Labcorp has a Quality Assurance Auditor -Molecular BioA position at 671 South Meridan Road, Greenfield, IN. 

Work Schedule: Monday -Friday, 8am – 5pm

Job Responsibilities:

Conduct, but not limited to protocol review, single department report/data audits, in-lab phase audits where applicable for multiple business areasDevelopment and delivery of training to operational groupsDelivery of training in performance of auditsProvide advice and guidance on aspects of quality and complianceProvide consultation to the operational team on quality issueCross-site QA and operational relationship, provide recommendations for improving compliance and/or efficiencyWork with operational management to support Quality topics and/or working on projects with QA team on other sites [showing development of collaboration skills] Manage local Quality initiatives aimed at improving compliance and/or efficiency of the local QA organizationEnsure Regulatory Compliance and Quality Assurance responsibilities, as indicated in applicable controlled documents, are followed

Minimum Qualifications:

Minimum: Bachelor’s Degree in Life Sciences preferred (or equivalent Life Science experience)3 years in a regulatory environment (experience in GLC/GCP roles)1 year experience in Molecular BioA

Additional Qualifications:

Knowledge of GLP/GCP auditingAble to influence QA strategyKnowledge of industry quality systems/standards and able to apply (applicable) regulations to monitor complianceExperienced in process improvementDemonstrated ability to apply critical thinking skillsClear communication skills, including ability to provide clear feedbackAble to clearly articulate processes to provide trainingAble to influence process improvement initiatives and offer solutions Job Description 3 Working Conditions:

The individual in this role verifies compliance with standard operating procedures (SOPs) and regulations by performing study protocol, report/data and in-lab phase audits where applicable for multiple business areas. The auditor leads internal and external facility/process and/or supplemental inspections, provides recommendations for improving compliance, and prepares and delivers training in performance of audits. 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), Good Manufacturing Practice (GMP), and Good Laboratory Practice (GLP) in the performance of their role.

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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