Associate Scientist - Analytical Development Bioassay

The work we do at Eurofins matters, and so do our employees. At Eurofins, 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, apply with us today!

Job Description

We’re seeking a skilled Analytical Development Scientist to join a client team dedicated to ensuring the consistency, safety, and efficacy of biologic therapies, including innovative cell and gene treatments. This role will specifically support the iPSC-induced islet cell therapy program within the Analytical Development Bioassay Team.

The scientist will work closely with bioprocessing, formulation, and data science groups to support manufacturing and quality control across the development pipeline. Key responsibilities include: 

• Design and execute bioanalytical assays including flow cytometry, cell counting, dPCR/qPCR, ELISA, and cell-based bioassays.
• Perform routine sample testing for in-process testing and lot release.
• Optimize assay parameters (specificity, sensitivity, precision, accuracy, linearity, etc.).
• Support assay qualification and lifecycle management.
• Document experiments and protocols using electronic lab notebooks (e.g., Benchling).
• Troubleshoot assay and instrument issues.
• Collaborate cross-functionally with Process Development, R&D, and Quality teams.
• Author technical documentation: protocols, test methods, reports, SOPs.

Qualifications

Minimum

Qualifications

• B.S. in Biology or related field with 3–4 years of experience in drug development labs, or M.S. with 1–2 years of experience.
• Hands-on experience with bioanalytical methods, including multi-color flow cytometry (minimum 4–6 colors preferred).
• Proficiency in mammalian cell culture techniques.
• Strong ability to troubleshoot, interpret data, and present conclusions effectively.
• Flexibility to take on additional responsibilities, including occasional weekend work.

Preferred

Qualifications

• Experience with dPCR/qPCR and cell-based bioassays (e.g., glucose-stimulated insulin release, ELISA, live-cell plate assays).
• Demonstrated ability to increase assay throughput using multi-color flow cytometry, automated liquid handlers (e.g., Hamilton), and plate-based sample prep.
• Direct experience with iPSC differentiation and handling iPSC-derived cells.
• Proficiency in method development and qualification.
• Skilled in data analysis tools (e.g., GraphPad Prism, FlowJo) and digital platforms (e.g., Benchling, SharePoint, Veeva).
• Strong troubleshooting and continuous improvement mindset.
• Knowledge of regulatory standards and ICH guidelines.
• Excellent time management and organizational skills, with the ability to balance multiple priorities under tight deadlines.
• Clear and effective communication skills, with the ability to work independently and thrive in a collaborative, matrixed environment.

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 Meeting in Person to Meet the Team 

Position is  Full Time, Monday-Friday, First Shift, Monday through Friday from 8 am-5 pm.  Candidates currently living within a commutable distance of Boston, MA,  are encouraged to apply

Excellent full-time benefits include: 

• Medical Coverage:  Comprehensive medical insurance options
• Dental & Vision:  Full dental and vision coverage available
• Life & Disability Insurance:  Employer-sponsored plans
• Retirement:  401(k) plan with company match
• Paid Time Off:  Vacation days, paid holidays, and additional PTO options
• Compensation:  $35.00-$40.00 per hour 

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