Principal Software Engineer – TeraWave RF and Optical Systems Blue OriginPrincipal Software Engineer – TeraWave RF and Optical SystemsSan Diego, Washingtonand/or transports placardable amounts of hazardous materials by ground in any vehicle on a public road while in commerce, may be subject to additional Federal Motor Carrier Safety Regulations including: Driver Qualification Files, Medical Certification (obtained before onboarding), Road Test, Hours of Service, Drug and Alcohol Testing, vehicle inspection requirements, CDL requirements (if applicable) and hazardous materials transportation/shipping training. Required for Certain Job Profiles: Drivers who operate Commercial Motor Vehicles with a Gross Vehicle Weight (GVW), Gross Vehicle Weight Rating (GVWR) or combination of power unit and trailer that meets or exceeds 10,001 lbs.
Senior Machine Learning Engineer LeidosSenior Machine Learning EngineerVista, California$107,900–$195,050 / yearWe are seeking a Senior Machine Learning Engineer to work on MLOPS that support the testing, and release of object detection algorithms for our portfolio of products that help safeguard the flow of cargo and vehicles through ports and borders worldwide. Leidos’ Security Enterprise Solutions (SES) operation is seeking a motivated and talented Senior Machine Learning Engineer to join our multidisciplinary, highly energized, and expert data science team.
Senior Machine Learning Engineer Leidos Holdings Inc.Senior Machine Learning EngineerVista, CA$107,900–$195,050 / yearWe are seeking a Senior Machine Learning Engineer to work on MLOPS that support the testing, and release of object detection algorithms for our portfolio of products that help safeguard the flow of cargo and vehicles through ports and borders worldwide. Leidos' Security Enterprise Solutions (SES) operation is seeking a motivated and talented Senior Machine Learning Engineer to join our multidisciplinary, highly energized, and expert data science team.
Engagement Manager Inizio Partners CorpEngagement ManagerSan Diego, CaliforniaPartner closely with the manual underwriting team to build a hybrid risk framework that integrates analytical strategies with expert manual review, ensuring consistent execution and continuous feedback loops. 7+ years of hands-on experience designing, calibrating, and managing credit strategies for cash advance / short-duration small business credit products; prior MCA credit strategy experience.
In Vivo Operations Specialist PharmaronIn Vivo Operations SpecialistCarlsbad, CA$80,000–$100,000 / yearFull timeWhat We're Looking For:Bachelor's degree + 5 years relevant experience, or Master's degree + 1–3 years relevant experienceExperience in laboratory, preclinical, CRO, or vivarium environmentsExperience coordinating operations or projects in fast-paced settingsStrong organizational and communication skillsProficiency with Microsoft Office (Excel, Word, Outlook)Anesthesia, analgesia, and peri-operative care experienceProtocol/report writing experienceSponsor-facing or client-facing experienceWhy Pharmaron? 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.
Engineer III Scientific Research CorporationEngineer IIISan Diego, CaliforniaFull timeExperience/knowledge with the following data and communications link equipment and related systems: Link-16, Link-11, Tactical Digital Data Information Link (TADIL-J), Common Shipboard Data Terminal Set (CSDTS), Joint Range Extension (JRE), Link Monitoring and Management Tool (LMMT), Joint Tactical Radio System (JTRS), and Tactical Network Targeting Topology (TTNT). About Us: Scientific Research Corporation is an advanced information technology and engineering company that provides innovative products and services to government and private industry, as well as independent institutions.
Decision Analytics Consultant- Emerging Pharma ZSDecision Analytics Consultant- Emerging PharmaSan Diego, CaliforniaYou’ll work directly with client leadership on critical decisions ranging from first product launches to portfolio and growth strategy, leveraging advanced analytics, structured problem-solving, and strategic thinking to drive commercial success in fast-evolving healthcare markets. As a management consulting and technology firm focused on improving life and how we live it, we transform ideas into impact by bringing together data, science, technology and human ingenuity to deliver better outcomes for all.
Comp Bio voyant-bio.comComp BioSan Diego, CaliforniaThe Role: We are looking for a founding Machine Learning/Computational Biology scientist to lead our technical efforts, focusing on multi-modal single-cell geomics, spatial data analysis, and method development. This role requires hands-on experience in Python for microscopy data analysis and single-cell genomics, as well as expertise in large-scale data management in cloud environments.
Sample Management Technician BioAgilytixSample Management TechnicianSan Diego, CALight to moderate lifting and carrying (or otherwise moving) objects, including laboratory samples, laboratory equipment, and laptop computer, with a maximum lift of 30 pounds. Repetitive hand movement of both hands with the ability to make fast, simple, repeated movements of the fingers, hands, and wrists to operate lab and office equipment.
Lab Assistant - Undergraduate Internship Eitr Biologics, Inc.Lab Assistant - Undergraduate InternshipSan Diego, CA$36,920Eitr has fostered a robust and highly collaborative worldwide network of academic and government laboratories that share our scientific goal to address unmet public health needs. Bending, Stooping, and Reaching: Employees may be required to bend, stoop, and reach to access equipment, samples, or materials on upper or lower shelves or within laboratory hoods.
Senior Software Engineer SatomicSenior Software EngineerSan Diego, CaliforniaStrong Python (backend) and TypeScript/React (frontend) required , paired with genuine enthusiasm for the craft of software engineering and a demonstrated ability (or clear eagerness) to pick up new languages and reach for the right tool, whether that's Rust, Go, C++, or something else. The strongest engineers we know treat languages as instruments, comfortable across the stack today and equally ready to pick up a performance-oriented language like Rust, Go, or C++ (or something else entirely) when a problem calls for it.
Associate Director, In-Vivo Pharmacology Bristol Myers SquibbAssociate Director, In-Vivo PharmacologySan Diego, CA$190,539–$230,888 / yearBased on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day. The ideal candidate combines deep expertise in oncology in‑vivo pharmacology with a strong sense of ownership, practical decision‑making, and comfort operating at the intersection of science, operations, and compliance in a fast‑moving biotech environment.
Associate Director, Business Insights and Analytics Crinetics PharmaceuticalsAssociate Director, Business Insights and AnalyticsSan Diego, CaliforniaEnable senior management to make informed, data-based driven decisions by providing business analysis and analytical support, particularly in areas where data is difficult to assess/unreliable and a high level of analytical skill is required. 12 years of professional experience with 7 years of related experience working in marketing sciences, forecasting, or business analytics function within a biotech/pharmaceutical company or consulting firm.
Director, Biology Group Lead Bristol Myers SquibbDirector, Biology Group LeadSan Diego, CA$227,418–$275,577 / yearThe role will also provide strategic leadership in the development of quantitative pharmacology and target engagement platforms, ensuring robust biochemical and cellular characterization of drug-target interactions to support target validation, lead optimization, and candidate selection across the radiopharmaceutical portfolio. Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day.
Medical Director, Enfortumab Vedotin PfizerMedical Director, Enfortumab VedotinSan Diego, PennsylvaniaWorking in close partnership with Clinical Scientists, Worldwide Medical, Translational Oncology, Biostatistics, Safety, Regulatory, and other cross-functional stakeholders, the Medical Director will help generate evidence that addresses both regulatory requirements and the evolving needs of patients, healthcare providers, and healthcare systems. Candidate demonstrates a breadth of diverse leadership experiences and capabilities including: the ability to influence and collaborate with peers, develop and coach others, oversee and guide the work of other colleagues to achieve meaningful outcomes and create business impact.
Senior Product Analyst Flock FreightSenior Product AnalystEncinitas, CaliforniaFlock Freight is the largest Shared Truckload (STL) freight brokerage in the U.S., transforming underutilized truckload capacity into tangible value: cost savings for shippers, increased earnings for carriers, and a smaller carbon footprint. Their AI-powered, patented pooling technology optimizes across Flock’s entire customer network, combining shipments from thousands of businesses into efficient Shared Truckloads.
Sr/Exec Director Clinical Development ErascaSr/Exec Director Clinical DevelopmentSan Diego, CAThis person will work closely with cross-functional teams in the management and execution of the Clinical Development Plan (CDP), in developing innovative and efficient solutions to medical and scientific clinical trial issues, and in ensuring the successful execution and completion of clinical trials. Key clinical deliverables include document development (INDs, Protocols, IBs, applicable regulatory documents, etc.), medical and scientific input into the development of deliverables required for study activation and study conduct (CRFs, SAP, data listings, etc.), data review, and other deliverables as needed.
POSTDOCTORAL ASSOCIATE - Andersen Lab Scripps ResearchPOSTDOCTORAL ASSOCIATE - Andersen LabSan Diego, CA$70,304–$75,353 / yearPart timeThe Andersen lab is working on diverse projects using genomics approaches and high-throughput experiments to study emerging viruses and the outbreaks they cause, including arenaviruses, filoviruses, coronaviruses, influenza viruses, orthopoxviruses, and arboviruses. Of most interest are candidates with experience in developing computational frameworks and tools for multimodal data integration, projection of infectious disease trends, optimization of response strategies, or LLM-assisted analyses and visualizations.
POSTDOCTORAL ASSOCIATE - Andersen Lab - Translational Medicine Scripps ResearchPOSTDOCTORAL ASSOCIATE - Andersen Lab - Translational MedicineSan Diego, CA$70,304–$75,353 / yearPart timeWe are looking for a computational postdoc with experience and/or interest in developing AI-enabled large-scale surveillance tools that integrate genomic data with functional in vitro and in silico readouts, including high-throughput deep mutational scanning, and deploying these tools through outbreak.info. D. in computational biology, epidemiology, applied mathematics, computer science, or related field, or an equivalent combination of education, training and/or experience from a recognized institution of higher learning.
Director, Drug Safety & Pharmacovigilance Xencor, Inc.Director, Drug Safety & PharmacovigilanceSan Diego, CARemote$206,000–$255,000 / yearThorough understanding of the drug development process in relation to safety surveillance activities in clinical trialsAbility to establish effective working relationships with people in a wide variety of disciplines and backgroundsAbility to manage and prioritize multiple projects and demands simultaneously, rapidly adjust to changing priorities, and work effectively under pressureKnowledge and understanding of all relevant global PV regulations, FDA, EU and ICH guidelines, initiatives and regulations governing clinical trial safety environmentsFamiliarity with Argus safety databaseKnowledge and training on MedDRA dictionary with relevance to adverse event codingExcellent interpersonal skills and professionalismExcellent time management and organizational skillsStrong analytical, assessment and problem-solving skillsAbility to read, analyze and interpret complex clinical data and informationAbility to demonstrate competencies applicable for job based on Xencor's Leadership Competency ModelAbility to effectively manage others through coaching and supervision, in accordance with company policies and practices. Reviews and provides safety functional input for development of protocols, IBs, ICFs, CSRs and other relevant study documentsActs as lead author for aggregate safety reports (e.g., DSURs)Leads efforts related to ad hoc and routine signal evaluationProvides Drug Safety/PV subject matter expertise on cross-functional platforms and teams throughout the companyProvides end to end Drug Safety/PV support for assigned products including study start up activities, vendor plans, signal detection plans, SAE review, aggregate data review, signaling, aggregate authoring including DSURs, annual core product document updates (IB, ICF), and CSR authoring as well as informed consent forms, integrated summaries of safety, marketing applications and other regulatory submission documents on assigned products.