Eurofins Scientific is an international life sciences company which provides a unique range of analytical testing services to clients across multiple industries. The Group believes it is the world leader in food, environment and pharmaceutical products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and for supporting clinical studies. In addition, Eurofins is one of the key emerging players in specialty clinical diagnostic testing in Europe and the USA.
Group's key figures are approx. 6.7 billion Euros turnover, over 940 laboratories across 59 countries and about 61,000 staff.
Responsibilities include reviewing work for research and development under CGMP and/or GLP guidelines for studies, documentation, etc. Assisting in reviewing, monitoring and reporting studies to ensure data accuracy and report quality. Providing somewhat complex analytical review work on projects and studies using a knowledge of analytical techniques and instruments. Working with increasing independence on studies and assignments.
The ideal candidate would possess:
Position is a full time Monday-Friday, 8 a.m.-4:30 p.m., with overtime as needed.
As a Eurofins employee, you will become part of a company that has received national recognition as a great place to work.
To learn more about Eurofins, please explore our website
Eurofins is a M/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer.
All your information will be kept confidential according to EEO guidelines.
Eurofins is a M/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer.
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