At STADA we pursue the purpose of "Taking care of people's health as a trusted partner." Generics, Consumer Healthcare and Specialties, we offer patients, doctors and pharmacists a wide range of therapeutic options.
Dealing with pharmaceutical technical enquiries in global quality compliance regarding the responsibility of STADA AG as MAH, Batch Releaser etc.
*Coordination of Tasks related to a certain process of a Quality Team to ensure compliance with Health Authorities requirements and company standards.
*Active participation in Quality System Processes, such as GMP documentation management, change control, investigation, deviation, CAPA activities and others as well as maintenance of the systems that manages the product, process, and packaging information as well as master data as applicable
*Execution and providing training according to area of responsibility.
*Tracking of actions, review and communication of timelines, escalation of delays and documentation of aliment meetings (project management)
*Administration of the change process within the electronic tool, e.g. through the creation and assignment of actions and impact assessments or the summaries / assessment of the generated data within the different steps according to current guidelines and GMP principles
*Advanced level of knowledge of MS Office package
*STADA offers a competitive environment for personal and professional development in a growing company full of opportunities.
Our future project requires dynamic and proactive professionals, capable of adding value in a changing environment.