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 Organisation 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 Organisations. It also has a rapidly developing presence in highly specialised 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 decentralised 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.

Job Summary: Eurofins Medical Device is seeking a Data Review 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
• Perform analysis of proteins and the impurities or raw materials associated with their production using various analytical techniques
• 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
• Diagnose problems, solve simple problems, and suggest solutions to complex problems in professional area; perform complex calculations
• Troubleshoot method and instrumentation problems
• Use office and instrumentation specific computer software
• Produce written reports (e.g., SOP, OMC, client reports)

Minimum Qualifications:

• Bachelor's degree in a scientific concentration (chemistry, physics, etc.).
• 1 year of experience
• Ability to work in the U.S. without restriction or sponsorship.
• Good communication and attention to detail.

Experience with chromatography, mass spec, CCIT, method development/validation is preferred

Working schedule will be Mon-Fri, 8:00am-5:00pm with occasional overtime as required. Candidates currently living within a commutable distance of Lancaster, PA are encouraged to apply.

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 holiday

Eurofins USA BioPharma Services is a M/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer.