Development BioTrace

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.

Assist with data integrity of analytical data for bioproducts

Ordering reagents/disposables

Entering reagents into a database

Assist with inspection readiness

Data and trend charting

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In addition to the above, we are looking for candidates with the following  skills:

DNA based methods (PCR/Gel Electrophoresis), ELISA, HPLC, Cell culture, cell counting, familiarity with AAV a plus.

Participate in document review and conducting and assisting with investigations, writing quality events, and putting effective CAPAs in place

Familiarity with GMP/cGMP in the pharmaceutical field. 

Applies GLP in all areas of responsibility, as appropriate.

Making sure all compliance standards are followed and proper documentation is maintained

Bachelors degree in biochemistry, cell biology, molecular biology 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

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 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

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