Job Description

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. Job Summary: Eurofins Microbiology is seeking an Associate Scientist to support data quality by reviewing laboratory data for accuracy, precision, and adherence to GMP and/or GLP regulations. This position does not require previous experience in the pharmaceutical industry and provides opportunities for career growth. This role is not a coding or data science role. We are not currently seeking computer science or IT-background applicants for these roles. Ensure that the client receives quality data by reviewing laboratory data for accuracy, clarity, and adherence to GMP and/or GLP regulations Review simple and complex routine and non-routine data (for three or more areas) according to departmental, corporate, and client SOPs; read and understand analytical procedures; ensure all work is performed according to GLP/GMP requirements and apply GLP/GMP in all areas of responsibility as appropriate Determine if data is compliant and defendable based on industry regulations and methodology Verify data is of sound quality following all method, industry, and client requirements where applicable Identify problems, solve simple problems, and suggest solutions to complex problems in professional area; perform complex calculations Use office and instrumentation specific computer software Review written reports (e.g., SOP, OMC, client reports) PLEASE NOTE: The shift for this role is as follows Tuesday-Saturday 1st shift (8am-4pm) Training will occur on first shift M-F 8a-4p Minimum Qualifications: Bachelor's degree in biology, microbiology, or related degree concentration. Ability to work in the U.S. without restriction or immediate/future sponsorship. Good communication and attention to detail. Working schedule will be Full-Time, First Shift, Tues-Sat 8am-4pm. Candidates currently living within a commutable distance of Lancaster, PA are encouraged to apply. No relocation assistance will be given. This position is NOT remote. What we Offer: 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. Eurofins

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