Documentation Review and Sample Management Specialist at Eurofins in Indianapolis, Indiana

Job Description:

Company 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 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.


In 2021, Eurofins generated total revenues of EUR 6.72 billion, and has been among the best performing stocks in Europe over the past 20 years.



Job Description




Employee Responsibilities:

• Complete data integrity review of analytical data reporting records for the client's portfolio, which includes Synthetic molecules, Peptides, and Bioproducts


• Support development stability studies which include handling, storing, delivering samples, and documenting per relevant procedures


• Assist domestic and international shipping of material, such as development samples or consumables


• Must be able/authorized to handle Controlled Drugs or Controlled Substances under the guidance of DEA requirements

• Strong computer and organizational skills


• Excellent communication (oral and written) and attention to detail


• Ability to work independently and as part of a team, and have self-motivation, adaptability, and a positive attitude


• Ability to learn complex processes and procedures, prioritize multiple tasks, keep accurate records, follow instructions, and comply with company policies

• Bachelor's degree in Science or other related degree concentration, or equivalent directly-related experience (two years of directly related industry experience is equivalent to one full-time year of college in related major)


• Authorization to work in the United States indefinitely without restriction or sponsorship

• Position is full-time, working Monday-Friday 8:00 a.m.-5:00 p.m


• overtime as needed


• Candidates currently living within a commutable distance of Indianapolis, IN 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


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• Authorization to work in the United States indefinitely without restriction or sponsorship