The role: 

We are seeking a motivated and creative Research Associate I/II to join our Platform Discovery team. You will work closely with more senior team members to evaluate and optimize methods for the delivery of our novel gene editing systems in therapeutically relevant cell types. This includes developing robust high-throughput workflows in biochemical and/or cell-based systems. Your work will be critical for enabling new therapeutic opportunities.

The ideal candidate will have extensive experience with molecular cloning, mammalian cell culture techniques, and assay development. This is an excellent opportunity to work cross-functionally with a diverse team of experts across AI and machine learning, protein design, cell biology, and gene editing.   

Responsibilities:

• Design, execute, and automate robust molecular and/or cell-based workflows for evaluation of delivery modalities for our novel gene editing tools. 
• Execute assays to measure on- and off-target activity of novel gene editing systems using a combination of targeted and genome-wide analytical methods.
• NGS library preparation, purification, quantitation, and final quality evaluation. 
• Analyze data, interpret results, and present findings to team members to arrive at critical go/no-go decisions.

Qualifications: 

• BS or MS in molecular biology, biochemistry, or a related field.
• 0-5 years of academic or biotechnology industry research experience.
• Extensive hands-on experience with molecular cloning and mammalian cell culture. 
• Experience with molecular or cell-based assay development and execution, including qPCR/dPCR, NGS, and/or flow cytometry techniques
• Hands-on experience and/or a deep understanding of key concepts and challenges related to genetic medicine, gene editing systems, DNA repair, etc.  

Preferences (but not required):

• Experience with process automation and scaling to develop high throughput workflows, ideally in a biotechnology/industry research setting.
• Experience or high-level familiarity with methods for ex vivo and in vivo delivery of genome editing systems 

What we offer at Profluent

• A high-growth opportunity with meaningful impact
• Competitive compensation package
• Health insurance (health/dental/vision)
• Generous paid time off (PTO) policy
• Commitment to physical and mental well-being
• More benefits and perks to be added!

Profluent Bio, Inc is an equal opportunity employer promoting diversity and inclusion in the workspace. We do not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical conditions, veteran status, sexual orientation, gender (including gender identity and gender expression), sex (which includes pregnancy, childbirth, and breastfeeding), genetic information, taking or requesting statutorily protected leave, or any other basis protected by law.

Work Authorization Requirement

Applicants must have ongoing work authorization in the United States that does not require employer sponsorship. Sponsorship will not be provided now or at any time in the future for this position.

Employment Eligibility Verification

Legal authorization to work in the United States is required. In compliance with federal law, all persons hired must verify their identity and work eligibility and complete the required employment verification form upon hire.