Senior Imaging & Testing Specialist JBL ResourcesSenior Imaging & Testing SpecialistFremont, CAWorking here means joining a team of top technical professionals bringing cutting-edge products to the forefrontoffering driven individuals the opportunity to make a meaningful impact every day. JBL Resources is proud to have earned the reputation of being a premier provider of top talent professionals in the fields of engineering, human resources, logistics, operations, and supply chain management.
Bioinformatics Engineer, QDI Qiagen N.VBioinformatics Engineer, QDIRedwood City, CA$130,000–$150,000 / yearAs a Bioinformatics Engineer in the Content Development team, you will play a critical role in maintaining and extending QIAGEN's biomedical knowledge base by integrating new knowledge from public data sources and facilitating capture of unstructured data into existing and new semantic models, as well as leveraging our Knowledge Graph to deliver data, interpretations, and inferences to our applications and customers. Familiarity with bioinformatics tools in genome biomedical research (e.g., genomic databases, genome browsers, mutation repositories), or integrative data analysis as it relates to genetics, multiomics, cell biology, physiology and pathology.
Biomechanics Researcher 1XBiomechanics ResearcherSan Carlos, CaliforniaDefine what human-level performance means in quantitative, engineering-relevant terms and translate those insights into specifications that guide the development of humanoid robots. We are rigorous about identifying the gap between current robotic performance and human capability, then developing the technologies required to close it.
Senior Manager, Quality Assurance Vera Therapeutics Inc.Senior Manager, Quality AssuranceBrisbane, CAQualifications: Bachelor's degree with 10+ years of experience in biomedical engineering, chemical engineering, pharmaceutical sciences, or a related field or a Master's degree with 7+ years of experience in biomedical engineering, chemical engineering, pharmaceutical sciences, or a related field. Excellent written and verbal communication skills, including demonstrated ability to effectively communicate in a project team environment, within department, among functional groups and among external collaborators.
Sr. Quality Engineer Inquis Medical, Inc.Sr. Quality EngineerSan Francisco, CA$120,000–$145,000 / yearThis role partners closely with Engineering, Manufacturing, Operations, Regulatory Affairs, Supply Chain, and R&D to ensure products are designed, manufactured, and maintained in compliance with FDA regulations, ISO 13485, ISO 14971, and other applicable regulatory requirements. Lead Design Assurance activities in accordance with Design Controls (21 CFR Part 820/ISO 13485), including: design reviews, design verification & validation; design transfer, and Design History File (DHF) documentation.
Part-time Newborn Hearing Screener Infant Hearing Screening SpecialistsPart-time Newborn Hearing ScreenerOakland, CA$23–$25 / hourWhile performing hearing screens, the Newborn Hearing Screener will follow IHSS and hospital policies and procedures, including, but not limited to infection prevention and control, safety awareness, and quality assurance. When possible, perform hearing screens on infants in the best possible testing conditions (while infant is sleeping, testing environment is quiet, lights are dimmed).
NewDirector of Regulatory Affairs Epia NeuroDirector of Regulatory AffairsAlameda, CaliforniaWe're looking for a Director of Regulatory Affairs, based in our Alameda, California office, to own the regulatory strategy and execution for Epia Neuro's Class III implantable neurotechnology - end-to-end, from early FDA engagement through IDE and PMA submission, approval, and commercialization. Partner directly with engineering on design and software decisions during active development, not reviewing after the fact, and help cross-functional alignment across development, clinical, quality, and operations to ensure activities support the regulatory strategy and requirements.
Post Doctoral Fellow Mass General BrighamPost Doctoral FellowBelmont, CaliforniaMcLean Hospital is seeking a Postdoctoral Research Fellow with a primary focus on investigating the neurobiology of posttraumatic stress disorder (PTSD) and related emotional disorders using magnetic resonance imaging (MRI), including functional MRI. The position offers substantial opportunities for scientific development, including leading manuscripts, presenting findings at national and international conferences, contributing to grant applications, developing new research questions using existing datasets, and building an independent program of research.
NewData Engineer UCSF Medical CenterData EngineerSan Francisco, CASpecifically, the Data Analyst will work with EIA (Enterprise Information Analytics), data governance staff, business analysts, end users, data owners, and technical teams to: Collaborate with business and technical stakeholders to understand data, reporting, and analytics needs. The Enterprise Analytics Information - Health Operations department functions as the liaison between the customer or partners in the organization and technical resources to provide optimal analytic solutions to solve problems, answer questions, deliver insights, and meet the needs of our customers.
Technical Lead - Software Developer, Data Foundry Eli Lilly and CompanyTechnical Lead - Software Developer, Data FoundrySan Francisco, CA$151,500–$244,200 / yearData Foundry is a multidisciplinary team within DTP that enables AI-native drug discovery through four integrated pillars: Architecture4Insight (data infrastructure and scientific software), Methods4Insight (analytical and computational methods), Automation & Scale4Insight (lab automation and agentic workflows), and Preparedness4Insight (data governance and readiness). Our current groups include: Africa, Middle East, Central Asia (AMECA), Black Employees at Lilly (BE@Lilly), Chinese Culture Network (CCN), EnAble, Evolve, Lilly Indian Network (LIN), Organization of Latinx at Lilly (OLA), Pride (LGBTQ+ Allies), Veterans Leadership Network (VLN) and Women's Initiative for Leading at Lilly (WILL).
Scientist, Drug Product Development NewLimitScientist, Drug Product DevelopmentSouth San Francisco, CA$113,000–$171,000 / yearThe ideal candidate possesses a deep technical understanding of LNP assembly via various mixing methods, expertise in downstream purification, and hands-on experience with advanced analytical characterization techniques. Learn more at: https://www.newlimit.com/careers *This compensation and benefits information is based on Company's good faith estimate as of the date of publication and may be modified in the future.
Sr. Principal Chemist Eli Lilly and CompanySr. Principal ChemistConcord, CA$115,500–$169,400 / yearOur current groups include: Africa, Middle East, Central Asia (AMECA), Black Employees at Lilly (BE@Lilly), Chinese Culture Network (CCN), EnAble, Evolve, Lilly Indian Network (LIN), Organization of Latinx at Lilly (OLA), Pride (LGBTQ+ Allies), Veterans Leadership Network (VLN) and Women's Initiative for Leading at Lilly (WILL). Headquartered in Indianapolis, Indiana, our over 50,000 employees around the globe take on complex challenges to discover and deliver life-changing medicines, strengthen how health is understood and managed, and support the communities we serve.
Senior Scientist, Cardiac Modeling InsitroSenior Scientist, Cardiac ModelingSouth San Francisco, CA$156,000–$166,000 / yearIn this role, you will own the development and application of iPSC-derived cardiomyocyte (iPSC-CM) models to study the genetic and molecular underpinnings of cardiovascular disease - working at the intersection of human stem cell biology, cardiac physiology, and scalable experimental platforms to generate the datasets that fuel our ML-driven drug discovery efforts. We work hard to bring together diverse teams-grounded in a wide range of expertise and life experiences-and work even harder to ensure those teams thrive in inclusive, growth-oriented environments supported by equitable company and team practices.
Principal Hardware Engineer - Fluidics - Pleasanton, CA CalyxoPrincipal Hardware Engineer - Fluidics - Pleasanton, CAPleasanton, CA$250,000–$270,000 / yearIndividually contribute to mechanical/electromechanical design for critical fluidics subsystem components and assemblies and provide expert design review of other team-members designs. This role focuses on the design and control of irrigation and aspiration systems, combining pumps, valves, sensors, tubing sets, and embedded software into safe and reliable products.
SMB Account Executive BenchlingSMB Account ExecutiveSan Francisco, CALife science background required - either a bachelor's degree in a life science discipline (e.g., molecular biology, biotechnology, biomedical engineering, biochemistry) or direct experience selling into pharma, biotech, or life science organizations). Proactively identify and engage new business opportunities across your territory, connecting with multiple personas - from bench scientists to business stakeholders - using outbound outreach, events, and creative prospecting strategies.
Customer Success Manager ZifoCustomer Success ManagerSan Francisco, CABe the Zifo Champion for Requests for Proposals from Customers; Work closely with Client Partners and/or own the response to RFP’s and work collaboratively with cross-functional stakeholders from Zifo including but not limited to Customer Success teams, Service Delivery Leadership, Product Partnership team, Subject Matter Experts etc., across geographies. We are looking for an individual who demonstrates strong commitment to proactive account management, maintains current revenue streams, consistently develops the revenue pipeline within the customer portfolio, and fosters successful, long-term partnerships with our clients.
Mfg. Engrs - Project Manager Viant MedicalMfg. Engrs - Project ManagerFremont, CAProduct areas (example: interventional/diagnostic medical devices; intravascular devices; bioelectronics devices)Risk Management, Manufacturing Quality and OperationsFinancial Budgetary Tracking and Reporting. COMPANY OVERVIEWViant Medical is a global medical device design and manufacturing services provider that partners and innovates with customers to provide the highest quality, life enhancing medical devices.
Director, Regulatory Affairs Companion Diagnostics (Cdx) Revolution Medicines, Inc.Director, Regulatory Affairs Companion Diagnostics (Cdx)Redwood City, CA$201,000–$251,000 / yearRequired Skills, Experience and Education: Advanced degree or bachelor's degree in life sciences, molecular biology, biomedical engineering, pharmacy, medicine, or related scientific discipline with a minimum of 12+ years of pharmaceutical, biotechnology, diagnostics, or combination product experience, including at least 8 years in Regulatory Affairs supporting companion diagnostics or in vitro diagnostics. This individual will serve as the regulatory lead for companion diagnostic development programs, partnering closely with Clinical Development, Translational Medicine, Biomarker Sciences, Regulatory Science, Commercial, and external diagnostic partners to ensure successful co-development and global registration of therapeutic products and associated companion diagnostics.
Post Doctoral Fellow Massachusetts General Physicians OrganizationPost Doctoral FellowBelmont, CaliforniaMcLean Hospital is seeking a Postdoctoral Research Fellow with a primary focus on investigating the neurobiology of posttraumatic stress disorder (PTSD) and related emotional disorders using magnetic resonance imaging (MRI), including functional MRI. The position offers substantial opportunities for scientific development, including leading manuscripts, presenting findings at national and international conferences, contributing to grant applications, developing new research questions using existing datasets, and building an independent program of research.
NewSr Prod Spec Cell Therapy Cell Culture - Berkeley, CA Bayer AGSr Prod Spec Cell Therapy Cell Culture - Berkeley, CABerkeley, CA$93,840–$140,760 / yearBayer seeks an incumbent who possesses the following: Required Qualifications: Bachelor's degree in a relevant life science or engineering discipline (e.g., Biotechnology, Cell Biology, Biochemistry, Biomedical Engineering or related field); 5-7 years of relevant experience in cell therapy, biologics, or advanced therapy medicinal product (ATMP) manufacturing, including hands‑on experience with mammalian cell culture and aseptic processing in a cGMP environment; Demonstrated expertise in end‑to‑end cell culture operations such as solution preparation, cell expansion and differentiation, cell banking, and drug product filling and packaging, including experience with single‑use technologies (SUT); Strong understanding of cGMP regulations, quality systems, documentation practices, and compliance expectations for clinical and launch‑stage products; Proven experience supporting or leading new product introductions (NPIs) and/or technology transfers into manufacturing, working closely with development and MSAT or equivalent functions; Proficiency in using data analysis and, where applicable, statistical process control tools to monitor, troubleshoot and optimize manufacturing processes; Experience authoring, reviewing and approving controlled documents (e.g., SOPs, batch records, work instructions) and supporting equipment commissioning and qualification activities. Preferred Qualifications: Advanced degree (e.g., Master's or PhD) in a relevant scientific or engineering discipline; More than 7 years of experience in clinical or commercial cell therapy manufacturing, including exposure to late‑stage and launch activities; Experience designing and delivering technical training curricula and acting as SME trainer for manufacturing teams; Demonstrated ability to lead cross‑functional initiatives, influence stakeholders outside of manufacturing, and represent manufacturing in audits, investigations and project forums; Strong communication, collaboration and coaching skills, with the ability to work effectively in a fast‑paced, highly regulated, and multidisciplinary environment; Experience with automation, electronic systems (e.g., MES, LIMS, electronic batch records) and continuous improvement methodologies to drive process robustness and efficiency; Willingness and ability to work flexible hours, including modified shifts and occasional off‑hours or weekend work, to support time‑critical manufacturing and surgical schedules.