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Apidel Technologies is seeking a local contract Pharmacist Level II for a local contract job in San Diego, California. Job Description & Requirements • Specialty: Pharmacist, • Discipline: Allied Health Professional, • Start Date: ASAP, • Duration: 26 weeks, • 25 hours per week, • Shift: 8 hours, days, • Employment Type: Local Contract Job Description Position: Pharmacist Location: San Diego, CA 92103 Duration: 05+ months (with higher possibilities of extension) Note: This is a Part time position: 3 to 4 days a week, 8-hour shifts. Duties • This position is responsible for dispensing prescriptions and coordinating clinical services for specialty drugs serviced at the branch location., • This position is responsible for interacting with the health care professionals in the provision and coordination of customer care., • Must also translate prescriptions, perform compounds and dispense prescribed pharmaceuticals. Must be comfortable communicating by telephone or mail, with patients and physicians for patient care., • Will also be responsible for resolving orders via the EA (External Adjudication) queue., • Reviewing patient profile, drug interactions, sensitivities and drug usage database in relation to patient's prescription., • Determines if prescription requires physician clarification or if it should be forwarded to therapeutic intervention or doctor phone calls for follow-up., • Enters prescription in to the computer. Assists in patient services as required, taking incoming prescription medication questions/concerns from patients., • Assists in the doctor phone call area and/or therapeutic intervention as assigned and contacts physicians to resolve any questions or concerns., • Maintains established procedures concerning quality assurance, security of controlled substances, and disposal of hazardous waste drugs., • Works with other members of the pharmacy to ensure accuracy of prescriptions., • Dispenses prescription medication and performs final dispensing quality check on all prescriptions for accuracy and dosage. Experience • Previous pharmacy experience in retail or hospital preferred., • Appropriate state license required., • Basic computer skills required., • Strong organizational skill, interpersonal skills and detail orientation important for this position., • Minimum of one year's pharmacy experience in a retail or hospital setting preferred. Education • Bachelor's degree in pharmacy or Pharm D. also preferred to have one year of experience as a pharmacist., • Must have an active license in good standing. Part time: 3 to 4 days a week, 8 hour shifts.\n About Apidel Technologies At Apidel Technologies LLC, we specialize in delivering high-impact healthcare staffing solutions that empower organizations to maintain operational excellence and deliver exceptional patient care. With our headquarters in Illinois and regional offices in New Jersey, California, and Georgia, we offer both nationwide reach and local insight to support the dynamic workforce needs of healthcare providers across the U.S. We deliver unmatched expertise in placing top-tier healthcare professionals, including Registered Nurses, Licensed Practical Nurses/Licensed Vocational Nurses, Certified Nursing Assistant/Certified Medical Assistant, and Nurse Practitioners, Medical Laboratory Scientist, Phlebotomist, Histologists, across a diverse spectrum of care settings such as hospitals, clinics, rehabilitation centers, long-term care facilities, correctional institutions, and more. Our deep talent network and sector-specific understanding position us as a valuable partner to client platforms, enabling a scalable and seamless workforce experience for healthcare employers and job seekers. Since our founding in 2012, Apidel has earned the trust of Fortune 500 healthcare organizations, mid-sized providers, and government agencies at the county and state levels. We provide end-to-end staffing services, contingent workforce solutions, direct hire, temp-to-hire, and executive search, designed to align with your clinical and operational objectives. As a certified WBENC firm, we are committed to Diversity, Equity, Inclusion & Belonging (DEI&B) and take a client-centric approach that combines industry insight, agile delivery models, and culturally competent staffing to help our clients thrive in today’s fast-evolving healthcare Benefits • 401k retirement plan, • License and certification reimbursement, • Medical benefits, • Dental benefits, • Vision benefits, • Referral bonus, • Sick pay

Job DescriptionDo You Want to Improve the Future of Healthcare? • Want to enable the world's top scientist to deliver impactful healthcare solutions faster?, • Do you believe that the best team wins?, • Do you thrive on providing innovative solutions to unique challenges? This position is an onsite role in San Diego, CA The Automation Engineer will help design, build, and deliver world-changing laboratory automation systems. The role will assemble automation workcells and custom engineering projects, conduct instrumentation operational and Green Button Go driver testing, assist with the electrical system design and implementation of the workcells, develop and test Green Button Go workcell processes, and periodically assist with the site-installation of the project. Responsibilities: • Conduct Operational Acceptance Testing of components for our projects, • Assemble automation workcells and custom engineering projects, • Assist with the electrical and control system design of automation projects and products, • Configure electrical, pneumatic, and communications on automation workcells and custom engineering projects, • Conduct Green Button Go instrumentation driver testing, • Develop and test Green Button Go application processes for automation workcells and custom engineering projects, • Bachelor’s degree in Bioengineering, Mechanical Engineering, or comparable field required, • Experience in Pharma/Life Sciences industry and using laboratory instrument from Beckman, Tecan, Agilent, etc. is preferred., • Experience working with hand tools (drills, saws, wrenches, etc.) is a plus, • Experience in robotic automation (SCARA or 6 DOF robot arms) is is a plus, • Experience working through a project engineering (from initial requirements setting, design, procurement, build, testing, and delivery), • EE knowledge around safety and power circuits is a plus, • Software/programming skills, especially with C#, preferred, • Ability to write professional technical reports and procedures, • Must be task focused and have a results-oriented attitude and approach to the job responsibilities Total Compensation target is $75,000 - $85,000 annually. Benefits include 401K with company match, Flexible Vacation Policy, Health Benefits, Investment in Professional and Personal Development, and much more. Biosero provides equal employment opportunities to all employees and applicants without regard to race, color, religion, sex, sexual orientation, national origin, age, disability, veteran status, gender identity, or any other factor protected by applicable federal, state, or local laws. In addition, Biosero complies with applicable state and local laws governing nondiscrimination in employment in every location in which it has facilities. This policy applies to all terms and conditions of employment, including, but not limited to, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation, and training. Biosero is committed to diversity and inclusion. We seek individuals from all backgrounds and appreciate and celebrate the diversity of our growing team. Powered by JazzHR HChRhrQ8eR

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 4:00 pm to 12:30 am, • 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 California Employee Privacy Notice - Millennium Health LLC 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 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 Position: Senior Scientist, In Vivo - Cell & Gene Therapy Salary Range: $100,000 - $125,000 / yr Location: Carlsbad, CA (on-site) About Pharmaron 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 • Design, execute, and lead in vivo studies evaluating CNS-targeted therapies-including cell and gene therapy candidates-with a focus on biodistribution, efficacy, and toxicity assessments, • Perform and optimize stereotaxic surgeries (ICV, IT, etc.) in rodents, • Conduct and interpret a broad range of behavioral assays (e.g., motor, cognitive, pain, etc.), • Act as Study Director on GLP/non-GLP studies, ensuring study execution aligns with applicable guidelines, • Prepare and maintain IACUC protocols and ensure animal welfare compliance in all procedures, • Author detailed study protocols, technical reports, and regulatory documents, • Train and mentor junior staff in surgical, behavioral, and technical procedures, • Maintain accurate documentation and data integrity in compliance with internal SOPs and external regulations, • Experience with neuroimaging, electrophysiology, or molecular techniques a plus, • Provide subject matter expertise in animal handling, restraint, dosing, and surgical procedures in rodents., • 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., • PhD. in a relevant scientific field with 3+ years of laboratory animal research experience., • Proven track record as Study Director 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., • Hands-on experience developing and characterizing in vivo models of CNS diseases., • 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 Description Research Scientist, Antibody Discovery and Research Job #25-07A 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 Job Description: We are seeking a highly motivated and qualified individual to join our Discovery Chemistry Department as a Principal Scientist, Conjugation 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 Principal Scientist, Conjugation will support ongoing RNA-based drug discovery projects in several therapeutic areas. Essential Responsibilities: • Develop and promote a workplace culture that values diversity of thought, promote integrity and create an atmosphere that supports coaching and fosters accountability., • 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., • 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., • Manage CROs., • Contribute to the preparation of research reports and presentations for internal project teams, leadership team, and external audience., • Maintain updated and well-organized individual and team’s lab notebooks and batch records., • Manage and maintain equipment, reagents and dedicated laboratory environment needed to carry out assignments., • 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, • 4-8 years of bioconjugation-related industry experience., • Team management experience is required., • 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., • Broad knowledge of scientific experience with track record of scientific achievement demonstrated by peer-reviewed publications., • Previous experience with RNA/oligonucleotide therapeutics., • A track-record of impacting drug discovery programs through driving projects to key decision points., • 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, • Gym Membership, • Paid Vacation, • Paid Holidays, • United States (Required), • Background Check, • As a condition of employment, you must successfully complete all post-offer, pre-employment requirements, including but not limited to a background check. Company Overview: We are a late-stage clinical biotechnology company dedicated to transforming cutting-edge science into next-generation RNA medicines across a wide range of therapeutic areas. Our goal is to control the expression of specific disease drivers with highly selective RNA targeted therapies, delivering life-changing treatments for patients with urgent unmet medical needs. 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., • Data: Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations., • Recruiters & Staff Agencies: ADARx Pharmaceuticals (ADARx) does not accept unsolicited resumes from any source other than candidates. The submission of unsolicited resumes by recruitment or staffing agencies to ADARx or its employees is strictly prohibited unless contacted directly by the Company’s internal Talent Acquisition team. Any resume submitted by an agency in the absence of a signed agreement will automatically become the property of ADARx and the Company will not owe any referral or other fees with respect thereto., • Compensation: 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., • Conditional Offer of Employment: 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 Job Summary We are seeking an experienced and highly motivated Principal Scientist to support growth into a late-stage clinical and commercial manufacturing environment. Reporting to the Senior Director of Biologics Development and Manufacturing, this role focuses on upstream process development and manufacturing-related activities. The ideal candidate will bring hands-on expertise in mammalian cell culture (CHO) and primary recovery, with a strong foundation in process development and characterization. Key Responsibilities * Establish upstream process development capabilities, including laboratory infrastructure, analytical equipment, and utilities. * Recruit, mentor, and lead a process development team. * Implement key unit operations such as solution preparation, shake flask culture, rocking cell bag, stirred-tank bioreactors, centrifugation, and depth filtration. * Set up data acquisition and management systems (e.g., ELN templates). * Develop and qualify scale-down models to support process development and characterization. * Establish internal media and feed platforms to enable high-yield CHO processes. * Apply Design of Experiments (DoE) to optimize and characterize upstream processes. * Produce bench- and pilot-scale material to support downstream, analytical, and toxicology studies. * Support external manufacturing activities, including technology transfer and troubleshooting process-related issues. * Review and manage development, manufacturing, and validation documents. * Author technical reports and present findings at departmental and cross-functional meetings. * Ensure compliance with FDA, EMA, ICH, GMP, and company policies and procedures. Qualifications * Bachelors degree in Chemical Engineering, Biochemical Engineering, Bioengineering, or related field required; advanced degree preferred. * Ph.D. with 3+ years, M.S. with 6+ years, or B.S. with 8+ years of industry experience in upstream process development. * Direct experience with mammalian cell culture bioreactors, including at least 2 years with ambr250 systems. * Strong background in process characterization studies preferred. * Knowledge of upstream process impact on product quality attributes desired. * Experience with analytical methods for cell culture processes. * Proven ability to analyze, interpret, and trend complex process data. * Experience collaborating with CDMOs and supporting technology transfer desirable. * Strong communication and interpersonal skills with the ability to drive problem-solving and teamwork. * Ability to manage multiple priorities in a fast-paced environment. * Detail-oriented with a focus on strategic objectives. * Familiarity with programming languages or AI/ML tools to support process analysis is a plus.

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 Job Summary The Associate Scientist, Analytical Development will play a key role in developing and executing mass spectrometry methods to support research and clinical programs. This is a hands-on laboratory position involving experimental design, data analysis, and interpretation to guide decision-making across cross-functional teams. The individual will contribute to analytical method development, qualification, and troubleshooting, while maintaining a strong focus on data quality, innovation, and compliance. Key Responsibilities * Design and perform experiments to develop, optimize, and qualify analytical methods for release, stability, and extended characterization testing. * Analyze experimental data, interpret results, and propose next steps to improve methods or resolve analytical challenges. * Implement novel analytical and mass spectrometry techniques for characterization of biologics and complex molecules. * Document experiments in electronic laboratory notebooks and prepare detailed technical reports summarizing findings. * Present data and updates regularly in team and project meetings. * Ensure all work adheres to regulatory standards and internal policies, including FDA, EMA, ICH, and GMP requirements. * Collaborate with cross-functional teams to support research, development, and technical operations initiatives. * Contribute to a culture of innovation, teamwork, and scientific excellence. Qualifications * Masters degree in Chemistry, Biology, or Pharmaceutical Sciences, or a Bachelors degree with at least 4 years of relevant experience in mass spectrometry analysis of biologics. * Hands-on experience with LC-MS/MS, HPLC, CE, and related analytical techniques. * Strong knowledge of antibody and/or oligonucleotide analytical characterization. * Demonstrated ability to analyze complex data and solve technical problems independently. * Excellent communication, organizational, and interpersonal skills. * Ability to work collaboratively in a fast-paced, multidisciplinary environment while managing multiple priorities effectively.

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 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 About 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. About the Role We are seeking a highly skilled Formulation Scientist to join Capricor Therapeutics and drive the development of stable, lyophilized exosome-based formulations for our groundbreaking therapies. In this critical scientific role, you will lead formulation design, optimization, and characterization, ensuring compliance with cGMP and supporting IND-enabling studies. You will collaborate with cross-functional teams, including analytical sciences, process development, and regulatory affairs, to advance our novel exosome-based drug delivery platforms. This role offers a unique opportunity to shape the future of exosome therapeutics, contributing directly to Capricor’s mission to transform the biotech industry and improve lives. Responsibilities Strategic Scientific Leadership • Develop and execute innovative formulation strategies for exosome-based drug products, aligning with Capricor’s mission to deliver transformative therapies for rare diseases, including DMD., • Stay ahead of advancements in exosome, lipid nanoparticle (LNP), and lyophilization technologies, implementing cutting-edge solutions to maintain a competitive edge., • Design and optimize exosome-based formulations for therapeutic modalities (e.g., nucleic acids, proteins, biologics), ensuring stability at 4°ree;C or room temperature for enhanced shelf-life., • Lead lyophilization process development for drug substances (DS) and drug products (DP), optimizing excipients, cryoprotectants, and thermal characterization (e.g., DSC, Freeze-Dry Microscopy) to extend stability., • Develop storage buffers (e.g., LNP-based) to support flexible storage conditions (4°ree;C, room temperature, -20°ree;C) and improve DS/DP integrity., • Perform physicochemical and biophysical characterization using techniques such as DLS, TEM, HPLC, LC-MS, DSC, and fluorescence-based assays to assess formulation performance., • Develop and validate quality control (QC) methods to evaluate stability, particle size, encapsulation efficiency, and biological activity of exosome-based DS/DP., • Collaborate with analytical scientists, process engineers, and regulatory affairs teams to define critical quality attributes (CQAs) and support IND submissions., • Partner with process development to transition formulations from R&D to clinical and commercial scale, ensuring scalability and GMP compliance., • Drive advanced formulation optimization to enhance exosome stability and delivery, leveraging data-driven approaches to meet regulatory and clinical demands., • Monitor and analyze key performance indicators (KPIs) for formulation processes, implementing corrective actions to improve efficiency and reliability., • Stay current with scientific literature and industry trends, contributing to Capricor’s innovation in exosome-based therapeutics. Requirements Minimum Qualifications • Education: Ph.D. in Pharmaceutical Sciences, Biochemistry, Bioengineering, Chemical Engineering, or a related field with 4+ years of biopharmaceutical industry experience; Master’s degree with 6+ years of relevant industry experience considered., • Experience: 4+ years of hands-on experience in biologics or vesicle-based formulation (e.g., exosomes, LNPs, liposomes, mAbs, peptides) in the biopharmaceutical industry., • Lyophilization Expertise: Direct experience with lyophilization process development, including excipient selection, thermal characterization, and cycle optimization for DS/DP stability., • Stability Optimization: Proven expertise in optimizing formulation stability at 4°ree;C or room temperature through forced degradation, real-time, and accelerated stability studies., • Analytical Skills: Proficiency in analytical techniques, including HPLC, LC-MS, DLS, TEM, and DSC, for formulation characterization., • Scientific Leadership: Demonstrated ability to plan and lead initiatives as a hands-on bench scientist in a fast-paced research environment., • Regulatory Knowledge: Strong understanding of cGMP, ICH guidelines, and compliance with 21 CFR Part 1271 and cGTP for injectable formulations., • Skills: Exceptional problem-solving, attention to detail, and communication skills, with a collaborative approach to cross-functional teamwork., • Direct experience with exosome-based therapeutics or vesicle-based systems (e.g., LNPs, liposomes)., • 5+ years of industry experience in biopharmaceutical or regulated environments within GMP or QC settings., • Expertise in GMP manufacturing, scale-up, and technical transfer to CMOs., • Experience authoring CMC sections for IND submissions or supporting regulatory interactions., • Proficiency in data analysis tools (e.g., Microsoft Excel, statistical software) and familiarity with process monitoring techniques., • Strong scientific communication and technical writing skills for reports, publications, and patent filings. Location Policy This position is based in San Diego, CA, with flexibility for occasional remote work as needed. Work Environment/Physical Demands • Physical Requirements: Ability to sit and stand for extended periods, lift/carry laboratory equipment and materials up to 40 pounds, move about the lab, and communicate effectively via telephone or in person. Capricor Therapeutics is headquartered in San Diego, California. We offer competitive compensation, generous vacation and parental leave, flexible working hours, and a collaborative work environment. If you are excited about joining a team that’s transforming the biotech industry through exosome-based therapeutics, we’d love to hear from you!

Job Description Invivoscribe is an industry pioneer, dedicated to Improving Lives with Precision Diagnostics®. Invivoscribe has been the global leader in driving international standardization of testing and accelerating patient access to the newest and best cancer treatments for over 30 years. Headquartered in sunny San Diego, California with locations across the world, we offer a comprehensive portfolio of products and services. We work with key collaborators to develop molecular assays, reagents, controls and bioinformatics tools under ISO 13485 design control that are used by over 700 clinical laboratories in over 160 countries. Our global network of laboratories offers internationally standardized next generation molecular and flow cytometry panels to support drug development and accelerate drug approvals worldwide. We work with pharmaceutical partners and international regulatory agencies across the globe to develop companion diagnostics, which are necessary to gain approval of new drugs and treatments for cancer patients. Our harmonized ISO15189 accredited and CLIA/CAP clinical laboratories offer a test menu focused on biomarkers which are clinically actionable to support therapeutic decisions, measurable residual disease (MRD) testing, patient stratification, and trial enrollment, all designed to accelerate approvals of new oncology drugs and treatments. For 30 years, we have been at forefront of precision diagnostics, and we’re just getting started! We are looking to add a Clinical Laboratory Scientist II for performing specialized high complexity testing of biological specimens. This position provides professional customer service to our clients. CLS works in a team environment to ensure timely and quality test results. The CLS II works with guidance as needed to changes in the workflow. Core Responsibilities Include: • Performs all assigned duties in compliance with internal SOPs and external regulations. Brings compliance issues to the attention of management., • Performs all aspects of pre-analytic workflow to ensure orders are entered correctly, specimens collected are appropriate for the test ordered and are correctly processed. Evaluates specimens for appropriateness and takes necessary corrective action. Appropriately documents unacceptable specimens., • Performs all aspects of the clinical testing workflow including:, • Semi-automated and manual DNA isolations., • Quantify and normalize isolated DNA., • Operate laboratory equipment, such as Thermocyclers, Next Generation testing platforms, cell counters, UV-Vis Spectrophotometer, fluorometer, electrophoresis testing platforms, etc. Use automated equipment that analyzes multiple samples at the same time., • Performs NGS Library Preparation which can then be sequenced on an NGS Testing Platform., • Performs complex gene panel NGS tests., • Verifies reagents and supplies, meets defined acceptability criteria upon receipt and prior to use and acts to ensure unacceptable items are removed from use., • Assist with inventory counting., • Prioritizes testing based on assignment or established priorities; completes testing within defined turn-around times., • Performs technical review, data analysis and interpretation. Reviews results for completeness, correctness and consistency within defined test system., • Performs moderate to advanced troubleshooting and repair. Escalates issues when necessary., • Recognizes when unresolved problems need to be escalated and takes necessary follow-up action., • Performs all aspects of the post-analytic workflow appropriate to ensure accurate results are reported within established time frames, specimens are retained appropriately, test results and/or current status are available upon inquiry., • Assists with required Quality Management System responsibilities including initiating Quality Occurrence Reports., • Follows all required safety procedures, assumes a proactive role in laboratory safety. Follows all required privacy, safety, and biohazard procedures and standards., • May assist with training of new employees., • Responsible for monitoring and troubleshooting temperature excursions on cold storage units., • Follows all proficiency testing (PT) policies and guidance., • Performs Phase-ins (also known as Prequalification of Reagents or Reagent QC)., • Ensures HIPPA laws are followed. Ensures patient, and employee confidentiality., • Ensures supply and reagent levels are at the appropriate levels and notifies appropriate personnel when new supplies are needed., • BS in Clinical Laboratory Science or scientifically related field with, typically, 2+ years of industry experience in a Clinical Laboratory. Equivalent combination of education and experience will be considered., • Licensed in California as a Clinical Laboratory Scientist., • A beautiful modern facility centrally located in San Diego County, with many jobs conducive to a hybrid work from home arrangement., • A safe, fully-vaccinated, work environment., • A diverse and inclusive work environment where you will learn, grow, and make new friends.

Key Requirements and Duties: The Clinical Laboratory Scientist I (CLS I) will perform analytical testing as well as general laboratory processes, in a high complexity clinical molecular laboratory in compliance with policies, procedures and regulations. Responsibilities: • Performs clinical testing of patient samples, which includes set-up of molecular assays., • Adheres to the laboratory’s quality control processes and document quality control activities, instrument and equipment verifications, and instrument maintenance and preventive maintenance., • Supports the Corporate and Laboratory Operations Goals and Objectives., • Follows the laboratory's policies and procedures whenever test systems are not within the laboratory's established performance specifications., • Identifies and documents problems that may adversely affect test performance and notifies the manager or director., • Documents all corrective actions taken when test systems deviate from the laboratory's established performance specifications., • Participates in activities required to support all necessary licensure for the clinical laboratory, including maintaining quality systems and test records and supporting on-site inspections of the laboratory., • Utilizes an in-house Lab Information System (LIS)., • Complies with all local, state, and federal laws and regulations governing clinical laboratory operations., • Maintains records that demonstrate that proficiency testing samples are tested in the same manner as patient specimens., • May be required to monitor the activities of non-licensed personnel., • May be required to assist in assay development activities., • Performs other duties as assigned. Minimum Education/Experience Requirements: • Clinical Genetics Molecular Biologist (CGMBS) or Generalist Clinical Laboratory Scientist (CLS) License from the State of California, • Bachelor’s Degree in Medical Technology or Biological Sciences., • Must meet the requirements for Testing Personnel under CLIA 88 (42 CFR, part 493), • Highly organized, able to work independently, follow standard operating procedures., • Experience in a high complexity CLIA/CAP environment strongly preferred, • Experience in Molecular Biology, Molecular Pathology, and/or Medical Genetics preferred Required Training/Certification: • On the job training including, but not limited to: HIPAA, and safety procedures.

Clinical Laboratory Scientist I (CLS I). Generalist Clinical Laboratory Scientist (CLS) License. Corporate and Laboratory Operations Goals and Objectives.

Clinical Lab Scientist - Part Time. Clinical Laboratory Scientist (CLS).

Must have current Clinical Laboratory Scientist issued by the State of California, Department of Public Health. Two (2) years of applicable clinical laboratory experience. Six (6) years of applicable clinical laboratory experience.

SIO is a world-renowned center of marine research with approximately 200 principal investigators leading research programs on all aspects of earth, ocean, biological, and atmospheric sciences. The positions require a PhD in a relevant field/related fields in Physical Oceanography or Climate Sciences

Tuesday and Friday, and each Saturday for a total of 4 days per week, 10 hours per day.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 m

Job DescriptionDo You Want to Improve the Future of Healthcare? • Want to enable the world's top scientist to deliver impactful healthcare solutions faster?, • Do you believe that the best team wins?, • Do you thrive on providing innovative solutions to unique challenges? Onsite Role Position Summary: The Automation Technician will assemble automation work cells and work on customer engineering projects. This position will assist in shipping and receiving components for projects and the automation engineers with the operational testing of instrumentation on the projects. Responsibilities: • Assemble automation workcells and custom engineering projects., • Configure electrical, pneumatic, and communications on automation workcells and custom engineering projects based on design schematics., • Label and organize all workcell wiring., • Unpack, arrange, level, and secure automation workcell tables., • Mount instrumentation and shelves to workcells., • Assist Shipping/Receiving to keep components organized and the shop clean., • Assist engineering team with operational testing on instrumentation., • High School Diploma., • Relevant trade-skill school degree desirable., • At least 1-2 years of experience with hand-tools (drills, saws, wrenches, etc), including cutting, drilling, and tapping aluminum or similar., • Experience working with extruded aluminum profile (such as 80/20) is preferred., • Excellent attention to detail and drive for quality., • Ability to read Engineering drawings., • Able to use electric and pneumatic tools., • Basic computer skills are required, including Microsoft Word and Excel., • Ability to operate a forklift is desired, Total Compensation target is $24.00 - $27.00 an hour; actual pay will vary based on experience. Benefits include 401K with company match, Flexible Vacation Policy, Health Benefits, Investment in Professional and Personal Development, and much more. Biosero provides equal employment opportunities to all employees and applicants without regard to race, color, religion, sex, sexual orientation, national origin, age, disability, veteran status, gender identity, or any other factor protected by applicable federal, state, or local laws. In addition, Biosero complies with applicable state and local laws governing nondiscrimination in employment in every location in which it has facilities. This policy applies to all terms and conditions of employment, including, but not limited to, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation, and training. Biosero is committed to diversity and inclusion. We seek individuals from all backgrounds and appreciate and celebrate the diversity of our growing team. Powered by JazzHR ddwzwRd0sf

Clinical Laboratory Scientist I (CLS I). Generalist Clinical Laboratory Scientist (CLS) License. Corporate and Laboratory Operations Goals and Objectives.

Assistants provide general support functions within the pre-analytic and analytic laboratory departments such as clerical and laboratory assistant duties to support overall operation of the lab. Pride Health is hiring a Laboratory Pre-Analytical Services Associate I to support our client’s medical

Careers With Purpose At Sanford Health, we are proud to offer development and advancement opportunities to our nearly 50,000 members of our family.Together, we are dedicated to the work of health and healing across our broad footprint.Take pride in your profession and provide quality care to your co

Clinical Laboratory Scientist I (CLS I). Generalist Clinical Laboratory Scientist (CLS) License. Corporate and Laboratory Operations Goals and Objectives.

The Principal Research Scientist will focus on targeted drug delivery including nucleic acid therapies.

Clinical Laboratory Scientist I (CLS I). Generalist Clinical Laboratory Scientist (CLS) License. Corporate and Laboratory Operations Goals and Objectives.

Are you a visionary scientist ready to lead antibody innovation from discovery to clinic? iBio is looking for a Principal Scientist, Protein Sciences to head our protein sciences group and drive cutting-edge therapeutic antibody development, with a focus on bispecific formats. Our core mission is to

They will also be responsible for mentoring internal process chemistry scientists and promote the department through publications in peer reviewed journals and participation in external conferences. They will have a strong interest in laboratory work and will be key to driving the development of saf

US Navy Ship Anti-Submarine Warfare (ASW) Readiness and Effectiveness Measuring (SHAREM) at Surface and Mine Warfighting Development Center (SMWDC) in.This position is associated with an upcoming contract that THOR is pursuing, with an estimated award/work start late 2025.We are conducting prelimina

Maintain safe, compliant laboratory operations and good housekeeping (5S); participate in EHS initiatives. Onsite laboratory role with routine handling of chemicals and analytical instrumentation.

Lab Services Field Operations Manager.It's fun to work in a company where people truly believe in what they're doing!.We're committed to bringing passion and customer focus to the business.The pay rate or range for this position is: $70,000 per year.This position has ownership and accountability to

Maintain safe, compliant laboratory operations and good housekeeping (5S); participate in EHS initiatives. Onsite laboratory role with routine handling of chemicals and analytical instrumentation.

Assist during internal and external laboratory inspections, to ensure compliance with applicable federal, state and local regulations and company standards. Ensure Laboratory Occurrence Management (LOM) forms are completed for anomalies; organize and implement corrective action procedures as necessa

Maintain safe, compliant laboratory operations and good housekeeping (5S); participate in EHS initiatives. Onsite laboratory role with routine handling of chemicals and analytical instrumentation.

The Lab Manager will manage a team of Mold and Asbestos Analysts and other Laboratory staff, provide leadership and be responsible for ensuring compliance of laboratory operations. Assists in pursuing, receiving, and maintaining necessary laboratory accreditations. Minimum 3 years of previous hands

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 soluti

Engineering Services (Lab Manager).Lab Specialist to oversee the daily operations of our test labs that support Tactical Data Link (TDL) contracts.The Lab Manager will be responsible for ensuring compliance with all safety and regulatory standards, maintaining equipment, managing supplies, and suppo

Design and execute laboratory testing according standard procedures, make observations and interpret findings Conduct experiments under defined conditions to verify/reject various types of hypotheses using refined scientific methods Organize and store all chemicals substances, fluids and compressed

Assistants provide general support functions within the pre-analytic and analytic laboratory departments such as clerical and laboratory assistant duties to support overall operation of the lab. Summary: The main function of a laboratory pre-analytics services assistant is to be responsible for proc

Come join our collaborative and creative group of AI scientists and machine learning engineers and build models that directly affect hundreds of thousands of our customers.

Provide technical guidance and mentorship to junior scientists and quality engineers. Proficient in laboratory techniques relevant to Hologic’s products (e. We are hiring a highly motivated Scientist 2 in our Diagnostic division, Quality Technical Investigations (QTI) team.

The Principal Data Scientist Machine Learning/Deep Learning is a primary driver in the design and development of state-of-the-art Artificial Intelligence solutions for medical applications. This position works closely with senior data scientists, machine learning engineers, software engineers and su

Work with software engineers and data scientists to develop and utilize data pipelines to develop algorithms and/or ML models applicable to the stated sensor domains. Leidos currently has an exciting opportunity for a Principal Scientist to lead the development of Human-Machine Teaming solutions for

Records all experimental findings in a laboratory notebook, and analyzes and interpret experimental findings.

The Principal Data Scientist Machine Learning/Deep Learning is a primary driver in the design and development of state-of-the-art Artificial Intelligence solutions for medical applications. This position works closely with senior data scientists, machine learning engineers, software engineers and su

Zoologist Job Duties: Conducts research on animal behavior, habitats and population trends.Contributes to scientific journals through research and scholarly articles.Studies effects of

Director/Senior Director, Clinical Scientist. Applied Sr Data Scientist - Fintech Foundation. Data Scientist – Python | PySpark | MLflow | Predictive Maintenance | Audit Analytics (Hybrid).