Quality Control Reviewer I

LAB Labcorp Early Development Laboratories Inc.; Madison (WI); On-site; USD 34,000 - 36,000; Full time

Benefits offered by this job

Health benefits

401(k)

Paid time off

Tuition reimbursement

Employee stock purchase plan

Job summary

Labcorp is seeking a detail-oriented data reviewer for an onsite, day-shift role in Madison, WI. You will verify data quality and regulatory compliance, interpret GLP/SOP guidance, and support colleagues across teams in maintaining SOP adherence.

The position emphasizes meticulous data review, attention to deadlines, and working in a regulated environment with strong written and verbal communication skills.

Qualifications

• Bachelor of Science/Arts degree required or substituted with 2-year degree plus experience
• Experience in a laboratory setting preferred
• Proven attention to detail and accuracy in data review

Responsibilities

• Reviews data to ensure quality standards and regulatory compliance
• Interprets and explains regulatory requirements (GLPs, SOPs) to colleagues
• Maintains SOP knowledge and applies regulatory requirements
• Expands knowledge of regulatory/sop requirements and guidance documents
• Collects error tracking data for reviewed items
• Monitors citation trends and follows up to prevent recurrences

Skills

Attention to detail

Regulatory knowledge

Data review

Written and verbal comms

Education

BS/BA in science

Job description

Labcorp is a global leader in laboratory services, providing the insights and answers that help healthcare providers, patients, researchers, pharmaceutical companies and health systems make confident decisions and improve outcomes. Through our unparalleled science, data, technology and laboratory network, we advance diagnostics, accelerate innovation and help address some of the world’s most important health challenges. As we shape the future of healthcare, we are leveraging advanced technologies, intelligent digital solutions and data-driven innovation across our operations to enhance how work gets done and deliver greater value to customers and patients. With our global scale and deep expertise, you’ll have the opportunity to do meaningful work, grow your career and make a real impact on people’s health around the world. Together, we’re improving health and improving lives.

Work Schedule: Monday – Friday, Day Shift (onsite)

Job Responsibilities:

• Reviews data to ensure quality standards are met and to verify compliance to applicable SOP and regulatory requirements
• Assists co-workers and internal customers with interpretation and understanding of regulatory requirements (e.g., GLPs - Good Laboratory Practice, SOP -Standard Operating Procedure etc.) and other guidance documents
• Maintains and applies a working knowledge of SOPs and requirements
• Maintains, seeks to expand and applies a strong working knowledge of regulatory requirements (e.g. GLPs), SOP requirements, and other guidance documents.
• Collects error tracking data for items reviewed
• Monitors citation trends, performs follow-up actions with respondents, management, or others, if needed, to prevent recurring citations, problems, or errors

Minimum Qualifications:

• Bachelor of Science/Arts (BS/BA) degree
• Experience may be substituted for education. (i.e. a two-year Associate degree plus 2 years applicable experience may be substituted for a BS/BA degree.)
• One-year experience in a laboratory setting

Preferred Qualifications:

• Bachelor of Science/Arts (BS/BA) degree in chemistry or a related degree.
• 1 year experience or more, in Laboratory administration.
• 1 year or more experience GxP experience.
• 2 years or more of Data review work experience.

Additional Job Standards:

• Proof reading experience is necessary.
• Excellent written and verbal skills
• Attention to detail
• Ability to work within tight time constraints /deadlines
• Working with clients in a regulated environment
• Knowledge of current office software (e.g., Word, Excel, PowerPoint)

Pay Range: $25-$26 per hour All job offers will be based on a candidate’s skills and prior relevant experience, applicable degrees/certifications, as well as internal equity and market data.

Application Window: 8/14 thru 8/23/26

Benefits:

Employees regularly scheduled to work 20 or more hours per week are eligible for comprehensive benefits including:

• Medical, Dental, Vision, Life, STD/LTD, 401(k), Paid Time Off (PTO) or Flexible Time Off (FTO), Tuition Reimbursement and Employee Stock Purchase Plan.
• Employees regularly scheduled to work less than 20 hours, Casual, Intern, and Temporary employees are only eligible to participate in the 401(k) Plan.

Labcorp is proud to be an Equal Opportunity Employer: Labcorp strives for inclusion and belonging in the workforce and does not tolerate harassment or discrimination of any kind.

We make employment decisions based on the needs of our business and the qualifications and merit of the individual.

Qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex (including pregnancy, childbirth, or related medical conditions), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic.

Additionally, all qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable law.

We encourage all to apply If you are an individual with a disability who needs assistance using our online tools to search and apply for jobs, or needs an accommodation, please visit our accessibility site or contact us at Labcorp Accessibility. For more information about how we collect and store your personal data, please see our Privacy Statement. We believe in the power of science to change lives. Labcorp is a leading global life sciences company that provides vital information to help doctors, hospitals, pharmaceutical companies, researchers, and patients make clear and confident decisions. Through our unparalleled diagnostics and drug development capabilities, we provide insights and accelerate innovations to improve health and improve lives. Here, you can join our nearly 70,000 employees, serving clients in more than 100 countries, as we work together to transform approaches to patient care.