QC Data Review & Compliance Associate at Eurofins

Lexington, Massachusetts, United States -

Full Time

Start Date

Immediate

Expiry Date

09 Feb, 26

Salary

34.0

Posted On

11 Nov, 25

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Data Review, Compliance, Documentation, QC Testing, GMP Principles, Regulatory Compliance, Analytical Development, Communication Skills, Time Management, Multitasking, Troubleshooting, Collaboration, Technical Reports, Data Accuracy, Stability Studies, Certificates of Analysis

Industry

Medical and Diagnostic Laboratories

Description

Company Description At Eurofins Professional Scientific Services (PSS), the work we do matters—and so do our employees. We’re committed to supporting your professional development while offering meaningful opportunities to grow within the biopharmaceutical industry. Our collaborative teams and robust resources empower you to thrive, while maintaining work-life balance and enjoying a competitive benefits package. Eurofins Scientific is a global life sciences company providing a comprehensive range of analytical testing services across industries. From food and water safety to pharmaceutical and environmental testing, Eurofins partners with leading companies to ensure product integrity, regulatory compliance, and public health. Join us in shaping a safer, healthier, and more sustainable world. Job Description This hybrid, non-laboratory role supports Quality and Analytical functions with a focus on data review, compliance, and documentation. The QC Data Review & Compliance Associate will work closely with internal teams and external vendors to ensure data accuracy, regulatory alignment, and timely execution of deliverables. Key Responsibilities Review and interpret analytical data; support technical reports and regulatory documentation. Evaluate QC testing data for small molecule and/or biologics methods from external labs. Enter GMP data into validated systems with precision and efficiency. Verify data and trending tables for inclusion in regulatory submissions. Build and manage stability studies within validated systems. Ensure GMP data aligns with specifications; generate Certificates of Analysis (COAs) as needed. Monitor and trend reference standards and analytical data. Identify and escalate technical issues or vendor concerns. Troubleshoot basic data-related issues using available resources. Collaborate with cross-functional teams under supervision. Travel between Lexington and Cambridge, MA sites as required. Qualifications Bachelor’s degree in Chemistry, Biology, or related field. Minimum 2 years of relevant industry experience. Experience in QC, QA, or GMP-regulated environments required. Analytical Development experience preferred. Familiarity with biologics or small molecule analytical methods is a plus. Strong understanding of GMP principles and regulatory compliance. Effective communication and documentation skills. Strong time management and multitasking abilities. Must be authorized to work in the U.S. 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 60 Minute Onsite Meeting with Team Additional Details: This is a full-time, onsite position based on a first-shift schedule (Monday through Friday, 8:00 AM to 5:00 PM), with overtime required as needed. Candidates located within a commutable distance to Lexington, MA, are strongly encouraged to apply. Occasional travel (approximately 1–2%) to the Cambridge, MA site may be required. Excellent full-time benefits include: comprehensive medical coverage, dental, and vision options Life and disability insurance 401(k) with company match Paid vacation and holidays Hourly rate is between $30-$34, depending on education and experience Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Responsibilities

The QC Data Review & Compliance Associate will review and interpret analytical data, ensuring compliance and accuracy in documentation. They will collaborate with internal teams and external vendors to support regulatory submissions and manage stability studies.