Eurofins QC Data Review & Compliance Associate \\\| SmartRecruiters Google Chrome Microsoft Edge Apple Safari Mozilla Firefox . QC Data Review & Compliance Associate Full-time Compensation: USD 30 \- USD 34 \- hourly Company Description At Eurofins Professional Scientific Services (PSS), the work we do mattersand so do our employees. Were 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 Bachelors 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 12%) 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. I'm interested I'm interestedCookies Settings I'm interested Refer a friend Posted by Samantha Goularte share this job Share on LinkedIn Share on Facebook Share on Twitter Share via email Share on Xing Share on WeChat Share to WeChat × Copy the link and open WeChat to share. Copy to clipboard Open WeChat Share to WeChat × Use Scan QR Code in WeChat and click ··· to share. QC Data Review & Compliance Associate Lexington, MA, USA Full-time I'm interested I'm interested

A Bachelor's degree in Chemistry, Biology, or a related field is required. The role necessitates a minimum of two years of relevant industry experience, with a strong background in QC, QA, or GMP-regulated environments. Familiarity with biologics or small molecule analytical methods is considered a plus. A solid understanding of GMP principles and regulatory compliance is essential, alongside effective communication, documentation, time management, and multitasking abilities.