Research Associate Jobs in San Diego, CA

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!

Research Associate I, ASSAY DEVELOPMENT REPORTS TO: Senior Manager, Assay Development STATUS: Full Time At EXOKĒRYX, we are committed to creating cutting-edge platforms and tests that leverage extracellular vesicles, the body's concentrated, information-dense cellular communication system. Toward this end, we are growing the Assay Development team. This Research Associate position is a key hands-on role, requiring an individual capable of executing, interpreting, and discussing the results of experiments. This individual is an organized, analytical, and hard-working team player . She/he tackles novel assays and information methodically to make measurable progress and enjoys gaining a deep understanding of the system(s) being studied/developed. This individual has excellent communication skills, a goal-oriented mentality, and a strong sense of ownership and drive to meet project goals and timelines. ESSENTIAL DUTIES § Execute biochemistry and molecular biology-based assays § Perform and analyze assay development experiments, making use of immunochemistry, fluorescence-based detection systems, statistical analysis, and other methods/tools § Carry out mammalian cell culture § Troubleshoot workflows and experiments proactively and communicate results effectively to team § Partner with other team members in support of project objectives § Author work instructions and other QMS-compliant documentation § Generate slides to effectively communicate experimentation and findings § Other duties as assigned EDUCATION/EXPERIENCE/SKILLS Minimum Qualifications § Research Associate I: Bachelor's degree or Master's degree in Biology, Biochemistry, Bioengineering, or a closely-related field § Lab experience in pipetting, running assays/test methods, and analyzing results § Strong verbal and written skills § Strong ownership of technical success Preferred Qualifications § Experience with cell culture § Experience with immunoassays (ELISAs, Western blots, microtiter plates, etc)

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

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We're looking for people who are determined to make life better for people around the world. Actual compensation will depend on a candidate's education, experience, skills, and geographic location. The anticipated wage for this position is $122,250 - $179,300. The HSE Lead will provide health and safety and environmental support to expanding west coast R&D sites with a goal to harmonize HSE programs, safety culture and execution processes across our San Diego, Pasadena, and South San Francisco sites including current and future acquisition opportunities. The position will work closely with the LRL HSE Regional Team and will be responsible to assess risk, prioritize needs and grow HSE at West Coast sites. Do you have at least 5 years of HSE experience in a pharma laboratory environment? Apply today to join the Lilly Team! Partner with LRL HSE Regional Team and site contract HSE personnel to ensure activities at LRL west coast sites maintain HSE compliance with State, local and federal regulations and achieve adherence to applicable Lilly HSE standards within appropriate timeframes. Support site HSE and operations personnel both remotely and on site as needed for external inspections and internal audits, and for emerging HSE issues or incidents that need additional HSE support. Work with LRL HSE regional technical hub personnel to prioritize and perform HSE project work across west coast research sites. Gain knowledge of and serve as a technical resource for core H&S tools and Lilly processes such as SciShield, Prior Approval, Event Management, SDS Management, Exposure Assessment Database, and other tools. Maintain an ongoing understanding of the H&S liabilities, risks and capabilities for each west coast site, including using site connections and business and HSE systems to anticipate changes in site risk profiles based on site growth, capital projects, changes to modalities and the evolution of science at west coast sites. Address identified gaps, grow safety culture, develop & implement HSE roadmaps and achieve prioritized goals through connections with site HSE resources, LRL HSE Regional Technical Hub, and LRL HSE technical resources. Assist sites in understanding appropriate timing and help implement core LRL HSE systems and processes for notification to management, incident response, corporate reporting, lab inspections, and other systems used across the LRL network. Provide recommendations to the LRL HSE Regional Team and assist with development and implementation of simplified, right-sized HSE programs for regional research sites. Network with LRL HSE technical resources and recommend arrangements for specialized HSE contract assistance and as needed for project work that lies outside existing site capabilities. Serve as augmented HSE technical support for West Coast incubator/accelerator research facilities as needed. Enable desired behaviors throughout the organization through clear communication and respect for people. Lead or support special projects as assigned by the LRL HSE Regional Site Integration and Execution Lead, LRL HSE. Responsible for informing, educating, and collaborating with scientific staff and management leaders within LRL organization regarding site HSE issues, programs and needs. Provide health and safety and environmental support for HSE programs including but not limited to the following systems/programs across the west coast sites: support for San Diego, South San Francisco and Pasadena facilities including acquisitions, chemical hygiene plan and programs, exposure assessment, hazard communication & risk assessment, HSE risk profile and leading and lagging metrics, site self-assessments, safety culture growth and progression, contractor safety, subpart BB and CC, LDAR compliance programs, CARB emission reporting program and hazardous materials and business plan (HMBP) program management. Minimum Qualifications: Bachelors degree or higher in a scientific or pharmaceutical development-related field 5+ years of HSE experience Additional Skills: Knowledge of basic HSE regulations and regulatory framework (OSHA, EPA, DOT, etc.) Strong communications skills Excellent self-management and organizational skills; able to manage workload, set priorities and adjust as needed Strong interpersonal and team building skills; able to develop effective teamwork between team members with diverse interpersonal styles across functional areas Flexibility to adjust quickly and effectively to frequent change and altered priorities Ability to conduct efforts across multiple sites, including travel (20-30%) Additional Preferences: Pharma, biotech or laboratory based HSE experience Certification in an HSE field (Industrial hygiene, safety, etc.) Familiarity with industrial safety programs (equipment lockout, machine guarding) Familiarity with waste solvent collection systems Experienced in interaction with external inspectors on the local and/or federal level. Previous team leadership or coaching experience Experience with or knowledge of scientific laboratory instrumentation. Experience in ensuring compliance with regulatory requirements in a research environment. Demonstrated ability to engage and influence scientists and/or business partners to achieve business results. Qualified candidates must be legally authorized to be employed in the United States. Lilly does not anticipate providing sponsorship for employment visa status (e.g., H-1B or TN status) for this position. Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form (******************************************************** for further assistance. Lilly is an EEO/Affirmative Action Employer and does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status. Full-time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance). In addition, Lilly offers a comprehensive benefit program to eligible employees, including eligibility to participate in a company-sponsored 401(k); pension; vacation benefits; eligibility for medical, dental, vision and prescription drug benefits; flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts); life insurance and death benefits; certain time off and leave of absence benefits; and well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities). #J-18808-Ljbffr

Macdonald & Company has been exclusively retained by a leading national real estate investment, development, and management company focused on the Multifamily sector to appoint a Capital Markets Associate for either their San Diego or Torrance office. The Capital Markets Associate will support the team in sourcing, negotiating, closing, and managing construction debt, JV equity, and project refinancing across the 21 markets where the company develops, builds, and acquires properties. Essential Functions & Responsibilities Prepare construction debt financing strategies and financing solicitation packages. Assist in closing debt and equity for new development and acquisition communities, with a focus on the Western U.S. offices. Support debt modifications and refinancing efforts for development and acquisition communities. Track debt solicitation processes, assist in lender due diligence, and ensure timely loan closings. Draft and review Investment Committee Meeting memos and ensure accuracy. Review loan documents and exhibits for accuracy. Work with Capital Markets and internal teams to track interim property tests, guaranty burn-offs, loan extensions, and other portfolio management requirements. Assist with lender and equity partner reporting, questions, and requests related to financed projects. Engage in financing discussions with equity partners, Asset Management, Portfolio Management, Development, and Accounting teams. Support Development, Accounting, and Treasury teams in executing loan draw requests, payments, covenants, and other requirements. Conduct detailed sensitivity analysis for loan covenants and extension tests. Prepare interest rebalancing projections and assist in negotiating loan rebalancing requests. Assist with interest rate hedging for construction loans. Coordinate lender approvals for retail leases nationwide. Maintain a lender contact relationship management database. Develop and maintain relationships with providers of construction debt, bridge, and permanent financing. Education & Experience Undergraduate degree required. Minimum of 3 years of real estate finance experience. Experience in commercial real estate lending or construction lending preferred. Multifamily experience preferred. Skills & Knowledge Strong attention to detail. Excellent analytical skills with an understanding of risk/reward relationships. Ability to create compelling and detailed materials for lenders. Proficiency in Word, PowerPoint, and Excel. Strong written and verbal communication skills. Ability to assess critical issues in complex financial situations. Effective team player with the ability to collaborate across functional and geographic lines. Highly organized, deadline-driven, and self-motivated. Strong interpersonal skills with the ability to manage conflict and influence outcomes. Ability to thrive in high-pressure environments. Operates with integrity, motivation, and intellectual curiosity. Work Environment Work settings include office environments and active construction sites. Travel required up to 25% of the time.

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

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.

Since 1980, NAI has been a leader in nutritional health, bringing whole food-based supplements to a global population. NAI is a leading expert and manufacturer of dietary supplements. We are involved in every facet of the industry, including research, development, manufacturing and marketing and advocacy. As a company, we continue to grow with manufacturing locations in Vista and Carlsbad, CA. We are looking for seasoned and entry level candidates that are interested in working for a great company with opportunities to grow, competitive pay and benefits. Benefits Free medical (one plan) and other medical plan options Dental, vision, life insurance and other voluntary benefit options. $1,000 Employee Referral Bonus 3 weeks' vacation and 11 paid holidays 401K including company matching and profit sharing Opportunities for advancement Comprehensive training Tuition Reimbursement and more! **PLEASE HAVE NUTRACEUTICAL EXPERIENCE PRIOR TO APPLYING** Summary Responsible for the successful technical transfer of product formulas from pilot lab to commercial equipment and through to cGMP production scale. Collaborate with R&D Team and Operations Team on formula development, providing technical expertise on reformulation needs through the product development process to achieve successful scale up. Create and maintain technical transfer documentation and history. Evaluate and refine product formulas as needed after commercial production, while maintaining customer requirements. Well versed on dietary supplement tablet, capsule and powder delivery formats. Essential Duties & Responsibilities Formulation: Provide technical expertise and support to ensure successful transfer of customer formulas from concept to pilot lab and on to commercial equipment and cGMP production. Collaborate with R&D Formulation Team and Technical Operations team on optimization of existing formulas to improve production efficiencies. Be readily available to perform quick and timely adjustments to optimize production runs at all stages of the production process Design and conduct appropriate formulation experiments to facilitate and ensure successful technical transfer of customer products to commercial production equipment, collaborating with R&D Formulation team, R&D Pilot Lab team and Director of Technical Operations. Present relevant findings following technical transfer trials and formula adjustments to provide guidance to R&D Formulation and R&D Pilot Lab team as needed. Provide technical expertise in review of initial formula concepts going through quoting process for any concerns around processability on commercial equipment Collaborate with R&D Formulation Team on development of new product concepts that would be suitable for commercialization Create and maintain relevant history and documentation on product formula transfer from pilot lab to commercial equipment: Pilot lab trial reports Commercial equipment trial reports First commercial production reports Modifications to equipment settings, blend instructions, and formulas during product trials Present technical transfer trial data/findings to senior management, Business Development and Client Management teams as needed Create and/or act as additional R&D reviewer as needed to ensure accuracy and/or maintain accurate records of technical documents for product development projects, including but not limited to: Draft formulas Final formulas Product specifications Product justifications Master batch records Testing requests for finished products Testing requests for prototypes Document change requests for formulas Pilot batch records Assist R&D Formulation team in evaluation of out-of-specification results on finished products Act as an additional reviewer and signoff of formula formula-related documents for others on the R&D team Maintain awareness of and update training as needed Proper use of laboratory and manufacturing equipment Development of new techniques, testing, and other areas related to product development Provide technical and scientific input, support and assistance to other technical disciplines Follow efficient operations in assigned project areas in accordance with NAI requirements, SOP's and GMP's Take leading role for projects as assigned Works independently while understanding the necessity for effective communication and coordination of work efforts with cross-functional team and external partners Participates in project meetings Support other projects as needed within the formulation team Raw Materials: Collaborate with and assist R&D Formulation Team, R&D Technical Services Team, Purchasing and Quality with qualification and replacement of new and alternate raw materials and suppliers. Collaborate with the R&D Formulation Team to identify raw material needs for prototypes and pilots for R&D Technical Services and Purchasing teams. Collaborate on specification development with R&D Technical Services and Formulation teams. Provide on-going internal and external technical support to ensure that production needs are met and customer requests are satisfied Manage and troubleshoot raw materials related products by understanding the potential ramifications caused by raw material and specification changes, such that appropriate actions are taken Build strategic relationships and maintain effective communications with vendors Foster professional knowledge of market and supplier information Collaborate with R&D Formulation Team and Purchasing as needed to help support a consistent supply of our raw materials, as well as avoid market price fluctuations Other Duties Maintain awareness of current developments within the functional discipline Develop a network of outside contacts such as vendors, consultants, educators, and attend appropriate continuing education courses Collaborate with and support cross-functional NAI teams Present ideas and suggestions for product or process improvements, and improvements to pilot laboratory operations Perform other related duties as assigned Qualifications Requires a four year college or university degree or its equivalent in Pharmacy, Chemistry, Food Science, Chemical Engineering or other science-related field In-depth knowledge of formula development in hard shell capsules, tablets, powder fills and/or other dietary supplement dosage forms Successful track record of developing/commercializing new products in manufacturing environment Requires a minimum of five years direct industry formulation development experience, ideally with an additional three years of related experience Possess comprehensive knowledge and practical experience with product/process development, and a firm foundation in chemistry, mathematics, pharmaceutics and/or food science Proficient in oral and written communication skills as well as effective organizational skills and the ability to make presentations and recommendations in the area of responsibility Must be able to communicate effectively in a cross functional team environment and have the ability to statistically analyze data Must have computer literacy, including word processing and spreadsheet software Must have strong critical thinking, sound judgment, planning, organizing and problem-solving skills Ability to work as a team member and interact at all levels Supervisory Responsibilities No direct supervisor responsibilities, but may guide and assign the work of others, such as technical support scientists, as well as provide technical guidance and support to formulation scientists. Physical Demands Manufacturing and general office environment Exposure to disagreeable elements is negligible Frequent work in pilot plant and production facilities Training The incumbent must be able to perform this job safely in accordance with standard operating procedures and good manufacturing practices, without endangering the health or safety of self or others. Work Environment General office, pilot plant and manufacturing environment A portion of the work will take place in the encapsulation, powder and/or tableting areas of the manufacturing facility, where one will be exposed to computerized equipment, moving mechanical parts, forklifts, heavy pallets, moderate to loud noise level, and air-borne dust and powders While working in the manufacturing area, one will be required to wear various personal protective equipment (e.g., clothing, hair net, face mask, gloves, goggles, etc NAI is an Affirmative Action/Equal Opportunity Employer and will consider all applications without regards to race, sex, age, color, religion, national origin, veteran status, physical or mental disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. Following a conditional offer of employment, satisfactory completion of a background check (including criminal records check) is required prior to beginning employment. Any offer of employment may be rescinded if the background check reveals disqualifying information, and/or it is discovered that the candidate knowingly withheld or falsified information. Failure to satisfactorily complete the background check may affect the continued employment of a current NAI employee who was conditionally offered the position.

Tektonyx Bio is focused on the use and optimization of a semi-synthetic E. coli organism for the production of novel protein therapeutics. We harness the power of a revolutionary technology based on E. coli that has been engineered to utilize an expanded genetic alphabet composed of the four natural nucleotides and two additional, synthetic nucleotides. This technology allows the encoding and production of custom proteins with site-specific functionalities for the discovery and development of novel protein-based therapeutics. We are seeking an analytical scientist/mass spectrometrist to utilize and help develop novel analytical, proteomic, and metabolomic methods to optimize unnatural protein production as well as to further optimize the semi-synthetic organism. Key Responsibilities Ability to serve as the analytical subject matter expert and work closely with colleagues across the company. Develop chromatography and mass spectrometry methods for characterizing the expressed proteins and assessing expression yields and the fidelity with which various non-canonical amino acids are incorporated. While use of the semi-synthetic organism for industrial scale therapeutic protein production has been validated, many aspects of the organism's physiology remain to be further optimized, and the successful applicant will work with colleagues focused on optimizing the organism's physiology. This will include both metabolomics and proteomics. Tektonyx Bio places a premium on intra-company collaboration, and thus the desire to interact closely with all facets of the effort to develop and use the semi-synthetic organism for novel therapeutic protein production is a must. The successful applicant should also enjoy and excel at working collaboratively on fast paced projects with rapidly evolving goals. Basic Qualifications PhD in a field related to analytical chemistry, proteomics, or metabolomics. Additional postdoctoral/industry experience is a benefit but not a requirement. Strong background in chromatographic separation, biophysical characterization (SPR, DLS, DSF, circular dichroism), and spectrophotometric techniques for proteins and protein conjugates. Familiarity with Agilent instrumentation (LC & Q-TOF LC/MS) and OpenLab/Chromeleon software is a benefit. Familiarity with the routine use of mass spectrometry for the characterization of proteins is essential. Familiarity with the use of mass spectrometry proteomics/metabolomics is beneficial, but not essential. Excellent written and oral communication skills; strong organizational skills and attention to detail. The salary range for this role is $125,000 - $170,000 and is based on a number of factors including qualifications and experience. Tektonyx also offers a comprehensive benefits package. To apply for this position, submit a resume and cover letter describing your experience, interests, why you are interested in joining us, and any other information that you would consider relevant to ***********************

Avalon BioVentures is a biotech venture capital firm that builds on Avalon's 40-year success in pursuing disruptive ideas to improve life. From its established offices and labs on the Torrey Pines Mesa, in La Jolla, California, Avalon BioVentures leverages its Accelerator, which provides operational infrastructure and support, and the team's extensive experience to identify promising science, build agile companies, and advance breakthrough therapeutics. Position Overview: We are seeking a highly motivated and skilled Immunologist to join our team in the development of cutting-edge Regulatory T cell therapies. This role will involve researching and advancing innovative therapeutic approaches utilizing regulatory T cells to treat inflammatory and pulmonary diseases. The ideal candidate will have a strong background in immunology, cellular biology, therapeutic development, and molecular techniques with a specific focus on regulatory T cell biology. Key Responsibilities: Research & Development: Design and conduct cutting-edge research to understand the biology of regulatory T cells (Tregs), their function, and their therapeutic potential in various diseases. Develop and optimize protocols for isolating, expanding, and modifying Tregs ex vivo for therapeutic applications using viral and non-viral modification Investigate the mechanisms by which Tregs interact with other immune cells and modulate immune responses. Study the effects of engineered Tregs in preclinical in vitro and in vivo models and assess their safety, efficacy, and biological activity. Analyze immune profiles, cytokine production, and T cell tissue homing and function to optimize T cell-based therapies. Conduct immune cell characterization using flow cytometry, ELISA, PCR, and other relevant techniques. Contribute to the generation of data for regulatory filings, research publications, and presentations at scientific conferences. Stay updated on the latest developments in regulatory T cell biology, cellular therapies, and immunotherapy research to inform product development strategies. Analyze experimental data using bioinformatics tools and statistical methods to assess the effectiveness of Treg therapies. Maintain detailed records of experiments, including data analysis and results, in accordance with Good Laboratory Practice (GLP). Communicate research findings to internal stakeholders, including senior management, and external collaborators. Qualifications: Ph.D. in Immunology, Cell Biology, Cellular Engineering, Molecular Biology, or a related field. Experience in Treg biology or immunotherapy is highly desirable plus 1-5+ years lab experience OR MS degree with 5+ years industry experience Hands-on experience with primary human immune cell isolation, culture, and expansion techniques, as well as flow cytometry and other immunological assays. Experience with in vitro cell culture models, flow cytometry, and functional assays (e.g. T cell phenotyping, T cell suppression, cytokine secretion assays). Strong problem-solving and critical thinking abilities. Proficiency in data analysis software and ELN systems (e.g., GraphPad, Flow Jo, Benchling). Excellent written and verbal communication skills. Passion for developing next-generation therapies with a focus on immune modulation. Ability to work independently and collaboratively in a fast-paced, multidisciplinary environment. Strong organizational skills and attention to detail, particularly in maintaining experimental integrity and compliance with regulatory standards Preferred Skills: Strong background in regulatory T cell biology and cell therapy. Experience with cell engineering via viral gene delivery and/or gene editing technologies (e.g., Lentivirus, CRISPR) . Hands-on experience in regulatory T cell isolation, activation, expansion, and engineering Experience establishing 3D organoid or air-liquid-interface cultures a bonus Compensation: In addition to a competitive compensation package with stock options, the company also offers a comprehensive benefits package for our employees and their families, which includes medical, dental, vision, and supplemental disability insurance. The above description is intended to describe the general nature of the job and may include other duties as assumed or assigned; it is not intended to be all inclusive or limit the duties of the position. Job Type: Full-time Benefits: 401(k) Dental insurance Employee assistance program Flexible schedule Equity Flexible spending account Health insurance Life insurance Paid time off Parental leave Retirement plan Vision insurance Holiday shutdown Supplemental pay types: · Bonus pay

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 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 required. Flow Cytometry experience required and Tissue Culture experience highly Required.

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.

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.

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.

Staff Scientist, Clinical Development Function: Clinical Development and Operations Company: Phanes Therapeutics, Inc. Phanes Therapeutics is a clinical stage biotech company focused on innovative discovery research and clinical development in oncology. The company has three programs in clinical stage: spevatamig (PT886) for pancreatic, gastroesophageal junction (GEJ) and gastric cancers, peluntamig (PT217) for small cell lung cancer (SCLC) and neuroendocrine carcinoma (NEC), mavrostobart (PT199) for non-small cell lung cancer (NSCLC) and pancreatic cancer. Both PT886 and PT217 have received Orphan Drug and Fast Track designations from the FDA. We are looking for motivated and passionate people to join us to help discover and develop new medicines and improve healthcare. We believe that innovative thinking, seamless execution, teamwork, and integrity are key values for building success. Our mission is to become a major source of innovation in the biotech and pharma industry. At Phanes, we understand that scientific innovation is a challenging task and that's why we are looking for exceptionally talented people to join us on our mission. We are committed to fostering an innovative and fun working environment where individuals can pursue creative ideas and deliver results, because we know that our success depends on how to realize the true potential of our people. Job Summary: The position is on-site full time. This position is in the clinical development team located at our R&D site in San Diego, CA. The candidate should have solid training and/or broad experience in a scientific discipline. The candidate will be trained by the company on various scientific and operational aspects of clinical trials, and gradually provide scientific support in all aspects of the clinical programs, such as literature review, scientific writing, data analysis, presentation, and summary. This candidate will be part of the overall support for the clinical teams in rationalizing scientific and clinical findings, implementing study efficiency, and communication of clinical data. The candidate must be a team player and is expected to work with other scientific and clinical staff in advancing our programs through the clinic. Key Responsibilities: Clinical Strategy: Provide clinical support and scientific opinion to study teams. Provide input on clinical trial documents, milestones and timelines. Maintain scientific and clinical knowledge in the specific therapeutic and disease area(s) of assignment, including performing rigorous literature reviews. Data Analysis: Analyze, review, and curate key clinical trial data in a timely manner. Organize and manage key clinical trial data. Contribute to the ongoing scientific review of clinical trial data. Presentation and Documentation: Help review and analyze results of clinical trial data for internal and external presentation (including external partners and stakeholders, including clinical investigators, study coordinators/CRAs and KOLs), and regulatory submission. Help with updating clinical research protocols, ICFs, pharmacy manuals, lab manuals and regulatory submission documents. Assist in the generation of Clinical Development Plans, and adherence to plans. Support and assist the Clinical Development team in delivering regulatory submission activities and ensure flow and accuracy of key data for clinical module sections of the IND. Qualifications: An advanced degree in a related Life Sciences discipline (e.g. Pharm D, PhD, or MD) is required. Fresh PhD graduates or current postdoctoral researchers are encouraged to apply. Proven track record of scientific publications. Ability to understand and critically evaluate scientific literature. Working knowledge of Microsoft suite of software products is required. Ability to work in a highly collaborative, matrix environment, with cross-functional teams. Excellent problem-solving skills, a strong sense of urgency and keen attention to detail. Well organized with the ability to effectively manage multiple priorities in a dynamic, cross-functional teamwork environment under time and resource pressures. Excellent oral and written communication skills and strong organizational skills are required. Our Benefits Include: Competitive compensation package including bonus opportunities and stock options opportunities. Retirement 401(k) savings plan with employer match. Exceptional career growth opportunities. Excellent medical, dental and vision plans. Generous vacation and sick leave plans. 18 paid company holidays per year including a Winter Holiday Break. An opportunity to do truly meaningful work to make a lasting impact. On-site gym, ample parking including complimentary EV charging stations, company-sponsored events, etc. Flexible spending accounts (FSAs) for eligible out-of-pocket health care and dependent day care expenses. Health savings accounts (HSAs) a trust or custodial account to pay or reimburse certain medical expenses. Life and AD&D insurance, short- and long-term disability plans. Employee assistance program (EAP) provides employee counseling programs and various online resources. Additional voluntary benefits including pet insurance, auto and home insurance, commuter benefits, legal plans, and more. The annual base salary we reasonably expect to pay is $80,000.00 - $100,000.00. Individual pay decisions depend on various factors, such as primary work location, complexity and responsibility of role, job duties/requirements, and relevant experience and skills.

Isto Biologics, a 100% biologics-focused company dedicated to helping patients heal faster, is seeking a Scientist in their Carlsbad, CA facility. With a portfolio comprised of the market-leading autologous concentration device as well as a differentiated bone grafting portfolio that offers functional solutions to meet patient and procedural challenges, Isto is equipped to offer a range of customizable options to surgeons of varying specialties.Biomedical engineer or similar focusing on specific tasks, experiments, and studies under guidance geared towards developing products with tissue engineering / regenerative medicine applications to improve patient outcomes in at least one of the following: sports medicine, orthopedics, general surgery, and / or wound healing. This position requires a deep functional understanding of various disciplines, including but not limited to immunology, biochemistry, biologics, biomaterials, tissue engineering, and regenerative medicine, along with a passion for advancing cutting-edge science into clinical applications. Day-to-day activities range from running and overseeing experiments to answer technical questions, designing and detailing solutions, managing direct reports, and project management aspects. Research experience specifically in bone, skin or allograft and allograft processing is required. Essential duties and responsibilities include: Research and Development Apply engineering and biology-based principles to translate scientifically proven concepts into commercially viable products or to develop new technology platforms for medical applications, under the supervision of Director / CSO. Develop laboratory protocols for fabrication of prototypes of medical devices under an existing project with known product specifications. Choose or develop appropriate assays or models to characterize product characteristics or predict product performance. With or without the assistance from direct reports and with little supervision, execute experiments and studies, collect data, and analyze results. Troubleshoot any unexpected results or issues with assay / model reliability. Product Development and Sales and Marketing Support Work with process engineering to transfer laboratory processes to manufacturing instructions. Manage work to create preclinical data packages for use by sales and marketing in the form of brochures, presentations, etc. Answer technical questions from sales personnel that arise from the field. This may include running experiments for sales and marketing support to help drive sales post launch. Documentation Document the appropriate evidence necessary to distinguish the relationship among materials, processes, design and product performance in order to build economically efficient systems directed toward a specific medical application. Review and approve laboratory documentation of direct reports. Publish results in internal reports and present results to upper management and possibly outside collaborators. Relationships Take ownership of all technical aspects of data generation for an existing project. This includes scheduling to stay within a prescribed deadline and keeping budget conscious of overall costs. Report results to supervisor / upper management on a bi-weekly to monthly basis. Supervise one or more research associates to assist in projects, as well as provide mentorship and career development. Interface with other lab members / groups in R&D to keep a safe, efficient, organized, and cost-conscious laboratory. Interface with other departments, including Process Engineering, Operations, and Sales and Marketing, when necessary. Skills Has mastery over experimental design, including but not limited to the concepts of well controlled experiments, statistical power, etc. Has mastery of data analysis, including various methods of statistical analysis and meta-analysis, as well as handling large data sets with high levels of accuracy. Has mastery over day-to-day logistics of lab operation, including but not limited lab safety, hazardous waste disposal, best lab practices, etc. Has mastery over pre-clinical models of various biological processes including but not limited to bone formation, wound healing, angiogenesis, inflammation/immune response required. Is familiar with clinical procedures and applications of medical devices in at least one of the following required: sports medicine, orthopedic surgery, general surgery, and / or wound care. Is familiar with FDA regulations and able to apply guidelines to designing products and/or processes. Is familiar with allograft processing and tissue banking. Is familiar with the competitive landscape of similar products and technologies. Stays up to date on state of the art in basic science and the commercial landscape. Excellent verbal and written communication skills required Education/Experience · Ph.D. in bioengineering/ biomedical engineering or related field and up to five years of relevant working post grad experience required. · M.S. degree in bioengineering/biomedical engineering or related field and a minimum of 5 years relevant experience may also be considered. · Travel may be required two or more times annually, either for attendance at technical conferences, trips to collaborators for technical support, or trips to customers to serve as a technical expert to customers.

is budgeted for $25.00 per hour and is non-negotiable. This is a part-time, 90-day temporary role with the possibility of an extension. The Department of Career Services is a unit in the Division of Student Affairs and Campus Diversity. It is an innovative, reputable, and globally recognized leader that supports education, workforce, and economic development. The Career Services Department serves students by supporting their career development journey through the following activities: Career exploration Professional development Employment preparation and experiential learning Industry engagement and employment outcomes The Career Services Department serves industry partners by supporting their talent acquisition and business needs through the following activities: Workforce development planning and consulting Professional development Direct services and resources to support talent acquisition The purpose of this position is to serve as lead over the design, deployment, and presentation of the department's data outcomes strategy and to keep the department current on workforce and economic development policy trends. The role involves analyzing student, employer, and stakeholder outcomes and trends and works on integrating evidence-based decision making into grant proposals and concepts. This role recommends and utilizes emerging technology and innovative tools to streamline research processes and to enhance reporting capabilities. This role addresses complex challenges, ensuring the effectiveness and impact of career services programs across the campus community and beyond. Responsibilities Data and Policy Trends Research 70% Lead comprehensive research on student, employer, and stakeholder outcomes using advanced statistical methods. Track and evaluate policies related to workforce development, economic trends, and career development at local, state, and federal levels. Analyze economic indicators, such as employment and inflation, to provide insights on labor market trends. Utilize technology and data tools to streamline research processes and enhance reporting capabilities. Develop and evaluate systems to support program outcomes and ensure regulatory compliance. Support the implementation and maintenance of data collection systems within the department. Ensure effective data collection and reporting for grants and special projects, meeting all requirements and deadlines. Conduct departmental assessments by analyzing large data sets to prepare relevant proposals and analyses. Provide expert advice based on data analysis to inform departmental decision-making. Design and implement data collection systems and analytical models to assess the impact of career services programs. Evidence-Based Reporting and Strategic Planning 20% Communicate data outcomes through various channels, including detailed reports, updates, news, visualizations, social media, and campus-wide efforts to promote evidence-based practice. Collaborate with campus partners to ensure Career Services research aligns with institutional and cross-divisional data and priorities. Collaborate with internal and external stakeholders to ensure data-driven insights are effectively disseminated and utilized across the university community. Independently determine approaches to research projects and priorities, with accountability for delivering high-impact results. Participate in high-level planning and development activities, providing expert analysis and recommendations to influence key objectives and long-term goals. Develop strategic solutions to complex problems by understanding and applying broad, interactive perspectives on policy and economic trends. Other Duties as Assigned 10% Qualifications Knowledge & Abilities Working knowledge of and ability to apply standard theories, principles, practices, and techniques applicable to the program and/or administrative specialty to develop conclusions and make recommendations. Expertise in investigating and analyzing problems with a broad administrative impact and implications. Ability to anticipate problems and address them proactively. Thorough knowledge of and ability to apply extensive expertise to complex programs and/or administrative specialties, including pertinent laws and regulations. Demonstrated expertise in and advanced knowledge of the principles, problems, and methods of public and business administration and operational and fiscal management. Expertise in administrative survey techniques, operations and systems analysis, statistical and research methods, and the ability to interpret and evaluate results to develop sound conclusions and recommend new or revised policies. Ability to analyze data and make accurate projections using business mathematics and basic statistical techniques. Ability to organize and plan work and projects including handling multiple priorities. Ability to make independent decisions and exercise sound judgment. Ability to compile, write, and present reports related to program or administrative specialty. Ability to take initiative and independently plan, organize, coordinate, and perform work in various situations where numerous and diverse demands are involved. Demonstrated ability to effectively interpret, organize, and present information and ideas in written or presentation form. Ability to train others on new skills and procedures and provide lead work direction. Ability to understand problems from a broad, interactive perspective and discern applicable underlying principles to conceive of and develop strategic solutions. Ability to work with representatives from public and private entities and handle potentially sensitive situations. Demonstrated consultative skills in working with internal and external constituent groups. Ability to effectively present ideas and concepts in written or presentation format and use consultative and facilitation skills to gain consensus. Minimum Education & Experience Completion of sufficient lower division coursework OR - Equivalent of one year related experience in lieu of coursework Preferred Qualifications & Special Skills Strategic planning for data collection, analysis, and presentation. Additional Applicant Information Candidate must reside in California and live within a commutable distance from SDSU at time of hire. Job offer is contingent upon satisfactory clearance based on background check results (including a criminal record check). San Diego State University Research Foundation is an equal opportunity employer. #J-18808-Ljbffr

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.

An international Top 10 AM Law Firm is seeking a Corporate Capital Markets Associate to join their award- winning practice group in San Diego. This is a hybrid role. You will be practicing in the areas of capital markets, corporate governance, securities regulation and working day to day with public companies. The ideal candidate will have: Minimum 5 years' capital markets experience Direct and applicable AM Law 100 law firm experience Juris Doctor- qualified candidate must be licensed to practice in California The yearly salary range for this position is $365 000- $420 000. The firm also offer an excellent benefits package. If you are interested in this position, and you meet the requirements of the role, please click 'apply now' to forward an up-to-date copy of your CV. Alternatively, if you would like to discuss this opportunity further, please contact Nikita Hari for a confidential discussion. Our advertisements use salary and experience as a guide only. Interlink Recruitment is an equal opportunities employer. *Please Note: Due to the high volume of applications we are currently receiving we are unable to contact applicants who have been unsuccessful.