QA Auditor

Join our Labcorp Quality department as a Quality Auditor in Madison, WI.

Are you wanting to move your career into the Quality department? This is a full-time benefitted, day position at the Madison, Wisconsin facility in the Quality department auditing the Immunology and Immunotoxicology work. Take your career to another level maintaining Quality!

Join an exceptional organization and an exceptional Quality department.

Job Summary:

• The individual in this role verifies compliance to standard operating procedures (SOPs) and regulations by performing study protocol, data, report, and in-lab phase audits where applicable for specific study types, participate in internal facility/process and/or supplemental inspections, and peer review QA SOPs. The statements below reflect the general responsibilities and requirements of the identified position but may not describe all the work requirements that may be inherent in the job. It is the responsibility of all employees to comply with all applicable regulations e.g. Good Clinical Practice (GCP), and 21 CFR Part 58 Good Laboratory Practice (GLP) in the performance of their role.

Job Duties:

• Conduct, but not limited to protocol review, report/data audits, and internal facility/process inspections
• Peer review QA SOPs
• Support operational liaison meetings representing QA function
• Report on relevant quality metrics (for single topics/departments) and highlight trends
• Ensure Regulatory Compliance and Quality Assurance responsibilities, as indicated in applicable controlled documents, are followed

Minimal Experience and Education:

• Bachelor’s Degree in Life Sciences preferred (or equivalent Life Science experience)
• Experience may be substituted for education
• Experience with plate reading technologies (e.g. MesoScale, EliSpot, BioPlex)
• Understanding of cell viability and cell potency testing
• General understanding of principles of flow cytometry
• 2 years in a regulatory environment
• Knowledge of and ability to interpret apply (applicable) regulations to monitor compliance
• Able to interpret data and identify quality critical problems
• Able to convey regulatory expectations

Why People choose to work at Labcorp?

At Labcorp, it’s our people that make us great – it’s what our clients, our partners and, most importantly, what our employees say. Here, you’ll have the opportunity to work with extraordinary people with diverse viewpoints. You’ll discover your own outstanding potential as we build an even stronger organization with industry leaders from early development to the clinic and beyond. We help our clients develop medicines that improve health and improve lives of their family and friends.

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. Casual, PRN & Part Time employees regularly scheduled to work less than 20 hours are eligible to participate in the 401(k) Plan only. For more detailed information, please click here.

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

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