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Job Description Test Technician - Medical Device Industry QUICK FACTS • Location: Irvine, CA, 92618, • Pay range: $75,000 – $110,000, • Shifts: Standard full-time, hours may include occasional off-hours, • Duration: Permanent EXPERIENCE/EDUCATION YOU WILL NEED • 2–5+ years of hands-on mechanical testing experience, • Experience working with laboratory equipment such as Instron machines and fluid systems, • Knowledge of Good Laboratory Practices (GLP) in a regulated environment, • Preference for candidates from medical device or regulated industries, • Engineering degree is not required but candidates with an engineering background open to technician roles are acceptable MAIN DUTIES OF THE JOB • Conduct mechanical testing on pumps and small plastic components, • Operate specialized lab equipment and measure flow rates, • Assemble small parts under a microscope and perform detailed mechanical assembly, • Maintain lab organization, label samples, and manage inventory, • Document testing and ensure compliance with protocols The company is an equal opportunity employer committed to providing employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, sex, national origin, age or disability, or any other class protected by Federal, State or local laws. Company DescriptionMedical Device Manufacturer in the Diabetes spaceMedical Device Manufacturer in the Diabetes space

As a QC Technician, you will support the testing and documentation needs of the Quality Control department during the manufacture and release of Bio-Rad control products. This position will work both independently and in a team-oriented environment. Location: This position must be based in Irvine, California and requires the employee to be located within commuting distance of the office. How You'll Make An Impact: • Operate, maintain, and troubleshoot QC laboratory instruments., • Follow good laboratory practices., • Order supplies and maintain instrument preventative maintenance schedule., • Interface with other departments when required., • Evaluate assay runs for accuracy and acceptability to Quality Control procedures., • Associate's degree or higher in a science field or equivalent clinical lab experience., • Any experience working in QC or a clinical laboratory are a plus., • Strong knowledge of Quality Systems and Good Documentation Practices (GDP). Experience in the use of clinical laboratory techniques and equipment. Experience in running. chemistry, hematology, and immunoassay analyzers a plus., • Experience with Microsoft Office Suite (Outlook, Excel, Word) is required. Experience with a LIS is a plus., • Excellent verbal and written communication skills to effectively interact with team members, supervisors, and other departments., • Strong attention to detail and accuracy of data. Benefits: We're proud to offer a variety of options, including competitive medical plans for you and your family, free HSA funds, a new fertility offering with stipend, group life and disability, paid parental leave, 401k plus profit sharing, an employee stock purchase program, a new upgraded and streamlined mental health platform, extensive learning and development opportunities, education benefits, student debt relief program, pet insurance, wellness challenges and support, paid time off, Employee Resource Groups (ERG's), and more! Compensation: The estimated hourly rate for this position is $23.13 to $31.78 at the time of posting. Actual compensation will be provided in writing at the time of offer, if applicable, and is based on several factors we believe fairly and accurately impact compensation, including geographic location, experience, knowledge, skills, abilities, and other job permitted factors. This position is eligible for a variable annual bonus, which is dependent upon achievement of your individual objectives and Company performance. Who We Are: For 70 years, Bio-Rad has focused on advancing the discovery process and transforming the fields of science and healthcare. As one of the top five life science companies, we are a global leader in developing, manufacturing, and marketing a broad range of high-quality research and clinical diagnostic products. We help people everywhere live longer, healthier lives. Bio-Rad offers a unique employee experience with collaborative teams that span the globe. Here, you are supported by leadership to build your career and are empowered to drive change that makes an impact you can see. EEO Statement: Bio-Rad is an Equal Employment Opportunity/Affirmative Action employer, and we welcome candidates of all backgrounds. Veterans, people with physical or mental disabilities, and people of all race, color, sex, sexual orientation, gender identity, religion, national origin and citizenship status are encouraged to apply. Agency Non-Solicitation:Bio-Rad does not accept agency resumes, unless the agency has been authorized by a Bio-Rad Recruiting Representative. Please do not submit resumes unless authorized to do so. Bio-Rad will not pay for any fees related to unsolicited resumes. Fraud Alert: Bio-Rad has received reports of individuals posing as Bio-Rad recruiters to obtain information, including personal and financial, from applicants. Beware of these fake "recruiters" and job scams. ___ for more information on this scam and how to avoid it. #LI-KD2 Legal Entity: (USA_1000)Bio-Rad Laboratories, Inc.

Job DescriptionAbout the Company:Harrington Geotechnical Engineering Inc. (HGEI), a QAI company, has over 50 years of experience in the geotechnical engineering field. With our experts, professional skilled staff, and diverse experience, we offer reliable services in an integrated, efficient, and cost-effective service to clients in the public and private sectors. Our services include Geotechnical Engineering, Geotechnical Engineering Laboratory Materials Testing, Engineering Geology, and Environmental Engineering. We are growing and looking for an experienced and motivated Soil Technician to join our team. Salary Range: $21 to $30 per hour (Depending upon experience) About the Job:As a Soil Technician, you will be conducting field work and utilizing computer software for the input/output of soil data and geographical information. This position is also responsible for collecting and analyzing soil samples, conducting quality control inspections, and providing valuable insights to support projects. You will also need to demonstrate excellent verbal and written communication skills, positive attitude, good organizational skills, with a strong work ethic. Responsibilities: • Collect, log and prepare soil samples for laboratory analysis using various techniques and equipment, • Conduct soil testing in the field and lab as needed to determine soils properties such as moisture content, density and composition., • Perform field observation of soils and construction materials onsite, and collect soil samples for laboratory testing as required per the project plans and specifications, • Maintain accurate records of samples, tests, and findings and prepare field daily inspection reports, • Maintain field equipment to ensure proper function and calibration due dates, • Proficiency in using lab, field test equipment and software for data analysis, • Adhere to strict safety standards and protocols in the field and laboratory, • Maintain professional working relationships and communication with office staff, clients, engineers, contractors, etc., • Obtain and/or maintain certifications required by employer, • A minimum of 2 to 3 years of proven experience as a Soil Technician or in a similar role., • Strong knowledge of soil surveying techniques and data collection methods, • Familiarity with construction inspection processes and procedures, including the ability to read construction plans and specifications, • Proficiency in analyzing soil samples in a laboratory setting., • Excellent attention to detail and the ability to accurately record and interpret data., • Ability to interpret engineering plans and specifications related to soil conditions., • Strong communication skills, with the ability to effectively collaborate with engineers, construction teams, and other stakeholders., • Must have nuclear gauge certification per The Nuclear Regulatory Commission (NRC), • Written and verbal communication skills

Job DescriptionAsana Recovery is seeking a compassionate and dedicated team member to join our Outpatient Program in Fountain Valley, operating Monday through Sunday. This dynamic role involves facilitating group sessions, conducting client intakes, and providing transportation as needed. If you're passionate about helping individuals on their journey to recovery and thrive in a supportive, team-oriented environment, we invite you to become part of the Asana team—where meaningful work meets purpose every day. Required • Valid Driver's License with NO restrictions or SR-22 Waivers, • RADT, SUDRC or equivalent, • Can work Saturday-Tuesday SUMMARY: The Health Technician works closely with each of the clients and clinical, on an individual basis, providing assistance in the areas of group facilitation, providing transportation and medical appointment scheduling, as well as overall client health.JOB DUTIES AND RESPONSIBILITIES: • Observation of clients, charting and reporting changes in clients' conditions, such as adverse reactions to medication or recording a change in treatment, and taking any necessary action, • Record withdrawal symptoms, and record collected data, • Collecting UA samples to prepare for the lab, • Educate clients regarding prescriptions and medication management (Licensed Personnel Only), • Measure and record clients’ vital signs, • Ensure accurate documentation on medication observations orders and monitor medication audits/counts and inventory, • Record data and communicate with physician for medical clearance in relation to treatment, planning and discharge, • Observe client concerns and recommend client to emergency medical care when necessary, • Perform inventory check and maintenance of supplies and over the counter medication supplies, responsible for requesting inventory and requisitioning supplies/instruments, • Client documentation and summary reporting at shift end, • Maintain compliance with HIPAA regulations, ADA and Joint Commission policies and procedures, boundaries and client and company confidentiality, • Other duties as requested by leadership, • Attends in-service training, educational workshops, and staff meetings, • Assist client with filling/refilling prescriptions, • Assist client with making outside appointments for medical care/management, • Behavioral Health Technicians have a valid RADT-1 Certification or equivalent upon hire, • Must have valid California driver’s license, • Vision, hearing, manual dexterity and hand-eye coordination must be adequate for the performance of job duties, • Able to sit at a desk, use keyboard, write and physically perform other job duties, • Able to move about the facility to observe clients and staff, • One year of experience is preferred. Experience in a residential healthcare facility, behavioral health, mental health, hospital or other related fields preferred, • Basic computer skills, proficiency in electronic medical record systems preferred, • Work Conditions: The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of the job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions., • Ability to move 25 lbs, • Ability to remain working at a fixed computer workstation

As a Quality Control Technician II, you will support the testing and documentation needs of the Quality Control department during the manufacture and release of Bio-Rad control products. This position will work both independently and in a team-oriented environment. This position is for a first-shift technician (Hours: 7:00 am to 3:30 pm) Location: This position must be based in Irvine, California and requires the employee to be located within commuting distance of the office. How You'll Make An Impact: • Operate, maintain, and troubleshoot QC laboratory instruments., • Follow good laboratory practices., • Order supplies and maintain instrument preventative maintenance schedule., • Interface with other departments when required., • Evaluate assay runs for accuracy and acceptability to Quality Control procedures., • Associate's degree or higher in a science field or equivalent clinical lab experience., • 3+ years of QC or clinical laboratory experience., • Strong knowledge of Quality Systems and Good Documentation Practices (GDP). Experience in the use of clinical laboratory techniques and equipment. Experience in running chemistry, hematology, and immunoassay analyzers a plus., • Experience with Microsoft Office Suite (Outlook, Excel, Word) is required. Experience with a LIS is a plus., • Excellent verbal and written communication skills to effectively interact with team members, supervisors, and other departments., • Strong attention to detail and accuracy of data. Benefits: We're proud to offer a variety of options, including competitive medical plans for you and your family, free HSA funds, a new fertility offering with stipend, group life and disability, paid parental leave, 401k plus profit sharing, an employee stock purchase program, a new upgraded and streamlined mental health platform, extensive learning and development opportunities, education benefits, student debt relief program, pet insurance, wellness challenges and support, paid time off, Employee Resource Groups (ERG's), and more! Compensation: The estimated hourly rate for this position is $27.00 to $37.74 at the time of posting. Actual compensation will be provided in writing at the time of offer, if applicable, and is based on several factors we believe fairly and accurately impact compensation, including geographic location, experience, knowledge, skills, abilities, and other job permitted factors. This position is eligible for a variable annual bonus, which is dependent upon achievement of your individual objectives and Company performance. Who We Are: For 70 years, Bio-Rad has focused on advancing the discovery process and transforming the fields of science and healthcare. As one of the top five life science companies, we are a global leader in developing, manufacturing, and marketing a broad range of high-quality research and clinical diagnostic products. We help people everywhere live longer, healthier lives. Bio-Rad offers a unique employee experience with collaborative teams that span the globe. Here, you are supported by leadership to build your career and are empowered to drive change that makes an impact you can see. EEO Statement: Bio-Rad is an Equal Employment Opportunity/Affirmative Action employer, and we welcome candidates of all backgrounds. Veterans, people with physical or mental disabilities, and people of all race, color, sex, sexual orientation, gender identity, religion, national origin and citizenship status are encouraged to apply. Agency Non-Solicitation:Bio-Rad does not accept agency resumes, unless the agency has been authorized by a Bio-Rad Recruiting Representative. Please do not submit resumes unless authorized to do so. Bio-Rad will not pay for any fees related to unsolicited resumes. Fraud Alert: Bio-Rad has received reports of individuals posing as Bio-Rad recruiters to obtain information, including personal and financial, from applicants. Beware of these fake "recruiters" and job scams. ___ for more information on this scam and how to avoid it. #LI-KD2 Legal Entity: (USA_1000)Bio-Rad Laboratories, Inc.

Now hiring Lab Technician Location Santa Ana, CA Pay Rate: $23.00 per hour 1st Shift Join Staffmark and discover a Lab Technician position where your work matters and your contributions are truly appreciated. Looking for a Lab Technician job where you're more than just a number on a clipboard? Here's the deal: we're hiring dependable team members who keep everything running - and we know the work doesn't happen without you. The day begins. You step in with purpose. Here's what it takes to succeed with us. • High school diploma or GED, • 1+ years of manufacturing experience, • Technical aptitude, • Able to lift 50 lbs., • Operate and maintain mechanical testing equipment in accordance with established procedures., • Perform testing to defined specifications, ensuring accurate data collection and documentation., • Support material processes including lay-up, curing, cutting, and sample preparation (training provided)., • Safely operate cutting and high-temperature equipment., • Maintain compliance with all safety, quality, and lab standards., • Keep work areas clean and organized to meet daily housekeeping expectations., • Coordinate with supervision to manage testing schedules and communicate resource needs., • Solid Weekly Pay - Direct deposit or payment card, your choice., • Real Benefits - Medical, dental, and vision to keep you (and your family) covered. Join a Team That Works for You At Staffmark, we're more than just a staffing company-we're your career partner. As part of RGF Staffing and Recruit Group, anHR powerhouse behind big names like Indeed and Glassdoor, we've got the muscle and the know-how to get you where you want to go. With more than half a century of experience and a track record of putting hundreds of thousands of people to work every year, we've got your back. Whether you're looking to level up, switch gears, or just get to work fast, we make it happen. Join us and experience the advantage of working with a trusted name in recruiting-because your success is our success. The base pay range listed reflects what we reasonably expect to offer for this role. Actual pay may vary based on location, experience, and performance. Depending on the position, benefits may include medical, dental, and vision coverage; retirement and savings plans; paid holidays and time off; supplemental insurance; and additional wellness or incentive programs. At Staffmark, we connect hardworking people with great companies, creating opportunities that make a lasting impact. Staffmark is an equal opportunity employer. Allapplicants will receive consideration without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status, or any other legally protected status. Staffmark offers reasonable accommodations for qualified individuals with disabilities; contact your local branch for inquiries. Staffmark is an E-Verify employer. See our Privacy Notice for Candidates and Employees/Contractors at . By applying, you consent to receive AI-generated and non-AI-generated calls, texts, or emails from Staffmark Group, its affiliates, and partners. Frequency varies and message/data rates may apply. Reply STOP to cancel or HELP for help.

At Induce Biologics USA Inc., we are focused on developing and providing advanced technologies for bone regeneration. With a foundation based on science, clinical evidence, and clinical experience, our Natural Matrix Protein® (NMP®) products support healing across a wide range of spine, dental, and orthopedic procedures. By joining Induce Biologics USA Inc., you’ll be part of a mission-driven team working with revolutionary technology that’s reshaping the future of bone regeneration—and making a real difference in patients’ lives. The Sterile Processing and Materials Management Technician is responsible for the day-to-day operations of the sterile processing department, which includes processing, sterilization, and preparation of materials and components required for daily manufacturing activities. This role will also be responsible for management of manufacturing inventory and support manufacturing by coordinating the receipt, inspection, transfer of donor tissue, raw materials, supplies and finished products where needed. Essential Functions & Responsibilities Sterile Processing • Responsible for the daily activities of sterile processing, ensuring compliance with all relevant policies, procedures, and regulations., • Ensure the workflow processes of decontamination, cleaning, assembly, packaging, sterilization, storage, and distribution of tissue processing instrumentation and equipment., • Ensure proper sterilization procedures and monitoring processes, including daily biological and chemical indicator verification., • Maintain accurate and original records of sterilization procedures, equipment maintenance, and inventory levels., • Operation and maintenance of reprocessing equipment, including ultrasonic baths, washer decontaminators, and autoclaves, ensuring proper function and maintenance., • Promote and maintain a safe sterile environment, adhering to strict infection control protocols and procedures., • Responsible for manufacturing support and controlled environment maintenance during routine production. Material & Inventory Management • Receive, inspect, and verify incoming donor tissue, reagents, and processing supplies to ensure compliance with tissue banking standards., • Accurately log all incoming and outgoing materials using inventory management systems to maintain traceability., • Monitor stock levels of critical materials such as cleanroom supplies, sterile packaging, and lab consumables and communicate with the Supply Chain Manager as needed., • Conduct routine cycle counts and support physical audits to ensure inventory accuracy and regulatory compliance. Logistics & Material Transfer Coordination • Coordinate the timely transfer of raw materials, parts, and finished products between suppliers, warehouses, cleanrooms, laboratories, and production areas., • Prepare materials for shipment, including labeling, packaging, and ensuring compliance with cold chain logistics or other storage conditions as needed., • Arrange and track shipments with third-party logistics providers, ensuring timely and accurate delivery. Warehouse and Storage Management • Monitor and manage inventory levels of supplies, reagents and equipment, ensuring adequate stock and timely replenishment, • Organize and maintain warehouse and storage areas for efficient material retrieval and workflow., • Operate pallet jacks, and other material handling equipment as needed., • Ensure proper storage conditions (e.g., refrigerated or frozen storage) for temperature-sensitive materials., • In collaboration with Manufacturing and Supply Chain Management, troubleshoot and resolve inventory discrepancies, material shortages, and storage capacity issues. Cross-Functional Coordination • Collaborate with Manufacturing, Quality, and Supply Chain teams to meet material demands and production schedules., • Support product traceability efforts by ensuring accurate lot tracking and chain of custody documentation., • Participate in process improvements to enhance material flow, inventory accuracy, and efficiency. Education/Experience Required • High school diploma or GED, • 2+ years of experience in material handling, warehouse/manufacturing operations, or inventory management in a hospital, surgery center, or regulated GMP biotech environment., • Thorough knowledge of sterile processing principles, procedures, and regulations. Education/Experience Preferred • Associate’s or Bachelor’s degree in biotechnology, life sciences, supply chain, or logistics is a plus, • Certified in Sterile Processing, e.g., CST, CSPD, or RCST, • Prior experience in a biotech, pharmaceutical, tissue banking, or regenerative medicine company is highly preferred, • Ability to operate specialized material handling equipment (e.g., , biohazard containment units, cleanroom carts)., • Familiarity with handling biological materials, cryopreserved products, and controlled-temperature shipments (e.g., fresh/frozen tissues, stem cells, or other human-derived materials)., • Prior experience working under FDA 21 CFR Part 1271 regulations and AATB (American Association of Tissue Banks), • Basic understanding of regulatory requirements, such as GMP, GDP, and other industry standards. Skills, Knowledge, and Abilities • Strong attention to detail for material tracking, documentation, and compliance reporting., • Strong communication and teamwork skills to collaborate with manufacturing, purchasing, and customer service., • Knowledge of ISO 13485 and FDA regulations preferred., • Ability to work in a fast-paced, evolving environment, with flexibility to adapt to new processes., • Must be able to adhere to Health, Safety and GMP requirements., • Ability to work weekends, overtime and holidays, if required., • Proficient in using MS Office suite. For California, the base pay range for this position is $25.00 to $27.00 / hour. The pay for the successful candidate will depend on various factors (e.g., qualifications, skills, education, prior experience). Equal Employment Opportunity Statement Induce Biologics is an equal-opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. Third-Party Recruiters Please note that Induce Biologics does not accept unsolicited resumes or inquiries from third-party recruiters or staffing agencies. Any resumes submitted to our team without a prior agreement will be considered the property of Induce Biologics, and we will not be obligated to pay any fees related to unsolicited submissions.

HCLTech is looking for a highly talented, self-motivated and Lab Technician to join it in advancing the technological world through innovation and creativity. Job Title: Electrical Lab Technician Job ID: 22496 Position Type: Fulltime Location: Irvine, CA Core Responsibilities • Perform electrical testing using multimeters, oscilloscopes, and spectrum/network analyzers., • Conduct mechanical testing using calipers, force gauges (Mark‑10), and Instron systems., • Carry out THT/SMT soldering and PCBA prototype assembly., • Assemble mechanical and plastic parts for prototypes and engineering builds., • Support system‑level electro‑mechanical assembly, integration, and debugging. Required Skills & Experience • 3–5 years of hands‑on experience in electro‑mechanical or technician roles, • Proficiency with electrical test equipment: multimeter, oscilloscope, spectrum/network analyzer, • Experience with mechanical tools: caliper, Mark‑10 force gauge, Instron fatigue/force test systems, • Strong PCBA soldering skills (THT & SMT), • Experience in mechanical and plastic parts assembly, • Ability to read engineering drawings, schematics, and work instructions, • Strong troubleshooting and analytical skills, • Good communication and documentation skills Pay and Benefits Pay Range Minimum: $73000 per year Pay Range Maximum: $80000 per year HCLTech is an equal opportunity employer, committed to providing equal employment opportunities to all applicants and employees regardless of race, religion, sex, color, age, national origin, pregnancy, sexual orientation, physical disability or genetic information, military or veteran status, or any other protected classification, in accordance with federal, state, and/or local law. Should any applicant have concerns about discrimination in the hiring process, they should provide a detailed report of those concerns to for investigation. Compensation and Benefits A candidate’s pay within the range will depend on their work location, skills, experience, education, and other factors permitted by law. This role may also be eligible for performance-based bonuses subject to company policies. In addition, this role is eligible for the following benefits subject to company policies: medical, dental, vision, pharmacy, life, accidental death & dismemberment, and disability insurance; employee assistance program; 401(k) retirement plan; 10 days of paid time off per year (some positions are eligible for need-based leave with no designated number of leave days per year); and 10 paid holidays per year. How You’ll Grow At HCLTech, we offer continuous opportunities for you to find your spark and grow with us. We want you to be happy and satisfied with your role and to really learn what type of work sparks your brilliance the best. Throughout your time with us, we offer transparent communication with senior-level employees, learning and career development programs at every level, and opportunities to experiment in different roles or even pivot industries. We believe that you should be in control of your career with unlimited opportunities to find the role that fits you best.

The Composite Lab Technician performs composite materials processing & characterization of Axiom products. Follows directions provided by the materials/chemical engineers in the Technical/R&D department. Follows all company policies and procedures to ensure product integrity and quality control. This position requires proactiveness, precision and attention to detail. Essential Functions 1. Carry out composite processing tasks (Layup, Kitting, Bagging, Curing, Machining)., 2. Safely operate laboratory & composite processing equipment (Autoclave, Vacuum Oven, Furnace, Analytical, Mechanical & Machining Equipment)., 3. Conduct lab-scale resin mixing & coating trials and maintain detailed records., 4. Carry out physical, mechanical, and analytical testing to predefined specifications and standards, maintaining clear and concise records of the testing, and ensuring associated equipment meets the needs of specifications and the business alike., 5. Work directly with supervision to maintain a clearly defined schedule, ensuring resource requirements are communicated to all affected departments. Provide feedback on processes and documentation., 6. Create and maintain close working relationships with all other lab employees, support the needs of the business as communicated by supervision, and ensure the communicated 'Lab Rules' are followed at all times. Environment Lab, office environment with some exposure to factory floor. This is largely a standing position. This would require the ability to lift, push, and pull up to 50 pounds. Ability to wear a NIOSH approved respirator. Required Education and Experience 1. High school diploma, General Education Degree or Equivalent, with 2 years of related experience., 2. Industrial lab or production shop experience., 3. Some analytical testing experience (DSC, DMA, Rheology, FTIR, HPLC, Particle size analyzer, or others), 4. Proficiency using MS Office software (Excel required)., 5. Ability to write routine reports and correspondence. Preferred Education and Experience Bachelor’s degree in chemistry/chemical engineering/materials science or 1-3 years of composites processing/testing experience preferred. Resin mixing and research lab experience a plus (especially in composites, polymers and adhesives). AAP/EEO Statement Axiom is proud to be an Equal Employment Opportunity and Affirmative Action employer. We do not discriminate based upon race, religion, color, national origin, gender (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, gender expression, age, status as a protected veteran, status as an individual with a disability, or other applicable legally protected characteristics.

Description Senior Laboratory Assistant at Providence Mission Hospital in Mission Viejo, CA. This position is full-time and will work 8-hour, Night shifts. Providence Mission Hospital in Mission Viejo has received Magnet designation in 2012, 2017, 2021 and are in the process of earning our fourth designation in 2025! This is a prestigious designation from the American Nurses Credentialing Center (ANCC), which recognizes organizations that provide the highest-quality care. Only eight percent of hospitals nationwide have achieved Magnet designation. We are also recognized as one of the best regional hospitals in 18 types of care by U.S. News & World Report, including orthopedic and gastroenterological care. Our hospital is also honored with awards for cardiac surgery, gastrointestinal surgery, and excellence in women's services by Healthgrades and Newsweek. The Senior Laboratory Assistant is responsible for the collections and processing of blood specimens, providing assessment and care for neonate, pediatric, adult, and geriatric in-patients, emergency room patients, and patients from other hospital services as needed. He/she will assist as necessary with outpatient specimen collection and processing. The inoculation of microbiology specimens onto primary media and the processing of specimens for referral testing are also responsibilities of the position. He/she is proficient in required competencies. Age-Related Competencies: Not Applicable. Providence caregivers are not simply valued – they’re invaluable. Join our team at Mission Hospital Regional Medical Center and thrive in our culture of patient-focused, whole-person care built on understanding, commitment, and mutual respect. Your voice matters here, because we know that to inspire and retain the best people, we must empower them. Required Qualifications: - Upon hire: California Certified Phlebotomy Technician I License Or - Upon hire: California Certified Phlebotomy Technician II License Preferred Qualifications: - 1 year of Laboratory phlebotomy experience. Why Join Providence? Our best-in-class benefits are uniquely designed to support you and your family in staying well, growing professionally, and achieving financial security. We take care of you, so you can focus on delivering our Mission of caring for everyone, especially the most vulnerable in our communities. About Providence At Providence, our strength lies in Our Promise of “Know me, care for me, ease my way.” Working at our family of organizations means that regardless of your role, we’ll walk alongside you in your career, supporting you so you can support others. We provide best-in-class benefits and we foster an inclusive workplace where diversity is valued, and everyone is essential, heard and respected. Together, our 120,000 caregivers (all employees) serve in over 50 hospitals, over 1,000 clinics and a full range of health and social services across Alaska, California, Montana, New Mexico, Oregon, Texas and Washington. As a comprehensive health care organization, we are serving more people, advancing best practices and continuing our more than 100-year tradition of serving the poor and vulnerable. Posted are the minimum and the maximum wage rates on the wage range for this position. The successful candidate's placement on the wage range for this position will be determined based upon relevant job experience and other applicable factors. These amounts are the base pay range; additional compensation may be available for this role, such as shift differentials, standby/on-call, overtime, premiums, extra shift incentives, or bonus opportunities. Providence offers a comprehensive benefits package including a retirement 401(k) Savings Plan with employer matching, health care benefits (medical, dental, vision), life insurance, disability insurance, time off benefits (paid parental leave, vacations, holidays, health issues), voluntary benefits, well-being resources and much more. Learn more at providence.jobs/benefits. Applicants in the Unincorporated County of Los Angeles: Qualified applications with arrest or conviction records will be considered for employment in accordance with the Unincorporated Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act. About the Team The Sisters of Providence and Sisters of St. Joseph of Orange have deep roots in California, bringing health care and education to communities from the redwood forests to the beach shores of Orange county - and everywhere in between. In Southern California, Providence provides care throughout Los Angeles County, Orange County, High Desert and beyond. Our award-winning and comprehensive medical centers are known for outstanding programs in cancer, cardiology, neurosciences, orthopedics, women's services, emergency and trauma care, pediatrics and neonatal intensive care. Our not-for-profit network provides a full spectrum of care with leading-edge diagnostics and treatment, outpatient health centers, physician groups and clinics, numerous outreach programs, and hospice and home care, and even our own Providence High School. Providence is proud to be an Equal Opportunity Employer. We are committed to the principle that every workforce member has the right to work in surroundings that are free from all forms of unlawful discrimination and harassment on the basis of race, color, gender, disability, veteran, military status, religion, age, creed, national origin, sexual identity or expression, sexual orientation, marital status, genetic information, or any other basis prohibited by local, state, or federal law. We believe diversity makes us stronger, so we are dedicated to shaping an inclusive workforce, learning from each other, and creating equal opportunities for advancement. Requsition ID: 415932 Company: Providence Jobs Job Category: Clinical Laboratory Job Function: Clinical Care Job Schedule: Full time Job Shift: Night Career Track: Clinical Support Department: 7500 MH CLINICAL LAB Address: CA Mission Viejo 27700 Medical Ctr Rd Work Location: Mission Hospital Mission Viejo Workplace Type: On-site Pay Range: $24.82 - $37.98 The amounts listed are the base pay range; additional compensation may be available for this role, such as shift differentials, standby/on-call, overtime, premiums, extra shift incentives, or bonus opportunities. PandoLogic. Category:Healthcare, Keywords:Medical Laboratory Assistant (MLA), Location:Laguna Beach, CA-92651

Job DescriptionAbout UsField AI is transforming how robots interact with the real world. We are building risk-aware, reliable, and field-ready AI systems that address the most complex challenges in robotics, unlocking the full potential of embodied intelligence. We go beyond typical data-driven approaches or pure transformer-based architectures, and are charting a new course, with already-globally-deployed solutions delivering real-world results and rapidly improving models through real-field applications. Assembly Technician RoleAs an Assembly Technician for Perception & Compute Payloads, you will be a hands-on contributor responsible for assembling, integrating, and validating Field AI’s sensing and compute payloads. You will build electro-mechanical subsystems, integrate sensors and embedded compute platforms, perform harnessing and power system checks, support functional testing, and ensure every payload is field-ready and reliable. This role bridges mechanical assembly, electrical integration, and practical system-level debugging. You will support both prototype development and production workflows while working closely with engineers to improve build processes and increase system reliability.What You Will Get To Do • Payload Assembly & Integration, • Assemble perception payloads including LiDAR, cameras, IMUs, GPS receivers, and auxiliary sensors using engineering drawings and build instructions., • Install and integrate CPU/GPU compute modules, carrier boards, and microcontroller-based subsystems., • Build and route wire harnesses for power, high-speed data, synchronization, and control., • Install mounts, enclosures, gaskets, seals, thermal components, and structural hardware. 2. Electrical, Power, and Communication Bring-Up • Perform continuity checks, grounding/EMI checks, and power-rail validation., • Assist in bring-up of Linux- or ROS2-based embedded compute systems., • Validate communication links across Ethernet, USB, CAN, GMSL, and other interfaces., • Verify correct connectorization, pinouts, and harness strain-relief practices. 3. System Testing & Quality Assurance • Run functional tests including sensor bring-up, calibration checks, compute boot/health tests, and network verification., • Document test results, deviations, rework, and repair actions with high accuracy., • Support environmental, vibration, mechanical alignment, and thermal characterization tests led by hardware engineers., • Conduct inspections for workmanship quality, mechanical stability, and electrical safety. 4. Debugging & Continuous Improvement • Diagnose wiring faults, mechanical misalignments, intermittent communication issues, thermal faults, and other integration failures., • Work closely with electrical, mechanical, and compute engineers to root-cause issues and improve build processes., • Provide feedback on assembly workflows, documentation clarity, and opportunities to streamline production. 5. Field & Operations Support • Prepare, stage, and service payloads for real-world deployment., • Support integration and troubleshooting activities during lab tests, field trials, and live demonstrations., • Perform rapid repairs and reconfigurations in dynamic testing environments.What You Have, • 2+ years of hands-on technician experience in robotics, aerospace, electronics, automotive, or related electro-mechanical assembly environments., • Proficiency with hand tools, power tools, torque drivers, and basic machine-shop tools., • Ability to read and follow wiring diagrams, mechanical drawings, and assembly instructions., • Experience building wire harnesses and working with low-voltage electrical systems., • Familiarity with embedded compute systems, sensors, or robotics hardware., • Strong attention to detail, documentation discipline, and ability to deliver reliable assemblies., • Ability to lift up to 50 lbs. and work in workshop, lab, or field environments. What Will Set You Apart, • Experience working with perception systems such as LiDAR, cameras, radar, or IMUs., • Familiarity with Linux, ROS2, or embedded system bring-up workflows., • Soldering, crimping, or IPC-certified workmanship skills., • Understanding of thermal management, weather sealing, EMI/EMC basics, and ruggedized mechanical design., • Experience supporting prototype builds, rapid iteration cycles, or field test deployments., • Ability to design or suggest simple fixtures or jigs to improve assembly and repeatability.

Job DescriptionBenefits: • Health insurance, • Paid time off, • Dental insurance, • Training & development Qualifications: Associate degree in Electronics or computers is acceptable with some experience. Degree in Electronics is a plus, basic electronics knowledge is preferable. Excellent communication skills both verbal and written are required. Ability to take detailed and accurate notes. The individual must be punctual, organized and dependable and possess a willingness to learn and grow with the company. Salary: Salary will commensurate with education, knowledge, and experience. We do pay overtime not the commission.

Primary Duties and Responsibilities.The EEG Technician performs basic neurodiagnostic testing across Hoag locations assessing the functional integrity of the peripheral and/or central nervous system.The EEG Technician obtains patient identification and medical history, preps patient and conducts neu

One-year lab tech experience in a fast paced acute care setting in Chemistry, Reference lab and/or Microbiology sections.

Welcome to Verdantas, where innovation meets sustainability, and your career finds purpose!.At Verdantas, we're redefining environmental consulting and sustainable engineering through our use of cutting-edge modeling and digital technology and our genuine commitment to people.Our work spans high-gro

Decontaminates, cleans, and cares for operating room equipment utilizing clean/sterile technique used in a procedural setting. Successful completion of an accredited Surgical Scrub Technician program or equivalent military medical core training (not required for GI Lab). Solid computer technical ski

University of California, Irvine, and the only academic health system based in Orange County.UCI Health is comprised of its main campus, UCI Medical Center, a 459-bed, acute care hospital in in Orange, Calif.UCI Health Community Network in Orange and Los Angeles counties and ambulatory care centers

Job Description Autonomous Medical Devices Incorporated (AMDI), based in California, is a fast-growing company on a mission to transform point-of-care diagnostics. Our team of world-class engineers, scientists, clinicians, and manufacturing experts is pioneering breakthrough technologies in microfluidics, protein engineering, and cloud-connected data systems. We’re gearing up to launch our inaugural products from our ISO 13485-certified, 110,000-square-foot facility in Santa Ana, CA — and we're looking for passionate individuals to join us in shaping the future of healthcare. Location: This is an onsite position located at our Santa Ana, CA office. Candidates living within a 25 mile range preferred. Summary of Position The Clinical Operations Technician plays a key role in supporting clinical studies and the biocollection program. This hands-on role manages clinical samples and study supplies, maintains accurate records, and performs basic molecular biology testing (PCR/RT-PCR) in a BSL-2 lab environment. The ideal candidate is detail-oriented, collaborates with internal teams and external partners, and ensures strict compliance with regulatory standards, Good Clinical Practice, and patient data confidentiality. Essential Duties and Responsibilities • Supports the external clinical studies, including, • working closely with R&D and Operations personnel and external clinical research organizations (CROs) on clinical studies., • managing investigational devices inventory and clinical study supplies., • organizing all applicable records for clinical studies and clinical samples., • receiving clinical samples from clinical sites and transferring to the appropriate R&D collaborators and/or storage., • proper storage of clinical samples following Clinical SOPs., • Ensuring all activities are conducted in accordance with all applicable regulatory requirements, Good Clinical Practice (GCP) guidance and AMDI’s policies and procedures., • Supports the internal biocollection program, including, • collecting and maintaining samples under the biocollection program (e.g., nasal swab samples, urine, saliva, etc.), including addressing R&D requests and managing the check-in/ check-out of stored specimens., • prepares reagents for and executes PCR testing on clinical samples., • provide written and/or oral updates to the team regarding data, progress, technical issues, etc., • receiving clinical samples from the biocollection program and transferring to the appropriate R&D collaborators and/or storage., • proper storage of clinical samples following Clinical SOPs., • collecting and maintaining all the records for the biocollection program., • coordinate and ensure inventory of critical lab reagents and supplies used for Clinical sample testing., • Safeguards the clinical samples, clinical data and records, ensuring that the confidentiality, integrity and security of the clinical samples and clinical records are maintained, and PHI information is protected., • Maintains all regulatory, legal, and financial disclosure documents per guidelines and regulations of the sponsor and IRB., • Supports regulatory inspection activities., • Works on other projects within QA & RA not related to clinical studies as assigned by management., • Minimum of an Associate degree in chemistry, biology or related field., • Minimum of 6 months of hands-on experience with nucleic acid preparation, amplification and detection technologies using proper unidirectional molecular laboratory workflow., • Experience with Good Laboratory Practices (GLP) and Good Documentation Practice (GDP) preferred., • Cooperative and motivated team player with a positive attitude and solid work ethic., • Sets specific goals and objectives to complete tasks on time in an organized manner., • Effectively communicates in both written and oral presentations on data generated., • Excellent attention to detail, record keeping and a passion for accuracy and precision., • Ability to work in a fast-paced environment with deadline-driven workflows., • Proficient in Microsoft Office Suite, specifically Word, Excel, PowerPoint, and Outlook., • Demonstrates a strong ability to work collaboratively and shows a consistent willingness to support team members when needed., • Ability to uphold strict protocols to preserve the confidentiality, integrity, and security of clinical samples and clinical records at all times. Work Environment • Work requires some time in front of the computer., • In-person position that requires working indoors in a BSL2 facility and testing laboratory environment., • Requires the use of personal protective equipment to prevent exposure to biohazardous waste and chemicals., • Some exposure to warehouse environment. Autonomous Medical Device Incorporated offers a comprehensive compensation and benefits package to eligible employees. The following is available for temporary employees: • Free lunch to all employees when working at one of AMDI’s on-site locations., • Casual dress code., • Employee discounts on activities such as theme parks, movie theaters, hotels, rental cars, etc. Autonomous Medical Devices Incorporated (AMDI) will not accept unsolicited resumes from any source other than directly from a candidate. An Agency must obtain advance written approval from AMDI’s internal Human Resources team to submit resumes only in conjunction with approved valid fully executed contracts. We are not currently entertaining Staffing agency assistance for this position. Our commitment to an inclusive workplace: We are an equal opportunity employer and encourage people from all backgrounds to apply. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, gender identity, sexual orientation, national origin, disability, protected veteran status, or any other protected characteristic under federal, state, or local law. Powered by JazzHR 0LS80GVqul

Job Description NO EXTERNAL RECRUITERS PLEASE No Sponsorship/Transfer Available Company Summary: For over 60 years, MeriCal has been at the forefront of innovation in the dietary supplement industry, delivering custom manufacturing and packaging solutions with passion and precision. With state-of-the-art facilities in Southern California and Ogden, UT, we transform ideas into high-quality products—from research and development to the finished products. Our team, with over 30 years of combined experience, is dedicated to crafting exceptional gummies, probiotics, tablets, capsules, chewables, and powders using clinically backed ingredients. At MeriCal, we don’t just meet expectations—we exceed them, every time. Join us and be part of a dynamic, forward-thinking team shaping the future of nutrition! The Opportunity: The Manager, R&D will lead dry dose formulation and lab technician teams to deliver high-quality products on time, which will lead to successful large-scale manufacturing. Leveraging and collaborating with external partners, the successful candidate will be responsible for identifying new technologies to improve existing formulations and incorporate into novel innovation. This role will oversee RFQs, internal formulations, bench top and pilot deliverables for new product development. What You’ll Do: • Lead R&D Projects: Manage new and existing projects, assign formulation requests, and oversee product development from benchtop to commercialization., • Team Management: Supervise employees to meet deadlines, provide support, and foster a culture of innovation, learning, and constructive feedback., • Cross-Functional Collaboration: Maintain internal communication and alignment with departments such as quality, procurement, sales, operations, and project management., • Formulation & Documentation: Create formulations, calculate potencies, document raw materials, product specification and manufacturing direction, and manage costing., • Production Oversight: Ensure smooth transitions from lab to pilot to full-scale production, working closely with operations and quality teams on the floor., • Format Expertise: Develop supplement format with primary focus on tablets, capsules, and powders., • Customer Engagement: Participate in customer visits and trials, and work directly with clients to develop customized formulations., • Technical Leadership: Provide guidance and troubleshooting support post-launch, and evaluate technical feasibility of new products., • Innovation & Strategy: Drive innovation programs, evaluate new ingredients and technologies, and align product opportunities with business priorities., • Professional Standards: Demonstrate professionalism, attention to detail, and strong organizational, mathematical, and communication skills., • Additional Duties: Accept other responsibilities as assigned by leadership. What You’ll Bring:. • Additional Duties: Accept other responsibilities as assigned by leadership., • 5-10 years' experience in the development of nutritional products., • Quality: Demonstrates accuracy and thoroughness; Looks for ways to improve and promote quality; Applies feedback to improve performance; Monitors own work to ensure quality., • Ability to read, write and speak English fluently. (Bilingual Spanish a plus)., • Knowledge of cGMP regulations a must., • Knowledge of dietary supplement ingredients and their efficacy of use., • Ability to effectively interact with all levels of personnel with the utmost professionalism., • Ability to handle multiple, rapidly changing and conflicting priorities., • Knowledge of manufacturing processes and technology used to accomplish product performance results., • Ability to work minimal supervision while remaining productive at all times., • Physical requirements include standing for long periods of time and lifting up to 25 lbs. Education Requirements: • Bachelor's degree in Food Science, Nutrition, Chemistry, or a related field with 5 to 10 years of experience. The Perks: • No-cost vision insurance (yes, you read that right!), employer-paid life insurance, paid company holidays, generous paid time off, sick leave, employee assistance program, and a comprehensive wellness program., • Affordable medical and dental insurance plans are tailored for you and your dependents., • Exceptional supplemental benefits, including Accident, Critical Illness, Hospitalization indemnity plans, and pet insurance., • 401(k) matching plan and more! A reasonable estimate of the current base pay range for this position is $125,000. - $160,000. The compensation offered may vary depending on the candidate’s geographic region, job-related knowledge, skills, and/or education. MeriCal is an equal opportunity employer and is committed to providing a workplace that is inclusive and free of discrimination and harassment. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability status, protected veteran status, or any other characteristic protected by law. We encourage individuals of all backgrounds to apply. We believe in creating a diverse and inclusive workplace where all employees feel valued and respected, and where differences are embraced as strengths. We are dedicated to fostering an environment that promotes equality and celebrates diversity. Qualified applicants with disabilities may be entitled to reasonable accommodation under the terms of the Americans with Disabilities Act and/or certain state or local laws. Please contact if you need an accommodation due to a disability to complete an application, job interview, and/or to otherwise participate in the hiring process. This email does not respond to non-accommodations related requests. MeriCal uses E-Verify to confirm authorization to work in the United States. For more information on E-Verify, please visit the following website: For more information about the categories of personal information we collect from you and how we use, sell, and share that information, please see our Privacy Notice for California Contractors and Privacy Notice for California Employees.

Job Description POSITION SUMMARY The Quality Engineer is responsible for developing, implementing, and maintaining quality standards, methods, instructions, and quality planning on assigned programs. The role includes performing supplier surveys, internal audits, and process audits. The Quality Engineer will support engineering, manufacturing, program management, and quality groups, and will be actively involved in continuous improvement initiatives and customer/supplier interactions. POSITION DUTIES/RESPONSIBILITIES · Review customer Purchase Order and Contract requirements to communicate quality requirements to responsible departments. · Perform internal and process audits, as assigned. · Provide technical direction and support to inspection. · Review and approve drawings and product build (work orders) documentation. · Review product discrepancies in manufacturing, perform investigations and coordinate with manufacturing and engineering to resolve problems. · Document, track and communicate Quality Plans, test results, analysis & unresolved problems. · Perform AS9102 First Article Inspection Reports · Represent Quality Assurance in day-to-day communication with customers and suppliers, including certifications, data, and corrective actions. · Perform supplier surveys, as assigned. · Review supplier purchase requisitions and apply appropriate quality requirements. · Support assigned Quality Assurance tasks, as required. · Support the company’s training program by creating, reviewing, and updating training materials. · Participate in and lead continuous improvement and Lean Manufacturing initiatives. SKILLS & ABILITIES · Excellent verbal and written communication skills. · Excellent interpersonal and customer service skills. · Excellent organizational skills and attention to detail. · micrometers, height gauges, etc. · Working knowledge of Mil-Spec and government contract requirements. · Working knowledge of ISO 9001 and AS9100 Quality Management Systems requirements. · Analytical and problem-solving ability · Excellent time management skills with a proven ability to meet deadlines. · Ability to function well in a high-paced and at times stressful environment. · Proficient with Microsoft Office Suite or related software. Education and Experience Education: Bachelor's Degree (four-year college or technical school) Preferred. Or equivalent experience. Field of Study: or related field and/or equivalent experience. Experience: Minimum of 3 years of experience as a Quality Engineer, in a manufacturing environment. PHYSICAL DEMANDS N (Not Applicable) Activity is not applicable to this position. O (Occasionally) Position requires activity up to 33% of the time (0 - 2.5+ hrs/day) F (Frequently) Position requires activity from 33% - 66% of the time (2.5 - 5.5+ hrs/day) C (Constantly) Position requires activity more than 66% of the time (5.5+ hrs/day) Physical Demands Lift/Carry • 10 lbs or less O, • 11-20 lbs O, • 21-50 lbs N, • 51-100 lbs N, • Over 100 lbs N Push/Pull • 12 lbs or less O, • 13-25 lbs O, • 26-40 lbs N, • 41-100 lbs N Other Physical Requirements · Must be able to remain in a stationary position such as working at a desk on a computer for prolonged periods of time. · This position requires you to occasionally move about the office to access filing cabinets, office machinery, etc. · Constantly operates a computer and other office productivity machinery, such as a calculator, copy machine, and computer printer. · The ability to communicate information and ideas so others will understand. Must be able to exchange accurate information in these situations. · The ability to observe details at close range (within a few feet of the observer). · This position requires the ability to navigate and access all areas of our campus. · Ability to wear Personal Protective Equipment (PPE) - Required Safety Glasses WORK ENVIRONMENT This position requires an on-site presence. Working conditions are 50% a normal office/lab environment and 50% a manufacturing environment and may be noisy at times. Work may require occasional weekend and/or evening work. The company has reviewed this job description to ensure that essential functions and basic duties have been included. It is intended to provide guidelines for job expectations and the employee's ability to perform the position described. It is not intended to be construed as an exhaustive list of all functions, responsibilities, skills, and abilities. Additional functions and requirements may be assigned by supervisors as deemed appropriate. This document does not represent a contract of employment, and the company reserves the right to change this job description and/or assign tasks for the employee to perform, as the company may deem appropriate. Company DescriptionApex Space and Defense prides itself on delivering the highest quality, large- and small-scale composite structures for our aerospace, defense, and commercial customers. APEX, Santa Ana, has over 50 years of experience from our roots in auto racing through years of supporting aerospace and defense. The key to our success is largely dependent on our dedicated family of hard-working team members with a can-do attitude. We’re currently searching for a Service Technician to join our ranks and continue our tradition of success.Apex Space and Defense prides itself on delivering the highest quality, large- and small-scale composite structures for our aerospace, defense, and commercial customers. APEX, Santa Ana, has over 50 years of experience from our roots in auto racing through years of supporting aerospace and defense. The key to our success is largely dependent on our dedicated family of hard-working team members with a can-do attitude. We’re currently searching for a Service Technician to join our ranks and continue our tradition of success.

Job Description Stanbridge University is seeking an energetic and detail-oriented Assistant Director, Vocational Nursing (Evenings/Weekends) to help lead and grow our VN program. Working alongside the Program Director, this role drives curriculum delivery, supports faculty, ensures compliance, and champions student success. With a focus on our evening and weekend cohorts, you’ll provide the leadership and support needed to create an outstanding learning experience that matches the quality of our daytime program. Key Responsibilities: • Oversee daily operations of the VN program, with emphasis on evening and weekend cohorts., • Recruit, train, and evaluate faculty., • Manage curriculum delivery, faculty schedules, instructional resources, and course planning., • Maintain adherence to the approved curriculum and ensure consistent instructional quality., • Utilize ATI resources and promote active learning strategies to drive student engagement., • Support student success by monitoring performance and implementing support strategies., • Provide timely feedback on students, faculty, and facilities during weekend clinicals., • Ensure grading, evaluations, and required reports are completed and submitted on time., • Ensure compliance with BVNPT regulations and accreditation standards., • Coordinate clinical site assignments and maintain partner relationships., • Collect and report program data for compliance and continuous improvement., • Establish strong two-way communication between the university and clinical facilities to ensure student requirements (e.g., health records, qualifications, paperwork) are met and to maintain healthy partnerships that drive student success.Qualifications:, • Licensure: Current, active, and unencumbered Registered Nurse (RN) license in California., • Education: Bachelor’s degree from a BVNPT-approved school required; Master’s degree in nursing, education, or administration preferred., • Experience:, • Minimum of three (3) years as a Registered Nurse., • At least one (1) year of teaching or clinical supervision in a state-approved nursing program (VN, RN, or psychiatric technician) within the last five years; or, • Three (3) years in nursing administration or education within the last five years., • Professional Preparation: Coursework in administration, teaching, and curriculum development from an approved school., • Skills: Strong organizational skills, effective communication, and a collaborative leadership style; ability to support program outcomes and student achievement., • $110-$125,000/yr. Compensation is commensurate with education, experience, and internal equity considerations. Conditions of Employment:, • A job-related assessment may be required during the interview process., • Must be able to perform each essential duty satisfactorily and be physically present in the office (unless otherwise noted)., • Employment verification will be conducted to validate work experience per accreditation standards., • Offers of employment are contingent upon the successful completion of a background check., • Official transcripts are required prior to hire. Degrees earned outside the United States must be evaluated by a recognized credential evaluation service to determine U.S. degree equivalency and applicable subject-area coursework., • Must be legally authorized to work in the United States at the time of hire and maintain such authorization throughout employment without the need for employer-sponsored work authorization now or in the future., • Reasonable accommodations may be made to enable individuals with disabilities to perform essential functions.Work Environment:, • Standard office/classroom/lab or clinical setting., • Duties are typically performed while sitting at a desk or computer workstation., • May include time spent in skills labs or bedside environments as required by the program., • Subject to frequent interruptions, noise from talking or office equipment, and demanding timelines. Physical Demands:, • Regularly sits for extended periods., • Physical ability to perform program- or department-related duties., • Proficient in using electronic keyboards and office equipment., • Effective verbal communication via phone and in person., • Ability to read fine print, operate computers, and understand voices clearly., • Able to lift, carry, and/or move objects weighing 10–25 pounds as needed. Employee Benefits:, • Health Care Plan (Medical, Dental & Vision), • Retirement Plan (401k), • Exciting university events, • Seasonal motivational health and wellness challenges, • Work/Life Balance initiatives, • Onsite wellness program / Staff Chiropractor, • Life Insurance (Basic, Voluntary & AD&D), • Paid Time Off (Vacation, Sick & Public Holidays), • Family Leave (Maternity, Paternity) Institutional Values:, • Diversity and Inclusion: Stanbridge University’s motto, “Strength through Diversity,” reflects our deep commitment to honoring the diverse backgrounds of our students, faculty, staff, and surrounding communities. We strive to build an inclusive learning environment and uphold anti-discrimination practices in all aspects of university life., • Innovation and Technology: We embrace cutting-edge technology to enhance student learning through interactive, hands-on experiences, including virtual reality and simulation labs—ensuring students are prepared for the demands of modern healthcare practice.

Job Description The Meiji Group was founded in Japan in 1916. For nearly a century, it has provided a broad range of products built upon the accumulated knowledge and skills of its talented workforce. Meiji America Inc., founded in 2011, as the United States division distributes a variety of unique confectionery and snack products including HELLO PANDA™, YAN YAN™ and CHOCOROOMS®. Hello Panda and Yan Yan are fun portable treats that are perfect for on-the-go snacking. Hello Panda has a crème center and a crunchy shell with drawings of cute Pandas enjoying various sports. Quality Assurance Technician - Seasonal Position (6 months) POSITION SUMMARY: Supports food safety and quality throughout receiving, storage, processing, baking, packaging, sanitation, and release for shipping. Properly documents and completes GMP & Absolute Safety Violation reporting, internal audits, sanitation inspections & verification, critical & preventive control verifications, product evaluations, holds of non-conforming materials, and investigations of supplier & customer complaints. Participates in hold investigation and resolution, meetings as required, product reviews, production data analysis, root cause analysis, and identification of corrective and preventive actions. Maintains laboratory instrumentation, lab procedures, recordkeeping, calibration, 6S, and high level of Good Laboratory Practice compliance. PRINCIPLE ACCOUNTABILITIES: • 35% - Interacts with Operations, Maintenance, Sanitation and Engineering to investigate and resolve production issues. Participates in daily meetings as required, coordinate’s product evaluation, and facilitates the evaluation and timely closure of non-conforming issues and finished product holds. Provides data analysis, product summaries, and inspection results to management for appropriate product review and disposition., • 35% - Provides Quality support to the operation through inspection and verification activities. Verification activities include monitoring critical processing information regularly to tie to finished product attributes and characteristics to ensure compliance to Manufacturing Specifications. Inspection activities include observation, measurement, and inspection at key points in the production process (i.e. taste, visual inspection, analytical measurements, and physical characteristics)., • 15% - Facilitates the collection, organization, storage, and retention of the Quality System documentation including Operations paperwork packets, COAs, lab analytical reports, etc. Collects, analyzes, and prepares monthly scorecard data as required as well as Operations and Quality metric tracking., • 10% - Participates as an active member on continuous improvement projects; 6S teams, Kaizen events, PDCA, Safety audits, Sanitation audits, GMP walks, internal food safety team, etc., • Performs quality support through observation, verification, and inspection at critical processing steps. Tasks may be operator procedure verifications, inspections of equipment and cleaning performance, as well as raw material, in-process product, or finished product evaluations., • Analyzes key product and process variables/attributes to understand process capability, identify process drift, and effects on finished product quality., • Collaborate with Operations, Quality, Maintenance, Engineering, and Sanitation to troubleshoot a product defect or processing issue. Participate in the discussion of potential root causes and assist with the implementation of effective corrective and preventative actions., • GED, Diploma, Food Safety/ Quality certification, or minimum 1 year of food industry experience., • Strong technical acumen - ability to troubleshoot a problem, involve other stakeholders as necessary, and brainstorm potential root causes, • Strong verbal and written communication skills, • Strong interpersonal skills, • Computer skills necessary, proficient with Microsoft Office Computer Skills While performing the duties of this job, the employee is regularly required to sit; use hands to grasp, handle or feel; reach with hands and arms; talk and hear. The employee frequently is required to walk, stand, stoop, kneel, climb stairs, and crouch. Specific vision abilities required by this job include close proximity and color vision. The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. The noise level in the work environment is usually moderate. • Pay Rate: $21.79/ hour, • Monday thru Friday plus weekends as needed, • Position Type: Hourly, • This is a temporary position for 6 months, • Seasonal employees, do not qualify for any benefits · Facilitates the collection, organization, storage, and retention of the Quality System documentation including Operations paperwork packets, COAs, reports, etc. Collects, analyzes, and prepares monthly scorecard data as required as well as Operations and Quality metric tracking. · Participates as an active member on continuous improvement projects; 5S teams, Kaizen events, PDCA, Safety audits, Sanitation audits, GMP walks, internal food safety team, design, and development of Quality Information System, etc. · All other duties as assigned. ACCOUNTABILITY: A Quality Assurance Technician will be accountable to the Quality Assurance Supervisor for fulfillment of his or her duties. The performance of a Quality Assurance Technician will be measured to the degree of his or her production levels and quality of work performed in these assigned areas. EXPERIENCE: · Strong technical acumen - ability to troubleshoot a problem, involve other stakeholders as necessary, and brainstorm potential root causes · Strong verbal and written communication skills · Strong interpersonal skills · Computer skills necessary, proficient with Microsoft Office · Statistical background a plus · Computer skills including proficiency with Microsoft Office software, and able to master other software. · Practitioner of SQF Quality Systems, HACCP Methodology, cGMP’s and statistical tools EDUCATION: 4-year BS degree science or related discipline is desired or minimum 5 years of progressive food industry experience PHYSICAL DEMANDS AND WORK ENVIRONMENT: While performing the essential duties of this job, the employee is regularly required to sit; use hands to grasp, handle or feel; reach with hands and arms; talk and hear. The employee frequently is required to walk, stand, stoop, kneel, crouch, climb and lift up to 50lbs and shared weight up to 100lbs. Specific vision abilities required by this job include close vision and color vision. Occasional exposure to airborne dust, high humidity and extremes of hot and cold are possible. The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. The noise level in the work environment is usually moderate. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Equal Opportunity Employer: Meiji America/ D.F. Stauffer’s is an Equal Opportunity Employer M/F/Disabled/Vets Notice to Staffing Agencies, Placement Services, and Professional Recruiters Meiji America Inc. / D.F. Stauffer Biscuit Co., Inc. has an internal Staffing Department. Recruiters are hereby specifically directed NOT to contact Meiji America employees directly in an attempt to present candidates. Meiji America will not accept unsolicited resumes from any source other than directly from a candidate. Any unsolicited resumes sent to Meiji America, including unsolicited resumes sent to a Meiji America mailing address, fax machine or email address, directly to Meiji America employees, or to Meiji America’s resume database will be considered Meiji America’s property. Meiji America will NOT pay a fee for any placement resulting from the receipt of an unsolicited resume. Meiji America will consider any candidate for whom a Recruiter has submitted an unsolicited resume to have been referred by the Recruiter free of any charges or fees. Job Type: Seasonal Full-time (Seasonal 6 months) Powered by JazzHR gBKowNg05w

Job DescriptionMechanical Engineering Technician Position Purpose To ensure reliable, high-quality production performance by building, maintaining, and troubleshooting mechanical systems while performing quality inspections, supporting field investigations, and validating product performance in real-world environments. Onsite position with occasional field work- Local Candidates only being considered for this role. No sponsorship offered Key Responsibilities Mechanical / Manufacturing Support • Assemble, install, and maintain mechanical systems, jigs, fixtures, and automated equipment., • Perform preventive and corrective maintenance on production machinery, tooling, and fixtures., • Support engineering with equipment setup, calibration, and functional testing for new product introduction (NPI)., • Troubleshoot mechanical issues, including pneumatics, hydraulics, and mechanical drive systems., • Conduct in-process, incoming, and final inspections using calipers, micrometers, CMM, gauges, and/or other metrology tools., • Validate mechanical and cosmetic characteristics against engineering drawings and GD&T requirements., • Support root cause analysis (RCA) and participate in corrective and preventive actions (CAPA)., • Maintain documentation such as defect logs, inspection reports, NCRs, and control charts., • Travel to customer sites, contract manufacturers, suppliers, or field environments to investigate quality or performance issues., • Perform onsite inspections, failure analysis, and operational assessments under real-world conditions., • Collaborate with customer service, engineering, and quality teams to address field defects or recurring issues., • Capture field data, photos, measurements, and feedback for engineering review and continuous improvement., • Identify opportunities to improve mechanical reliability, process capability, and product quality., • Suggest design-for-manufacturability improvements based on production and field learnings., • Participate in Lean, Kaizen, 5S, and continuous improvement activities., • Technical degree or certification in Mechanical Engineering Technology, Mechatronics, Industrial Maintenance, or equivalent experience., • 3–7 years in a manufacturing, mechanical, or quality technician role; consumer tech or electronics environment preferred., • Strong mechanical troubleshooting skills with experience in pneumatics, hydraulics, tooling, and fixtures., • Proficient with precision measurement tools (calipers, micrometers, gauges, torque tools, CMM)., • Understanding of GD&T, engineering drawings, and mechanical tolerances., • Familiarity with quality systems such as ISO 9001, IATF 16949, or similar., • Ability to travel occasionally for field investigations (5–20%)., • Mechanical aptitude with a strong quality mindset, • Analytical and detail-oriented, • Effective communicator in both production and field environments, • Root cause problem-solving, • Strong teamwork across Quality, Engineering, and Operations, • Safety-focused and disciplined in documentation, • Adaptable — able to shift between factory, lab, and field needs All qualified applicants will receive equal consideration for employment without regard to race, color, national origin, religion, sex, pregnancy, marital status, sexual orientation, gender identity, age, physical or mental disability, or covered veteran status.

Job Description TRL11 is a venture backed startup looking to bring cutting edge video technology to the space economy. We are based in Irvine, CA. This candidate will be working on-site. Position Overview: We are seeking to hire an experienced Electronics Technician to join our team. As a member of our engineering team, you will be responsible for assisting other engineers build prototypes and final products. This person will be involved in the assembly, testing, and maintenance of electronic systems and components essential for space exploration missions. This position offers the opportunity to work at the forefront of space technology. If you are passionate about cutting-edge technology, this is an excellent opportunity for you to participate in the new space economy. Requirements Essential: • Experience with assembling, testing, and maintaining electronic systems and components., • Experience with debugging electrical issues and reworking PCBs, • Comfortable with soldering irons, wire cutters, bench supplies, and other lab tools., • Familiar with multimeters, oscilloscopes, function generators, and other testing equipment, • Collaborate with engineers and other team members to ensure reliability and functionality of electronic systems and all products, • Experience operating environmental testing chambers, such as thermal chambers and TVAC chambers, • Applicable certifications such as IPC-A-610, IPC-A-620, IPC-7711, J-STD-001, • Experience working with cameras or optical systems

Job Description Join a team where your impact reaches beyond the stars! At Terran Orbital, you're not just part of the system – you're a vital force propelling our mission forward. As trailblazers in satellite manufacturing and aerospace innovation, we shatter boundaries daily to deliver groundbreaking solutions that power our nation's defense and commercial missions. We are a unique, fast growing, and trusted team dedicated to swiftly and efficiently designing, building, launching, and operating state of the art satellites for advanced mission constellations. If you're driven by purpose, inspired by challenges, and ready to leave your mark on the universe, you'll find a home and endless opportunities for growth here. Together, let's redefine what is possible in orbit and beyond! Terran Orbital is seeking an experienced AIT Technician – Vehicle Integration to join our dynamic team. Reporting to the Production Supervisor the AIT Technician – Vehicle Integration will responsible for the hands-on manufacturing and assembly of sub-assemblies essential for spacecraft vehicle integration. The ideal candidate should possess a keen understanding of quality control and AS-9100 standards. This role is on our Weekend shift (Friday - Sunday) from 6:00AM - 7:00PM Key Duties and Responsibilities • Follow detailed procedures to assemble complex electronic and mechanical modules., • Operate hand tools such as screwdrivers, torque wrenches, and light power tools., • Ability to quickly change priority while working in a fast-paced environment., • Communicate statuses, issues, and suggestions effectively to the support engineering team., • Updating documentation and hardware statuses through online services., • Basic avionics and the electrical troubleshooting., • Assist in spacecraft integration related activities., • Must possess a strong work ethic, be able to work with limited supervision, and meet the requirements of the attendance policy., • Must perform all functions of the job in a safe and professional manner., • Must keep work area(s) in a neat, clean, safe, and orderly condition., • Ability to stand for most of the working day., • Perform miscellaneous lab duties, including kitting, inventory, and organization tasks., • High school diploma or GED, • 2+ years of professional experience working hands-on as a technician within electromechanical assembly or spacecraft/spacecraft hardware manufacturing, • Experience with wire harness routing and/or space flight integration., • Ability to read, understand and follow detailed work instructions for assembly and testing flight product including blueprints and schematic drawings, • Proficiency with Windows 10, Microsoft Office products, and internet browser applications, • Good written and verbal communication skills, • Knowledge of soldering tools and practices (J-STD-001 certification preferred but not required), • Ability to maintain a clean and organized workspace, • Familiarity with cleanroom cleanliness standards and ESD precautions, • Must have excellent visual acuity to perform detailed inspections and quality control tasks, • Ability to accurately distinguish a wide range of colors, which is essential for success in this role Benefits • 100% Company-paid comprehensive medical, dental, and vision coverage for you and your dependents, • 401(k) Match, • Flexible Time Off (FTO), • Education Reimbursement Terran Orbital is a leading manufacturer of satellite products primarily serving the aerospace and defense industries. Terran Orbital provides end-to-end satellite solutions by combining satellite design, production, launch planning, mission operations, and on-orbit support to meet the needs of the most demanding military, civil, and commercial customers. Learn more at Physical Demands An employee must meet the physical demands described to perform the essential functions of this job successfully. In performing the duties of this job, the employee is routinely required to sit or stand for long durations of time, in addition to bending, reaching, and walking. This would require the ability to lift or move objects up to 10 pounds and occasionally lift or move objects up to 25 pounds. This position is generally sedentary, with substantial computer usage. Work Environment The job operates in a professional office environment but in a manufacturing company. This job routinely uses standard office equipment such as computers, phones, photocopiers, and scanners. Disclaimers To comply with U.S. Government space technology export regulations, the applicant 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. In addition, please note that this position may require a current United States National Security clearance or eligibility for such a clearance. Terran Orbital is an Equal Opportunity/Affirmative Action Employer. We consider applicants without regard to race, color, religion, age, national origin, ancestry, ethnicity, gender, gender identity, gender expression, sexual orientation, marital status, veteran status, disability, genetic information, or membership in any other group protected by federal, state, or local law. If you need assistance or accommodation due to a disability, you may contact us at . Terran Orbital does not accept unsolicited resumes from recruiters, employment agencies, or staffing firms. To conduct business with Terran Orbital, a Master Services Agreement (MSA) must be executed and confirmed prior to submitting any information relating to a potential candidate. Without a signed MSA, Terran Orbital shall not be responsible to any individual or entity for any payment relating to any form of fee or compensation. And, in the event that a resume or candidate is submitted by a recruiter, an employment agency, or a staffing firm without a fully executed MSA, Terran Orbital has the unrestricted right to pursue and hire any of those candidate(s) without any legal or financial responsibility to the recruiter, agency, and/or firm.

Job Description At Turion Space, we’re building spacecraft to secure Earth and expand humanity’s reach beyond it. As a Senior Wire Harness Designer at Turion Space, you will responsible for the design, development, and integration of electrical harnesses for aerospace systems. This role involves creating detailed harness layouts, routing, and assembly drawings to meet stringent aerospace standards and program requirements. This is a full-time, exempt position based on-site at our Irvine, California headquarters. Key Responsibilities * Own harness design and documentation from concept through launch across multiple spacecraft projects * Create and maintain harnessing documentation including drawings, and wire diagrams * Write harness instructions and iterate based on technician feedback * Serve as the wire harnessing subject matter expert (SME) and consult with other disciplines * Select and manage vendors for aerospace electrical components including connectors, crimps, shielding, overwrap, and wires * Manage harness vendors and build processes and priorities * Define test acceptance procedures, own final acceptance and lead troubleshooting and root cause analysis * Perform harness routing within complex assemblies and ensure compliance with space constraints and environmental requirements * Support and participate in space vehicle integration in clean room * Maintain effective communication with all the functional groups to ensure manufacturability and project success (including mechanical, manufacturing, software, test, and supply chain) Minimum Qualifications * Associate or Bachelor’s degree in Electrical Engineering, Mechanical Engineering, or related field; or equivalent technical experience. * 7+ years of hands-on experience designing and assembling wire harnesses in a high-reliability environment. * Proficiency in tools for harness design (Altium, CATIA Electrical, Creo Cabling, or similar). * Knowledge of wire selection, shielding, EMI/EMC considerations. * Confidence working in the lab automated test equipment, hipot testers, DMMs, and power supplies. * Ability to read and interpret electrical schematics and mechanical drawings; excellent attention to detail. Preferred Qualifications * Familiarity with aerospace standards (AS50881, NASA-STD-8739.4, IPC/WHMA-A-620) * IPC/WHMA-A-620 certification * Hands on experience assembling harnesses, soldering and crimping, with D-sub, micro-D, nano-D, MIL-DTL-38999, Harwin Datamate, and other connectors * Experience with PLM systems (Teamcenter, Windchill) * Ability to obtain and maintain a Secret and/or a TS/SCI clearance. Senior Wire Harness Designer Salary: $90,000 - $130,000 USD. ITAR Requirements: This position may include access to technology and/or software source code that is subject to U.S. export controls. To conform to U.S. Government export regulations, applicant must be a (i) U.S. citizen or national, (ii) U.S. lawful, permanent resident (aka green card holder), (iii) Refugee under 8 U.S.C. § 1157, or (iv) Asylee under 8 U.S.C. § 1158, or be eligible to obtain the required authorizations from the U.S. Department of State. Benefits: We offer a comprehensive compensation and benefits package designed to support the well-being and professional growth of our employees. In addition to a competitive base salary and company stock, determined by factors such as job-related knowledge, education, skills, experience, and market demand, full-time employees are eligible for: * Equity: Receive equity in Turion Space, letting you benefit from the company's success * Health Insurance: Comprehensive medical, dental, and vision coverage for employees and their dependents. * Retirement Plans: Access to a 401(k) plan to help you plan for your future. * Paid Time Off: Generous vacation days, personal days, sick days, and holidays to ensure you have time to recharge. * Professional Development: Opportunities for ongoing training, workshops, and courses to advance your skills and career growth. * Team Building Activities: Regular social events, team outings, and company-sponsored activities to foster a positive work environment. We are dedicated to providing a supportive and enriching environment for our team members, recognizing that our collective success is built upon the well-being and satisfaction of each individual. Turion Space is an Equal Opportunity Employer; employment with Turion Space is governed on the basis of merit, competence and qualifications and will not be influenced in any manner by race, color, religion, gender, national origin/ethnicity, veteran status, disability status, age, sexual orientation, gender identity, marital status, mental or physical disability or any other legally protected status. Compensation Range: $90K - $130K

Job Description TRL11 is a venture backed startup looking to bring cutting edge video technology to the space economy. We are based in Irvine, CA. This candidate will be working on-site. Position Overview: We are seeking to hire an experienced Electronics Technician to join our team. As a member of our engineering team, you will be responsible for assisting other engineers build prototypes and final products. This person will be involved in the assembly, testing, and maintenance of electronic systems and components essential for space exploration missions. This position offers the opportunity to work at the forefront of space technology. If you are passionate about cutting-edge technology, this is an excellent opportunity for you to participate in the new space economy. Requirements Essential: • Experience with assembling, testing, and maintaining electronic systems and components., • Experience with debugging electrical issues and reworking PCBs, • Comfortable with soldering irons, wire cutters, bench supplies, and other lab tools., • Familiar with multimeters, oscilloscopes, function generators, and other testing equipment, • Collaborate with engineers and other team members to ensure reliability and functionality of electronic systems and all products, • Experience operating environmental testing chambers, such as thermal chambers and TVAC chambers, • Applicable certifications such as IPC-A-610, IPC-A-620, IPC-7711, J-STD-001

Job Description Join a team where your impact reaches beyond the stars! At Terran Orbital, you're not just part of the system – you're a vital force propelling our mission forward. As trailblazers in satellite manufacturing and aerospace innovation, we shatter boundaries daily to deliver groundbreaking solutions that power our nation's defense and commercial missions. We are a unique, fast growing, and trusted team dedicated to swiftly and efficiently designing, building, launching, and operating state of the art satellites for advanced mission constellations. If you're driven by purpose, inspired by challenges, and ready to leave your mark on the universe, you'll find a home and endless opportunities for growth here. Together, let's redefine what is possible in orbit and beyond! Terran Orbital is seeking an experienced AIT Technician – Vehicle Integration to join our dynamic team. Reporting to the Production Supervisor the AIT Technician – Vehicle Integration will responsible for the hands-on manufacturing and assembly of sub-assemblies essential for spacecraft vehicle integration. The ideal candidate should possess a keen understanding of quality control and AS-9100 standards. This role is on our Weekday shift (Monday - Thursday) from 6:00AM - 4:30PM. Key Duties and Responsibilities • Follow detailed procedures to assemble complex electronic and mechanical modules., • Operate hand tools such as screwdrivers, torque wrenches, and light power tools., • Ability to quickly change priority while working in a fast-paced environment., • Communicate statuses, issues, and suggestions effectively to the support engineering team., • Updating documentation and hardware statuses through online services., • Basic avionics and the electrical troubleshooting., • Assist in spacecraft integration related activities., • Must possess a strong work ethic, be able to work with limited supervision, and meet the requirements of the attendance policy., • Must perform all functions of the job in a safe and professional manner., • Must keep work area(s) in a neat, clean, safe, and orderly condition., • Ability to stand for most of the working day., • Perform miscellaneous lab duties, including kitting, inventory, and organization tasks., • High school diploma or GED, • 2+ years of professional experience working hands-on as a technician within electromechanical assembly or spacecraft/spacecraft hardware manufacturing, • Experience with wire harness routing and/or space flight integration., • Ability to read, understand and follow detailed work instructions for assembly and testing flight product including blueprints and schematic drawings, • Proficiency with Windows 10, Microsoft Office products, and internet browser applications, • Good written and verbal communication skills, • Knowledge of soldering tools and practices (J-STD-001 certification preferred but not required), • Ability to maintain a clean and organized workspace, • Familiarity with cleanroom cleanliness standards and ESD precautions, • Must have excellent visual acuity to perform detailed inspections and quality control tasks, • Ability to accurately distinguish a wide range of colors, which is essential for success in this role Benefits • 100% Company-paid comprehensive medical, dental, and vision coverage for you and your dependents, • 401(k) Match, • Flexible Time Off (FTO), • Education Reimbursement Terran Orbital is a leading manufacturer of satellite products primarily serving the aerospace and defense industries. Terran Orbital provides end-to-end satellite solutions by combining satellite design, production, launch planning, mission operations, and on-orbit support to meet the needs of the most demanding military, civil, and commercial customers. Learn more at Physical Demands An employee must meet the physical demands described to perform the essential functions of this job successfully. In performing the duties of this job, the employee is routinely required to sit or stand for long durations of time, in addition to bending, reaching, and walking. This would require the ability to lift or move objects up to 10 pounds and occasionally lift or move objects up to 25 pounds. This position is generally sedentary, with substantial computer usage. Work Environment The job operates in a professional office environment but in a manufacturing company. This job routinely uses standard office equipment such as computers, phones, photocopiers, and scanners. Disclaimers To comply with U.S. Government space technology export regulations, the applicant 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. In addition, please note that this position may require a current United States National Security clearance or eligibility for such a clearance. Terran Orbital is an Equal Opportunity/Affirmative Action Employer. We consider applicants without regard to race, color, religion, age, national origin, ancestry, ethnicity, gender, gender identity, gender expression, sexual orientation, marital status, veteran status, disability, genetic information, or membership in any other group protected by federal, state, or local law. If you need assistance or accommodation due to a disability, you may contact us at . Terran Orbital does not accept unsolicited resumes from recruiters, employment agencies, or staffing firms. To conduct business with Terran Orbital, a Master Services Agreement (MSA) must be executed and confirmed prior to submitting any information relating to a potential candidate. Without a signed MSA, Terran Orbital shall not be responsible to any individual or entity for any payment relating to any form of fee or compensation. And, in the event that a resume or candidate is submitted by a recruiter, an employment agency, or a staffing firm without a fully executed MSA, Terran Orbital has the unrestricted right to pursue and hire any of those candidate(s) without any legal or financial responsibility to the recruiter, agency, and/or firm.

Job DescriptionBenefits: • 401(k), • 401(k) matching, • Company parties, • Dental insurance, • Free food & snacks, • Free uniforms, • Health insurance, • Paid time off, • Training & development IMPORTANT REQUIREMENT: Local candidates with reliable transport to work. Wednesday to Sunday 8:30 am -5:30 pm About the Role We are seeking a reliable and motivated Entry-Level Lab Technician to support daily operations in a medical device laboratory environment. This is an excellent opportunity for individuals interested in hands-on work. Formal education is not required candidates must be dependable, able to follow instructions, and committed to performing assigned tasks under supervision. This position focuses on assisting technical staff with laboratory activities while maintaining compliance with company procedures and quality standards. Key Responsibilities Follow instructions from supervisors and technical staff to complete assigned duties Assist with setup, cleaning, and organization of laboratory equipment and workspaces Perform basic laboratory support tasks under supervision Prepare materials, samples, or equipment as directed Maintain accurate documentation and follow standard operating procedures (SOPs) Support testing activities and general lab operations Maintain cleanliness and safety of the laboratory environment Follow safety guidelines and company quality procedures Assist with inventory organization and stocking of lab supplies Perform additional tasks as assigned Qualifications High school diploma or equivalent preferred but not required Ability to follow detailed instructions and work under supervision Strong attention to detail and reliability Willingness to learn and adapt in a technical environment Basic organizational skills Ability to work independently and as part of a team Preferred (Not Required) Previous experience in a laboratory, manufacturing, or technical environment Interest in medical devices, engineering, or science-related work Familiarity with clean work practices or regulated environments Physical Requirements Ability to stand for extended periods Ability to lift up to 25 lbs Manual dexterity for handling small components Why Join Us Entry-level opportunity with training provided Exposure to medical device development and laboratory operations Supportive team environment Opportunity to gain technical skills and grow professionally Equal Opportunity Employer We are an equal opportunity employer and welcome applicants from diverse backgrounds. Candidates will be evaluated based on qualifications, reliability, and ability to perform job responsibilities.

Job Description Express Lens Lab is currently seeking to hire lab technicians in both our surfacing and finishing departments. Responsibilities In this role, you will be responsible for performing optical laboratory duties, including adjusting, repairing, and fabricating eyeglasses•Adjust, repair, and fabricate eyeglasses according to customer needs•Follow technical instructions accurately and efficiently•Maintain up-to-date knowledge of optical laboratory processes and techniques•Provide excellent customer service and communication skills•Utilize appropriate tools and equipment to complete tasks•Ensure accuracy of all products before releasing to customers•Maintain a clean and organized working environment•Adhere to safety protocols and procedures•Assist other technicians with optical-related tasks, if needed | Job descriptionWe are currently seeking a highly motivated and detail-oriented Technician, Optical Laboratory to join our team at Express Lens Lab. In this role, you will be responsible for performing optical laboratory duties, including adjusting, repairing, and fabricating eyeglasses. The ideal candidate for this position will possess a combination of technical and customer service skills, as well as the ability to work in a fast-paced environment. If you have a passion for providing quality optical care and are ready to join a team of dedicated professionals, we encourage you to apply. Qualifications:• Previous experience as an optical laboratory technician preferred• Excellent customer service and communication skills• Ability to work accurately and efficiently• Working knowledge of optical laboratory processes and techniques• Ability to read and follow technical instructions• Ability to lift up to 25 pounds Responsibilities: Adjust, repair, and fabricate eyeglasses according to customer needs. Follow technical instructions accurately and efficiently. Maintain up-to-date knowledge of optical laboratory processes and techniques. Provide excellent customer service and communication skills. Utilize appropriate tools and equipment to complete tasks. Ensure accuracy of all products before releasing to customers. Maintain a clean and organized working environment. Adhere to safety protocols and procedures. Assist other technicians with optical-related tasks, if needed. Lift up to 25 pounds when necessary. Express Lens Lab, Inc. is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. We do not discriminate based upon race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a protected veteran, status as an individual with a disability, or other applicable legally protected characteristics

Job DescriptionJob Title: Composite Lab Technician Location: Santa Ana, CA Employment Type: Full-Time (Placement through Pathway Group) Pay: $23–$27/hour DOE Schedule: Monday–Friday, 8:00 AM – 5:00 PM About the Opportunity: Pathway Group, a recruiting and placement firm, is assisting a leading manufacturing company specializing in advanced composite materials. We are seeking a detail-oriented Composite Lab Technician with machining experience to perform composite materials processing and testing. This is a hands-on, fast-paced role that requires precision, proactiveness, and strong attention to detail to support product quality and integrity. Key Responsibilities: • Perform composite processing tasks: layup, kitting, bagging, curing, and machining., • Safely operate lab and composite processing equipment, including autoclaves, vacuum ovens, furnaces, analytical instruments, mechanical equipment, and machining tools., • Conduct lab-scale resin mixing and coating trials, maintaining detailed records., • Perform physical, mechanical, and analytical testing to defined specifications and standards., • Maintain clear and concise records of testing and ensure equipment meets specifications., • Collaborate with supervision to maintain schedules, communicate resource needs, and provide process feedback., • Follow all lab rules, company Health & Safety policies, and Quality System requirements., • Maintain daily housekeeping to meet company standards.Qualifications:, • High school diploma/GED or equivalent; 2+ years of related experience., • Industrial lab, production shop, or machining experience required., • Some analytical testing experience (DSC, DMA, Rheology, FTIR, HPLC, Particle Size Analyzer) preferred., • Proficiency in MS Office (Excel required)., • Ability to write routine reports and correspondence.Preferred Qualifications:, • Bachelor’s degree in chemistry, chemical engineering, or materials science., • 1–3 years of composites processing, testing, and machining experience., • Experience with resin mixing and research labs, particularly with composites, polymers, or adhesives.Physical Requirements:, • Mostly standing; ability to lift, push, and pull up to 50 lbs., • Ability to wear a NIOSH-approved respirator.Work Environment:, • Lab and office environment with some exposure to the factory floor.Why Apply Through Pathway Group:, • Placement with a leading manufacturing company in advanced composites., • Competitive pay ($23–$27/hour DOE) with hands-on experience in lab processing, testing, and machining.

Job DescriptionCompany Description Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organization services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organizations. It also has a rapidly developing presence in highly specialized and molecular clinical diagnostic testing and in-vitro diagnostic products. In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralized and entrepreneurial network of 900 laboratories in over 54 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products. In 2024, Eurofins generated total revenues of EUR € 6,515 billion, and has been among the best performing stocks in Europe over the past 20 years. Job Description The EMC Technician is responsible for performing electromagnetic compatibility (EMC) testing on electrical and electronic products in accordance with applicable regulatory and international standards. This role supports compliance engineers by setting up test configurations, executing test plans, collecting data, and ensuring accurate and repeatable results in an accredited laboratory environment. EMC Technician Responsibilities & Duties Include but are not Limited to the Following: Test Execution • Perform EMC testing including:, • Radiated Emissions (RE), • Conducted Emissions (CE), • Immunity testing (ESD, EFT, Surge, Radiated Immunity), • Execute test plans in accordance with standards such as:, • FCC Part 15, • CISPR 32, • IEC 61000-4-2, • Record test data accurately and completely, • Capture test configurations, photos, and observations, • Maintain clear and traceable test records in accordance with lab proceduresQualifications Basic Minimum Education Requirements: • Minimum 0-3 years of experience in EMC/EMI testing, • Comfortable with using Spectrum Analyzers and Receivers, • Experience working with FCC/CISPR EMC Standards, • Understanding basic lab safety, • Basic understanding of EMC principles (Emissions vs Immunity, Conducted vs Radiated Disturbances), • Equipment and Lab Skills, • Basic computer skills (Excel, word), • Ability to assist in test setup and results reporting., • Ability to move and setup test equipment (25-50 lbs) Additional Information Position is full-time working Monday - Friday 9:00am - 5:00pm, with overtime as needed. Candidates currently living within a commutable distance of Irvine, CA are encouraged to apply. • Compensation: $80,000 - $90,000, • Excellent full-time benefits including comprehensive medical coverage, dental, and vision options, • Life and disability insurance, • 401(k) with company match

Job DescriptionSalary: $85,000 - $102,300 The Company TelemetryX, formerly Access Control Group, is now a wholly owned subsidiary of Pacific Rim Capital. TelemetryX is a fast-growing provider of agnostic telemetry data and third-party asset management services. TelemetryX centralizes fleet intelligence to transformdata into operational power driving continuous improvement across every asset and aspect of fleet operations. Our solutions help clients optimize total cost of ownership, performance, and safety. Job Summary A Senior Electronics Engineering Technician plays a critical role in supporting engineers and maintaining complex electronic systems and equipment. This position typically requires advanced technical skills, significant experience, and the ability to work independently on challenging projects. Key Responsibilities The primary duties often include: • Product Development Support, • Following FRS/PRD for end to end product validation, • Develop and update test cases., • Building, testing, modifying, and assembling prototypes from schematics and design specifications., • Install prototype/pre-production devices on material handling equipment., • Travel to test sites to perform field test and validation when required, • Prepare test reports, update JIRA, and support development team to fix bugs, • Perform regression testing, • Testing and Troubleshooting, • Conducting diagnostic tests using oscilloscopes, multimeters, and spectrum analyzers to locate and resolve complex component-level failures., • Calibrate and validate electronic equipment to meet performance standards., • Repairing and refurbishing PCBs and sub-assemblies., • Documentation and Reporting:, • Maintain accurate records of testing procedures, results, component inventory, and repair history., • Write technical reports and contribute to the development of test procedures and maintenance manuals., • Collaboration:, • Work closely with key stakeholders throughout the testing process to ensure alignment and successful outcomes., • Partner with engineering, software development, technical support, and field technicians to gather insights, troubleshoot issues, and validate solutions., • Communicate findings and recommendations clearly to cross-functional teams to support continuous improvement and product quality. Success Measurements: • Prototype Delivery & Accuracy: Complete electronic prototypes within agreed timelines, achieving 95% compliance with design specifications and zero critical defects., • Testing & Troubleshooting Impact: Reduce equipment downtime by 20% through timely diagnosis and resolution of component-level issues (within 48 hours of identification)., • Quality & Reliability: Maintain calibration and testing accuracy to meet or exceed industry standards, with less than 1% rework rate on validated assemblies., • Documentation & Reporting Excellence: Achieve 100% accuracy and timeliness in test reports, repair logs, and inventory records to support engineering and compliance requirements., • Continuous Improvement & Cost Efficiency: Identify and implement at least two process enhancements per quarter that reduce material waste or improve assembly efficiency by measurable percentages., • Safety & Compliance: Maintain zero safety incidents and full adherence to OSHA and internal safety standards during all lab operations. Requirements • Associates degree in electronics technology or related field, bachelors degree preferred, • 5+ Years of hands-on experience as electronics technician, • Technical Skill: Proficiency in analog and digital circuits and microcontrollers. Must understand installation of product and testing as it relates to functionality and safety., • Proficient in reading and interpreting schematics, block diagrams, and assembly drawings. Advanced soldering and rework skills, • Tool Proficiency: Expert-level operation of test equipment (e.g., oscilloscope, signal generator, DMM). Familiarity with lab software (e.g., LabVIEW). JIRA project management experience., • Soft Skills: Strong troubleshooting and problem-solving abilities. Excellent communication and documentation skills. Ability to work independently and manage project deadlines. Compensation and Benefits • Salary: $85,000-$93,000, • Performance Bonus: Eligible for a quarterly bonus of up to 10%, bringing the total compensation range to $93,500-$102,300, • Health Benefits: Comprehensive medical, dental, vision, and life insurance, along with an Employee Assistance Program and 401(k) plan with company match, available for full-time employees., • Paid Time Off: Accrue three weeks of PTO annually., • Holidays: Enjoy 15.5 paid holidays throughout the year. TelemetryX is an equal opportunity employer and is committed to fostering an inclusive and diverse workplace. We welcome and encourage applicants from all backgrounds to apply, regardless of race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, veteran status, or any other protected characteristic under applicable law. If you require a reasonable accommodation during the application or interview process, please contact the People and Culture department. We believe that diversity of thought, background, and experience makes us stronger and helps us better serve our employees, customers, and communities.

Job Description Job description: Shift: 8:00am-4:30pm M-F , OT and occasional weekend hours as needed Pay Rate: $23 - $27/hr. DOE Temp-to-hire Job Summary: We are seeking a Composite Technician to perform processing and characterization of composite materials in a Technical/R&D lab. This temp-to-hire role works under the direction of engineers, ensuring product quality, process accuracy, and adherence to safety standards. Key Responsibilities: • Perform composite processing tasks: Layup, Kitting, Bagging, Curing, Machining., • Operate lab and processing equipment including Autoclave, Vacuum Oven, Furnace, and Machining tools., • Conduct lab-scale resin mixing and coating trials., • Perform physical, mechanical, and analytical testing, maintaining accurate records., • Utilize Microsoft Office (Excel, Access) for documentation and reporting., • Maintain lab housekeeping and follow all Health, Safety, and Quality policies., • 1–3 years of composites processing or machining experience preferred., • Analytical lab or quality testing experience a plus., • Strong attention to detail and ability to follow precise instructions., • Temp-to-hire opportunity with potential for permanent placement., • Hands-on technical experience in an R&D lab., • Develop expertise in composites and advanced manufacturing processes. #PROD1 Job Type: Full-time Benefits: • 401(k), • 401(k) matching, • Dental insurance, • Health insurance, • Life insurance, • Paid time off, • Vision insurance Experience: • composite processing: 1 year (Preferred), • composite machining: 1 year (Preferred)Company DescriptionPathway Group is a Recruitment and Staffing service dedicated to the Manufacturing Industry. We pride ourselves on being expert recruiters in the space staying true to our manufacturing recruitment vertical. The vast majority of our placements are contract to hire and direct hire placements. Our goal is to add value to the client and candidate. Placing the right candidate into their next career. We focus on positions like mechanical assemblers, electrical assemblers, CNC operators, CMM operators, composite technicians, quality technicians, engineers, managers, etc.Pathway Group is a Recruitment and Staffing service dedicated to the Manufacturing Industry. We pride ourselves on being expert recruiters in the space staying true to our manufacturing recruitment vertical. The vast majority of our placements are contract to hire and direct hire placements. Our goal is to add value to the client and candidate. Placing the right candidate into their next career. We focus on positions like mechanical assemblers, electrical assemblers, CNC operators, CMM operators, composite technicians, quality technicians, engineers, managers, etc.

Job DescriptionDescription: Job Title: Laboratory Technician Department: Anatomic Pathology Reports To: Laboratory Manager Location: Laguna Hills, CA Hours: 1:00pm-9:30pm Tues-Sat. Job Purpose The Lab Tech is responsible for a multitude of pre-analytical and post-analytical support services in a high complexity testing CLIA certified laboratory. Essential Responsibilities • Prioritize and monitor cases throughout the day, • Routinely interface with Pathologists, • Troubleshoot missing or delayed cases, • Provide status updates of cases as required, • Ensure that all actions taken on behalf of a client or a patient are appropriately documented in the current information systems and are according to standard operating procedures', • Support services for the laboratory, sales and clients, • Responsible for client services duties as assigned by the supervisor, • Label, scan slides and prepare slide boxes for shipment, • Maintain organized pathology reports, • Responsible for specimen accessioning and data entry in the LIS, • Responsible for logistics duties as assigned by the supervisor, • Use personal protective equipment appropriately and demonstrate safe work practices in accordance with laboratory and company policy. Maintain a clean and safe work environment, • Demonstrate excellent customer service skills, • Organize and file slides that have been stained and reviewed, • Extract and synthesize clinical data from pathology reports into format that can be used in a clinical database, • Knowledge of Histotechnology and Immunohistochemistry in a clinical setting, • High School Diploma required, • Associate’s Degree or Bachelor’s Degree preferred, • Working knowledge of MS Office, • Ability to adapt to changing procedures, policies and work environment, • Good data entry skills, • Ability to communicate effectively and follow written and verbal instructions, • High level of accuracy and attention to detail, • Ability to work in a fast paced team environment, • Ability to multitask and prioritize with little supervision

Job Description The Quality Control Lab Technician III – Chemistry ensures company standards are met for all functions as they pertain to the QC Laboratory. Overtime is required to meet business needs. Responsibilities: • Processes paperwork and logbook receipts associated with raw material, in-process/finished products testing., • Performs raw material testing assignment and release functions in the ERP system., • Operates general analytical instruments during testing with raw material, IP, FP, and ST sample testing, such as an automatic titrator, FTIR, and dissolution testing., • Labels, transcribes, reports sheets and laboratory notebooks and records documentation as required by APs and SOPs., • Performs physical testing, such as particle size., • Creates finished product certificates of analysis., • Washes glassware as needed to minimize dirty glassware in the lab., • Verifies test results against specifications promptly, alerting management of any specification excursions., • Verifies vendor’s specifications and vendor’s results to ensure specifications are met., • Schedules, coordinates, and tracks raw material, in process, and finished product testing., • Coordinates with outside labs to ensure prompt delivery of results., • Maintains the chemical inventory database, and associated MSDS., • Receives incoming lab supplies and chemicals., • Works with QC Management to determine and implement production and quality control standards., • Ensures project deadlines and performance standards are established and met., • Ensures compliance with all Company policies and procedures, including safety rules and regulations., • Maintains strict standards of hygiene in the production area and throughout the facility., • Follows/adheres to the Standard Operating Procedures (SOP’s), Good Manufacturing Practices (cGMP’s),, • Standard Safety Practices, and all company policies/procedures., • Performs other projects and tasks as assigned by management., • You must be available to work overtime every other weekend (Sat or Sun) Qualifications: • 3 - 4 years of lab experience in a manufacturing environment is a plus., • Adaptability/Flexibility - able to adapt in changing circumstances/environments and to embrace new ideas., • Knowledge of laboratory techniques, terminology, equipment, and supplies., • Communication Skills (Oral/Written) - able to speak clearly, concisely, and accurately in order to ensure effective department operations., • Continuous Improvement - willingness to learn new things and comply with continuous improvements in procedures and processes., • Detail Oriented - pays close attention to detail, accuracy, and completeness, double-checking their work., • Honesty/Integrity - follow through with company values and provide exceptional quality products., • Safety Minded - follows/demonstrates awareness of all safety policies/procedures of self and others., • Teamwork/Cooperation - ability to work well with others in a group and cooperate with others. What We Offer: • Competitive Wages, starting at $25.00-$29.00/hour, depending on experience., • Medical & Dental (company pays 75% of employees' HMO plans), • Discounted Vision, • 401k match dollar for dollar up to 3% of your salary, • Paid Holidays, • Vacation Days, • Sick Days Our HR department will contact applicants who meet the required selection criteria and most closely match the requirements of an open opportunity either by phone or email. Should your skills and experience align with our current needs, we will contact you to discuss the next steps in the recruitment process. Please note: You will only be contacted if your application is selected for the next stage of the recruitment process. Robinson Pharma is committed to providing equal employment opportunity without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, or any other protected status with respect to recruitment, hiring, promotion, and other terms and conditions of employment. Robinson Pharma takes affirmative action in support of this policy to employ and advance in employment individuals who are minorities, women, individuals with disabilities, and veterans. Robinson Pharma, Inc will conduct a background check by using a third-party vendor to conduct such background investigations. After acceptance of an offer, you will be asked to complete and deliver authorization, consent, and release of all background information. Employment will be 'at-will' and may be terminated at any time, with or without notice, by either party in writing. Company DescriptionWe are a full-service contract manufacturer of softgels, tablets, capsules, powders, gummies and liquids for dietary supplements and personal health care.We are a full-service contract manufacturer of softgels, tablets, capsules, powders, gummies and liquids for dietary supplements and personal health care.

Job Description Are you fascinated by microbiology and eager to apply your skills? Look no further- Tentamus California is looking for a highly motivated Microbiology Lab Technician to join our team in Irvine, CA, to support critical quality and safety testing in a start-up lab environment. This role offers hands-on experience with microbial analysis, laboratory procedures, and data management in an industry-leading lab. You will be involved in key microbiological testing, including USP 61 & 62 for microbial enumeration and pathogen detection, ensuring the safety and compliance of various products. How you will contribute as a vital part of our team: Under the direction of the Microbiology Manager, duties include but are not limited to: • Prioritize and process samples; Perform media preparation, sample weighing, plating, and counting., • Perform microbial testing, including USP 61 & 62, for microbial limits and pathogen screening., • Basic setup, troubleshooting, and routine equipment maintenance; Perform routine checks of instruments such as balances, refrigerators, and incubators, • Receive and log in reagents, along with certificates of analysis and SDSs, • Maintain notebooks and other relevant documentation to GDP (Good Documentation Practices) standards, • Prepare reports and summarize large amounts of data using Excel, instrument software and LIMS., • Cleaning and sanitizing throughout the Microbiology Laboratory; Properly handling and disposing of laboratory hazardous waste., • Assist with inventory management and restocking of lab supplies; contribute to improving laboratory efficiency and cost-effectiveness., • Execute projects as assigned to meet changing laboratory needs and requirements., • Other duties as assigned Position Type & Expected Schedule This is a full-time, 40-hour-per-week position based onsite at Tentamus California in Irvine, California. The regular schedule is Tuesday - Saturday or Sunday - Thursday, 10:00 AM to 7:00 PM or 11:00 AM to 8:00 PM, with a lunch break included. Weekend and holiday availability may be required as needed. Qualifications Our ideal candidate will be authorized to work in the United States, indefinitely, without restriction or sponsorship, hold a Bachelor's degree in Microbiology, Biology, Food Science or a related science field preferred; Possess experience with microbiological testing methods, laboratory equipment, and strong understanding of Good Laboratory Practices (GLP). Other qualifications include: • Experience working in a commercial lab setting is preferred, • Knowledge of LIMS, Microsoft Word, Excel, and Outlook is a plus., • Possess strong attention to detail, • Ability to memorize different testing types, Media, Dilutions, SOPs, etc., • Ability to work in a fast-paced environment and stand for long periods; to work independently and within a team. What's in it for you? Hourly pay between $24 to $26, comprehensive and low-cost benefit plans (medical, dental, vision, disability, life insurance) Ample PTO, 40 hours of sick time, and a matching 401k! About Tentamus: Labs for Life®. We are a global network of full-service accredited analytical laboratories providing crucial quality and safety analysis for clients locally, nationally, and beyond using proven methods of chemistry and microbiology. Many of the products you use and consume daily rely on Tentamus labs. With 20 labs in the Americas and growing (100 globally), we celebrate having talented diverse scientific and service-oriented professionals. Visit us at Tentamus.com|Follow Tentamus on LinkedIn|Follow Tentamus CA on LinkedIn Job Posted by ApplicantPro

Radiology / Cardiology/Cath Lab Technician. Cath Lab Tech position in a 488-bed. Perform cath lab technical duties during 4x10-hour shifts.

Allied Technician - Cath Lab Tech.

Cath Lab Technicians are vital team members who assist doctors during invasive cardiovascular procedures such as angioplasty, cardiac catheterization, and electrophysiology. Weekly amount stated in the job postings is scaled based on estimated hourly wages and potential stipends available for the

We're currently looking for individuals across the country to take part in remote paid research, including remote focus groups, product trials, and consumer studies.Earn up to $750 a week in your free time by providing feedback on everyday products and services.If you're comfortable sharing your opi

Under general minimal supervision, independently and in collaboration with other others; analyze, organize, and prepare publications; maintain current knowledge of appropriate related scientific literature; assist with research training for undergraduate and graduate students, and post-docs. Collabo