QC Manager

Job Responsibilities

1. Responsible for managing QC personnel, including recruitment, training, performance evaluation, daily work arrangements, continuously improving work processes, and enhancing work efficiency;
2. Responsible for managing the QC documentation system, formulating departmental management procedures, and reviewing laboratory-related SOPs, testing methods, quality standards, validation plans, etc.;
3. Supervise the verification (confirmation) of inspection instruments and methods in the department to ensure the accuracy of test results;
4. Ensure that necessary inspections are completed before the release of materials and products, confirming that they meet quality requirements;
5. Responsible for the timely and accurate issuance of inspection reports and reviewing inspection report forms;
6. Manage QC-related projects to ensure projects are completed as planned;
7. Ensure the effective operation and continuous optimization of the quality control management system;
8. Supervise and participate in departmental changes, CAPA, and investigations related to laboratory OOS/OOT/abnormal test data;
9. Ensure the completeness, reliability, and authenticity of QC laboratory data;
10. Complete other tasks assigned by the superior supervisor.

Job Requirements

1. Bachelor's degree or above in chemistry, biology, pharmacy, or related fields;
2. Understand principles and operations of inspection; Familiar with pharmaceutical GMP regulations and domestic and international pharmacopeia-related testing descriptions;
3. Good English reading ability and proficient in computer operation;
4. At least 5 years of work experience in the pharmaceutical industry and over 2 years of management experience.

HR Email: hr@biotech-pack.com (If interested, please contact us through this email or directly send your resume)