NewPrincipal Clinical Scientist DanaherPrincipal Clinical ScientistLos Angeles, CA$120,000–$165,000 / yearThe essential requirements of the job include: Bachelor's degree in Life Sciences, Healthcare, or a related field with 9+ years of experience in clinical research, specifically with significant experience in US and/or EU trials, or a Master's degree with 12+ years of experience or Doctoral degree with 4+ years of same experience. It would be a plus if you also possess previous experience in: Experience in study designs for diagnostic technologies (IVD) is highly preferred, specifically for Clinical Chemistry, Immunoassays, Hematology, Urinalysis, Flow Cytometry, and/or Biomarkers.
Relationship Manager Business Banking Sr City National BankRelationship Manager Business Banking SrEncino, CARemote$92,114–$156,880 / yearThis may be accomplished through active calling efforts and referrals from existing customers and line colleagues from Personal & Business Banking and other divisions and by providing the CNB exemplary level of service identifying and promoting solutions to customer needs and maintaining an active calling program. Additional Qualifications: Preferred to be in good standing under The Secure and Fair Enforcement for Mortgage Licensing Act of 2008 (Safe Act) and be registered/licensed with the Nationwide Mortgage Licensing System and Registry (NMLS) or must be able to be registered under the Safe Act.
Technical Specifications Manager - Raw Materials AmgenTechnical Specifications Manager - Raw MaterialsThousand Oaks, CaliforniaIn addition to the base salary, Amgen offers a Total Rewards Plan, based on eligibility, comprising of health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities that may include: A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts. The Technical Specifications Manager works closely with Process Development, Material Sciences, Engineering, Quality Assurance, Quality Control, Supply Chain, Regulatory Affairs, and external suppliers to translate technical and manufacturing requirements into clear, compliant, and effective raw material specifications.
National Account Director (GPO): Cencora/Cardinal Les Laboratoires Servier SASNational Account Director (GPO): Cencora/CardinalCA$204,000–$249,000 / yearThe NAD will be able to leverage existing relationships with individuals in leadership and purchasing decision-making roles to inform clinical and financial decisions impacting access to and utilization of Servier's portfolio of current and future medicines. Leverage insights derived from customer interactions and cross-functional collaboration within Servier as a cornerstone to leading strategic oncology portfolio account planning, alignment with field sales, and identification of areas for collaboration.
Project Management Coordinator Lief LabsProject Management CoordinatorValencia, CA$26–$35 / hourOur world-class R&D and Product Development teams create innovative, great-tasting formulations, while our state-of-the-art cGMP manufacturing facility delivers scalable, turnkey solutions that help entrepreneurial companies build and grow successful brands. This is an exciting opportunity to partner with teams across Product Development, Finance, Quality, Operations, and Regulatory Affairs while building your project management expertise and making a meaningful impact on innovative product launches.
Global Patient Safety Business Excellence, Senior Manager AmgenGlobal Patient Safety Business Excellence, Senior ManagerThousand Oaks, CaliforniaRemoteIn addition to the base salary, Amgen offers a Total Rewards Plan, based on eligibility, comprising of health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities that may include: A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts. As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients.
Senior GCP Auditor ImmunityBio IncSenior GCP AuditorEl Segundo, CAImmunityBio, Inc. (NASDAQ: IBRX) is a commercial-stage biotechnology company developing cell and immunotherapy products that are designed to help strengthen each patient's natural immune system, potentially enabling it to outsmart the disease and eliminate cancerous or infected cells. ImmunityBio is developing cutting-edge technology with the goal to transform the lives of patients with cancer and develop next-generation therapies and vaccines that complement, harness and amplify the immune system to defeat cancers and infectious diseases.
Manager, Quality Assurance - Microbiology and Sterility Assurance Cardinal Health IncManager, Quality Assurance - Microbiology and Sterility AssuranceCA$105,100–$150,100 / yearEnvironmental Monitoring Program Management: Managing and continuously improving the Environmental Monitoring Program, which involves data review, trend analysis, investigations, and CAPA implementation for Environmental Monitoring results including establishing, maintaining, and periodically assessing environmental monitoring alert and action limits to ensure effective process control. Subject Matter Expertise: Serve as the microbiology and sterility assurance Subject Matter Expert (SME) for Quality, Compliance, Product Development and Manufacturing, providing technical leadership and guidance while supporting regulatory inspections, customer audits, and internal corporate assessments.
Patient Access Liaison - Long Beach, CA AmgenPatient Access Liaison - Long Beach, CAThousand Oaks, California$158,394–$193,988 / yearIn addition to the base salary, Amgen offers a Total Rewards Plan comprising health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities including: Comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts. The Patient Access Liaison (PAL) is a field-based patient access and reimbursement specialist responsible for supporting patients, caregivers, healthcare providers, and sites of care in navigating insurance coverage and reimbursement pathways for Amgen therapies.
Nplate Patient & Growth Marketing AmgenNplate Patient & Growth MarketingThousand Oaks, CaliforniaChampion Lifecycle Value Lab (LVL) innovation by participating in commercial experiments on behalf of the Nplate brand, evaluating marketing performance and customer insights, documenting key learnings, and identifying opportunities to optimize commercial execution and inform scalable best practices for the group. Reporting to the Nplate Brand Director, you will play a highly visible role partnering across Marketing, Medical, Sales, Market Access, Advocacy and Commercial Data & Analytics (CD&A) teams to accelerate growth, enhance customer engagement, and develop scalable commercial capabilities for the future.
NewClinical Project Manager Abbott LaboratoriesClinical Project ManagerSylmar, CA$100,000–$200,000 / yearFacilitates communication between R&D, Regulatory Affairs, Sales and Marketing, Training, Senior Management and investigational sites by conducting team meetings, drafting and sending routine correspondence (e.g., newsletters) and by presenting regular updates to mgmt staff. Whether it's glucose monitoring system, innovative therapies for treating heart disease, or products that help people with chronic pain or movement disorders, our medical device technologies are designed to help people live their lives better and healthier.
Design Control Process Manager iRhythm Holdings IncDesign Control Process ManagerCARemote$151,000–$196,000 / yearCreate a scalable implementation plan for deployment of new and updated design control requirements across new product development, sustaining engineering, remediation, and product-change activities. Evaluate the effectiveness of design control processes and recommend updates based on product-development needs, quality data, regulatory expectations, audit observations, and industry best practices.
Chemist II LancesoftChemist IINorthridge, CA$40In this role, you will support analytical testing, method development, validation, and troubleshooting activities for pharmaceutical and/or medical device products. Required Qualifications Bachelor's degree in Chemistry, Analytical Chemistry, Biochemistry, Pharmaceutical Sciences, or a related scientific discipline.
Associate Director, Communications and Public Relations Pepperdine UniversityAssociate Director, Communications and Public RelationsCalabasas, CaliforniaThe University conducts such screenings in compliance with applicable laws and with the objectives of evaluating risk and supporting a safe environment for students, faculty, staff, and guests; safeguarding key University assets including people, property, information, and the University’s reputation; and providing comprehensive job-related information to University leaders to enable them to make prudent hiring decisions. Integrated Marketing Communications is directly tasked with supporting the University’s mission and strategic plan by building brand equity, elevating the University’s national reputation, providing strong and consistent institutional message leadership, and implementing effective integrated marketing and communications strategies.
Director Product Quality Leader AstraZeneca PlcDirector Product Quality LeaderSanta Monica, CA$167,595.20–$251,392.80 / yearThe Cell Therapy Product Quality Leader (PQL) is a matrixed leader responsible for the end-to-end product quality strategy and lifecycle management of autologous, allogeneic, and in-vivo cell therapy products. Work cross-functionally to develop and implement platform approaches for specifications, comparability, and stability to enable consistent, scalable practices across multiple cell therapy products.
NewDirector, Safety Physician Summit Therapeutics IncDirector, Safety PhysicianCA$190,000–$237,000 / yearHARMONi: Phase 3 clinical study which was intended to evaluate ivonescimab combined with chemotherapy compared to placebo plus chemotherapy in patients with EGFR-mutated, locally advanced or metastatic non-squamous NSCLC who were previously treated with a 3rd generation EGFR TKI. Primary responsibilities include medical review of individual case safety reports (ICSRs), strategic input for adverse event monitoring and signal detection, ensuring global pharmacovigilance regulatory requirements are met, and safeguarding patients enrolled in our trials or administered our products.
NewClinical Trial Liaison, Director - West AstraZeneca PlcClinical Trial Liaison, Director - WestCA$211,111.20–$316,666.80 / yearThe role is accountable for recommending priority site selection, and setting up a clear field plans consistent engagement expectations across US strategic research centers increasing the consistency, impact, and speed of site-facing medical support for new and ongoing clinical studies across AstraZeneca marketed products, new indications, and compounds in development, including priorities across Cardiovascular, Renal and Metabolic; Respiratory, Immunology; and Vaccines and Infectious Disease. The Regional Director, Clinical Trial Liaison Team will lead and manage a field-based Clinical Trial Liaison team responsible for strengthening scientific engagement with strategic clinical research sites, improving investigator understanding of AstraZeneca trials and pipeline, and helping reduce practical barriers to study start-up, screening, enrollment, referral, and retention.
Medical Science Liaison - West Revance Therapeutics IncMedical Science Liaison - WestCA$175,000–$190,000 / yearMinimum Required: Minimum of 3 years MSL experience (5 years preferred); preferably with expertise in neuromodulators (botulinum toxin/neurotoxins/movement disorders) and/or other relevant specialties, and minimum of 5 years post professional degree, practice, or relevant transferrable experience (e.g., clinical practice, academic research, regulatory/scientific). Responsibilities/Essential Duties: Identify and develop relationships with international, national, regional, local, and emerging medical / scientific Thought Leaders (TLs), academic centers, and researchers consistent with the strategy and objectives of Revance Medical Affairs.
Director of Licensing Valar AtomicsDirector of LicensingTorrance, California$204,545–$300,000 / yearThe Director sets regulatory strategy, builds and leads the licensing organization, owns the licensing processes and infrastructure, and serves as the senior company interface with regulators across DOE and NRC engagement pathways. Fifteen (15) or more years of nuclear licensing and regulatory affairs experience, or related experience, including leadership of licensing teams and direct interaction with regulators.
Scientific Director Amgen Inc.Scientific DirectorThousand Oaks, CAIn addition to the base salary, Amgen offers a Total Rewards Plan, based on eligibility, comprising of health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities that may include: A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts. As the Scientific Director and functional leader for Product Stewardship Toxicology, you will provide strategic scientific direction while building and continuously improving toxicology programs that support Amgen's product portfolio from early development through commercialization and post-market lifecycle management.