Associate Scientist, Gene Editing and iPSC Engineering
- Full-time
Company 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 diabetes team. This position will play a key lab-based role in advancing iPSC stem cell engineering and will contribute to the development of the next generation of islet cell therapies. Successful candidates will have experience with gene editing, molecular biology techniques, assay development, and human iPSC cell culture, differentiation, and banking.
Key Responsibilities:
- Enabling and advancing iPSC gene editing, cell line development, and evaluation of differentiated cells.
- Routine iPSC cell culture, passaging, and media making.
- Optimize workflows for iPSC CRISPR based gene-editing, gRNA screening, and delivery.
- Optimize and perform assays for on-/off-target analysis via PCR and NGS workflows.
- Generate clonal gene edited iPSC lines and characterize via flow cytometry, ddPCR, dPCR and qPCR.
- Culture and execute routine directed differentiation of human iPSCs to pancreatic islets performing drug substance assessments such as cell counts, viability, and metabolite assessments.
- Assist scientists in the team to evaluate and design mitigation strategies to ensure genomic stability of the iPSC lines and drug substance.
- Collaborate cross-functionally to support transfer of R&D assays to GMP.
- Maintain accurate and detailed records of all experiments, synthesize results, prepare reports, and present in meetings. Contribute to SOP development.
- Work seamlessly in executing workplans and meeting deadlines.
Qualifications
Minimum Required Qualifications:
- B.S. in Stem Cell Biology, Cell Biology, Bioengineering or a related field with 3-4 years relevant industry experience in gene editing and cell therapy. M.S. in Stem Cell Biology, Cell Biology, Bioengineering or related field with 1-2 years relevant industry experience in gene editing and cell therapy.
- Extensive hands-on experience with human iPSC culture, gene editing, and molecular biology techniques.
- Proficiency in CRISPR gene editing and cell line development, including optimization of protocols, familiarity with flow-based sorting.
- Proficiency in molecular biology techniques including construct design, PCR, ddPCR, dPCR, and NGS.
- Hands-on experience with assay development including luciferase assays, ELISA, and flow cytometry.
- Hands-on experience with cell delivery methods of gene editing tools.
- 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 experience in pancreatic islet directed differentiation.
- Hands-on experience in transitioning research-grade processes to GMP-grade.
- Familiarity with electronic lab notebook (ELN) documentation.
- Authorization to work in the United States indefinitely without restriction or sponsorship.
Additional Information
Position is Full Time, Monday-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 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
What We Offer:
- Target pay range: $37-41/hr
- 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
Eurofins Lancaster Laboratories Professional Scientific Services® (PSS) is a global, award-winning insourcing solution that places our people at our clients’ sites dedicated to running and managing laboratory services while eliminating headcount, co-employment, and project-management worries.
We infuse our 55-year track record of scientific and laboratory operations expertise, as well as HR, and a great place to work best practices, to recruit, hire, train, and manage highly qualified scientists to perform laboratory services using our client’s quality systems and equipment.
To learn more about Eurofins Lancaster Laboratories, please explore our website www.eurofinsus.com
Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.