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9 Hours AgoSaved
In-Office
Redwood City, CA, USA
Mid level
Mid level
Biotech
The Logistics Coordinator supports Lab Operations by managing external sample logistics, coordinating with project leads, and maintaining sample inventory and registration.
Top Skills: BenchlingElectronic Laboratory Notebook SystemsProficient With Ms Office
2 Days AgoSaved
In-Office
Redwood City, CA, USA
Senior level
Senior level
Biotech
Lead quality assurance activities for cell and viral banks and drug products, ensuring compliance with cGMP and regulatory requirements, and collaborate cross-functionally for lot disposition.
Top Skills: CgmpElectronic Quality Management SystemsIch GuidelinesMastercontrol
4 Days AgoSaved
In-Office
Redwood City, CA, USA
Senior level
Senior level
Biotech
The Technical Development Scientist will design experiments for gene therapy product development, optimize processes, analyze data, and collaborate cross-functionally to ensure compliance and quality.
Top Skills: AavAnalytical AssaysBioreactorsCgmpInsect Cell-Baculovirus Expression TechnologyPcr
Reposted 12 Days AgoSaved
In-Office or Remote
Redwood City, CA, USA
Senior level
Senior level
Biotech
Support design and execution of clinical development activities for ophthalmology trials: protocol writing, vendor/CRO oversight, medical monitoring, data review/interpretation, regulatory document contributions, and cross-functional collaboration.
Top Skills: Electronic Data CaptureJ-ReviewExcelMicrosoft PowerpointMicrosoft WordRave
Reposted 21 Days AgoSaved
In-Office or Remote
Redwood City, CA, USA
Senior level
Senior level
Biotech
Manage end-to-end clinical cold-chain logistics for cGMP materials—design shipping lanes, oversee couriers, customs, temperature control, inventory, excursion investigations, SOPs, vendor performance, and ensure regulatory compliance for international shipments.
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Reposted 21 Days AgoSaved
Hybrid
Redwood City, CA, USA
Expert/Leader
Expert/Leader
Biotech
Provide QA leadership and independent oversight of QC activities for drug substance/product and release testing. Ensure cGMP compliance, data integrity, method lifecycle management, investigations, change control, CAPAs, and inspection readiness while partnering with QC and cross-functional teams.
Reposted 21 Days AgoSaved
In-Office or Remote
Redwood City, CA, USA
Senior level
Senior level
Biotech
Lead design, validation, and lifecycle management of IRT systems for clinical trials. Translate protocol into IRT specifications, govern change control, manage vendor relationships, lead UAT/validation, monitor live performance, troubleshoot shipments and inventory, ensure regulatory inspection readiness, and align cross-functional teams on supply strategy and IRT operations.
Top Skills: Data Analytics ToolsIrt
23 Days AgoSaved
Hybrid
Redwood City, CA, USA
Expert/Leader
Expert/Leader
Biotech
The QA Project Manager leads quality assurance efforts for clinical projects, ensuring compliance with regulations and effective cross-functional collaboration.
Top Skills: Cell CultureGmp ComplianceProject Management ToolsQuality AssuranceRisk Management PrinciplesViral Vector Manufacturing
25 Days AgoSaved
Hybrid
Redwood City, CA, USA
Mid level
Mid level
Biotech
The Quality Control Analyst will conduct release testing for clinical products, analyze data, guide junior staff, and engage in method validation and troubleshooting.
Top Skills: Ce-SdsDlsElisaEmpower SoftwareHplcMass SpectrometryQpcrSec
25 Days AgoSaved
Hybrid
Redwood City, CA, USA
Senior level
Senior level
Biotech
The QC Project Manager will manage Quality Control project timelines, coordinate cross-functional activities, identify risks, facilitate meetings, and ensure effective communication among stakeholders in a GMP environment.
Top Skills: MS OfficeMicrosoft Project
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