Associate Manager Quality Compliance

Independently planning and conducting research on good manufacturing, good laboratory, and good clinical practices pertinent to FDA regulated industries to support the development of Altria's Quality Requirement Manual (AQRM), Quality Management System (QMS) and general quality practices.
  • Providing regulatory expertise in development of quality requirements for e-vapor product devices and components.
  • Assisting in the development, implementation and continuous monitoring of objectives, procedures, tracking and trending mechanisms to ensure that management is consistently informed on the status and effectiveness of compliance activities.
  • Planning, conducting and reporting the results of internal, supplier, and/or clinical related quality audits to departmental and operational management.
  • A Bachelor's Degree in a Physical Science, Engineering or a related field.
  • Strong written, verbal and presentation skills along with demonstrated ability to collaborate with others.
  • The ability to perform assignments in an independent and autonomous manner with minimal direct supervision.
  • Comfortable working during non-core hours as required to assess multiple shifts and operations spanning lengthy periods.
  • In addition to the opportunity to apply and develop your skills toward key business objectives, we offer an excellent compensation package including a competitive base salary, comprehensive health/vision/dental insurance, participation in our incentive compensation and deferred profit sharing programs as well as a relocation assistance package.