质量专员(轮岗培养)
On-site · Shanghai, Shanghai, China
Job Summary
Support the daily operations of the SQM and Quality Processes teams while rotating through QC, QA, QS&C and Affiliate Quality within PT China. The rotation aims to familiarize with responsibilities across different quality functions and to develop future talent in quality management. Key duties include quality risk management (QRM) per GMP/GSP standards, monitoring quality metrics, coordinating Quality Council activities, providing quality and compliance oversight for external GxP suppliers, ensuring on-time batch dispositions for API/materials, frontline QA activities in plants, handling quality-related investigations, and overseeing outsourced GMP activities in CMO sites. Manage analytical method validation, instrument maintenance/calibration, and transfer/troubleshooting of methodologies. Contribute to QMS execution and regulatory compliance, document management, change control, and inspection/audit readiness. Qualifications include a Bachelor’s Degree (or higher preferred), fresh graduates or up to 1 year of experience, and strong knowledge of GMP, quality systems, and English proficiency (CET6). This role is based in Shanghai, China with full-time engagement and rotation across various quality functions.
Required Qualifications
- Bachelor’s Degree in Pharmaceutical, Chemistry, Biochemistry, Bio-engineering or relevant disciplines
- Fresh graduates or within 1-year working experience acceptable
- Good knowledge of Quality System and Compliance principles in pharmaceutical industry
- Knowledge of cGMP/regulations
- Proficiency in English (CET6)
- Proficient with office software (Word, Excel, PowerPoint)
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