QC Reviewer - Entry Level

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

Basic Minimum Qualifications :

Ability to read, write and interpret documents such as safety rules, standard operating procedures, maintenance instructions, and procedure manuals.

High attention to detail and quality

Ability to write read and interpret technical and scientific reports and correspondence.

Ability to perform mathematical calculations

Ability to speak effectively before customers and employees.

Ability to perform statistical analysis and interpretation of data.

Ability to solve practical problems and deal with a variety of concrete variables in situations where only limited information is available.

Ability to construct, communicate and interpret a variety of instructions furnished in written, oral, diagram, or schedule form

Watson LIMS experience preferred

Authorization to work in the United States indefinitely without restriction or sponsorship

Basic Minimum Education Requirements :

Associate’s Degree in a science-related field

OR minimum 2 years related experience and/or training

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.

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.