Stability Data Specialist

At Eurofins Professional Scientific Services, we prioritize your professional growth while offering work-life balance and a competitive benefits package. Eurofins Scientific is an international life sciences company providing analytical testing services to ensure safety, health, and sustainability across food, water, medicines, and more. We are a global leader in testing and laboratory services for multiple industries.

About the role

This is a hybrid, non-laboratory role supporting Quality and Analytical functions. The successful candidate will collaborate with internal teams and external partners to ensure data integrity, regulatory compliance, and timely execution of deliverables.

Responsibilities

• Collaborate with departmental colleagues to complete assignments under supervision.
• Review and interpret analytical data with client support; contribute to technical reports and regulatory documentation.
• Evaluate QC testing data for small molecule and/or biologics methods from external vendor laboratories.
• Enter GMP data into validated database systems accurately and efficiently.
• Verify data and trending tables for inclusion in regulatory submissions.
• Build and manage stability studies within validated systems, as applicable.
• Ensure GMP data aligns with current specifications; generate Certificates of Analysis (COAs) when required.
• Monitor and trend reference standards and analytical data.
• Identify and escalate routine technical issues or vendor-related concerns.
• Troubleshoot basic issues using available resources and guidance.
• Travel between Lexington and Cambridge client sites as needed.

Requirements

• Bachelor’s degree in Chemistry, Biology, or a related field.
• Minimum of 2 years of relevant industry experience.
• Prior experience in Quality Control, Quality Assurance, or a GMP-regulated environment is required.
• Experience in Analytical Development is preferred.
• Familiarity with analytical methods for biologics or small molecule products is a plus.
• Solid understanding of GMP principles and regulatory compliance.
• Strong communication skills; able to document and report issues clearly and promptly.
• Effective time management and multitasking abilities in a cross-functional team setting.
• Must be authorized to work in the U.S. permanently without restriction or sponsorship.

Candidates currently living within a commutable distance of Lexington, MA are encouraged to apply. Occasional travel (approximately 1–2%) to the Cambridge, MA site may be required.

Schedule

Full Time, Monday-Friday, 8am-5pm.

Pay

$31.00-$35.00 per hour based on education and related experience.

Benefits

• Comprehensive medical coverage, dental, and vision options.
• Life and disability insurance.
• 401(k) with company match.
• Paid vacation and holidays.
• Eligibility for yearly goal-based bonus & merit-based increases.