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:

Applies GMP/GLP in all areas of responsibility, as appropriate.

Perform verification of data and confirm resolution of issues identifiedAnticipate quality events or issues and elevate them to appropriate management attention immediatelyIndependently engage and collaborate with coworkers, customers, and management within a cGMP environmentMust be able to identify problems and know when to solve proactively and seek adviceContribute and participate in investigations, as neededSupport regulatory and client inspections, as needed

QualificationsProficiency in cGMP and FDA-regulated clinical services laboratory environmentStrong computer, scientific, and organizational skillsExcellent written and oral communication with attention to detailCapability to work well on a team and be able to troubleshoot and problem-solve in cross-functional team settingAbility to read, comprehend, and present complex subjects

Minimum Qualifications:

Bachelor's degree in biology, biochemistry, chemistry, 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)At least 3 years related GMP pharmaceutical experience in either operations or testing roleAuthorization to work in the United States indefinitely without restriction or sponsorshipEnsure adherence to highest quality and efficiency standards in laboratory operations

Additional Information

 

Position is Monday- Friday 8:00 am- 5:00 pm. 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 optionsLife and disability insurance401(k) with company matchPaid vacation and holidays#LI-EB1Authorization to work in the United States indefinitely without restriction or sponsorship

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