About this role
Job Description 1. Manage the Quality Systems of Grin Laboratories. 2. Manage the Documentation System and Qdoc System. 3. Ensure that all GMP-related documents at Grin Laboratories are created, reviewed, updated, and stored in accordance with applicable regulations. 4. Ensure that each generated document complies with the coding system for each document type. 5. Ensure the efficient use of the area's material resources. 6. Ensure that all documents are reviewed periodically and kept up to date. 7. Send the validity status of all documents to the responsible parties in each area. 8. 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. Competencies Collaboration Customer Centricity Developing Talent Innovation & Creativity Process Excellence Result Orientation Stakeholder Management Strategic Agility