdisciplinary environment with a high degree of ownership and drive milestones forward to unlock commercialization of the first mass-produced nuclear reactor. Responsibilities and Duties: • Architect, build, and maintain a variety of internal tools and platforms, • Help define and build our simulation and analysis stack to support the development of Digital Twins, • Collaborate across teams to integrate new and existing software with a variety of software and hardware platforms, • Mentor and be a technical leader: review code and provide feedback, establish best practices (documentation, testing, deployment automation) Required Qualifications and Skills: • Bachelor’s degree in computer science or engineering, • 5-8+ years of professional experience in Python, C++, C#, or similar object-oriented programming languages, • Familiarity with Git, Docker, and common CI/CD frameworks Desired Qualifications and Skills: • Highly self-motivated with strong communication skills, • Experience testing software and hardware systems, • Experience with embedded and distributed software development and familiarity with common design patterns, • Interest in physics, hardware and electrical engineering Additional Requirements: • Must be willing to work extended hours and weekends as necessary to accomplish our mission., • Must work 100% onsite at El Segundo HQ. Total Compensation and Benefits Radiant's new hire compensation package includes base salary, substantial equity grants, and comprehensive benefits. Total compensation and level are determined through a holistic evaluation of your interview performance, experience, education, and qualifications. Benefits and Perks for Eligible Employees: • Stock: Substantial incentive stock plan for all full-time employees., • Medical: 100% up to base silver level plan for employee + 50% dependents, offers up to Platinum plans., • One Medical: Sponsored memberships for employees and their dependents., • Vision: 100% top tier plan coverage + 50% for dependents., • Dental: 100% top tier plan coverage, orthodontia extra, 50% for dependents., • Voluntary life, accident, hospital, critical illness, commuter and FSA/HSA are offered as employee contributed benefits., • 8-weeks of paid parental leave for all parents. Additional paid pregnancy leave for CA employees., • Daily catered lunch. Free snacks and drinks., • Flexible PTO policy. Remote workday allocation., • Company and team-bonding events, happy hours and in-person camaraderie., • Beautiful El Segundo headquarters close to the Pacific Ocean. We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity or expression, pregnancy, age, national origin, disability status, genetic information, protected veteran status, or any other characteristic protected by law. Unfortunately, we are unable to provide visa sponsorship at this time. This position involves access to technology that is subject to U.S. export controls. Any job offer made will be contingent upon the applicant’s capacity to serve in compliance with U.S. export controls.

Duration: 10 Months Start Date: 2/23/2026 Pay: $76.64/hr Location: El Segundo, CA 90245 The Company requires the services of a Senior BSA Label Design & Implementation Contractor with deep expertise in Bartender label design software and Visual Basic (VB) scripting. The ideal candidate will support end‑to‑end label lifecycle activities—including design, configuration, testing, validation, and deployment—within a GxP-regulated biopharma, biotech, or cell therapy environment. This role requires strong collaboration with IT, Supply Chain, Quality, Manufacturing, and R&D or QC Lab teams to ensure compliant, reliable, and scalable labeling solutions. The candidate will work with the Company's commercial and clinical supply chain organizations, regulatory affairs, manufacturing and quality stakeholders to support requirements gathering, prototyping, and label design. The candidate will also work with cross functional IT teams on the implementation, testing, deployment, and support of labels. The candidate must be experienced working in GxP environment. The candidate must have strong collaboration and clear communication skills with ability to present technical concepts to non-technical audiences. The candidate must be comfortable to work with ambiguity, engage and align cross-functional stakeholders and delivery partners. The individual should have experience leading workshops and meetings, bringing people together, and ensuring structured process-driven approach to projects and support. The candidate will be a key point of contact for labeling ensuring projects and dependencies are tracked, risks escalated and mitigation strategies proposed in a timely manner, Essential Duties and Job Functions: Label Design & Development • Design, develop, configure, and optimize labels using Bartender, including advanced templates, dynamic data handling, automation, and printing logic., • Utilize Visual Basic scripting to support conditional logic, formatting, and integration with upstream systems., • Implement standardized label formats across systems and sites to support harmonization and reduce deviations. Label Lifecycle Management • Drive the full label lifecycle: requirement gathering, design, configuration, testing, validation, production deployment, and support., • Troubleshoot label-related issues across interconnected systems (e.g., MES, Robar, ERP/EBS, Bartender)., • Maintain documentation, SOP updates, and knowledge transfer materials. System & Process Integration • Collaborate with Supply Chain, Regulatory, Quality, Manufacturing, and IT teams to ensure alignment of label workflows with end‑to‑end business processes., • Participate in cross‑functional workshops to define future‑state process flows, roles, responsibilities, and support models., • Ensure solutions comply with cGMP, data integrity requirements, and regulatory standards. Testing, Validation & Compliance • Develop and execute test plans for label functionality, integrations, and printing performance., • Support validation deliverables and change control processes for regulated systems., • Ensure accuracy, security, and compliance throughout the label lifecycle. Support & Continuous Improvement • Provide hands-on support during transitions, system upgrades, and site enablement projects., • Assist with troubleshooting high‑priority incidents and participating in cross-team triage., • Identify opportunities to improve labeling processes, tooling, and documentation. Required Qualifications • Expert-level proficiency with Bartender, including design, automation, and server components., • Strong Visual Basic / VBScript skills applied to label automation and dynamic behavior., • Strong troubleshooting skills in complex labeling ecosystems involving MES, ERP, and printing hardware., • Experience in biotech, pharma, or cell therapy supply chain, with familiarity in materials management, batch/lot control, serialization, and regulated operations., • Ability to collaborate with global cross-functional teams and translate requirements into technical label specifications., • Experience supporting systems and processes within a GMP-regulated environment. Highly Desirable Qualifications • Experience implementing or supporting laboratory instruments in QC labs or research environments (e.g., , label printers, scanners, nucleocounters, cytometry instruments, and similar)., • Experience working in IT site support, particularly in environments managing lab, manufacturing, or supply chain systems., • Experience working with Robar labeling software (configuration, troubleshooting, integration)., • Experience with EBS (Oracle E‑Business Suite) for label data sourcing or workflow integration. Preferred Qualifications • Prior involvement in labeling system standardization, migration, or transformation initiatives., • Familiarity with validation documentation (URS, FRS, IQ/OQ/PQ)., • Experience supporting enterprise label architecture involving MES (e.g., PAS-X), ERP, or middleware integrations. Benefits Full-time employees (working an average of 30 hours or more) are eligible to select from different benefits packages. Packages may include medical, dental, and vision benefits, a 401(k) retirement savings plan with employer match (available after 1 year of employment), commuter benefits, employee discount and referral programs, and life and supplemental income insurance. Paid sick leave is provided in accordance with applicable state and local laws. Compensation Final offer amounts, within the base pay set forth above, are determined by factors including your relevant skills, education, and experience, as well as the benefits package you select. Work Authorization ATR International, Inc. cannot sponsor work visas (H-1B, F-1 STEM OPT with I-983, or similar). Candidates must have valid U.S. work authorization. ATR International, Inc. is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.

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