Job Description
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:
Qualifications
_ Basic Minimum Qualifications:_
Additional Information
Position is a full time Monday-Friday, 8 a.m.-4:30 p.m., with overtime as needed. Candidates currently living within commutable distance to Columbia, MO **** are encouraged to apply.
What we Offer:
Excellent full-time benefits including
To learn more about Eurofins, please explore our website www.eurofins.com
Eurofins USA BioPharma Services is a Disabled and Veteran Equal Employment Opportunity employer.