The primary objective is to guarantee the correct, controlled, and traceable receipt of materials and products according to medical device regulatory requirements
Job Summary
The primary objective is to guarantee the correct, controlled, and traceable receipt of materials and products according to medical device regulatory requirements.
Responsibilities include verifying supplier documentation, registering entries in the ERP system, and immediately reporting any discrepancies or damaged materials.
The role requires strict adherence to Good Manufacturing Practices (GMP), ISO 13485 standards, and maintaining proper segregation of materials based on their inspection status.
Matching Summary
The primary objective is to guarantee the correct, controlled, and traceable receipt of materials and products according to medical device regulatory requirements.