QA Auditor - BioA
Indexed description
Join our Labcorp Quality department as a Quality Auditor - BioA
Work Schedule: Monday Through Friday 8-5 pm in Madison, WI
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 Good Laboratory Practice (GLP) in the performance of their role.
Job Focus Areas
- 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
- Other duties as assigned by management
- A minimum of a Bachelor’s Degree in Life Sciences preferred
- Experience may be substituted for education.
- 2 years in regulatory environment (experience in GXP roles) BioA and/or LCMS
- 1-year expereince BioA and LCMS
- Understanding of chromatography (i.e. HPLC)
- Experience with mass spectrometry/hybrid tandem mass spectrometry instrumentation
- Knowledge of and ability to interpret and apply (applicable) regulations in order to monitor compliance
- Ability to interpret data and identify quality critical problems
- Able to convey regulatory expectations
- Support 'business partner' /liaison meetings representing QA function with operations (local)
- Report on relevant quality metrics (for single topics/departments) and highlight trends
- Adhere to required timeline on assigned activities
- Peer Review QA SOP's
- Ensure Regulatory Compliance and Quality Assurance (RC&QA) responsibilities, as indicated
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. 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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