GMP Spezialist (m/f/d)

Independent planning and implementation of internal system audits and external GxP supplier audits Interpretation, explanation and application of relevant GxP regulations, guidelines and procedures for pharmaceutical products Development of action plans to address compliance issues and quality assurance issues Providing advice and training on GxP requirements for colleagues and cross-functional teams Participation in the maintenance of the global audit plan, the list of suppliers and the further development of departmental procedures

Complete university studies, preferably in a scientific or engineering discipline Long-term professional experience in Regulatory Affairs, Quality Assurance or Pharmaceuticals Medical Devices Accreditation by a specialist organisation, e.g. CQA or CQM, desirable Funded and comprehensive understanding of the international GMP regulatory standards Detegratable leadership and technical expertise Secure application of common software Good knowledge of German in word and writing Careful and independent working Working time model: 37.5 hours/week

Attractive salary and long-term job security through corporate membership Extensive social benefits, including Christmas and holiday allowances Aid for occupational pensions after the end of the trial period Up to 30 days holiday per year Individual training with renowned partners Monthly changing employee offers, e.g. for technology, fashion, cars, etc. .