Research Technician Jobs in La Mesa, CA

Position Overview: We are seeking a Biomedical Engineer or a similar professional to support the development of products in the field of tissue engineering and regenerative medicine. This role involves assisting with lab-based research and preclinical studies under the supervision of a manager, aiming to enhance patient outcomes in areas such as sports medicine, orthopedics, general surgery, and wound healing. The ideal candidate will have a strong passion for advancing scientific knowledge and contributing to meaningful healthcare solutions. Key responsibilities include conducting experiments, documenting and analyzing results, maintaining the laboratory, and collaborating with the manager. Key Responsibilities: Research and Development Follow technical documents, including standard operating procedures and test protocols, to independently perform experiments aligned with project goals set by the manager. Record methodologies and results, conduct basic data analysis, and present findings to the manager for further discussion and planning of subsequent experiments. Lab Maintenance and Safety Perform general laboratory maintenance, including cleaning lab equipment and glassware, organizing the lab space, and conducting device preventative maintenance. Coordinate with internal teams and external vendors for ordering supplies and managing inventory. Work with third-party vendors for essential lab services, such as device calibration and hazardous waste disposal. Documentation Maintain accurate and detailed records of all experimental work in laboratory notebooks and other documents. Present experimental data in regularly scheduled lab meetings. Team Collaboration and Communication Meet regularly with the manager (daily to weekly) to receive assignments, discuss results, and plan next steps. Collaborate with other lab members and teams in R&D to maintain a safe, organized, and cost-effective laboratory environment. Required Skills and Qualifications: Proficiency in laboratory experimentation, including managing multiple samples and running concurrent experiments with minimal supervision. Expertise in maintaining a detailed laboratory notebook and documenting experiments in real-time. Strong data analysis skills, with the ability to handle large datasets with high accuracy. Understanding of experimental design, including concepts of controlled experiments and statistical power. Knowledge of daily lab operations, including lab safety, hazardous waste disposal, and best laboratory practices. Familiarity with various statistical analysis methods. Experience with the following laboratory techniques (preferred but not required): Sterile techniques training Buffer preparation Enzyme-linked immunosorbent assay (ELISA) Protein isolation from tissue Colorimetric assays (e.g., BCA) Dialysis SDS-PAGE/Western blot Tissue culture PCR

CAMRIS seeks a Research Laboratory Technician II to support the Naval Health Research Center (NHRC), Operational Infectious Diseases (OID) Directorate by executing critical laboratory procedures that directly contribute to the advancement of infectious disease research and operational readiness for military personnel. This role involves assisting in the preparation and execution of experiments, maintaining laboratory equipment, and ensuring compliance with safety and regulatory protocols. The OID Directorate conducts ongoing, laboratory-based surveillance of US military populations in unique environments to quantify and study the etiology of infectious illnesses. Test specimens are collected from ongoing surveillance programs and from special investigations of febrile illnesses and pneumonia among military personnel or civilians (recruits, forces afloat, deployed forces, outbreaks of concern, and border populations). In addition to the utilization of portable, rapid assay technologies to identify pathogens in the field, test specimens and limited epidemiologic data, when approved by the Institutional Review Board (IRB), are provided to the NHRC laboratory where diagnostics and, in some instances, in-depth pathogen characterization is conducted. Results are provided to sponsors, the Armed Forces Health Surveillance Center, local investigators and collaborators, and, when applicable, county health units to guide proper responses that ultimately affect both the readiness of US forces and the safety of public health. CAMRIS International, LLC, is a dynamic medical research and development firm that achieves innovative solutions to health and development challenges through high-quality, cost-effective programs and research management services. We combine our proven systems with today's most effective, evidence-based best practices. Our core practice areas include vaccine research, development, and production; microbiology and infectious disease research; biodefense; clinical research; global health security; and HIV/AIDS programs. Our employees enjoy a collegial environment where individual contributions matter at all levels. At CAMRIS, you will notably improve the lives of people at home and abroad. Responsibilities Laboratory Operations Support surveillance of operational infectious diseases that affect DoD personnel and civilians in coordination with federal agencies, local governments, research organizations, and universities at locations around the world. Provide operational support, including analytical evaluations and prospective clinical evaluations, for diagnostic evaluations, clinical studies, and/or clinical trials sponsored by Federal Agencies or private companies, subject to final GS or military approval. Oversee and maintain general laboratory infrastructure, including equipment maintenance, housekeeping, inventory management, and restocking. Follow Standard Operating Procedures (SOPs) and perform molecular biology-related experiments involving but not limited to total nucleic acid purification, real-time PCR, and next-generation sequencing. Assist in the development, review, and revision of laboratory protocols and Standard Operating Procedures (SOPs). Perform other duties and responsibilities as assigned or directed by the supervisor. Data Management and Analysis Accurately record experimental results and observations in laboratory notebooks and electronic systems according to Good Laboratory Practice (GLP) guidelines. Assist in analyzing data and preparing summary reports for review by senior scientists and research investigators. Compliance and Safety Follow all safety and regulatory guidelines, including proper handling and disposal of hazardous materials. Ensure compliance with the College of American Pathologists (CAP), Institutional Review Board (IRB), and other regulatory requirements as applicable. Participate in safety inspections and maintain necessary certifications, such as biosafety and chemical safety training. Qualifications Required A BA/BS in a science-related field (e.g., biology, microbiology, or molecular biology). Three to five years of laboratory experience, preferably in a research setting. Knowledge of molecular biology techniques, immunoassays, or microbial culture methods. Strong understanding of laboratory techniques and equipment, including handling of infectious materials. Familiarity with laboratory safety standards and Good Laboratory Practice (GLP). Excellent organizational and time-management skills, with attention to detail. US Citizenship and the ability to obtain and maintain a T3/Secret Clearance. Preferred Experience in infectious disease research or work within a medical/military research environment. Certification in laboratory safety or related fields (e.g., biosafety, chemical safety). Please submit your resume online at *************** CAMRIS is an Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, protected veteran status, disability status, political affiliation, marital status, military status, or any other characteristic protected by any applicable federal, state, or local law. CAMRIS offers a comprehensive benefits package, including medical, dental, and vision insurance for individuals and families, FSAs, HSA, life and AD&D insurance, short- and long-term disability, legal services, voluntary hospital indemnity, critical illness and accident insurances, EAP, pet insurance, 401(k) with employer match and Roth option, tuition and professional reimbursement, public transportation support in the DMV area, a referral bonus program, vacation with tenure-based increases, PTO, 11 paid holidays, paid bonding leave, and paid supplemental short-term disability. Employment is contingent upon successful completion of a secret-level background check, a requirement for this position under an active federal contract. The background check process may include, but is not limited to the following: (1) contacting your professional references; (2) verification of previous employment, education and credentials; (3) a criminal background check; (4) use/abuse of federally-controlled substances; and (5) a department of motor vehicle check. Candidates must be prepared to fully-complete any required background check questionnaire during initial onboarding.

Light Horse Therapeutics is a developer of first-in-class small molecule therapeutics based in San Diego, leading the way in precision genome editing applied to small molecule drug discovery and pioneering approaches to target the root causes of disabling and life-threatening diseases. Its advanced platform identifies cryptic chemically accessible functional domains within targets that play critical roles in disease biology. This high-throughput discovery platform systematically interrogates complex signaling pathways and uncovers unique sites of vulnerability in their native, cellular context to best ensure that discoveries in the lab translate into the clinic. Light Horse therapeutics was founded by leading academics Brian Liau, PhD (Harvard), Ben Cravatt, PhD (Scripps) and Nathanael Gray, PhD (Stanford) with financial backing from Versant Ventures and Mubadala Capital as well as three strategic investors: Bristol-Myers Squibb Co, AbbVie and Taiho Ventures. Light Horse Therapeutics is seeking a talented, motivated, and creative Research Associate to join the Functional Genomics Group as a contractor for a minimum of 6 months, renewable upon performance and business needs. The candidate will contribute to the design, execution, and analysis of CRISPR-based gene editing screens to study novel oncology targets. They will also perform mechanistic experiments to characterize these targets and the impact of various mutations on their function. The candidate will have the opportunity to employ multiple experimental techniques in cell biology to build an understanding of novel target biology in a dynamic start-up environment that employs cutting-edge tools in functional genomics and proteomic technologies. This is a temporary contract position, located in our San Diego office, with an expected duration of a minimum of 6 months. This role is not eligible for benefits. Job Description: Execute CRISPR-Cas9 mutagenesis screens using state-of-the-art technologies and multiple phenotypic readouts. Execute target and site validation studies in disease-relevant preclinical models using both high-throughput and in-depth cell biology experiments. Contribute to experimental planning and data analysis Position mostly requires benchwork responsibilities involving multitasking Present results regularly at team meetings Perform diligent and timely note-keeping and work process tracking Required Qualifications: Bachelor's and/or Master's degree in biological science with at least 2 years hands-on experience in a Biotech or Pharma setting Proficiency in mammalian cell line culture, especially large-scale projects Proficiency in standard molecular biology techniques, including DNA, RNA, and protein analysis, mammalian cell line transfection and lentiviral infection Track record of being able to multitask while working independently Excellent technical laboratory skills Attention to details in documenting, executing, and analyzing experiments Flexibility and eagerness to tackle new tasks and challenges, and meet aggressive timelines Ability to work closely with team members and across disciplines Preferred Qualifications Experience with CRISPR-Cas9 mutagenesis screens Experience with lentivirus production, infection and selection Experience constructing next generation sequencing libraries Experience with high throughput assay development for cell growth and gene/protein expression Experience with flow cytometry is a plus The anticipated pay rate for candidates who will work in San Diego, CA is $31.00 to $60.00/hour. The final pay rate offered to a successful candidate will be dependent on several factors that may include but are not limited to the type and length of experience within the job, type and length of experience within the industry, education, etc. This is a temporary contract position, located in our San Diego office, with an expected duration of a minimum of 6 months. This role is not eligible for benefits.

Research Associate II (Contract) ⏳ Schedule: Temporary Assignment, 20-30 Hours/Week 💰 Pay Rate: $32-37/hr About the Role BioPhase is seeking a Research Associate II for a temporary contract assignment with a cutting-edge life sciences company in San Diego. This role is ideal for candidates with hands-on research experience in biomarker discovery and ELISA-based assays who thrive in a collaborative, fast-paced environment. The position will focus on experimental work, data acquisition, and basic analysis supporting research and development programs. Key Responsibilities Conduct diverse biomarker discovery experiments, including ELISA-based assays and protein analysis. Perform protein-based assays, immunoassays, and other experimental techniques under the guidance of senior scientists. Assist with primary data analysis and contribute to research findings. Troubleshoot experiments and suggest practical solutions for technical challenges. Maintain accurate electronic lab records and documentation. Collaborate with scientists and engineers to optimize research methodologies. Ensure compliance with laboratory safety guidelines and best practices. Participate in research discussions and contribute to team projects as needed. Qualifications & Experience Bachelor's or Master's degree in a scientific discipline (Biology, Biochemistry, Molecular Biology, or related field). 18+ months of hands-on laboratory experience in an academic or industry setting. Proficiency with protein assays, immunoassays, and general lab techniques. Ability to analyze data, troubleshoot experiments, and communicate findings effectively. Strong organizational skills and attention to detail. Experience working in a regulated lab environment is a plus. 🔬 Interested? Apply today and take the next step in your research career!

Job Title: Research Associate-Scientific Duration: 12 months Schedule: M-F Standard Business Hours Job Title: Research Associate Molecular Biology, Next-Generation Sequencing and Operations Management Top 3-5 Skills: Molecular Biology Next-Generation Sequencing Bachelor's Degree is required Description: The Sequencing Research & Genomics (SRG) team at Client is seeking a dedicated, talented, and motivated molecular biologist to support our Next-Generation Sequencing (NGS) projects within the Protein Homeostasis Thematic Research Center (TRC). This role involves a blend of hands-on laboratory work and project management, including tracking NGS collaborative research inquiries and organizing supporting information to facilitate lead target discovery and assay development. The successful candidate will have the unique opportunity to collaborate with diverse cross-functional scientific teams and contribute to groundbreaking drug discoveries that directly impact patient health. This is a 1-year contract position with the potential for extension. Responsibilities: Ensure smooth day-to-day lab operations, including RNA/DNA extraction/purification, NGS library preparation & QCs, and loading sequencers (e.g., Illumina, Oxford Nanopore, etc.) Track projects and develop new project organizational guidelines as part of our sequencing pipelines Review sequencing run and data quality control statistics and document them for future reference Provide technical and project-level guidance to internal and external stakeholders Generate, organize, and maintain meticulous records of all experiments conducted Work independently or with supervision from team members on new assay and protocol development Requirements: Bachelor's degree with 0-3 years of professional experience in molecular biology, biotechnology, or biochemistry Experience with Electronic Lab Notebooks and project management tools like JIRA and Confluence Demonstrated experience in managing external vendors and CROs for NGS or other research services Proficiency in molecular biology techniques, including DNA/RNA extraction & purification, NGS library preparation & QC, PCR, qPCR, cloning, etc. Strong understanding of theory behind techniques, with proficient reasoning skills in experimental design and optimization of wet lab techniques, coupled with exceptional attention to detail Excellent communication skills, both written and oral Strong team player with a proactive and positive attitude Ability to use technical skills and effective time management to perform work efficiently and meet project timelines Exposure to cell biology techniques such as cell culture, along with functional assays for drug responses, is a plus Application Requirements: Cover Letter Curriculum Vitae

Qureator, Inc. About Us Headquartered in San Diego, California, we are an early-stage, well-funded Techbio company specializing in innovative drug discovery solutions. Our proprietary 3D organ-on-a-chip platform, Curiochips, offers significant advantages in accurately recapitulating both normal and disease states of the human body. This capability has been validated through multiple ongoing collaborations with hospitals, government institutions, and major pharmaceutical companies. Our Mission At Qureator Inc., we are committed to revolutionizing the drug discovery process. Our mission is driven by the Qureator platform's unparalleled ability to replicate complex disease phenotypes, surpassing the limitations of traditional preclinical models. By bridging the gap between laboratory research and real patient outcomes, we aim to accelerate the development of treatments for a wide range of conditions, from cancers to rare diseases. Our Approach We tackle diseases that lack clear in vitro models, setting new standards in preclinical research. Our comprehensive approach to phenotypic analysis includes detailed disease tissue phenotyping, which is essential for observing complex drug responses. This effort is crucial for advancing treatments informed by the complexities of human biology. Position: Research Associate 1 We are looking for a highly motivated individual to join us as a Research Associate and assist in developing platforms for drug discovery and safety testing on Qureator's proprietary 3D organ-on-a-chip technology. The successful candidate will be self-motivated with the ability to collaborate effectively in a team-oriented environment. Your work will be crucial in supporting the development of our in vitro disease models. In this position you will be able to: · Obtain hands-on experience with Qureator's organ-on-chip systems · Set up equipment and apply innovative ideas to processes for drug discovery · Participate in close discussions with engineers, biologists, and data scientists · Learn and grow with the company Key Responsibilities: · Perform reagent and cell experiments and manage related data · Assist in prototyping and process development · Perform general laboratory duties such as: sample aliquotting/storage, inventory management, and up-to-date experiment documentation About You: Education and Experience · Bachelor's degree in Cell/Molecular Biology, Bioengineering, or a related field, with 1-2+ years of relevant laboratory experience in an academic or industry setting Personal Qualities · Good written and verbal communication skills for communicating ideas and presenting results · Willingness to adapt and learn new concepts or techniques · Detail-oriented and organized Technical Skills and Knowledge · Demonstrated knowledge of and adherence to standard chemical and biological safety protocols · Proficiency in a range of laboratory techniques, including but not limited to: · Mammalian cell culture · ELISA and/or other colorimetric assays · Microscopy - brightfield and IF imaging · Literature review of scientific papers Additional Preferred Qualifications · Experience with advanced high-content 3D imaging techniques · Experience with automated liquid handlers · Experience with electronic lab notebook and/or inventory system (Benchling preferred) · Proficiency in 3D cell culture models (spheroids, organoids, or tumoroids) Salary and Benefits · Competitive salary commensurate with experience · Health, dental, vision and AD&D insurance · Paid time off

Job Title: Quality Control Specialist Duration: 6 months (possibility of extension) Shift: 1st shift / 8-4:30 M-F Payrate: $28 /hr. on W2 Description: Interviews in person Onboarding & background must be completed & cleared prior to starting Ensure applicants have hands on Flow experience. This is required skillset, and they are finding that many of the candidates do not have this background or are not familiar or lack the knowledge of flow. Must have: BA/BS degree in a related scientific discipline or some related college coursework with a minimum of 2 year's experience in a biotech lab environment. The QC Associate I is responsible for routine, accurate and timely testing of QC samples according to standard protocols and operating procedures, such as flow cytometry related protocols. The QC Associate I will prioritize daily workload and work independently. They will participate in the review of data, report results, and complete all required documentation and database entries. QC Associate I will receive specific instructions and ongoing guidance regarding required tasks and expected results. JOB RESPONSIBILITIES • Trains and becomes proficient in all the required techniques, operation of relevant equipment and software packages associated with testing, data analysis, and data reporting. • This may require working with human blood, human or mammalian cell culture and/or animals and animal tissues. • Routine, accurate and timely completion of all assigned QC tests under supervision and according to standard protocols or operating procedures. • Will prioritize daily workload and develop skills to work independently. • Analyze data and report test results including completion of all required documentation and database entries as required by QC protocols or operating procedures. • Calibrate and maintain equipment. Report problems to QC Supervisor or Manager. • Maintain logs and required documentation, as necessary. • Prepare lab supplies, reagents, and assist with laboratory maintenance, as needed. • Promote a safe work environment. May provide recommendations on maintaining the safety of the work environment. • Participate in Environmental, Health & Safety programs. • Address corrective actions whenever a hazard is identified. • Notify supervisor and Safety Officer(s) of all observed hazardous conditions or unsafe work practices. • Keep abreast of the basic requirements for safety compliance in own area of work and complies with those requirements. • Participate in group or intra-department teams and projects as required. • Participate in assigned cross-training. • Perform other related duties and assignments, as required. EDUCATION AND EXPERIENCE: • BS/BA in a related scientific discipline or some related college coursework with a minimum of 2 years related experience in a biotech lab environment. • Experience in an industrial or research laboratory preferred. • Flow Cytometry experience required and Tissue Culture experience highly preferred. KNOWLEDGE AND SKILLS • Basic computer skills: MS Excel & Word. • Knowledge of general laboratory safety. • Effective interpersonal, written and oral communication skills. • Demonstrated ability to follow established policies/procedures, and ability to keep neat, accurate, and complete records and logs. • Effective analytical and problem-solving skills. Net2Source is an Equal Opportunity Employer. We believe that no one should be discriminated against because of their differences, such as age, disability, ethnicity, gender, gender identity and expression, religion or sexual orientation. Our rich diversity makes us more innovative, more competitive, and more creative, which helps us better serve our clients and our communities. All employment decisions shall be made without regard to age, race, creed, color, religion, sex, national origin, ancestry, disability status, veteran status, sexual orientation, gender identity or expression, genetic information, marital status, citizenship status or any other basis as protected by federal, state, or local law.

About Us Seawolf Therapeutics is a Series A company based in San Diego, CA. We are an innovative and collaborative team developing DNA-based medicines that will be first-in-class and best-in-class long-acting therapeutics for patients living with unmet medical needs. Come join our team and be an agent of change. Overview of the Role We are seeking a Research Associate/Sr. Research Associate to join our Payload Production team. This is a hands-on, on-site laboratory role, with approximately 80% lab-based work and 20% dedicated to data entry and experiment planning. This individual will play a critical role in the preparation, purification, and quality control of nucleic acid materials for in vivo applications. The ideal candidate will possess the skills necessary to independently prepare, purify, and QC our payload materials, while also supporting the development of new processes and methods. This role additionally requires good organization and record keeping, cross-functional collaboration, and the ability to present and discuss work across teams. Key Responsibilities Purify RNA and DNA samples using AKTA chromatography systems and tangential flow filtration (TFF). Perform quality control (QC) analysis on nucleic acid materials, utilizing gel electrophoresis, UV-VIS spectrophotometry, HPLC, and plate-based assays. Prepare samples for internal studies, ensuring timely and accurate transfer to other teams. Maintain and troubleshoot purification equipment, including AKTA systems. Accurately document experimental procedures, results, and process optimizations. Collaborate across departments to meet research and development goals. Adapt to evolving project needs in a fast-paced, data-driven environment. Qualifications Education & Experience Bachelor's degree in biochemistry, chemical biology, chemistry, or a related field. At least 1 year of experience in a laboratory research setting (industry experience preferred). Technical Skills Hands-on experience with nucleic acid purification using chromatographic techniques (e.g., IEX, affinity, HIC, TFF, AKTA). Proficiency in biomolecule quality assessment methods (HPLC, gel electrophoresis, endotoxin assays, ELISA, qPCR). Experience in DNA/RNA production methods (e.g., cloning, PCR, RCA, IVT). Strong troubleshooting and problem-solving skills for experimental and equipment-related issues. Proficiency in Microsoft Suite (Excel, Word) for data documentation and analysis. Organizational & Soft Skills Strong organizational skills, attention to detail, and meticulous data documentation. Ability to prioritize multiple tasks while maintaining accuracy. Effective verbal and written communication skills for cross-functional collaboration. Flexibility to adapt to evolving project priorities. A team-oriented, startup mentality, willing to take on multiple responsibilities. Scientifically curious, paired with a strong work ethic and grit Authorization Applicants must have authorization to work in the U.S. The anticipated salary range for candidates who will work in San Diego, CA is $60,000 to $100,000. The final salary offered to a successful candidate will be dependent on several factors that may include but are not limited to the type and length of experience within the job, type and length of experience within the industry, education, etc. Seawolf provides competitive salaries and an excellent benefits package including medical, dental, vision, life insurance, 401K, stock options and bonus.

Key Responsibilities: Perform routine testing in a cGMP environment (Environmental Monitoring, Bioburden testing, Growth Promotion, Bacterial and Fungal IDs). Maintain and calibrate laboratory equipment; manage inventory and stock materials. Analyze and interpret data against protocol specifications and alert limits. Participate in laboratory investigations for invalid assays and out-of-spec results. Ensure cleanliness of the lab and equipment. Complete training and maintain accurate records. Train QC analysts on test methods. Qualifications: BA or BS degree required. Minimum 1-3 years of laboratory experience, preferably in Quality Control. Familiarity with equipment maintenance, calibration, inventory management, and submitting orders. Proficient in MS Office (Word, Excel). Skills: Strong understanding of GMP/GLP practices. Ability to analyze data and interpret results. Excellent organizational and communication skills.

We are a San Diego-based biotech company that provides cell cultures, growth media, and cell biology products for research use. We are seeking candidates for the GROWTH MEDIA TECHNICIAN role. The ideal Technician candidate is energetic, positive, adaptable, dependable, responsible, and takes pride in performing at a high level. Your work directly impacts the life sciences community, as renowned researchers at universities, biotech, and pharmaceutical companies worldwide depend on our products and services to make new discoveries. ========================================= GROWTH MEDIA TECHNICIAN RESPONSIBILITIES INCLUDE, BUT ARE NOT LIMITED TO Basal and Growth Media preparation and filtering. Buffer and reagent preparation. Cleaning of glassware, autoclaving, inventory, and stocking. Maintenance and organization of accurate records. Labeling and sealing of products. Quality Control testing. GROWTH MEDIA TECHNICIAN CANDIDATE REQUIREMENTS A B.S. degree in cell biology, chemistry, or closely related field. 1-2 years laboratory experience is preferred. Possess a great work ethic. Track record of completing tasks in precise and punctual fashion. Possess manual dexterity and be able to carry out aseptic work. Be able to carry out scientific calculations necessary for determining molarity, percentages, cell doubling time, cell concentration, seeding density, etc. Working knowledge of standard laboratory procedures and safety. Working knowledge of laboratory equipment (i.e. pH meter, scale, pipetting). Comfortable with what can sometimes be repetitive work. Extremely neat and detail-oriented. Candidate must be a team player and have good communication skills. Candidate must be organized and have the ability to closely follow direction. Basic computer skills (Word, Excel, Google searches).

BPS Bioscience's purpose is to advance new scientific discoveries that lead to therapies by creating innovative solutions for research. Breakthroughs in research rely on dependable model systems that accurately reflect biological systems. We are experts in protein design, expression, purification, and characterization, cell line and lentivirus engineering, and biochemical and cellular assay development. Our products and services have enabled thousands of researchers to advance biological discoveries across a wide variety of disciplines, including epigenetics, cell signaling, immunotherapy, adoptive cell therapies, and many more. Science never stands still. We focus on emerging research needs and rapidly deliver solutions. Job Overview The position requires the ability to perform and interpret molecular cloning and protein expression experiments. The successful candidate will be tasked with duties in molecular biology, cell culture and transfection techniques. These include standard cloning, PCR techniques, and plasmid preparation and analysis. The primary expression systems of focus will be mammalian and E. coli, but the candidate may also assist with the HEK293 or SF9 expression if needed. This position will include assisting other researchers with their experiments and with lab maintenance. This position will also be required to perform QC assays such as cell based, ELISA, Flow Cytometry and immuno-magnetic cell isolation assays. Responsibilities: Assist other researchers with various tasks, including aid in experiments, data entry, sample storage, organization, and ordering. Recombinant protein expression in E. coli (HEK293 and SF9 if needed) while maintaining sterility, preparation, organization, and storage of virus and cells for expression. Accurate design and generation of genes of interest for cloning; analyze and confirm DNA sequence of recombinant plasmid for proper protein expression Maintain supply stocks for the common lab area including reagents, DNA, equipment, and consumables.· Perform internet searches to gather relevant information, record and present any relevant findings in a manner pursuant to facility protocol. Prepare reagents and solutions as needed. Prepare documentations for project validation and research quality control; keep an updated database record with project details and information. Ensure lab cleanliness and safety by maintaining equipment and technician attire, and keeping all samples properly labeled and stored. Perform QC and assembly of kit components including those for immune-magnetic cell isolation and cell cytotoxicity assay kits. Recombinant protein expression, as well as preparation of cultures, reagents, and competent cells for expression. Accurate design and generation of genes of interest for cloning; analyze and confirm DNA sequence of recombinant plasmid for proper protein expression. Ensures lab cleanliness and safety by maintaining equipment and technician attire, and keeping all samples properly labeled and stored. Maintains supply stocks for the common regarding area including reagents, DNA, equipment, and consumables; communicates with sales representatives for appropriate pricing. Prepares reagents and solutions as needed. Handles documentation needed for project validation and research quality control; keeps an updated database record with project details and information. Performs internet searches to gather relevant information, record and present any relevant findings in a manner pursuant to facility protocol. Other duties as assigned. Requirements: Bachelor's degree in a relevant Life Sciences field Good communication, interpersonal, and teamworking skills are essential Minimum of 2-4 years of experience working in a molecular biology or biochemistry lab in either industry or academia. Hands on experiences in recombinant protein expression, molecular cloning, cell culture, and protein characterization assays are required. Experiences in Flow cytometry and immune-magnetic cell isolation is a plus. Benefits! 401k with company match Medical/Dental/Vision health insurance plans Vacation and paid holidays BPS Bioscience is an equal opportunity employer, without regard to race, color, religion, age, gender, sexual orientation, disability, or any other characteristic protected by applicable law.

Research Associate, Fixed Income The Research Associate works as part of the Fixed Income Research team, covering bond managers. The primary responsibility of the analyst is to research and analyze fixed income investment managers. This role supports the development and communication of Fixed Income research to our consultants and clients. In addition, the Associate will conduct investment market research on a broad array of topics (e.g. assist with writing white papers and other internal or external facing content) and utilize investment and statistical software programs to aid in the monitoring and identification of Fixed Income strategies. The Research Associate is expected to progressively increase his or her level of knowledge regarding capital markets broadly, public markets manager research, and firm-specific practices. The Research Associate works closely with other research professionals and other investment analysts in carrying out the position's duties. The position reports to the Head of Fixed Income and is based in our Carlsbad, CA office. Roles and Responsibilities: • Attend and / or conduct manager research meetings • Draft or help draft comprehensive manager meeting notes and prepare manager analyses • Monitor the performance of investment managers and identify potential areas of concern • Conduct performance review conference calls with existing managers • Identify promising new managers in the relevant asset class • Work with senior manager research analysts and consultants to help coordinate the manager search process (RFPs, data collection, search document creation, etc.) • Assume asset class coverage responsibilities as needed Skills, Qualifications, Experience Preferred: • Progress towards the CFA designation • Strong proficiency in Microsoft Excel • Familiarity with CRM databases and AI tools • Familiarity with eVestment, Diligence Vault, and other investment related tools • An individual who is a committed team player, has strong communication skills, is well organized and is willing to learn, and is detail-oriented, are other desirable attributes Skills, Qualifications, Experience Required: • Minimum of 2 years of relevant work experience for external applicants • Minimum of 1 year of relevant work experience for internal applicants • Ability to gather, organize, and coordinate data from disparate sources • Professional and effective verbal communication skills • Solid understanding of economic and investment theory and practices • Strong quantitative and analytical skills, including facility with financial and statistical concepts • Superior written and verbal communication skills • Excellent attention to detail • Ability to work efficiently and accurately under pressure and to meet commitments • Independently and to proactively seek new responsibilities • Work well with employees from other company departments • Solid interpersonal and presentation skills • A bachelor's degree Measure of Success: • Accuracy and timeliness of client-related work product • Ability to use independent judgment and exercise discretion in selecting and evaluating appropriate managers • Growth in knowledge base, including general investment and economic topics, and client-related issues of strategy and implementation • Degree to which knowledge is communicated and available to other investment staff • Level of proficiency with investment-related software • Effectiveness of communication, both verbal and written, in conveying knowledge, eliciting necessary information, and meeting predefined objectives • Contribution to improvements in the quality of the company's advisory services • Contribution to improvements in the efficiency of the company's analytical processes and procedures About Meketa Investment Group Meketa recognizes that our workforce is a reflection of our company, and we operate in an inclusive environment that accepts and promotes diversity. We believe our employees can best serve our clients in an atmosphere where individuals are treated fairly, where professional growth is developed and encouraged, and where a healthy balance between work and home life is respected and preserved. To support employees, Meketa offers a competitive compensation structure, a wide range of benefits from core insurance benefits to time-based benefits, as well as flexible schedules and support for continuing education. Meketa is an Equal Employment Opportunity and Affirmative Action Employer. If reasonable accommodation is needed to participate in the job application or interview process, to perform essential job functions, and/or to receive other benefits and privileges of employment, please contact us

The purpose of the In Vivo Research Associate I position is to provide support on In vivo studies within the In Vivo Pharmacology group meeting Company's goals, objectives and quality standards. PRIMARY RESPONSIBILITIES: * Works closely with Study Directors, Study Coordinators, In Vivo Managers, and cross functional team members to ensure all assigned studies are conducted in accordance with study protocols, standard operating procedures and company policies * Collection of body weight data * Collection of tumor volume measurements * Collect tissue samples and process for shipment to sponsor as well as internal purposes * Preparation of animals for procedures, including shaving, ear tagging and other tasks as directed * Performance of clinical observations and humane euthanasia in mice * Collect relevant data and provide feed back to team members regarding progress of assigned projects * Performance of basic in vivo procedures, including PO, SC and IP dosing * May be trained on more complex procedures * Providing general group support by cleaning, general supply stocking and sample shipping * Responsible for tracking time spent on projects (project logs) MINIMUM REQUIREMENTS * Bachelor's degree or 4 years of relevant work experience in the life science/biotech industry * Comfortable working in a laboratory animal research environment PREFERRED REQUIREMENTS * At least 6 months of experience handling mice and/or rats in a Vivarium environment is preferred * Prior CRO or research experience is preferred * Knowledge and interest in oncology is preferred * Planning, organizational skills and flexibility in a reactive environment * Demonstrated accountability and responsibility for own work * Ability to follow standard operating procedures, observe safety and security procedures WORKING CONDITIONS and PHYSICAL REQUIREMENTS: * Requires physical dexterity of fingers, hands, wrists, and arms * Requires overtime hours to be worked, as well as possible work on weekends and holidays * Picking up and moving materials and supplies * Sitting for long periods of time * Standing for long periods of time * Prolonged computer usage * Able to lift up to 25lbs * Frequently required to use repetitive hand/wrist/arm motion * BSL-2 Lab Environment * Normal office environment The California salary range for this position is: Research Associate I: $23- $27.82 This salary (or salary range) is merely an estimate and may vary based on an applicant's skills and prior relevant experience. Crown Bioscience is committed to a diverse and inclusive workplace. Crown Bioscience is an equal opportunity employer and does not discriminate based on race, national origin, gender, gender identity, sexual orientation, protected veteran status, disability, age, or other legally protected status. KBI Biopharma is committed to providing a safe and healthy workplace. Any employee entering a KBI site located in the US must inform KBI Biopharma of their vaccination status and must submit their vaccination status. All vaccinated employees are required to provide proof of their COVID-19 vaccination, with a COVID-19 vaccination which has been granted FDA approval or Emergency Use Authorization. KBI Biopharma, Inc. is an EEO/AA employer and actively seeks to diversify its work force. Therefore, all qualified applicants, regardless of race, color, national origin, religion, gender, gender identity, sexual orientation, age, disability or veteran status, are strongly encouraged to apply. I understand that neither the completion of this application nor any other part of my consideration for employment establishes any obligation for KBI Biopharma, Inc. to hire me. If I am hired, I understand that either KBI Biopharma, Inc. or I can terminate my employment at any time and for any reason, with or without cause and without prior notice. I understand that no representative of KBI Biopharma, Inc. has the authority to make any assurance to the contrary. I attest with my signature below that I have given to KBI Biopharma, Inc. true and complete information on this application. No requested information has been concealed. I authorize KBI Biopharma, Inc. to contact references provided for employment reference checks. If any information I have provided is untrue, or if I have concealed material information, I understand that this will constitute cause for the denial of employment or immediate dismissal.

Research Biologist needs 1 or more years of research experience in an academic institute, biotechnology or pharmaceutical industry Research Biologist requires: Bachelors degree in biology, biochemistry, molecular biology or similar discipline with 1 or more years of research experience in an academic institute, biotechnology or pharmaceutical industry Experience in running biochemical and immunological assays. Highly motivated and agile biochemist Research Biologist duties: Perform experiments to characterize protein-protein interactions using PAGE, Western Blot, ELISA & SPR technologies Perform basic tasks to support tissue culture and maintenance of immune competent cell lines Perform basic cell-based assays with immunology research-related technologies (e.g. human whole blood, primary human leukocyte isolation, cellular activation and differentiation, FACS, cytokine assay, etc.) Work with a cross-disciplinary team for data analysis Independently execute experiments, analyze, interpret and present experimental data

In Vivo Research Associate II FLSA status: Non-Exempt Pay Rate: $28 - $32 /hr Pharmaron (San Diego) is seeking to hire an outstanding candidate to join our Medical Device department at the Research Associate II level. The Research Associate will play an important role by supporting in vivo studies to test medical devices. This position requires a broad knowledge of animal anatomy, physiology, and biochemistry to help develop and support in vivo models to screen therapeutics and devices being developed for various indications. Responsibilities: * Experience in the administration of test substances by various basic methods (i.e., oral gavage, SQ, IV, dermal, etc.) * Manage and observe animals for general health and overall wellbeing. * Experience in the collection of biological specimens (i.e., blood from appropriate vessels from all species of laboratory animals at the site) * Able to perform study related activities in compliance with Good Laboratory Practice Regulations (GLPs), study protocols, and company policies and Standard Operating Procedures (SOPs) * Review documentation to ensure functions performed meet quality control requirements. * Handle, restrain, and provide care for all species of laboratory animals at the site. * Perform study preparation activities, including collection tube labeling and room setup. * Perform catheter placements in large animals. * Perform surgical procedure: intubation, anesthesia, pain recognition and analgesia. * Monitor animals under anesthesia and during post-operating monitoring and recovery. * Perform biopsies and skin excisions. * Perform necropsies and tissue collection. * Interface with different teams, including study director, principal investigator, QC/QA, and Account Managers/Sales. * Maintain accurate records in various internal databases. * Support internal research projects to optimize service offerings. Perform aseptic techniques. * Perform other duties as directed by management. What We're Looking For: * We're seeking individuals who have strong communication skills with attention to detail who thrive in fast-paced environments. * Associates degree (preferred) in veterinary technology with 3 years relevant experience. * BS with at least 2 years relevant experience. * Education level requirements could be amended based on relevant years of experience. * Certification as a registered veterinarian technician (RVT) is a plus. * Background in lab animal (in vivo) research is a must. * Working knowledge of preclinical techniques and modalities will be a plus. * Position requires good communication skills and attention to detail. * Strong work ethic, self-motivation, and ability to adapt to a dynamic team environment. Why Pharmaron? Pharmaron is a premier service provider for the life sciences industry. Founded in 2004, Pharmaron has invested in its people and facilities and established a broad spectrum of research, development, and manufacturing service capabilities throughout the entire drug discovery, preclinical, and clinical development process across multiple therapeutic modalities, including small molecules, biologics, and CGT products. With over 21,000 employees and operations in the U.S., the U.K. and China. Pharmaron has an excellent track record in delivering R&D solutions to its partners in North America, Europe, Japan, and China. Collaborative Culture: You'll thrive in our inclusive and collaborative environment, where teamwork and innovation go hand in hand. Here, your voice matters, and your contributions make a real impact. "Employees Number One" and "Clients Centered" are the core cultural values at Pharmaron. Our culture, which sets Pharmaron apart from other organizations, has evolved from our deep commitment to our employees, partners and collaborators. Benefits: As part of our commitment to your well-being, we offer a comprehensive benefits package: * Insurance including Medical, Dental & Vision with significant employer contributions * Employer-funded Health Reimbursement Account * Healthcare & Dependent Care Flexible Spending Accounts * 100% Employer-paid Employee Life and AD&D Insurance, Short and Long Term Disability Insurance * 401k plan with generous employer match * Access to an Employee Assistance Program How to Apply: Ready to seize this incredible opportunity? Join us at Pharmaron and be part of a dynamic team driving innovation and excellence in biopharmaceutical research and development. Apply online today! As an Equal Employment Opportunity and Affirmative Action employer, Pharmaron values diversity and inclusion in the workplace, fostering an environment where all individuals are empowered to succeed. Join us in our mission to make a difference in the world of life sciences. #LI-MC1

Job Title: Research Associate/Senior Research Associate Reports To: Principal Scientist Department: Research OBJECTIVES: In this role you will be a member of the biology team developing cellular assays to discover novel targets and treatments for inflammatory and autoimmune diseases. The ideal candidate will have a range of skills and be open to learning new techniques to answer key biological questions. The colleague will be an enthusiastic and self-motivated candidate that enjoys working in a highly collaborative and fast-paced team environment. RESPONSIBILITIES, KNOWLEDGE AND SKILLS: · Being part of a team focused on profiling primary immune cells and cell lines to move projects forward · Knowledge of immunology, cellular biology is preferred · Familiarity with cellular and molecular biology assays, including ELISA, HTRF, CRISPR, flow cytometry, and Q-PCR · Outstanding organizational skills and experience in preparing scientific and technical documents including detailed protocols · Experience using data analysis programs such as Prism, Excel, FlowJo · Document and deliver high-quality data in a time-efficient manner · Comfortable presenting data at internal review meetings EDUCATION AND EXPERIENCE: · A minimum of a BS in Biology or related discipline with 2+ years post-graduate experience is required fields · Industry experience is preferred but not required · Willingness to work in a dynamic and changing environment · High level of motivation to grow as a scientist · Excellent communication and interpersonal skills PHYSICAL DEMANDS: · Manual dexterity required to operate office equipment (i.e. computers, phones, etc.) · Carrying, handling and reaching for objects (up to 25 lbs) · Onsite office, lab environment Further Information: Salary range: $98k-$117k Trotana is a biotechnology company based in San Diego. In addition to a competitive compensation package with stock options, the company offers a comprehensive benefits package for our employees and their families, which includes medical, dental, vision, life insurance, disability insurance and a 401(k) plan. The company is an Equal Opportunity employer. We do not discriminate based upon race, religion, color, national origin, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender, gender identity, gender expression, transgender status, sexual stereotypes, age, status as a protected veteran, status as an individual with a disability, or other applicable legally protected characteristics. To be considered as an applicant, please submit your resume/CV referencing the specific position of interest to *******************. Applicants whose qualifications and experience most closely match the requirements of the position will be reviewed.

We are a San Diego-based biotech company that provides cell cultures, growth media, and cell biology products for research use. We are seeking candidates for the CELL CULTURE TECHNICIAN role. The ideal Technician candidate is energetic, positive, adaptable, dependable, responsible, and takes pride in performing at a high level. Your work directly impacts the life sciences community, as renowned researchers at universities, biotech, and pharmaceutical companies worldwide depend on our products and services to make new discoveries. ========================================= CELL CULTURE TECHNICIAN RESPONSIBILITIES INCLUDE, BUT ARE NOT LIMITED TO Isolation, growth, subculture of mammalian cell cultures. Tissue dissection and small animal surgery. Lab maintenance, stocking, cleaning. Digital and hardcopy recordkeeping. Microscope work. Quality Control testing, data collection, and analysis. Depending on personal aptitude, the candidate may also be involved in cell isolation and other cell-based research & development projects. CELL CULTURE TECHNICIAN CANDIDATE REQUIREMENTS A B.S. degree in cell biology or closely related field. 1-2 years laboratory experience, or equivalent, is preferred. Possess a great work ethic Track record of completing tasks in precise and punctual fashion. Possess outstanding manual dexterity and be able to carry out aseptic work. Be able to carry out calculations necessary for determining cell doubling time, cell concentration, seeding density, molarity, etc. Be comfortable with what can sometimes be repetitive work, including extended use of microscopes. Be extremely neat and detail-oriented. Be familiar with life science laboratory equipment.

The purpose of the In Vivo Research Associate I position is to provide support on In vivo studies within the In Vivo Pharmacology group meeting Company's goals, objectives and quality standards. PRIMARY RESPONSIBILITIES: Works closely with Study Directors, Study Coordinators, In Vivo Managers, and cross functional team members to ensure all assigned studies are conducted in accordance with study protocols, standard operating procedures and company policies Collection of body weight data Collection of tumor volume measurements Collect tissue samples and process for shipment to sponsor as well as internal purposes Preparation of animals for procedures, including shaving, ear tagging and other tasks as directed Performance of clinical observations and humane euthanasia in mice Collect relevant data and provide feed back to team members regarding progress of assigned projects Performance of basic in vivo procedures, including PO, SC and IP dosing May be trained on more complex procedures Providing general group support by cleaning, general supply stocking and sample shipping Responsible for tracking time spent on projects (project logs) MINIMUM REQUIREMENTS Bachelor's degree or 4 years of relevant work experience in the life science/biotech industry Comfortable working in a laboratory animal research environment PREFERRED REQUIREMENTS At least 6 months of experience handling mice and/or rats in a Vivarium environment is preferred Prior CRO or research experience is preferred Knowledge and interest in oncology is preferred Planning, organizational skills and flexibility in a reactive environment Demonstrated accountability and responsibility for own work Ability to follow standard operating procedures, observe safety and security procedures WORKING CONDITIONS and PHYSICAL REQUIREMENTS: Requires physical dexterity of fingers, hands, wrists, and arms Requires overtime hours to be worked, as well as possible work on weekends and holidays Picking up and moving materials and supplies Sitting for long periods of time Standing for long periods of time Prolonged computer usage Able to lift up to 25lbs Frequently required to use repetitive hand/wrist/arm motion BSL-2 Lab Environment Normal office environment The California salary range for this position is: Research Associate I: $23- $27.82 This salary (or salary range) is merely an estimate and may vary based on an applicant's skills and prior relevant experience. Crown Bioscience is committed to a diverse and inclusive workplace. Crown Bioscience is an equal opportunity employer and does not discriminate based on race, national origin, gender, gender identity, sexual orientation, protected veteran status, disability, age, or other legally protected status. KBI Biopharma is committed to providing a safe and healthy workplace. Any employee entering a KBI site located in the US must inform KBI Biopharma of their vaccination status and must submit their vaccination status. All vaccinated employees are required to provide proof of their COVID-19 vaccination, with a COVID-19 vaccination which has been granted FDA approval or Emergency Use Authorization. KBI Biopharma, Inc. is an EEO/AA employer and actively seeks to diversify its work force. Therefore, all qualified applicants, regardless of race, color, national origin, religion, gender, gender identity, sexual orientation, age, disability or veteran status, are strongly encouraged to apply. I understand that neither the completion of this application nor any other part of my consideration for employment establishes any obligation for KBI Biopharma, Inc. to hire me. If I am hired, I understand that either KBI Biopharma, Inc. or I can terminate my employment at any time and for any reason, with or without cause and without prior notice. I understand that no representative of KBI Biopharma, Inc. has the authority to make any assurance to the contrary. I attest with my signature below that I have given to KBI Biopharma, Inc. true and complete information on this application. No requested information has been concealed. I authorize KBI Biopharma, Inc. to contact references provided for employment reference checks. If any information I have provided is untrue, or if I have concealed material information, I understand that this will constitute cause for the denial of employment or immediate dismissal.

Research Biologist needs 2-3 years experience Research Biologist requires: Degree in biology Laboratory equipment and procedures. MS Office Lab techniques Research Biochemistry Cell biology Experience in running biochemical and immunological assays. Research Biologist duties: Ø Conduct experiments to identify and validate drug targets. Ø Support assay design, optimization, validation, and data analyses. Ø Design and execute molecular and cell biology experiments. Ø Troubleshoot and analyze complex data in support of drug discovery projects. Ø Presentation of results and conclusions both orally and written.