Principal Quality Associate | Principle Associate (m/w/d)

Job Summary

As a Principal Quality Associate in Penzberg, you will play a vital role in developing and harmonizing quality control concepts within a leading international life sciences environment. Your daily responsibilities include collaborating with subject matter experts to create GMP and non-GMP (R&D) regulations, managing planned events, CAPAs, and deviations within the Veeva QMS system. You will also support data integrity assessments for R&D equipment and maintain master data in SAP. This position is particularly unique due to its international scope, involving the harmonization of processes between the Penzberg site and Philadelphia. It offers a high degree of responsibility in ensuring compliance and operational excellence within a cutting-edge research and innovation hub. The role is ideal for professionals who enjoy cross-functional collaboration and technical documentation in a highly regulated environment.