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Senior Scientist, Synthetic & Molecular Biology

BeiGene

San Carlos, CAOnsitePosted 1 day ago$136,600 - $170,700 annually
Full TimeSenior LevelResearch & ScientistBiotechnology
Original posting ↗

Summary

BeOne Institute extends BeOne's execution strength with a dedicated innovation engine, bringing agility and scientific depth to transform uncertainty into actionable and high-impact therapeutic opportunities. We are seeking a highly skilled and driven Senior Scientist with expertise in Molecular Biology and Synthetic Biology to join our early discovery group within our agile biotech ecosystem.

Job description

In this role, you will design, build, and optimize the next-generation genetic payloads that drive our cell therapy and RNA medicine platforms. You will serve as a core molecular biology expert, designing everything from individual targeted constructs to high-throughput pooled libraries for pooled screens and circuit optimization. While molecular biology is your primary core capability, you will work iteratively with cell biologists, immunologists, and cross-functional project teams to ideate and rapidly advance lead constructs from in silico concept to in vitro functional validation.

Essential Functions of the Job

  • Proactively propose and implement innovative synthetic biology strategies (e.g., gene circuits, inducible promoters, dual-vector logic, novel cell-surface receptors) to address therapeutic hurdles in oncology and immunology.
  • Design, execute, and troubleshoot modular molecular cloning workflows (Gibson, Golden Gate, site-directed, high-throughput assembly) spanning individual targeted constructs to large-scale pooled/arrayed DNA libraries for functional screens.
  • Design, transcribe, and characterize in vitro transcribed (ivT) RNA and optimize viral vector architectures (lentivirus, AAV) to maximize payload capacity, expression kinetics, and payload stability.
  • Evaluate and manage external vendor and CRO workflows (e.g., DNA synthesis, custom cloning, high-throughput plasmid preps, whole-plasmid sequencing), strategically balancing internal bench execution with outsourcing to optimize project timelines, cost, and bandwidth.
  • Maintain clean, traceably documented plasmid archives and map registries for team constructs, ensuring seamless cross-functional handoffs.
  • Work closely with cell biologists, immunologists, and screening teams to translate payload designs into mammalian functional assays (flow cytometry, qPCR, NGS, reporter readouts) and evaluate lead candidates.
  • Lead design reviews, incorporate cross-functional feedback to refine payload iterations.
  • Communicate results to project teams and discovery leadership.

Requirements

  • Ph.D., M.S., or B.S. degree in Molecular Biology, Synthetic Biology, Bioengineering, Cell Biology, Immunology, or a related scientific field, with 2+ years (Ph.D.), 7+ years (M.S.), or 9+ years (B.S.) of relevant industry, academic, or postdoctoral experience.
  • Advanced proficiency in molecular cloning strategy, high-throughput assembly methods, construct design, and library generation (regulatory elements, UTRs, promoters, synthetic receptors).
  • Demonstrated mastery of construct design software and electronic inventory management (Benchling, SnapGene), with exceptional organizational skills to track and maintain large libraries of plasmids and map files.
  • Strong practical knowledge of lentiviral vector design principles and mRNA ivT workflows.
  • Demonstrated experience interfacing with molecular biology vendors and CROs, with sound judgment on when to leverage external synthesis/cloning capabilities versus driving complex construct assembly in-house.
  • Proven track record of generating new scientific concepts, defining research strategies, executing complex benchwork independently, and actively seeking and integrating feedback from multidisciplinary teams.
  • Demonstrated ability to independently design and execute experiments, rigorously analyze data, and present results clearly.
  • Ability to work on site in San Carlos, CA.

Preferred

  • Familiarity with basic protein biology, structure-function relationships, or protein engineering principles to support receptor and circuit design.
  • Hands-on experience in lentivirus generation, titering, and transduction optimization.
  • Prior experience working in drug discovery or translational biology environments.
  • Familiarity with primary cell culture (especially T cells or NK cells), CAR/TCR engineering, immuno-oncology targets, or cell therapy platform development.
  • Experience with quantitative molecular and cellular readouts, including NGS library preparation, flow cytometry (FACS), qPCR, and reporter assays.
  • Basic programming skills in R or Python for biological data processing and analysis.

Requirements

  • Ph.D., M.S., or B.S. degree in Molecular Biology, Synthetic Biology, Bioengineering, Cell Biology, Immunology, or a related scientific field
  • 2+ years (Ph.D.), 7+ years (M.S.), or 9+ years (B.S.) of relevant industry, academic, or postdoctoral experience
  • Advanced proficiency in molecular cloning strategy, high-throughput assembly methods, construct design, and library generation
  • Demonstrated mastery of construct design software and electronic inventory management (Benchling, SnapGene)
  • Strong practical knowledge of lentiviral vector design principles and mRNA ivT workflows
  • Demonstrated experience interfacing with molecular biology vendors and CROs
  • Proven track record of generating new scientific concepts, defining research strategies, and executing complex benchwork independently
  • Demonstrated ability to independently design and execute experiments, rigorously analyze data, and present results clearly
  • Ability to work on site in San Carlos, CA

Benefits

  • Medical, Dental & Vision
  • 401(k)
  • FSA/HSA
  • Life Insurance
  • Paid Time Off
  • Wellness
  • Annual bonus plan
  • Discretionary equity awards
  • Employee Stock Purchase Plan

Company overview

BeiGene, Ltd., now rebranding as BeOne Medicines, is a global commercial-stage biotechnology company specializing in the discovery, development, manufacturing, and commercialization of innovative oncology medicines. Founded in 2010 by John V. Oyler and Xiaodong Wang, the company has grown into a multinational organization with headquarters in Cambridge, Massachusetts, Beijing, China, and Basel, Switzerland. BeiGene focuses on developing targeted and immune-oncology therapies for cancer treatment, with a diverse pipeline that includes internally discovered products like BRUKINSA (zanubrutinib), a Bruton's tyrosine kinase inhibitor, and Tevimbra (tislelizumab), a PD-1 inhibitor. The company operates across six continents with over 45 countries participating in clinical trials and has enrolled more than 30,000 patients in its research programs. With approximately 12,000 employees worldwide, BeiGene has established itself as a significant player in global oncology, particularly with strong market presence in China and expanding operations in the United States and Europe. The company's mission centers on expanding access to high-quality cancer therapies worldwide through persistent innovation and challenging traditional approaches to drug development.

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