Research Associate, Reprogramming
- Validate processes to generate iPSCs at scale and within clinically-driven time constraints.
- Generate and characterize iPSCs ensuring their high quality for preclinical safety studies.
- Perform primary cell isolation from patient’s starting material.
- Support tech transfer of iPSC protocols into GMP manufacturing.
- Contribute to establishing scalable manufacturing process of GMP-grade iPSCs.
- Maintain detailed and accurate records of experimental procedures and results.
- Maintain electronic records in GMP manufacturing and contribute to supporting documents, such as SOPs.
- Generate and characterize iPSCs for clinical use.
- Be part of a rotational weekend work schedule.
- Have a B.S or an M.S. in biology or a related field and at least 2 years of hands-on experience generating, maintaining and characterizing iPSC lines.
- Have experience with gene delivery into primary cells ex vivo.
- Learn quickly and follow protocols precisely.
- Strive to continuously optimize practices for high speed and accuracy.
- Enjoy working cross-functionally with specialists with various backgrounds (cell biologist, quality control scientists, operational and logistic specialists).
- Are familiar with good manufacturing practices or/and have experience working in a GMP environment.
- Have experience with process development and scaling iPSC production for cell therapies.
- Have experience in isolating cells from human samples.
- Have experience with cell characterisation techniques (eg FACS/flow cytometry, IF/microscopy, karyotyping).
- Medical, dental, and vision insurance for you and your family
- 401(k) plan with 4% matching
- Flexible time off and 10 company holidays per year
- Paid parental leave
- Annual learning & development stipend
- Daily Retro-sponsored lunch and snacks
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