Lab Data Entry QC Review - Tues-Sat, 8:30am-5:00pm

Eurofins Clinical Diagnostics; Lenexa (KS); On-site; USD 32,000 - 42,000; Full time

Job summary

Eurofins Viracor LLC is seeking a Laboratory Data Entry QC Review associate in Lenexa, KS to audit order entry and accessioning, using LIMS and test ordering systems.

The role emphasizes accuracy, timely corrections, adherence to data management policies, and collaboration with laboratory staff to maintain quality, safety, and compliant documentation. Evening or weekend hours may be required as part of scheduling.

Qualifications

• High School diploma or equivalent required.
• Specimen processing experience preferred.
• Must be comfortable with raw specimen handling.
• Excellent verbal & written communication skills.
• Ability to read, interpret SOPs and policies.
• Position may require evening and weekend hours.
• 1 year of data entry experience preferred.

Responsibilities

• Review order entry information in LIMS and test ordering systems.
• Prioritize workflow and manage time efficiently.
• Maintain detailed records per good documentation practices.
• Resolve patient demographic issues or discrepancies.
• Process correction requests promptly.
• Adhere to data management policies and protocols.
• Prepare records for long-term storage.
• Verify samples for type, stability, volume, and other requirements.
• Label samples for delivery to correct areas.
• Maintain sample storage materials.
• Maintain quality control and QA records.
• Ensure laboratory safety compliance.
• Collaborate with lab staff to complete daily activities.

Skills

Time management

Attention to detail

Verbal & written communication

Interpersonal skills

Data entry proficiency

PC-based software proficiency

Education

High School diploma or equivalent

Job description

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 Organisation 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 Organisations. The Group also has a rapidly developing presence in highly specialised 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 decentralised 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.

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 Organisation 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 Organisations. The Group also has a rapidly developing presence in highly specialised 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 decentralised 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.

Job Description

Eurofins Viracor LLC is an equal opportunity employer and encourages individuals from all backgrounds to apply. By submitting your application, you acknowledge and agree to the following conditions:

• Drug Screen: Successful candidates will be required to pass a standard drug screen as part of the pre‑employment process.
• Background Check: A thorough background check will be conducted for all potential employees. This may include, but is not limited to, criminal history, education verification, and employment history.
• Visa Sponsorship: Eurofins Viracor LLC does not sponsor employment visas. All candidates must have the legal right to work in Lenexa, KS without requiring sponsorship. Unless approved by HR and supporting parties.

Basic Function and Scope of Responsibility

The Laboratory Data Entry QC Review associate is responsible for the review and audit of order entry information and performing duties with a high degree of proficiency. The Laboratory Data Entry QC Review associate is also responsible for performing duties related to accessioning and data entry.

Essential Job Duties

Level I - Minimum

• Demonstrate data entry proficiency with the Laboratory Information Management System (LIMS) and/or other test ordering systems.
• Ability to prioritize and organize efficient workflow, demonstrating excellent time management skills.
• Ability to maintain detailed and accurate records with great attention to detail, according to good documentation practices.
• Make appropriate internal or external contact to resolve patient demographic issues or discrepancies.
• Complete correction requests as needed in a timely manner.
• Adhere to all Data Management policies and protocols.
• Prepare completed records for long term/offsite storage as needed.
• Examine samples for accuracy and other requirements (sample type, stability, volume, etc.)
• Label samples for delivery to proper area(s)
• Use and maintain applicable sample storage materials (i.e., dry ice)
• Maintain quality control and quality assurance records as required.
• Adhere to all quality and safety standards, as well as ensuring compliance with all applicable regulatory agencies.
• Work closely and communicate with other lab associates to complete daily activities efficiently.
• Maintain other Clinical Laboratory databases as needed or assigned.
• Provide administrative support for Clinical Laboratory projects as needed.
• Represent department and the organization favorably and in accordance with established Company standards and associate attributes at all times.
• Ensure adherence to laboratory safety policies
• Other duties as assigned by management.

Level II – Fully meets the qualifications of Level I plus the following

• Manage issues and projects; resolve escalated issues as appropriate.
• Demonstrate superior understanding of Laboratory operations and department processes.
• Suggest potential improvements to existing systems and processes to immediate supervisor.

Level III – Fully meets the qualifications of Level II plus the following

• Help to develop and provide training to new and existing associates on department functions.
• Organize and analyze data entry errors to help determine opportunities for individual performance and process improvement.
• Participate in identifying solutions regarding data entry errors and concerns.

Qualifications

Essential Knowledge, Skills and Abilities

Level I - Minimum

• High School diploma or equivalent required
• Specimen processing experience preferred.
• Must be comfortable with raw specimen handling.
• Ability to read, interpret, and comply with documents such as internal SOPs, operating and maintenance instructions, and company policies.
• Position may require evening and weekend hours.
• Goal oriented, with excellent time management and organizational skills
• Excellent interpersonal skills, with ability to interact effectively and work efficiently with people at all levels in an organization.
• Excellent verbal & written communication skills
• Keenly attentive to detail
• Ability to keep sensitive information confidential.
• High level of proficiency with PC-based software programs; strong database skills; 1 year of data entry experience preferred.

Level II – Fully meets the qualifications of Level I plus the following

• Minimum of 2 years of clinical laboratory experience or 1 year as a Level I
• Demonstrate superior understanding of laboratory operations and department processes.
• Advanced problem-solving skills

Level III – Fully meets the qualifications of Level II plus the following

• Minimum of 3 years of clinical laboratory experience or 1 year as a Level II
• Demonstrate ability to manage workflow.
• Higher level understanding
• Demonstrated leadership abilities.
• Demonstrated effective training skills.
• Ability to direct other Associates as required.
• Ability to assist Management in providing overall direction of workflow for Support Services as needed.
• Ability to ensure applicable SOPs are being utilized and followed appropriately.
• Help with weekly scheduling of staff.
• Serve as the primary trainer for new LDEQCR or re‑training of existing LDEQCR
• Ability to accurately answer questions when Supervisor is unavailable.
• Ability to interact with other departments as necessary and develop relationships with other Lab Leadership and Management as it relates to work processes and workflow.
• Ability to communicate concerns/needs as necessary to Supervisor.
• Aid Supervisor with areas of improvement in workflow or organization

Physical Requirements

• Physical dexterity sufficient to use hands, arms, and shoulders repetitively to operate a keyboard and other office equipment, use a telephone, access file cabinets and other items stored at various levels, including overhead.
• Ability to speak and hear well enough to communicate clearly and understandably with sufficient volume to ensure an accurate exchange of information in normal conversational distance, over the telephone, and in a group setting.
• Ability to stand for extended periods of time as necessary in the laboratory (4 or more hours)
• Ability to lift and move items weighing up to 25 pounds. It is advised to obtain assistance for items over 25 pounds.
• Physical dexterity sufficient to move body frequently around laboratory equipment and instrumentation.
• Ability to continuously operate a personal computer for extended periods of time (4 or more hours)
• Mental acuity sufficient to collect and interpret data, evaluate, reason, define problems, establish facts, draw valid conclusions, make valid judgments and decisions.

The essential physical and mental requirements described here are representative of those that must be met by an employee to successfully perform the essential functions of the job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

Additional Information

Schedule

• Tues-Sat, 8:30am-5:00pm

What we offer

• 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 Diagnostics is a Disabled and Veteran Equal Employment Opportunity employer.