Excellent opportunity in the Quality Assurance Department at Labcorp! 

We have a position for a Quality Assurance Auditor III, GLP/GCP in the Quality Assurance department at Labcorp.

Do you have experience as an LCMS scientist, bioanalytical chemistry, and/or GLP/GCP auditing experience? Are you detail-oriented and have strong communication skills?   Do you love collaborating with others to solve problems and increase the efficiency of internal processes? If so, then this may be the position for you!!  See essential job duties below.

This position is at the Madison, WI. facility (This position is not remote).

Position Overview

Requires working knowledge of LC/MS bioanalysis, FDA Guidance for Industry: Bioanalytical Method ValidationAudits bioanalytical validation and sample analysisInterprets applicable quality regulations/standardsManages interactions with the operational management to support quality topicsEvaluates responses to inspection reports and performs follow-up with internal and external stakeholders to ensure resolution

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.

Work Schedule: 8am-5pm

Pay: This is an Hourly position

Work Location: 3301 Kinsman Blvd Madison, WI.

Essential Job Duties:
-Conduct audits as assigned and reviews audit responses for completeness

-Support business partner/liaison meetings representing QA function with operations

-Report of relevant quality metrics and highlights trends

-Peer Review QA SOPs

-Ensure Regulatory Compliance and Quality Assurance responsibilities, as indicated in applicable controlled documents, are followed

Minimum Required:

2 years in regulatory environment (experience in GXP roles)

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

Adaptability to an ever-changing work environment

Education/Qualifications/Certifications and Licenses Recommended:

A minimum of a Bachelor’s Degree in Life Sciences preferred (or equivalent Life Science experience)

Experience may be substituted for education.

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:

As an EOE/AA employer, Labcorp strives for diversity and inclusion 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 of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), 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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