Scientist jobs in San Diego, CACreate job alerts

Job Description Join Dr. Athanasia Panopoulos and her research group as a Project Scientist in the Cedars-Sinai Regenerative Medicine Institute! The Cedars-Sinai Board of Governors Regenerative Medicine Institute brings together research faculty and clinicians to provide a true "bench to bedside" organization. Regenerative medicine is a new and developing field that aims to restore function in diseased or aged tissues through either revitalizing existing cells or transplanting new ones. At the Board of Governors Regenerative Medicine Institute, researchers are turning stem cells into therapies for treating a multitude of prevalent diseases and conditions. The Panopoulos Laboratory at the Cedars-Sinai Regenerative Medicine Institute is a seeking a highly motivated postdoc to join our new, dynamic research group. The laboratory studies fundamental and clinically relevant research questions that are at the intersection of the fields of stem cell biology, blood cell development, and cancer. The long-term research goals of the Panopoulos Laboratory are to harness the power of stem cells to provide innovative and clinically relevant advances in targeted cancer therapeutics and regenerative medicine. Our work focuses on utilizing human somatic cell reprogramming to identify and target novel embryonic mechanisms that are exploited in cancer, and as an avenue to discover fundamental aspects of normal and aberrant hematopoietic development. To learn more, please visit Panopoulos Research Lab | Cedars-Sinai Are you ready to be a part of breakthrough research? The Project Scientist will plan and conduct experiments with pluripotent stem cells and cancer cells. The Project Scientist works independently and in cooperation with the Principal Investigator to make significant and creative contributions to a research or creative project in any academic discipline. The Project Scientist may be an ongoing member of a research team or may be employed for a limited period of time to contribute high-level skills to a specific research or creative program. Project Scientists are not required to carry out independent research or to develop an independent research reputation and do not have teaching responsibilities. Ordinarily, the Project Scientist title will carry out research or creative programs as well as administration of day-to-day lab operations with supervision by a member of the Professorial Series. Primary Job Duties and Responsibilities: • May assist in preparation of grant proposals, submissions, publications and presentations but is not responsible for generating grant funds., • May serve as PI for certain grants as approved by supervising member of the Professorial Series., • May participate in publications and presentations as author or co-author., • May develop, adapt and implement new research techniques and protocols., • Assists in lab experiments., • Analyzes, interprets, summarizes and compiles data., • May lead or train Staff Research Associates and Research Fellows., • Will assist in day-to-day laboratory activities., • No experience is required. Completion of postdoctoral appointment in the area of specialization, as applicable., • Demonstrated significant, original, and creative contributions to a research or creative program or project., • Experience in organ-on-chip and/or cell signaling is a plus., • Expertise in one or more of the following areas is required: primary and mammalian cell culture, flow cytometry, animal work/bone marrow transplantation, basic techniques in cell biology, molecular biology, and biochemistry., • Knowledge of PI’s area of research specialization., • Scheduling flexibility, including evening, weekend, and holiday rotation commitment, may be necessary. Travel may be required., • Function efficiently and cooperatively with a team of faculty, research associates, technicians, and students.

Job Description Principal Investigator, Dr. Ryan Urbanowicz, is seeking a Postdoctoral Scientist to join the Department of Computational Biomedicine! The primary focus of the URBS Lab (Unbounded Research in Biomedical Systems) is the development, evaluation and application of machine-learning (ML) and artificial intelligence (AI) tools/methods targeting various biomedical data types and problems. We develop and apply methods that (1) automate and provide rigor to machine-learning analyses, (2) can detect complex patterns of association, (e.g., epistasis and heterogeneity), (3) are interpretable/explainable to promote trust and translational adoption, as well as to identify and address sources of bias, (4) scale to “big data” and (5) flexibly adapt to common data challenges, (i.e., missing values, class imbalance, consideration of covariates). We aim to make ML and AI tools that are applicable to a wide variety of biomedical problems and that are accessible, reliable, reproducible, flexible, user-friendly, computationally efficient and transparent. Our lab holds particular interest in the research of rule-based ML, automated ML, feature selection and evolutionary algorithms. To learn more, please visit: Cedars-Sinai | Urbanowicz Lab Are you ready to be a part of breakthrough research? The URBS-lab focuses on the development and application of machine learning, artificial intelligence, and statistical methodologies targeting a variety of domains and data types within biomedical research. Emphasis is placed on developing methods that are interpretable/explainable, scalable to ‘big data’, and capable of detecting complex patterns of association. Current research focuses on automated machine learning, rule-based modeling, feature selection, and evolutionary optimization. Other areas of interest include (but are not limited to) rare-variant analysis, data simulation, data integration, heterogeneous patient subgroup identification, time-series analysis, deep learning, and identifying and correcting for biases. We are a highly collaborative lab with access to EHR, genomic, and other ‘omics’ data in areas of research such as obstructive sleep apnea, congenital heart disease, pancreatic cancer, transplantation donor-recipient matching, and hospital readmission. Working independently but in close cooperation and in consultation with Dr. Ryan Urbanowicz and other research scientists, the Postdoctoral Scientist will perform routine and complex computational, mathematical, and statistical procedures throughout the training period. As a Postdoctoral Scientist you may develop, adapt, and implement new techniques, algorithms, analysis pipelines, and software, as well as analyze, interpret, summarize, and compile data. Primary Duties and Responsibilities: • May assist in the preparation of grant proposals, but is not responsible for generating grant funds., • May participate in publications and presentations as author or co-author., • Designs and performs experiments. Will keep appropriate experimental records and documentation and analyze the results with the Principal Investigator., • Analyzes interpret, summarizes, and compiles data., • Operates and maintains equipment and instruments., • Competitive candidates will be proficient in scientific writing having published in more than one of the areas mentioned as well as experience with algorithm development/application., • Including a cover letter and publication examples (first authorship) are preferred, but not required., • Independently works on research projects designed in collaboration with one or more mentors within an area of specialization., • Acquires thorough technical and theoretical knowledge of research projects and objectives during one to five (1-5) year post-doctoral appointment., • Demonstrated aptitude to perform experimental protocols and procedures, including detailed data collection.

Job Description Join Dr. Athanasia Panopoulos and her research group as a Postdoctoral Scientist in the Cedars-Sinai Regenerative Medicine Institute! The Cedars-Sinai Board of Governors Regenerative Medicine Institute brings together research faculty and clinicians to provide a true "bench to bedside" organization. Regenerative medicine is a new and developing field that aims to restore function in diseased or aged tissues through either revitalizing existing cells or transplanting new ones. At the Board of Governors Regenerative Medicine Institute, researchers are turning stem cells into therapies for treating a multitude of prevalent diseases and conditions. The Panopoulos Laboratory at the Cedars-Sinai Regenerative Medicine Institute is a seeking a highly motivated postdoc to join our new, dynamic research group. The laboratory studies fundamental and clinically relevant research questions that are at the intersection of the fields of stem cell biology, blood cell development, and cancer. The long-term research goals of the Panopoulos Laboratory are to harness the power of stem cells to provide innovative and clinically relevant advances in targeted cancer therapeutics and regenerative medicine. Our work focuses on utilizing human somatic cell reprogramming to identify and target novel embryonic mechanisms that are exploited in cancer, and as an avenue to discover fundamental aspects of normal and aberrant hematopoietic development. To learn more, please visit Panopoulos Research Lab | Cedars-Sinai Are you ready to be a part of breakthrough research? The Postdoctoral Scientist will plan and conduct experiments with pluripotent stem cells and cancer cells. Working independently but in close cooperation and in consultation with the Principal Investigator and other Research Scientists, the Research Fellow will perform routine and complex laboratory procedures throughout the training period. Analyzes and interprets data. May develop, adapt, and implement new research techniques and protocols. May assist in the preparation of grant proposals. Not responsible for generating grant funds. Primary Job Duties and Responsibilities: • May participate in publications and presentations as author or co-author., • Designs and performs experiments. Will keep appropriate experimental records and documentation and analyze the results with the Principal Investigator., • Analyzes, interprets, summarizes, and compiles data., • Operates and maintains equipment and instruments., • Acquires thorough technical and theoretical knowledge of research project and objectives during one to five (1-5) year post-doctoral appointment., • Works independently on research projects designed by a mentor (typically the PI) within area of specialization., • Expertise in one or more of the following areas is required: primary and mammalian cell culture, immunofluorescence/imaging analysis, basic techniques in cell biology and biochemistry., • Experience in organ-on-chip and/or cell signaling is a plus., • Demonstrated aptitude to perform experimental protocols and procedures, including detailed data collection, analysis, and operation and maintenance of specialized equipment., • Scheduling flexibility, including evening, weekend, and holiday rotation commitment, may be necessary. Travel may be required., • Function efficiently and cooperatively with a team of faculty, research associates, technicians, and students., • Excellent written and oral communication skills are essential.

Faro Health aims to improve lives by helping life sciences companies design optimal clinical trials.Our AI powered software platform optimizes and orchestrates complex clinical development by providing powerful insights about trial design and outcomes.Faro empowers researchers to design more intelli

They collaborate across the business with collaborators in Dexcom Labs, Strategy, Behavioral Science, HEOR, Clinical Affairs, Data Science and Integrated Evidence Planning, both US and internationally. Where you come in: As a member of the Medical Affairs team, you will contribute the development of

Description Are you a motivated Principal Resilient Systems Scientist with a technical vision and hands-on knowledge of mission-focused systems? The Leidos Innovations Center’s newly established Information and Data Science Division is seeking a Senior Resilient Systems Scientist to help lead strategic solution developments and projects. This role will drive capture of strategic customer-funded software R&D. The ideal candidate will have a proven track record in developing technology-based approaches that yield novel, innovative capabilities while advancing the state of the art. We are looking for a proven researcher who can develop and lead a groundbreaking research portfolio using both internal and customer funding. Please note: This is an on-site role. The ideal candidate will be able to work out of our San Diego, CA; Arlington, VA or Dayton, OH offices. Occasional opportunity to telework may be available. Primary Responsibilities • Develop innovative solutions to challenging problems of interest to the Defense Applied Research Projects Agency (DARPA) and U.S. Department of Defense (DoD)., • Engaging R&D customers and transition partners to understand technical gaps and needs for resilient systems solutions in mission critical systems., • Lead and execute research in areas of naval surface platforms, autonomy, and resilient systems., • Develop and deliver software products., • Leading teams of researchers and engineers in the development, adaptation, and extension of innovative approaches to resilient systems solutions across a range of technical areas and application domains to advance the state of the art while addressing long-term problems of importance to national security such as embedded systems., • Develop novel approaches for the generation of assurance evidence for critical software, at scale, • Collaborate in cross-discipline teams to deliver innovations that provide measurable resilient mission impact., • To ensure technical relevancy, they will track software technology trends in the customer community and broader R&D communities as well as identify future software R&D funding opportunities. Basic Qualifications • Bachelor’s degree in Computer Science, Mathematics, or a related field and 12+ years prior relevant experience, M.S degree with 10+ years of prior relevant experience, or Ph.D. with 8+ years of experience (Ph.D. preferred)., • Must be a US Citizen., • Qualified candidates MUST possess a Secret clearance as well as have the ability to obtain a TS/SCI., • Proven track record in proposing, winning, and executing work with customers such as DARPA, IARPA or similar agencies within the last 5 years., • Proven track record in developing and delivering software products., • Experience with surface platforms, autonomous concepts, and naval applications., • Industrial and/or academic experience advancing the state of the art in FPGA development, embedded systems, formal verification, developing technologies such as program analysis, constraint-solving, symbolic execution, or theorem proving., • Experience with autonomous systems., • Experience with naval systems and specifically surface vessels., • Proven track record in proposing, winning, and executing Contract R&D., • At least 4 years of experience with programming languages such as Java, Scala, C/C++, Ruby, Rust, or Python., • Experience with test and evaluation, software analysis and software specification., • Strong verbal and written communication skills, with experience engaging with senior leadership and technical teams as well as ability to present complex software solutions in a clear, understandable manner. Preferred Qualifications • Ph.D. in Computer Science, Mathematics, or related degree, • FPGA development and testing, embedded systems design and innovation, applying formal methods, using technologies such as theorem provers for first-order logic and higher-order logic, proof assistants, solvers, or other automated reasoning tools, • Experience conducting applied research areas of CPS such as autonomous vehicles, smart sensors, or Internet of Things, fusing data collected from cyber and physical systems to develop novel approaches to address emerging technical challenges in domains relevant to U.S. national security, • Experience in semantic analysis of software, • Strong and proven customer relationship skills including the ability to discover the true technical challenges and requirements associated with opportunities, recommending alternative technical approaches, and shaping future opportunities, • Experience applying and leading the application of formal methods in fundamental research contexts, to problems in complex domains, under conditions of uncertainty, and dynamic and evolving technical challenges, • Ability to work in a fast-paced environment, • Excellent written and oral skills in communicating technical information with an ability to present complex technical information clearly and coherently, • Proven experience forming strong teams composed of members from academia and industry for competitive research and development opportunities, • Experience developing software for critical applications that require software certification LInC July 18, 2025 For U.S. Positions: While subject to change based on business needs, Leidos reasonably anticipates that this job requisition will remain open for at least 3 days with an anticipated close date of no earlier than 3 days after the original posting date as listed above. Pay Range $126,100.00 - $227,950.00 The Leidos pay range for this job level is a general guideline only and not a guarantee of compensation or salary. Additional factors considered in extending an offer include (but are not limited to) responsibilities of the job, education, experience, knowledge, skills, and abilities, as well as internal equity, alignment with market data, applicable bargaining agreement (if any), or other law.

Northridge Hospital Medical Center is seeking a highly skilled and experienced Clinical Laboratory Scientist to join our dynamic team in Clinical Laboratory Services. This position plays a crucial role in providing accurate and timely diagnostic testing to support patient care across various hospitals • Perform a wide range of laboratory tests in multiple disciplines, including:, • Hematology: Complete blood counts, coagulation studies, blood bank procedures, • Chemistry: Electrolytes, enzymes, hormones, drug levels, • Microbiology: Bacterial culture and identification, antimicrobial susceptibility testing, • Immunology: Autoantibody testing, serological markers, • Urinalysis and Body Fluids: Microscopic examination, chemical analysis, • Molecular Diagnostics: PCR testing, genetic analysis, • Operate and maintain complex laboratory equipment, including analyzers, microscopes, and automated systems, • Ensure proper specimen handling, processing, and analysis, • Maintain accurate and detailed records of all tests performed, • Adhere to strict quality control procedures and safety protocols, • Participate in departmental quality assurance activities and proficiency testing, • Collaborate effectively with other laboratory personnel, physicians, and nurses, • Assist with training and mentoring of new staff members, • Contribute to the development and implementation of new laboratory procedures Qualifications • Minimum one year of experience in an acute care facility required., • Required training in Hematology, Chemistry, Blood Bank, Microbiology, Immunology, and Serology as applicable., • B.A./B.S. required, • Windows Operating System., • Knowledge of MS Word and MS Excel is helpful., • California Clinical Laboratory Scientist License or Limited California Clinical Laboratory Scientist License, California Clinical Immunohematologist Scientist License, California Clinical Microbiologist Scientist License are required, and ASCP registry preferred, • Current Los Angeles County fire card is required., • For direct patient care, AHA BLS certification is required for CLS drawing blood donors only.

Pride Health is hiring a Clinical Laboratory Scientist I or II to support our client’s medical facility based in San Juan Capistrano CA 92675, This is a Contract job with a possible extension opportunity and a great way to start working with a top-tier healthcare organization! Job Title: Clinical Laboratory Scientist I or II Work Location: San Juan Capistrano CA 92675 Pay: 45/Hr To 55/Hr + Tax Free Stipend available for travelers (Included) Contract : 5 to 6 months Shift : 1ST: 7 AM-3:30 PM PST or 8pm-4:30AM PST or 2PM- 10:30PM Days : tue to sat or mon to Fri Summary Dedicated Clinical Laboratory Scientist with experience performing moderate to high complexity clinical laboratory tests in accordance with established procedures and policies. Committed to accuracy, quality assurance, and maintaining regulatory standards. Skilled in troubleshooting, equipment maintenance, and data analysis, with a focus on laboratory efficiency and patient safety. Duties and Responsibilities • Perform moderate to highly complex clinical laboratory tests independently, including newly introduced tests requiring specialized skills., • Prepare and oversee preparation of reagents, stock solutions, standards, and controls. Test new reagents/controls and evaluate their effectiveness., • Determine specimen acceptability and ensure accurate data calculations via manual or computerized methods., • Accurately enter and verify test results; monitor reporting accuracy and maintain turnaround times., • Evaluate and release results of routine and complex analyses. Address and document critical or unexpected results., • Conduct preventive maintenance, troubleshooting, and calibration of lab equipment., • Perform and evaluate instrument checks, linearity, accuracy, and precision testing., • Run Quality Control and calibrations; assess results for compliance before releasing data., • Select/evaluate control materials, initiate corrective actions as necessary., • Accurately participate in and document proficiency testing., • Detect and resolve technical and operational issues, escalating to supervisors or field support as needed., • Maintain accurate labeling and tracking of reagents and supplies., • Keep a clean, organized, and safe work area., • Communicate effectively with team members, supervisors, and internal/external stakeholders., • Actively participate in team meetings and Quality Improvement initiatives., • Undertake special projects such as evaluating new procedures, cost analysis, reference range establishment, and SOP writing., • Follow company policies and safety protocols, including infection control and waste disposal., • Uphold confidentiality and professional integrity at all times., • Supervise and train unlicensed staff, support training programs as needed., • Maintain continuing education per California state licensure requirements., • Answer phones, relay messages, and perform other administrative tasks as needed., • Use personal protective equipment and comply with health/safety standards., • 0–3 years of direct experience in a clinical laboratory setting., • Frequently lift/carry 1–10 lbs; occasionally 11–25 lbs; rarely 26–50 lbs (with assistance if over 50 lbs)., • Perform repetitive tasks and fine motor manipulation; good hand-eye coordination required., • Must be able to sit or stand for extended periods., • Proficient in Microsoft Office (Word, Excel, Outlook), • Strong typing skills, • Bachelor’s Degree in Medical Technology or related Life/Physical Science (from an accredited institution) – Required, • Current State Clinical Laboratory Scientist (CLS) License – Required (California only; no substitutions accepted), • Mass Spectrometry experience – Preferred, • Chemistry background – Preferred

Source One is a consulting services company and we’re currently looking for the following individual to work as a consultant with our direct client, a global pharmaceutical manufacturing client in La Jolla, CA. This role will be onsite and available to candidates local to the La Jolla, CA area. We are interested in every qualified candidate who is eligible to work in the United States. Unfortunately, we are not able to sponsor visas or employ corp-to-corp Title: Scientist II Research & Development (Oligonucleotide Analytics) Location: La Jolla, CA Onsite (Mon-Fri, 40 hours) Contract Duration: 12 months, with likely extension Pay Rate: $52.26 per hour (w2) Key Responsibilities: 30% • Operating LC-MS systems to perform in-process and final QC of various scales of highly modified oligonucleotides, including siRNA and ASO, to support both discovery portfolio and pre-portfolio projects 20% • Optimize methods and improve analytical capabilities for Client Oligonucleotide synthesis 10% • Analyze and optimize methods in a project-specific way (i.e. GalNAc vs Cholesterol vs C16) by denaturing and non-denaturing HPLC methods. In addition, phosphoramidites or lipids by HPLC and LCMS. 20% • Establish and automate high throughput analytical capabilities and coordinate those efforts with higher synthesis throughput. 5% • Analyze oligonucleotides by HPLC-SEC, RP-IP and Ion-Exchange Chromatography. • Continue optimizing siRNAs using best-in class analytical chemistry methodologies such as different column matrixes for optimal siRNA characterization, • Support integrity confirmation requests (such as concentration) by assay development and biology teams 3% • Conduct QC for lipid nanoparticle (LNP) formulations of mRNA 5% • Ensure the supply of laboratory consumables and reagents are in stock as needed • Maintain a high level of productivity in the laboratory setting. 2% • Present data and reports on project status at individual, group, and departmental meetings. Qualifications • Ph.D.. with 1-3 years of experience, performing progressively advanced duties at the Scientist level, or the equivalent training/experience is required., • Prior experience in the characterization of oligonucleotides and/or nucleoside/nucleotide analytes is required. Top Three Skills: Operate LC-MS systems - Analyze and optimize methods - establish and automate high throughout analytical capabilities Role is 100% onsite

Location: San Diego, CA Seniority Level: Scientist (Mid-level) Employment Type: Full-time About OliX Pharmaceuticals OliX Pharmaceuticals is a clinical-stage biotechnology company dedicated to developing next-generation RNA interference (RNAi) therapeutics. Founded in 2010 and now publicly traded in Korea, our vision is to be recognized as a pioneer in next-generation nucleic acid medicines, combining advanced science with global partnerships. At the heart of OliX’s innovation is our proprietary asymmetric siRNA (asiRNA) platform, which enables precise, durable gene silencing with minimized off-target effects. Building on this foundation, we have developed specialized delivery platforms: • GalNAc-asiRNA for liver-targeted therapies Our clinical pipeline is advancing rapidly: • OLX75016 – in Phase I for metabolic dysfunction-associated steatohepatitis (MASH) and liver fibrosis, partnered with Eli Lilly, • OLX72021 – completed Phase I in androgenetic alopecia (hair loss), demonstrating strong safety By joining OliX, you will become part of a company where cutting-edge RNAi science, small-molecule innovation, and global collaboration intersect—all aimed at creating transformative therapies for patients worldwide. Job Summary OliX is seeking a Scientist I/II, Medicinal Chemistry to lead small-molecule design and synthesis in support of our expanding RNAi therapeutic pipeline. The successful candidate will focus on creating novel small molecules—including delivery enhancers, conjugation partners, and pharmacological modulators—that complement and advance OliX’s RNAi medicines. This role offers the opportunity to apply classical medicinal chemistry expertise in a cutting-edge environment, directly contributing to discovery and clinical programs arising from partnerships with Eli Lilly, L’Oréal, and Hansoh Pharmaceutical. Key Responsibilities • Design and synthesize novel small molecules to support RNAi therapeutic development, including delivery enhancers, conjugation partners, and pharmacological modulators, • Execute synthetic strategies for nucleoside and nucleotide building blocks, • Develop innovative bio-conjugation strategies linking RNAi molecules with small molecules or peptides, • Perform advanced analytical characterization (UHPLC, LC/MS, NMR, UV-Vis), • Operate, maintain, and troubleshoot laboratory instrumentation, • Document research results in SOPs, batch records, technical reports, and presentations, • Collaborate across multidisciplinary teams spanning medicinal chemistry, RNAi chemistry, and biology, • Maintain safe and efficient laboratory operations Qualifications • Ph.D. in Medicinal Chemistry, Organic Chemistry, or a related field (0–3 years of postdoctoral or industry experience), or M.S. with 5+ years of relevant small-molecule industry experience, • Strong background in synthetic organic chemistry and small-molecule drug design, • Demonstrated ability to apply medicinal chemistry principles to optimize molecules for potency, selectivity, and ADME properties, • Proficiency with analytical methods (UHPLC, LC/MS, NMR, UV-Vis), • Excellent record-keeping, communication, and teamwork skills, • Experience drafting SOPs or batch records is a plus Why Join OliX? At OliX, you will contribute to programs that sit at the intersection of small-molecule medicinal chemistry and RNAi therapeutics, helping to shape the next generation of RNA medicines. With active Phase I clinical programs, global partnerships with Eli Lilly, L’Oréal, and Hansoh, and strong grant and institutional support, OliX offers a secure, collaborative, and innovation-driven environment where your work will directly impact future therapies for patients worldwide. We also provide a competitive compensation and benefits package, including: • Base salary range of $85,000 – $145,000 (depending on experience and qualifications), • Comprehensive Medical, Dental, and Vision insurance, • 401(k) retirement plan, • Paid year-end company shutdown and generous holiday time off, • Stock option grants, • Collaborative lab environment with opportunities for professional growth

Eli Lilly and Company seeks a Principal Scientist – Automation (R3-R4) to lead the transformation of scientific workflows from manual processes to fully automated systems. Conduct basic engineering research, design, and support across the automated sample management, biology, and chemistry platforms supporting Discovery Chemistry. Integrate advanced automation technologies including machine learning, 3D printing, computer vision, and robotic manipulators. Translate scientific concepts into actionable engineering specifications. Develop and implement automation solutions and enhance laboratory performance. Train operators on the use and maintenance of robotics to ensure safe operation and rapid troubleshooting. #LI-DNI Position requires a Bachelor’s degree in Bioengineering, Chemical Engineering, Computer Science, Robotics or a related field and 2 years of academic or employment experience with applying innovative robotic solutions to drive efficiency and effectiveness in early-stage drug-discovery labs. Academic or employment experience must include a minimum of: 2 years of experience with operation, maintenance, troubleshooting, and scripting for robotics; 2 years of experience with scheduling and training fully integrated robotic systems; 2 years of experience implementing effective and reliable automation systems; and 2 years of experience with C#, Java, Python, and VB.NET. 10% domestic and international travel required. #LI-DNI Job Location: San Diego, CA. Rate of Pay: $105,000.00 - $175,000.00 per year. To apply, please visit and enter job requisition number R-91525 when prompted. Alternatively, please send your resume, cover letter, and a copy of the ad to: Matthew Tenaglio, Lilly Corporate Center, Indianapolis, IN 46285.

Job Title: Senior Associate Scientist Location: La Jolla, CA Compensation: $38.82 - $43.41 Work schedule: Sunday thru Thursday Type: Contract Overview Leading pharmaceutical company looking for a Senior Associate Scientist. Ideal candidates should have a BS degree with 2-3 years of in vivo experience in pharmaceuticals or related field. Responsibilities Support the project teams in both Research and Development by performing in vivo technical procedures in the conduct of experiments and protocols and by collecting, recording and exporting data in the delivery of studies. Interact with the key in vivo contacts in project teams to understand their needs, engaging them in a flexible and constructive manner. Contribute to operational excellence by the collation of metrics showing the efficient delivery of support across projects teams, including alignment with colleagues in CM in the delivery of technical support and its associated metrics when required. Provide support in basic veterinary medical treatment as prescribed by the veterinary staff. Maintains appropriate records in compliance with regulatory and departmental standards, this may include maintaining animal study related records and ensuring flawless animal care and welfare in conducting research studies. Operate and maintain laboratory equipment's. Requirements BS with 2-3 years of in vivo experience in pharmaceuticals or related field. AALAS certification preferred. Required: Basic handing of animals (rodents); In vivo techniques including dosing of animals, collection and processing of blood samples; tissue collection, recording data and basic analysis using Excel and Word. Preferred: Tumor cell implantation, tumor volume measurements in vivo imaging and anesthesia set-up. Animal handling, dosing and blood collections experience (PO, IP and SubQ) Invio experimentation (Mice) Benefits System One offers eligible employees health and welfare benefits coverage options, including medical, dental, vision, spending accounts, life insurance, voluntary plans, and participation in a 401(k) plan. Ref: #558-Scientific

A client of Innova Solutions is immediately hiring for a Bench Scientist. Position type: Full-time– Contract Duration: 6 Months Location: La Jolla, CA (ONSITE) Work Schedule: Sunday thru Thursday As Bench Scientist, you will: Job Description: You will also be responsible for maintaining inventory of animal supplies and provide basic technical assistance (i.e., restraint, anesthesia, injections, blood collections etc.) in support of research studies. Position Responsibilities Support the project teams in both Research and Development by performing in vivo technical procedures in the conduct of experiments and protocols and by collecting, recording and exporting data in the delivery of studies. Interact with the key in vivo contacts in project teams to understand their needs, engaging them in a flexible and constructive manner. Contribute to operational excellence by the collation of metrics showing the efficient delivery of support across projects teams, including alignment with colleagues in CM in the delivery of technical support and its associated metrics when required. Provide support in basic veterinary medical treatment as prescribed by the veterinary staff. Maintains appropriate records in compliance with regulatory and departmental standards, this may include maintaining animal study related records and ensuring flawless animal care and welfare in conducting research studies. Operate and maintain laboratory equipment's. Organizational Relationships As part of the Comparative Medicine (CM) team, you will work with extended team members including the CM operations, veterinary, science and technology and research unit colleagues and scientists. Education And Experience BS with 2-3 years of in vivo experience in pharmaceuticals or related field. AALAS certification preferred. Technical Skills Requirements Required: Basic handing of animals (rodents); In vivo techniques including dosing of animals, collection and processing of blood samples; tissue collection, recording data and basic analysis using Excel and Word. Preferred: Tumor cell implantation, tumor volume measurements in vivo imaging and anesthesia set-up. Hard Skills Animal handling, dosing and blood collections experience (PO, IP and SubQ) Invio experimentation (Mice) Qualified candidates should APPLY NOW for immediate consideration! Please hit APPLY to provide the required information, and we will be back in touch as soon as possible. We are currently interviewing to fill this and other similar positions. If this role is not a fit for you, we do offer a referral bonus program for referrals that we successfully place with our clients, subject to program guidelines. ASK ME HOW. Thank you! Lailun Sheikh Phone: 412-763-1477 PAY RANGE AND BENEFITS: Pay Range*: $36.00-$41.00 per hour. *Pay range offered to a successful candidate will be based on several factors, including the candidate's education, work experience, work location, specific job duties, certifications, etc. Benefits: Innova Solutions offers benefits( based on eligibility) that include the following: Medical & pharmacy coverage, Dental/vision insurance, 401(k), Health saving account (HSA) and Flexible spending account (FSA), Life Insurance, Pet Insurance, Short term and Long term Disability, Accident & Critical illness coverage, Pre-paid legal & ID theft protection, Sick time, and other types of paid leaves (as required by law), Employee Assistance Program (EAP). ABOUT INNOVA SOLUTIONS: Founded in 1998 and headquartered in Atlanta, Georgia, Innova Solutions employs approximately 50,000 professionals worldwide and reports an annual revenue approaching $3 Billion. Through our global delivery centers across North America, Asia, and Europe, we deliver strategic technology and business transformation solutions to our clients, enabling them to operate as leaders within their fields. Recent Recognitions: Named One of America’s Best Employers for New Grads by Forbes (2024 Named One of the Best Companies to Work For by U.S. News & World Report (Private Companies List, 2024-2025) One of the Largest IT Staffing Firms in the US – Ranked #3 by Staffing Industry Analysts (SIA, 2024) One of the Largest Staffing Firms in the US – Ranked #13 by Staffing Industry Analysts (SIA, 2024; includes Innova Solutions, Volt, & HireGenics) Named One of the Top Ten Private Companies in Atlanta by the Atlanta Business Chronicle (2023) One of the Largest Certified Minority Business Enterprises (MBEs) in the United States (NMSDC, 2024) AWS Advanced Tier Services Partner with 100+ certifications Website: Innova Solutions offers a referral bonus for qualified Ambassadors who refer eligible referrals. Submit referrals at and earn $250-$1,000 per referral. Innova Solutions is an Equal Opportunity Employer and prohibits any kind of unlawful discrimination and harassment. Innova Solutions is committed to the principle of equal employment opportunity for all employees and to providing employees with a work environment free of discrimination and harassment on the basis of race, color, religion or belief, national origin, citizenship, social or ethnic origin, sex, age, physical or mental disability, veteran status, marital status, domestic partner status, sexual orientation, or any other status protected by the statutes, rules, and regulations in the locations where it operates. If you are an individual with a disability and need a reasonable accommodation to assist with your job search or application for employment, please contact us at or (770) 493-5588. Please indicate the specifics of the assistance needed. Innova Solutions encourages all interested and qualified candidates to apply for employment opportunities. Innova Solutions (HireGenics/Volt) does not discriminate against applicants based on citizenship status, immigration status, or national origin, in accordance with 8 U.S.C. § 1324b. The company will consider for employment qualified applicants with arrest and conviction records in a manner that complies with the San Francisco Fair Chance Ordinance, the Los Angeles Fair Chance Initiative for Hiring Ordinance, and other applicable laws.

Job Description When you join Groundwater & Environmental Services, Inc. (GES), you are not a number – you become the reason for our success. You’ll have the opportunity to carve your own career path while working shoulder-to-shoulder with some of the most talented and dedicated professionals in the industry. By combining our unique talents and expertise, we help the world’s leading organizations solve their most complex environmental challenges. We work hard, and we have a lot of fun while we’re at it. Our core values are centered on doing what’s right – for our clients, our employees, and our community. Our employees benefit from a supportive, collaborative culture and an entrepreneurial spirit that promotes new ideas and shared learning. Groundwater & Environmental Services, Inc. (GES), an industry leader with a reputation for excellence in providing environmental consulting, engineering, compliance, and technical field services to clients in diverse market sectors, seeks an experienced Geologist or Environmental Scientist to support environmental remediation project activities in Southern California. • Under general supervision, provides project management support including client involvement, work plan and proposal preparation, project scheduling and deadline tracking, budget evaluation and analysis, and technical editing and report finalization., • Must be a detail-oriented team player able to multi-task, and possess strong communication, analytical, organizational, problem-solving, planning, technical writing, delegation, mentoring, and time management skills., • Executes, supervises, and documents field aspects of environmental site assessment and remediation activities using standard operating procedures (SOPs). Conducts compliance assessment (e.g., facility response plan compliance), remedial testing, operation, maintenance, and monitoring (OM&M), short-term remedial events (e.g., chemical injection, groundwater and vapor extraction), and other project-support field activities., • Self-performs or directs junior staff in the installation of soil borings, monitoring wells, remediation activities, waste management and disposal, and other field requirements using standard operating procedures (SOPs). Self-performs and may direct junior staff in the performance of engineering design, permitting, OM&M, remedy process optimization, and environmental compliance., • Acts as the primary author for site work plans and proposals for routine scopes of work on low/medium priority projects, and co-author for complex scopes of work including comprehensive site characterizations and remedial actions. Co-authors comprehensive site characterizations and remedial action plans. These reports contain multiple level and interrelated interpretations and conclusions as well as provide recommendations based upon conclusions with focus on conceptual site model development., • May manage various level priority projects by providing technical, regulatory, and financial project support. Technical responsibilities may include monitoring contaminant concentrations, fate and transport analysis, QA/QC of data collected and documents generated, and ensuring compliance with applicable regulations., • Provides technical, regulatory, and financial project support for O&M sites. Technical responsibilities may include monitoring contaminant concentrations, site remediation activities, quality of data collected and documents generated, and ensuring compliance with applicable regulations., • Knowledgeable of pertinent regulations and their application to the compliance and progression of the projects., • Performs hydrogeological assessments regarding groundwater flows to identify contamination impact and related concerns., • Researches information relating to identifying geological formations and soil delineation studies and prepares reports and geological maps based on the findings., • Participates in the identification of viable remedial solutions consistent with all federal, state, and local regulations, • Procures and manages subcontractors and vendors for completion of project tasks (e.g., trenching and excavation, system construction, and electrical work), including supplier bid package development. Skills & Requirements: • A Bachelor's degree or higher in geology, environmental science, engineering or related scientific discipline., • 4+ years of related experience., • GIT or EIT a plus, • Must be detail-oriented, and a team player with good communication, analytical, organization, and time management skills. Our comprehensive benefits include: medical, dental, vision, prescription, 401k, FSA, LTD, STD, New Parent Leave, 529 CollegeBound Fund, Continuing Education/Training Course Assistance, Bonus Plan, and more. Groundwater & Environmental Services, Inc. (GES) believes that diversity and inclusion among our staff is critical to our success, and we seek to recruit, develop and retain the most talented people from a diverse candidate pool. At GES, we are committed to providing an environment of mutual respect where equal employment opportunities are available to all applicants and employees without regard to race, color, religion, gender, pregnancy, national origin, age, disability, marital status, sexual orientation, gender identity or expression, military and veteran status, and any other characteristic protected by law.

Job Description Job Responsibilities: • Test & report test results, • Ensure accuracy & quality of test results, • Enter data & perform standardized tests on samples, • Maintain accurate records of test results, • Ensure tests adhere to QC procedures, • Troubleshoot & resolve issues with test results, • Document lab issues, • Train & support Technicians and Accessioners, • Prepare & maintain reagents & supplies, • Help maintain lab equipment, • Support internal lab audits, • Adhere to all safety procedures, policies, precautions, HIPAA & QA, • 2+ years of CLS experience in a CLIP/CAP environment, • Active California CLS Generalist License Required, • Strong verbal & written communication skills, • Strong attention to detail and organizational skillsCompany DescriptionWith over two decades of internal recruitment support, RedBrick Staffing has been able to fine-tune a tried and true strategy of locating talent through a personalized recruitment process. With a background in finding highly qualified candidates ranging from startup to fortune 500 companies, we tailor our search to your individual requirements. A minority & veteran-owned & operated staffing firm.

Job DescriptionDescription: SUMMARY Responsible for all aspects of purification process development from process definition to process characterization for support of pipeline projects. Designs a series of experiments that contribute to project objectives. Develops new processes and technologies to achieve improved product quality and reduce production cost. Interacts with management on advanced technical matters. JOB RESPONSIBILITIES ESSENTIAL FUNCTIONS • Applies engineering and scientific principles in the process definition, process optimization, scale-up, technology transfer, process characterization, and process validation activities associated with the purification of biopharmaceuticals., • Designs, implements, and conducts a series of scientific experiments which contribute to project objectives. Leads troubleshooting processes, instrumentation, and equipment., • Serves as a technical resource in technology transfer from process development to clinical cGMP manufacturing including definition of bill of materials, batch record drafting/review, and discrepancy resolution. Serves as a process development representative during purification operations. Provides technical troubleshooting and recommends process equipment improvements., • Designs and perform a series of bench scale experiments such as sterile membrane filtration, depth filtration, tangential flow filtration, viral clearance filtration, as well as chromatography., • Develop and recommend new processes and technologies to achieve cost effectiveness and improved product quality. Proactively identifies purification issues and suggests solutions., • Collaborates with cell culture, formulation, analytical, MSAT, Quality, and Validation for achievement of project objectives. May manage external collaborators., • Effective communicator of ideas, project goals and results across functions., • Interacts with management on advanced technical matters., • Authors and reviews regulatory filing documentation as well as process validation and characterization reports. Authors internal reports at appropriate milestones. JOB REQUIREMENTS Education and Experience • Proficient in programming, operating, and troubleshooting the following chromatography systems: AKTA pure, AKTA ready, and AKTA pilot., • Proficient in designing and conducting chromatography development studies., • Proficient in designing and conducting filtration studies using Scilog FilterTec and labscale TFF systems., • Understands purification process design limits for implementation in a clinical manufacturing environment., • Initiates, designs, and executes experiments independently. Capable of independent data interpretation. May apply advanced modeling or statistical analysis tools where appropriate., • Highly skilled communicator of ideas, project goals, and results., • Capable of working effectively in teams., • Knowledge of cGMP and familiarity with large scale manufacturing support.Requirements:

Job Description Are you passionate about advancing the field of bioinformatics and helping researchers make groundbreaking discoveries? Join our team to lead the charge in developing innovative methods and analyses for the rapidly emerging field of epitranscriptomics. This high-impact role will place you at the intersection of cutting-edge science, technology development, and customer success. Alida Biosciences is a VC-backed startup in San Diego pioneering innovative technologies in epigenomics to empower researchers. Our mission is to provide solutions that enable scientific breakthroughs in understanding gene regulation and epitranscriptomics, driving advancements in both fundamental research and clinical applications. In this role, you will be responsible for the analysis and interpretation of internal and external epitranscriptomic data sets, leveraging our EpiScout analysis software and ad hoc analysis approaches inspired by your experience in tertiary data analysis and computational systems biology. You’ll collaborate with world class researchers on impactful science and directly support customers to maximize the potential of our state-of-the-art technologies. From custom analysis to co-authoring scientific publications, your work will push the boundaries of epigenomics research and empower customers to make breakthrough discoveries. Key Responsibilities • Conduct custom bioinformatics analyses and design novel methods and algorithms for epigenomics research., • Provide data interpretation of disease samples through the lens of a systems biologist., • Collaborate with internal and external researchers and developers to analyze and interpret assay-generated datasets using innovative techniques., • Liaise with customers to understand how they use our software outputs. Customize the outputs to fit customer needs and work with engineers to develop optimized data outputs as standard software features., • Drive continuous software improvements including data visualization, implementation of new secondary and tertiary data analysis tools and data interactivity., • Work with the commercial team to support customers in developing new methods to unlock the full potential of our technology for scientific breakthroughs., • A Ph.D. in Bioinformatics, Computational Biology, Systems Biology or a related field., • A minimum of 6 years of postgraduate experience conducting bioinformatics analysis of complex genomic data sets., • Proficiency in Python and R programming and familiarity with Unix-based environments. C++ is a plus., • A strong foundation in bioinformatics algorithms, machine learning, statistics and data visualization., • Familiarity with established methods for differential gene expression, transcript assembly, splicing and gene fusion analysis, RNA editing and epitranscriptomic analysis, demonstrating both breadth and depth of understanding. Examples include:, • Methods like MeRIP-seq for RNA modification profiling or CHIP-Seq for histone modification detection and MACS2 for peak calling., • DNA or RNA methylation detection using conversion chemistries (e.g. bisulfite or GLORI), • Experience with nanopore direct RNA sequencing., • Motif analysis, mutation and deletion calling., • Differential enrichment analysis to identify biologically significant changes. We offer a competitive and comprehensive employee benefits package including medical, dental, and vision, LTD, paid vacation, 401k and a stock plan. Alida Biosciences is an Equal Opportunity Employer. We do not discriminate in recruitment, hiring, training, promotion, or other employment practices for reasons of race, color, religion, gender, pregnancy, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status.

Job DescriptionSalary: $90,000 - $100,000/year Job Overview BPS Bioscience Inc. is a leading provider of recombinant proteins, assay kits, and recombinant cell lines for drug discovery. We are seeking an exceptional scientist, with a strong background in enzymology, enzyme kinetics, protein/protein interactions, and fluorescence and luminescence-based assays. The Scientific Communications Manager will support BPS Bioscience through product marketing efforts and scientific content. More specifically, this rolewill provide in-depth scientific and technical support in relation to solutions for the marketplace and product marketing. Responsibilities: • Creates and develops product/portfolio marketing strategies., • Participates in or leads problem solving and troubleshooting activities., • Writes and coordinates the development of scientific content for: product pages, webinars, technical notes, posters, blog posts, marketing collateral., • Ensures customer needs are identified and addressed via creation and updates to product literature and service guides., • Finalizes new product launches daily with technical review and editing of product inserts and web content., • Partners closely with product management and scientific teams to gain an understanding of product features and relevance to market segments., • Participates in writing of Standard Operating Procedures (SOPs) for the Marketing team., • Creates sales enablement tools including webinars, support content and other relevant content., • Monitors and reports scientific/technical knowledge of scientific fields and their potential impact to products in the market., • Keeps up to date with new trends in drug discovery., • Attends scientific meetings to support business objectives., • Other duties as assigned. Requirements: • Ph.D. in Immunology, Cancer Biology, or Molecular Biology & Cell Biology, • A minimum of 2+ years of experience in the Life Science industry, • Must be able to build credibility and relationships across functions and levels, • Ability to communicate with and influence internal and external audiences, using both oral and written communication skills highly effectively, • Excellent writing skills, • High level of organization, multi-tasking, and attention to detail Benefits! • 401k with 4% company match, • Medical/Dental/Vision health insurance plans, • Vacation and paid holidays, • Companywide lunches provided quarterly 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.

Job DescriptionPosition: Business Development Manager / Director - Toxicology & Safety Assessment (Preclinical Studies) Location: Home-based - West Coast (San Diego preferred) Salary: $150,000 to $200,000 Pharmaron is a global CRO (Contract Research Organization) helping pharma and biotech companies bring new therapies to life. With over 21,000 employees worldwide across 23 locations in the US, UK, and China, we support drug discovery through to manufacturing with fully integrated, high-quality services. We're proud of the impact we make. Just last year, we supported over 1,000 preclinical safety studies, helping our clients advance their drug candidates with confidence. Our teams work across small molecules, ADCs, biologics, and gene therapies, partnering with more than 3,000 global customers. To learn more, visit . About the Role Are you a toxicologist or preclinical scientist who enjoys connecting great science with real-world impact? This could be your next step. We're looking for a scientifically minded Business Development Manager or Director to join our U.S. team, covering the West Coast, with a preference for candidates based in San Diego. This role is ideal for someone with a strong background in toxicology, safety pharmacology, or preclinical development who's ready to move beyond the bench and into a more strategic, client-facing role. You'll work closely with our internal scientists to shape proposals, ensure client expectations are realistic and achievable, and help translate complex safety assessment needs into tailored solutions. Your scientific insight will be key to building trust with clients and turning conversations into successful, long-term partnerships. It's a remote role with regular travel across the region and perfect for someone who wants to stay close to the science while stepping into a more commercial, outward-facing position. We are interviewing for this role on an ongoing basis. So don't miss out on this opportunity and apply as soon as possible. Key Responsibilities • Lead business development efforts across the West Coast, identifying and securing new opportunities with biotech and pharma clients in the toxicology and safety assessment space., • Build and maintain strong relationships with senior stakeholders, positioning Pharmaron as a trusted, long-term partner., • Collaborate with internal scientific and operational teams to develop tailored proposals and ensure successful project delivery., • Drive cross-functional initiatives to expand Pharmaron's market presence and service adoption., • Represent Pharmaron at key industry events, conferences, and client meetings., • Maintain a robust pipeline of qualified opportunities and consistently meet or exceed revenue targets., • Provide market insights and competitive intelligence to inform strategic planning.Candidate Profile, • Advanced degree in Toxicology, Pharmacology, Biology, or a related scientific discipline (PhD preferred)., • 8+ years of experience in the pharmaceutical or CRO industry, including hands-on experience in preclinical safety assessment., • Proven success in business development or client-facing roles within preclinical development., • Strong understanding of the CRO landscape and GLP-compliant safety studies., • Excellent communication, negotiation, and relationship-building skills., • Strategic thinker with a results-driven mindset and high level of self-motivation. Benefits: • 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, • 401(k) plan with generous employer match If you have any questions about the role or application process, please contact Elisa Di Caterino - Talent Acquisition Partner on Linkedin ED1-#LI

Job Description Job Description: We are seeking a highly motivated and qualified individual to join our Conjugation-Discovery Chemistry Department as a Senior Scientist I and work as part of a team to drive success. Ideal candidates will be self-motivated, independent, committed to the generation of high-quality data within a fast-paced and innovative research team. The Senior Scientist I will support ongoing RNA-based drug discovery projects in several therapeutic areas. Essential Responsibilities: • Design, synthesis, purification and analysis of oligonucleotide-conjugates on antibodies and other modalities. Develop and optimize conjugation protocols using novel chemistries and technologies for target drug delivery., • Evaluate SAR on the conjugates and drive the program by collaborating cross-functionally with the teams., • Track progress against project timelines, generate regular status updates, and communicate progress to the team., • Carry out assigned laboratory functions applying knowledge and skill in an accurate, timely manner., • Establish and maintain excellent working relationships with critical collaborative partners throughout the company to advance discovery research activities to pre-clinical development., • Contribute to the preparation of research reports and presentations for internal project teams, leadership team, and external audience., • Manage and maintain equipment, reagents and dedicated laboratory environment needed to carry out assignments., • Maintain updated and well-organized lab notebooks and batch records., • Execute daily laboratory operations with an approach designed to minimize risks and hazard waste streams., • Maintain all appropriate corporate standards for facility safety and hazardous material management. Reasonable accommodation(s) may be made to enable qualified individuals with disabilities to perform the essential functions of a job, on a case-by-case basis. On-Site Protocol: Physical presence at the ADARx Pharmaceuticals worksite is a necessary job function of this role, which the Company deems critical to collaboration, innovation, productivity, employee well-being and engagement, and it enhances the Company culture. Qualifications: • Ph.D. in Chemistry, or related scientific discipline, • 3-5 years bioconjugation-related industrial experience., • Understanding of project timelines and deliverables and plans/coordinate project work accordingly with departmental, functional, and external stakeholders., • Strong problem-solving skills and a proactive attitude towards exploring new approaches., • Excellent written and verbal communication skills and effective presentation of complex scientific data to cross-functional and senior management teams are essential for this role., • In-depth knowledge of modern bioconjugation methods on antibodies (ADC, AOC), proteins, peptides, and other biomolecules., • Hands-on experience in the analytical characterization of the conjugates with strong analytical mindset. Proficiency in purification techniques such as RP-HPLC, FPLC, SEC, and IEX., • Team management experience, • Previous experience with RNA/oligonucleotide therapeutics is preferred but not essential., • A track-record of impacting drug discovery programs through driving projects to key decision points., • Positive attitude and high personal and ethical standards. A strong team player with a passion for science and drug discovery., • Must be able to work independently as well in cross-functional team settings with supervision as needed., • Adaptable / Flexible - willing and able to adjust to multiple demands and shifting priorities as well as an ability to meet day-to-day challenges with confidence and professionalism., • This is a full-time position, Monday-Friday, occasional overtime., • Pay is commensurate with experience., • Equity-based compensation, • Performance-based bonuses, • 401(k) with Company Match, • Medical, Dental, Vision, • Flexible Spending Account, • Life Insurance, • Employee Assistance Program, • Employee Discounts, • Paid Vacation, • Paid Holidays, • United States (Required), • Background Check Company Overview: ADARx Pharmaceuticals, Inc., (the “Company” or “ADARx”) located in San Diego, is a clinical stage biotechnology company committed to turning cutting-edge science into life-saving therapeutics. ADARx has developed proprietary RNA targeting platforms and technology for silencing or editing target mRNA. ADARx has a growing pipeline of RNA targeting therapeutics for treating diseases across a range of therapeutic areas including genetic, cardiometabolic, complement-mediated diseases and central nervous system. ADARx currently has multiple active programs in development with the lead candidate in the clinic. We are well-financed by a syndicate of renowned VC firms. ADARx Pharmaceuticals is an EEO employer committed to an exciting, diverse, and enriching work environment. We prohibit discrimination and harassment of any kind based on race, color, sex, religion, sexual orientation, national origin, disability, genetic information, pregnancy, or any other protected characteristic as outlined by federal, state, or local laws. Disclosure Statement: • The above statements are intended to describe the general nature and level of work being performed by employees assigned to this classification. They are not intended to be construed as an exhaustive list of all responsibilities, duties and skills required of employees assigned to this position., • Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations., • The range provided is based on what we believe is a reasonable estimate for the base salary pay range for this job at the time of posting. This role is eligible for an annual target bonus and annual equity awards. Some roles may also be eligible for overtime pay, in accordance with federal and state requirements. Actual base salary pay will be based on a number of factors, including skills, competencies, type and length of experience within the industry, and other job-related factors permitted by law., • Total Compensation includes base salary; benefits: medical, vision, and dental insurance; life insurance; 401(k) matching program; paid time off; paid holidays; Employee Assistance Program; and other employee benefits. This role may also be eligible for short-term or long-term incentive compensation, including but not limited to cash bonuses., • 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.

Job Description Under direct supervision, will be responsible for performing pre-analytical and assisting with the analytical procedures for patient testing. REQUIREMENTS Bachelor Degree in a Hard Scientific Field 1+ Years of experience in a professional laboratory JOB LOCATION Rancho Bernardo, CA WORK SCHEDULE • 5 days a week, Tuesday thru Saturday - 8 hours per day, • Shift time is 8pm to 4:30 a.m., • 10% Shift differential on hours worked between 9pm and 4am, • $200.00 weekend differential when hours are worked on Saturday and Sunday ESSENTIAL FUNCTIONS The following are intended to be examples of the accountabilities for which the person in this position is responsible. This position is not intended to be complete or all-inclusive and does not preclude management from assigning other or related functions for which the individual has demonstrated competency through performance. Laboratory • Assists with testing all test methods approved by CAP and CLIA under Clinical Laboratory Scientist (CLS) Supervision., • May provide training and guidance to other Laboratory Technicians, Laboratory Assistants and Data Entry personnel as well as other laboratory personnel as appropriate, • Assists in process improvement activities such as quality, safety, document management and control, and proficiency testing, • May assist with the implementation of test methods from internal and external sources, • May interact with vendors on special projects such as test method validations and new equipment, • May participate in technical studies designed to improve or validate clinical laboratory testing methods, • Required to work closely with CLSs and report all problems to Lead, laboratory operations; Supervisor and/or Director, • Assists with instrument maintenance and repair, • Performs preventative maintenance and calibrations on laboratory equipment and instruments, • Perform instrument troubleshooting, repairs and quality control procedures, • Monitors reagent and supply inventory, • May prepare laboratory reagents and assay materials according to SOPs, standard laboratory recipes/formulas under CLS supervision, • Organizes patient specimen and assay worksheets/printouts for testing and CLS review, • Assists in writing Laboratory documents such as Standard Operating Procedures and departmental forms, • Required to follow all safety procedures, policies, precautions, and Quality Assurance, • Other duties as required SECONDARY ACCOUNTABILITIES Remains aware of evolving needs and opportunities, showing flexibility in doing whatever is appropriate to support the Company’s success. Pursues educational opportunities to maintain advanced and up-to-date knowledge in the field. Performs all other related duties as required and assigned and understands that the items in this description are not all-inclusive. Requirements EDUCATION Requires BS or BA in a Hard Scientific Field EXPERIENCE • 1+ years of general laboratory. Knowledge of laboratory terminology a plus., • Work in a repetitive environment at a fast pace, • Excellent communication skills (verbal and written), • Ability to be a team player as well as work independently, • Must be dependable and reliable, • Must have the ability to establish effective working relationships with peers and managers, • Ability to ensure HIPAA, Confidentiality and Compliance policy, procedures, and standards are always adhered to. ESSENTIAL PHYSICAL & MENTAL REQUIREMENTS: • This position will require the following physical requirements; sitting (20 %), walking (10 %), standing (70 %), lifting up to 20 lbs on an occasional basis., • Employee is exposed regularly to moderate pressure/moderate stress situations, and therefore must be able to thrive in this type of environment., • Employee must be able to tolerate a moderate noise level., • $45,760.00 - $48,880.00 Benefits Benefits Offered: • Medical, Dental, Vision, Disability Insurance, • 401k with Company Match, • Paid Time off and Holidays, • Tuition Assistance, • Behavioral and Health Care Resources, • Opportunity to apply to our Clinical Toxicologist Scientist training program

Job Description SCHEDULE: Night Shift This position offers four 10 hour shifts with an 8pm PT start time. The 4 days will be between Tuesday and Sunday. Hours worked between 9pm and 4am will receive a 10% night shift differential. Additionally, if scheduled to work hours on both Saturday and Sunday, a $200 weekend differential will be provided. LOCATION: San Diego, CA While the work schedule will be mostly remote, employee needs to live within the San Diego area to come onsite for occasional training. Why Millennium Health? Millennium Health LLC is an accredited specialty laboratory with more than a decade of experience in medication monitoring and drug testing services, helping clinicians monitor the use and misuse of prescription medications and illicit drugs. The testing is used by healthcare professionals to obtain objective information about patients’ recent use of prescription medications and/or illicit drugs and helps monitor the effectiveness of treatment plans. Everyone that joins our team is key to our ability to support the clinicians and patients. GENERAL SUMMARY The Clinical Laboratory Scientist, Data Review will review chromatographic data and calculated results obtained from a variety of standardized urinalysis tests in a toxicology laboratory for the detection of prescription and illicit drugs using advanced LC-MS-MS technology and EIA; applies toxicological and chromatographic rule sets to determine acceptability of results; requests additional testing as necessary; approves reports and patient results to ordering physicians. ESSENTIAL FUNCTIONS The following are intended to be examples of the accountabilities for which the person in this position is responsible. This is not intended to be complete or all-inclusive and does not preclude management from assigning related functions for which the individual has demonstrated competency through performance. • Responsible for testing to troubleshoot result issues., • Reports laboratory test results for all test methods approved by CAP, NY and CLIA., • Ensures accuracy and quality of test results meeting required turnaround times., • Enters testing data and reviews chromatography and calculated results from a variety of standardized tests on urine samples using advanced LC-MS-MS technology and EIA for the detection of prescription and illicit drugs., • Evaluates the validity of results obtained, maintains proper records of results and creates a report of results., • Maintains quality control and LC-MS-MS chromatographic data prior to release or results to physicians., • Ensures that testing methods follow established quality control procedures., • Identifies, troubleshoots, documents and resolves test result issues., • Documents issues using the Laboratory Occurrence Management (LOM) form., • Acts as a resource to laboratory technicians, laboratory assistants and associate scientists., • Follows safe laboratory practices and participates in operational support activities necessary to maintain and optimize testing capabilities., • May oversee the duties of clinical laboratory technicians, clinical laboratory assistants and associate scientists who prepare specimens or perform other less complex procedures. Remains aware of evolving needs and opportunities, showing flexibility in doing whatever is appropriate to support the Company’s success. Pursues educational opportunities to maintain advanced and up-to-date knowledge in the field. Performs all other related duties as required and assigned and understands that the items in this description are not all-inclusive. Requirements SKILLS/KNOWLEDGE/ABILITIES • 2+ years’ experience in high complexity testing; CLIA/CAP environment, • Must maintain continuing education units required by California Department of Health Services, • Knowledgeable in laboratory methods and techniques, • Knowledgeable of equipment and supplies used in a laboratory, • Proficient in MS applications (Word/Excel/PowerPoint/Outlook), • Strong interpersonal skills and ability to communicate with all levels of employees, • Effective attention to detail with high degree of accuracy, • Bachelor’s degree with current California CLS license, • Physical: Primary functions require sufficient physical ability to work in an office setting and operate office equipment. Continuous sitting and upward and downward flexion of neck; fine finger dexterity; fast paced data entry with finger pressure to manipulate keyboard. Have the ability to speak and listen to customers on fast-paced phone calls., • Medical, Dental, Vision, Disability Insurance, • 401k with Company Match, • Paid Time off and Holidays, • Tuition Assistance, • Behavioral and Health Care Resources POTENTIAL HIRING RANGE: • Hourly Position: $45-$50, • 10% Night Shift Differential applied to hours worked between 9pm and 4am, • $200 Weekend differential is added per weekend worked, • Offers are based on skills, knowledge, and abilities of the selected candidate. Millennium Health is an Equal Opportunity/Affirmative Action employer and E-Verify participant. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, gender identity, sexual orientation or protected veteran status California Employee Privacy Notice - Millennium Health LLC

Job DescriptionTHOR Solutions is actively seeking a Mid-Level Data Scientist to support the US Navy Ship Anti-Submarine Warfare (ASW) Readiness and Effectiveness Measuring (SHAREM) at Surface and Mine Warfighting Development Center (SMWDC) in San Diego, CA. This position is associated with an upcoming contract that THOR is pursuing, with an estimated award/work start late 2025. We are conducting preliminary, “contingent” hiring for roles associated with this contract. The work start is dependent upon THOR being awarded this contract. Typical Responsibilities: • System administration for Naval Ship Tracking, Reporting and Analysis Tool (NSTRAT) System, to monitor the application and/or services and troubleshoot issues affecting availability, • Software Engineering and testing to develop data analysis tools and event reconstruction, • Performs database entry, management, and monitors automated back-up Travel Requirements: Up to 10% travel is anticipated. Typical Physical Activity: Primarily desk/computer work in an office environment. Periodic visits to waterfront/shipboard environments. May involve: repetitive motion, traversing shipboard environments (e.g., confined spaces, ladders, hatches), speaking or vision. Typical Pay Range: The anticipated pay range for this position in the identified location(s) is $63,750 - $89,250/year. Actual compensation offered will be based upon individual factors including education, qualifications, and experience. Existing Security Clearance Required: This position requires a DoD Secret security clearance. A qualified candidate must already possess an active or interim security clearance. A candidate with especially strong, relevant experience but no active security clearance may still be considered, but work start would be dependent upon a new Secret clearance being awarded. Typical Knowledge, Skills, and Abilities: • High School diploma, GED, or equivalent, • Five (5) years of Navy experience managing Navy computer networks, • Three (3) years of experience using Python and other programming tools to script data analysis products, • Hold and maintain certifications and/or training to maintain FLANKSPEED IL6 AZURE Privileged Access to include:, • Scripting language such as Python with SQL server relational database, • Security+ certification, • AZURE Administrator Associate AZ-104, • Proficient with common productivity software, including the Microsoft Office suite., • Paid Time Off (accrued), • Paid Holidays, • 401(k) with employer match and traditional/Roth options, • Medical Insurance (3 plan options) + TRICARE Supplemental Coverage, • Dental Insurance (2 plan options), • Vision Insurance Plan, • Healthcare and Dependent Care Flexible Spending Accounts, • Commuter/Transit Benefits, • Basic Life/AD&D, Short-Term and Long-Term Disability Insurance, • Supplemental Life Insurance, • Pet Benefits, • Legal Resources, • ID Theft Benefits, • Employee Assistant Plan and Work-Life Program, • Voluntary Leave Transfer Program, • Tuition Reimbursement Program Founded in 2009, THOR Solutions, LLC (THOR) is a rapidly growing Center for Veteran’s Excellence (CVE) verified Service-Disabled Veteran-Owned Small Business (SDVOSB) providing mission critical support across the Department of Defense, Department of Homeland Security, federal civilian agencies and commercial maritime industry, worldwide. THOR provides innovative and tailored expertise in multidisciplinary engineering, project and program management, business and financial management, technical support, integrated logistics support, training support, fleet support, corporate operations support, assessments and studies. THOR is privileged to deliver service solutions to the nation’s most complex military, public sector and industry challenges. THOR is proud to be an Equal Opportunity Employer, including veterans and individuals with disabilities. THOR considers all qualified applicants for employment without regard to legally protected characteristics. This policy applies to all terms and conditions of employment. If you are an individual with a disability and would like to request a reasonable accommodation as part the employment selection process, please contact us at or (571) 215-0077. Powered by JazzHR m1JkAUDHPf

Job DescriptionAbout Capricor Therapeutics Capricor Therapeutics is a biotechnology company dedicated to developing transformative therapies for rare diseases, with a primary focus on Duchenne muscular dystrophy (DMD). We are pioneers in cell therapy and exosome-based technology, leveraging our proprietary StealthX™ platform to engineer innovative treatments. Our team is committed to harnessing cutting-edge science and advanced technologies to meet the unmet needs of patients living with DMD and other challenging medical conditions. Join us on our journey as we push the boundaries of medical science and pave the way for a healthier future. Position Overview The PK/PD Scientist plays a pivotal role in advancing Capricor’s innovative therapeutic pipeline by designing, executing, and analyzing preclinical pharmacokinetics (PK) and pharmacodynamics (PD) studies. Reporting to the Preclinical Research Lead, this position is responsible for conducting in vivo studies, including compound dosing, sample collection, and data analysis, to generate high-quality PK/PD data to inform therapeutic development. The ideal candidate is a highly skilled scientist with expertise in animal models, PK/PD study design, and data interpretation, coupled with a passion for scientific discovery. This role offers the opportunity to work alongside a dynamic and collaborative team to develop a novel therapeutic modality, contributing to Capricor’s mission of delivering transformative treatments for rare diseases. Responsibilities * Design and conduct in vivo PK/PD studies, including rodent dosing via intravenous (IV), intraperitoneal (IP), subcutaneous (SC), intramuscular (IM), and intratumoral (IT) injections, to evaluate the pharmacokinetics, pharmacodynamics, and efficacy of therapeutic candidates. * Perform animal husbandry tasks, including breeding setups, genotyping sample collection, and general animal care, ensuring compliance with IACUC-approved protocols, policies, and procedures. * Collect and process biological specimens, including blood (via submandibular and/or cardiac puncture), necropsies, and tissue samples, for downstream PK/PD and biomarker analysis. * Develop and optimize genotyping assays and manage sample processing to support preclinical studies. * Analyze experimental data, including animal weight, blood analyses, and other project-specific tests, to generate PK/PD profiles and support data-driven decision-making. * Perform and interpret protein-based assays (e.g., Western Blots, ELISA, flow cytometry) to support PK/PD and efficacy studies, as needed. * Utilize IVIS imaging for in vivo studies to assess biodistribution and therapeutic effects, if applicable (preferred but not required). * Maintain detailed laboratory notebooks, analyze complex PK/PD datasets, and present findings at internal project team meetings to communicate insights and drive project strategy. * Execute, troubleshoot, and optimize standard and novel protocols for in vivo procedures, ensuring scientific rigor and adherence to research guidelines. * Collaborate with cross-functional teams, including R&D, clinical, and regulatory, to integrate PK/PD data into broader therapeutic development plans. * Contribute to the preparation of regulatory documents and scientific publications, ensuring accurate representation of PK/PD study results. * Perform additional duties as assigned to support the preclinical research team and organizational objectives. Requirements * Advanced degree (PhD preferred; Master’s considered with significant experience) in pharmacology, biology, biochemistry, bioengineering, molecular biology, or a related discipline. * Minimum of 3-5 years of experience in preclinical PK/PD studies within the biotech, pharmaceutical, or related industry, with a focus on animal models and therapeutic development; candidates with 5-7 years of experience may qualify for a Senior PK/PD Scientist level. * Demonstrated expertise in designing and conducting in vivo studies, including proficiency in dosing techniques (IV, IP, SC, IM, and IT injections) and biological specimen collection (e.g., blood via submandibular and/or cardiac puncture, necropsies, tissue collection). * Experience with protein-based assays (e.g., Western Blots, ELISA, flow cytometry) and familiarity with IVIS imaging preferred. * Strong knowledge of IACUC protocols, policies, and procedures, with a commitment to ethical animal care practices. * Proficiency in PK/PD data analysis and interpretation, with experience using relevant software (e.g., Phoenix WinNonlin, GraphPad Prism) and basic statistical analysis. * Advanced proficiency in Microsoft Office Suite (Excel, Word, PowerPoint) for data analysis, reporting, and presentations. * Exceptional written and verbal communication skills, with the ability to document experiments rigorously, present complex data clearly to internal teams, and contribute to scientific publications. * Highly motivated, collaborative, and adaptable, with a passion for scientific discovery and the ability to thrive in a fast-paced, multidisciplinary environment. * Strong organizational and project management skills, with the ability to multitask, prioritize work, and adapt to a flexible schedule as needed. * Hybrid role based in San Diego, CA, with flexibility for remote work; occasional travel (up to 10%) for scientific conferences or collaborations may be required. Work Environment and Physical Demands * Professional laboratory and office setting with a hybrid work model (remote and onsite). * Ability to work in a controlled laboratory environment, including handling animals and biological samples. * Capability to sit, stand, and use laboratory equipment for extended periods. * Occasional lifting of materials or equipment up to 20 pounds. * Willingness to adhere to safety protocols and wear personal protective equipment as required. Why Capricor? Capricor Therapeutics is an industry leader in cell and exosome therapy, pushing boundaries to create innovative treatments that raise the standard of care. Grounded in integrity and driven by science, our team is committed to making a meaningful impact through patient-centered innovation. Join us and be part of a team that’s changing lives—help us shape the future of healthcare. Compensation (USD) * Salary Range: Competitive, commensurate with experience. * Benefits: Comprehensive benefits package, including health insurance, retirement plans, equity awards, and opportunities for professional development. Come work with us! At Capricor, we offer a collaborative work environment that supports your professional growth. Join a passionate team committed to transforming the lives of patients and pushing the boundaries of medical science.

Job Description Research Scientist, Antibody Discovery and Research Job #25-06A Mapp Biopharmaceutical, Inc. "Mapp" is a San Diego based, innovative biopharmaceutical company focused on addressing unmet medical needs through the development of life-saving monoclonal antibody treatment options to combat a variety of neglected and tropical infectious diseases, and in support of biodefense programs. The Early Research and Development Group (ERDG) and the Advanced Research and Development Group (ARDG) at Mapp Biopharmaceutical are responsible for the execution of high quality Research and Development activities to ensure the achievement of a robust portfolio through CMC, Nonclinical, Regulatory, Project Management, and Clinical activities consistent with Mapp's product development objectives. The Research Scientist works in the antibody discovery group which is responsible for isolating novel antibodies that may be used in future drug products. This includes creating and producing the antigens necessary to isolate these antibodies and assessing the antibodies for their potential as therapeutics. The Research Scientist, Antibody Discovery and Research will provide overall support for our projects including design, execution, supervision, analysis and interpretation of results. Basic Qualifications • PhD or equivalent in biology, molecular biology, biochemistry, virology, and/or related field, • Post doc experience or other appropriate scientific experience, • Author on scientific publications in respected peer reviewed journals, • Demonstrated excellence in the following competency areas:, • Protein expression in bacterial, mammalian and insect cell systems, • Protein purification, including experience with automated HPLC and FPLC systems, fluency in GE Unicorn FPLC software, • Flow cytometry and single B-cell sorting techniques, • Experience in leading scientific personnel to execute against program deliverables, • Experience with ForteBio Octet technology and isothermal titration calorimetry, • Hands-on experience operating IncuCyte and similar high-content live-cell imaging systems, • Experience with primer design and RT-PCR particularly for monoclonal antibody isolation and cloning from single B-cells, • Experience expressing and purifying viral proteins, • Experience with reverse genetics and pseudo typed viral vector systems., • Command of in-silico workflows for antibody and protein engineering and optimization, • Development of functional cell based assays/immunoassays to assess mechanism of action and potency of new antibody candidates (e.g. reporter assay, internalization assay, neutralization assay, shedding assay ADCC-assay, ADCP-assay, multi-color flow etc.), • Optimizes and designs expression constructs for protein stability, solubility and expression levels, • Designs and optimizes strategies to generate and purify proteins of interest for subsequent in vitro and in vivo applications, • Designs and develops novel in vitro assays to assess antibodies for binding and activity, • Supervises research scientists at various levels as needed, • Reviews and synthesize new research findings regularly, • Maintains detailed records of all experiments performed This position is an on-site position located in Mapp's new state-of-the-art San Diego facility. Willingness to Travel (Domestic Travel = Approximately 2x per year + International Travel = Approximately 1x per year) will be required for this position. Mapp wants you to join their team and invites you to apply by submitting your information through the Mapp Biopharmaceutical, Inc. Job Openings website page. This job will remain open for twenty (20) days after being posted on Mapp's Job Openings website page. No Solicitors, agents or placement agencies please. Mapp utilizes E-Verify. Mapp is an equal opportunity employer and employment decisions are not based on any protected status. Mapp uses a wide variety of advertising and outreach to find qualified applicants for employment. Mapp is an Equal Opportunity Employer/Veterans/Disabled. Job Posted by ApplicantPro

Job Description Valspec—a global provider of system validation and lifecycle services—provides commissioning and qualification of computerized systems for clients in the Life Sciences industry. Established in 1999, Valspec's mission is to provide a wide spectrum of services that help its clients meet their capital project and lifecycle maintenance goals. Valspec's projects are critical to the industry, and to the people who rely on its products. Many projects ensure that life-changing drugs are available to those who need them; others streamline production to meet demand at a lower cost, allowing for the discovery of new and innovative therapies. Process Validation Engineer (Contract) Location: California Duration: 8-12 months Job Description: We are seeking a highly skilled and motivated Process Validation Engineer to join our team on a contract basis and serve as a bridge between R&D and manufacturing. This is an excellent opportunity for anyone who is a Scientist in Vaccine Manufacturing Science and Commercialization – Bioreactor & Fermentation Development to become more involved on the design side. The successful candidate will represent validation as a Subject Matter Expert (SME) and provide validation oversight monitor project results and drive sustainability. Equipment includes Chromatography columns, Wave rockers, and Bioreactors (50-2K L). Key Responsibilities: • Develop validation plans, protocols, and summary reports to perform shakedowns and functional testing. This role offers a unique chance for scientists to engage in the design and validation of critical equipment., • Work closely with the Manufacturing Sciences and Technology (MSAT) team to develop technical documents for the drug product line. This collaboration provides an excellent opportunity for scientists to contribute to the design and optimization of drug product lines., • Provide hands-on process and equipment support for the upstream area of an egg-based vaccine manufacturing facility, including execution of project start-ups for Harvesters, Centrifuge skid, Clarification, and Tangential Flow Filtration., • Provide technical leadership and subject matter expertise for Equipment and Process Qualification (SAT, IQ, OQ, PQ) activities., • Review and execute protocols, operate and troubleshoot automation equipment, and coordinate project management with vendors and contractors., • Work independently and interface directly with personnel from multiple departments, including Technical Development, Manufacturing, Engineering, Manufacturing Support, MSAT, Quality Control (QC), and Quality Assurance (QA). This role allows scientists to engage with various teams and gain experience in the design and validation processes., • Process Validation: Support industrialization, validation studies, and pre-approval inspections for drug products. Equipment includes Chromatography columns, Wave rockers, Bioreactors (50-2K L)., • Technical Support: Provide day-to-day assistance to manufacturing for process improvements, troubleshooting, and ensuring compliance with cGMP and regulatory standards., • Technology Transfer: Enable the transfer of processes from development to manufacturing while driving innovation. Qualifications: • Bachelor's degree in Engineering, Life Sciences, or a related field., • Proven experience in process validation within a pharmaceutical or biotechnology environment., • Strong knowledge of GMP regulations and validation principles., • Excellent problem-solving and analytical skills., • Ability to work independently and as part of a team. This role is a contract position lasting 8-12 months, based in California. The successful candidate will have the opportunity to work with a leading pharmaceutical company and contribute to the development and validation of critical processes and equipment. Valspec offers a standout culture, fantastic work environment, and has very competitive benefits to include premium medical, 401K match, tuition reimbursement, and other unique incentives. When receiving e-mails from a Proconex or Valspec recruiter, you will only receive e-mails from addresses ending in @proconexdirect.com or @valspec.net. Any other domains are impersonations and should be ignored. Candidates must be legally eligible to work in the United States without company sponsorship. Also, we are not interested in working on a corp-to-corp basis with other companies at this time. Any third-party unsolicited resume submission(s) will immediately become the property of Valspec. Valspec will not pay any fee to a submitting employment agency, person, or entity unless a signed agreement is established. Valspec is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to sex, race, color, religion, national origin, age, sexual orientation, gender identity, disability, protected veteran status or any other protected class. We are committed to providing a professional environment free of any discrimination or harassment, and we are proud to be a Drug-Free Workplace.

Job DescriptionSalary: About Artiva: Artiva is clinical-stage, publicly-traded biotechnology company focused on developing natural killer (NK) cell-based therapies for patients suffering from devastating autoimmune diseases and cancers. Artivas lead program, AlloNK, is an allogeneic, off-the-shelf, non-genetically modified NK cell therapy candidate designed to enhance the antibody-dependent cellular cytotoxicity effect of monoclonal antibodies to drive B-cell depletion. AlloNK is delivered in the outpatient setting with no required hospitalization. AlloNK is currently being evaluated in three ongoing clinical trials for the treatment of B-cell driven autoimmune diseases. This includes two company-sponsored trials, one in systemic lupus erythematosus for patients with or without lupus nephritis, and a basket trial across autoimmune diseases (Rheumatoid Arthritis, Systemic Sclerosis, Idiopathic Inflammatory Myopathies and Sjgrens Disease), as well as an investigator-initiated basket trial in B-cell driven autoimmune diseases. Artivas pipeline also includes CAR-NK candidates targeting both solid and hematologic cancers. Artiva was founded in 2019 as a spin out of GC Cell, formerly GC Lab Cell Corporation, a leading healthcare company in the Republic of Korea, pursuant to a strategic partnership granting Artiva exclusive worldwide rights (excluding Asia, Australia and New Zealand) to GC Cells NK cell manufacturing technology and programs. Artiva is headquartered in San Diego, California. For more information, visit. Job Summary: The Associate Scientist, Process Development Analyticswill be responsible for completing analytical testing in support of the development of off-the-shelf, allogeneic, natural killer (NK) cell-based therapies. Operating in a cross-functional and dynamic environment, the individual will work closely with the Analytical Development team to transfer and conduct in-vitro testing for Process Development activities. The ideal candidate should have a proven track record of conducting analytical testing for cell therapy products. This is a temporary position. Duties/Responsibilities: • Conduct routine in-vitro testing to support Process Development experiments and enhance process understanding., • Analyze data, interpret results, trend data and maintain detailed records., • Provide data for technical reports, standard operating procedures, and regulatory submissions in support of process development activities, • Manage assay transfer from internal Artiva functional groups to Process Development as needed., • Identify potential problems, investigate, troubleshoot assays, and work to resolve any issues., • Coordinate activities within a collaborative work environment across functional teams to support process development as well as the characterization of Artivas products., • Train Process Development personnel on analytical testing procedures as needed. Requirements: • B.S. with 8+ years or M.S in a biological field with a minimum of 5+ years of relevant laboratory experience., • Hands-on experience (equipment and software) with flow cytometry, plate readers, and automated cell counters required., • Experience with functional assays, IncuCyte a plus, • Strong organizational, recording keeping, time management, and communication skills are required., • Previous exposure to analytical testing in a Pharma/Biotech, regulated (GxP) environment is preferred., • Experience in cell therapy, immunology, or oncology is strongly preferred. Why you should apply: We have a fantastic team and philosophy! We are passionate we deeply care about our team, our science, and improving the lives of patients. We are tenacious laser-focused on our mission and undeterred in our commitment to deliver life-saving medicines for cancer patients.We are innovative - pushing into new frontiers for patient benefit.We are transparent - believers in flat, accessible, and open communication paths.We are inclusive committed to the diversity of our team and ensuring that all voices are heard. Base Salary: $103,000 - $125,000. Exact compensation may vary based on skills and experience.

Job Description The Sr. Air Quality Engineer / Scientist (Environmental Permitting and Compliance Specialist) performs professional engineering work, leading and executing the compliance and permitting functions in relation to Air Quality Regulations and Compliance. This candidate will be reviewing processes and equipment, analyzing permit-related technical and regulatory issues, and communicating those analyses within Yorke, the client organization, with government agencies and with the public at large. The work is challenging, broad in scope, and variable from project to project. The position involves effective communication, decision-making, and time management. The candidate performs other duties as required or assigned. This is a Senior to Principal level position. Positions at this level are assigned to perform the more complex and sensitive duties in the occupational field. The employee in this position may be assigned to train and mentor other employees and/or monitor work produced by other employees. The candidate qualifications we are seeking include: • 10-20+ years of work experience in the Air Quality and/or Environmental industry in an engineering role (preferably in a consulting environment);, • Experience in the environmental services industry focusing on leading Air Quality services:, • Process and equipment review;, • Air quality permitting under SCAQMD and other Air Districts, including Title V Permitting;, • RECLAIM implementation and reporting;, • Annual Emissions Reporting;, • Air Dispersion Modeling;, • Air Quality Assessments including Data Analysis and Emission Inventories;, • General Air Quality Compliance for facilities in CA., • Ability to manage and lead active team members on project teams towards project completion within project scope, budget and schedule and ensure quality work product and deliverables;, • Ability to manage successful relationships with clients, staff, and regulators through effective communication and expertise by fostering a collaborative environment without losing focus of quality;, • Proven track record or desire to engage in successful regulatory work in dealing with the SCAQMD, EPA, CARB and/or other similar regulatory agencies;, • Experience working on-site at client facilities;, • Prepare reports and submissions in timely manner;, • Experience with handling highly technical data and technical data interpretation;, • Highly motivated to continue working in Air Quality environmental field and expand their knowledge and experience;, • B.S or M.S. degree in Chemical Engineering, Environmental Engineering, or Mechanical Engineering, or other relevant technical degrees from an accredited college (minimum GPA of 3.0);, • Ability to work collaboratively in a team fashion, handle several projects at once, prioritize work, and work efficiently;, • Desire to train and share technical expertise in environmental rules and regulations with clients and team members;, • Excellent oral and written communications skills;, • Experience in conflict resolution and crisis management;, • Track record of successful analysis, interpretation, and application of rules and regulations towards practical solutions;, • Ability to think critically and develop solutions;, • Software Knowledge:, • Strong Microsoft Excel, Word, Outlook, and Powerpoint skills (required);, • Microsoft 365 Applications, including Sharepoint (a plus), • P.E. Certification (a plus);Company DescriptionJoin Yorke Engineering, LLC, an Environmental Consulting leader in California that implements Environmental Engineering and Compliance solutions for our clients throughout California. Our mission is to solve environmental compliance problems for industrial and governmental/infrastructure facilities. We are a growing and dynamic organization of highly respected professionals. Yorke Engineering, LLC has assisted over 2,000 client organizations with their Air Quality and Environmental Compliance, Engineering, and Permitting needs. Our philosophy is to efficiently help government and industrial customers with the complex array of environmental laws and regulations. From simple permits to complex agency negotiations, from small companies to the largest of California’s organizations, Yorke successfully solves our clients’ Air Quality and Environmental challenges. Our team has over 1,000 years of combined environmental experience and consists of engineers and scientists that specialize in Air Quality, Waste, Water, CEQA, Safety, and Industrial Hygiene.Join Yorke Engineering, LLC, an Environmental Consulting leader in California that implements Environmental Engineering and Compliance solutions for our clients throughout California. Our mission is to solve environmental compliance problems for industrial and governmental/infrastructure facilities. We are a growing and dynamic organization of highly respected professionals. Yorke Engineering, LLC has assisted over 2,000 client organizations with their Air Quality and Environmental Compliance, Engineering, and Permitting needs. Our philosophy is to efficiently help government and industrial customers with the complex array of environmental laws and regulations. From simple permits to complex agency negotiations, from small companies to the largest of California’s organizations, Yorke successfully solves our clients’ Air Quality and Environmental challenges. Our team has over 1,000 years of combined environmental experience and consists of engineers and scientists that specialize in Air Quality, Waste, Water, CEQA, Safety, and Industrial Hygiene.

Job Description We are seeking a highly experienced Senior Data Scientist to lead advanced analytics, machine learning model development, and data-driven decision support within a Department of Defense (DoD) program environment. This role involves architecting and deploying end-to-end data solutions that enhance operational effectiveness, readiness forecasting, and mission-critical insights for Navy enterprise systems. Key Responsibilities • Design, develop, and deploy predictive models, natural language processing (NLP), and optimization algorithms, • Lead data ingestion, cleaning, transformation, and exploratory analysis from diverse structured and unstructured data sources, • Create interactive dashboards and visualizations to communicate analytical findings to technical and non-technical audiences, • Collaborate with cross-functional teams including software engineers, data engineers, and subject matter experts, • Translate mission needs into analytical frameworks, model requirements, and implementation strategies, • Validate and tune models for performance, explainability, and operational relevance, • U.S. Citizenship with an active or interim Secret clearance, • Bachelor's degree in Data Science, Computer Science, Statistics, Mathematics, or related field (Masters preferred), • 10+ years of professional experience in data science and leadership or senior technical role, • Security+ Certification, • Proven experience with:, • Python, R, SQL, and Spark for data analysis and modeling, • Machine learning libraries such as scikit-learn, TensorFlow, PyTorch, or XGBoost, • Data visualization tools like Power BI, Tableau, or Plotly, • Cloud platforms (AWS, Azure, or Google Cloud) and MLOps workflows, • Experience developing AI/ML solutions in support of Navy or defense logistics, sustainment, or readiness analytics, • Familiarity with DoD data governance, data labeling, and ethical AI guidelines, • Strong understanding of model operationalization, A/B testing, and production monitoring, • Knowledge of data engineering concepts including ETL pipelines, data lakes, and data mesh architectures, • Agile/Scrum experience or certifications (e.g., Certified Scrum Master, SAFe Practitioner), • Ability to mentor junior data scientists and lead cross-disciplinary technical teams

Job Description About Capricor Therapeutics Capricor Therapeutics, Inc. (NASDAQ: CAPR) is a cutting-edge biotech company based in San Diego, CA, focused on the discovery and development of novel cell and exosome-based therapeutics for the treatment and prevention of various diseases and disorders. Our lead product candidate, allogeneic Cardiosphere-Derived Cells (CDCs), known as deramiocel, is under investigation as a treatment for Duchenne muscular dystrophy and COVID-19. We are also advancing our exosome platform technology for several indications, including a novel COVID-19 vaccination approach. Capricor offers exciting opportunities and invites qualified professionals to join our expanding team. We offer competitive compensation and benefits packages. Position Overview: Process Development Associate The Process Development Associate will play a key role in advancing Capricor’s biomanufacturing efforts by evaluating, improving, and scaling processes for therapeutic production. This position focuses on optimizing product yield, reducing costs, and ensuring scalability—from small experimental batches to large-scale manufacturing—while maintaining quality and efficiency. Reporting to the Process Development Director or Associate Scientist, the associate will collaborate with cross-functional teams to support the production of cell -based therapeutics, troubleshoot challenges, and implement innovative solutions. This role is ideal for a hands-on, detail-oriented professional eager to contribute to cutting-edge biotech advancements. Responsibilities: • Evaluate and improve biomanufacturing processes to enhance product yield and reduce overall production costs., • Scale up cell and tissue culture processes for larger batches of materials and work on small batches as needed, adapting techniques to meet increasing production demands., • Evaluate impact of new equipment and processes on production yield and potency., • Assist in characterization of product for identity, purity and potency to ensure quality standards are met., • Troubleshoot and resolve problems associated with different phases of full-scale biomanufacturing production., • Participate in researching, developing, and implementing new methods and technologies to improve production processes., • Collaborate with team members to document findings, maintain accurate records, and support process development goals. Requirements: Education: Bachelor’s degree in a scientific discipline (e.g., biology, biotechnology, or related field) required Experience: Minimum of 2-4 years (or 0-2 with a Master’s degree) in a research laboratory, process development, or biomanufacturing environment. Technical Expertise: Proven skills in cell and tissue culture, with experience troubleshooting biomanufacturing challenges. Tissue dissection experience preferred but not required. Process Improvement: Demonstrated ability to evaluate and enhance biomanufacturing processes, improving yield or reducing costs. Aseptic Handling: Familiarity with aseptic processes and maintaining contamination-free environments. Equipment Maintenance: Hands-on experience assisting with production equipment upkeep and basic operational troubleshooting. Assay Development: Practical knowledge of flow cytometry, RNA isolation, qRT-PCR and other basic molecular biology techniques . Closed System (Preferred): Experience with closed systems for biomanufacturing in a process development setting is a plus. Collaboration: Ability to work effectively with cross-functional teams to support process development goals. Work Arrangement: Onsite role in San Diego, CA, with occasional flexibility based on project needs. Work Environment and Physical Demands: • Professional lab and office environment., • Ability to stand or sit for extended periods while working with lab equipment or computers., • May require occasional lifting of materials or equipment up to 50 pounds., • Ability to work in a laboratory environment adhering to safety and contamination protocols. Why Capricor? Capricor Therapeutics is an industry leader in cell and exosome therapy, pushing boundaries to create innovative treatments that raise the standard of care. Grounded in integrity and driven by science, our team is committed to making a meaningful impact through patient-centered innovation. Join us and be part of a team that’s changing lives—help us shape the future of healthcare. Compensation (USD): • Salary Range: Competitive, based on experience and education level., • Comprehensive benefits package, including health insurance, retirement plans, and opportunities for professional development. Come work with us! At Capricor, we offer a collaborative work environment that supports your professional growth. Join a passionate team committed to transforming the lives of patients and pushing the boundaries of medical science.

Job Description Job Description: We are seeking a highly motivated and qualified individual to join our Discovery Biology Department as a Senior Scientist I and work as part of a team to drive success. The Senior Scientist I will support ongoing RNA-based drug discovery projects in several therapeutic areas. The successful candidate will have experience in neuroscience drug discovery and a deep understanding of human neurobiological processes that drive CNS disease pathophysiology. The Senior Scientist I will employ a variety of in vivo, ex vivo, and in vitro techniques to advance oligonucleotide therapeutics for CNS indications. Essential Responsibilities: • Carry out assigned laboratory functions applying knowledge and skill in an accurate, timely manner., • Support the establishment and maintenance of primary and IPSC-derived neuronal cell models., • Support in vivo studies by performing basic animal handling and specialized CNS techniques (e.g. intracerebroventricular and intrathecal injection), • Perform brain and spinal cord dissections and tissue processing. Collect bodily fluids, e.g. blood and cerebrospinal fluid., • Implement multiple state-of-the-art techniques in molecular biology, biochemistry, and microscopy to determine drug distribution, efficacy, safety, and mechanism of action., • Critically evaluate, interpret, summarize, and present data to internal project teams and leadership., • Maintain a current knowledge of relevant literature, competitive landscape, and methodologies specific to oligonucleotide-based therapeutics targeting CNS disorders., • Contribute to the preparation of research reports and presentations for internal project teams, leadership team, and external audience., • Maintain updated and well-organized lab notebooks., • Establish and maintain excellent working relationships with critical collaborative partners throughout the company., • Execute daily laboratory operations with an approach designed to minimize risks and hazard waste streams to carry out assignments., • Maintain all appropriate corporate standards for facility safety and hazardous material management. Reasonable accommodation(s) may be made to enable qualified individuals with disabilities to perform the essential functions of a job, on a case-by-case basis. On-Site Protocol: Physical presence at the ADARx Pharmaceuticals worksite is a necessary job function of this role, which the Company deems critical to collaboration, innovation, productivity, employee well-being and engagement, and it enhances the Company culture. Qualifications: • Ph.D. in Neuroscience, Pharmacology, or related scientific discipline, • 3+ years post-doctoral or biotech/pharmaceutical industry experience in neuroscience research and drug discovery., • In-depth knowledge in the field of neuroscience, CNS disease and therapeutic modalities., • Expertise in the rodent stereotaxic surgery techniques including intracerebroventricular and intrathecal injection, • Expertise in rodent brain and spinal cord dissection., • Experience with tissue processing, embedding and microtomy of brain tissues, fixation and immunohistochemistry., • Experience in gene expression analysis using qPCR and protein analysis techniques., • Broad knowledge of scientific experience with track record of scientific achievement demonstrated by peer-reviewed publications., • Understanding of project timelines and deliverables and plans/coordinate project work accordingly with departmental, functional, and external stakeholders., • Strong problem-solving skills and a proactive attitude towards exploring new approaches., • Excellent written and verbal communication skills and effective presentation of complex scientific data to cross-functional and senior management teams are essential for this role., • Ability to work as part of a team with a drive to partner effectively with internal and external leaders., • Experience with oligonucleotide-based therapeutics is highly desirable., • Prior experience in biotech/pharmaceutical industry a plus., • Experience in primary neuronal cell cultures and human iPSC-derived neural cells is a plus., • Experience in collection of cerebrospinal fluid samples is a plus., • Must be able to work independently as well in cross-functional team settings with supervision as needed., • Adaptable / Flexible - willing and able to adjust to multiple demands and shifting priorities as well as an ability to meet day-to-day challenges with confidence and professionalism., • This is a full-time position, Monday-Friday, occasional overtime., • Pay is commensurate with experience., • Equity-based compensation, • Performance-based bonuses, • 401(k) with Company Match, • Medical, Dental, Vision, • Flexible Spending Account, • Life Insurance, • Employee Assistance Program, • Employee Discounts, • Paid Vacation, • Paid Holidays, • United States (Required), • Background Check Company Overview: ADARx Pharmaceuticals, Inc., (the “Company” or “ADARx”) located in San Diego, is a clinical stage biotechnology company committed to turning cutting-edge science into life-saving therapeutics. ADARx has developed proprietary RNA targeting platforms and technology for silencing or editing target mRNA. ADARx has a growing pipeline of RNA targeting therapeutics for treating diseases across a range of therapeutic areas including genetic, cardiometabolic, complement-mediated diseases and central nervous system. ADARx currently has multiple active programs in development with the lead candidate in the clinic. We are well-financed by a syndicate of renowned VC firms. ADARx Pharmaceuticals is an EEO employer committed to an exciting, diverse, and enriching work environment. We prohibit discrimination and harassment of any kind based on race, color, sex, religion, sexual orientation, national origin, disability, genetic information, pregnancy, or any other protected characteristic as outlined by federal, state, or local laws. Disclosure Statement: • The above statements are intended to describe the general nature and level of work being performed by employees assigned to this classification. They are not intended to be construed as an exhaustive list of all responsibilities, duties and skills required of employees assigned to this position., • Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations., • The range provided is based on what we believe is a reasonable estimate for the base salary pay range for this job at the time of posting. This role is eligible for an annual target bonus and annual equity awards. Some roles may also be eligible for overtime pay, in accordance with federal and state requirements. Actual base salary pay will be based on a number of factors, including skills, competencies, type and length of experience within the industry, and other job-related factors permitted by law., • Total Compensation includes base salary; benefits: medical, vision, and dental insurance; life insurance; 401(k) matching program; paid time off; paid holidays; Employee Assistance Program; and other employee benefits. This role may also be eligible for short-term or long-term incentive compensation, including but not limited to cash bonuses., • 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.

Job Description We are Herrera Envision yourself at a growing, employee-owned company that inspires and empowers you to deliver your best performance while making a difference in the world. We are Herrera, a science, planning, and design consulting firm dedicated to working with clients to develop holistic solutions that provide social and environmental benefit. We protect the environment every day by providing a diverse range of consulting services to cities, counties, state and federal agencies, Tribes, non-profits, and private clients throughout Washington, Oregon, California, Montana, Wyoming, Alaska, and western Canada. For over 40 years, Herrera has cultivated a collaborative, caring, and values-driven culture that empowers our employee-owners to achieve excellence while ensuring we have fun along the way. By providing our employee-owners with the autonomy to pursue their professional interests and through encouraging them to grow, we benefit from high employee-owner retention that contributes to our longstanding partnerships with clients. Our Values • Treat everyone with respect and dignity, always., • Insist on integrity, objectivity, and social and environmental ethics in our work., • Act as stewards of the environment upon which we depend., • Research and outreach, learn and teach. We are hiring a senior level Water Resources Engineer or Scientist to join our growing Water practice in California. Do you have a passion for innovative problem-solving and collaboration with your clients and partners? Do you enjoy teaching others, learning from some of the most cutting-edge science and engineering projects on the west coast, and co-creating meaningful and impactful projects? If so, we have the perfect opportunity for you! In this role, we will count on you to: • Manage diverse projects such as stormwater, green infrastructure designs, water resource planning, water quality studies, BMP performance assessments, etc., • Serve as a conduit for Herrera’s diverse Water practice knowledge, helping share valuable lessons and solutions up and down the west coast., • Play an integral role in ongoing refinement and implementation of our strategic business development initiatives in California. Education, Experience, & Licensure/Certifications • Bachelor’s degree in engineering or science, • 10+ years of experience in stormwater management and/or stormwater quality, • If you are an engineer, a PE license in California, • Extensive project management experience in Southern California, • Collaborator and team builder with capacity to work with a team of interdisciplinary professionals and manage multi-disciplinary projects, • Experience developing scopes of work and budgets, • Strong business development skills and the ability to lead proposals, • 15+ years’ experience in stormwater management and/or stormwater quality Supervisory and mentorship experience This is a remote opportunity for candidates located within the broader San Diego / San Diego County region. We are proud to support our employee-owners by offering the following compensation and benefits: • This position is salaried and exempt from overtime; the salary ranges are as follows:, • Engineer V: $135,000 - $175,000, • Engineer VI: $150,000 - $190,000, • Scientist V: $120,000 - $160,000, • Scientist VI: $140,000 - $180,000, • Level is determined during the interview process and will vary based on multiple factors, including but not limited to years of experience, type/relevance of experience, skillset, and fit for the role, • Flexible hybrid work culture, • Medical/prescription drug/dental/vision insurance for employees and dependents; employees covered at no cost on base plan with buy-up options available; company contribution for dependents, • Section 125 flexible benefits plans – healthcare and dependent care, • Company-paid life insurance for employees; option to purchase additional life insurance for employees and dependents at employees’ expense, • Company-paid long term disability insurance for employees; option to purchase short-term disability insurance at employees’ expense, • Employee Assistance Program (EAP), • Employee Stock Ownership Plan (ESOP) – we are 100% employee owned!, • 401(k) retirement plan, • Paid vacation, accrued bi-weekly, equivalent to 15 days per year for a 40 hour/week employee and prorated for employees working 24-39 hours/week, • Paid sick leave, accrued bi-weekly, equivalent to 10 days per year for a 40-hour/week employee and prorated for employees working 24-39 hours per week, • Flexible paid holidays (10), • Paid volunteer time (8 hours annually), • Company-paid annual membership dues for one professional organization, • Professional development / continuing education allowance, • Discretionary annual bonus Reliable internet service is required for remote work, with acceptable types including cable, DSL, or fiber and minimum speeds of 30 Mbps download and 5 Mbps upload. A wired Ethernet connection is strongly preferred. Dial-up, satellite, wireless bridges, range extenders, and outdated or weak Wi-Fi connections are not supported. We Are Committed to Equal Opportunity, Diversity, Equity, and Inclusion At Herrera, we celebrate our differences as much as our similarities. We know the best outcomes come from interdisciplinary, diverse, and inclusive teams. Our values are ever-present in the people, culture, and work we do, they are not just a few sentences on our website. We treat people with respect and act with integrity and objectivity. Our employment decisions are based on knowledge, skills, and abilities, and have nothing to do with your race, color, gender, age, religion, national origin, disability, sexual orientation, medical history, reproductive health decisions, political ideology, veteran status, or physical appearance. As an equal opportunity and affirmative action employer, we encourage women, minorities, veterans, disabled veterans, and individuals with disabilities to apply for our open positions. We are also a member of E-Verify. To learn more about E-Verify, read the E-Verify Notice and the Right to Work Notice. Powered by JazzHR 5PovDH05ps

Job DescriptionAbout Capricor Therapeutics Capricor Therapeutics is a biotechnology company dedicated to developing transformative therapies for rare diseases, with a primary focus on Duchenne muscular dystrophy (DMD). We are pioneers in cell therapy and exosome-based technology, leveraging our proprietary StealthX™ platform to engineer innovative treatments. Our team is committed to harnessing cutting-edge science and advanced technologies to meet the unmet needs of patients living with DMD and other challenging medical conditions. Join us on our journey as we push the boundaries of medical science and pave the way for a healthier future. Position Overview We are seeking a highly motivated and skilled Scientist or Senior Scientist with strong expertise in in vitro assay development to support therapeutic programs focused on rare muscle diseases. The ideal candidate will play a critical role in designing and executing cellular assays to evaluate exosome-based delivery of therapeutic agents, including protein, mRNA, siRNA, ASO, and PMO. A demonstrated ability to troubleshoot complex biological systems and a passion for advancing innovative therapies are essential. Experience with iPSC genome editing and differentiation into myoblasts is a significant advantage. This hands-on, lab-based role involves strong cross-functional collaboration with molecular biology, cell biology, and translational research teams to advance Capricor’s mission of developing transformative treatments for rare diseases. Responsibilities * In Vitro Assay Development: * Design, develop, and validate mechanism-of-action and functional assays to evaluate the efficacy, potency, and safety of therapeutic candidates. * Establish pharmacokinetic/pharmacodynamic (PK/PD) assay platforms to characterize cellular uptake, expression, and downstream effects. * Employ advanced techniques such as high-content imaging, flow cytometry, qPCR, Western blot, and ELISA to support assay development. * Exosome-Based Drug Substance Delivery: * Develop and optimize loading and delivery protocols for therapeutic payloads (protein, mRNA, siRNA, ASO, PMO) into exosomes or lipid nanoparticles. * Characterize loading efficiency, payload integrity, delivery kinetics, and functional outcomes in vitro using rigorous analytical methods. * Cell Culture and Molecular Biology: * Maintain and manipulate various mammalian cell types, including primary cells, immortalized lines, and preferably induced pluripotent stem cells (iPSCs). * Perform nucleic acid delivery, transfection, and transduction, followed by molecular and functional analyses. * Support genome engineering using CRISPR/Cas9 or related gene editing platforms. * Disease Relevance: * Develop and use in vitro models relevant to rare muscle diseases, including muscle-derived or iPSC-differentiated myoblasts. * Correlate cellular phenotypes with disease-relevant biomarkers and therapeutic mechanisms. * Troubleshooting and Optimization: * Rapidly identify and solve technical challenges in assay workflows and delivery approaches. * Adapt protocols to accommodate evolving project needs and new delivery modalities. * Data Analysis and Reporting: * Analyze and interpret complex data sets; communicate findings clearly through presentations and written reports. * Maintain high standards of documentation and data integrity in a collaborative environment. * Collaboration and Innovation: * Work cross-functionally with research, bioanalytics, and translational teams to ensure alignment of assay strategies with therapeutic goals. * Stay abreast of emerging technologies in drug delivery, nucleic acid therapeutics, and assay platforms, and apply innovative thinking to accelerate discovery. Requirements * Education: Ph.D. in Cell Biology, Molecular Biology, Biochemistry, or a related field with 0–3+ years of postdoctoral or industry experience (or M.S. with 5+ years). * Experience: * Hands-on expertise in in vitro assay development and validation for drug evaluation. * Hands-on expertise in exosome or similar delivery platform-based delivery of therapeutic agents. * Hands-on expertise in mammalian cell culture, assay troubleshooting, and protocol optimization. * Preferred Qualifications: * Experience with iPSCs, including CRISPR-based genome editing and myogenic differentiation (e.g., into myoblasts). * Familiarity with rare muscle disease models and relevant functional biomarkers. * Knowledge of therapeutic modalities including siRNA, ASO, PMO, mRNA, and proteins. * Proficiency in data analysis tools (e.g., GraphPad Prism, FlowJo). * Soft Skills: * Strong troubleshooting and problem-solving capabilities. * Highly organized and detail-oriented with excellent documentation skills. * Effective communicator and collaborative team player. Work Environment and Physical Demands * Professional laboratory setting with a focus on hands-on experimental work. * Ability to perform laboratory tasks, including standing for extended periods, operating delicate equipment, and working in controlled lab environments. * Ability to lift/carry up to 20 pounds and gown for classified cleanroom areas as needed for GMP compliance. * Primarily an on-site role at our San Diego headquarters, with occasional flexibility for remote work based on project needs. Compensation (USD) Salary Range: $85,000 - $125,000 (commensurate with experience). Benefits: Comprehensive benefits package, including health, dental, and vision insurance, retirement plans with company match, equity awards, generous paid time off, parental leave, and opportunities for professional development. Why Capricor? Capricor Therapeutics is an industry leader in cell and exosome therapy, pushing boundaries to create innovative treatments that raise the standard of care. Grounded in integrity and driven by science, our team is committed to making a meaningful impact through patient-centered innovation. Join us and be part of a team that’s changing lives—help us shape the future of healthcare. Come Work with Us! At Capricor, we offer a collaborative work environment that supports your professional growth. Join a passionate team committed to transforming the lives of patients and pushing the boundaries of medical science. Apply today to contribute to our mission of developing transformative therapies for rare diseases like DMD.

Job DescriptionDescription: GeoEngineers, Inc. Staff Geotechnical Engineer San Diego, California Duties: Performs geotechnical engineering activities. Leads or coordinates the observation of field explorations and construction projects, ensuring that work performed is consistent with project plans and specifications as well as in accordance with safety guidelines. Completes detailed, accurate field reports and assists with coordination of field exploration programs. Assists with training junior technical and technician staff. Supports project management tasks such as budget planning, general field report reviews, and proposal development. Manages small projects under the supervision of a certified professional engineer or scientist as required. Gathers field data and field samples for related projects. Coordinates samples for testing. Supports the completion of permit applications according to appropriate local, state and federal guidelines. Completes engineering analyses and/or calculations within assigned discipline. Complete complex numerical modeling analysis using PLAXIS and FLAC. Develops moderately complex conceptual models under the supervision of a licensed engineer. Prepares deliverables such as memos and reports and provides occasional quality assurance/control support. Ensures that deliverables are submitted to the project manager in a timely manner and are completed as estimated. Develops project-related deliverables related to GIS/CAD (Geographic Information System / Computer Aided Design) data such as maps, database organization, etc. under the supervision of a licensed engineer. Assists project team members in making basic design decisions from detailed criteria provided by the senior engineer or project manager. Assists with the generation of technical reports; completes portions of technical reports and generates figures, tables, charts, etc. Domestic travel to project sites may be required up to 10% of the time. Requirements: Applicants must have a Bachelor’s degree or the foreign equivalent in Civil Engineering or a closely related engineering field and 1 year of experience as a Research/Teaching Assistant, Engineer, Engineering Intern or in a related geotechnical /civil engineering occupation. Experience must include 6 months using Ensoft (LPile and APile), Rocscience (Settle3), Bluebeam, MathCAD, GeoStudio Suite, Microsoft Studio Suite, SupportIT, FLAC, Civil 3D, Plaxis, or other software related to the discipline of geotechnical engineering. The position also requires completion of coursework (at either an undergraduate or graduate level) covering the following topics: • Advanced Soil Mechanics;, • Foundation Engineering; and, • either Numerical Modeling or Finite Elements. All education, training and experience may be gained concurrently. Applicants must be U.S. workers (includes U.S. citizens, permanent residents, foreign nationals granted temporary residence under one of the 1986 legalization programs, refugees, and asylees. To Apply: Salary offered: $86,690/year for 40+ hours/week. Interested applicants may submit resume and cover letter online at . GeoEngineers is an Equal Opportunity Employer that values workplace diversity. At GeoEngineers, investing in our people is a top priority. In addition to competitive and equitable pay, we are proud to offer a wide range of benefits to support employees and their families, including healthcare (with travel benefit for care not locally available), 401(k) with company match, short-term and long-term disability, life insurance, wellbeing benefits, paid vacation and sick time and paid holidays, among others. View our full listing of benefits at . GeoEngineers is also committed to working with and providing reasonable accommodation to individuals with physical and mental disabilities. If you need special assistance or accommodation while seeking employment, please contact Human Resources at or by phone at (425) 861-6000. We will then make a determination regarding your request for reasonable accommodation on a case-by-case basis. We care about your privacy. Read GeoEngineers’ Privacy Notice for details on our personal data policies. Requirements:

Job Description JOB SUMMARY We are seeking a skilled and highly motivated Research Scientist to join our Computational Sciences group at the Iambic Therapeutics headquarters in San Diego. You will be a key player in the application of advanced ML techniques to drive our drug discovery efforts. You will play an active role in the research teams pursuing important therapeutics across multiple indications. You will work in a cross-functional team, collaborating closely with computational chemists, medicinal chemists and biologists to apply ML models across hit identification, lead optimization, and candidate selection phases. This is a hands-on application scientist role, requiring technical expertise in ML, familiarity with the drug discovery process and a drug-hunter mindset. KEY RESPONSIBILITIES * Design, train, evaluate and deploy ML models for predicting drug-target interactions and molecular properties * Apply ML models to the prioritization of virtual molecules: including de novo design ideas, HTE libraries and commercial collections * Partner with computational chemists, medicinal chemists and biologists to leverage ML insights for decision-making * Serve as a bridge between the bench and our computational platforms * Translate scientific questions into computational workflows and deliver actionable results * Present results to project teams and senior leadership, explaining methods, implications and recommendations * Collaborate with ML group to optimize model performance and evolve platforms QUALIFICATIONS Required: * PhD or equivalent degree in a computational field, or commensurate job experience * Skills: Python programming, statistics, drug discovery * Able to locate in San Diego Strongly preferred: * PhD or equivalent degree in computational chemistry or machine learning * 2+ years of experience working in a drug discovery project * Experience with molecular modeling/structure-based drug design and cheminformatics ABOUT IAMBIC THERAPEUTICS Iambic is a clinical-stage life-science and technology company developing novel medicines using its AI-driven discovery and development platform. Based in San Diego and founded in 2020, Iambic has assembled a world-class team that unites pioneering AI experts and experienced drug hunters. The Iambic platform has demonstrated delivery of new drug candidates to human clinical trials with unprecedented speed and across multiple target classes and mechanisms of action. Iambic is advancing a pipeline of potential best-in-class and first-in-class clinical assets, both internally and in partnership, to address urgent unmet patient need. Learn more about the Iambic team, platform, pipeline, and partnerships at iambic.ai. MISSION & CORE VALUES Our mission is to deliver better medicines through innovations in AI-based discovery technologies. The culture and work at Iambic Therapeutics are profoundly strengthened by the diversity of our people and our differences in background, culture, national origin, religion, sexual orientation, and life experiences. We are committed to building an inclusive environment where a diverse group of talented humans work together to discover therapeutics and create technologies. PAY AND BENEFITS We offer industry leading competitive pay, company paid healthcare, flexible spending accounts, voluntary life insurance, 401K matching, and uncapped vacation to our team. We are in a brand-new state-of-the art facility in beautiful San Diego with an onsite gym, dining, and easy access to great places to live and play. Compensation Range: $110K - $138K

Job DescriptionJob Title: Senior Platform Applications Scientist Reports to: VP, Translational Research FLSA: Exempt Location: San Mateo/San Diego Position Summary: At ClearNote Health, we combine novel epigenomic technologies with our innovative machine learning architecture to tackle the most urgent challenges in cancer care. We are looking for a highly motivated and experienced scientist with similar passion to join our mission to develop next-generation non-invasive cancer diagnostics for better patient outcomes. As an accomplished scientist with skill in design and execution of complex multidisciplinary projects toward molecular diagnostic tests in the treatment of cancer, you will contribute to the design and management of projects that employ the company’s novel platform technologies in drug development in collaboration with pharma partners. The projects will enable the company to formulate clinical questions that contribute to the care of cancer patients. Responsibilities: • Lead relationships with external collaborators and pharma partners to drive projects from inception to completion., • Lead and manage research projects with pharma partners that address fundamental questions using our state-of-the-art platform technology in diagnostic and therapeutic areas in oncology., • Ensure high data quality and the requisite scientific background and knowledge to navigate the complexity of experimental design and interpretation., • Build a continually expanding knowledge base in cancer biology, biomarker discovery and development., • Work in a collaborative and project-oriented manner with interdisciplinary teams composed of laboratory scientists, data scientists and bioinfomaticians as well as commercial and marketing personnel, and ensure that members contribute to their highest potential., • Ability to manage cross-functional projects and timelines., • Support, nurture, and help close sales opportunities., • Role requires 10% travel., • Exemplify our core values:, • Put Patients First: Focused on serving patients and their support system, we direct all our efforts toward the area of greatest impact by discovering and building with speed, excellence, and purpose., • Redefine the Possible: We are daring, imaginative, and focused in our pursuit of the next big idea. We take calculated risks to grow our business and improve patients’ lives., • Together We Win: We encourage and challenge each other to achieve the greatest positive impact on those we serve: our customers, patients, colleagues, and stakeholders.Requirements:, • M.D./Ph.D. or Ph.D. in Oncology, Cancer Biology, Epigenetics and Genomics or related field with 6+ years’ relevant experience in positions of increasing responsibilities with 3-6 years of in industry., • Experience in leading and working in teams with a history of successful project management., • Experience in the field of oncology and its underlying biology, along with genomics and epigenomics expertise, as demonstrated by publications, involving impactful tools or data sets as well as presentations at international conferences., • Understanding existing large data sets and modern tools in cancer genomics for processing and analysis of primary data. Proficiency in programming languages such as R or python is a plus., • Experience in biomarker development or molecular diagnostics in industry is strongly preferred., • Experience with experimental design in population based clinical studies., • An understanding of experimental limitations of next generation sequencing experiments as applied broadly in cancer., • Demonstrated ability to apply these skills to uncover new biological insights., • Excellent interpersonal, teaming, written and spoken communication skills.Individual compensation is determined based on several factors, including job-relevant skills, expertise, and experience; applicable education or training; a demonstrated track record of exceeding expectations; and geographic location. The typical salary range for this position is estimated at $126,000–$164,000 for candidates based in the San Francisco or San Diego metro areas. Exceptions to this range may occur from time to time based on the depth of technical experience and other job-relevant qualifications.Come join us in addressing large healthcare needs through precision epigenomic medicine! Come join us in addressing large healthcare needs through precision epigenomic medicine! ClearNote Health is an exciting life science company that is reinventing non-invasive molecular diagnostic testing using next generation epigenomic technologies. We are passionate and dedicated to discovering and developing medicines that will make a significant difference in cancer and other epigenomic-driven diseases. Our technologies provide novel insight and quantitation of human health and disease, with our focus on precision medicine applications improving both clinical and health system outcomes. Our company was founded based on pioneering work in the Stanford laboratory of Stephen Quake, with advisors from Stanford and UCSF. We look for extraordinary lifelong learners with a passion and growth mindset for these areas, and for combining biological ingenuity with AI and data analysis. Led by a team with decades of experience bringing products from concept to market, we are an equal opportunity employer and value diversity at our company. We provide generous benefits to all employees including stock options. We are building a world-class company, based in San Diego and San Mateo. Our commitment to Diversity, Equity, Inclusion, and Belonging: We celebrate diversity in perspectives and backgrounds, and this is reflected in our innovation, our mission, and values. Our differences make us unique, help us innovate, and allow us to persevere. We strive to achieve representation and inclusion and redefine the possible in patients living longer lives. Powered by JazzHR ZAHKsbMaGt

Job Description Arrowhead Pharmaceuticals, Inc. (Nasdaq: ARWR) is a clinical stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead therapies trigger the RNA interference mechanism to induce rapid, deep, and durable knockdown of target genes. RNA interference, or RNAi, is a mechanism present in living cells that inhibits the expression of a specific gene, thereby affecting the production of a specific protein. Arrowhead's RNAi-based therapeutics leverage this natural pathway of gene silencing. Arrowhead is focused on developing innovative drugs for diseases with a genetic basis, typically characterized by the overproduction of one or more proteins that are involved with disease. The depth and versatility of our RNAi technologies enables us to potentially address conditions in virtually any therapeutic area and pursue disease targets that are not otherwise addressable by small molecules and biologics. Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates. Arrowhead's corporate headquarters is in Pasadena, CA with research and development teams in Madison, WI & San Diego, CA, and a state of the art manufacturing facility in Verona, WI. Our employees are nimble, science-driven innovators who are collaborating to bring new therapies to patients in need. The Position Arrowhead Pharmaceuticals is seeking a talented and motivated Scientist or Senior Scientist in Computational Drug Design to join our interdisciplinary drug discovery team. This role is ideal for a creative, independent thinker with strong technical skills in machine learning and a passion for applying computational approaches to advance next-generation therapeutics. The successful candidate will contribute to the design and optimization of novel antibody-siRNA conjugates using cutting-edge AI/ML methodologies. Responsibilities • Develop and curate large biological datasets by integrating internal and publicly available data sources., • Design, train, and apply predictive models for antibody-siRNA conjugate drug design., • Apply AI techniques to extract insights and generate testable biological hypotheses from model outputs., • Monitor and critically assess emerging developments in AI/ML for therapeutic discovery., • Ph.D. in Computational Chemistry, Computational Biology, Bioinformatics, Computer Science, or a related discipline., • Strong programming skills in Python (or equivalent), with experience using common scientific libraries and proficiency in UNIX-based environments., • Practical experience with deep learning frameworks such as TensorFlow, PyTorch, or JAX., • Proven experience applying machine learning to solve complex biological or chemical problems., • Hands-on experience in RNA and/or protein structure prediction and relevant in silico design tools., • A strong track record of scientific impact as evidenced by publications, conference presentations, or patents. All applicants must have authorization to work in the US for a company. California Applicant Privacy Policy

Job DescriptionAbout the Client Our client is a rapidly growing technology company at the intersection of healthcare and artificial intelligence. Founded by a team of industry veterans and academic leaders, this organization is on a mission to make high-quality clinical data more accessible for innovation in AI-driven healthcare. They are building a next-generation platform to support the development, training, and validation of responsible AI models with a strong emphasis on data quality and patient safety. About the Role The company is looking for a skilled Data Scientist to help shape, validate, and refine large-scale healthcare datasets for use in clinical research and AI product development. This role plays a crucial part in harmonizing complex, multimodal data from diverse healthcare environments into usable, well-documented formats for clinical and AI teams. Responsibilities * Design and maintain robust data transformation pipelines using tools such as dbt and Snowflake, prioritizing data integrity and transparency. * Normalize and integrate various types of clinical data—including structured records, unstructured notes, imaging, and more—into a unified ontological model. * Collaborate with engineering teams to optimize de-identification and ETL workflows from multiple cloud-hosted healthcare data sources. * Partner with NLP experts to develop methods for extracting structured clinical information from text-based sources. * Apply CI/CD and version control best practices within analytics codebases. * Translate complex research and modeling requirements into scalable data engineering solutions in collaboration with technical stakeholders and external partners. Requirements Required: * At least 3 years of experience in analytics or data engineering. * Strong proficiency with SQL and dbt. * Bachelor's degree in a technical or quantitative field. * Hands-on experience with cloud platforms (especially Snowflake and/or AWS). * Competency in Python for data wrangling and feature generation. * Familiarity with AI/ML workflows and deployment pipelines. * Commitment to clean, modular, and well-documented code using software engineering best practices. * Comfort working in a dynamic, fast-paced startup setting. * Clear communication skills and the ability to advocate for robust data practices. * Passion for advancing healthcare through trustworthy and scalable data infrastructure. Preferred: * Experience with healthcare data standards such as HL7, FHIR, or DICOM. * Background in academic medical research. * Visualization experience using tools like Tableau, Power BI, Hex, or Python libraries. * Exposure to integrating LLM tools and frameworks (e.g., RAG, agent workflows) within analytics pipelines. Benefits & Why Join * Competitive compensation package: base salary in the $145K–$160K range plus equity. * Opportunity to work at the forefront of AI and healthcare innovation. * Collaborative and mission-driven team environment. * Flexibility to work remotely or from the company’s office in New York. * A chance to make a real-world impact by shaping the future of clinical AI and healthcare research.

Job Description Are you highly motivated, hard-working, and seeking to join a growth-focused consulting & engineering firm? Are you looking for a company that will invest in your development and grow your professional skills? If so, consider a career with Apex! Powered by record sales, extraordinary client retention, strategic acquisitions, and an entrepreneurial spirit, Apex Companies is one of the fastest growing engineering and environmental consulting firms in the US. We were recently recognized by the Zweig Group as one of the fastest growing firms in the AEC industry. We take pride in providing our clients with exceptional service and have earned numerous awards for project excellence. We continue to grow, and we want you to grow with us. Your Responsibilities as an Environmental Scientist: • Provide staff level technical support for Phase I/II Environmental Site Assessments, Remediation projects, and Tank permitting, inspection, and compliance projects in Southern California., • Field duties include performing soil, soil vapor, and groundwater sampling prepare detailed soil/well boring logs, inspect and maintain in-situ remediation equipment, inspect hazardous waste storage tanks, and oversee subcontractor activity., • Office duties include preparing concise, detailed, and accurate data tables, figures, draft work plans, sampling and analysis plans, quality assurance/quality control plans, site-specific health and safety plans, permits, and work-performed reports, and maintaining project files and client-specific databases., • Work with and at the direction of a multi-disciplinary team of expert engineers, geologists, industrial hygienists, environmental scientists, and related professionals., • Actively engage in managing site safety through developing job hazard analyses, performing site safety inspections, and contributing "good catches" in support of best practice., • BS degree in civil engineering, geology, or related science., • Current 40-Hour HazWoper Certification, • 2+ years relevant experience including soil, soil vapor, and groundwater sampling., • Experience drafting detailed data tables and work-performed reports., • Detail-oriented, focused professional, with strong organization, analytical, technical writing skills demonstrating focus, clarity, and accuracy., • Excellent safety awareness and a good record and understanding of safe work practices., • Team-oriented but able to work independently., • Interest and commitment to cross-training and professional development., • A valid driver's license, good driving history and reliable transportation are required., • Medical, dental and vision plan options., • Company-paid life, short, and long-term disability insurance., • 401k plan., • Paid time-off and holidays., • Cross-training and the ability to work on a variety of projects., • Other perks and incentives., • Working with the best and brightest in the industry., • Visibility and recognition for your contributions and success. TO ALL RECRUITMENT AGENCIES: Apex Companies does not accept unsolicited agency resumes. Please do not forward resumes for any of our job postings to our career's sites, or to any employees of Apex Companies or affiliates. Apex Companies is not responsible for any fees related to unsolicited resumes.

Job Description SCHEDULE: Night Shift This position offers four 10 hour shifts with an 8pm PT start time. The 4 days will be between Tuesday and Sunday. Hours worked between 9pm and 4am will receive a 10% night shift differential. Additionally, if scheduled to work hours on both Saturday and Sunday, a $200 weekend differential will be provided. LOCATION: San Diego, CA While the work schedule will be mostly remote, employee needs to live within the San Diego area to come onsite for occasional training. Why Millennium Health? Millennium Health LLC is an accredited specialty laboratory with more than a decade of experience in medication monitoring and drug testing services, helping clinicians monitor the use and misuse of prescription medications and illicit drugs. The testing is used by healthcare professionals to obtain objective information about patients’ recent use of prescription medications and/or illicit drugs and helps monitor the effectiveness of treatment plans. Everyone that joins our team is key to our ability to support the clinicians and patients. GENERAL SUMMARY The Clinical Laboratory Scientist, Data Review will review chromatographic data and calculated results obtained from a variety of standardized urinalysis tests in a toxicology laboratory for the detection of prescription and illicit drugs using advanced LC-MS-MS technology and EIA; applies toxicological and chromatographic rule sets to determine acceptability of results; requests additional testing as necessary; approves reports and patient results to ordering physicians. ESSENTIAL FUNCTIONS The following are intended to be examples of the accountabilities for which the person in this position is responsible. This is not intended to be complete or all-inclusive and does not preclude management from assigning related functions for which the individual has demonstrated competency through performance. • Responsible for testing to troubleshoot result issues., • Reports laboratory test results for all test methods approved by CAP, NY and CLIA., • Ensures accuracy and quality of test results meeting required turnaround times., • Enters testing data and reviews chromatography and calculated results from a variety of standardized tests on urine samples using advanced LC-MS-MS technology and EIA for the detection of prescription and illicit drugs., • Evaluates the validity of results obtained, maintains proper records of results and creates a report of results., • Maintains quality control and LC-MS-MS chromatographic data prior to release or results to physicians., • Ensures that testing methods follow established quality control procedures., • Identifies, troubleshoots, documents and resolves test result issues., • Documents issues using the Laboratory Occurrence Management (LOM) form., • Acts as a resource to laboratory technicians, laboratory assistants and associate scientists., • Follows safe laboratory practices and participates in operational support activities necessary to maintain and optimize testing capabilities., • May oversee the duties of clinical laboratory technicians, clinical laboratory assistants and associate scientists who prepare specimens or perform other less complex procedures. Remains aware of evolving needs and opportunities, showing flexibility in doing whatever is appropriate to support the Company’s success. Pursues educational opportunities to maintain advanced and up-to-date knowledge in the field. Performs all other related duties as required and assigned and understands that the items in this description are not all-inclusive. Requirements SKILLS/KNOWLEDGE/ABILITIES • 2+ years’ experience in high complexity testing; CLIA/CAP environment, • Must maintain continuing education units required by California Department of Health Services, • Knowledgeable in laboratory methods and techniques, • Knowledgeable of equipment and supplies used in a laboratory, • Proficient in MS applications (Word/Excel/PowerPoint/Outlook), • Strong interpersonal skills and ability to communicate with all levels of employees, • Effective attention to detail with high degree of accuracy, • Bachelor’s degree with current California CLS license, • Physical: Primary functions require sufficient physical ability to work in an office setting and operate office equipment. Continuous sitting and upward and downward flexion of neck; fine finger dexterity; fast paced data entry with finger pressure to manipulate keyboard. Have the ability to speak and listen to customers on fast-paced phone calls., • Medical, Dental, Vision, Disability Insurance, • 401k with Company Match, • Paid Time off and Holidays, • Tuition Assistance, • Behavioral and Health Care Resources POTENTIAL HIRING RANGE: • Hourly Position: $45-$50, • 10% Night Shift Differential applied to hours worked between 9pm and 4am, • $200 Weekend differential is added per weekend worked, • Offers are based on skills, knowledge, and abilities of the selected candidate. Millennium Health is an Equal Opportunity/Affirmative Action employer and E-Verify participant. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, gender identity, sexual orientation or protected veteran status California Employee Privacy Notice - Millennium Health LLC

Job Description JOB SUMMARY Iambic Therapeutics is seeking a machine‑learning scientist to extend Enchant—our multimodal transformer—by incorporating genomics, transcriptomics, proteomics, metabolomics, and other omics signals. Your work will focus on target selection and biomarker discovery. You will create robust data pipelines, curate benchmarking datasets, and develop models that combine multi‑omics information with existing context in Enchant. An understanding of causal experimental design and the interactions among diverse molecular modalities is essential. This position is remote, with a preference for candidates on the East Coast. KEY RESPONSIBILITIES * Identify, prioritize, and acquire multi-omics datasets. * Build, maintain, and document data pipelines that ingest, quality‑control, and harmonize large multi‑omics datasets from public and proprietary sources. * Design schemes for pretraining and finetuning Enchant on multi-omics data. * Define benchmarks for target‑selection and biomarker tasks; source or assemble reference datasets to measure progress. * Apply causal‑inference principles to propose experiments that disambiguate biological mechanisms and validate model outputs. * Write high‑quality, tested code and deploy models across multi‑GPU or HPC environments; monitor performance and iterate. * Stay current with advances in machine learning and computational biology; prototype promising ideas and share findings with the team. * Mentor colleagues in best practices for data engineering, modeling, and experimental design. REQUIRED QUALIFICATIONS * PhD (or equivalent experience) in machine learning, computational biology, bioinformatics, computer science, or a related field, plus 3+ years of relevant experience. * Demonstrated expertise applying deep learning to omics data at scale. * Proficiency in Python and modern deep‑learning frameworks (PyTorch, JAX, or similar). * Experience designing and operating data pipelines for genomics, transcriptomics, proteomics, or metabolomics. * Solid grasp of causal inference, experimental design, and statistics. * Familiarity with software engineering best practices, version control, code review, and continuous integration. PREFERRED QUALIFICATIONS * Experience working in cloud or HPC environments and with distributed training. * Familiarity with multimodal transformers. ABOUT IAMBIC THERAPEUTICS Iambic is a clinical-stage life-science and technology company developing novel medicines using its AI-driven discovery and development platform. Based in San Diego and founded in 2020, Iambic has assembled a world-class team that unites pioneering AI experts and experienced drug hunters. The Iambic platform has demonstrated delivery of new drug candidates to human clinical trials with unprecedented speed and across multiple target classes and mechanisms of action. Iambic is advancing a pipeline of potential best-in-class and first-in-class clinical assets, both internally and in partnership, to address urgent unmet patient need. Learn more about the Iambic team, platform, pipeline, and partnerships at iambic.ai. MISSION & CORE VALUES Our mission is to deliver better medicines through innovations in AI-based discovery technologies. The culture and work at Iambic Therapeutics are profoundly strengthened by the diversity of our people and our differences in background, culture, national origin, religion, sexual orientation, and life experiences. We are committed to building an inclusive environment where a diverse group of talented humans work together to discover therapeutics and create technologies. PAY AND BENEFITS We offer industry leading competitive pay, company paid healthcare, flexible spending accounts, voluntary life insurance, 401K matching, and uncapped vacation to our team. We are in a brand-new state-of-the art facility in beautiful San Diego with an onsite gym, dining, and easy access to great places to live and play. Compensation Range: $152K - $215K

Job DescriptionDescription: Founded in 2010, Terraphase Engineering is a dynamic, privately owned environmental consulting firm seeking a Principal Environmental Compliance Consultant (Scientist, Geologist, or Engineer) with 16+ years of professional experience to help grow and support our Compliance Services Division, one of Terraphase’s four core Service Areas—alongside Environmental, Site Engineering, and Water Resources. The Compliance Division offers significant career growth as one of our fastest growing service areas and is central to Terraphase’s long-term growth strategy, with dedicated resources and leadership focused on expanding our reach and capabilities. This is a senior leadership opportunity for a proven seller–doer—a consultant who combines deep technical expertise with a strong record of cultivating and sustaining client relationships while delivering practical compliance solutions. At Terraphase, you’ll enjoy the personal attention and entrepreneurial culture of a small-to-mid-sized firm (fewer than 200 people), backed by the technical depth, multidisciplinary resources, and geographic reach of a company with offices across the U.S. You’ll have the platform to shape strategy, mentor emerging talent, and deliver tailored, high-value service to clients in a variety of industries—all while contributing to the continued growth of our compliance practice through your network and technical expertise. Our compliance professionals help clients meet critical environmental and safety standards, contributing to healthier communities and sustainable operations. The Role • Maintain comprehensive knowledge of federal, state, and local environmental regulations (CWA, RCRA, CAA, EPCRA, etc.)., • Lead large-scale and multi-state compliance programs., • Serve as a trusted advisor to clients, guiding regulatory negotiations and agency interactions., • Manage diverse projects—compliance audits, gap analyses, discharge monitoring, tank programs, litigation support, and permitting efforts., • Develop proposals, scopes, budgets, and schedules while ensuring client satisfaction and profitability., • Lead teams for responses to small and large RFPs/SOQs, • Oversee and mentor a team of consultants, scientists, and engineers, while managing subcontractors and vendors., • Provide quality assurance and technical reviews of deliverables, including reports, plans, and specifications., • Support project bidding, contract solicitation, and business development opportunities., • Collaborate across disciplines to deliver innovative, cost-effective compliance solutions., • 16+ years of consulting experience with a focus on environmental compliance., • Bachelor’s degree in Engineering, Geology, Environmental Science, or related discipline., • Demonstrated ability to lead compliance programs and manage client portfolios., • Recognized expertise in federal and multi-state regulatory frameworks., • Strong record of client development and relationship management., • Professional licensure such as CHMM or proven leadership in subject matter areas (Hazardous Waste, Stormwater, Air), • Experience using many government platforms such as US EPA CDX, CERS, RCRAInfo / myRCRAid, TRI-MEweb, ECHO, E-Plan, and similar compliance systems. Terraphase offers an extensive benefits package including; Medical, Dental, Vision, Employer Paid Life Insurance, Long-Term Disability, a generous 401(k) match, Commuter Benefits, TerraLunches, TerraTalks, Tuition/Licensing/Professional Development Reimbursement, Flexible Work Schedule, ongoing company-sponsored events. Terraphase is a privately-owned S-Corp with a path to ownership. EOE Statement Terraphase is an Equal Opportunity Employer, committed to an inclusive & diverse work environment where individual strengths and diverse viewpoints are respected and complement each other to achieve common goals. (EOE M/V/F/D) Salary Compensation for this position is based on years of experience, technical expertise, technical education, and geographic location with a range of $135,000-$200,000. Requirements:

Job DescriptionSalary: $24.00 - $30.00/hr About BPS Bioscience BPS Biosciences 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, SARS-CoV-2, immunotherapy, adoptive cell therapies, and many more. Science never stands still. We focus on emerging research needs and rapidly deliver solutions. BPS Bioscience Inc. is a leading provider of recombinant proteins, assay kits, lentiviruses, and recombinant cell lines for drug discovery. We are currently seeking a diligent and highly motivated scientist to join our cell biology group to assist in production and new product development. Responsibilities: • Perform routine tissue culture of mammalian cell lines including human induced pluripotent stem (iPS) cells and establishment of stable cell lines., • Perform molecular biology techniques including PCR, cloning, and plasmid preparation., • Maintain accurate and detailed records of experimental procedures and results, • Ensures lab cleanliness and safety by maintaining equipment and keeping all samples properly labeled and stored., • Maintains supply stocks for the common lab area including reagents, DNA, equipment, and consumables; communicate with sales representatives for appropriate pricing., • Handles documentation needed for project validation and research quality control; keep an updated database record with project details and information., • Performs literature review and summarizes the relevant information for the preparation of product datasheets., • Assists other researchers with various tasks, including aid in experiments, data entry,sample storage, and organization., • Other duties may include transfections, lentivirus production, performing cell-based assays in 96 well plates, assisting with order fulfillment, and other duties as assigned. Requirements: • A Bachelor's with 0-1 years., • Detail oriented, well organized, possess excellent lab skills and maintain meticulous records., • Ability to work in cross-functional teams. Strong teamwork, written and oral communication skills are essential., • Due to stem cell maintenance protocols, some weekend work (less than 1 hour) may be required. Benefits! • 401k with 4% company match, • Medical/Dental/Vision health insurance plans, • Vacation and paid holidays, • Companywide lunch provided quarterly 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.

Job DescriptionAbout Radionetics Radionetics Oncology, Inc. is a clinical stage radiopharmaceutical company focused on the discovery and development of novel radiotherapeutics for the treatment of a wide range of oncology indications and is poised to capitalize on the increasing demand for novel radiotherapeutics. Radionetics Oncology spun out of Crinetics Pharmaceuticals (Nasdaq: CRNX) and is supported by Frazier Life Sciences, 5AM Ventures, DCVC Bio, Crinetics Pharmaceuticals, and GordonMD Global Investments. Radionetics is advancing a pipeline of novel small molecule radioligands targeting G-protein coupled receptors for the treatment of a broad range of cancers, including adrenocortical carcinoma, breast cancer, lung cancer, among others. For more information, visit . The Director/Senior Director, Clinical Scientist reports directly to the Chief Medical Officer and plans, implements, and manages assigned clinical research studies in collaboration with internal and external stakeholders to ensure trial integrity and success. The Clinical Scientist provides strategic input and development support for clinical plans, evaluating and interpreting clinical data reviewing and authoring study-related documents, monitoring patient data and data collection status, and delivering protocol-related training to CROs and clinical trial sites. The Clinical Scientist provides support for preparation of regulatory submissions necessary for the initiation of clinical studies. This position is a key cross-functional team member contributing to the design and execution of the company’s clinical trials. Essential job functions and duties • Support the creation of the clinical development plan in partnership with cross- functional team members as well as KOLs and CROs., • Author, manage, and review study materials for competent authorities’ submissions; gain insights from clinical and scientific experts (e.g. protocol, regulatory documents, study report, safety review and communication)., • Analyze and interpret clinical trial data, collaborating with clinical operations to conduct data review., • Troubleshoot internal and external conflicts to ensure trial integrity and success., • Develop and present protocol training for CROs and trial sites., • Engage with trial sites and CROs on an on-going basis to monitor subject data and data collection status, ensure adherence to protocol, and evaluate consistency of data., • Maintain knowledge of the therapeutic area, current medical practice, and pharmaceutical regulations to help ensure best practices., • Establish excellent communication and collaboration with the cross-functional partners within the company and outside of the company., • Deliver timely, high-quality clinical study data, working in concert with external and internal partners., • Collaborate with clinical operations to identify, recruit, qualify, manage, and maintain relations with clinical trial sites, including collaborating with Principal Investigators to prioritize enrollment and ensure timely and high-quality execution of clinical studies., • Support clinical operations in the selection, contracting, and oversight of CROs and vendors in assigned projects., • Work closely with clinical department team members and other stakeholders to develop and drive patient accrual strategy to meet appropriate corporate timelines., • In assigned projects, lead or assist in writing, reviewing, and/or approving clinical project deliverables such as scope definition documents, investigational product labeling/kitting, Pharmacy Manuals, informed consent, IRB/EC and HA submissions/approvals, site activations, monitoring plan and tools, CRF’s, DMP edit checks, safety plan, Safety Management Team and DMC charter, close-out plans, inspection readiness plans, and CSRs., • Lead the development of study presentations, handouts, and coordination of Investigator Meetings, Advisory Boards, Study Monitoring boards., • Lead in writing publications and scientific presentations., • Perform other responsibilities as required by business needs.Minimum required qualifications, • Advanced degree in life sciences/ healthcare (or clinically relevant degree) is required. Master’s, PharmD, MPharm, PhD, MBBS, BDS, MD strongly preferred., • Minimum 10 years (director) or 12 years (Senior director) of experience with 5+ years as a Clinical Scientist or comparable role., • Solid knowledge of set-up, organization and execution of global clinical studies in a pharmaceutical company or contract research organization (CRO), or comparable experience within academic research institution., • Experience in a scientific discipline with clinical drug development experience and strategic planning specifically in the pharmaceutical or biotech industries is preferred; however, other relevant experiences and skills may be considered., • Experience in oncology is preferred, radiopharmaceutical experience is a plus., • Highly motivated and thrives working in a fast-paced innovative environment while remaining flexible, proactive, resourceful, and efficient., • Excellent working knowledge of ICH GCP guidelines, CFR, EMA, and HIPAA regulations., • Self-starter who can lead and manage function independently, while utilizing sound judgment.Non-standard work schedule, travel or environmental requirements, • The position is based in San Diego, CA; a portion of the job duties may be performed remotely. Pay Range: $208,000 - $240,000 (director range); $250,000 - $280,000 (sr. director range) Radionetics evaluates a variety of factors in determining individual pay decisions, which may include relevant education, experience, and skills; internal equity; complexity and responsibility of the role; and market demand relative to the position. Geographic location may also be a consideration in evaluating salary when candidates work in states outside of California. Important notices Radionetics Oncology, Inc. is committed to a policy of equal opportunity in which all qualified applicants receive equal consideration for employment without regard to race, color, national origin, ancestry, religion, sex, pregnancy, marital status, sexual orientation, gender, gender identity and expression, age, physical and medical disability, medical condition, genetic information, military or veteran status, or any other federal, state or local protected class. The job description specifics provided above are intended to describe the general nature and level of work performed by people assigned to this classification. They are not intended to be construed as an exhaustive list of all responsibilities and requirements. Radionetics retains the right to add or change duties, education, experience, skills or any other requirements of the position at any time. Radionetics does not accept unsolicited referrals from employment agencies for position vacancies unless written authorization is provided from the Human Resources department before any candidates are referred for specific identified positions. In the absence of such written authorization, any actions taken by the employment business/agency shall be deemed to have been performed without consent or contractual agreement, and Radionetics shall not be liable for any fees arising from such actions or referrals for position vacancies at Radionetics. Powered by JazzHR PVMo2sgj5Z

Job DescriptionDescription: As a Project Environmental Engineer or Scientist, you will be responsible for planning, performing, and managing fieldwork to collect environmental data (soil, sediment, groundwater, and vapor), performing and managing oversight of cleanup construction, lead efforts related to multimedia compliance, evaluating and interpreting environmental data, performing engineering and scientific analysis and evaluation, preparing cleanup documents including work plans, reports and design (design drawings, specifications, and engineers estimate), managing projects/tasks, and mentoring junior staff. Performs duties in collaboration with senior engineers/geologists. Essential Duties and Responsibilities • Plan, perform, and manage field explorations and environmental data (soil, sediment, groundwater, and vapor) collection efforts. Field explorations may include drilling and test pitting to collect soil samples, sediment grab sampling and coring, and monitoring well installation and collection of groundwater samples., • Lead efforts related to multimedia compliance (predominantly construction and industrial stormwater, but air and wastewater are included). This includes permitting, monitoring, and reporting across construction and operational phases., • Evaluate and interpret field and laboratory environmental data, perform engineering/scientific analysis and evaluation, and develop solutions to complex problems., • Evaluate the fate and transport of environmental contaminants in various media including soil, sediment, groundwater, and vapor, and develop conceptual site models to evaluate contaminant exposure pathways to receptors., • Prepare remedial investigation work plans, sampling and analysis plans, data reports, remedial investigation/feasibility study (RI/FS) reports, cleanup action plans, and remedial action completion reports on environmental remediation projects involving multiple contaminated media including soil, sediment, groundwater, and vapor., • Prepare design documents and supporting deliverables, including engineering calculations, design drawings, specifications, and engineers' estimate., • Prepare permit applications and coordinate with regulatory agencies in obtaining project permits., • Support clients with project bidding/contract solicitation, and contractor selection process for cleanup construction., • Perform management and oversight of cleanup construction involving remedial excavation, dredging of contaminated sediment and wood debris, installation of sediment caps, installation, operations and maintenance of in-situ remediation systems and site restoration activities., • Provide project closeout and long-term monitoring support on environmental remediation projects., • Perform project and task management duties, such as developing scopes of work and budgets, coordination with clients, subcontractor solicitation, invoicing, cost control, and contract reviews., • Communicate effectively with clients, regulators, contractors and project staff through the lifecycle of a project., • Mentor and train junior staff., • Bachelor’s degree in civil/environmental engineering or geology. Master’s degree preferred., • 5 to 10 years of environmental consulting or related professional experience., • QSD or QSP certification preferred., • PE license required., • Ability to prepare proposals, work plans, data reports, remedial investigation/feasibility study (RI/FS) reports, and design (design drawings, specifications and engineers' estimate) under a senior engineer’/geologist’s supervision., • QISP certification is preferred., • Familiarity with Local, State, and Federal permitting processes applicable to environmental cleanup projects is preferred., • Strong project management and technical environmental skillset preferred., • Ability to consistently meet tight deadlines in a fast-paced work environment., • Works well independently and collaboratively as part of project teams and GeoEngineers’ environmental group., • Strong verbal and written communication and technical writing skills., • A valid driver’s license is required., • All candidates are subject to completing a background check, and reference check., • All candidates are required to participate in our medical surveillance program., • Ability to perform a wide range of physical activities and do heavy work including exerting up to 50 pounds of force on occasion., • Ability to perform consistent work on a PC with prolonged sitting and view of a monitor/screen., • Ability to travel for short-term and long-term assignments as needed. At GeoEngineers, investing in our people is a top priority. In addition to competitive and equitable pay, we are proud to offer a wide range of benefits to support employees and their families, including healthcare (with travel benefit for care not locally available), 401(k) with company match, short-term and long-term disability, life insurance, wellbeing benefits, paid vacation and sick time and paid holidays, among others. View our full listing of benefits here. Our Commitment to Belonging at GeoEngineers When people feel they can bring their whole selves to work, that they have a voice and are supported and respected, it creates trust and a feeling of belonging— employees then flourish, grow their careers, and do the best work of their lives. A culture of belonging allows our employees to thrive and our company to prosper. This is a journey, and we are committed to doing the work, learning and evolving as we go. GeoEngineers is proud to be an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to age, ancestry, color, family or medical care leave, gender identity or expression, genetic information, marital status, medical condition, national origin, physical or mental disability, political affiliation, protected veteran status, race, religion, sex (including pregnancy), sexual orientation, or any other characteristic protected by applicable laws, regulations, and ordinances. GeoEngineers is also committed to working with and providing reasonable accommodation to individuals with physical and mental disabilities. If you need special assistance or accommodation while seeking employment, please contact Human Resources at or by phone at (425) 861-6000. We will then make a determination regarding your request for reasonable accommodation on a case-by-case basis. We welcome and encourage individuals from all backgrounds and experiences to apply for openings on our team. We would love for you to join us! We care about your privacy. Read GeoEngineers’ Privacy Notice for details on our personal data policies. Requirements:

Job Description Position: Senior Scientist, In Vivo - Cell & Gene Therapy Salary Range: $100,000 - $125,000 / yr Location: Carlsbad, CA About Pharmaron Pharmaron is a global CRO (Contract Research Organization) helping pharma and biotech companies bring new therapies to life. With over 21,000 employees worldwide across 23 locations in the US, UK and China, we support drug discovery through to manufacturing with fully integrated, high-quality services. We're proud of the impact we make and just last year, we supported over 780 discovery projects, 1,000+ CMC programmes, and 1,000+ clinical trials across all phases. Our teams are involved in everything from small molecules, ADC's, biologics, and gene therapies and we work with more than 3,000 global customers. To learn more, visit . Job Overview: Pharmaron is seeking a Senior Scientist / Study Director to join our In Vivo team. In this role, you will lead preclinical in-vivo studies as the single point of control, ensuring scientific rigor, compliance, and effective collaboration. You'll design, oversee, and interpret studies that advance pharmaceutical and cell and gene therapy programs, with a focus on immunocompromised mouse models. As a key liaison between sponsors, scientists, veterinary staff, and business partners, you will shape study strategies across therapeutic areas such as toxicology, biodistribution, oncology, immunology (B- and T-cells), and CNS research - driving innovative solutions that accelerate drug development. Key Responsibilities • Lead the design, conduct, analysis, and reporting of in-vivo studies, ensuring scientific rigor and regulatory compliance., • Partner with sponsors to develop scientifically sound and cost-effective study designs that meet project needs., • Oversee study scheduling and resource allocation in coordination with in vivo scientists, veterinary staff, and QA/QC teams., • Prepare study protocols and reports, maintaining high standards of accuracy and clarity., • Provide subject matter expertise in animal handling, restraint, dosing, and surgical procedures in rodents and large animals., • Act as a liaison between sponsors and internal teams, fostering transparent communication and timely responses to sponsor requests., • Ensure all study activities adhere to regulatory guidelines (USDA, FDA, AAALAC, OSHA) and IACUC protocols., • Contribute to internal research projects aimed at expanding and optimizing service offerings., • Ph.D. in a relevant scientific field with 3+ years of laboratory animal research experience., • Proven track record in study direction and team leadership within a preclinical or CRO environment., • Strong background in cell and gene therapy programs, with hands-on expertise in animal models and surgical procedures., • Technical expertise in immunology, cell culture, flow cytometry, and experience establishing new laboratory capabilities., • Proficiency in Microsoft Office and statistical analysis software., • Skilled in technical writing of study protocols, reports, and documentation for GLP studies., • Solid foundation in physiology, anatomy, and pharmacology with application in preclinical settings. 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 will 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 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 DescriptionJob Title: Bioinformatics Scientist I/II FLSA: Exempt Location: San Diego, CA (Onsite) Position Summary: ClearNote Health is an early cancer detection company focused on the development and commercialization of non-invasive epigenomic tests to detect cancer through a standard blood draw, earlier than existing methods and when the disease is still treatable. Leveraging its novel liquid biopsy technology, ClearNote Health is initially focused on high-mortality cancers with the greatest need for early detection, starting with pancreatic and ovarian cancers. In this high-impact position, you will work as part of a collaborative team to analyze epigenomic and genomic features from cell-free DNA and develop classification algorithms for early cancer detection. You’ll contribute across the full lifecycle—from experimental design and data analysis to production-ready code and results presentation to cross-functional teams. Responsibilities: • Design and analyze experiments using ClearNote’s epigenomics platform, • Develop and apply machine learning techniques tailored to the platform’s unique data characteristics, • Analyze clinical genomics data to train models that make clinically relevant predictions (e.g., cancer detection from epigenomic profiles), • Apply appropriate statistical methods to support rigorous, scientifically sound decision-making, • Evaluate and recommend software tools for epigenomic data analysis, • Write clean, maintainable code following software engineering best practices, • Present findings clearly, concisely, and quantitatively to cross-functional stakeholders, • Communicate hypotheses, data insights, and experimental designs to colleagues, collaborators, and advisors, • PhD or equivalent experience in Biophysics, Genetics, Genomics, Biochemistry, Molecular Biology, or a related field with a strong computational focus, • Experience working with genomics technologies, preferably with cell free DNA, • Ability to interpret biological data quantitatively using principles of molecular biology and biochemistry, • Proficiency in statistical methods for supervised machine learning, • Experience developing neural network models, particularly multi-layer perceptrons (MLPs), • Understanding of common parametric and non-parametric statistical tests, • Strong programming skills in Python and/or R, • Experience using Git for version control in a collaborative environment (branching, merging, pull requests), • Strong communication skills — both written and verbal — with the ability to explain complex concepts to cross-functional teams, • Proficiency in relational databases and SQL ClearNote Health offers a competitive salary and benefits package. Come join us in addressing large healthcare needs through precision epigenomic medicine! ClearNote Health is an exciting life science company that is reinventing non-invasive molecular diagnostic testing using next generation epigenomic technologies. We are passionate and dedicated to discovering and developing medicines that will make a significant difference in cancer and other epigenomic-driven diseases. Our technologies provide novel insight and quantitation of human health and disease, with our focus on precision medicine applications improving both clinical and health system outcomes. Our company was founded based on pioneering work in the Stanford laboratory of Stephen Quake, with advisors from Stanford and UCSF. We look for extraordinary lifelong learners with a passion and growth mindset for these areas, and for combining biological ingenuity with AI and data analysis. Led by a team with decades of experience bringing products from concept to market, we are an equal opportunity employer and value diversity at our company. We provide generous benefits to all employees including stock options. We are building a world-class company, based in San Diego and San Mateo. Our commitment to Diversity, Equity, Inclusion, and Belonging: We celebrate diversity in perspectives and backgrounds, and this is reflected in our innovation, our mission, and values. Our differences make us unique, help us innovate, and allow us to persevere. We strive to achieve representation and inclusion and redefine the possible in patients living longer lives. Powered by JazzHR M82g5qtwGI

Job DescriptionDescription: This position is contingent upon successful contract proposal submission and award. At Prevailance, we deliver high-impact results with integrity and purpose. Our professionals support mission-critical efforts across defense and national security domains, guided by excellence and trust. We are seeking an experienced and mission-focused professional to join our team as a Data Scientist. Responsibilities include, but not limited to: • Administer the Naval Ship Tracking, Reporting, and Analysis Tool (NSTRAT) system, including monitoring application performance and troubleshooting issues affecting availability, • Perform software engineering and testing to develop data analysis tools and event reconstruction capabilities, • Conduct database entry and management while ensuring monitoring of automated backups, • Security+ Certification, • Five (5) years of Navy experience managing Navy computer networks, • Three (3) years of experience using Python and other programming tools to develop data analysis products, • Proficiency with scripting languages such as Python and SQL Server relational databases, • Microsoft Azure Administrator Associate (AZ-104) certification, • Experience with database design, optimization, and advanced query development, • Familiarity with large-scale data analytics, data visualization, and statistical modeling Prevailance, Inc. proudly supports veterans as a member of the V3 (Virginia Values Veterans) program and the Hire Vets initiative. Prevailance provides a comprehensive benefits package to eligible employees, designed to support health, wellness, and financial security. Our benefits include: • Medical Insurance, • TriCare Supplemental, • Dental Insurance, • Vision Insurance, • Life & Accidental Death & Dismemberment (AD&D) Coverage, • 401(k) Plan with Company Matching Contributions, • Paid Time Off (PTO), • 11 Paid Holidays, • Education Reimbursement Program