Scientist - iPSC Gene Editing

Job Description

Job DescriptionCompany Description

The work we do at Eurofins Professional Scientific Services matters, and so do our employees. At Eurofins PSS, we put a focus on your professional growth. We provide our employees the ability to break into the biopharmaceutical industry and grow from the bottom up. We have the supportive teams and tools available to invest in you while also affording you work-life balance and a competitive benefits package.

Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies.

If you’re looking for a rewarding career, a place to call home, apply with us today

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 Expect 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 84,000-86,000 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.