1. Manage the Quality Systems of Grin Laboratories.
- Manage the Documentation System and Qdoc System.
- Ensure that all GMP-related documents at Grin Laboratories are created, reviewed, updated, and stored in accordance with applicable regulations.
- Ensure that each generated document complies with the coding system for each document type.
- Ensure the efficient use of the area's material resources.
- Ensure that all documents are reviewed periodically and kept up to date.
- Send the validity status of all documents to the responsible parties in each area.
- Manage the logbook lifecycle.
Qualification and Experience
Bachelor's degree in Chemical Engineering, Pharmaceutical Chemistry, Pharmaceutical Engineering, or equivalent. Skills: Initiative, Teamwork, Adaptability, Integrity, Planning, and Goal-oriented.
2 years of experience in Quality Assurance or Quality Systems.