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Research Associate/Senior Research Associate (Stem Cells)

Employer
4D Molecular Therapeutics
Location
94608, Emeryville
Start date
Jan 14, 2019

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Job Details

We seek a talented and passionate Research Associate/Senior Research Associate to assist in the development of human in vitro models to characterize and study novel Adeno Associated Virus (AAV) variants to support our goal to offer transformative gene therapeutic products to patients in need.  In this role, you will have the unique opportunity to work on culturing and differentiating human pluripotent stem cells and conduct cellular reprogramming, in addition to performing immunocytochemistry and more.  Thus, you will have the special opportunity to expand your skillsets in the gene therapy arena. You will be a part of history in helping discover and develop novel AAV therapeutic vectors to treat a wide range of diseases.   

Responsibilities:

  • Conducting independent scientific experiments following defined laboratory technical procedures
  • Culturing and differentiating human pluripotent stem cells
  • Cellular reprogramming
  • Performing immunocytochemistry
  • Performing tissue histological procedures involving specimen processing, embedding, sectioning, and staining
  • Using fluorescent microscopy for cellular and tissue imaging and analysis
  • Using basic molecular biology techniques, DNA and RNA purification, PCR, qPCR, gene cloning, and western blotting
  • Contributing to establishing human in vitro disease models
  • Maintaining accurate and well-organized laboratory records, worksheets and notebooks
  • Maintaining current training requirements
  • Maintaining compliance to company Environmental Health and Safety policies, procedures, and practices

Requirements:

  • B.S. or M.S. degree in biology, bioengineering, or a related field
  • 3+ years prior experience in biological laboratory experimentation
  • Prior experience working with human pluripotent stem cells
  • Ability to conduct research with strong attention to detail
  • Highly organized and motivated, ability to work independently in a collaborative team-oriented setting, and have strong analytical, organizational, and communication skills
  • Working knowledge of Microsoft Word, Excel, PowerPoint, and Adobe Photoshop

We are 4D Molecular Therapeutics (4DMT) -- a global leader in gene therapy product research & development using scientific innovation to unlock the full potential of gene therapy for patients with genetic diseases. Our goal is to design and develop transformative gene therapy products using our proprietary adeno-associated virus variants platform to treat serious unmet medical conditions.   While AAV gene therapy pioneers are making great strides with the first wave of products, hurdles still exist with the use of 1st & 2nd generation vectors (naturally occurring primitive viral capsids).  4DMT’s next-generation Therapeutic Vector Evolution platform generates targeted, optimized and proprietary AAV vectors that have the potential to overcome the delivery and immunological challenges currently facing the field, ultimately unlocking the full potential of gene therapy. We invite all of you who share our passion and vision in creating the ultimate gene therapy products to cure severe genetic and rare diseases with high unmet medical need.  We seek the best people in the industry who identify with our mission and innovative results-driven approach. We offer an inspiring and collaborative environment that encourages individual contributions, recognizes performance in multiple ways, offers uniquely generous benefits and provides challenging opportunities for career development.

Company

4DMT is a gene therapy company with a transformative discovery platform --Therapeutic Vector Evolution --that enables our “disease first” approach to product discovery and development, thereby allowing us to customize our AAV vectors to target specific tissue types associated with the underlying disease.


At 4DMT we are creating and developing optimized “biopharmaceutical grade” AAV vectors that will allow us uniquely to unlock the full potential of gene therapy. Our customized and proprietary AAV vectors are each designed, according to a 4DMT Target Vector Profile, to deliver genes to specific cells and tissues in the body to eradicate both rare and large market diseases.


While AAV gene therapy pioneers are making great strides with the first wave of products, hurdles still exist with the use of conventional vectors. The most commonly used AAV capsids (e.g., AAV2, 5, 8 and 9) were identified either 1) as contaminants in lab stocks of adenovirus, or 2) through monkey tissue processing. Therefore, these conventional vectors are not targeted specifically to any tissue in the body. This can lead to inefficient and non-specific delivery, thus requiring extremely high doses and potentially resulting in toxicities (including inflammation), high manufacturing burdens and suboptimal efficacy. In addition, suboptimal routes of delivery can be required for delivery to the right tissues (e.g., subretinal delivery to the retina). Finally, pre-existing neutralizing antibodies in many patients can limit efficacy, clinical trial enrollment and market sizes. 4DMT Innovation empowers us to create new and improved next generation AAV capsids to allow targeted delivery of our products by the optimal clinical route of administration.


At 4DMT we use our robust discovery platform, termed “Therapeutic Vector Evolution,” to create customized and proprietary gene delivery vehicles (novel AAV vectors) to deliver genes to specific tissues and cells in the body by the optimal route of administration. We use the power of evolution to create and refine these optimized vectors through genetic diversification and then natural selection in vivo.


4D Purpose Statement:  Boldly Innovating to Unlock the Full Potential of Gene Therapy for Countless Patients


GUIDING PRINCIPLES

 

  • Dare to Cure - Patients are waiting. Create big dreams for patients and take calculated risks to achieve them
  • Break Boundaries - Question the status quo and innovate beyond conventional approaches
  • Beyond Yourself - It's about patients, their families, our team, our families. We strengthen each other.
  • Prepare and Execute Relentlessly - Start with the end in mind, over-prepare and make contingency plans to your contingency plans


We invite all of you who share our passion and vision in creating the ultimate gene therapy products to cure genetic and rare diseases in children and adults. We seek the best people in the industry who identify with our mission and innovative results-driven approach. We offer an inspiring and collaborative environment that encourages individual contributions, recognizes performance in multiple ways, offers generous benefits and provides challenging opportunities for career development. 
 

Company info
Website
Phone
510-505-2680
Location
5858 Horton St. Suite 455
Emeryville
California
94608
United States

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