Job Responsibilities:

1. Responsible for verifying the formulation and revision of related SOPs, and continuous improvement of related processes;

2. Carry out the company's verification management, formulate the company's annual verification master plan, organize implementation and process monitoring;

3. Circulation, management, and completion of verification documents. Preparation before implementation of verification projects. According to user needs, regulations, SOPs and other documents, formulate verification evaluation, IQ/OQ/PQ, process verification and cleaning verification programs;

4. Establish a verification/verification project team, review verification plans, verification/verification plans and reports, and guide and coordinate risk assessment;

5. Investigation and handling of deviations in confirmation/verification;

6. Change management during confirmation/verification;

job requirements:

1. Major in pharmacy, pharmaceutical engineering, chemistry, bachelor degree or above;

2. More than five years of practical experience in drug production and quality management;

3. Experienced FDA, EU, China and other official GMP inspections;

4. Production, QC and other departments have rich experience in transformation, QA can also be considered;

Work location: No. 5, Donghai Fourth Avenue, Toumen Port Economic Development Zone, Zhejiang Province

Please call: 0576-85589365 E-mail:hr@ausunpharm.net