Government, Regulatory and Code, Pharmaceutical, Quality, Quality Engineering
Required Education:
4 Year Degree
The individual will promote a quality driven culture across Covance Central Laboratory Services through the conduct of internal audits and through the interactions with operational departments.
Essential job duties listed below;
Performs internal audits according to applicable standards.
Identifies opportunities for improvement within the organization.
Acts as a liaison for an operational department.
Executes existing interpretation of regulatory requirements and quality standards.
Delivers training material to QA teams.
Creates local procedures.
Provides support to client audit hosts.
Trains auditors on the regulatory requirements.
Other essential job duties as assigned by management.
BA/BS four year degree in medical, technical or laboratory-related science
Minimum of 4 Years of experience Preferred
Extensive Covance specific database knowledge.
Formal GLP and GCP training.
Participated in external continuing educational programs in quality assurance related sessions.
Internal Number: 2020-50013
About Covance
Covance, the drug development business of LabCorp, is the world’s most comprehensive drug development services company. Because of our broad experience, from early research to commercialization, our more than 20,000 employees from across the globe are in a unique position to supply insights that go above and beyond testing. Our team’s impact on healthcare is remarkable. Through their everyday work they’ve supported 100% of the top 50 drugs on the market and all the oncology drugs approved in 2016. Even though we span multiple businesses, we operate as one, sharing our knowledge to improve our efficiency and deliver on the promise of a healthier world.
