Job Description

We are seeking a highly skilled, passionate, and motivated scientist to join our Bioproduct Research and Development team. This position will play a key lab-based role in iPSC gene editing and will contribute to the development of next-generation islet cell therapies. Ideal candidates will have extensive hands-on experience with human iPSC culture, CRISPR-based gene editing, molecular biology, and assay development.

The successful candidate will be responsible for daily R&D and GMP gene-editing operations, including iPSC culture, gene editing platform development and optimization, documentation preparation (SOP and batch record drafting and review), deviation investigation, raw material screening, clone characterization, and as well small-scale iPSC derived islet differentiation.

Key Responsibilities:

• Lab-based role focused on advancing CRISPR-based iPSC gene editing and iPSC cell line generation to enable GMP readiness.
• Develop and optimize gene-editing workflows, including gRNA design, RNP delivery, knock-in cargo design, clone genetic screening, and cell banking.
• Characterize edited iPSC clones using DNA-based assays (PCR, qPCR, ddPCR), sequencing, flow cytometry, and next-generation sequencing (NGS).
• Evaluate and implement iPSC culture media optimization and gene editing strategies to ensure genomic stability of iPSC lines.
• Support and refine directed differentiation of iPSCs into islet cells and characterize resulting drug product attributes.
• Perform hands-on iPSC gene editing within GMP settings to generate clinical-grade cell lines.
• Draft, review, and execute SOPs and master batch records; ensure compliance with GMP, regulatory, and quality standards; support deviation investigations and maintain thorough documentation.
• Participate in supplier qualification and sourcing of critical raw materials and consumables to ensure GMP readiness.
• Demonstrate strong teamwork, communication, and organizational skills to manage multiple projects and timelines effectively.

Qualifications

_ Minimum Required Qualifications:_

• Ph.D. in biology, bioengineering, or a related field with 0-1 years of relevant industry experience in iPSC gene editing and cell therapy.
• Extensive experience with human iPSC culture, gene editing, and molecular biology techniques.
• Proficiency in CRISPR gene editing, including optimization of protocols
• Proficiency in gene editing workflows and molecular biology techniques including construct design, cell delivery methods, PCR, ddPCR, flow cytometry, and NGS.
• Ability to troubleshoot and interpret experimental results and effectively present conclusions.
• Excellent communication and interpersonal skills, with the ability to work effectively in a team-oriented environment.
• Strong organizational skills and diligent record keeping.

_ Preferred Qualifications:_

• Hands-on GMP gene editing operational experience.
• Experience in direct differentiation and scale-up of iPSC-derived cells.
• Familiarity with electronic lab notebook (ELN) documentation.
• Authorization to work in the United States indefinitely without restriction or sponsorship.

Additional Information

What to Exp ect in the Hiring Process:

• 10-15 Minute Phone Interview with Region Recruiter
• 45-60 Minute Virtual Interview with Manager and/or Group Leader
• 45-60 Minute In-Person Meeting over Coffee for a Casual Discussion of the Role

The Position is full-time, Monday through Friday, 8am-5pm, with occasional weekends (on a rotational basis to support cell culture) . Candidates currently living within a commutable distance of Boston, MA, are encouraged to apply.

What We Offer:

• Excellent full-time benefits, including comprehensive medical coverage, dental, and vision options
• Life and disability insurance
• 401(k) with company match
• Paid vacation and holidays
• Yearly goal-based bonus & eligibility for merit-based increases
• Compensation is 84,000-91,000 anually

Ready to make an impact?
Join a team where your scientific skills matter, and your growth is supported. If you're passionate about quality, collaboration, and continuous improvement, we want to hear from you. Apply today and take the next step in your career with Eurofins PSS!

Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.