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\n Description\n \n \n \n \n The research lab of Sanaz Memarzadeh, MD, PhD, focuses on understanding the molecular basis of the formation, progression and treatment of gynecologic epithelial cancers. The Gynecologic Oncology (GO) Discovery lab (godiscoverylab.com) investigates the molecular pathways in chemotherapy-resistant ovarian and aggressive endometrial tumor cells that are candidates for therapeutic intervention via small molecule inhibitors and/or immunotherapy. Knowledge gained from this translational research will then be used to design and test strategies for cancer therapeutics that will move onto clinical trials. \n \n Dr. Memarzadeh and the GO Discovery Lab (godiscoverylab.com) are seeking a full-time Staff Research Associate III to join their team. As a member of our cutting edge gynecologic oncology research laboratory (G.O. Discovery Lab), you’ll under the mentorship of Dr. Sanaz Memarzadeh to focus on determining the molecular basis of epithelial cancer formation, progression and treatment. More specifically, you will work with cell lines, animal models, viruses, DNA, RNA , proteins, and other diagnostic and functional assays towards understanding the molecular, cellular and genetic events involved in the formation and progression of gynecologic diseases. You design, optimize and perform procedures and protocols that cross and connect scientific disciplines at the fully operational level. You will also consult with Dr, Memarzadeh and scientific literature to find and bring new ideas to the lab. Additional responsibilities will include also taking on a portion of the lab management duties, including supply management, ordering and equipment upkeep, and coordinate general lab support activities. You will also help obtain and process human samples from operating rooms at UCLA. \n \n Hourly salary range: $36.13 - $58.10. The department’s target hourly rate is $36.13. \n \n \n\n\n Qualifications\n \n \n Required: \n \n • Knowledge of laboratory equipment and safety\n, • Knowledge of cell biology and previous experience working with human cells, preferably primary patient samples\n, • Knowledge in molecular biology and laboratory experiments\n, • Knowledge of specimens and tissue collection\n, • Knowledge of consent form\n, • Excellent skill in verbal and written communication. Proper utilization of English in the written word and conversation.\n, • Skill in tact and diplomacy\n, • Skill in working with disparate faculty\n, • Knowledge of contract and grant application process\n, • Skill in organizing and coordinating meetings\n, • Advanced skill and knowledge of computer applications including those for imaging, data analysis and manuscript figures (ImageJ, FloJo, Prism, Biorender, etc.)\n, • Ability to be self-motivated, minimal supervision, handle multi-tasks and prioritize workload\n, • Ability to handle sensitive & confidential information\n, • Ability to operate various office equipment, Ability to setup and maintain filing system and office supplies\n, • Ability to read and understand scientific publications, judge them based scientific merit, technical innovation and relevance to lab projects\n, • Master’s of Science degree in a life/biomedical science discipline, PhD degree preferred\n \n \n Preferred: \n · Knowledge of UCLA Policies and procedures \n \n

\n Description\n \n \n Under the supervision of the Manufacturing Manager of the Center for Advanced Biotherapies (CAB), the CAB Lead Manufacturing Scientist is responsible for the manufacturing of human gene and cell therapy products under Good Manufacturing Practices (GMP), quality control testing of these products to ensure that the products meet the required quality, oversee other manufacturing associates and overall management of all projects. The purpose of the CAB is to manufacture clinical grade gene and cellular therapy products for novel patient treatments in clinical trials, and to perform scholarly research and development when appropriate. These objectives are to be met within the limits of resources available with an emphasis on cost effectiveness and innovation. \n \n The Lead Manufacturing Scientist must have advanced tissue culture expertise, preferably including human cell line and stem cell culture. This position requires experience with GMP-grade culture and formulation of various human cell types, including peripheral blood mononuclear cells (PBMCs), T cells, dendritic cells, mesenchymal stromal cells, human embryonic stem cells, and induced pluripotent stem cells. In addition, the candidate must possess strong project and personnel management skills and have experience conducting and managing quality control testing. \n \n \n \n Annual Salary Range: $90,720.00 - $194,040.00 \n \n \n\n\n Qualifications\n \n \n Required: \n \n • Bachelor of Science or Master of Science or Ph.D. Degree in Biology, Chemistry, or related field and a minimum of 2 years of manufacturing experience in GMP setting.\n, • Knowledge and practical experience in aseptic technique/tissue culture.\n, • Understanding of GMP requirements and regulations. Previous experience directly involved with federal regulations regarding GLP and GMP.\n, • Knowledge of Standard Operating Procedures and Quality Control requirements in a GMP laboratory setting.\n, • Work independently, with emphasis on the ability to closely follow SOPs.\n, • Ability to wear protective clothing for extended periods of time including: gowns, coveralls, gloves, masks, face shields, goggles, sleeves and head covers.\n, • Ability to work flexible hours, various hours on short notice (including covering staff shortages and holiday shifts); determine workload priorities for completion of job assignments in a timely manner to meet critical deadlines\n, • Ability to serve as a resource for complex procedure or equipment troubleshooting in areas of expertise, and/or solicits same as necessary in areas where expertise is deficient.\n, • Work under regular exposure to zoonotic diseases, anesthetic agents, and cleaning chemicals.\n, • Strong interpersonal communication skills to effectively and diplomatically interact with physicians, staff, administration & sponsors.\n, • Experience managing complex projects is required as well\n, • Advanced knowledge of cell culture, cell line development, bioreactor operation and scale-up, centrifugation and ultracentrifugation, tangential flow and normal flow filtration\n, • Expert in flow cytometry, protein, mRNA, DNA characterization\n, • Excellent record keeping skills and good documentation practices.\n, • Demonstrated ability to work independently and collaboratively with multiple departments while utilizing innovation to elicit compliance.\n, • Demonstrated ability to carry out analytical tasks, to identify and define issues and alternatives, to resolve problems, and to draw logical conclusions.\n, • Demonstrated skill in gathering pertinent data, preparing narrative reports, statistical reports, charts, graphs, and tables.\n, • Demonstrated skill in reviewing documents, data and material compiled by others for completeness and accruacy to ensure that incorrect/incomplete data is corrected.\n, • Ability to deal with and maintain confidential and sensitive information with discretion.\n, • Demonstrated skill in good decision making and taking appropriate action in situations where no established criteria exists or where answers to problems are not readily available.\n, • Ability to work on a diverse variety of projects simultaneously, organize multiple projects for efficiency and cost-effectiveness.\n, • Demonstrated skill in prioritizing workflow to meet deadlines, often under pressure of conflicting demands, while maintaining accuracy and effectiveness of work.\n, • Ability to attend off-site staff meetings, conferences and investigator meetings.\n, • Ability to write concise and accurate administrative reports, policies, procedures, and correspondence.\n, • Working knowledge of some medical and scientific terminology for protocol abstracting and conversation with research personnel.\n, • Demonstrated skill in records management. Skill in establishing and maintaining complex filing systems.\n, • Demonstrated skills with personal computers, spreadsheets, databases and word processing applications for the maintenance of records, analysis of data, and the preparation of reports.\n \n \n \n

Job Description Summary: The histotechnician will perform all routine and special paraffin histotechnology duties in our state of the art, CAP-certified pathology laboratory. Under the guidance of a Senior or Lead Histotechnologist, you will provide high quality diagnostic material within established turn-around-times. Position Responsibilities: Embeds, cuts, stains and performs other tasks required to process tissue in the Immunohistochemistry laboratory. Performs accurate gross description on tissue samples.Perform quality control procedures established for each method and maintains accurate records. Operates all instruments/ equipment according to accepted written procedures and recognizes and identifies instrument/ equipment problems. Meets acceptable turnaround time and productivity standards for the section. Recognizes testing errors/discrepancies or problems and notifies appropriate personnel; assists in problem resolution. Record, transcribe, and maintain records of patient test results according to protocol. Assist other personnel with identifying and analyzing inconsistent and abnormal results. Review accuracy and completeness of results prior to releasing in the Laboratory Information System. Complete routine and STAT testing within acceptable turn-around time guidelines. Required: Associate degree in medical technology, chemistry, biology, or related life scienceFormal training in Histology from an accredited program (720 hours)State Licensure, where applicable (CA, FL, NY require licensing)Meets CLIA personnel standard criteria.Skills in microtomy, grossing, processing, embedding, cutting and routine special staining techniques.2-4 years of experience

\n Description\n \n \n This position will be comprised of roughly 70% research duties and 30% administrative duties. \n In collaboration with Principal Investigator, the candidate will be expected to perform research projects (molecular, biochemical and cellular) related to understanding the molecular, immunologic and genetic events involved in the formation and progression of gynecologic diseases. Knowledge gained from this research is then used to design and test strategies for cancer treatment and will move to clinical trials. This work requires experience in cell biology, molecular biology, and involves the use of human samples and animal models. Responsibilities will include: preparation of data management forms per protocol, tissue culture work, preparation of RNA, DNA, protein and viruses, PCR, immunohistochemistry, overseeing laboratory and equipment maintenance, ordering materials and preparation of data and manuscripts for publication. \n \n The ideal candidate must have excellent record keeping skills, be able to function well within a team environment, have strong communication skills, be able to work independently, is scientifically creative and an independent thinker. Knowledge of contract and grant application process. Skill in organizing and coordinating meetings. Excellent skill in verbal and written communication. Proper utilization of English in the written word and conversation. \n \n \n \n \n The full hourly salary range for this position is: $32.79 - $52.75 \n \n\n\n Qualifications\n \n \n Required: \n \n \n • Bachelors degree and/or equivalent combination of education and experience.\n, • Previous lab experience of at least 2 to 4 years of related experience or training\n, • Experience in molecular, biochemical and cellular research. Ability to perform biochemical techniques as well as molecular biology techniques. Experience isolating tissues and doing tissue culture work.\n, • Ability to perform euthanasia on animals for research purposes.\n, • Ability to work independently and to take direction. Interpersonal skills to effectively interact with faculty, staff, and students. Ability to establish and maintain positive working relationships with other team members and collaborators.\n, • Ability to maintain accurate inventory of supplies and laboratory instruments. Ability to use lab equipment including PCR machine, centrifuges, etc. Skill in troubleshooting and making minor repairs of laboratory instruments/equipment.\n, • Ability to make innovative contributions pertaining to laboratory procedures. Ability to read abstracts or scientific articles pertaining to prosecution of broad research problems. Ability to analyze research findings and prepare clear, concise and accurate technical/statistical reports. Ability to conduct literature search. Ability to participate in planning strategies to accomplish goals.\n, • Experience with tissue culture. Experience with RT and real time PCR.\n, • Ability to prepare samples for analysis using standard methods.\n, • Skill in writing legible, concise and grammatically correct documentation.\n \n \n Preferred:\n \n \n \n \n, • Master's degree\n \n \n

Job Description Overview Ansible Government Solutions, LLC (Ansible) is currently recruiting Medical Technologists to support the VA Medical Center located at 11301 Wilshire Blvd, Los Angeles, CA 90073. Services will be delivered to both the Anatomic Pathology and Clinical Pathology divisions of the facility. Exceptional compensation packages with full benefits are available. Ansible Government Solutions, LLC (Ansible) is a Service-Disabled Veteran-Owned Small Business (SDVOSB) providing Federal customers with solutions in many arenas. Our customers face wide-ranging challenges in the fields of national security, health care, and information technology. To address these challenges, we employ intelligent and committed staff who take care of our customers’ success as if it is their own. Responsibilities • Rotate on a regular basis through the areas in which they have been trained and are competent, • Perform a broad range of laboratory procedures in Chemistry, Hematology, Coagulation, Urinalysis, Microbiology, and Transfusion Medicine, • Perform advanced and complex laboratory procedures, recognizing deviation from expected results, analyzing and correcting problems using scientific principles, • Recognize and communicate pre-defined critical results affecting patient care, • Maintain the optimal functioning of laboratory equipment and keep appropriate records for documentation; operate, calibrate, identify malfunctions, repair and perform preventive maintenance of laboratory analyzers, • Perform and document quality control, quality assurance and corrective actions related to test performance using sound statistical principles and theories of performance improvement, • Enter and verify laboratory results in the computer system; recognize deviations from expected results, analyze and correct problems using scientific principles, • Perform other duties as assigned relating to the responsibilities of a Medical Technologist Qualifications • Accredited Bachelors degree in medical laboratory science, medical technology, clinical laboratory science, or a related science (i.e. biology, chemistry, etc.) AND completion of an accredited medical technology clinical practice program (i.e. NAACLS, CAAHEP, ABHES) OR • Accredited Bachelors degree including 16 semester hours in biological science (one course in microbiology), 16 semester hours in chemistry (one course in organic or biochemistry), and one course in mathematics AND two (2) years of post-certification clinical laboratory experience within the last ten (10) years as a certified Medical Laboratory Technician (ASCP-BOC), • A minimum of one (1) year of Medical Technologist experience within the last three (3) years, • Demonstrated knowledge of laboratory medicine techniques and practices, • Demonstrated education and clinical training in the practice of laboratory medicine, • No sponsorship available Pay Range: $28.97 - $52.41 hourly All candidates must be able to: • Sit, stand, walk, lift, squat, bend, twist, and reach above shoulders during the work shift, • Lift up to 50 lbs from floor to waist, • Lift up to 20 lbs, • Carry up to 40 lbs a reasonable distance, • Push/pull with 30 lbs of force All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran. Powered by JazzHR knj80tbhLJ

Job DescriptionBenefits: • 401(k), • Competitive salary, • Dental insurance, • Health insurance, • Paid time off, • Vision insurance Rare opportunity to learn and grow with our company! Liberty EnviroLab is currently seeking Full Time Experienced Laboratory Analysts specializing in wildfire, structure fire, asbestos, and mold analysis. Liberty EnviroLab is located in San Marcos in the northern San Diego County. Liberty offers a variety of analytical testing services to support environmental investigations focused on wildfire, structure fire, asbestos, mold (microbiology). Our management team has over 71 years of combined experience in particulate analysis and trace evidence examination. We believe in empowering our customers with accurate and defensible analytical results. Some Responsibilities Include: · Safely perform analyses on samples according to Liberty’s Standard Operating Procedures (SOPs) using advanced instruments. · Follow all laboratory QA/QC requirements · Record data using computer software and programs. · Maintain equipment according to manufacturer guidelines and company procedures. · Perform other assigned duties, as requested by supervisor. Requirements: · Associates or Bachelor’s Degree in a life science (biology, chemistry, environmental science, etc.) preferred. · 1-2 years of Polarized light microscopy (PLM) experience required. · 1 year of Phase contrast microscopy (PCM) experience required. · Self-motivated, independent, and team oriented. · Must be able to work in a fast-paced setting, multi-task, and prioritize assignments. · Good communication, computer, typing, and organizational skills. . Visit our website for more information about our company. www.libertyenvirolab.com Please submit your resume, or call us at 760-539-7024 for assistance! About UsOur experience and cutting-edge, high-performance instruments combined with our solutions-focused customer service empower our clients with accurate and defensible analytical results. We Don’t Settle For Anything But The Best Our investment employing the most advanced, state-of-the-art instruments and uniquely experienced scientists and analysts, provides an unparalleled opportunity and experience for our customers. Our court approved experts have decades of experience in particulate analysis and trace evidence examination using various techniques of light microscopy, electron microscopy, infrared microspectroscopy and Raman spectroscopy. Our highly experienced staff have instructed forensic microscopy courses in university science graduate programs and have distinguished careers in developing and implementing quality assurance/quality control programs for laboratories across the nation.

Job Description:\n\n Certified Group is committed to partnering with customers to deliver innovative scientific solutions and expertise – So The World Can Trust In What It Consumes™. Our network of 30+ North American and European laboratories serves the food & beverage, dietary supplements, cosmetics, OTC, tobacco/nicotine, cannabis, and hemp industries.\n \n Our Brands\n Certified Group is comprised of a set of specialized brands that collectively deliver laboratory testing, regulatory consulting, and certification & audit services across highly regulated industries:\n \n Certified Laboratories – Provides comprehensive analytical and microbiological testing, primarily supporting food, beverage, cosmetics, OTC, and dietary supplement industries.\n Food Safety Net Services (FSNS) – A leading network of ISO-accredited laboratories across North America, focused on food safety testing, operational support, and technical services for the food industry.\n Labstat – A global leader in contract research and testing for nicotine, tobacco, cannabis, hemp, and next-generation products, with deep expertise in analytical chemistry and toxicology.\n EAS Consulting Group – A regulatory consulting firm offering expert guidance, training, and auditing support across FDA, USDA, and other regulated sectors, powered by a large network of independent advisors.\n FSNS Certification & Audit – Provides accredited third-party auditing and certification services, including food safety, animal welfare, and GMP programs.\n \n \n\nJob Summary:\nThe Microbiology Laboratory Manager is responsible for the day-to-day operations of the Burbank Microbiology laboratory, ensuring accurate, compliant, and timely testing for the local and national customer base. Burbank is a GMP-registered facility supporting microbiological testing of OTC drug products, cosmetics/personal care products, antibiotic products, and sterility-related . The Manager is accountable for all quality, customer, people, financial, and workflow activities within Microbiology. The role operates with a strong general manager mindset, balancing scientific rigor and cGMP discipline with business acumen, resource optimization, customer engagement, and continuous improvement. Particular focus is required on on-time delivery (OTD), backlog control, timely PET/stability/sterility starts, method suitability readiness, and accurate execution in LabWare.\nPurpose: So the world can trust in what it consumes.\nMission: Partner with customers to deliver innovative scientific solutions and expertise.\nValues: start with the customer, commit to safety and quality, drive to deliver, act with integrity and support the team.\nLeadership Accountabilities:\n\n Quality Excellence: Promote a culture where cGMP compliance, data integrity, technical accuracy, and adherence to approved methods and SOPs are embedded into every action. Ensure the laboratory remains audit- and inspection-ready.\n Customer-Focus: Ensure timely, high-quality results and proactive, factual communication on delays, study starts, technical concerns, and revised timelines to build trust and protect key customer relationships.\n People-Centricity: Maintain a safe, engaging, accountable environment. Be present and accessible, ensuring supervisors and analysts are trained, supported, cross-trained, and developed to perform at their best.\n Profitability: Manage labor, overtime, inventory, supplies, capacity, and other controllable costs while improving OTD, productivity, utilization, and sustainable laboratory contribution.\n Innovation: Drive continuous improvement through root-cause problem solving, standard work, LabWare workflow improvement, automation, and cross-site best-practice sharing.\n\nBehavioral & Functional Competencies:\n\n Strategic Leadership: Think beyond daily execution to align resources, capability, and capacity with Burbank and broader COS objectives; anticipate risks before they become customer or compliance issues.\n Quality Champion: Use sound microbiological and regulatory judgment to ensure work is technically defensible, methods are appropriate, and issues are escalated and corrected promptly.\n Customer Orientation: Build confidence through reliable commitments, transparency, responsiveness, and professional management of technical or service escalations.\n Team Empowerment: Develop supervisors, technical leads, and analysts; create clear accountability while building bench strength and reducing single-point dependencies.\n Operational & Financial Acumen: Use OTD, backlog aging, turnaround time, productivity, staffing, quality, and financial metrics to set priorities and make timely business decisions.\nResponsibilities:\nCore Operations\n\n Foster a high-performing Microbiology laboratory environment aligned with Certified Group standards, Burbank cGMP expectations, and customer commitments.\n Lead daily operations using a balanced scorecard that includes OTD, backlog volume and aging, test starts, turnaround time, late work, staffing/capacity, quality events, and customer-critical commitments.\n Conduct daily huddles with supervisors and technical leads to set priorities, rebalance work, remove bottlenecks, and ensure available resources are properly utilized.\n Actively manage sample flow from receipt/intake and SME review through test start, incubation/reading, technical review, and result release; eliminate avoidable queue time between steps.\n Ensure timely initiation and execution of PET/AET, stability, sterility, microbial limits, specified-organism, suitability, growth-promotion, and other microbiological work within the site's approved scope.\n Maintain accurate and timely use of LabWare for Microbiology status, holds, scheduling, test initiation, result entry, and internal visibility.\n Maintain technical competence across the department and ensure sufficient SME coverage and cross-training for critical methods, shifts, and review functions.\n Proactively manage organisms, media, reagents, controls, sample quantities, and other prerequisites so procurement or readiness issues do not repeatedly delay testing.\n\nQuality & Safety\n\n Lead operations in accordance with applicable cGMP requirements, the Corporate Quality Management System, ISO/IEC 17025 requirements where applicable, approved SOPs, validated/verified methods, and customer-specific requirements.\n Ensure the laboratory is inspection-ready for FDA, customer, accreditation, and internal audits. Be present during audits and ensure supervisors and SMEs can clearly explain their processes, controls, investigations, and records.\n Partner with Quality and R&D/Validation on method suitability, verification, validation, transfer, deviations, and technical risk assessments; testing must remain within the site's qualified and approved scope.\n Ensure deviations, OOS/OOT results, laboratory investigations, CAPAs, and quality events are initiated promptly, scientifically sound, and completed within established timelines.\n Maintain appropriate aseptic, contamination-control, environmental, cleaning/disinfection, and material-flow practices for sterility and other sensitive microbiological activities.\n Monitor incubators, autoclaves, biosafety/clean-air equipment, environmental-monitoring devices, and other critical systems to ensure qualification, calibration, maintenance, and readiness.\n\nCustomer Engagement\n\n Represent Certified Group with professionalism and care in all customer interactions, with a focus on trust, retention, and growth.\n Ensure timely and accurate responses to customer questions and concerns, especially around test suitability, study starts, delays, technical risk, and revised completion dates.\n Provide clear, factual, and consistent updates when results or study starts are at risk; avoid unsupported timelines and ensure commitments reflect actual laboratory capacity and technical requirements.\n Participate in customer calls, investigations, technical reviews, audits, and business reviews as needed; coordinate closely with Client Experience to present one consistent message.\n\nPeople Leadership\n\n Anticipate staffing needs based on volume and test mix, and design schedules across shifts, weekends, PET/sterility/stability activities, and customer commitments.\n Recruit, interview, select, onboard, train, and retain high-quality talent; maintain structured qualification and cross-training plans for methods, equipment, systems, and cGMP responsibilities.\n Coach supervisors and technical leads to create a high-performance environment with clear accountability for safety, quality, productivity, training, communication, attendance, and customer commitments.\n Reduce single-point dependencies by building technical depth across critical methods and shifts, including succession planning for supervisors, SMEs, and review functions.\n Maintain a visible daily presence in the laboratory to observe operations, reinforce standards, recognize performance, and provide real-time coaching and feedback.\n Partner with Human Resources on performance management and employee-relations matters, ensuring documentation is timely, thorough, and consistent.\n\nProfitability\n\n Manage Microbiology financial performance by aligning labor, overtime, staffing, supplies, inventory, vendor costs, and operating plans with budget and laboratory contribution expectations.\n Use workload, productivity, utilization, backlog, and turnaround data to support staffing decisions and optimize resources before adding cost.\n Understand the cost of repeat testing, delayed starts, poor first-pass execution, excessive overtime, and customer escalations; implement corrective actions that improve both service and profitability.\n Proactively manage outside vendors and service providers to minimize waste while maintaining appropriate quality and compliance standards.\n\nInnovation and continuous improvement\n\n Actively contribute to cross-site best-practice sharing across the Certified Group network and support overflow testing, resource sharing, method transfer, and training where appropriate.\n Use OTD, backlog, discrepancies, OOS/OOT, customer complaints, repeat work, and equipment downtime trends to prioritize and verify continuous-improvement actions.\n Identify opportunities for workflow redesign, standardization, scheduling improvements, LabWare enhancements, and automation that increase throughput without compromising quality or compliance.\nQualifications:\n\n Bachelor's degree in Microbiology, Biology, Biological Sciences, or a closely related scientific field required; master's degree preferred.\n Minimum five years of progressively responsible experience in a microbiology laboratory supporting GMP-regulated testing; experience in OTC/drug, pharmaceutical, cosmetics/personal care, antibiotic, or contract testing environments strongly preferred.\n Minimum three years of direct people-leadership experience; experience leading supervisors or technical leads who oversee hourly laboratory staff strongly preferred.\n Demonstrated experience with cGMP microbiology and compendial/validated methods, including several of the following: microbial limits/enumeration, specified organisms, PET/AET, method suitability, growth promotion, sterility testing, and aseptic/environmental controls.\n Prior experience in a high-volume, customer-facing third-party laboratory strongly preferred, with demonstrated ability to manage OTD, backlog, capacity, customer escalations, and competing priorities.\n Working knowledge of laboratory investigations, deviations, CAPA, OOS/OOT, change control, audit readiness, training/qualification, and document control.\n Experience with LIMS-based laboratory operations required; LabWare experience preferred.\n Proven track record of using operational and financial KPIs to improve productivity, service, quality, and laboratory performance.\n Strong written and verbal communication skills, with the ability to interpret complex business, technical, quality, and regulatory documents.\n Confident in presenting to and engaging with senior leadership, peers, customers, Quality, and cross-functional teams.\n\nMathematical Skills:\n\n Work with mathematical concepts such as probability, statistical inference, trend analysis, and basic laboratory performance metrics.\n Apply concepts such as fractions, percentages, ratios, proportions, and basic financial measures to practical laboratory situations.\n\nSupervision\n\n Lead Microbiology supervisors, technical leads, and/or designated staff and indirectly lead the broader Burbank Microbiology team; supervisory span may vary with business demand and organizational structure.\nPhysical Demands & Work Environment\n\n Potential exposure to odors, fumes, airborne particles, hazardous chemicals, disinfectants, and microbiological organisms/pathogens.\n Use of required PPE and controlled-area/aseptic gowning where applicable.\n Noise level varies from quiet to loud and temperature may vary by laboratory area.\n The environment is interactive and fast-paced, requiring frequent standing, walking, speaking, hearing, computer work, and use of hands.\n Occasionally lift and/or move up to 25 pounds.\n Night, weekend, or holiday work may be required based on customer demand, PET/sterility/stability schedules, audits, or laboratory events.\n Ability to travel occasionally as required.\n\n \nSchedule: Monday-Friday, 8:00AM-5:00PM\n \n \n \n\n \n \n \n \n \n \n \n \n \n The compensation details provided below reflect the expected pay range for this role, based on the selected compensation structure and applicable guidelines. Actual pay within this range may vary depending on factors such as experience, skills, qualifications, and geographic location. Additional components of total rewards—such as bonuses, benefits, or incentives—may also apply where applicable.\n \n \n \n \n \n \n \n \n \n \n \n \n Salary Range for Pay Transparency\n \n \n $100,000—$135,000 USD\n \n\n By applying, you acknowledge that Certified Group will process your personal information for recruitment and hiring purposes in accordance with our Applicant Privacy Policy. California residents may review additional information about how we collect and use personal information, including retention and rights, in our California Notice at Collection. To view our Privacy Policy, click the link here: Certified Group Privacy Policy\n We are an Equal Opportunity Employer and make employment decisions without regard to protected characteristics under applicable law.

Job Description Mission Driven, Community Focused About | Charles R. Drew University of Medicine and Science (cdrewu.edu) Charles R. Drew University is located in the Watts-Willowbrook area of south Los Angeles and was founded in 1966 in the wake of the Watts uprising. CDU was founded to address inadequate medical care in the region and to provide equitable medical education opportunities for underrepresented students. CDU is strongly invested in the local and regional community. The university leads multiple partnerships and programs to provide equitable healthcare resources in a variety of south Los Angeles neighborhoods. This role includes a CDU College of Medicine faculty appointment. Please ensure to include the following in your application; application will not be considered unless all requested documents are attached: • Academic Curriculum Vitae (as an attachment): CV format template can be found at the following link: CV Template.pdf (cdrewu.edu), • Academic Credentials (as an attachment) – Medical License, Cert/Training, Board(s) Certificate(s) and Fellowships (if any)., • List of 2-3 Evaluators (Provide contact information for evaluators/references during application questions), • Personal Statement (as a one page attachment): Personal Statement format template can be found at the following link: Self-Statement Sample.pdf (cdrewu.edu) The requested documents listed above will be compiled and presented to the appointments and promotions committee for review as part of our peer review process. Job Summary: Under the general direction of Principal Investigator, performs independent research in support in molecular endocrinology, diabetes and obesity research laboratory. Current projects involve endocrine effects of e-cigarettes. Responsibilities includes project planning, data collection, experimental protocols and procedures; bench work involving lab techniques focused on molecular biology, and small animal studies. Essential Duties and Responsibilities: • Design and plan research in collaboration with the Principal Investigator, • Organizing and implementing complex research plans, the development of methods of research, testing and data collection, analysis and evaluation, and writing reports containing descriptive, analytical and evaluative content., • Responsible for conducting analyses and submission of findings for peer review publication., • Provide formal mentorship support to students and trainees., • Enhance opportunities for students and trainees to participate in research when possible., • Designs, analyzes, implements, and reports findings on targeted statistical research studies; provides consultation to investigators and researchers on experimental design and statistical research approaches, requirements, and scientific standards to advance medical knowledge and improve research in public health., • Works with investigators to formalize analysis plans and reporting specifications; advises as to choice of statistical analysis strategies, reliability of measurements and identifiability of models, and interpretation and presentation of statistical results., • Builds and sustains collaborative relationships with individuals in different disciplines and serves as subject-matter expert for research teams, internal and external committees, and other constituencies and collaborators., • Plans and documents computer data file structure; develops, programs, manages, and maintains complex statistical databases; performs or supervises data entry., • Conduct literature searches, gather and summarize relevant findings from the published scientific literature., • Engage weekly meetings with PI and other research team members., • Assist with writing papers for submission to peer-reviewed journals. Other Duties and Responsibilities: • Performs other duties as assigned. Qualifications/Requirements: EDUCATION: • MD, PhD or equivalent degree from an accredited institution required. EXPERIENCE: • Three (3) years as a postdoctoral fellow and experience in an academic research laboratory, • Experience communicating research in peer-reviewed publications, scientific meetings, and interdisciplinary stakeholder, regulatory, or policy related meetings., • Prior experience writing and publishing peer-reviewed manuscripts., • Evidence of successful grant applications preferred., • Past evidence of designing and leading research studies preferred. KNOWLEDGE/ABILITY/SKILLS (depending on research interests): • Knowledge of scientific approach and methodologies., • Knowledge and understanding of the principles, concepts, methods, and standards of statistical research., • Protein and RNA extract from mouse tissues and mammalian cells., • Mammalian tissues culture, • siRNA transfection in vivo and in vitro, • Real time RT-PCR, • Western blot, • Immunohistochemistry, • DNA cloning and plasmid purification, • Perform animal studies including diabetic animal model generation and treatment., • Animal tissue collection, • Knowledge of scientific reporting and manuscript preparation requirements and standards., • Ability to work in a team environment to design, analyze, and report on research projects., • Strong analytical communication, critical thinking and problem solving skills., • Ability to provide technical guidance and leadership to professional personnel in area of expertise., • Excellent time management skills and ability to prioritize projects., • In-depth knowledge and understanding of probability and medical statistics theory., • Knowledge of data management principles and regulatory requirements for clinical trials and medical research., • Strong focus and quality and timely delivery of work. COMPLEXITY: • The ability to perform highly detailed work with sustained attention and care while providing/obtaining information on numerous inquiries is paramount to success in this position. PHYSICAL DEMANDS: • 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. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions., • Occasional stooping. Frequent standing. Constant walking, sitting, climbing, reaching high/low levels, finger movement, feeling, speaking clearly, hearing conversationally, and seeing far and near. WORK ENVIRONMENT: • The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions., • Occasionally required to work in confined space. MENTAL DEMANDS: • The mental demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions., • Frequent work on a variety of unrelated tasks. Constant calculating interrupted work, work on a variety of interrelated tasks, and use of sustained concentration, reasoning, judgment, resourcefulness, analytical ability, and ingenuity. Special Requirements: • As a health professions institution of higher education, Charles R. Drew University of Medicine and Science seeks to protect the health and safety of the University community. As a condition of enrollment and employment, students, faculty, and staff must comply with the current CDU COVID-19 requirements as described on the CDU COVID-19 webpage. Please visit the CDU Return to Campus website https://www.cdrewu.edu/covid-policy/ or email the Campus Nursing Office at nurseofficer@cdrewu.edu., • Ability to work effectively with a diverse community. Compensation: • $90,000 annually Position Status: • Full Time Work Location: • On-site Conditional Statement: The employment status of this position is classified as “Conditional.” Conditional employment means that the job exists contingent upon continued funding and limitations of restricted funds or, the duration of a specific program, project, grant, or contract. Since this position is funded by AIM, End Date: 07/31/2025 and R35, End Date: 04/30/2026, this position is contingent upon the continued receipt of these funds. Continuation of this position is dependent, in part, upon funding availability. Furthermore, no work may be performed after the grant end date(s) unless the position receives an extension in writing from a Dean, Division VP, or Human Resources. EEO Statement: Charles R. Drew University is committed to Equal Employment Opportunity. Applicants will be considered without regard to gender, race, age, color, religion, national origin, sexual orientation, genetic information, marital status, disability or covered veteran status. Fair Chance Statement: Charles R. Drew University of Medicine and Science will consider qualified applicants, including those with criminal histories, in a manner consistent with state and local “Fair Chance” laws.

Job Description Quality Assurance Lab Technician Recent food science grads wanted! 2nd Shift times: 11am-7:30pm 1pm-9:30pm 5pm-1:30am Job Description The Quality Assurance Lab Technician performs microbiological, chemical, and physical testing on raw materials, in-process products, environmental samples, and finished goods to ensure they meet food safety, quality, and regulatory standards. This role supports production operations by conducting laboratory analyses, documenting results accurately, and contributing to GMP, HACCP, FSMA, and SQF programs. The technician partners closely with production and other operational teams to maintain consistent product quality and support a safe, compliant food manufacturing environment. Responsibilities • Perform microbiological, chemical, and physical testing on raw materials, in-process products, environmental samples, and finished products in accordance with established procedures., • Collect and prepare samples following defined sampling plans and protocols., • Accurately document laboratory results, maintain testing records, and ensure all data is complete and traceable., • Verify product specifications, including pH, viscosity, temperature, weight, and other quality parameters, and report any deviations promptly., • Conduct environmental monitoring and sanitation verification activities, including swabbing and ATP testing., • Support product hold and release decisions by providing timely and accurate test results., • Calibrate, operate, and maintain laboratory equipment to ensure reliable performance and accurate measurements., • Perform line inspections on the production floor and verify compliance with food safety and quality standards., • Complete GMP-compliant documentation and records in accordance with regulatory and company requirements., • Participate in investigations, root cause analysis, and corrective and preventive action (CAPA) activities to resolve quality and food safety issues., • Support internal and external audits and regulatory inspections by providing documentation, test results, and process explanations as needed., • Contribute to the maintenance and continuous improvement of HACCP, SQF, FSMA, and GMP programs., • Collaborate with production, sanitation, maintenance, warehouse, and other cross-functional teams to ensure consistent product quality and food safety., • Assist with sensory testing, allergen and pathogen testing, and other specialized analyses as required., • Perform routine tasks such as glassware washing and general lab housekeeping to maintain a clean, organized, and safe laboratory environment. Essential Skills • Science-based degree or 13 years of experience in quality assurance, laboratory, or food manufacturing., • Experience performing laboratory testing and documenting data accurately., • Understanding of Good Manufacturing Practices (GMPs) and food safety requirements., • Ability to interpret product specifications, test methods, and standard operating procedures., • Strong attention to detail and commitment to precise documentation., • Basic computer proficiency and data entry experience for recording and managing test results., • Effective communication skills with the ability to work collaboratively across departments., • Foundational knowledge in biology, food science, microbiology, or chemistry relevant to food manufacturing., • Ability to perform and interpret tests related to pH, viscosity, and other analytical parameters. Additional Skills & Qualifications • Associates or Bachelors degree in Food Science, Microbiology, Chemistry, Biology, or a related scientific discipline., • Experience in dairy manufacturing or broader food manufacturing environments., • Familiarity with SQF, HACCP, FSMA, and sanitation programs within a food facility., • Experience supporting audits, investigations, and corrective action processes., • Hands-on experience with microbiological techniques, swabbing, ATP testing, and environmental monitoring., • Exposure to quality assurance and quality control (QA/QC) practices in a laboratory or production setting., • Experience with sensory testing, allergen testing, and pathogen testing., • Ability to work in a fast-paced, growing company with a long-term mindset and interest in career development., • Openness to learning and developing expertise in analytical testing and food safety systems., • Recent graduates with science degrees who are eager to build a long-term career in food quality and safety are encouraged to apply. Work Environment This role is based in a laboratory environment attached to a food manufacturing facility, providing direct exposure to production operations and product development activities. Occasional overtime may be required on Saturdays based on production and testing needs. The work involves routine use of laboratory instruments and equipment for microbiological, chemical, and physical testing, as well as time spent on the production floor conducting line inspections and environmental monitoring. The environment is stable and growth-oriented, with opportunities for advancement, overtime, and company-paid healthcare benefits. Job Type & Location This is a Permanent position based out of Sun Valley, CA. Pay and Benefits The pay range for this position is $47840.00 - $54080.00/yr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors. company paid medical for the employee. yearly raises. opportunity for growth Job Type & Location This is a Permanent position based out of Sun Valley, CA. Application Deadline This position is anticipated to close on Nov 17, 2026. Workplace Type This is a fully onsite position in Sun Valley,CA. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options. San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records. Massachusetts Lie Detector: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability. Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.

Job DescriptionDescription: Position Summary The Staff Physician works with the Center Leadership Team at assigned Center, and under the direction of the Chief Medical Officer directs the Center's medical policies and programs ensuring the delivery of affordable, efficient, responsible, and accountable occupational healthcare of the highest quality to business, industry and patients in accordance with Agile’s policies, practices and procedures. Schedule: Monday through Friday, 8:00 AM to 5:00 PM Compensation: Starting compensation range is $250,000.00-$300,000.00 annually. Exact compensation may vary based on skills, experience, and location. Responsibilities • Spends 100% of time in a center providing direct patient care, leading by example, enhancing processes and procedures to minimize visit times, and creating an exceptional patient experience, • Ensures day-to-day execution as the Primary Treating Physician (PTP) for all injuries collaborating with therapists and specialists to drive optimal clinical outcomes and expedite case closure, • Manages clinicians and support staff and complies with all supervisory physician requirements for PA/NPs, • Creates a professional and collaborative working environment with full colleague participation that promotes teamwork, quality, exceptional outcomes, and patient safety, • Works with medical leadership to identify and implement changes to ensure continuous clinical improvement and efficiency, • Masters use of clinical systems to ensure efficiency, excellent supportive documentation, appropriate and optimal coding levels, charge capture, and follow through on all patient care orders, • Ensures compliance with individual State Practice Act/Rules and Regulations/WC Regulations, • Calls and communicates to employers on all new injuries and other significant clinical changes, • Actively participates in team meetings with Center Manager and Center Therapist to improve quality, patient safety, case management, and ensures the ongoing development and growth of the center's business, • Maintains and cultivates relationships with center clients and payers while responding to requests within 24 hours, • Works with medical and clinical leadership to manage clinical and support staffing levels and proficiencies that will optimize patient satisfaction, workflows, and efficiencies, • Develops and supports colleague success through all aspects of the talent life cycle for staff clinicians and support staff within the center, • Fosters an environment of collaboration, professionalism, patient/colleague safety, quality care, continuous improvement and reward and recognition, • Promotes center initiatives and workflows that are consistent with those in other centers, • Possesses financial awareness and provides input to center budget and key business metrics, • This job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job. Duties, responsibilities, and activities may change at any time with or without notice.Requirements: Education/Credentials • Doctor of Medicine (M.D.) or Doctor of Osteopathic Medicine (D.O.) degree from an accredited medical school., • Current, unrestricted California medical license (or license in progress), • Board certification or board eligibility preferred., • Active DEA registration required., • Current BLS, AED, and ACLS certifications required., • NRCME (DOT Medical Examiner) certification required, or ability to obtain within 30 days of hire. Job-Related Skills/Competencies • Ability to make decisions or solve problems by using logic to identify key facts, explore alternatives, and propose quality solutions, • Outstanding customer service skills with tact and professionalism, • Ability to handle sensitive and confidential information (HIPAA/PHI) in compliance with federal, state, and company policies, • Knowledge of occupational medicine requirements and clinical operations, including OSHA and DOT standards, • Solid foundation in medicine, biology, chemistry, systems evaluation, and human behavior, • Customer and personal service knowledge including needs assessment, meeting quality standards for services and evaluation of customer satisfaction, • Critical thinking, judgment, and effective communication skills, • Skilled in diagnosing and treating human injuries, with understanding of professional practice standards, • Leadership, supervision, and staff development abilities, • Promotes a cooperative, team-oriented environment and fosters high morale, • Patient-focused with a professional, approachable demeanor, • Commitment to Agile’s core practices, policies, and procedures, • Willingness to learn and continuously improve, to be audited, observed, and reviewed; is positively responsive to feedback, • Basic computer skills; experience with electronic medical records preferred, • Ability to coach, instruct, and mentor team members Benefits • Comprehensive benefits package, including medical, dental, vision, life, and disability insurance, • 401(k) plan with employer match, • Annual CME stipend with dedicated paid CME time off, • Employer-paid medical malpractice insurance, • Paid time off and company-paid holidays, • Excellent work-life balance - no required nights, weekends, or holidays, • Collaborative, fast-paced and dynamic work environment, • Opportunity to make a meaningful impact on patient care and clinic performance Why You Should Join Our Team Agile Occupational Medicine is a leading occupational medicine group with a network of 42 centers dedicated to providing comprehensive healthcare services to businesses and their employees across California and Yuma, Arizona. We specialize in ensuring the health and well-being of workers through a range of medical services, including work injury care and employer services. We are a rapidly growing organization with a fun and collaborative work environment. We are passionate about disrupting the world of occupational medicine, and we are committed to providing our customers and patients with the best possible experience. Agile Occupational Medicine is an Equal Opportunity Employer. Agile does not discriminate on the basis of race, religion, color, sex, gender identity, sexual orientation, age, non-disqualifying physical or mental disability, national origin, veteran status or any other basis covered by appropriate law. All employment is decided upon qualifications, merit, and business need.

Job Description We are seeking a Care Manger - CA to join our team at Independent Living Systems (ILS). ILS, along with its affiliated health plans known as Florida Community Care and Florida Complete Care, is committed to promoting a higher quality of life and maximizing independence for all vulnerable populations. About the Role: The Care Manager in California plays a pivotal role in coordinating and managing comprehensive care plans for individuals requiring health and social support services. This position ensures that members receive personalized, effective, and timely care by collaborating with healthcare providers, social workers, and family members. The Care Manager acts as a liaison to facilitate communication among all parties involved, advocating for the client’s needs and preferences. They monitor client progress, adjust care plans as necessary, and ensure compliance with regulatory standards and organizational policies. Ultimately, the role aims to improve client outcomes, enhance quality of life, and optimize resource utilization within the care continuum. Minimum Qualifications: • Bachelor’s degree in social work, Psychology, Biology, Public Health, Nursing, Community Health, or Health related field or equivalent experience required., • Requires at least 5 years of experience working with people who need assistance with complex health and social issues., • Requires knowledge of and experience working with community agencies and programs., • Requires experience with Medi-Cal eligibility guidelines, application, and renewal/redetermination process., • Requires strong problem-solving and customer service skills., • Must be a CA Resident and must reside in CA while employed., • Current and valid California (CA) Driver’s License., • Must use personal vehicle and current vehicle registration required., • Proof of auto insurance required, must maintain CA minimum insurance coverage., • BCLS CPR Certification required. Preferred Qualifications: • Master’s degree in Nursing, Social Work, Public Health, or Healthcare Administration., • Certified Case Manager (CCM) credential or equivalent certification., • Experience working with diverse populations including elderly, disabled, or chronically ill clients., • Bilingual abilities, particularly in Spanish or other commonly spoken languages in California. Responsibilities: • Develop and manage Individualized Care Plans for members in assigned caseload and provide consistent and effective care coordination as indicated by the Care Plan., • Assess psychosocial and social determinants of health needs for high-risk members and document assessment results or augment available information in appropriate systems, • Consult with or refer members to licensed staff (social worker, nurse case manager etc.) as required based on member social, health risk and medical complexity., • Establish relationships and partner with community resources, health plans and providers by participating in community engagement activities with local agencies e.g. faith-based organizations, community centers, government agencies, parks, recreation centers and schools, • Assist members with problem solving barriers to high complexity health conditions by identifying, locating, connecting to and navigating needed community and medical system services, including visiting members at their homes, accompanying members to medical appointments and assisting members with completing forms to access needed services, • Actively engage, build rapport, establish trusting relationships and facilitate collaborative communication with members and member family support systems, • Identifies social determinants of health concerns/ gaps, develops and documents a plan to address complex social and health disparities, • Documents member updates and progress notes in appropriate systems, submits timely reports, and provides recommendations for improved member outcomes tracking, • Identifies gaps in community resources and medical systems, makes recommendations to close gaps and implements new services or solutions to close identified gaps

Job Description Overview Ansible Government Solutions, LLC (Ansible) is currently recruiting Medical Technologists (Medical Laboratory Scientists, Clinical Laboratory Scientists) to support the VA Long Beach Healthcare System located at 5901 E 7th St, Long Beach, CA 90822. Services will be delivered to both the Anatomic Pathology and Clinical Pathology divisions of the facility. Exceptional compensation packages with full benefits are available. Ansible Government Solutions, LLC (Ansible) is a Service-Disabled Veteran-Owned Small Business (SDVOSB) providing Federal customers with solutions in many arenas. Our customers face wide-ranging challenges in the fields of national security, health care, and information technology. To address these challenges, we employ intelligent and committed staff who take care of our customers’ success as if it is their own. Responsibilities • Rotate on a regular basis through the areas in which they have been trained and are competent, • Perform a broad range of laboratory procedures in Chemistry, Hematology, Coagulation, Urinalysis, Microbiology, and Transfusion Medicine, • Perform advanced and complex laboratory procedures, recognizing deviation from expected results, analyzing and correcting problems using scientific principles, • Recognize and communicate pre-defined critical results affecting patient care, • Maintain the optimal functioning of laboratory equipment and keep appropriate records for documentation; operate, calibrate, identify malfunctions, repair and perform preventive maintenance of laboratory analyzers, • Perform and document quality control, quality assurance and corrective actions related to test performance using sound statistical principles and theories of performance improvement, • Enter and verify laboratory results in the computer system; recognize deviations from expected results, analyze and correct problems using scientific principles, • Perform other duties as assigned relating to the responsibilities of a Medical Technologist Qualifications • Accredited Bachelors degree in medical laboratory science, medical technology, clinical laboratory science, or a related science (i.e. biology, chemistry, etc.) AND completion of an accredited medical technology clinical practice program (i.e. NAACLS, CAAHEP, ABHES) OR • Accredited Bachelors degree including 16 semester hours in biological science (one course in microbiology), 16 semester hours in chemistry (one course in organic or biochemistry), and one course in mathematics AND two (2) years of post-certification clinical laboratory experience within the last ten (10) years as a certified Medical Laboratory Technician (ASCP-BOC), • A minimum of one (1) year of Medical Technologist experience within the last three (3) years, • Demonstrated knowledge of laboratory medicine techniques and practices, • Demonstrated education and clinical training in the practice of laboratory medicine Pay Range: $28.97 - $62.40 hourly All candidates must be able to: • Sit, stand, walk, lift, squat, bend, twist, and reach above shoulders during the work shift, • Lift up to 50 lbs from floor to waist, • Lift up to 20 lbs, • Carry up to 40 lbs a reasonable distance, • Push/pull with 30 lbs of force All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran. Powered by JazzHR QqAWu62lWN

Job Description About California Custom Fruits and Flavors Founded in 1986, California Custom Fruits & Flavors (“CCFF”) is a leading developer and manufacturer of custom-formulated specialty ingredients & flavors. CCFF develops tailored solutions for its diverse customer base of brands, retailers, and co-manufacturers across numerous food products and channels. With world-class facilities in California and Indiana, CCFF has served as a leading partner and innovator of industry-leading flavors and formulations for nearly four decades. CCFF is backed by Peak Rock Capital, a leading middle-market private investment firm that makes equity and debt investments in companies in North America and Europe. Peak Rock's equity investment platform focuses on opportunities where it can support senior management to drive rapid growth and performance improvement, with expertise in corporate carve-outs and partnering with families and founders seeking first-time institutional capital. About the role: Looking for a full-time and driven candidate, preferably with flavor compounding experience. Assist Flavor Chemist with new and existing flavor projects. Responsibilities: • Accurately weigh and compound keys and flavors according to the formulas, • Maintaining, organizing, cleaning and stocking supplies in the flavor lab and flavor library, • Generating and maintaining documentation; product specifications, nutritionals, safety data sheets, etc., • Assist Flavor Chemist with receiving, setting up flavoring ingredients for evaluation., • Participate in organoleptic evaluations of flavors in application and in finished product., • Prepare samples for customers, including packing and shipping, • Follow all safety policies, food safety standards and procedures, • Developing knowledge of aroma chemicals, essential oils, and other flavor ingredients Candidate Requirements: • Bachelor of Science degree; Food Science, Chemistry, Biology or related scientific discipline required and/or at least three-year prior workplace laboratory experience, • Ability to use sensory skills (taste and smell) for evaluation, • Excellent verbal and written communication skills with ability to collaborate with R&D, Sales, Purchasing, Quality Assurance and other cross-functional teams, • Strong organization and problem-solving skills, • Ability to multitask while maintaining excellent attention to detail and accuracy, • Proficiency with Microsoft Office and perform other duties as assigned, • Complete projects in a timely manner Why Join Us: • Be part of a mission-driven food company focused on quality and innovation, • Competitive salary, benefits, and opportunities for career growth, • Supportive and collaborative work culture, • Commitment to sustainability, food safety, and ethical sourcing Equal Employment Opportunity All candidates are subject to a criminal background check and standard drug screen. All offers are contingent upon favorable results. California Custom Fruits and Flavors is committed to recruiting, selecting, and developing employees based on individual ability and job performance. \nCompany Description About California Custom Fruits and Flavors Founded in 1986, California Custom Fruits & Flavors (“CCFF”) is a leading developer and manufacturer of custom-formulated specialty ingredients & flavors. CCFF develops tailored solutions for its diverse customer base of brands, retailers, and co-manufacturers across numerous food products and channels. With world-class facilities in California and Indiana, CCFF has served as a leading partner and innovator of industry-leading flavors and formulations for nearly four decades. CCFF is backed by Peak Rock Capital, a leading middle-market private investment firm that makes equity and debt investments in companies in North America and Europe. Peak Rock's equity investment platform focuses on opportunities where it can support senior management to drive rapid growth and performance improvement, with expertise in corporate carve-outs and partnering with families and founders seeking first-time institutional capital. About California Custom Fruits and Flavors\nFounded in 1986, California Custom Fruits & Flavors (“CCFF”) is a leading developer and manufacturer of custom-formulated specialty ingredients & flavors. CCFF develops tailored solutions for its diverse customer base of brands, retailers, and co-manufacturers across numerous food products and channels. With world-class facilities in California and Indiana, CCFF has served as a leading partner and innovator of industry-leading flavors and formulations for nearly four decades.\n\nCCFF is backed by Peak Rock Capital, a leading middle-market private investment firm that makes equity and debt investments in companies in North America and Europe. Peak Rock's equity investment platform focuses on opportunities where it can support senior management to drive rapid growth and performance improvement, with expertise in corporate carve-outs and partnering with families and founders seeking first-time institutional capital.\n

Job Description Summary The Sr. Quality Control Specialist works under the general direction of Head of Quality as the lead for Quality Control laboratory. The primary responsibilities are: timely disposition of Raw Materials, In-Process and Customer Supplied Bulks and efficient operation of Quality Control laboratory. Hours would be : 2pm to 10:30pm M-F onsite. This is a temporary position up to end of November. Position is location in El Segundo, CA Essential Responsibilities Help Develop, implement and maintain QC systems and measures • Inspect and test Raw Materials, Fragrances, In-Process and Customer supplied bulk, against specification to ensure quality standards are met., • Establish priorities to ensure timely job completion., • Issue adjustments to In-Process Bulk if necessary, • Complete Inspections forms for Finished Bulk/Intermediate and /or Raw Materials and Fragrances., • Update status of Raw Materials and /or Bulk/Intermediate in ERP system, • Communicate quality control information to all relevant organizational departments, outside vendors or contractors, • Produce and communicate reports regarding nonconformance of products, • Assist in investigations related to Nonconformance or OOS, Customer Complaint, • Provide Department related data, trends etc. for Management Review, • Resolve production and manufacturing problems to minimize cost and delay, • Maintain the raw material retains for the Department, • Maintain all Quality Systems logs related to the Department, • Monitor Performance of QC systems to ensure effectiveness, efficiency and compliance to company SOPs and regulatory requirements, • Assist in updating or writing Department related SOPs and Work Instructions or other Department related documents., • Review statistical studies, technological advances or regulatory standards and trends to stay abreast of issues in the field of quality control, • Identify and implement training needs for the production team to meet quality standards, • Instruct staff in QC and analytical procedures, • Assist in Raw Materials and Bulk /Intermediate Cycle Counts and Full Inventories, • Consistently demonstrates excellent interpersonal skills and professionalism to company management, all levels of staff and vendors and outside agencies Qualifications To perform this job successfully, an individual must be able to perform each essential responsibility satisfactorily using the skills and abilities outlined in this job description. The requirements listed below are representative of the knowledge, skills and/or abilities required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions • Discretion in handling confidential and sensitive matters, • Knowledge of drug cGMPs, SOPs and regulatory guidelines including FDA requirements Education, Experience and Licensure • Bachelor’s degree in science (chemistry, pharmacy, or biology) or equivalent work experience., • 5+ years Quality Control related experience in a cGMP OTC manufacturing environment. Skills • Proficient use of Microsoft Office products including Word, Excel, Outlook and PowerPoint., • Experience using common laboratory equipment such as pH Meter; Refractive Index; Pycnometer; Brookfield Viscometer; Color Matching; Scales; and lab mixers, • Must be able to clearly and concisely communicate verbally and in writing in English, • Ability to speak and understand Spanish is a plus, • Must be able to analyze and present quantitative data., • Able to accurately compute basic mathematical equations such as addition, subtraction, division, multiplication and percentages Reasoning Ability Must be able to analyze and interpret data relating to various projects and resolve issues and problems that arise including: • Resolve issues of a general, routine and complex nature and exercise appropriate judgment to escalate issues to senior management., • Effectively prioritize routine and non-routine work assignments to ensure goals and timelines are met., • Apply knowledge of Quality Control best practices, cGMPs, regulations, and Company policies to problems and provide appropriate resolution. Physical Demands and Work Environment The physical demands and work environment described here are representative of those an employee encounters while performing the essential functions of this job. • Must have good visual/organoleptic alertness., • Must be able to sit for up to eight hours per day, lift and carry up to 20 lbs with or without assistance, reach above shoulder height, bend, stoop, and crawl to retrieve items from under a desk or floor level cabinet or drawer; push and pull, use a computer keyboard throughout the workday, stand while filing or performing other essential responsibilities., • Exposure to standard chemicals used in an office environment is expected and includes but is not limited to toner, glue and liquid paper or white out. Additionally, the incumbent will be exposed to chemicals used in the manufacturing process of nutritional supplements, cosmetics, and prescription drugs., • Must have reliable transportation and valid driver’s license and be able to drive to appointments. Must maintain current, in-force vehicle insurance. Local candidates only. No Recruiters please.

Job DescriptionBenefits: • 401(k), • Competitive salary, • Opportunity for advancement Job Description Hello! We are Premier Academy Walnut, a tutoring center committed to providing students with an enriching, well-rounded experience to help them achieve their academic goals. As we continue to grow, we are looking for passionate and dedicated individuals to join our team and contribute to our mission. Expectations As a private AP Chemistry & Physics tutor, you are expected to be proficient in the core concepts and exam formats of both subjects, including: • Cell structure and function, cellular energetics, genetics and information transfer, natural selection and evolution, ecology, and biological systems interactions., • AP Chemistry: atomic structure, chemical bonding, stoichiometry, thermodynamics, kinetics, equilibrium, and lab-based problem solving, • AP Physics (1 & 2 or C): mechanics, electricity and magnetism, waves, and data analysis aligned with College Board requirements, • AP Biology: You should also be familiar with AP Biology lab investigations, data analysis, and free-response question strategies, as outlined by the College Board curriculum framework., • AP Environmental Science: Key topics such as ecosystems, biodiversity, population dynamics, earth systems, resource use, pollution, and climate change What We’re Looking For in a Teacher: • Demonstrates strong work ethic: well-organized, well-prepared, and punctual., • Ability to develop and implement engaging lesson plans., • Adaptability in teaching methods to meet the diverse needs of learners., • Ability to build meaningful relationships and mentor students effectively., • Long-term commitment (for the full school year or summer session)., • Flexible availability to accommodate students’ schedules, with coordination around your availability., • At least 2+ years of teaching or tutoring experience., • Bachelor’s degree or higher in a relevant field., • Bonus Qualifications:, • CBEST certification or a primary/secondary teaching credential., • Experience with the Walnut Valley Unified School District (WVUSD).Responsibilities, • Provide 1:1 instruction (maximum of 1:3 students, though most sessions will be 1:1)., • Develop and implement customized lesson plans, tailored to individual students’ needs., • Assign and review homework and quizzes as appropriate., • Keep detailed records of tutoring sessions using Premier-provided forms., • Motivate students by setting clear expectations, conducting progress checks, and offering regular feedback., • Submit periodic progress reports for each student., • Collaborate with the Campus Director to address and improve students’ academic progress.Support from Our Team: Our Front Office team will handle parent communication and scheduling, allowing you to focus on teaching and supporting your students! Position Type: Part-time • typically 2–30 hours per week, depending on tutor’s availabilityHow to apply: please complete our application at premieracademywalnut.com/join-our-team Flexible work from home options available.

Job DescriptionJob Details: • Position: Brain Bank Technician (FT) Laboratory Skills Required., • Brain Bank Technician with Biological laboratory bench work., • This job is ONSITE in Los Angeles. Remote work is not available for this position., • Biological laboratory bench work. Knowledge of medical terminology., • RESUMES MUST CONTAIN YOUR NAME AND BE SUBMITTED AS A PDF FILE. Summary: • The Brain Bank Technician under the direction of the Bank Director helps in Brain Bank biological laboratory work., • General duties include but are not limited to the following and more detailed specific directions, prioritization and updates are provided on a regular basis., • This position requires rotating on-call responsibilities as needed, including nights, weekends, and holidays. Essential Duties And Responsibilities include any combination of the following. Other duties may be assigned: • Be flexible to accommodate special projects that come up regularly and are related to the work., • Set up, operate, adjust, calibrate, troubleshoot, and maintain laboratory instruments and equipment., • Participate in conducting a battery of laboratory analyses utilizing standard lab methods, on human specimens., • Isolate, dissect, and prepare specimens for standardized quality assessment/assurance., • Participate in conducting and monitoring molecular biology experiments, make observations, and calculate and record operational data and complete results to submit for discussions., • Assist in banking human specimens while working with the donor coordinator for timely processing and preservation of incoming all brain/spinal cord tissue and fluid specimens., • Participate in on-call rotating schedule duty without schedule restrictions. This includes evenings, weekends and after-hours receiving and preservation of incoming brain/spinal cord tissue and fluid specimens., • Assist in a timely shipment of prepared quality assessment/assurance tested banked specimens to the requesting researchers., • Participate in the research and development scientific processes of the Brain Bank., • Use computers, computer-interfaced equipment, robotics or high-throughput equipment and computer applications to perform work duties. Qualifications: • To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform essential functions., • Strong database entry skills to accurately enter detailed medical and social history and lab notes., • Excellent knowledge of word processing tools and spreadsheets (MS Office Word, Excel etc.)., • Excellent interpersonal, written/oral communication and organizational skills., • Ability to work independently as well as part of a team., • Ability to design experiments and troubleshoot technical hurdles independently., • Typically, such skills are the result of a combination of education (e.g., courses in Biology, Molecular Biology, Biochemistry, or related Biological Science area, medical terminology, personal computer operations) and working experience in a research laboratory., • The incumbent must be able to perform this job safely, without endangering the health or safety of him/herself or others. Education and/or Experience: • Bachelor’s Degree., • Biological laboratory bench work. Knowledge of medical terminology is desirable. Language Skills: • Superior command of writing, proofreading, and communicating in the English language. Mathematical Skills: • Ability to calculate figures and amounts such as discounts, interest, proportions, percentages, area, etc. Ability to apply concepts of business mathematics and statistical analysis. Reasoning Ability: • Ability to deal with problems involving multiple variables in non-standard situations. Physical Demands: • 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., • Reasonable accommodations may be made to enable individuals with disabilities to perform essential functions., • While performing the duties of this job, the employee is frequently required to sit; use hands; and talk or hear., • The employee is occasionally required to stand and walk., • The employee must occasionally lift and/or move up to 10 pounds., • Specific vision abilities required by this job include close vision, color vision, and the ability to adjust focus. Work Environment: • The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job., • Reasonable accommodations may be made to enable individuals with disabilities to perform essential functions., • While performing the duties of this job, the employee is occasionally exposed to moving mechanical parts such as the case of using a paper shredder, copier, or other standard office equipment that contains said parts., • The noise level in the work environment is usually moderate.

Job Description Aptask Global Workforce (AGW) is seeking a Research Scientist for a Hybrid position with a Global Biotechnology Company located in Santa Monica, CA. This is a 12+ month contract opportunity. The Research Scientist will support biomarker and translational strategy for the clinical development of chimeric antigen receptor (CAR-T) programs in Multiple Myeloma. As a member of the Translational Medicine team, you will be at the intersection of Research and Clinical Development, providing valuable insight into the function of CAR-T cells in patients and the development of potential prognostic tools. Regulatory filing experience and a demonstrated ability to facilitate clinical trial execution, synthesize scientific data, and communicate key findings cross-functionally is required. Responsibilities: • Directs and establishes pharmacokinetic and pharmacodynamic (PK/PD) analysis to support clinical pharmacology for CAR T clinical trials in Multiple Myeloma, • Serves as Biomarker lead on clinical study teams to oversee delivery of pharmacology data and documentation required for pivotal and registrational study filings, • Reviews and contributes to clinical protocol design and study activities, • Identify and establish agreements with contract research organizations (CRO) and support the transfer of established methods, • Collaborates with Clinical development teams including Clinical Operations, Regulatory, Clinical Data Management and Biometrics/Stats to advance data acquisition and analyses of clinical trial data, • Leads the resolution of clinical pharmacology/translational queries from regulatory agencies, supports writing and reviewing responses to regulatory queries, • Support the preparation of data packages for publication with medical writers, presentation and/or submission to regulatory agencies, • Collaborates with Translational Medicine, Bioinformatics and Statistical teams for exploratory biomarker correlative studies and deeper analysis of tumor biology and CAR T functionality, • Contribute to external scientific discussions/research collaborations and publications and engagement with key opinion leaders in the field Requirements: • Advanced scientific degree (i.e. MD, PharmD, PhD) and 3+ years in industry OR Master's Degree and 5+ years of scientific experience OR Bachelor's Degree and 7+ years of scientific experience, • Strong background in cancer immunotherapy, immunology and/or oncology with experience focusing on Multiple Myeloma, • Prior experience in Regulatory filings, • In-depth understanding of multiple myeloma, knowledge of clinical landscape, evolving therapy, competitive scenarios, • Strong understanding of clinical, translational, and mechanistic data, • Familiarity and experience with clinical and biomarker operations, • Understanding of early or late-stage drug and translational development process; including clinical trial experience in industry or academia, • Familiarity with bioanalytical assay development and validation in a GxP environment, • Experience working with engineered T cells, immunophenotyping, and NGS-based approaches to profile the function of tumor and immune cells, • Comfortable in a matrixed and fast-paced company environment and able to adapt to changing priorities, • Strong collaboration, excellent interpersonal and communication skills, • Proficient with data presentations to communicate to a diverse cross-functional audience, • Maintain a high degree of accuracy and attention to detail, • Ph.D. degree in biology-related field (immunology, cancer biology, bioinformatics or a closely related field) Pay range: up to $47.35 per hour Only candidates available and ready to work directly as Aptask Global Workforce (AGW) employees will be considered for this position. If you have the described qualifications and are interested in this exciting opportunity, apply today! Aptask Global Workforce (AGW) ApTask Global Workforce (AGW) is a certified Minority and Veteran workforce solutions company. AGW delivers operational, clinical, lab and professional talent with a strong focus on healthcare and life sciences. The company supports clients with reliable staffing, program expertise and a commitment to quality, speed and consistent delivery. Benefits of working with ApTask Global Workforce include: • Medical, • Dental, • Vision, • Sick Pay (for applicable states/municipalities) Our team stays close to the process and is here to guide you every step of the way. To learn more, please visit our website https://www.agwtalent.com/. ApTask Global Workforce is an Equal Opportunity Employer. Candidates will receive consideration without regard to their race, color, religion, sex, sexual orientation, gender identity, national origin, disability or status as a protected veteran.

Job DescriptionDescription: AVITA Medical® is a therapeutic acute wound care company focused on transforming how patients heal. We develop and deliver innovative technologies that harness the body’s own healing capabilities to accelerate recovery and improve clinical outcomes. Our flagship technology, RECELL®, uses a patient’s own skin to create Spray-On Skin™ at the point of care, enabling faster healing for patients with serious wounds, including burns and trauma. In the U.S., we also bring forward advanced wound care solutions such as Cohealyx® and PermeaDerm®, expanding our ability to support clinicians across the continuum of care. At AVITA Medical, we are united by a shared purpose: to help patients heal faster - and to make a meaningful difference when it matters most. Position Summary: The Medical Science Liaison (MSL) is a key contributor to the company’s clinical and commercial development with responsibility for establishing, developing, and maintaining relationships with prominent experts in the therapeutic areas where AVITA Medical skin regeneration products are sold. This role works with customers, internal stakeholders, and outside vendors on clinical research in support of pre-market and post-market initiatives. Additionally, the MSL will provide the latest emerging data in response to healthcare professional inquiries, as well as interpret and translate dense clinical and scientific information into engaging, persuasive messages. Key Responsibilities: • Build Awareness of AVITA Medical skin regeneration products in key accounts across the acute wound division which includes burns and soft tissue reconstruction., • Attendance at key conferences (burns, trauma, plastics) focusing on gathering competitive information as well as other information with implications for clinical development of AVITA Medical products., • Proactively identifies and engages with upcoming and established key opinion leaders in the acute wound space., • Promotion of conference abstract submission and content development in support of conference podium and poster presentations., • Contributor to publication planning and journal manuscript submissions., • Establish and maintain relationships with key opinion leaders to facilitate the execution of clinical studies., • Engagement with heath care professionals and review of investigator-initiated research protocols and results., • Support commercial team with translation of clinical and scientific information into marketing and education tools., • Assist with the review and approval of customer facing materials., • Provide sales training and field activity support as needed (customer meetings, device training, and case coverage)., • Assist with development of company sponsored clinical study protocols in alignment with demonstration of key product benefits as well as pre-clinical studies., • Responsible for customer inquiries and network for peer-to-peer communication., • Support the translation of VOC into medically relevant product design specifications as well as usability testing., • Stay abreast of current scientific trends, opinions of company data, and competitor products., • Drive departmental project prioritization, time and workload management activities.Requirements:, • Advanced degree in medical field, life sciences, or public health preferred., • 2+ years in clinical education, clinical research, MSL, or medical affairs position., • Medical writing (study protocols, abstracts, posters, and manuscripts)., • Experience in management of acute wounds (burn injuries/soft tissue injuries) preferred., • Up to 50% of travel time may be required. Special Knowledge/Skills: • Understanding of clinical research and GCP., • Familiarity with skin cell biology and pre-clinical models of wound healing., • Excellent written and oral communication skills., • Advanced knowledge of Microsoft word, PowerPoint, and Excel., • Knowledge of aseptic techniques, bloodborne pathogens, and operating room etiquette., • Ability to work independently and as a member of a team., • Capable of managing multiple projects simultaneously.

Job Description Nova Biomedical: One Global Brand. One Vision. Together under one name. Advanced Instruments and Nova Biomedical are now united under one brand, Nova Biomedical, marking a major milestone in our journey to deliver greater value to our customers. By combining our strengths, we're accelerating innovation, supporting critical workflows, and delivering world-class service across the biopharmaceutical and clinical markets. Job Summary: The Clinical Applications Specialist provides post-sales training, validation, and support related to the implementation and ongoing use of Nova Point-of-Care monitors, as well as Nova Blood Gas and Critical Care analyzers, to ensure customers achieve optimal use of these technologies. Responsibilities: • Performs on-site application studies for Nova POC and HBTA products, including StatStrip, StatSensor, Prime, products., • Conducts on-site application activities, including correlation to alternative reference methods, precision studies, linearity studies, and customer training., • Works with new customers after the sale to streamline validation requirements for Nova products and support a successful, smooth transition to Nova technology., • Reviews and prepares data outputs and presents performance data obtained during on-site or remotely supported application studies to current customers, as appropriate., • Demonstrates the ability to understand and educate end users on instrument use and application-related issues, and to perform data analysis in support of Clinical Applications department objectives., • Manages customer calls that are escalated to the Clinical Applications group from the Technical Support Hotline., • Timely, detailed documentation of all onsite activities and callbacks within Nova’s CRM system., • Maintains data files for all linearity, precision, and correlation data per department policy., • Serves as a resource to field support peers., • Must be willing to travel within or outside the assigned territory approximately 50% to 75% of the time by car, air and/or train, including overnight stays. Must be able to travel on short notice., • Valid United States driver’s license required. Experience Requirements: • Bachelor’s or Associate degree in Medical Technology required. Degrees in Biology, Chemistry, or Biochemistry may also be considered with relevant clinical laboratory experience., • 2+ years of medical diagnostic industry or hospital related experience., • Clinical laboratory bench experience and/or point-of-care testing experience is strongly preferred., • Experience with beside glucose and blood gas systems is preferred., • A solid understanding of statistical data is required., • Proficiency with Microsoft Excel is required., • Communication and Training Skills., • Strong presentation and telephone communication skills are required., • Excellent communication, teaching, and interpersonal skills are required. Physical Requirements and Working Conditions: • Willingness to travel as required (including air and ground transportation)., • Valid driver’s license and ability to safely operate a motor vehicle as needed for job responsibilities., • Able to store, transport materials, samples, or demonstration equipment (up to ~25 pounds)., • Comfort with standing and engaging with customers for extended periods., • Ability to adapt to varying work environments (e.g., customer sites, laboratories, offices). Why Work for Nova Biomedical • Flexible Medical, Dental, & Vision Coverage, • Competitive 401k company match, • Bonus Program, Generous PTO and paid holidays, • Generous Tuition reimbursement, • Hybrid and flexible work arrangements, • Professional development, engagement and events, • Company marketplace for lunch and snacks in our Norwood, MA, Billerica, MA and Westbrook, ME offices, • Company subsidized cafeteria in our Waltham, MA office Work Location: Field (Los Angeles, CA) Targeted Salary Range: $95,000 - $100,000 a year Nova Biomedical believes in transparency and integrity throughout all we do, including compensation. The provided salary range for this role represents the expected base salary or hourly rate for this opening. Actual compensation will be commensurate with the candidate’s experience and may vary based on individual factors such as location, skills, and education. About the Company At Nova Biomedical, we’re not just building instruments, we’re powering breakthroughs that improve lives. Our smart, science-driven solutions are trusted in over 100 countries to speed drug development and enhance patient care. Our integration brings together more than 70 years of scientific excellence with Nova’s cutting-edge innovation, forming a powerhouse of precision, purpose, and possibility. With FDA-registered, ISO-certified manufacturing, more than 125 FDA approvals, and industry-trusted diagnostics, we’re setting new standards in quality and reliability. Nova Biomedical is proud to be a global leader in osmolality testing and biotechnology and in vitro diagnostic (IVD) instrumentation, dedicated to advancing patient care and scientific discovery with a legacy that continues to shape the future of life sciences. With headquarters in Norwood and Waltham, Massachusetts, and a global team of nearly 2,000 employees, we’re building a collaborative, empowered culture grounded in shared values: Customer Centricity, Ingenuity, Ownership & Accountability, Collaboration, and Integrity. Working at Nova Biomedical means joining a mission-driven organization where your contributions matter. Whether you're in engineering, science, manufacturing, or support, you’ll be part of a team that values innovation, invests in your growth, and is committed to making a real-world impact on global health. Explore what’s next with us at novabiomedical.com EEO Statement: Nova Biomedical takes pride in being an equal opportunity employer committed to hiring a diverse and inclusive workforce. As a part of our commitment to a diverse and inclusive workforce, Nova Biomedical will continue to take steps to assure that recruitment, hiring, assignment, promotion, compensation, and all other personnel decisions are made and administered without regard to race, religion, color, national origin, citizenship, sex, sexual orientation, gender identity, gender expression, veteran status, age, mental or physical disability, genetic information or any other protected class. Privacy Policy https://www.novabiomedical.com/privacy-policy/

Job Description Job Title: Biologist Location: Pasadena, CA Work Model: Onsite Hours: M-F 8am-5pm Compensation: $45.00 - $48.00/hr Type: 12-month contract, Potential for extension or conversion to permanent Responsibilities • As a tissue culture biologist, you will be responsible for maintaining and expanding various cell lines, performing and troubleshooting cell-based assays, and optimizing protocols., • You will work with human whole blood and primary cells, including their isolation, culture, and use in downstream assays., • You will also provide automation support and data analysis for high-throughput in-vitro assays using liquid handlers., • You will work closely with other scientists and engineers on the Protomer team to ensure and continuously improve the quality and efficiency of the tissue culture and automation processes. Requirements, • Bachelor's degree or higher in biology, biotechnology, or related field., • Experience in tissue culture with mammalian cells; at least one year preferred., • Experience in using automation platforms, such as Tecan, Hamilton, or Beckman Coulter preferred., • Proficiency in data analysis and reporting tools, such as Excel, R, or Python., • Excellent communication and teamwork skills., • Attention to detail and problem-solving skills. System One, and its subsidiaries including Joulé and Mountain Ltd., are leaders in delivering outsourced services and workforce solutions across North America. We help clients get work done more efficiently and economically, without compromising quality. System One not only serves as a valued partner for our clients, but we offer eligible employees health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan. System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law. #M- #LI- Ref: #558-Scientific

Job Description SUMMARY The marine husbandry Aquarist II (Invertebrate Focus) is responsible for the daily care and health management of all marine livestock with a focus on the invertebrate livestock in the facility. These duties include but are not limited to distributing feeds to all marine livestock, water quality sampling and testing, tank cleaning, inventory control, and recognition and treatment of diseases, making and distributing saltwater, and other husbandry-related tasks as assigned. Primary RESPONSIBILITIES & DUTIES • Remove deceased animals from the holding systems, • Water testing and data entry, • Mix and distribute chemicals, • Oversee and manage coral fragging processes, • Prepare and distribute feeds to livestock, • Clean and maintain tanks, systems, and work areas5848, • Administer treatments to maintain coral health, • Update and maintain accurate inventory records, • Prepare arrival and holding spaces for incoming shipments Secondary RESPONSIBILITIES & DUTIES • Assist livestock acclimation, freshwater husbandry, fish husbandry, packing and picking, facility maintenance teams., • Other responsibilities as assigned Qualification/Requirements • Bachelor’s degree in biology or related field or equivalent experience, • Weekend and holiday work required, • Strong verbal and written communication skills, • Working knowledge of Microsoft Office suite, • Ability to multi-task, prioritize responsibilities, work under pressure, meet deadlines and be able to thrive in a fast-paced work environment, • Knowledge of marine fishes and invertebrates required, • Fish pathology, coral husbandry, and coral propagation a plus, • Aquarium keeping, preferred (Ever kept a fish tank? Let us know!) Physical Requirements Standing for more than 7 hours per day. Able to lift 60 lbs.

Job Description Patent Prosecution Associate – AmLaw 100 Firm Locations: Various Full-Time Direct Counsel represents an AmLaw 100 firm seeking a Patent Prosecution Associate with 1–4 years of experience to join its intellectual property practice. The ideal candidate will have experience in patent prosecution, patent bar membership, and a strong technical background in the life sciences, chemistry, or related disciplines. This role involves supporting patent prosecution matters for innovative clients across biotechnology, pharmaceutical, and emerging health technology sectors. Qualifications: • 1–4 years of patent prosecution experience at a law firm, • Registration with the U.S. Patent and Trademark Office (Patent Bar required), • Advanced degree required in one of the following fields: cell or molecular biology, immunology, biochemistry, bioinformatics, bioengineering, organic chemistry, medicinal chemistry, cancer biology, pharmacology, biophysics, or digital health-related disciplines, • Prior patent agent experience preferred, • Strong academic credentials, • Excellent written, verbal, and interpersonal communication skills Compensation & Benefits The expected salary range is $225,000–$310,000, depending on experience and year classification. Discretionary merit-based bonuses may also be awarded. The firm offers a competitive benefits package, including healthcare coverage, retirement benefits, paid parental leave, wellness programs, professional development support, paid CLE and bar expenses, and additional employee benefits. Direct Counsel is conducting a confidential search for qualified candidates.

Job DescriptionDescription: About Us: We are a startup revolutionizing beauty with a purpose; create the industry standard of “clean”. Our premium skincare, makeup, and body care formulations combine uncompromising safety, efficacy and environmental responsibility. And our vision transcends products. We are committed to inspiring confident women (and others) to recognize their collective power to create meaningful change. Our innovative community-commerce ecosystem connects customers, beauty enthusiasts, and loyalists, allowing each person to align with our brand in ways that authentically reflect their values and aspirations. From our formulas to our advocacy efforts to our community connection, we lead clean. In this role you will: · Establish and develop quality control processes, protocols, and documentation standards. · Monitor and ensure compliance with all applicable state and federal regulations and Company Policies & Procedures · Implement and improve quality systems and processes. · Manage day-to-day operations of the Quality Department. · Ensure process is maintained for control of documents. Develop and maintain company change control system. · Evaluate and approve new identified suppliers through the Supplier Approval process. · Ensure that products meet the company’s standards and specifications. · Review quality control test results, documenting and distributing interpretation and feedback to relevant parties. Perform release of bulk and packaged products. · Manage and track various quality testing. · Provide support and participate in resolving customer inquiry/complaint. · Ensure adequate receipt of response for observations, deviations and non-conformances, including investigations and corrective/preventive action plans, and perform effectiveness checks and closure. · Report on key quality metrics to management. · Perform other duties as assigned by management. EXPERIENCE: · A minimum of five (5) years’ experience in Quality in a federally regulated field. · Scientific or technical discipline to perform data collection, extraction and analysis. EDUCATION: · Bachelor’s degree in Life Sciences or a related field (e.g., Chemistry, Biochemistry, Biology, or related science) SKILLS: • Proficient in digital quality tracking and reporting tools, including Microsoft office suite (including Excel, PowerPoint, and SharePoint). · Ability to work to deadlines, set priorities and manage multiple projects simultaneously without compromising quality. • Must take directions well and pay attention to detail with a high degree of accuracy., • Strong interpersonal skills for collaboration with various departments within the company., • Comfortable in both virtual and in-person settings., • Ability to travel as required for quality-related activities. Requirements:

Job DescriptionJob Title: Research Scientist, Multiple Myeloma Duration: 12 Months Location: Santa Monica, CA Hybrid Schedule: M-F 8:00-17:00 Summary The Research Scientist will support biomarker and translational strategy for the clinical development of chimeric antigen receptor (CAR-T) programs in Multiple Myeloma. As a member of the Translational Medicine team, you will be at the intersection of Research and Clinical Development, providing valuable insight into the function of CAR-T cells in patients and the development of potential prognostic tools. Regulatory filing experience and a demonstrated ability to facilitate clinical trial execution, synthesize scientific data, communicate key findings cross-functionally is required. Key Responsibilities: Directs and establishes pharmacokinetic and pharmacodynamic (PK/PD) analysis to support clinical pharmacology for CAR T clinical trials in Multiple Myeloma Serves as Biomarker lead on clinical study teams to oversee delivery of pharmacology data and documentation required for pivotal and registrational study filings Reviews and contributes to clinical protocol design and study activities Identify and establish agreements with contract research organizations (CRO) and support the transfer of novel methods Collaborates with Clinical development teams including Clinical Operations, Regulatory, Clinical Data Management and Biometrics/Stats to advance data acquisition and analyses of clinical trial data Leads the resolution of clinical pharmacology/translational queries from regulatory agencies, supports writing and reviewing responses to regulatory queries. Support the preparation of data packages for publication with medical writers, presentation and/or submission to regulatory agencies Collaborates with Translational Medicine, Bioinformatics and Statistical teams for exploratory biomarker correlative studies and deeper analysis of tumor biology and CAR T functionality Contribute to external scientific discussions/research collaborations and publications and engagement with key opinion leaders in the field Education Level Advanced scientific degree (i.e. MD, PharmD, PhD) and 3+ years in industry OR Master's Degree and 5+ years of scientific experience OR Bachelor's Degree and 7+ years of scientific experience Experience Preferred Qualifications: Strong background in cancer immunotherapy, immunology and/or oncology with experience focusing on Multiple Myeloma Prior experience in Regulatory filings In-depth understanding of multiple myeloma, knowledge of clinical landscape, evolving therapy, competitive scenarios Strong understanding of clinical, translational, and mechanistic data Familiarity and experience with clinical and biomarker operations Understanding of early or late-stage drug and translational development process; including clinical trial experience in industry or academia Familiarity with bioanalytical assay development and validation in a GxP environment Experience working with engineered T cells, immunophenotyping, and NGS-based approaches to profile the function of tumor and immune cells Comfortable in a matrixed and fast-paced company environment and able to adapt to changing priorities Strong collaboration, excellent interpersonal and communication skills Proficient with data presentations to communicate to a diverse cross-functional audience Maintain a high degree of accuracy and attention to detail Ph.D. degree in biology-related field (immunology, cancer biology, bioinformatics or a closely related field)

Job DescriptionJoin a Global Leader in Workforce Solutions – Net2Source Inc. Who We Are Net2Source Inc. isn't just another staffing company, we're a powerhouse of innovation, connecting top talent with the right opportunities. Recognized for 300% growth in the past three years, we operate in 34 countries with a global team of 5,500+. Our mission? To bridge the talent gap with precision—Right Talent. Right Time. Right Place. Right Price. Title-Research Scientist, Multiple Myeloma - Translational Medicine Location-Santa Monica,California,USA,90404 Duration- 12 months contract Location: Hybrid Schedule: M-F 8:00-17:00 Job Description • The Research Scientist will support biomarker and translational strategy for the clinical development of chimeric antigen receptor (CAR-T) programs in Multiple Myeloma., • As a member of the Translational Medicine team, you will be at the intersection of Research and Clinical Development, providing valuable insight into the function of CAR-T cells in patients and the development of potential prognostic tools., • Regulatory filing experience and a demonstrated ability to facilitate clinical trial execution, synthesize scientific data, communicate key findings cross-functionally is required.Key Responsibilities:, • Directs and establishes pharmacokinetic and pharmacodynamic (PK/PD) analysis to support clinical pharmacology for CAR T clinical trials in Multiple Myeloma, • Serves as Biomarker lead on clinical study teams to oversee delivery of pharmacology data and documentation required for pivotal and registrational study filings, • Reviews and contributes to clinical protocol design and study activities, • Identify and establish agreements with contract research organizations (CRO) and support the transfer of Client methods, • Collaborates with Clinical development teams including Clinical Operations, Regulatory, Clinical Data Management and Biometrics/Stats to advance data acquisition and analyses of clinical trial data, • Leads the resolution of clinical pharmacology/translational queries from regulatory agencies, supports writing and reviewing responses to regulatory queries., • Support the preparation of data packages for publication with medical writers, presentation and/or submission to regulatory agencies, • Collaborates with Translational Medicine, Bioinformatics and Statistical teams for exploratory biomarker correlative studies and deeper analysis of tumor biology and CAR T functionality, • Contribute to external scientific discussions/research collaborations and publications and engagement with key opinion leaders in the field Education Level • Advanced scientific degree (i.e. MD, PharmD, PhD) and 3+ years in industry OR Master's Degree and 5+ years of scientific experience OR Bachelor's Degree and 7+ years of scientific experience. Preferred Qualifications:, • Strong background in cancer immunotherapy, immunology and/or oncology with experience focusing on Multiple Myeloma, • Prior experience in Regulatory filings, • In-depth understanding of multiple myeloma, knowledge of clinical landscape, evolving therapy, competitive scenarios, • Strong understanding of clinical, translational, and mechanistic data, • Familiarity and experience with clinical and biomarker operations, • Understanding of early or late-stage drug and translational development process; including clinical trial experience in industry or academia, • Familiarity with bioanalytical assay development and validation in a GxP environment, • Experience working with engineered T cells, immunophenotyping, and NGS-based approaches to profile the function of tumor and immune cells, • Comfortable in a matrixed and fast-paced company environment and able to adapt to changing priorities, • Strong collaboration, excellent interpersonal and communication skills, • Proficient with data presentations to communicate to a diverse cross-functional audience, • Maintain a high degree of accuracy and attention to detail, • Ph.D. degree in biology-related field (immunology, cancer biology, bioinformatics or a closely related field) Why Work With Us? We believe in more than just jobs—we build careers. At Net2Source, we champion leadership at all levels, celebrate diverse perspectives, and empower you to make an impact. Think work-life balance, professional growth, and a collaborative culture where your ideas matter. Our Commitment to Inclusion & Equity Net2Source is an equal opportunity employer, dedicated to fostering a workplace where diverse talents and perspectives are valued. We make all employment decisions based on merit, ensuring a culture of respect, fairness, and opportunity for all, regardless of age, gender, ethnicity, disability, or other protected characteristics. Awards & Recognition • America's Most Honored Businesses (Top 10%), • Fastest-Growing Staffing Firm by Staffing Industry Analysts, • INC 5000 List for Eight Consecutive Years, • Top 100 by Dallas Business Journal, • Spirit of Alliance Award by Agile1

Job Description We are seeking a Housing Navigator to join our team at Independent Living Systems (ILS). ILS, along with its affiliated health plans known as Florida Community Care and Florida Complete Care, is committed to promoting a higher quality of life and maximizing independence for all vulnerable populations. About the Role: The Housing Navigator plays a critical role in connecting individuals and families experiencing housing instability with appropriate housing resources and support services within the healthcare sector. This position focuses on assessing client needs, identifying suitable housing options, and facilitating access to community resources to promote long-term housing stability and improved health outcomes. The Housing Navigator collaborates closely with healthcare providers, social service agencies, and landlords to coordinate care and ensure seamless transitions into safe and affordable housing. By providing personalized guidance and advocacy, the Housing Navigator helps reduce barriers to housing and supports clients in maintaining their housing arrangements. Ultimately, this role contributes to enhancing the overall well-being and quality of life for vulnerable populations through effective housing solutions integrated with healthcare services. Minimum Qualifications: • Bachelor’s degree in social work, Psychology, Biology, Public Health, Nursing, Community Health, or Health related field or equivalent experience required., • Requires at least 5 years of experience working with people who need assistance with complex health and social issues., • Requires knowledge of and experience working with community agencies and programs., • Requires experience with Medi-Cal eligibility guidelines, application, and renewal/redetermination process., • Requires strong problem solving and customer service skills., • Must have a strong understanding of the DHCS housing and tenancy program and services and requirements., • Must demonstrate proficiency in or willingness to learn HMIS and other data entry systems., • Must be a CA Resident, and must reside in CA while employed., • Current and valid California (CA) Driver’s License., • Must use personal vehicle and current vehicle registration required., • Proof of auto insurance required, must maintain CA minimum insurance coverage., • BCLS CPR Certification required. Preferred Qualifications: • Certification in case management or housing navigation., • Experience working within healthcare settings or with interdisciplinary care teams., • Familiarity with electronic health records (EHR) and case management software., • Bilingual abilities or proficiency in additional languages relevant to the community served., • Training in trauma-informed care and cultural competency. Responsibilities: • Conduct comprehensive assessments of clients’ housing needs and barriers to stable housing and collaborates to develop Individualized Service Plan (ISP) that addresses housing goals, maintaining/increasing income and other personal goals identified by the participant including medical, mental health, substance use, financial resources, vocational, and social support needs, • Provides referrals, linkages, information, and support to resources that help participants to achieve their ISP goals, • Completes program specific assessments., • Evaluates strengths and challenges to addressing short term and long-term goals, conducts a 90-day review with the participant after initial intake., • Develop individualized housing plans in collaboration with clients and multidisciplinary teams., • Identify and maintain up-to-date knowledge of available housing resources, subsidies, and community programs., • Advocate on behalf of clients with landlords, housing authorities, and service providers to secure housing placements. Also must focus on landlord engagement and retention that involves negotiation and advocacy., • Provide ongoing support and follow-up to ensure housing stability and address any emerging challenges., • Coordinate with healthcare providers to integrate housing solutions with clients’ health and social care plans., • Maintain accurate documentation of client interactions, housing plans, and outcomes in compliance with organizational policies., • Participate in community outreach and education efforts to raise awareness of housing resources and services.

Job Description Marine Husbandry Aquarist SUMMARY The marine husbandry aquarist I (Operational Focus) is an entry level position. The marine husbandry aquarist I is responsible for maintaining clean and healthy aquariums for livestock. These duties include but are not limited to: livestock health management, siphoning and cleaning livestock holding, and distribution of feeds to marine fishes and invertebrates. Primary RESPONSIBILITIES & DUTIES • Check invoices and get counts for spacing, • Prepare arrival and holding spaces for incoming shipments, • Handling and moving livestock as needed, • Remove deceased animals from the holding systems, • Prepare and distribute feeds, • Clean tanks, systems, and work areas, • Water testing and data entry Secondary RESPONSIBILITIES & DUTIES • Assist livestock acclimation, freshwater husbandry, invert husbandry, packing and picking, facility maintenance teams., • Other responsibilities as assigned Qualification/Requirements • Weekend and holiday work required, • Entry level - no prior experience required, • Working knowledge of Microsoft Office suite, • Ability to multi-task, prioritize responsibilities, work under pressure, meet deadlines and be able to thrive in a fast-paced work environment, • Keeping aquariums, a plus – tell us about it! Physical Requirements Standing for more than 7 hours per day. Able to lift 60 lbs. SUMMARY The marine husbandry aquarist II is responsible for the daily care and health management of all marine fishes in the facility. These duties include but are not limited to: distributing feeds to marine fishes, water quality sampling and testing, tank cleaning, inventory control, and recognition and treatment of diseases, making and distributing saltwater, and other husbandry-related tasks as assigned. Primary RESPONSIBILITIES & DUTIES • Remove deceased animals from the holding systems, • Prepare and distribute feeds to livestock, • Maintain system organization and move fish as needed, • Water testing and data entry, • Administer livestock treatments, • Remove animals in need of treatment and place in hospital systems, • Identify and remove healthy animals from the treatment system, • Clean and maintain tanks, systems, and work areas, • Mix and distribute chemicals, • Count and adjust inventory as required Secondary RESPONSIBILITIES & DUTIES • Assist livestock acclimation, freshwater husbandry, invert husbandry, packing and picking, facility maintenance teams., • Other responsibilities as assigned Qualification/Requirements • Bachelor’s degree in biology or related field or equivalent experience, • Weekend and holiday work required, • Strong verbal and written communication skills, • Working knowledge of Microsoft Office suite, • Ability to multi-task, prioritize responsibilities, work under pressure, meet deadlines and be able to thrive in a fast-paced work environment, • Knowledge of marine fishes and invertebrates required, • Fish pathology, coral husbandry, and coral propagation a plus, • Aquarium keeping, preferred (Ever kept a fish tank? Let us know!) Physical Requirements Standing for more than 7 hours per day. Able to lift 60 lbs.

Job Description Charcuterie and Chats, LLC is seeking experienced California Licensed Clinical Laboratory Scientists (Generalist I & II) to support a statewide regulatory laboratory oversight program. This position offers an opportunity to work in a professional environment supporting laboratory compliance, inspections, quality assurance, and public health initiatives throughout California. Locations • Los Angeles, CA Employment Type: Full-Time Compensation: $50.00–$58.00 per hour, based on experience and qualifications. Position Summary Clinical Laboratory Scientists will perform laboratory inspection, compliance, and quality assurance activities for licensed clinical laboratories and physician office laboratories. Responsibilities include conducting inspections, reviewing laboratory operations, evaluating regulatory compliance, preparing technical reports, and providing consultation on laboratory standards. Travel throughout California, including occasional overnight travel, is required. Responsibilities • Conduct onsite laboratory inspections and compliance reviews., • Perform complaint investigations and follow-up inspections., • Review laboratory policies, procedures, and quality systems., • Prepare inspection reports and corrective action documentation., • Conduct exit interviews and communicate inspection findings., • Provide technical guidance on laboratory regulations and compliance., • Maintain accurate records and electronic documentation., • Participate in quality assurance and quality improvement activities., • Collaborate with laboratory professionals and internal leadership., • Travel throughout California as required. Minimum Qualifications • Current California Clinical Laboratory Scientist (Generalist) License, • Bachelor's degree in Clinical Laboratory Science, Biology, Chemistry, or a related scientific discipline, • Minimum three (3) years of experience in clinical or public health laboratory sciences, laboratory supervision, technical specialty areas, or laboratory regulatory compliance, • Working knowledge of CLIA and California laboratory regulations, • Strong written, verbal, and organizational skills, • Ability to travel throughout California Preferred Qualifications • Laboratory inspection or accreditation experience, • Public health laboratory experience, • Experience interpreting laboratory regulations, • Excellent technical writing and communication\nCompany Description Charcuterie and Chats, LLC, formerly operating as EverythingWellness LLC, is a California-based professional services company specializing in healthcare staffing, workforce management, regulatory support, and government contracting. We provide highly qualified professionals to federal, state, and local government agencies, as well as private-sector organizations, with a focus on delivering dependable, compliant, and customer-focused staffing solutions. Our expertise includes recruiting, credentialing, onboarding, and managing licensed healthcare professionals, including California Licensed Clinical Laboratory Scientists (CLS), to support regulatory oversight, laboratory operations, public health initiatives, and specialized healthcare programs. We maintain rigorous quality assurance processes to ensure personnel meet all required licensure, education, and experience standards while complying with applicable federal, state, and local regulations. Charcuterie and Chats, LLC has demonstrated success supporting large-scale government and healthcare initiatives requiring workforce coordination, contract administration, quality assurance, and operational oversight. Our experience includes managing nationwide staffing programs for the U.S. Department of the Treasury – Internal Revenue Service (IRS) and coordinating California Licensed Clinical Laboratory Scientists for healthcare testing operations under licensed laboratory supervision. Our core capabilities include: Healthcare Staffing and Workforce Management Clinical Laboratory Scientist (CLS) Staffing Government Contract Staffing Recruitment and Credential Verification Regulatory and Compliance Support Contract Administration and Program Management Quality Assurance and Performance Monitoring Administrative and Operational Support Charcuterie and Chats, LLC is committed to delivering responsive service, qualified personnel, and operational excellence while helping our clients achieve their mission through reliable staffing, regulatory compliance, and exceptional customer service. Charcuterie and Chats, LLC, formerly operating as EverythingWellness LLC, is a California-based professional services company specializing in healthcare staffing, workforce management, regulatory support, and government contracting. We provide highly qualified professionals to federal, state, and local government agencies, as well as private-sector organizations, with a focus on delivering dependable, compliant, and customer-focused staffing solutions.\r\n\r\nOur expertise includes recruiting, credentialing, onboarding, and managing licensed healthcare professionals, including California Licensed Clinical Laboratory Scientists (CLS), to support regulatory oversight, laboratory operations, public health initiatives, and specialized healthcare programs. We maintain rigorous quality assurance processes to ensure personnel meet all required licensure, education, and experience standards while complying with applicable federal, state, and local regulations.\r\n\r\nCharcuterie and Chats, LLC has demonstrated success supporting large-scale government and healthcare initiatives requiring workforce coordination, contract administration, quality assurance, and operational oversight. Our experience includes managing nationwide staffing programs for the U.S. Department of the Treasury – Internal Revenue Service (IRS) and coordinating California Licensed Clinical Laboratory Scientists for healthcare testing operations under licensed laboratory supervision.\r\n\r\nOur core capabilities include:\r\n\r\nHealthcare Staffing and Workforce Management\r\nClinical Laboratory Scientist (CLS) Staffing\r\nGovernment Contract Staffing\r\nRecruitment and Credential Verification\r\nRegulatory and Compliance Support\r\nContract Administration and Program Management\r\nQuality Assurance and Performance Monitoring\r\nAdministrative and Operational Support\r\n\r\nCharcuterie and Chats, LLC is committed to delivering responsive service, qualified personnel, and operational excellence while helping our clients achieve their mission through reliable staffing, regulatory compliance, and exceptional customer service.

Job Description Title: Data Scientist 2 Location: West Hills, CA 91304 (Onsite) Duration: 6 months W2 contract with high possibility of extension based on performance and depending on business needs Shift time: Day shift Pay rate: 40/hour on W2 Position Summary This is a key position in the Client team. The successful candidate will have the opportunity to work with a broad team of lab scientists and software engineers to build cutting-edge technologies and develop innovative molecular diagnostics products for improving organ transplantation outcomes. The successful candidate will assist in streamlining computation workflows for sequencing analysis and report generation. This role will work in collaboration with the research staff and other departments, and requires knowledge of bioinformatics, biostatistics, molecular biology, as well as the ability to quickly grasp new disciplines. Key Responsibilities • Maintaining and optimizing existing analysis workflow pipelines, • Collect, clean, and manage data from various sources., • Collaborate with the internal bioinformatics and data science teams to identify computational bottlenecks in existing workflows and assist in process efficiency where needed., • Light scripting and programming work are expected.Education, • Bachelors or Master's degree in Computer Science, Bioinformatics, Biological Sciences, or similar fields with 2+ years of meaningful experience.Experience and Skills, • Proficiency in programming/scripting with C/C++, Python, R, SQL, Client or other languages, • Able to interact with organization system hardware, software, infrastructure, and IT individuals regularly, • Experience working in Linux environment, building and maintaining NGS bioinformatics analysis pipelines, knowledge of the common bioinformatics tools and databases strongly preferred, • Statistical analysis and data visualization with large datasets preferred, • Understand basic biological concepts preferred

Job DescriptionBenefits: • 401(k), • Paid time off, • Health insurance Clinlab.AI is seeking a talented and detail-oriented Clinical Lab Scientist (CLS) to join our team. At Clinlab.AI, our mission is to revolutionize patient care by aggregating and delivering insightful information rather than just numerical results. We empower Physician Office Laboratories to provide the same high-quality care that leading reference or hospital labs offer nationwide, right within the Physician Office itself. In this position, you will perform testing and lead a team of other technicians to perform testing in the Chemistry, Special Chemistry, Hematology and/or Coagulation Departments. Responsibilities: Team Leadership: • Build and maintain strong customer relationships, providing a positive and empathetic understanding to all physicians and their staff., • Collaborate with the Lab Staff and Office Staff to ensure timely and accurate testing., • Train and onboard and lead lab assistants and technicians in performing their jobs., • Travel to neighboring labs to provide support and coverage as needed. Test Administration: • Perform lab tests, including Chemistry, Immunoassay, Hematology, Molecular accurately., • Follow laboratory procedures for specimen handling, processing, test analysis, reporting, and record-keeping of patient test results., • Demonstrate excellent troubleshooting skills on automated instruments., • Provide accurate test results within the expected turnaround time. Compliance & QA: • Maintain proficiency testing records, with experience in CAP, API, AAB, MLE, or other CLIA approved proficiency testing., • Adhere to the laboratory's quality control policies, document all quality control activities, instrument and procedural calibrations, and maintenance., • Comply with CLIA, HIPAA, OSHA, and safety guidelines., • Identify and address problems that may impact test performance or result reporting promptly., • Document all corrective actions taken when test systems deviate from the laboratory's established performance specifications. Qualification Requirement: • Bachelor's Degree in Biology, Chemistry, Medical Technology or related life science., • Valid California Clinical Laboratory Scientist license with ASCP certification -must possess for position., • 2+ years previous work experience in a clinical laboratory as a CLS., • Effective communication skills in English, both verbal and written., • Exceptional organizational skills with the ability to set priorities., • Proficiency in computer skills and experience with a laboratory information system., • Experience as a Generalist in Chemistry, Immunology, and Hematology., • Familiarity with the Beckman AU Systems, Beckman Access Systems, or Roche Cobas System is a plus. We are pleased to offer the following benefits to our employees: • 401K: We provide a comprehensive 401K retirement plan to help our employees plan for their future financial security., • Sick Time and Vacation: We understand the importance of work-life balance, which is why we offer generous sick time and vacation benefits. Take the time you need to recharge, relax, and spend quality time with your loved ones., • Healthcare Benefits: We prioritize the well-being of our employees by providing a contribution to your healthcare coverage. Join our team and enjoy these valuable benefits that contribute to your overall happiness, financial stability, and peace of mind. Please note that additional details and eligibility criteria for these benefits will be provided during the interview process. We look forward to receiving your application and welcoming you to our company!

Job DescriptionBenefits: • Health insurance, • Paid time off, • Parental leave, • Profit sharing, • Vision insurance, • 401(k), • Bonus based on performance, • Competitive salary, • Dental insurance, • Flexible schedule HETI is currently searching for full-time Certified Industrial Hygienists/Industrial Hygienists to add to our expanding operations. These positions will be responsible for providing industrial hygiene (IH)/environmental consulting services, including: • Indoor air quality assessment and other IH program design/implementation, • Fungal and microbial contamination investigations, • Human health risk assessments, • Service a wide range of clients, particularly within the insurance industry, • Provide expert witness testimony and litigation support services., • Assist our Director of Business Development in expanding the regional business for their respective offices.The ideal candidate will have:, • Advanced degree in Biology, Chemistry, Industrial Hygiene or Occupational Safety, as well as a Certified Industrial Hygienist (CIH) professional registration (or equivalent work experience), • Ten or more years’ relevant experience in environmental/IH consulting, health & safety, and/or insurance, • Strong written/verbal communications, presentation and interpersonal skills, • Prior business development experience, • Expertise in providing environmental/indoor air quality risk assessment and/or claim services in or to the insurance industry required.Founded in 1986, HETI is a full-service, nationwide environmental services company specializing in environmental and indoor air quality site assessment, site remediation, risk characterization, occupational health and safety services, and litigation/expert witness support. Through our network of offices throughout the U.S., we serve a variety of large and small businesses. We are an Equal Opportunity Employer and offer a competitive benefit package and a friendly, flexible work environment. Flexible work from home options available.

Job DescriptionInternal Title: Research Scientist, Multiple Myeloma - Translational Medicine Schedule: M-F 8:00-17:00 Job Description Summary The Research Scientist will support biomarker and translational strategy for the clinical development of chimeric antigen receptor (CAR-T) programs in Multiple Myeloma. As a member of the Translational Medicine team, you will be at the intersection of Research and Clinical Development, providing valuable insight into the function of CAR-T cells in patients and the development of potential prognostic tools. Regulatory filing experience and a demonstrated ability to facilitate clinical trial execution, synthesize scientific data, communicate key findings cross-functionally is required. Key Responsibilities: Directs and establishes pharmacokinetic and pharmacodynamic (PK/PD) analysis to support clinical pharmacology for CAR T clinical trials in Multiple Myeloma Serves as Biomarker lead on clinical study teams to oversee delivery of pharmacology data and documentation required for pivotal and registrational study filings Reviews and contributes to clinical protocol design and study activities Identify and establish agreements with contract research organizations (CRO) and support the transfer of Client methods Collaborates with Clinical development teams including Clinical Operations, Regulatory, Clinical Data Management and Biometrics/Stats to advance data acquisition and analyses of clinical trial data Leads the resolution of clinical pharmacology/translational queries from regulatory agencies, supports writing and reviewing responses to regulatory queries. Support the preparation of data packages for publication with medical writers, presentation and/or submission to regulatory agencies Collaborates with Translational Medicine, Bioinformatics and Statistical teams for exploratory biomarker correlative studies and deeper analysis of tumor biology and CAR T functionality Contribute to external scientific discussions/research collaborations and publications and engagement with key opinion leaders in the field Education Level Advanced scientific degree (i.e. MD, PharmD, PhD) and 3 years in industry OR Master's Degree and 5 years of scientific experience OR Bachelor's Degree and 7 years of scientific experience Experience Preferred Qualifications: Strong background in cancer immunotherapy, immunology and/or oncology with experience focusing on Multiple Myeloma Prior experience in Regulatory filings In-depth understanding of multiple myeloma, knowledge of clinical landscape, evolving therapy, competitive scenarios Strong understanding of clinical, translational, and mechanistic data Familiarity and experience with clinical and biomarker operations Understanding of early or late-stage drug and translational development process; including clinical trial experience in industry or academia Familiarity with bioanalytical assay development and validation in a GxP environment Experience working with engineered T cells, immunophenotyping, and NGS-based approaches to profile the function of tumor and immune cells Comfortable in a matrixed and fast-paced company environment and able to adapt to changing priorities Strong collaboration, excellent interpersonal and communication skills Proficient with data presentations to communicate to a diverse cross-functional audience Maintain a high degree of accuracy and attention to detail Ph.D. degree in biology-related field (immunology, cancer biology, bioinformatics or a closely related field)

Job Description The Quality Control Manager oversees all laboratory and QC line operations and personnel responsible for testing raw materials, in-process samples, in-line finished goods and finished OTC products, packaging components, and stability studies. This role ensures compliance with FDA cGMP regulations (21 CFR Parts 210, 211 and 700), USP standards, and internal quality procedures to support the release of safe, compliant, and high-quality Cosmetic and OTC drug products. The Quality Control Manager works under the general direction of Quality Control Director. Essential Responsibilities • Manage, train, and develop QC analysts, chemists, Line Inspectors and microbiologists to ensure efficient, compliant operations., • Schedule and prioritize laboratory activities to support production and product release timelines., • Provide technical guidance and serve as the primary QC representative in cross-functional meetings (QA, R&D, Manufacturing)., • Help Develop, implement and maintain QC systems and measures., • Communicate quality control information to all relevant organizational departments, outside vendors or contractors., • Produce and communicate reports regarding nonconformance of products., • Assist in investigations related to Nonconformance or OOS, Customer Complaint etc., • Provide Department related data, trends etc. for Management Review., • Monitor Performance of QC systems to ensure effectiveness, efficiency and compliance to company SOPs and regulatory requirements., • Adhere to company policies and procedures and sets a positive example for others within the organization., • Participate in change control, CAPA, internal audits, and regulatory inspections (FDA, state boards, third-party auditors)., • Support method validation/verification, stability program management, and reference standard qualification., • Collaborate with QA to ensure timely release of materials and products that meet all quality standards., • Ensure laboratory SOPs, test methods, and specifications are up-to-date and properly controlled., • Assist in updating or writing Department related SOPs and Work Instructions or other Department related documents., • Evaluate and implement new analytical technologies, laboratory automation, or process improvements., • Enforce adherence to safety policies, chemical hygiene, and PPE requirements., • Maintain a clean, organized, and compliant laboratory environment., • Develop and conduct training programs for QC personnel on methods, SOPs, and cGMP principles., • Resolve production and manufacturing problems to minimize cost and delay., • Laboratory and Production:, • Oversee testing of raw materials, in-process, finished products, water, and stability samples in accordance with compendial (USP, EP, JP) and internal methods., • Review and approve laboratory test results, specifications, and Certificates of Analysis (CoA)., • Update status of Raw Materials, Bulk/Intermediate and Finished Goods in ERP system., • Communicate quality control information to all relevant organizational departments, outside vendors or contractors., • Ensure accurate execution and documentation of analytical and microbiological testing (e.g., assay, pH, viscosity, microbial limits, identification tests)., • Ensure environmental monitoring and microbiological controls for production and water, • Lead or support investigations of Out-of-Specification (OOS), Out-of-Trend (OOT), and laboratory deviations, including root cause analysis and CAPA implementation., • Complete all other additional tasks assigned by supervisor. Qualifications To perform this job successfully, an individual must be able to perform each essential responsibility satisfactorily using the skills and abilities outlined in this job description. The requirements listed below are representative of the knowledge, skills and/or abilities required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. • Discretion in handling confidential and sensitive matters., • Strong knowledge of FDA OTC regulations, USP/NF methods, and ICH stability guidelines. Education, Experience and Licensure • Bachelor’s degree in science (chemistry, pharmacy, or biology) or equivalent work experience., • 5+ years Quality Control related experience in a cGMP OTC manufacturing environment, including 2+ years in a supervisory or managerial capacity., • Strong experience with microbiological testing, method validation/verification, cleaning validation, OOS investigations, and audit preparation/response.

Job DescriptionVARITE is looking for qualified Research Scientist, Multiple Myeloma - Translational Medicine in Santa Monica, CA (Hybrid) WHAT THE CLIENT DOES? An American biotechnology company that develops cancer immunotherapy products with a primary focus on genetically engineered autologous CAR T cell therapy - a cell-based therapy which relies on chimeric antigen receptors and T cells. WHAT WE DO? Established in the Year 2000, VARITE is an award-winning minority business enterprise providing global consulting & staffing services to Fortune 1000 companies and government agencies. With 850+ global consultants, VARITE is committed to delivering excellence to its customers by leveraging its global experience and expertise in providing comprehensive scientific, engineering, technical, and non-technical staff augmentation and talent acquisition services. Job Title: Research Scientist, Multiple Myeloma - Translational Medicine Location: Santa Monica, CA 90404 (Hybrid) Contract Duration: 12 months with possible extension Pay Range: $45.00/hr. to $47.35/hr. on W2 HERE’S WHAT YOU’LL DO Summary: • The Research Scientist will support biomarker and translational strategy for the clinical development of Client's chimeric antigen receptor (CAR-T) programs in Multiple Myeloma., • As a member of the Translational Medicine team, you will be at the intersection of Research and Clinical Development, providing valuable insight into the function of CAR-T cells in patients and the development of potential prognostic tools., • Regulatory filing experience and a demonstrated ability to facilitate clinical trial execution, synthesize scientific data, communicate key findings cross-functionally is required. Key Responsibilities: • Directs and establishes pharmacokinetic and pharmacodynamic (PK/PD) analysis to support clinical pharmacology for CAR T clinical trials in Multiple Myeloma., • Serves as Biomarker lead on clinical study teams to oversee delivery of pharmacology data and documentation required for pivotal and registrational study filings., • Reviews and contributes to clinical protocol design and study activities., • Identify and establish agreements with contract research organizations (CRO) and support the transfer of Client methods., • Collaborates with Clinical development teams including Clinical Operations, Regulatory, Clinical Data Management and Biometrics/Stats to advance data acquisition and analyses of clinical trial data., • Leads the resolution of clinical pharmacology/translational queries from regulatory agencies, supports writing and reviewing responses to regulatory queries., • Support the preparation of data packages for publication with medical writers, presentation and/or submission to regulatory agencies., • Collaborates with Translational Medicine, Bioinformatics and Statistical teams for exploratory biomarker correlative studies and deeper analysis of tumor biology and CAR T functionality., • Contribute to external scientific discussions/research collaborations and publications and engagement with key opinion leaders in the field. Education Level: • Advanced scientific degree (i.e. MD, PharmD, PhD) and 3+ years in industry OR, • Master's Degree and 5+ years of scientific experience OR, • Bachelor's Degree and 7+ years of scientific experience Experience: Preferred Qualifications: • Strong background in cancer immunotherapy, immunology and/or oncology with experience focusing on Multiple Myeloma, • Prior experience in Regulatory filings, • In-depth understanding of multiple myeloma knowledge of clinical landscape, evolving therapy, competitive scenarios, • Strong understanding of clinical, translational, and mechanistic data, • Familiarity and experience with clinical and biomarker operations, • Understanding of early or late-stage drug and translational development process; including clinical trial experience in industry or academia, • Familiarity with bioanalytical assay development and validation in a GxP environment, • Experience working with engineered T cells, immunophenotyping, and NGS-based approaches to profile the function of tumor and immune cells, • Comfortable in a matrixed and fast-paced company environment and able to adapt to changing priorities, • Strong collaboration, excellent interpersonal and communication skills, • Proficient with data presentations to communicate to a diverse cross-functional audience, • Maintain a high degree of accuracy and attention to detail, • Ph.D. degree in biology-related field (immunology, cancer biology, bioinformatics or a closely related field) BENEFITS: We offer a comprehensive benefits package designed to support the health, well-being, and financial security of our employees and their families. Eligible employees may receive: • Health Insurance: Medical, dental, and vision coverage, • Retirement Plans: Participation in a company-sponsored retirement savings plan., • Legal Service Plans: Offering access to attorneys for legal advice and representation. If this opportunity interests you, please respond by clicking on EasyApply. Know someone who would be perfect for this role? Refer to us and if they are hired, you could be eligible for our employee referral bonus! Help us grow our team with top talent from your network. VARITE is committed to creating a diverse environment and is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, or veteran status.

Job Description Job Summary: Under the direct supervision of the Principal Investigator, Dr. Qiongyu Hao, the Laboratory Research Associate supports both the animal colony operations and the routine bench work of the laboratory's translational cancer research program. The successful candidate divides time between ensuring the highest standards of animal welfare and breeding management and performing routine cancer research procedures, including cell culture, molecular biology assays, and drug treatment/functional assays. This role is essential to maintaining the integrity and consistency of the laboratory's scientific output across both the in vivo and in vitro arms of the research program, which spans exosome biology, cancer metabolism, and small-molecule drug discovery in breast cancer and acute myeloid leukemia. Essential Duties and Responsibilities: • Oversee weaning and maintain accurate breeding records to ensure line sustainability., • Assist research staff with experimental procedures such as tail/ear snipping for DNA collection, injections (IP, SC), oral gavage, and tissue harvesting., • Perform routine PCR-based genotyping and maintain a digital database of animal strains and genetic statuses., • Conduct health checks and clinical observations; report any abnormalities or welfare concerns to the Principal Investigator and veterinary staff immediately., • Maintain and passage cancer cell lines (e.g., TNBC, AML) under sterile conditions; perform routine cell counting, viability assays, and cryopreservation., • Perform routine RNA/DNA/protein extraction, qRT-PCR, and Western blotting to support ongoing cancer research projects., • Assist with in vitro drug treatment experiments, proliferation/apoptosis assays, and routine data collection., • Assist with routine isolation and characterization of extracellular vesicles/exosomes using established core platforms, under supervision., • Ensure all activities strictly adhere to IACUC (Institutional Animal Care and Use Committee) protocols and institutional biosafety guidelines., • Maintain a clean and organized work environment, monitor room parameters (temperature/humidity), and ensure all surgical and procedural equipment is sterilized., • Maintain inventory of laboratory reagents, chemicals, and supplies needed for ongoing studies. Other Duties and Responsibilities: • Perform other related duties as assigned. Qualifications/Requirements: EDUCATION: • B.S. or Associate degree in Biology, Animal Science, Biochemistry, Molecular Biology, or a related life science field. EXPERIENCE: • Direct experience handling and restraining small rodents., • Hands-on experience with mammalian cell culture (cancer cell lines preferred) and standard molecular biology techniques (PCR, Western blot, ELISA)., • Proficiency in basic laboratory math and digital record-keeping., • Familiarity with aseptic techniques is highly preferred., • Prior experience with in vivo animal models (mouse/rat) is a plus., • Prior experience with extracellular vesicle/exosome isolation or characterization is advantageous but not required. KNOWLEDGE/ABILITY/SKILLS: • Exceptional reliability and punctuality, as consistent care is critical for animal welfare., • Strong communication skills for coordinating with diverse research teams., • Ability to follow complex Standard Operating Procedures (SOPs) with high precision., • Able to troubleshoot and resolve routine technical difficulties., • Committed to supporting a translational Cancer Research program. COMPLEXITY: • The ability to perform highly detailed work with sustained attention and care while providing/obtaining information on numerous inquiries is paramount to success in this position. PHYSICAL DEMANDS: • 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. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Frequent handling of small animals, standing, and walking. Constant sitting, climbing, reaching high/low levels, finger movement, feeling, speaking clearly, hearing conversationally, and seeing far and near. WORK ENVIRONMENT: • The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job, including animal facility and standard wet-laboratory settings. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. MENTAL DEMANDS: • The mental demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Frequent work on a variety of unrelated tasks. Constant calculating, interrupted work, work on a variety of interrelated tasks, and use of sustained concentration, reasoning, judgment, resourcefulness, analytical ability, and ingenuity. Special Requirements: • Ability to work effectively with a diverse community., • The ideal candidate will be seeking a career supporting translational Cancer Research and able to make a long-term commitment. Compensation: • $70,340 - $93,468 Position Status: • Full Time, Exempt EEO Statement: Charles R. Drew University is committed to Equal Employment Opportunity. Applicants will be considered without regard to gender, race, age, color, religion, national origin, sexual orientation, genetic information, marital status, disability or covered veteran status. Fair Chance Statement: Charles R. Drew University of Medicine and Science will consider qualified applicants, including those with criminal histories, in a manner consistent with state and local “Fair Chance” laws

Job DescriptionQA Laboratory Technician I Location: Commerce, CA 90040 Schedule 5pm - 1:30am - Candidate to be flexible for change of hours Working Days: Sunday, Wednesday, Thursday, Friday & Saturday) / Off days: Monday and Tuesday. The Supply Operations Los Angeles Milk/Culture Plant, located in Commerce, California, has a Plant Quality Control Technician position available. Is there possibility this assignment will be extended? No Is there a possibility this role will convert to full time? No Key Responsibilities include, but are not limited to: • Responsible for sampling, testing, plating, reading, and recording product test results., • Ensure that daily records are kept and maintained., • Data Entry and tracking, • Following QC Hold Procedures for out of specification products, • Must possess the ability to follow standard operating procedures (SOP's)., • Will assist in the discipline to maintain a 5-S rating of an " "A " "., • Be flexible in working hours., • Equipment calibration and troubleshooting, • Perform other duties as assigned., • Participate in driving continuous improvement., • Must meet with supervisor on a daily basis covering on any issues associated with production., • Possess the knowledge and understanding of Industry best practice maintenance on equipment. Qualifications: • Minimum Bachelor's degree ( Food Science, Biology, Microbiology or related science) or equivalent experience (Minimum 2 years in similar role), • Knowledge of Microbiological , Chemical and Physical, Organoleptic Testing, • Ensure policies, procedures, and workplace safety is adhered to., • Evaluate trends from test results and develop plans to correct deficiencies and communicate these plans to employees, and management., • Implement quality control processes/testing to meet the expectations of quality standards and ensure that the product(s) are within specification., • Excellent organizational skills with a high degree of initiative and flexibility., • Good analytical and problem solving skills., • Utilize laboratory supplies/items relating to plant sanitation/safety., • Good oral/written communication skills., • Able to multi-task in fast paced environment with limited supervision., • Proficient in window based PC programs., • Lab Test Equipment/Maintenance., • Ability to lift 50lbs., • Time Management, • Quick to learn new techniques, • Ability to work in cold and loud environments

Job DescriptionBenefits: • Life Insurance, • Health insurance, • Paid time off, • Vision insurance, • 401(k), • 401(k) matching, • Dental insurance The R&D Formulation Specialist performs various project duties supporting the product development of a contract manufacture of Nutraceuticals and Dietary Supplements. This includes FPS process, formulation, bill of materials database maintenance, and record retention SOPs and new product process. DUTIES & RESPONSIBILITIES: The following responsibilities would characterize the requirements of this position. Must possess the skills necessary to perform the majority of the listed functions: 1. Interpret customer’s explanations, descriptions and requests and convert them to the chemical components and formula combinations, 2. Meet with suppliers and technical experts for product information collecting newest developments and formulating appropriate applications., 3. Assemble chemicals and materials into laboratory batches and test formula for efficacy/performance, 4. Modify, substitute, and reformulate materials to meet highest level of customer expectations, and quality while maintaining lowest formulation costs, 5. Evaluate alternate chemical suppliers, 6. Enter and review formulas in computer system, 7. Trouble shoot formula issues related to manufacturing/compounding, 8. Revise priorities keeping all deadlines under control according to production demands, customer needs and company interests., 9. Maintain professional expertise through individual study, continuing education and professional development, 10. Must communicate progress, problems and needs with management, vendors, customers as appropriate, 11. Assist with managing the product development process from the concept phase to the post-launch analysis phase, 12. Involvement in new product concept brainstorming meetings, 13. Primary liaison with overseas vendors for Product Development from artwork to product specifications, sculpting, and sample approval, 14. Negotiate pricing with oversees vendors, 15. Set up item number and other development information in item master while updating and maintaining it, 16. Ensure the accuracy of product and packaging samples and seek approvals, 17. Guarantees deadlines are met to obtain samples for tradeshows & licensor, 18. Initiates collateral requests within the Creative Department and/or with outside service vendors, 19. Works with Quality Compliance department regarding compliance issues REQUIREMENTS: Competencies 1. M.S or B.S. degree in Chemistry, Biology, Food Science or other physical science, 2. 2-3 years’ experience in formulation of new and innovative personal care products, preferably in a contract manufacturing environment, 3. Ability to multitask handling 4-5 bench projects at a time, 4. Ability to thrive within a team environment, 5. Working knowledge of claim substantiation, 6. Current knowledge of ingredient technology and familiar with working within customer and international, 7. Extensive knowledge of laboratory procedures, test instrumentation, and experimental design, 8. Advance writing, reading, and math skills including statistical analysis, 9. Ability to interpret, analyze, reason, and plan

Job Description Job Summary: We are looking for a motivated R&D Laboratory Technician I to support product development activities in our Brea, CA facility. This role involves assisting engineers with laboratory testing, prototype evaluations, equipment setup, and documentation while ensuring compliance with laboratory safety and quality standards. Responsibilities: • Perform laboratory testing following approved procedures and engineering protocols., • Assist engineers with product development, validation, and prototype evaluations., • Prepare laboratory equipment, instruments, and materials for testing activities., • Record, organize, and maintain accurate laboratory data and technical documentation., • Support calibration, maintenance, and troubleshooting of laboratory equipment., • Assist with sample preparation, conditioning, and handling of testing materials., • Compile test observations and communicate findings to engineering teams., • Maintain laboratory cleanliness while adhering to safety and quality procedures., • Participate in continuous improvement initiatives for laboratory processes., • Report equipment issues or test abnormalities to supervisors promptly. Requirements: • High School Diploma or equivalent., • Minimum 6 years of laboratory, manufacturing, or regulated technician experience OR, • Associate or bachelor's degree in engineering, Biology, Chemistry, or another technical discipline with at least 1 year of laboratory or R&D experience., • Experience working in a regulated environment and following written procedures., • Strong organizational and documentation skills., • Comfortable working collaboratively in a team environment., • Basic computer proficiency, including Microsoft Office. Preferred Qualifications: • Experience supporting product development or engineering projects., • Familiarity with laboratory instruments and testing equipment., • Ability to interpret engineering instructions and test procedures., • Strong attention to detail with accurate data recording., • Excellent communication and problem-solving skills., • Experience in maintaining laboratory equipment and inventory., • Ability to assist in training junior laboratory personnel.

Job Description Job Summary: We are looking for a motivated R&D Laboratory Technician I to support product development activities in our Brea, CA facility. This role involves assisting engineers with laboratory testing, prototype evaluations, equipment setup, and documentation while ensuring compliance with laboratory safety and quality standards. Responsibilities: • Perform laboratory testing following approved procedures and engineering protocols., • Assist engineers with product development, validation, and prototype evaluations., • Prepare laboratory equipment, instruments, and materials for testing activities., • Record, organize, and maintain accurate laboratory data and technical documentation., • Support calibration, maintenance, and troubleshooting of laboratory equipment., • Assist with sample preparation, conditioning, and handling of testing materials., • Compile test observations and communicate findings to engineering teams., • Maintain laboratory cleanliness while adhering to safety and quality procedures., • Participate in continuous improvement initiatives for laboratory processes., • Report equipment issues or test abnormalities to supervisors promptly. Requirements: • High School Diploma or equivalent., • Minimum 6 years of laboratory, manufacturing, or regulated technician experience OR, • Associate or bachelor's degree in engineering, Biology, Chemistry, or another technical discipline with at least 1 year of laboratory or R&D experience., • Experience working in a regulated environment and following written procedures., • Strong organizational and documentation skills., • Comfortable working collaboratively in a team environment., • Basic computer proficiency, including Microsoft Office. Preferred Qualifications: • Experience supporting product development or engineering projects., • Familiarity with laboratory instruments and testing equipment., • Ability to interpret engineering instructions and test procedures., • Strong attention to detail with accurate data recording., • Excellent communication and problem-solving skills., • Experience in maintaining laboratory equipment and inventory., • Ability to assist in training junior laboratory personnel.

Job Description Mission Driven, Community Focused About | Charles R. Drew University of Medicine and Science (cdrewu.edu) Charles R. Drew University is located in the Watts-Willowbrook area of south Los Angeles and was founded in 1966 in the wake of the Watts uprising. CDU was founded to address inadequate medical care in the region and to provide equitable medical education opportunities for underrepresented students. CDU is strongly invested in the local and regional community. The university leads multiple partnerships and programs to provide equitable healthcare resources in a variety of south Los Angeles neighborhoods. Job Summary: The Clinical Research Program Manager is responsible for the overall operational management of clinical research, trial, study activities from design, set up, conduct, through closeout, and all administrative management duties. In this role, you will be responsible and oversee the implementation of research activities for multiple studies. Perform necessary tasks to manage projects and prioritize work to meet necessary deadlines. You will be responsible for planning and organizing necessary tasks to ensure adherence to the study protocol and applicable regulations, such as institutional policy and procedures, FDA Code of Federal Regulations (CFR), and ICH Good Clinical Practice (GCP). The Clinical Research Program Manager works closely with the Director, Principal Investigators (PI), ancillary departments, central research infrastructure teams, sponsors, institutions, and other entities as needed to manage the administration of all aspects of studies, including, but not limited to, compliant conduct, financial management, and adequate personnel support. This role includes supervision of research staff, coordination of resources, development of infrastructure, and implementation of strategies to expand the Center’s research capacity and impact. Essential Duties and Responsibilities: Administrative Responsibilities • Provide daily administrative, regulatory, financial, and business activities necessary to assist investigators in the conduct of clinical research at CDU. Serves as a point of contact for all faculty and staff., • Manage the day-to-day operations of the CTRC, including personnel supervision, scheduling, workflow management, and performance evaluation., • Independent study coordination including screening of potential patients for protocol eligibility, presenting non-medical trial concepts and details to the patients, and participating in the informed consent process., • Scheduling of patients for research visits and procedures., • Develop, implement, monitor, and maintain standard operating procedures (SOPs) to ensure efficient and compliant study conduct. While maintaining accurate source documents related to all research procedures., • Track and report key performance indicators (KPIs) related to study volume, participant enrollment, sponsor satisfaction, and financial performance., • Plans and coordinates strategies for increasing patient enrollment, and/or improving clinical research efficiency., • Develops, implements and maintains system records on employees, equipment inventories, and compliance activities, official minutes for all required administrative leadership meetings., • Develop and manage networks between an array of companies and organizations, including hospitals, pharmaceutical companies, government-based organizations, nongovernmental agencies, and clinical research organizations., • Maintains competency and keeps up with trends and changes in regulations and developments in clinical research, both internally and externally. Ensures information is disseminated to appropriate departments., • Supervises other research staff. Clinical and Compliance Oversight • Ensures site compliance with research protocols by reviewing all regulatory requirements to confirm implementation of appropriate methods, practices, and procedures for all research activities, • Ensure that all CTRC activities comply with FDA, ICH-GCP, NIH, HIPAA, and institutional policies., • Oversee preparation and maintenance of regulatory documentation, study logs, and institutional correspondence., • Schedules and maintains participant protocol activities while adhering to study protocol schedule of assessments, • Manages the regulatory staff in the maintenance of regulatory documents in accordance with SOP and applicable regulations, • Communicates and collaborates specific study requirements to the research team, including internal and external parties, sponsor, monitors, PI, and study participants, • Ensures compliance with research protocols by providing ongoing quality control audits, including maintaining ongoing investigational drug accountability, • Works closely with CDU’s Institutional Review Board (IRB) Administrator to submit Adverse Events, Serious Adverse Events, protocol deviations, and Safety Letters in accordance with local and federal guidelines., • Interfaces with research participants to support efforts to determine eligibility and consenting of study participants according to protocol, • Serve as the primary point of contact for regulatory inspections and sponsor monitoring visits., • Supports the disbursement investigational product and provides patient teaching regarding administration, as necessary., • Communicates and collaborates with study teams, including internal and external parties, sponsors, PI, and study participants. Data and Quality Management • Identify and prioritize the development of systems and infrastructure to maintain research quality and compliance., • Responsible for accurate and timely data collection, documentation, entry, and reporting including timely response to sponsor queries., • Responsible for compiling and reporting on each study including information related to protocol activity, accrual data, workload, and other research information; present this information at regular research staff meetings., • Notifies direct supervisor about concerns regarding data quality and study conduct., • Validate large subsets of clinical patient data., • Assist with designing database/data architecture transitions. QUALIFICATIONS: EDUCATION • Bachelor's Degree from an accredited institution in life sciences (biology, chemistry, microbiology), health sciences, public health, clinical research administration, or medical technology required. Master’s Degree Preferred. EXPERIENCE • 5 years of progressively responsible experience in clinical research, including at least 3 years in management or supervisory roles required., • Grant administration and operations experience is required, • 3 years’ experience managing the day-to-day operations of clinical trials, research programs, data management, and computer/related systems is required., • Ability to interpret and apply knowledge of State, Federal and Agency standards to comply with regulations., • Ability to use discretion and maintain privacy, confidentiality or anonymity., • 5 or more years of direct staff management experience, including recruitment and training, is preferred., • Experience managing multi-site, NIH, or industry-funded studies., • Experience developing and communicating detailed, technical-scientific, and administrative program information to various audiences in written and oral form. Strongly prefer experience and knowledge in the Biological Sciences, Health, and Health Disparities. KNOWLEDGE/ABILITY/SKILLS: • Proven ability to manage budgets, contracts, and personnel effectively., • Ability to work independently as well as communicate well with other professionals., • Strong written and verbal communication abilities and highly effective interpersonal skills., • Ability and/or experience supervising and training employees, including organizing, prioritizing, and scheduling work assignments., • Excellent customer service skills, • Current knowledge of GCP principles, HIPAA, compliant research conduct, and guidelines surrounding human subject research, • Proficiency in Microsoft Office Suite and electronic data capture systems (e.g., REDCap, OnCore)., • Conflict resolution experience with the ability to multitask, collaborate and prioritize., • Possess effective leadership abilities. Coaching/teaching abilities, • Ability and/or experience managing budgets, preferably research project budgets. Compensation: • $75,700 - $90,000 annual Position Status: • Full Time, Exempt COMPLEXITY: • The ability to perform highly detailed work with sustained attention and care while providing/obtaining information on numerous inquiries is paramount to success in this position., • The ability to perform highly detailed work with sustained attention and care while providing/obtaining information on numerous inquiries is paramount to success in this position., • Demonstrated competencies in strategic and systems thinking, project management, and knowledge of continuous improvement methods., • Ability to manage various projects and assignments with multiple priorities in a rapidly changing environment., • Experience with Center development/expansion, including in scientific areas, student training, clinical research areas, and community-based areas, as well as related grant proposal development, writing, and submission to federal agencies or foundations., • Ability to develop and maintain professional working relationships in complex program/organizational settings involving heterogeneous constituents such as academic and clinical faculty, staff, students, and community partners from diverse backgrounds., • Experience interpreting operating policies, and procedures, resolving minor discipline and other employee relations issues within an academic setting or institution. PHYSICAL DEMANDS: • 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. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions., • Occasional stooping. Frequent standing. Constant walking, sitting, climbing, reaching high/low levels, finger movement, feeling, speaking clearly, hearing conversationally, and seeing far and near. WORK ENVIRONMENT: • The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions., • Occasionally required to work in confined space., • Position is on-site unless specific authorization from the manager. MENTAL DEMANDS: • The mental demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions., • Frequent work on a variety of unrelated tasks. Constant calculating interrupted work, work on a variety of interrelated tasks, and use of sustained concentration, reasoning, judgment, resourcefulness, analytical ability, and ingenuity. SPECIAL REQUIREMENTS: • Ability to work effectively with a diverse community. Conditional Employment: The employment status of this position is classified as “Conditional.” Conditional employment means that the job exists contingent upon continued funding and limitations of restricted funds or, the duration of a specific program, project, grant, or contract. Since your salary is funded by Axis CTRC and Novartis Grant(s) and 2/28/2026, your position is contingent upon the continued receipt of these funds. Continuation of your position is dependent, in part, upon funding availability. Furthermore, no work may be performed after the grant end date(s) unless you have received an extension in writing from a Dean, Division VP, or Human Resources. EEO Statement: Charles R. Drew University is committed to Equal Employment Opportunity. Applicants will be considered without regard to gender, race, age, color, religion, national origin, sexual orientation, genetic information, marital status, disability or covered veteran status. Fair Chance Statement: Charles R. Drew University of Medicine and Science will consider qualified applicants, including those with criminal histories, in a manner consistent with state and local “Fair Chance” laws.

Job DescriptionBenefits: • Life Insurance, • LTD, • Health insurance, • Paid time off, • Vision insurance, • 401(k), • 401(k) matching, • Dental insurance The Research and Development Formulation Chemist performs various project duties supporting the product development of a contract manufacture of Nutraceuticals and Dietary Supplements. This includes FPS process, formulation, bill of materials database maintenance, and record retention SOPs and new product process. DUTIES & RESPONSIBILITIES: The following responsibilities would characterize the requirements of this position. Must possess the skills necessary to perform the majority of the listed functions: 1. Interpret customer’s explanations, descriptions and requests and convert them to the chemical components and formula combinations, 2. Meet with suppliers and technical experts for product information collecting newest developments and formulating appropriate applications., 3. Assemble chemicals and materials into laboratory batches and test formula for efficacy/performance, 4. Modify, substitute, and reformulate materials to meet highest level of customer expectations, and quality while maintaining lowest formulation costs, 5. Evaluate alternate chemical suppliers, 6. Enter and review formulas in computer system, 7. Trouble shoot formula issues related to manufacturing/compounding, 8. Revise priorities keeping all deadlines under control according to production demands, customer needs and company interests., 9. Maintain professional expertise through individual study, continuing education and professional development, 10. Must communicate progress, problems and needs with management, vendors, customers as appropriate, 11. Assist with managing the product development process from the concept phase to the post-launch analysis phase, 12. Involvement in new product concept brainstorming meetings, 13. Primary liaison with overseas vendors for Product Development from artwork to product specifications, sculpting, and sample approval, 14. Negotiate pricing with oversees vendors, 15. Set up item number and other development information in item master while updating and maintaining it, 16. Ensure the accuracy of product and packaging samples and seek approvals, 17. Guarantees deadlines are met to obtain samples for tradeshows & licensor, 18. Initiates collateral requests within the Creative Department and/or with outside service vendors, 19. Works with Quality Compliance department regarding compliance issues REQUIREMENTS: Competencies 1. M.S or B.S. degree in Chemistry, Biology, Food Science or other physical science, 2. 2-3 years’ experience in formulation of new and innovative personal care products, preferably in a contract manufacturing environment, 3. Ability to multitask handling 4-5 bench projects at a time, 4. Ability to thrive within a team environment, 5. Working knowledge of claim substantiation, 6. Current knowledge of ingredient technology and familiar with working within customer and international, 7. Extensive knowledge of laboratory procedures, test instrumentation, and experimental design, 8. Advance writing, reading, and math skills including statistical analysis, 9. Ability to interpret, analyze, reason, and plan

Job Description Overview Ansible Government Solutions, LLC (Ansible) is currently recruiting Medical Technologists to support the VA Medical Center located at 11301 Wilshire Blvd, Los Angeles, CA 90073. Services will be delivered to both the Anatomic Pathology and Clinical Pathology divisions of the facility. Exceptional compensation packages with full benefits are available. Ansible Government Solutions, LLC (Ansible) is a Service-Disabled Veteran-Owned Small Business (SDVOSB) providing Federal customers with solutions in many arenas. Our customers face wide-ranging challenges in the fields of national security, health care, and information technology. To address these challenges, we employ intelligent and committed staff who take care of our customers’ success as if it is their own. Responsibilities • Rotate on a regular basis through the areas in which they have been trained and are competent, • Perform a broad range of laboratory procedures in Blood bank., • Perform advanced and complex laboratory procedures, recognizing deviation from expected results, analyzing and correcting problems using scientific principles, • Recognize and communicate pre-defined critical results affecting patient care, • Maintain the optimal functioning of laboratory equipment and keep appropriate records for documentation; operate, calibrate, identify malfunctions, repair and perform preventive maintenance of laboratory analyzers, • Perform and document quality control, quality assurance and corrective actions related to test performance using sound statistical principles and theories of performance improvement, • Enter and verify laboratory results in the computer system; recognize deviations from expected results, analyze and correct problems using scientific principles, • Perform other duties as assigned relating to the responsibilities of a Medical Technologist Qualifications • Accredited Bachelors degree in medical laboratory science, medical technology, clinical laboratory science, or a related science (i.e. biology, chemistry, etc.) AND completion of an accredited medical technology clinical practice program (i.e. NAACLS, CAAHEP, ABHES) OR • Accredited Bachelors degree including 16 semester hours in biological science (one course in microbiology), 16 semester hours in chemistry (one course in organic or biochemistry), and one course in mathematics AND two (2) years of post-certification clinical laboratory experience within the last ten (10) years as a certified Medical Laboratory Technician (ASCP-BOC), • Demonstrated knowledge of laboratory medicine techniques and practices, • Demonstrated education and clinical training in the practice of laboratory medicine, • No sponsorship available Pay Range: $50- $60.42 hourly All candidates must be able to: • Sit, stand, walk, lift, squat, bend, twist, and reach above shoulders during the work shift, • Lift up to 50 lbs from floor to waist, • Lift up to 20 lbs, • Carry up to 40 lbs a reasonable distance, • Push/pull with 30 lbs of force All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran. Powered by JazzHR YS1yN6n6dy

Job Description About the job Mercor connects elite creative and technical talent with leading AI research labs. Headquartered in San Francisco, our investors include Benchmark, General Catalyst, Peter Thiel, Adam D'Angelo, Larry Summers, and Jack Dorsey. Position: Biology / environmental science Evaluator Type: Contract Compensation: $80–$120/hour Location: Remote Role Responsibilities • Evaluate AI-generated artifacts against domain-specific quality rubrics., • Identify factual, aesthetic, and presentation errors in AI-generated work products., • Provide clear, structured written feedback to improve AI model outputs., • Review and assess documents, spreadsheets, and slide decks for accuracy and domain quality., • Work independently and asynchronously to meet deadlines while enhancing AI model performance. Qualifications Must-Have • 5+ years of relevant professional experience in Biology / environmental science., • Native or professional fluency in English., • Highly proficient in Microsoft Office and Google Workspace, especially Slides. Preferred • Advanced degree (Master's or higher) from a reputable institution. Application Process (Takes 20–30 mins to complete) • Upload resume, • AI interview based on your resume, • Submit form Resources & Support • For details about the interview process and platform information, please check: https://talent.docs.mercor.com/welcome, • For any help or support, reach out to: support@mercor.com PS: Our team reviews applications daily. Please complete your AI interview and application steps to be considered for this opportunity. #hiringmercor

Job Description Design Engineer III - Civil Engineer CA - This position can sit out of Santa Cruz or Los Angeles. About Sherwood Sherwood is a civil and environmental engineering firm that is committed to investing in and embracing people, communities and the environment. Our team has delivered net zero energy and net zero carbon systems, net positive water systems, resilient coastlines, natural resource protection, green streets, living roofs and more for thousands of clients in the region and across the globe. We specialize in sustainable infrastructure, water management strategies, green building design, and systems based solutions for infrastructure and landscapes. Our focus is on the conservation and management of the consumption of all site resources — carbon, energy, water, and waste. We’ve worked on over thirty award-winning projects, and our work has been published locally and internationally. Founded in 2003, our award-winning projects include 843 N Spring Street in Los Angeles, (tallest cross laminated timber structure in Los Angeles), Hudson Yards in New York (the largest private real estate development in U.S. history), San Francisco Better Streets Plan, Greater New Orleans Urban Water Plan, revitalization of the iconic waterfront Brooklyn Bridge Park, and the 35 square-km Baietan Urban Area Plan in the heart of Guangzhou, China. Our mission is to engineer an environmentally and socially regenerative planet. Will you join us? Role Summary At Sherwood Design Engineers, we value collaboration that incorporates multiple perspectives, and believe that diverse ideas produce more robust and equitable solutions. We have an amazing opportunity for a driven and curious Design Engineer focused on site civil design to support our team. Minimum Qualifications • Typically 5+ years of industry experience, • Bachelor’s degree in Engineering - Civil and/or Environmental, • Experience with Site Grading, Earthwork Calculations, Road Design, Drainage (Calculations & Reports), Utility Layout & Sizing, Technical Report Writing, • Ability to research and interpret technical documents, • Experience in preparing and advancing plan set packages through all project phases including providing redlines for drafter, • Exercise sound judgment on design decisions and in application of standard methods, • Work with multiple site base files oriented in different coordinate frames and varying units, • Knowledge of civil design programs (AutoCAD, Civil 3D, Water Design Software, GIS), • Knowledge of Microsoft and Google Office applications (Word, Excel, GDoc, GSheet), • Ability to travel to project sites as needed Preferred Skills • Certifications or other sustainability-oriented accreditation preferred (LEED,PE, etc.), • Knowledge of natural systems, green infrastructure, hydrology, stormwater design, • Knowledge of Bluebeam, • Constructability understanding, • Local permitting pathways understanding (Low Impact Development, LA Hillside Grading Ordinance, A-Permit, B-Permit, Building Permit, Grading Permits, Fire Department Approvals) Expected Outcomes • Research, design, develop, and evaluate plans, specifications, and layouts for residential, commercial, and industrial development projects, public works improvements, or other capital improvement projects using applied knowledge of civil engineering, • Design naturally and physically built structures using knowledge of biology, statistics, dynamics, materials, kinematics, hydrology, hydraulics, and geotechnics, • Prepare technical reports, create design specifications, and determine cost estimates, • Oversee construction of projects to ensure adherence to design specifications, • Ensure projects comply with local zoning and ordinances, as well as national regulatory requirements, • Identify, evaluate, and document existing structures for signs for disrepair and provide design remedies as necessary, • Create and interpret blueprints, technical drawings, and schematics, • Use drafting tools or computer-aided design (CAD) equipment and software in design work. May manage project schedules and budgets, • May be required to approve designs that can impact the health, safety, and welfare of the general public, as required by law What We Offer • Own a part of the firm with ESOP eligibility after one year, • Flexible working - 9/80 schedule with every other Friday off, • Competitive Health plans, including PPO and HMO options, Dental and Vision plans, • Learning and Development stipend to use as you see fit, • Generous PTO and 8 paid holidays, • Automatic 401k enrollment, • Fun team events, lunches and happy hours to get to know colleagues outside of work, • A tangible opportunity to truly help the environment! Compensation: The wage range for this role takes into account the wide range of factors that are considered in making compensation decisions, including but not limited to: skill sets; experience and training; licensure and certifications; and other business and organizational needs. At Sherwood Design Engineers, it is not typical for an individual to be hired at or near the top of the range for their role and compensation decisions are dependent on the facts and circumstances of each case. A reasonable estimate of the current range is $97,000 to $119,000. The disclosed range estimate has not been adjusted for the applicable geographic differential associated with the location at which the position may be filled. Reasonable accommodations may be made to individuals with disabilities to perform the essential functions. We will consider for employment qualified applicants with arrest and conviction records. Employer will not sponsor visas for position. Applicants must be currently authorized to work in the United States on a full-time basis. Powered by JazzHR oXMeIsteeg

Job Description Under the general direction of Principal Investigator, provides technical support in molecular endocrinology, diabetes and obesity research laboratory. Responsibilities includes project planning, data collection, experimental protocols and procedures; bench work involving lab techniques focused in molecular biology, and small animal studies. Essential Duties and Responsibilities: • Protein and RNA extract from mouse tissues and mammalian cells., • Mammalian tissues culture, • siRNA transfection in vivo and in vitro, • Real time RT-PCR, • Western blot, • Immunohistochemistry, • ELISA, • DNA cloning and plasmid purification, • Perform animal studies including diabetic animal model generation and treatment., • Animal tissue collection Other Duties and Responsibilities: • Perform other related duties as assigned. Qualifications/Requirements: EDUCATION: • Undergraduate degree (B.A., B.S.) required in Biological Sciences or related filed., • Master’s degree preferred. EXPERIENCE: • 1-3 years experience in related field., • Strong background in biochemistry and/or molecular biology. KNOWLEDGE/ABILITY/SKILLS: • Familiar with molecular biology techniques/science including extraction of DNA, RNA and protein, Western blots, cell culture techniques, immunohistochemistry, and instrumentation., • Ability to follow protocol performing experiments., • Capability to work independently., • Knowledge of optics and microscopy is a plus but not essential, • Proficient with MS Word, MS Excel, PowerPoint and Internet Explorer. COMPLEXITY: • The ability to perform highly detailed work with sustained attention and care while providing/obtaining information on numerous inquiries is paramount to success in this position. PHYSICAL DEMANDS: • 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. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. WORK ENVIRONMENT: • The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions., • Ability to work effectively with a diverse community. MENTAL DEMANDS: • The mental demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions., • Frequent variety of unrelated tasks. Constant calculating interrupted work, a variety of interrelated tasks, and use of sustained concentration, reasoning, judgment, resourcefulness, analytical ability, and ingenuity. SPECIAL REQUIREMENTS: • Ability to work effectively with a diverse community. COVID-19 As a health professions institution of higher education, Charles R. Drew University of Medicine and Science seeks to protect the health and safety of the University community. As a condition of enrollment and employment, students, faculty, and staff must comply with the current CDU Covid-19 requirements as described on the CDU Covid-19 webpage. Please visit the CDU Return to Campus website https://www.cdrewu.edu/covid-policy/ or email the Campus Nursing Office at nurseofficer@cdrewu.edu. EXCELLENT BENEFITS: Your wellbeing is important to us, Charles R. Drew University of Medicine and Science (“CDU”) offers a comprehensive health and wellness benefits package to help you stay healthy and provide financial you protection. POSITION STATUS: • Full Time, Non-Exempt COMPENSATION • $22.10 - $26.52 an hour CONDITIONAL EMPLOYMENT: The employment status of this position is classified as “Conditional.” Conditional employment means that the job exists contingent upon continued funding and limitations of restricted funds or, the duration of a specific program, project, grant, or contract. Since 100% of your salary is funded by (Rodent Model Study Liver & Muscle Effects Nic), end date (06/30/2027), your position is contingent upon the continued receipt of these funds. Continuation of your position is dependent, in part, upon funding availability. Furthermore, no work may be performed after the grant end date(s) unless you have received an extension in writing from a Dean, Division VP, or Human Resources. EEO STATEMENT: Charles R. Drew University is committed to Equal Employment Opportunity. Applicants will be considered without regard to gender, race, age, color, religion, national origin, sexual orientation, genetic information, marital status, disability or covered veteran status. FAIR CHANCE STATEMENT: Charles R. Drew University of Medicine and Science will consider qualified applicants, including those with criminal histories, in a manner consistent with state and local “Fair Chance” laws.

Job DescriptionBiology Research Scientist Job Type: Contractor Location: Remote Hours: 10–20 hours/week Duration: 1–2 months minimum, with likely extension Start: Immediate Job Overview We are seeking experienced Biology Research Scientists to support a project focused on validating protein target assignments against primary scientific sources and UniProt records. You will review research papers and patents, identify target assignment errors, propose corrected UniProt accessions, and provide concise, evidence-based scientific reasoning. Key Responsibilities • Review primary research papers and patents to verify protein target assignments., • Compare target assignments against UniProt and identify discrepancies., • Classify target assignment errors using a structured taxonomy., • Propose accurate UniProt accessions where assignments are incorrect., • Document clear, concise, evidence-grounded reasoning for each determination., • Apply expertise in pharmacology, biochemistry, molecular biology, or chemical biology to evaluate target relationships.Required Skills, • Protein Target Identification, • UniProt, • Primary Literature Review, • Protein Biochemistry, • Molecular Biology, • Pharmacology, • Binding & Functional Assays, • Scientific Data Interpretation, • Evidence-Based Reasoning, • Technical DocumentationQualifications, • BA/BS + 5 years, MS + 2 years, or PhD with relevant industry/drug discovery experience., • Background in pharmacology, biochemistry, molecular biology, or chemical biology within biotech, pharma, or CRO environments., • Hands-on experience with assays such as SPR, TR-FRET, radioligand binding, kinase assays, or GPCR functional assays., • Experience interpreting IC50, Ki, and Kd data., • Currently active in a bench-based research, scientist, or associate scientist role., • Working knowledge of UniProt or related workflows such as SAR, HTS, target validation, biochemical profiling, or IND-enabling studies.Nice to Have, • Experience with ChEMBL, BindingDB, or PubChem., • Selectivity profiling or counterscreening experience., • Understanding of agonist/antagonist vs. activator/inhibitor distinctions.Screening Questions, • What is your highest relevant degree and how many years of industry research experience do you have?, • What is your experience with protein target identification and UniProt?, • Which binding or functional assays have you performed hands-on?, • Do you have experience interpreting IC50, Ki, or Kd data?, • Have you worked with ChEMBL, BindingDB, or PubChem?, • Are you currently bench-active in a research or scientist role?, • Are you available for 10–20 hours per week with an immediate start?

Job DescriptionJob Title: Molecular Production Lab TechnicianJob Description The Molecular Production Lab Technician plays a key role in the testing, packaging, and quality control of raw materials and molecular diagnostic products. This position supports the production of PCR-based test kits for conditions such as COVID-19, RSV, and influenza, ensuring all products meet defined specifications and regulatory requirements. The technician contributes to the development of specifications and protocols, performs routine laboratory procedures, and completes all documentation required for product testing and release in a fast-paced laboratory production environment. Responsibilities • Perform testing, packaging, and quality control of raw materials and finished molecular diagnostic products in a laboratory production environment., • Complete all required documentation related to product testing, quality control, and release in an accurate, timely, and compliant manner., • Contribute to the development and refinement of product specifications and testing protocols to ensure all distributed products meet established quality standards., • Support and adhere to applicable regulations, including but not limited to FDA, ISO, and CMD/CAS requirements., • Use pipettes consistently and accurately for repetitive laboratory procedures, maintaining precision and aseptic technique., • Handle microscope slides, operate plate readers, and analyze resulting data using computer-based software., • Generate tables, charts, graphs, and reports using Microsoft Excel and Microsoft Word to document and communicate test results and production data., • Perform ELISA tests and other immunoassays as part of product formulation and quality control processes., • Assist with various aspects of producing molecular test kits, including basic packaging, assembling kits, and supporting formulation activities as training progresses., • Conduct raw material and product testing to support production of molecular devices and ensure ongoing product quality., • Work effectively as part of a team of lab technicians, collaborating and communicating to meet production goals and timelines., • Multi-task and prioritize work in a fast-paced environment, adapting to changing production demands and schedules., • Follow laboratory safety procedures and good laboratory practices when working with mechanical equipment, biohazardous and infectious materials, and chemicals., • Participate in training on first shift and remain open to occasional second-shift and weekend work on a voluntary basis as business needs arise.Essential Skills, • Hands-on experience with PCR techniques, gained through academic or laboratory settings., • Foundational knowledge in molecular biology or microbiology applicable to a production laboratory environment., • Proficiency in pipetting with consistent accuracy, including high-volume repetitive pipette use., • Experience with aseptic technique in a laboratory setting., • Basic understanding of ELISA assays and immunoassay principles., • Ability to navigate microscope slides and operate plate readers to collect and interpret experimental data., • Working knowledge of Microsoft Excel for generating tables, charts, graphs, and data reports., • Working knowledge of Microsoft Word for preparing documentation and reports., • Ability to multi-task and manage several responsibilities simultaneously in a fast-paced environment., • Capacity to follow detailed protocols and standard operating procedures with strong attention to detail., • Willingness and ability to work standard first shift hours and occasionally support second shift and weekend work on a voluntary basis.Additional Skills & Qualifications, • Bachelors degree preferred in Biology, Biological Sciences, Biochemistry, Microbiology, or another bio-related discipline., • Academic laboratory experience with pipetting, PCR, or aseptic techniques, clearly demonstrated on the resume., • Familiarity with molecular cell biology concepts as they relate to diagnostic product development and testing., • Experience in a quality control (QC) technician or laboratory technician role is beneficial., • Exposure to ELISA assays and, preferably, IFA assays is an advantage., • Comfort working with regulatory standards such as FDA, ISO, and CMD/CAS requirements., • Strong organizational skills and ability to maintain accurate records and documentation., • Effective communication skills for working within a team of laboratory technicians and production staff.Work Environment This role is based in a laboratory production environment focused on molecular diagnostics and the manufacture of PCR test kits for RSV, influenza, and COVID. The position begins as a 36 month contract with potential for hire, aligned with a busy seasonal period. Initial training occurs on a first shift schedule from 9:00 a.m. to 5:00 p.m., followed by standard first shift hours of 6:00 a.m. to 2:30 p.m. with a 30-minute lunch break. Technicians are expected to be open to occasional second-shift assignments from 2:00 p.m. to 10:30 p.m. several times per month on a voluntary basis, as well as occasional weekend work as business needs require. The lab is a sterile environment where technicians assist with packaging and assembling kits, performing ELISA tests, and supporting formulations and raw material testing. The team consists of approximately 1520 lab technicians working collaboratively to support production of molecular devices. While performing duties, employees may occasionally be exposed to moving mechanical parts, fumes or airborne particles, biohazardous and infectious materials, and toxic or caustic chemicals. The noise level is typically moderate. Appropriate laboratory attire is provided, including a lab coat, safety glasses, and gloves, and strict safety protocols and good laboratory practices are followed at all times. The work is highly repetitive, particularly with frequent pipette use, and is best suited to individuals who thrive in a structured, process-driven environment. Job Type & Location This is a Contract position based out of Cypress, CA. Pay and Benefits The pay range for this position is $22.00 - $22.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: Medical, dental & vision Critical Illness, Accident, and Hospital 401(k) Retirement Plan Pre-tax and Roth post-tax contributions available Life Insurance (Voluntary Life & AD&D for the employee and dependents) Short and long-term disability Health Spending Account (HSA) Transportation benefits Employee Assistance Program Time Off/Leave (PTO, Vacation or Sick Leave) Job Type & Location This is a Contract position based out of Cypress, CA. Application Deadline This position is anticipated to close on Nov 6, 2026. Workplace Type This is a fully onsite position in Cypress,CA. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options. San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records. Massachusetts Lie Detector: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability. Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.

Job DescriptionTitle: Research Scientist, Multiple Myeloma - Translational Medicine Location: Santa Monica, CA Duration: 12+ Months Schedule: Monday - Friday, 8:00am - 17:00pm Pay Rate: $43/hr. - $47/hr. on W2 Job Description The Research Scientist will support biomarker and translational strategy for the clinical development of Client’s chimeric antigen receptor (CAR-T) programs in Multiple Myeloma. As a member of the Translational Medicine team, you will be at the intersection of Research and Clinical Development, providing valuable insight into the function of CAR-T cells in patients and the development of potential prognostic tools. Regulatory filing experience and a demonstrated ability to facilitate clinical trial execution, synthesize scientific data, communicate key findings cross-functionally is required. Key Responsibilities: • Directs and establishes pharmacokinetic and pharmacodynamic (PK/PD) analysis to support clinical pharmacology for CAR T clinical trials in Multiple Myeloma, • Serves as Biomarker lead on clinical study teams to oversee delivery of pharmacology data and documentation required for pivotal and registrational study filings, • Reviews and contributes to clinical protocol design and study activities, • Identify and establish agreements with contract research organizations (CRO) and support the transfer of Client methods, • Collaborates with Clinical development teams including Clinical Operations, Regulatory, Clinical Data Management and Biometrics/Stats to advance data acquisition and analyses of clinical trial data, • Leads the resolution of clinical pharmacology/translational queries from regulatory agencies, supports writing and reviewing responses to regulatory queries., • Support the preparation of data packages for publication with medical writers, presentation and/or submission to regulatory agencies, • Collaborates with Translational Medicine, Bioinformatics and Statistical teams for exploratory biomarker correlative studies and deeper analysis of tumor biology and CAR T functionality, • Contribute to external scientific discussions/research collaborations and publications and engagement with key opinion leaders in the fieldEducation Level, • Advanced scientific degree (i.e. MD, PharmD, PhD) and 3+ years in industry OR Master's Degree and 5+ years of scientific experience OR Bachelor's Degree and 7+ years of scientific experience.Preferred Qualifications:, • Strong background in cancer immunotherapy, immunology and/or oncology with experience focusing on Multiple Myeloma, • Prior experience in Regulatory filings, • In-depth understanding of multiple myeloma, knowledge of clinical landscape, evolving therapy, competitive scenarios, • Strong understanding of clinical, translational, and mechanistic data, • Familiarity and experience with clinical and biomarker operations, • Understanding of early or late-stage drug and translational development process; including clinical trial experience in industry or academia, • Familiarity with bioanalytical assay development and validation in a GxP environment, • Experience working with engineered T cells, immunophenotyping, and NGS-based approaches to profile the function of tumor and immune cells, • Comfortable in a matrixed and fast-paced company environment and able to adapt to changing priorities, • Strong collaboration, excellent interpersonal and communication skills, • Proficient with data presentations to communicate to a diverse cross-functional audience, • Maintain a high degree of accuracy and attention to detail, • Ph.D. degree in biology-related field (immunology, cancer biology, bioinformatics or a closely related field).