GE 通用电气，招聘全职应届生。理工科背景。
1. Reviewing of production documentation and assisting with batch release procedures 2. Liaising with Operations personnel to ensure regulatory and quality requirements are met during routine operations 3.Supporting the ongoing deviation / corrective action program 4. Liaising with other departments to allow closure of corrective actions 5. Participating in audits, together with follow up. 6. Responding to routine quality related queries from other departments 7. Monitoring and aiding the implementation of continuous improvements and process changes to ensure that these are implemented in compliance with GMP. 8.training of Operations personnel 9. Support the timely release of product to market. 10. Conducting QA activities including revision of SOPs, SAP QA work and the issuance of protocols. 11. Review, Approval and Reporting Activities related to the QMS 12. Attending a number of cross functional team meetings /projects

Qualifications Required:

1. B.S. Degree in business or technical field or equivalent experience 2. 1-year experience in a medical device or pharmaceutical industry. 3. 1-year experience with CA/PA systems, including complaint handling. 4. Thorough familiarity with cGMPs of sterile product manufacture 5. Knowledge of relevant Electronic Management Systems transactions and familiarity with Excel / Word packages

Desired Characteristics

1. Statistics education and or training 2. Experience developing and tracking quality metrics 3. Familiar with Continuous Improvement methodologies, including Six Sigma