CRISPR TherapeuticsNASDAQ: CRSP: Public biopharmaceutical developing gene-based medicines for patients with serious human diseases.
2+ YOEExperience in gene editing, immunology, cloning, ddPCR, flow cytometry, primary T cell culture, and quantitative biology; PhD or equivalent experience; strong teamwork and communication skills.
ATUM: Biotechnology contract research organization providing gene design, protein engineering, and cell-line development services to biopharma clients worldwide.
Bachelor's in Biology, entry-level experience, ability to follow SOPs, operate automated liquid handlers, work weekends, lift up to 25lbs, strong communication and organization.
Merge Labs: Private brain-computer interface research laboratory developing high-bandwidth, AI-integrated technologies for patients and broader human capability.
Ph.D. or equivalent research experience in bioengineering or related field; hands-on focused ultrasound gene delivery experience; expertise in gene delivery modalities, in vivo experiment design and evaluation; strong communication and collaboration skills.
Senior Scientist, Gene Editing Process Sciences (Contractor)
South San Francisco, California, United States
$60-$70/hrOnsiteContract
Allogene TherapeuticsNasdaq Global Select Market: ALLO: Clinical-stage biotechnology developing off-the-shelf allogeneic CAR T-cell therapies for cancer and autoimmune disease patients.
5+ YOEPhD and 5+ years, MS and 10+ years, or BS and 12+ years in biological sciences, engineering, or related fields; gene editing or delivery expertise, DOE, statistical analysis, data visualization, and cGMP knowledge.
Preventive: Private biotechnology research studying safe embryo gene editing to prevent severe genetic diseases before birth.
2+ YOEBS or higher in a relevant field,2+ years industry experience,demonstrated prime or base editing and molecular biology skills,proficiency in mammalian tissue culture,NGS and single-cell workflows,strong work ethic and ownership.
Senior Regulatory Affairs Director - Oncology Cell & Gene Therapy
South San Francisco, California, United States
$218k-$327k/yrHybridFull Time
AstraZenecaLondon Stock Exchange: AZN: Global science-led biopharmaceutical.
7+ YOEAdvanced science degree, 7–10 years of experience, cell or gene therapy regulatory strategy expertise, global regulatory knowledge, multiple myeloma development experience, and proven regulatory and cross-functional leadership.
Senior Regulatory Affairs Director - Oncology Cell & Gene Therapy
South San Francisco, California, United States
$218k-$327k/yrHybridFull Time
AstraZenecaLondon Stock Exchange: AZN: Global science-led biopharmaceutical.
7+ YOEAdvanced degree in a science field and 7+ years regulatory experience in cell and gene therapy; proven global regulatory strategy, leadership, health authority interaction, and product development experience (multiple myeloma preferred).
Cell and Gene Therapy Discovery Stage Project Manager
Stanford, California, United States
$120k-$153k/yrHybridFull Time
Stanford University: Private research university in Stanford, California.
7+ YOE5+ MgmtBachelor's degree plus 5+ years relevant experience (7+ preferred), 5 years team lead project management in research, knowledge of GLP and regulations, project management skills, budgeting, communication, and subject-matter expertise.
2027 Spring Intern - Product Technical Cell and Gene Therapy - Laboratory (Wet-Lab) Focus
South San Francisco, California, United States
$26-$40/hrOnsiteFull Time, Internship
Genentech: U.S.-headquartered biotechnology discovering and developing medicines for people with serious and life-threatening diseases.
Pursuing or holding an associate's, bachelor's, or master's degree in a listed science or engineering discipline; research lab or biotechnology experience preferred; strong communication and collaboration skills.
Scientist/Senior Scientist, CHO Cell Line Development
Newark, California, United States
$120k-$150k/yrOnsiteFull Time
ATUM: Biotechnology contract research organization providing gene design, protein engineering, and cell-line development services to biopharma clients worldwide.
0+ YOEPh.D. in a life sciences discipline, 0–3 years of experience, and demonstrated mastery of CRISPR, gene editing, molecular biology, and cell biology techniques.
Orca Bio: Late-stage biotechnology developing high-precision allogeneic cell therapies for patients with blood cancer and autoimmune diseases.
0+ YOEBachelor's degree in life sciences or a related scientific field; 0–2 years of experience; strong Excel and analytical skills; fluency with AI tools; interest in cell and gene therapy.
Microsoft Excel, Salesforce, Tableau, Microsoft Power BI, Enterprise Resource Planning (ERP), data warehouse, Customer Relationship Management (CRM), Claude, ChatGPT, Gemini, Python, SQL
Associate Director, Scientific & Medical Affairs (Contract)
Redwood City, California, United States
$65-$110/hrRemoteContract
Adverum BiotechnologiesNASDAQ: ADVM: Clinical-stage gene therapy targeting unmet medical needs in ocular and rare diseases.
5+ YOETerminal degree required, 5+ years industry experience preferred, publication experience, ophthalmology/gene therapy experience desired, strong scientific communication and presentation skills, Microsoft Office proficiency.
Microsoft Word, Microsoft PowerPoint, Microsoft Excel
Senti BioNasdaq: SNTI: Public clinical-stage biotechnology developing cell and gene therapies for patients with incurable diseases.
10+ YOEBA/BS in a scientific field, 10+ years regulatory CMC experience in pharma/biotech, strong knowledge of biologics regulations, leadership and agency interaction experience; gene/cell therapy experience preferred.
Senior Director / Executive Director, US Regulatory Strategy
United States or San Francisco
RemoteFull Time
VCLS (Voisin Consulting Life Sciences): Private life sciences consultancy helping biotech, pharmaceutical, and medical-device innovators develop products and reach regulated markets.
Degree in a life sciences discipline; significant industry experience with US FDA regulatory strategy for biologics, multiple BLA experiences, and experience with complex modalities (combination products, cell and gene therapies). Strong consulting and leadership skills.
5+ YOE5+ years industry experience in analytical development/characterization for biologics or cell/gene therapy; hands-on flow cytometry and functional assay development; IND-enabling study design, data documentation, and regulatory knowledge; advanced degree preferred.