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 Organization 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 Organizations. It also has a rapidly developing presence in highly specialized 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 decentralized 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 2024, Eurofins generated total revenues of EUR 6,515 billion, and has been among the best performing stocks in Europe over the past 20 years.
Quality Control Technician I responsibilities include, but are not limited to, the following:
The Quality Control Technician I, with direct supervision, is responsible for
ensuring that data reported to both internal and external customers is accurate
and reflects the work performed
- Conducts a QC review of all study generated documents
- Inspects assay worksheets for completeness with regards to Test Methods and SOP's
- Checks equipment documentation ensuring accuracy, completeness and appropriate approvals
- Conducts an inspection of Ancillary documentation
- Provides a determination of acceptance for assays and results
- Performs maintenance of data files and performs various data handling tasks as required
- Understands and follows all procedures and processes required for work performed under the appropriate regulatory body (i.e. GxP)
- Attends meetings and participates on teams as required
- Reads and understands training documents
- Checks-in and assists in scheduling projects through the QC department
- Creates where applicable and conducts 10% check of transfer files that are sent to client database
- Investigates discrepant data or client questions or concerns
- Completes other data related tasks as assigned, based on business needs
- Provides cross-functional support to other departments as required
- Adjusts work hours as needed to meet client deadlines
- Adheres to site employee health and safety (EHS) requirements
- Conducts all activities in a safe and efficient manner
- Demonstrates and promotes the company vision
- Regular attendance and punctuality
- Performs other duties as assigned
Position is full-time working Monday - Friday, 8:00am - 5:00pm. Candidates currently living within a commutable distance of Lenexa, KS 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
Eurofins USA Clinical Trial Solutions is a Disabled and Veteran Equal Employment Opportunity employer.