The role involves conducting incoming goods inspections and executing interim and final inspections of clinical trial samples during production
Job Summary
The role involves conducting incoming goods inspections and executing interim and final inspections of clinical trial samples during production.
Candidates will be responsible for preparing GMP-relevant documents such as SOPs, specifications, and test instructions while ensuring adherence to company processes.
The position requires developing CAPA measures and supporting the investigation and evaluation of GxP-relevant deviations to ensure quality conformity.
Matching Summary
The role involves conducting incoming goods inspections and executing interim and final inspections of clinical trial samples during production.
Skills & Requirements
Must-have
GMP standards compliance
Incoming goods inspection
Batch record review
SOP and specification creation
Deviation investigation
CAPA implementation
Nice-to-have
Team training support
Change control participation
Root cause analysis skills
Self-motivated attitude
Meaningful mission focus
Key Requirements
Vocational training in pharmaceutical fields or Bachelor's degree
First professional experience in quality control or assurance
Fluent German and English language skills
Knowledge of regulatory requirements in GMP and GDP environments