Praktikant*in im Bereich Qualifizierung (alle Geschlechter)
Core
Support the execution, documentation, and archiving of qualification activities and requalification tasks within a regulated pharmaceutical environment.
Role type
Intern (Qualification)
Builds
GMP documents, Standard Operating Procedures (SOPs), and supplier documentation.
Domain
Life Sciences / Pharmaceutical Manufacturing
Required skills
Technical or natural science degree (Pharmaceutical Engineering, Chemical Engineering), Microsoft Office, German (fluent), English (fluent)
Preferred skills
Experience in regulated environments, experience with qualification activities
Technologies
Microsoft Office
Responsibilities
Execute and document qualification and requalification activities, assist in creating and revising GMP documents and SOPs, review supplier documentation, support cross-functional projects, contribute to establishing team work standards.