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Staff Research Associate 2 Non-Exempt - Irvine, CA, Job ID 74113
University of California Agriculture and Natural Resources 3.6
Research Scientist Job 10 miles from Orange
The Staff Research Associate II (SRA II) will assist the Cooperative Extension Advisors (Advisors) with research and education in nurseries and greenhouse production in California, focusing on irrigation and water quality management, pest management, disease management, fertilization management and other topics. The projects' audience is composed of predominantly Hispanic population and Spanish language skills are important. Under supervision, incumbents perform a wide variety of standard repetitive laboratory and/or field experimental procedures at the full operational or journey level of skill in one field of specially; or perform a limited variety of non-standard laboratory and/or field experimental procedures requiring ingenuity, resourcefulness, and adaptability to special and changing needs of research in one specialized field. Incumbent will perform a wide variety of standard procedures without detailed technical supervision, in horticulture. They may also modify, vary or adapt standard procedures to meet the needs of research projects, or improve tests that are unsatisfactory, and after studying available literature, analyze and alter conditions under which determinations are made. The position is a full-time position requiring 40 hours per week, but flexibility is required according to travel schedule and seasonal work schedule. Occasionally it may be required to work during the weekend or on holidays. The position requires frequent travel to nursery and greenhouse operations in southern California and infrequent but regular travel to Central Valley, Ventura/Santa Barbara, Watsonville/Salinas/Gilroy, Sacramento. The expected frequency of travel for data collection and organizing trainings is 2 days per week. This position is a career appointment that is 100% fixed, with grant funding available through 10/01/2026. Pay Scale: $28.88/hour to $36.62/hour Job Posting Close Date: This job is open until filled. The first application review date will be 11/15/2024. Key Responsibilities: 10% Reporting and Writing Summarize research findings for use in articles (popular press, newsletter and journal) using MS Office suite programs and statistical programs. Assist in preparation of grant proposals and in summarizing literature and data needed for funding group reports and assist in writing publications and peer reviewed publications in scientific journals. Prepare graphical summaries, using Microsoft Excel, that will be used to demonstrate the discovered data in publications. Review studies, literature, attend workshops, seminars, training. Prepare travel reports in accordance with University policies. 15% Data Preparation Collect data and prepare initial reports. Modify, vary or adapt standard procedures to meet the needs of the research project. Convert raw data into testable value; conduct basic statistical analysis. Ensure that there is the necessary information to evaluate each trial. Generate summary and overview reports of program activities as needed. This includes educational event and field demonstration evaluations and monthly, quarterly, and annual reporting as needed. Manage survey data from training events. 40% Outreach Coordinate and collaborate with federal, state, county, and local agencies and community-based organizations on the delivery of programs to support program functional area. Produce educational videos which may include filming and editing Delivers trainings, with guidance and oversight from the Advisors, on the topic of irrigation and water management in English and Spanish for California nursery irrigators and production managers Organizes all aspect of trainings including booking travel and coordinating with cooperators. 35% Field Work/Research In consultation with the supervisor, plan and assist in coordination of project experiments. Ensure that sufficient materials are available to provide required safety training and documentation to assure safe work environment. Under direction of the Advisors, set up experiments and collect data at various nurseries throughout Southern California regarding irrigation and pest management Requirements: Demonstrated scientific/research experience or formal education in horticulture, agriculture, or related field. Experience with research and/or teaching, training, or workshops. Experience with scientific field studies including data collection, data management and data entry. Scientific knowledge and skill to make technical determinations and/or observations. Ability to deliver effective presentations in conjunction with Advisor coaching and guidance. Ability to set up scientific experiments and collect data with Advisor supervision. Knowledge of the principles of horticulture, which may include: irrigation and water quality, pest, disease, and fertilization management. Demonstrated ability to develop and outreach to community partners. Demonstrated experience with computers, software, and social media for the development and delivery of newsletters, presentations, and other educational materials. Experience using Microsoft Office. Excellent oral and written communication skills. Bilingual Spanish speaking, reading, and writing. Preferred Skills: Experience with data compilation in order to produce reports. Special Conditions of Employment: Ability to work a flexible work schedule including early mornings, evenings, and weekends and holidays as needed to meet project needs. Travel, including travel outside of normal business hours may be requested. Must possess valid California Driver's License to drive a County or University vehicle. Ability and means to travel on a flexible schedule as needed, proof of liability damage insurance on vehicle used is required. Reimbursement of job-related travel will be reimbursed according to University policies. The University reserves the right to make employment contingent upon successful completion of the background check. This is a designated position requiring a background check and may require fingerprinting due to the nature of the job responsibilities. UC ANR does hire people with conviction histories and reviews information received in the context of the job responsibilities. As of January 1, 2014, ANR is a smoke- and tobacco-free environment in which smoking, the use of smokeless tobacco products, and the use of unregulated nicotine products (e-cigarettes), is strictly prohibited. To apply, please visit: https://careerspub.universityofcalifornia.edu/psc/ucanr/EMPLOYEE/HRMS/c/HRS_HRAM_FL.HRS_CG_SEARCH_FL.GBL?Page=HRS_APP_JBPST_FL&JobOpeningId=74113&PostingSeq=1&SiteId=17&language Cd=ENG&FOCUS=Applicant Copyright ©2025 Jobelephant.com Inc. All rights reserved. Posted by the FREE value-added recruitment advertising agency jeid-8d9747651b1da24dac8438a5c1c90e14
$28.9-36.6 hourly 8d ago
Founding Head of AI Products
Clear Skies Partners
Research Scientist Job 35 miles from Orange
Clear Skies is incubating a stealth venture that uses an AI-powered platform to serve major stakeholders in private equity. We operate at the intersection of finance/AI to optimize deal flow, automate decisioning, and integrate networks into a seamless customer journey. Our team is composed of seasoned professionals from private equity, financial advisory, human capital, and AI engineering. We are seeking a Founding Head of AI Products to spearhead the development of AI-driven solutions that redefine how investments are sourced, evaluated, and executed. You will define the product and lead AI initiatives to solve real-world problems in a multi-billion-dollar industry. Key Responsibilities: Product Strategy Execute AI product strategies for market fit and business impact. Analyze customer needs and competitive landscape to uncover new product opportunities. Build business cases with market analysis, ROI projections, and scalability assessments. AI Product Development Define features and workflows to gather customer feedback and iterate on MVP development. Build AI-powered engines to transform large-scale unstructured data into actionable intelligence. Implement NLP techniques for semantic search and keyword matching from unstructured data. Utilize embedding models for vector-based search and context understanding. Workflow Automation Establish scalable AWS-based infrastructure and data pipelines. Develop automated communications, scheduling, and self-service AI tools. Implement best practices for AI model versioning, monitoring, and optimization. Leadership & Collaboration Lead and mentor AI and product teams, promoting innovation and learning. Collaborate with business leaders to align AI strategies with goals. Define and track KPIs to measure product success and guide development. Key Qualifications: 10+ years in product leadership with focus on AI/ML platforms and generative AI technologies. Expertise in AI/ML frameworks (TensorFlow, PyTorch, etc.) and cloud infrastructure. Experience in financial services or private equity is a plus. Application Process: Interested candidates are invited to submit their CV and cover letter detailing relevant experience and qualifications to ***************************. About Clear Skies: Clear Skies is a private equity investment firm that acquires middle-market businesses. We partner with management teams to drive growth and value through our global networks.
$86k-121k yearly est. 52d ago
Principal Applied AI Scientist
Gusto 4.5
Research Scientist Job 35 miles from Orange
Gusto is a modern, online people platform that helps small businesses take care of their teams. On top of full-service payroll, Gusto offers health insurance, 401(k)s, expert HR, and team management tools. Today, Gusto offices in Denver, San Francisco, and New York serve more than 400,000 businesses nationwide. Our mission is to create a world where work empowers a better life, and it starts right here at Gusto. That's why we're committed to building a collaborative and inclusive workplace, both physically and virtually. Gusto is looking for a Principal Applied AI Scientist to join our AI team and build out our Generative AI capabilities. About the Role: We're looking to accelerate AI investments across the business to solve customer pain points, and are growing our Applied AI team. You'll be a part of the core group of experts exploring big, innovative bets, quickly prototyping solutions and shipping to customers. You're also responsible for quickly iterating on improvements and eventually scaling to production-grade AI applications. You'll be working alongside a multidisciplinary group of Product Engineers, PMs, and Design. In this role, you'll be responsible for designing, building, evaluating, and shipping products that use proprietary and open source LLMs. You'll be responsible for all aspects of the AI development lifecycle: framing the problem, designing the system, making decisions on frameworks, building, evaluation, and deploying. As an Applied AI Scientist, you'll own the customer impact end-to-end. Here's what you'll do day-to-day: Design, develop and deploy innovative AI solutions Experiment with multi-agent frameworks to build autonomous systems Improve LLMs through pre-training, fine-tuning, and RLHF Build evaluation for LLMs and LLM based products, and assess best methods required to build LLMs suited for purpose Collaborate with the engineering team to determine technical requirements and SLAs for API-enabled services Research novel AI techniques and strategies that create magical customer experiences Here's what we're looking for: 8+ years experience designing, evaluating, and productionizing AI applications. Experience with Agentic AI frameworks (LangGraph and Llama-Index) and experience building, deploying and maintaining LLM-based applications in production are essential Demonstrated expertise in writing production-level Python code Proven ability to design and prototype AI solutions quickly Experience working on multi-agent AI systems to automate end to end workflows Our cash compensation amount for this role is targeted at $191,000-$237,000/year in Denver, Chicago, and Atlanta, $208,000-$258,000/year in Los Angeles and Seattle, and $225,000-$279,000/year for San Francisco and New York. Final offer amounts are determined by multiple factors including candidate experience and expertise and may vary from the amounts listed above. Gusto has physical office spaces in Denver, San Francisco, and New York City. Employees who are based in those locations will be expected to work from the office on designated days approximately 2-3 days per week (or more depending on role). Our customers come from all walks of life and so do we. We hire great people from a wide variety of backgrounds, not just because it's the right thing to do, but because it makes our company stronger. If you share our values and our enthusiasm for small businesses, you will find a home at Gusto. Gusto is proud to be an equal opportunity employer. We do not discriminate in hiring or any employment decision based on race, color, religion, national origin, age, sex (including pregnancy, childbirth, or related medical conditions), marital status, ancestry, physical or mental disability, genetic information, veteran status, gender identity or expression, sexual orientation, or other applicable legally protected characteristic. #J-18808-Ljbffr
$225k-279k yearly 17d ago
Holography Application Scientist
Metrolaser, Inc. 3.8
Research Scientist Job 15 miles from Orange
Candidates must be US citizens or US permanent residents as required by Government regulations for this position. MetroLaser, Inc. is a leading R & D company world-wide recognized for its laser-based measurement and diagnostic technologies for industrial, military, and space applications. Since its inception in 1988, MetroLaser has been at the forefront of state-of-the-art research and development as well as the commercialization of optical diagnostics systems to measure flow velocity, temperature, chemical composition, surface temperature, non-destructive inspection of components, etc. The core business of MetroLaser is in the defense sector, NASA and DOE and as a commercial provider of flow and combustion diagnostics. We have an exciting opening for a Holography Applications Scientist at our office in Laguna Hills, CA. The new appointee will support the scientific staff in implementation, investigation and analysis of laboratory-based experiments and various engineering problems. The successful candidate is expected to work under moderate supervision while using technical skills and judgment to solve problems encountered during the course of the experimental/analytical investigation. The appointee is expected to prioritize time to stay on schedule, be proactive in documenting the results and findings, and in communicating them to the scientific staff. He/she is expected to work as a part of a team and may also lead efforts with other engineers and technicians. Job Responsibilities Design, analysis and construction of optical systems using holography for measurements, right from inception to prototyping Application of holography for microscopy and microbial tracking for plant biology Application of holography for measurements in fluid mechanics and particle dynamics Interfacing holography with fluorescence-based spectroscopy Develop timelines and resources to implement solutions for the project execution Layout of breadboard for experimental work and instrument development Document findings/results and analyses for reporting Interface with other technical stuff to jointly investigate and solve engineering problems Prepare technical presentations for internal use, conferences and customers Qualifications MS/Ph.D. in optical sciences/engineering, mechanical/aerospace/structural engineering or equivalent, with 1 or more years of work experience after the PhD degree or 2 or more years of experience after the MS degree Good understanding of optics, lens design, optical systems design Working knowledge of holography, interferometry and Schlieren for instrument development and applications Good understanding of fluid mechanics and structural mechanics Good understanding of microbial tracking in plant biology Experience with lasers and optical detectors Experience with Zemax or a similar optical design software Experience in image processing and software coding using C/C++/Python/MATLAB Experience with LabVIEW and SOLIDWORKS programming Highly-motivated and a self-starter with ability to quickly absorb new concepts and subsequent application within prescribed timelines and resources Strong communication and inter-personal skills, and the ability to work in a team towards a larger company objective MetroLaser, Inc. offers highly competitive compensation and fringe benefit package that includes retirement plan, matching contributions; health, dental and vision benefits; generous paid time-offs; sick leaves and a highly intellectual, work environment. MetroLaser is an equal opportunity employer. Candidates must be US citizens or US permanent residents as required by Government regulations for this position .
$74k-116k yearly est. 3d ago
Associate Hardware Scientist (Mass Spec - Ion Traps)
Sciex 4.6
Research Scientist Job 4 miles from Orange
For over 50 years, SCIEX has been developing groundbreaking technologies and solutions in mass spectrometry and capillary electrophoresis. Our products enable our customers to quickly respond to environmental hazards, better understand biomarkers relevant to disease, improve patient care in the clinic, bring relevant drugs to market faster and keep food healthier and safer. At SCIEX, you'll find a rewarding role that amplifies your impact on the world and helps you realize life's potential. SCIEX is one of 10 Life Sciences companies of Danaher. Together, we accelerate the discovery, development and delivery of solutions that safeguard and improve human health. Learn about the Danaher Business System which makes everything possible Are you ready for the next step in your mass spectrometry career? The Associate Hardware Research Scientist (Mass Spectrometry- Ion Traps) is responsible for driving innovation around ion traps and mass analyzers. This position is part of the Hardware Research Department and will be located in Concord, Ontario. In this role, you will have the opportunity to: Defines and tests novel ion trap hardware to enable improved performance for customer workflows Performs different methodologies to verify or validate different aspects of hardware/software under the mentorship of more senior scientists Drives innovation by generating novel ideas to advance scientific technology Identifies and implements opportunities for product improvement within a defined research area Contributes to on-time delivery of different research projects and translates development or scientific risks into a tangible research plan The essential requirements of the job include: Higher level Science degree in a related field such as Physics, Chemistry, or similar required (Ph.D. preferred) Broad background and knowledge of ion movement, mass analyzer technology, ion trap technology and ion trap theory Proven publication record within the field related to hardware design Experience with various sample introduction techniques It would be a plus if you also possess previous experience in: Understands the link between project goals and company strategy Ability to work independently Proven track record of innovation and patent generation preferred The salary range for this role is $90-$120K CAD. This is the range that we in good faith believe is the range of possible compensation for this role at the time of this posting. This range may be modified in the future. SCIEX, a Danaher company, offers a broad array of comprehensive, competitive benefit programs that add value to our lives. Whether it's a health care program or paid time off, our programs contribute to life beyond the job. Check out our benefits at Join our winning team today. Together, we'll accelerate the real-life impact of tomorrow's science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life. For more information, visit . Danaher Corporation and all Danaher Companies are committed to equal opportunity regardless of race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law. We value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform crucial job functions, and to receive other benefits and privileges of employment. Please contact us at to request accommodation.
$90k-120k yearly 1d ago
Bioinformatics Scientist
燃石医学 Burning Rock Biotech
Research Scientist Job 10 miles from Orange
About Burning Rock Dx.: Burning Rock Dx. (NASDAQ:BNR) was foundedin 2014, and it is a leading innovator in next-generation sequencing (NGS) technologies, dedicated to advancing precision medicine, genomics research, and clinical diagnostics. We collaborate with global partners to deliver cutting-edge solutions for complex biological challenges. About the Role: We‘re seeking a highly skilled and motivated Clinical Bioinformatics Scientist to join our CAP-accredited molecular oncology laboratory. The candidate will play a crucial role in analyzing and interpreting Next-Generation Sequencing (NGS) data for cancer diagnostics, ensuring compliance with CLIA/CAP guidelines, and contributing to the development of robust bioinformatics pipelines for somatic and germline variant analysis. Key Responsibilities: Analyze and interpret NGS data for molecular oncology applications, including somatic and germline variant calling, copy number alterations, structural variations, and tumor mutational burden (TMB)/microsatellite instability (MSI) analysis. Develop, optimize, and maintain bioinformatics pipelines for clinical NGS testing, ensuring compliance with CAP, CLIA, and FDA regulatory requirements. Perform variant annotation, curation, and classification using public and proprietary databases (e.g., ClinVar, COSMIC, gnom AD, OncoKB). Support quality control (QC) and quality assurance (QA) activities by identifying and troubleshooting technical and computational issues. Collaborate with molecular pathologists, clinical scientists, and laboratory personnel to ensure accurate variant interpretation and reporting. Stay up to date with emerging bioinformatics tools, guidelines, and best practices for NGS-based oncology testing. Assist in validation and verification of new assays, software updates, and enhancements to bioinformatics workflows. Participate in CAP/CLIA audits, proficiency testing, and regulatory documentation. Maintain and develop Laboratory Information Management Systems (LIMS) to support efficient clinical sample tracking, data management, and workflow automation. Work closely with laboratory staff to ensure seamless LIMS integration with NGS pipelines and other bioinformatics tools. Qualifications: PhD in Bioinformatics, Computational Biology, Genomics, Molecular Biology, or a related field, OR MS with at least 3 years of relevant clinical experience. Strong experience with NGS data analysis in a clinical setting, preferably in molecular oncology. Proficiency in Python, R, Perl, Bash, and Linux-based environments for bioinformatics workflows. Familiarity with NGS analysis tools such as GATK, SAMtools, BCFtools, VarDict, Mutect2, Annovar, VEP, and other variant callers/annotators. Experience working with NGS assay validation, quality control metrics, and regulatory compliance (CAP/CLIA/FDA guidelines). Strong knowledge of human genetics, cancer genomics, and clinical variant interpretation (ACMG/AMP/ASCO guidelines). Ability to work in a collaborative, fast-paced clinical laboratory environment with strong analytical and problem-solving skills. Nice to Have: Prior experience working in a CAP/CLIA-certified clinical laboratory. Knowledge of cloud-based bioinformatics workflows (e.g., AWS, Terra, DNAnexus).Experience with database management, pipeline automation, and high-performance computing (HPC) environments. Understanding of laboratory information management systems (LIMS). Prior involvement in NGS assay development, validation, or FDA submission processes. Benefits & Perks: Competitive salary and performance-based bonuses Comprehensive healthcare, dental, and vision insurance 401(k) retirement plan with company matching Paid time off and flexible work arrangements Professional development and conference opportunities Join us in advancing precision oncology through cutting-edge clinical bioinformatics. Equal Opportunity Statement: It is the policy of Burning Rock Dx. LLC to provide equal employment and advancement opportunities to all colleagues and applicants for employment without regard to race, color, ethnicity, religion, gender, pregnancy/childbirth, age, national origin, sexual orientation, gender identity or expression, disability or perceived disability, genetic information, citizenship, veteran or military status or a person's relationship or association with a protected veteran, including spouses and other family members, marital or domestic partner status, or any other category protected by federal, state and/or local laws. As an equal opportunity employer, Burning Rock Dx LLC is committed to a diverse workforce.
$85k-130k yearly est. 20d ago
Research Associate - In Vivo
Hamlyn Williams
Research Scientist Job 35 miles from Orange
Partnered with a growing biotech startup dedicated to CNS drug delivery. As a Research Associate - In Vivo, you will play a crucial role in preclinical research and early drug development, assessing therapeutic candidates in animal models. Key Responsibilities Design and execute in vivo studies using rodent or other mammalian models. Handle and process blood and tissue samples for biochemical and histological assays. Collaborate with cross-functional teams to advance preclinical studies. Maintain laboratory equipment, generate documentation, and assist in data analysis. Present findings to multidisciplinary discovery teams. Adapt to evolving research needs and support various lab tasks as required. Basic Qualifications B.S. or M.S. in Life Sciences (Biology, Neuroscience, Pharmacology, or related field). Strong understanding of CNS disease biology. Hands-on experience with rodent or mammalian animal models. Skilled in tissue processing and sample handling with attention to precision. Familiarity with biochemical/histological analysis techniques and standard lab equipment. Excellent communication, multitasking, and problem-solving skills. Preferred Qualifications Experience with plate-based assays (e.g., ELISA, RT-qPCR). Knowledge of biologics delivery (antibody, oligonucleotide, peptide) in in vivo studies. Proficiency in animal handling techniques (behavioral experiments, perfusion) and tissue processing (sectioning, imaging). Commitment to a two-year tenure for team consistency and growth.
$47k-75k yearly est. 1d ago
Senior Research Associate In Vivo
Acurastem 3.3
Research Scientist Job 29 miles from Orange
AcuraStem is a patient-based biotechnology company pioneering the development of treatments for amyotrophic lateral sclerosis (ALS), Frontotemporal dementia (FTD), and additional neurodegenerative diseases. We are a purpose-driven company on a mission to get our promising treatments into patients' hands as quickly as possible. AcuraStem's best-in-class disease modeling platform, iNeuroRx , is the gold standard for discovering novel, effective, and broadly-acting treatments. The AcuraStem team's extensive expertise in ASO technology is accelerating the advancement of treatments to the clinic. At AcuraStem, we know that empowered and supported colleagues strengthen our commitment and significantly enhance our collective mission. We are committed to scientific excellence, impactful results, persistence, attention to detail, teamwork, sound decision-making, and continuous learning. We are seeking a highly skilled and well-organized Senior Research Associate to contribute to our research programs and drive scientific progress. The Senior Research Associate will work closely with AcuraStem scientists, executing and refining experimental protocols with precision. The ideal candidate will have experience handling rodents and be adept at following detailed protocols meticulously while also demonstrating the ability to propose improvements when necessary. Responsibilities: Design, execute and manage in vivo experiments assessing the efficacy and safety of test agents in various rodent models. Perform a range of in vivo techniques, including rodent handling, various routes of compound administration (IV, ICV, IT), tissue collection, and behavioral assessments. Manage mouse colonies and perform breeding, weaning, and genotyping. Conduct various laboratory assays, including immunohistochemistry, microscopy, and biochemistry/molecular biology. Analyze and interpret experimental data, and prepare scientific documents including study reports, protocols, and other related materials for presentations, regulatory submissions and publications. Maintain accurate records of experimental data and protocols in accordance with AcuraStem guidelines. Collaborate effectively with internal/external resources to schedule and execute tasks independently with minimal training/guidance from manager. Independently conducts multiple complex experiments and provides technical guidance and problem solving related to methods, procedures and processes, and obtain optimum solutions. Provide technical guidance and problem-solving related to methods, procedures, and processes to the work group. Mentor and train junior lab members, promoting a positive and collaborative research environment. Desired Skills and Experience: Minimum 6+ years of hands-on experience conducting in vivo research with mice or rats. B.S. in Biology, Neuroscience, Bioengineering, or a related discipline, with 4+ years of industry experience or 6+ years of academic research experience. Strong verbal and written communication skills for effective collaboration and documentation. Strong organizational and analytical skills to manage multiple projects simultaneously. Proven ability to work effectively both independently and as part of a team. Knowledge of and adherence to Environmental Health & Safety (EH&S) procedures. Additional Information: Scheduling Flexibility: Availability for late evening, weekend, and holiday work as needed to support animal welfare needs. Travel Requirement: Frequent travel (>50%) to various AcuraStem laboratory sites in Los Angeles. Work Authorization: Candidate must be currently in the USA and authorized to work immediately. Compensation/Benefits: The salary range for this position is $82,000 - $115,000 with actual compensation determined by factors such as experience, qualifications, location, and other role-specific requirements. AcuraStem offers a comprehensive and competitive benefits package tailored to attract top talent. All regular-status employees receive compensation, performance-based bonuses, equity, and extensive benefits, including health, dental, vision, life, and disability insurance. AcuraStem also provides paid time off, annual company holidays, 401K matching, and bi-weekly lunch for onsite staff. Diversity, Inclusion, and Recruitment Practices at AcuraStem: Applicants must be authorized to work in the United States. AcuraStem is an equal-opportunity employer and values diversity and inclusion throughout the hiring process. Employment decisions are made based on relevant qualifications, experience, and business needs, without regard to race, color, religion, sex, gender identity, sexual orientation, age, marital status, national origin, disability, veteran status, or any other protected characteristic. AcuraStem's commitment to diversity and inclusion extends to all areas of employment, including hiring, compensation, performance evaluations, promotions, training, and career development. We strive to provide a supportive and inclusive workplace, free from discrimination or harassment. For staffing inquiries, AcuraStem's Human Resources team manages all recruitment activities directly. We ask that external recruiters avoid contacting hiring managers or submitting candidates without prior authorization, as unsolicited resumes will not establish any contractual relationship with AcuraStem. Qualified candidates, please submit your CV/resume to ******************
$82k-115k yearly 47d ago
Transcriptomics Scientist - Wet Lab (mRNA Specialization)
Grittgene Therapeutics
Research Scientist Job 29 miles from Orange
Job Title: Transcriptomics Scientist - Wet Lab (mRNA Specialization) Type: Contract with potential to turn into full-time We are looking for an experienced and hands-on scientist to lead and execute mRNA-related wet lab experiments. The ideal candidate will have deep expertise in transcriptome profiling techniques, RNA isolation and quality control, and next-generation sequencing (NGS) library prep, with a particular focus on mRNA biology. This role is heavily experimental and requires a passion for lab work, molecular assay optimization, and data generation. Key Responsibilities: Design and execute experiments for transcriptomic profiling, including bulk and targeted mRNA analysis. Isolate high-quality RNA from a variety of sample types (e.g., tissues, cells, biofluids, extracellular vesicles) and perform quality assessments. Develop and optimize mRNA-focused protocols for RNA extraction, cDNA synthesis, qPCR, and NGS library preparation. Maintain and operate equipment such as Agilent Bioanalyzer, Qubit, thermal cyclers, illumina sequencers and nanopore sequencers , and automated liquid handlers. Interpret experimental results and troubleshoot technical issues in collaboration with cross-functional teams. Document experimental procedures, protocols, and results in lab notebooks and databases. Stay up to date on advancements in transcriptomics technologies and incorporate new methodologies as appropriate. Qualifications: PhD or MS in Molecular Biology, Biochemistry, Genetics, or related field with 2+ years (PhD) or 4+ years (MS) of hands-on wet lab experience in transcriptomics. Deep understanding of mRNA biology and transcriptomic workflows (e.g., polyA selection, rRNA depletion). Strong hands-on experience with RNA isolation, reverse transcription, qPCR, and NGS library prep. Familiarity with working with human or animal tissue and cell culture samples. Experience working in a fast-paced, collaborative research environment. Excellent organizational, communication, and data documentation skills. Experience with automation platforms or single-cell workflows is a plus but not required. The Company: GrittGene Therapeutics is a start-up company at the R&D preclinical stage aimed at the development of treatment for DM, particularly DM2. We are building a diverse team of highly motivated professionals from various fields of science and technology. We are building a diverse, interdisciplinary team of dreamers and doers. We're looking for fellow visionaries hungry for real impact in reimagining every facet of how we cure disease.
$69k-105k yearly est. 3d ago
Scientist
Akkodis
Research Scientist Job 10 miles from Orange
Akkodis is seeking a Scientist I for a contract to hire, onsite position with a client in Irvine, CA. / No Corp-to-Corp; No C2C; No Referrals from C2C accepted Rate Range: $25.00/hour to $28.00/hour; The rate may be negotiable based on experience, education, geographic location, and other factors. Job Title: Scientist I - Chemistry/Microbiology Location: Irvine, California Department: Advanced Research & Development Position Summary: We are seeking a highly motivated and detail-oriented Scientist I to join our Advanced Research & Development team. The successful candidate will support both routine and exploratory testing, method development, and process improvement initiatives. This hands-on laboratory role involves data collection, analysis, and collaboration with cross-functional teams to drive innovation and support the development of next-generation products. ________________________________________ Key Responsibilities: Under supervision and in accordance with applicable regulations (e.g., FDA, ISO) and company policies and procedures, the Scientist I will: •Conduct experiments to support the development and evaluation of new technologies for potential products, including biological and chemical studies involving materials, medical devices, and associated cleaning agents, disinfectants, sterilants, and processing technologies. •Execute research studies by following prepared protocols and experimental designs to support product development across feasibility, verification, and validation phases. •Perform data analysis, organize results, and prepare basic reports and summaries. •Prepare microbiology media/fluids and sterilize glassware and laboratory supplies as needed. •Participate in routine laboratory maintenance, instrument calibration, and inventory management. •Collaborate with internal stakeholders to meet project timelines and deliverables. •Clearly and effectively communicate experimental progress and testing outcomes to team members. •Support general lab functions and perform other duties as assigned. •Contribute to a collaborative and high-performing team environment. ________________________________________ Qualifications: •Bachelor's degree in Chemistry, Microbiology, Biochemistry, or a related scientific discipline is required. •At least 2 years of relevant laboratory experience in academic, research, or industrial settings is preferred. •Familiarity with standard analytical and/or microbiological techniques and instrumentation is required. •Strong attention to detail, organizational skills, and commitment to quality is required. •Ability to work independently as well as collaboratively within a team is required. •Excellent communication, documentation, and critical thinking skills are required. ________________________________________ Work Environment & Physical Requirements: •Ability to lift and carry a minimum of 25 lbs. •Position requires physical activity including: o Up to 80% standing o Up to 80% walking o Up to 50% sitting o Up to 10% kneeling •Frequent repetitive hand motions required, including pipetting, twisting, simple grasping, fine manipulation, and computer use. •Appropriate use of personal protective equipment (PPE) is required at all times. If you are interested in this role, then please click APPLY NOW. For other opportunities available at Akkodis go to **************** Equal Opportunity Employer/Veterans/Disabled Benefit offerings available for our associates include medical, dental, vision, life insurance, short-term disability, additional voluntary benefits, an EAP program, commuter benefits, and a 401K plan. Our benefit offerings provide employees the flexibility to choose the type of coverage that meets their individual needs. In addition, our associates may be eligible for paid leave including Paid Sick Leave or any other paid leave required by Federal, State, or local law, as well as Holiday pay where applicable. Disclaimer: These benefit offerings do not apply to client-recruited jobs and jobs that are direct hires to a client. To read our Candidate Privacy Information Statement, which explains how we will use your information, please visit ****************************************** The Company will consider qualified applicants with arrest and conviction records in accordance with federal, state, and local laws and/or security clearance requirements, including, as applicable: · The California Fair Chance Act · Los Angeles City Fair Chance Ordinance · Los Angeles County Fair Chance Ordinance for Employers · San Francisco Fair Chance Ordinance
$25-28 hourly 3d ago
Formulation Scientist (Nutraceuticals)
Captek Softgel International 4.2
Research Scientist Job 12 miles from Orange
Summary: The R&D Formulator develops and optimizes formulations, conducts testing, and ensures accurate documentation. Supports technology transfer, collaborates cross-functionally, and stays updated on industry trends. Maintains lab safety, mentors staff and participates in management meetings. Evaluates raw materials, improves formulations, and oversees special projects as assigned. Essential Duties and Responsibilities Formulation creation (bench mix, formulation sheet, product description sheet, sample measurement, color verification, etc.) Writes and/or reviews procedures, purchase orders, quotes, and specifications needed to support product development activities Develops and/or performs all formulation requirements on new formulas Documents test results, specifications, and final formula procedures in a standard format for inclusion in the master file Participates in the technology transfer from pilot scale to manufacturing Communicates, in a timely fashion, all information regarding formulation, project status, raw material research, results, etc. to all appropriate individuals in Purchasing, Sales, Customer Services, and Quality departments Conducts intellectual searches for technical information through a variety of resources Keeps abreast of current trends, practices, developments, and regulatory changes, which would impact products, procedures, or formulation Ensures the maintenance and/or adherence to good laboratory practices and all safety regulations both in laboratory and manufacturing areas Provides technical knowledge in guiding other assistants/technicians in the R&D Lab Develops and presents to the R&D Manager or Director, R&D matters requiring his/her decision Participates in scheduled Management and Sales meetings in the absence of the R&D Manager/Director Evaluate new and alternative raw materials for functionality and stability Assist in verification studies as required Reformulate to improve existing products as needed Special projects as needed and any other tasks assigned by the R&D Director or Manager. Qualifications/Education/Experience: Minimum Bachelor of Science in Chemistry or related field 2+ years' Experience in R&D, Quality Assurance, Quality Control or Manufacturing is required; nutritional, pharmaceutical or biotechnology experience preferred; Have strong eye for color, finish, and detail Must have proficient math skills; weights and volumes experience a plus Excellent communications (verbal/written) Excellent organizational and multi-tasking skills Proficient with MS Word, Excel, Teams, and Outlook 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. While performing the duties of this job, the employee is occasionally exposed to work near moving mechanical parts, fumes, or airborne particles and risk of electrical shock. The noise level in the work environment is usually moderate. 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. Physical demands require sitting for extended periods of time, walking, bending, reaching, carrying, and occasionally lifting and/or moving objects up to 25 pounds. Specific vision abilities required by this job include Close vision, Peripheral vision, and the ability to adjust focus. While performing the duties of this job, the employee is occasionally required to use hands to finger, handle, or feel; reach with hands and arms; climb or balance; stoop, kneel, crouch, or crawl and talk or hear.
$80k-116k yearly est. 25d ago
Formulation Scientist
Simply Biotech
Research Scientist Job 27 miles from Orange
Formulation Scientist- Simply Biotech Are you looking for a new career opportunity with an exciting biotech company?! Then we've got the right team for you! In this role, you're responsible for the duties listed below. Immediate opening for a Formulation Scientist with a biotech company in Torrance, CA who possesses: Bachelor's degree in chemical engineering, chemistry, food science/technology, or similar 2 years' experience in nutritional supplement industry or similar field (working with dietary supplements, pharmaceutical development, etc.) 1+ year experience in granulation techniques, processing, and property characterization Email resumes to ************************* or call ************ FULL DESCRIPTION : The Formulation Scientist is responsible for the development of new products, enhancement of existing formulations, and resolution of manufacturing challenges. This role involves evaluating new and alternative raw materials, identifying cost-saving opportunities, and ensuring compliance with regulatory standards. The scientist will formulate powders, tablets, capsules, and nutrient premixes tailored to customer specifications while considering application requirements, shelf life, processing conditions, and stability. Additionally, this position will contribute to ingredient assessments and provide internal blending instructions as needed. The selected candidate will be responsible for: Thorough understanding of solid dose product development and manufacturing scale-up. Operational understanding of wet and dry granulations, tablet presses, encapsulation machines, ribbon blenders, and V-blenders. Develop and make lab samples of custom dietary supplement blends. Interpret customer requests into prototypes, such as great-tasting powdered beverages or tablets designed with various properties. Work with R&D teams, Manufacturing, supply chain, etc. on scale-up and transfer of developed formulations to the plant. Provide customers with technical support on dietary supplement formulations. Maintain proper documentation of product development process and results and keep equipment logbooks in accordance with R&D guidelines. Comply with company procedural guidelines, laboratory procedures, and safety programs. The selected candidate will also possess: Bachelor's degree in chemical engineering, chemistry, food science/technology, or similar. 2+ years prior experience in a nutritional supplement industry or similar field. 2+ years working with dietary supplements, pharmaceutical development, or similar. 2+ years' experience in granulation techniques, processing, and property characterization. Ability to formulate nutraceutical and powdered functional food prototypes based on nutritional targets as well as to consumer sensory acceptance. Understanding of GMP manufacturing considerations and requirements. Good interpersonal and presentation skills to share development work within the organization and with customers. Ability to work in a physically challenging environment: lift 25 pounds and move up to 50 pounds when working with bulk ingredients, operate pilot scale equipment. Be authorized to work in the United States Salary Range: $75k-85k/yr For immediate and confidential consideration, please email your resume to ************************* or call ************. More information can be found at *********************
$75k-85k yearly 3d ago
Research Associate LT
Chapman University Careers 4.3
Research Scientist Job 10 miles from Orange
Under general supervision, the candidate should work effectively in a team environment and have demonstrated high productivity and reproducible technical skills, including mouse physiological assessments, mouse surgery, cell culture techniques, Western Blotting, DNA / RNA extraction and PCR , gene transfection, protein purification, and Immunofluorescence/Immunohistochemistry. This person is also expected to be detail-oriented and self-motivated, and knowledge of computers is essential for high volume research and maintenance of the data records. The candidate will be expected to present data in the weekly laboratory seminars after independent analysis and write the methodology and results for the manuscript and grant preparation. This person also provides trainings to undergraduate students and oversees their research on the day-to-day basis. Responsibilities Conduct research experiments independently and in consultation with supervisor. Perform mouse handling, tattooing, tail sampling, and genotyping. Should be willing to work long hours for completion of long and time-consuming experiments. Determine mouse body temperature (rectal thermometry). Perform mouse blood collection, mouse behavior analysis, mouse organ dissection, thyroidectomy and mouse brain sectioning. Prepare technical reports, papers, graphs and/or records and provides interpretations. Perform PCR , Western blot, ELISA , immunostaining, immunohistochemistry, and other techniques of molecular biology as needed. Maintain mammalian cell lines, perform transfections, and collect samples. Maintain mamalian cell lines, perform transfections, and collect samples. Perform bacterial transformation and plasmid purification. Histology sample preparation, confocal microscopy, data analysis, and presentation. · Collaborate with other faculty with similar research interests on this topic. Maintains and updates record of all experimental studies. Stores all biochemical data in digital format on computers and backs up regularly. Consult and assist Principal Investigator Work alongside Principal Investigator to determine method, details, and means of performing the experiments. Furnish regular updates to Principal Investigator. Laboratory Ensure the facility is well equipped with all necessary tools to conduct research Place request orders for equipment and lab supplies Use equipment and laboratory space accordingly to work contract Contribute to the development of research documentation for publication and/or presentation. Perform other duties as assigned. Required Qualifications Ph.D in the field of Biomedical Sciences, Molecular Biology, Biochemistry, Cell Biology or Pharmacy with molecular biology emphasis or its equivalent in research skill and subject matter knowledge. Must be available to work extended hours to be able to complete time consuming experiments. Proven experience working with rodents, and genotyping rodents Proven practical experience with techniques of molecular biology. Working experience with cell lines and/or primary culture Proficient in research methods, testing and data collection, analysis, evaluation, report writing, independent discretion and judgment. Knowledge of research and experimental methods as issued by Institutional Research Boards. Good organizational skills and ability to prioritize and handle multiple complex tasks independently. Ability to operate laboratory equipment and maintain a safe working environment. Ability to conduct research in a timely manner and document all data. Strong writing skills and computational knowledge. Ability to establish and maintain cooperative working relationships with co-workers, investigators and other research staff. Ability to work alone and/or with student (or laboratory) assistants.
$52k-88k yearly est. 60d+ ago
R&D Scientist
Nellson Nutraceutical, LLC 4.3
Research Scientist Job 23 miles from Orange
Join NELLSON and Become Part of a Winning Team of Professionals! We currently have an immediate opportunity for R&D Scientist to join the BAR DIVISION at our ONTARIO, CALIFORNIA location. Provide effective and functional technical support within the current R&D organization leadership. Responsible for the development of nutritional bar products for both new and existing Nellson customers. Provide data based technical leadership for innovation and product development from ideation to commercialization, utilizing standard best practices and procedures with hands on scale up and commercialization support. Collaborate with cross-functional disciplines to accomplish project goals. ESSENTIAL JOB DUTIES AND RESPONSIBILITIES: * Support and lead the development of commercially successful and innovative new products for the bar business. * Develop an effective relationship and work closely with the QA, Sales, Operations, and Nellson customers. * Gain full command of internal formulation system for food product development and commercialization. * Support and lead ideation and development of innovative products and platforms via formulation and/or process driven technologies using customer/marketing insights and existing/new technologies. * Maintain awareness of market trends and comparative products. * Ability to clearly present and articulate product ideas and innovations to internal and external customers. * Ability to identify and qualify new equipment and/or processes for new product commercialization (US only). * Ability to run and monitor bench-top and manufacturing scale-up batches. * Ability to conduct shelf-life testing protocols, including the preparation and/or review shelf-life testing protocols. Preparation and/or manufacture of shelf-life testing samples. Monitoring, evaluation, and summary of results for shelf-life test results. * Support R&D team through the identification and sourcing of new, novel ingredients. * Gain full command of process systems for effective and sustainable product commercialization and apply product development processes to ensure formulation robustness for commercialization. * Support and lead product transfers from other processing locations for maximizing schedule flexibility, efficiency, and lowest cost production. * Capture and analyze key process data to determine and communicate key process variables and execute corrective action steps. (US only) * Assist R&D project Sr Scientist in completing development and commercialization of new products. * Develop a network of outside contacts such as customers, vendors, consultants, and educators. * Performs Technical Reports writing as required. * Performs other related duties as assign. PERSONAL ATTRIBUTES: * Strong problem solving and critical thinking skills for trouble shooting and expanding current equipment capital for developing new product forms and formats. * Knowledge and practical experience with shelf stable water activity-controlled food products and/or functional foods product development, processing equipment and techniques and regulatory requirements. * Advance communication skills, both written and verbal (French and English for Canadian positions). Ability to speak effectively in front of groups of customers or employees. * Demonstrate attention to detail. * Must work will in group problem solving and exhibit sound judgement. * Ability to prioritize and use time effectively while managing competing demands. * Contribute to building a positive team spirit and display a high amount of professionalism. * Responds promptly to customer needs. * A firm foundation in food engineering and food science is required. * Strong product formulation skills. Firm understanding of ingredient functionality and nutrition. * High level of professionalism and diplomacy. * Experience conducting plant trials/ process validation testing. * Demonstrates self-management by consistently at work and on-time, takes responsibility for own actions, takes initiative, generates suggestions for improving work, meets productivity standards, and monitors own work to ensure quality. QUALIFICATIONS AND EXPERIENCE: * Requires a minimum of 3-5 years of experience in the food industry. * Requires a four-year college or university degree or its equivalent in Food Engineering Sciences, Food Science, or other relevant science degree. * Knowledge and Experience with Design of Experiment (DOE) techniques. At Nellson, we invest in highly talented individuals and provide them with opportunities to continuously learn and grow to realize their full potential. Our state-of-the-art facilities, warehouses, and corporate offices offer a knowledgeable and professional environment to employees. By joining our performance-oriented team, you will be able to put your expertise to use and positively impact many groups across our production process. Nellson offers competitive pay, career growth opportunities, and an outstanding benefits program that features: * Medical, Dental & Vision Coverage * Generous Paid Time Off * 401(k) with Company Match * Flexible schedules * Professional Development & Tuition Reimbursement * And Many More Employee-Friendly Programs! Nellson is proud to be an Equal Opportunity Employer. All applicants receive consideration without regard to race, color, religion, gender, national origin, age, disability, veteran status or any other status protected by law. You may visit our website at ****************** to view current job openings.
$83k-118k yearly est. 33d ago
Equity Research Associate
Hotchkis & Wiley 4.0
Research Scientist Job 35 miles from Orange
Hotchkis & Wiley is seeking a highly motivated individual with a genuine interest in learning about investing to become part of our Research Associate Program. Hotchkis & Wiley is a research-driven institutional asset management firm with a team-oriented, collegial culture. We have a strong track record of identifying attractive investment opportunities globally across the entire market capitalization range and across the capital structure for publicly traded securities. Our experienced team of investment professionals is committed to mentoring younger analysts and developing their ability to look through short term company issues to focus on the long term secular opportunity. The Research Associates support our Investment Team, which currently consists of 24 members. The program is a two year opportunity but the company may extend the position to incorporate increased exposure to fundamental company analysis. The position would provide an excellent foundation for someone who wants to pursue a long term career in finance as a highly skilled professional investor. The Research Associate program provides exceptional learning opportunities and mentoring, competitive compensation, strong exit opportunities, and an attractive work-life balance within a highly collegial culture. The Research Associate will work together with our equity analysts/portfolio managers in conducting in-depth fundamental research for companies within one or more industries, including financial modeling and preparation of investment memos. The position is located in Los Angeles and offers a hybrid of in-office and work from home flexibility. While this program was originally designed to give pre-MBA candidates the unique opportunity to experience the asset management business prior to Business School, we will not discount applications from interested MBA or MFin candidates whom we believe would derive benefit from our program. Note that the applicant must be able to legally work in the U.S. for the duration of our program without sponsorship. Specific Responsibilities Include · Research and analyze potential investments and monitor current portfolio investments · Construct and maintain detailed financial models including long term projections and valuation estimates · Engage with company management as well as conduct calls and meetings with analysts and industry experts · Compose investment updates and assist in creation of detailed investment presentations · Understand and incorporate relevant economic and industry trends · Provide analysis for client service as needed Skills & Experience Required · Bachelor's Degree (CFA a plus) with excellent academic credentials · A passion for investing combined with creativity, integrity, and intellectual honesty · Strong analytical and quantitative skills, including intermediate knowledge of Excel, accounting and finance. Experience with Bloomberg a plus · 1-3 years of relevant experience in investment banking, accounting, or related financial services · Strong communication skills, particularly written · A passion for equity investing combined with creativity, integrity, and intellectual honesty · Clients first mentality: a positive, energetic, and responsive attitude · Team oriented individual who is willing to take the initiative and accept increasing responsibility The expected base salary range for this position is generally between $100,000 to $130,000 per year. This position is eligible for a discretionary bonus as part of a total compensation package which also includes our company sponsored benefit programs. Base salary is determined on an individualized basis and may vary based on factors including but not limited to education, training, experience, and market factors. Link to apply: ************************************ About Hotchkis & Wiley Hotchkis & Wiley is an institutional asset management firm overseeing U.S. and global value equity and high yield portfolios for clients worldwide. The firm currently manages approximately $34 billion in assets and is majority owned by its management and employees. For more information refer to our website, ************* Hotchkis & Wiley is an Equal Opportunity employer (EEO), and all employees and applicants will be entitled to equal employment opportunities when employment decisions are made. Hotchkis & Wiley will take affirmative action to recruit, hire, train and promote individuals in all job classifications without regard to race, religion, color, age, sex, national origin, citizenship, pregnancy, veteran status, sexual orientation, physical or mental disability, gender identity, or membership in a historically under-represented group.
$100k-130k yearly 21d ago
Research Associate II - Pulmonary - Jiang Lab
Dev 4.2
Research Scientist Job 35 miles from Orange
Company DescriptionJobs for Humanity is partnering with CEDARS-SINAI to build an inclusive and just employment ecosystem. Therefore, we prioritize individuals coming from the following communities: Refugee, Neurodivergent, Single Parent, Blind or Low Vision, Deaf or Hard of Hearing, Black, Hispanic, Asian, Military Veterans, the Elderly, the LGBTQ, and Justice Impacted individuals. This position is open to candidates who reside in and have the legal right to work in the country where the job is located. Company Name: CEDARS-SINAI Job Description Working under direct supervision, as a Research Associate II, you will perform routine and increasingly complex laboratory tasks and procedures and develops technical expertise in one or more areas relevant to research projects. You will participate in research activities involving all aspects of the research process, to include, but not limited to; investigation, technical, testing/validation of results, and report findings. Will perform a variety of routine experimental protocols and procedures to support the objectives of laboratory research projects. You will observe and comply with safety standards and procedures, assist in preparation of data for publication and/or presentation at scholarly meetings, and assist in general laboratory maintenance. This position does not have supervisory responsibilities. Essential Job Duties and Responsibilities: Performs a variety of increasingly complex experimental protocols and procedures and assist in the design of new complex or unusual protocols and techniques. Keeps accurate and detailed records of experiments and results, and assist in identifying and troubleshooting of unexpected results. Orders laboratory supplies and supports laboratory operations. Maintains lab equipment and related records and may coordinate use of lab equipment. Assists in the operation of specialized equipment, as required by the area of research. Assists in preparation of data for publication and/or presentation at scholarly meetings. Observes and complies with safety standards and procedures. Orients research laboratory assistants or lower level research associates and undergraduate student researchers on day-to-day lab operations and routine procedures. Department-Specific Responsibilities: Associate Investigates molecular mechanisms of lung fibrosis, and participates in research projects including the role of innate immune, stem cells, extracellular matrix, resident mesenchymal cells, and fibroblast lineages in lung injury and repair. Experimental approaches employed in our lab include molecular biology, genetically modified mice, lineage tracing, lung injury models, prospective isolation and organoid culture of lung stem cells, single cell RNA-sequence, immunology, and genomics studies. Under minimal supervision, s/he is expected to maintain and carry out mouse husbandry, perform in vivo experiments including mouse lung injury models and sample collections, and in vitro experiments including molecular sub-cloning, cell culture, flow cytometry, mRNA analysis, protein analysis and biochemical studies. Trains other lab technician on related lab procedures. Other lab duties include: ordering lab supplies, record keeping, lab maintenance, and other duties as assigned. #Jobs Education: Bachelor's Degree in a Science related field is required. Experience: One (1) year of laboratory experience. Understanding of general research objectives. Familiar with routine laboratory procedures, experimental protocols, and overall lab organization. Applicant must be highly motivated and able to work independently. Must have superior interpersonal, communication and organization skills and the ability to work across company disciplines and functional units, and computer application experience. Must possess computer skills to include, but not limited to, Excel and Word. Ability to simultaneously manage multiple clerical trials, and attention to details. Working Title: Research Associate II - Pulmonary - Jiang Lab Department: Home Dept - Pulmonary Business Entity: Cedars-Sinai Medical Center Job Category: Academic/Research Job Specialty: Research Studies/Clinical Trials Position Type: Full-time Shift Length: 8 hour shift Shift Type: Day Base Pay:$21.26 - $36.14
$21.3-36.1 hourly 60d+ ago
Scientist, Optics R&D
Rxsight 3.4
Research Scientist Job 18 miles from Orange
RxSight is an ophthalmic medical technology corporation headquartered in Aliso Viejo, California that has commercialized the worlds first and only adjustable intraocular lens (IOL) that is customized after cataract surgery. The companys mission is to revolutionize the premium cataract surgery experience by allowing surgeons to partner with their patients to achieve optimized results for every unique eye. OVERVIEW: RxSight is a biomedical device company based in Aliso Viejo, California, is seeking candidates for a research position in its Optics R&D Division. This job involves working with a team of scientists to develop a light-adjustable intraocular lens for use in cataract and refractive surgery. The position requires a working knowledge of standard optical testing techniques (interferometry, MTF, profilometry, etc), experience with optical instrument design and assembly, and basic aberration theory. Experience with human vision is desired, but not required. Duties include the maintenance and calibration of equipment, optical measurements, design of experiments, and design of optomechanical fixtures. Successful candidates will have the ability to prioritize, work independently, and to get along with others. ESSENTIAL DUTIES AND RESPONSIBILITIES: * Confers with engineering and technical staff regarding fabrication and testing of prototype systems, and modifies design as required. * Work in the laboratory to assist with development of nomograms for the light adjustable lens. * Design and commercialize new products based on light adjustable materials technology. * Ensure that all laboratory equipment is properly maintained and calibrated * Modify hardware equipment as needed * Design and build test and manufacturing fixtures as needed Required Knowledge, SKILLS, and Abilities: * Theoretical and working knowledge of interferometric optical testing. * General knowledge of optical aberration theory and its application to the design and analysis of optical components. * Theoretical knowledge and practical experience with general optical testing techniques (e.g., MTF, ROC, etc.) * Experience with designing, engineering, fabrication, and alignment of optical systems. * Analytical - Synthesizes complex or diverse information; Collects and researches data; Designs work flows and procedures. * Problem Solving - Identifies and resolves problems in a timely manner; Develops alternative solutions; Works well in group problem solving situations. * Technical Skills - Strives to continuously build knowledge base and skills sets. * Proficient with data analysis tools such as Matlab, MathCAD, or MAPLE. * Written Communication - Presents numerical data effectively; Able to read and interpret written information. * Ability to read, analyze, and interpret complex documents. SUPERVISORY RESPONSIBILITIES: * None EDUCATION, EXPERIENCE, and TRAINING: * Successful candidates must have either a MS or BS degree in optics, optical engineering, Physics, Chemistry or a related field. * Training to be completed per the training plan for this position as maintained in the document control system * The training requirements on TRN-10007 Insider Trading Policy, TRN-10008 Global Anti-Bribery and Anti-Corruption Policy and TRN-10009 Code of Business Conducts and Ethics must be diligently completed within 30 days from the hiring date and on an annual basis CERTIFICATES, LICENSES, REGISTRATIONS: * N/A COMPUTER SKILLS: * Word Processing. * Spreadsheet Software. * Matlab or Mathcad or Mathematica or Maple * Project Management System SALARY RANGE: * $60,000 To $95,000 Per Year
$60k-95k yearly 60d+ ago
Associate Production Scientist
Polypeptide Laboratories
Research Scientist Job 27 miles from Orange
"The Associate Production Scientist is responsible for a upscaling R&D small scale work into GMP large scale manufacturing, Oversee production activities of the assigned projects, collect and analyze GMP data, Author and review quality documents such as MBPR, R.A, PPQ protocol, drive yield and process improvement projects, update the customer with the GMP activities, ensuring production processes meet quality standards, or maintaining equipment efficiency]. This role contributes directly to PolyPeptide's commitment to delivering exceptional quality and on-time delivery to our customers." Key Responsibilities: List the key tasks and duties for the role. Use action verbs and make each responsibility specific and measurable. Prioritize by importance. * Review and approve quality and validation documents as the production representative that does not need managers approval (MBPR, CC, SOP, PQE, PPQ related documents, educational certificates etc.) * Perform Operational assessments. * Prepare weekly slide deck presentations on project updates to internal and external stakeholders. * Lead and/or prepare and/or support product investigations using root cause analysis techniques (interviewing, fishbone diagram, 5 whys etc) and summarizing findings in written reports and oral presentations to internal and external stakeholders (QIRM, OOT, OOS, RCI, CAPA/Task) * Author, prepare and support Deviations, process change controls, CAPA during project execution. * Prepare Change Control Change Request and list of change document as part of MBPR generation (CC general and for MBPR) * Draft and review Standard Operating Procedures (QUMAS) * Conduct Risk Assessment (CRIA, RIA, FMEA) * Approve quality documents as the production representative that does not need managers approval (MBPR, ARM, CR, SOP, PQE, validation documents, educational certificates etc.) * Generate detailed Gannt chart of batch schedule. * BOM generation and Process mapping (soon to include route & formula) * Provide on-floor and remote 24/7 technical support to Production during project execution (including weekends, grave, and night shifts), e.g. make go/no go decisions on IPC-results regarding process steps or troubleshooting issues. * Project management of operation activities related to batch preparation/ execution (equipment/ IPC validation, hold time study, etc…) * Draft, format and improve MBPR template. * Support technology transfer activities (generation of comparability report, identification of CPPs, review and approve validation PPQ documents, generation of BPR etc). * Author and review campaign reports. * Raw material OOS assessment * Conduct Bottle neck analysis and Gap analysis of unit operations. * Prepare Process capability analysis. * Conduct cost analysis and forecasting. * Liaise with cross functional groups (Production, QA, QC, Development, Project Management, Sale, Regulatory, Supply Chain etc.) to support the planning and execution of manufacturing operations. * Collaborate with PD to Design small scale experiments to support investigations or process improvement initiatives. * Lead, mentor and train Operators and team members as part of upstream and downstream process knowledge transfer on MBPR and unit operations. * Support continuous improvement initiatives. * Manually Collect, trend, and analyze in process data as part of process monitoring to determine yields and change points. * Support QA and regulatory with responding to comments by clients on executed BPR and NDA/BLA, submission. * Support Validation activities during the planning execution of PPQ runs (prepare supporting PPQ document, e.g. equipment calibration and suitability, analytical methods, hold time study, PPQ strategy etc). * Support regulatory review of documents. * Process Mapping * Routes and Formula on AX to be added to our responsibilities Qualifications: Education & Experience * Required Education: Bachelor's degree in chemistry, Biochemistry, Engineering, or a related field. * Preferred Education: Masters degree preferred, advanced degree or certifications bachelor's degree in chemistry, Biochemistry, Engineering. * Experience: Minimum 3 years in pharmaceutical manufacturing GMP production or MS&T team, peptide manufacturing experience preferred. Skills & Competencies * Technical Skills: Basic understanding about SPPS GMP manufacturing, Proficiency in HPLC systems, cGMP processes, Data analysis (Minitab experience is preferred). * Soft Skills: Strong problem-solving, collaboration, Microsoft Data analysis (Minitab experience is preferred), Technical writing, and communication skills, and Microsoft office. Work Environment & Physical Demands: * Physical Requirements: N/A * Work Environment: able to adjust priorities based on business need, able to oversee multiple [projects/ processes arranging throughout SPPS manufacturing to product release. Performance Metrics (KPIs): * Meet or exceed 90% of on-time MBPR, technical reports, and quality related documents delivery targets. * Complete all assigned process mapping, route and formulas, & process evaluation. * This job might be entitled to a customer facing/ updates in a timely manner. * Completed all related data collection for the GMP projects and perform trending as needed. Salary: $75k-90k per year We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity or expression, pregnancy, age, national origin, disability status, genetic information, protected veteran status, or any other characteristic protected by law.
$75k-90k yearly 7d ago
Associate Production Scientist
Polypeptide Us
Research Scientist Job 27 miles from Orange
"The Associate Production Scientist is responsible for a upscaling R&D small scale work into GMP large scale manufacturing, Oversee production activities of the assigned projects, collect and analyze GMP data, Author and review quality documents such as MBPR, R.A, PPQ protocol, drive yield and process improvement projects, update the customer with the GMP activities, ensuring production processes meet quality standards, or maintaining equipment efficiency]. This role contributes directly to PolyPeptide's commitment to delivering exceptional quality and on-time delivery to our customers." Key Responsibilities: List the key tasks and duties for the role. Use action verbs and make each responsibility specific and measurable. Prioritize by importance. Review and approve quality and validation documents as the production representative that does not need managers approval (MBPR, CC, SOP, PQE, PPQ related documents, educational certificates etc.) Perform Operational assessments. Prepare weekly slide deck presentations on project updates to internal and external stakeholders. Lead and/or prepare and/or support product investigations using root cause analysis techniques (interviewing, fishbone diagram, 5 whys etc) and summarizing findings in written reports and oral presentations to internal and external stakeholders (QIRM, OOT, OOS, RCI, CAPA/Task) Author, prepare and support Deviations, process change controls, CAPA during project execution. Prepare Change Control Change Request and list of change document as part of MBPR generation (CC general and for MBPR) Draft and review Standard Operating Procedures (QUMAS) Conduct Risk Assessment (CRIA, RIA, FMEA) Approve quality documents as the production representative that does not need managers approval (MBPR, ARM, CR, SOP, PQE, validation documents, educational certificates etc.) Generate detailed Gannt chart of batch schedule. BOM generation and Process mapping (soon to include route & formula) Provide on-floor and remote 24/7 technical support to Production during project execution (including weekends, grave, and night shifts), e.g. make go/no go decisions on IPC-results regarding process steps or troubleshooting issues. Project management of operation activities related to batch preparation/ execution (equipment/ IPC validation, hold time study, etc…) Draft, format and improve MBPR template. Support technology transfer activities (generation of comparability report, identification of CPPs, review and approve validation PPQ documents, generation of BPR etc). Author and review campaign reports. Raw material OOS assessment Conduct Bottle neck analysis and Gap analysis of unit operations. Prepare Process capability analysis. Conduct cost analysis and forecasting. Liaise with cross functional groups (Production, QA, QC, Development, Project Management, Sale, Regulatory, Supply Chain etc.) to support the planning and execution of manufacturing operations. Collaborate with PD to Design small scale experiments to support investigations or process improvement initiatives. Lead, mentor and train Operators and team members as part of upstream and downstream process knowledge transfer on MBPR and unit operations. Support continuous improvement initiatives. Manually Collect, trend, and analyze in process data as part of process monitoring to determine yields and change points. Support QA and regulatory with responding to comments by clients on executed BPR and NDA/BLA, submission. Support Validation activities during the planning execution of PPQ runs (prepare supporting PPQ document, e.g. equipment calibration and suitability, analytical methods, hold time study, PPQ strategy etc). Support regulatory review of documents. Process Mapping Routes and Formula on AX to be added to our responsibilities Qualifications: Education & Experience Required Education: Bachelor's degree in chemistry, Biochemistry, Engineering, or a related field. Preferred Education: Masters degree preferred, advanced degree or certifications bachelor's degree in chemistry, Biochemistry, Engineering. Experience: Minimum 3 years in pharmaceutical manufacturing GMP production or MS&T team, peptide manufacturing experience preferred. Skills & Competencies Technical Skills: Basic understanding about SPPS GMP manufacturing, Proficiency in HPLC systems, cGMP processes, Data analysis (Minitab experience is preferred). Soft Skills: Strong problem-solving, collaboration, Microsoft Data analysis (Minitab experience is preferred), Technical writing, and communication skills, and Microsoft office. Work Environment & Physical Demands: Physical Requirements: N/A Work Environment: able to adjust priorities based on business need, able to oversee multiple [projects/ processes arranging throughout SPPS manufacturing to product release. Performance Metrics (KPIs): Meet or exceed 90% of on-time MBPR, technical reports, and quality related documents delivery targets. Complete all assigned process mapping, route and formulas, & process evaluation. This job might be entitled to a customer facing/ updates in a timely manner. Completed all related data collection for the GMP projects and perform trending as needed. Salary: $75k-90k per year We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity or expression, pregnancy, age, national origin, disability status, genetic information, protected veteran status, or any other characteristic protected by law.
$75k-90k yearly 6d ago
Research Chemist
Actalent
Research Scientist Job 9 miles from Orange
Gather and analyze pH buffering data across a variety of ingredients and formulations to understand pH behavior and its impact on product stability. Build and refine predictive models for pH behavior based on data collected from ingredient and formulation testing. Validate the accuracy and reliability of the predictive models through testing and comparison with experimental results. Provide data-driven insights and recommendations to support the commercialization of new products, ensuring the models align with product specifications and regulatory requirements. Work closely with R&D Services, R&D Developers, Quality Assurance, and other departments to ensure that the pH data and models contribute effectively to product development and scale-up activities. Responsibilities * Gather and analyze pH buffering data across various ingredients and formulations. * Build and refine predictive models for pH behavior based on collected data. * Validate the accuracy and reliability of predictive models through testing. * Provide data-driven insights and recommendations to support product commercialization. * Work closely with R&D Services, Developers, and Quality Assurance to ensure effective data and model contribution to product development. * Strategize ingredient testing and data analysis. * Input data into the ingredient library and improve the formatting of Excel sheets. * Follow priority task lists and perform necessary calculations. Essential Skills * Bachelor's or advanced degree in Chemistry, Food Science, or a related field. * Understanding of pH systems. * Experience with statistical analysis tools and software for data modeling and validation. * Experience with titration methods. * Strong math and statistical background. * Experience with pH titrations in a food manufacturing setting. * Understanding of basic Chemistry principles. Additional Skills & Qualifications * Bachelor of Science degree in Chemistry. * 1+ years of Chemistry experience in a food manufacturing company. * Experience in model validation and data analysis. Work Environment Shift: Monday - Friday with a flexible start time around 8am. Work in an office setting with an R&D prep kitchen. Collaborate with a team including a Microbiologist and another experienced team member. Pay and Benefits The pay range for this position is $24.00 - $30.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: * Medical, dental & vision * Critical Illness, Accident, and Hospital * 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available * Life Insurance (Voluntary Life & AD&D for the employee and dependents) * Short and long-term disability * Health Spending Account (HSA) * Transportation benefits * Employee Assistance Program * Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Brea,CA. Application Deadline This position is anticipated to close on Apr 30, 2025. 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 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. Diversity, Equity & Inclusion At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through: * Hiring diverse talent * Maintaining an inclusive environment through persistent self-reflection * Building a culture of care, engagement, and recognition with clear outcomes * Ensuring growth opportunities for our people 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.
$24-30 hourly 5d ago

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How much does a Research Scientist earn in Orange, CA?

The average research scientist in Orange, CA earns between $71,000 and $189,000 annually. This compares to the national average research scientist range of $58,000 to $137,000.

Average Research Scientist Salary In Orange, CA

$116,000

$71,00010%

$116,000Median

$189,00090%

What are the biggest employers of Research Scientists in Orange, CA?

The biggest employers of Research Scientists in Orange, CA are:

Solvay America Inc

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How much does a Research Scientist earn in Orange, CA?

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