Pharmacy Intern in Production for 2027 (all genders)

Creating and maintaining Standard Operating Procedures and risk analyses. Supporting GMP-compliant documentation. Maintaining and archiving documents in accordance with GMP requirements. Supporting the preparation of validation plans and reports and sample collection. Coordinating sample shipments. Processing change and CAPA measures. Supporting optimization projects within production. Working closely with experienced professionals.

Second state examination in pharmacy completed by the start of the internship. Initial work experience in a GMP environment is desirable. Willingness to learn about pharmaceutical production sites and GMP-regulated production processes, as well as an interest in scientific work. Dedicated, reliable, and communicative working style. Enjoyment of teamwork. Confident use of Microsoft Office. Very good written and spoken German and English.