Top Biotech Jobs in San Francisco, CA

The Regulatory Affairs Senior Specialist leads regulatory submissions and offers guidance on product development, ensuring timely launches and compliance with regulations.

The Clinical Sales Specialist provides technical sales support for medical products, conducts product demonstrations, training, and gathers customer feedback to enhance product offerings.

The Director of Executive Talent Planning will provide strategic talent insights, assess talent pipelines, and collaborate with HR and business leaders to align talent strategies with enterprise objectives.

The role involves developing cutting-edge AI/ML models for biology, leading research strategy, and mentoring. Requires expertise in machine learning methodologies and experience in biological data.

The Manager will oversee Genomics Hub operations, manage resources and teams, ensure workflow efficiency, and lead technology development and staff training.

As Head of Finance, you will oversee all financial operations, build scalable financial systems, and ensure transparency and efficiency while partnering with leadership.

As a Computational Protein Design Scientist, you will leverage generative AI to design proteins, improve models, and collaborate with lab teams for experimental validation.

Lead procurement and supply chain functions to develop and execute strategies for sourcing, supplier management, and logistics within Eikon Therapeutics.

Field-based pharmaceutical sales representative responsible for promoting and selling products within a defined territory, developing and executing territory plans, building relationships with physicians and healthcare providers, participating in sales meetings, and maintaining compliance and high ethical standards.

Develop and deploy computer-vision and ML pipelines for microscopy datasets, partner with biologists and engineers, benchmark and calibrate tools, extract disease-relevant phenotypes, and communicate results to cross-functional stakeholders.

The VP, Associate General Counsel will provide legal counsel on healthcare compliance, privacy, and regulatory matters, support commercialization efforts, and lead healthcare compliance programs while collaborating with executive teams.

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.

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.

Design and execute high-throughput molecular assay development studies, write SOPs and Design History File documentation, perform NGS data analysis and interpretation, implement assays for production (automation, QC, LIMS), transfer and train CLIA operators, mentor lab staff, and collaborate across automation, bioinformatics, clinical, regulatory, and marketing teams.

Perform hands-on assay development and optimization for high-throughput diagnostic platforms. Design experiments, write SOPs and Design History File documentation to meet FDA requirements, transfer assays to production, troubleshoot labs, and collaborate with automation, LIMS, bioinformatics, regulatory, and clinical teams.

Lead design, development, validation, and deployment of scalable NGS bioinformatics workflows for regulated diagnostics. Drive assay study design, ML/statistical evaluation, regulatory compliance, documentation, and mentor junior team members.