Senior Specialist Abweichungen (m/w/d)

With over 15 years of experience in the classic pharmaceutical industry, biotechnology, chemistry and medical technology, we know the key contact persons who write out demanding tasks with potential. The high demand for personnel opens up exciting opportunities for dedicated professionals and managers to develop professionally and work on their own careers. As a specialized staff consultancy with an international network, we offer you decisive advantages - and this is completely free of charge for you. Register and benefit from interesting and matching positions and projects. Function as owner for deviations and risk analyses: Responsibility for the planning, coordination and implementation of events Coordination of interfaces for example for production, MSAT and quality assurance Function as an expert in the applicable internal GMP standards to ensure the correct presentation of production documentation Working with the continuous optimization and standardization of the deviation process

Complete training for technicians Chemistry, Biotechnology or the like or a study with technical or scientific focus (e.g. Biotechnology, etc.) Found professional experience in the field of production and quality assurance in the GMP environment is absolutely necessary and indispensable Strong Quality Management Background flowing German and (at least) good English knowledge in word and writing IT Affinity and ability to work quickly into new tools Ability to adjust to different stakeholders

Annual holiday entitlement of 30 days Varied activity in a renowned company Demanding and varied tasks in a future-oriented and innovative industry Support in the ongoing project by our team Care in the entire application process