รายละเอียดงาน**กรุณาตรวจสอบสถานที่ปฏิบัติงานว่า สามารถเดินทางไปทำงานได้ ก่อนกดสมัคร
1. Translates the long-term goals for Quality System (QS) into tactical plans while maintaining oversight of the department’s operational and financial status.
2. Endorses the Standard Operating Procedures (SOPs) for plants and reviews validation plans and procedures, ensuring alignment with Current Good Manufacturing Practices (CGMPs) and regulatory requirements, respectively.
3. Defines the information required for new product registrations and facilitates registration applications to obtain approval for the release of biological products.
4. Responsible for building department personnel capability by initiating training programs, and developing strategies to facilitate operational improvements for the department.
5. Responsible for all QS activities within the organization.
6. Deep knowledge of regulatory requirements and expertise pertaining to verification of product and process quality for product release.
7. Leader who provides clear guidance on critical work activities and deliverables, and has the foresight to develop skills and capabilities within and beyond the department to optimize resources, talent and overall performance.
8. Ability to develop creative solutions to resolve problems.