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 laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organization services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organizations. It also has a rapidly developing presence in highly specialized and molecular clinical diagnostic testing and in-vitro diagnostic products. In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralized and entrepreneurial network of 900 laboratories in over 54 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products. In 2024, Eurofins generated total revenues of EUR € 6,515 billion, and has been among the best performing stocks in Europe over the past 20 years.   Provides Administrative support by + assisting with routine quality assurance activities + performing administrative functions within the QA group + supporting Quality-related Help Desk and e-mail requests + assisting in Analytical Subcontractor documentation maintenance Supports Data Reporting by: + reviewing, approving, and releasing laboratory data + assisting with review and approval of Certificates of Analysis and Cumulative Reports + assisting with review and verification of Technical Reports and Summaries Assists in Document Control by: + issuing Master Lists numbers + issuing Laboratory Notebooks and Logbooks + issuing and maintaining Controlled Copies + maintaining the Technical Library + maintaining Archival of Records Supports Stability activities as assigned Supports Manufacturing activities as needed by: + executing the quality assurance roles of batch records Other duties as assigned Required: a minimum of High School Diploma or Equivalent. Preferred Bachelor’s Degree and/or certifications in laboratory/quality/regulatory Required: Understanding of FDA requirements and Quality Systems Preferred: Must have good administrative skills (Microsoft Office Suite, LIMS, QMS) Preferred: 1 – 2 Years in a laboratory environment. Preferred: 3+ years of GLP/GMP environment in laboratory operations or QA, or combination of both Position is full-time, Monday - Friday 8:00am - 5:00pm . Candidates currently living within a commutable distance of Cary, NC are encouraged to apply. + 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 Eurofins USA BioPharma Services is a Disabled and Veteran Equal Employment Opportunity employer.