Principal Quality Associate | Principle Associate (m/w/d)
Randstad Professional
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.
Required Skills
Education
University degree in a scientific field (Bachelor/Master/Diploma) OR vocational training as a Lab Assistant/CTA/BTA/MTA with additional Technician certification.
Experience
- Several years of professional experience in a GMP environment
- Experience in processing technical changes, CAPAs, and deviations
- Professional experience in a scientific or laboratory environment
- Experience in quality control (preferred)
Languages
Additional
- The role requires the ability to work in a highly regulated GMP/non-GMP environment and involves collaboration with international sites (Philadelphia).
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