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 works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.

Eurofins is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organization services. Eurofins 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 Organizations. The Group also has a rapidly developing presence in highly specialized and molecular clinical diagnostic testing and in-vitro diagnostic products.

In over just 30 years, Eurofins has grown from one laboratory in Nantes, France to 55,000 staff across a decentralized and entrepreneurial network of 900 laboratories in over 50 countries. Eurofins offers a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products.

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

 Applies the highest quality standard in all areas of responsibility

 Meets all quality and productivity metrics and demonstrates strong teamwork and collaboration

 Reviews and approves/rejects completed client laboratory reports and like records for accuracy, traceability, and completeness. Evaluates addressed deficiencies for clarification and for potential impact on compliance status. Works with staff to correct any noted deficiencies/inconsistencies.

 Assist with implementation and monitoring of quality systems and procedures (e.g. CAPA, change controls, trainings, etc.)

 Reviews protocols, procedures, data, reports, and other documents to ensure accordance with specified regulatory requirements, protocol, and/or project plan, methods, and SOPs.

 Keeps supervisor informed of significant issues or developments identified during quality assurance activities.

 Learn new tasks and remember the processes associated with this role.

 Ability to communicate with Scientific staff for resolving comments

 Ability to complete tasks in situations that have a speed or productivity quota.

 Communicates effectively with client staff members

 Performs other duties as assigned

Basic Minimum Qualifications :

• Bachelor's degree is required. A degree in a relevant field such as chemistry, biochemistry, biology, chemical engineering, pharmaceutical science, or other directly related field or degree with comparable coursework is preferred.  In some cases, experience in the relevant area may be used to substitute the Bachelor's degree.
• Authorization to work in the United States indefinitely without restriction or sponsorship

Other Qualifications :

• Experience with reading and understandings protocols, SOPs, and technical guidelines.
• Ability to define and solve practical problems, present solutions, establish facts, and draw valid conclusions

Position is full-time, Monday-Friday, 8:00 a.m.-4:30 p.m. with additional hours, as needed. Candidates currently living within a commutable distance of Columbia, MO are encouraged to apply. 

 We offer excellent full-time benefits including:

• Comprehensive medical coverage,
• Life and disability insurance,
• 401(k) with company match,
• Paid holidays and vacation, 
• Dental and vision options.

Eurofins USA BioPharma Services is a Disabled and Veteran Equal Employment Opportunity employer.