Bayer is a global enterprise with core competencies in the Life Science fields of health care and agriculture. Its products and services are designed to benefit people and improve their quality of life. At Bayer you have the opportunity to be part of a culture where we value the passion of our employees to innovate and give them the power to change

Validation and GMP Inspection Supervisor -验证与自检主管 

YOUR TASKS AND RESPONSIBILITIES

• Update site VMP and maintain VMP database routinely, manage Sys. No., track the progress of qualification and validation execution.
• Is responsible for creating periodic qualification documents, coordinate departments for execution. Participate in review Q&V protocols and reports from compliance perspective, especially enhance the management to process validation and cleaning validation as new requirements from up-to-date GSOPs and guidances.
• Enhance qualification management of site self-inspectors and provide related training, enhance self-inspection's scope and extent, enhance the CAPA management.
• Provide dedicate trainings periodically at site level about those findings from self-inspections and qualification&validaiton.
• Add the on-site inspection of qualification and validation during execution, enhance the documentation management.
• Participate or organize related departments to do risk assessment when there is upgrading of current systems or new technical system.
• Organize Third Party to perform site monitoring and maintainence of pest control, coordinate departments for deviation investigation about pest control if applicable.
• Update SOP according to GSOP and local requirements; some related work like, to review monthly maintenance report.

WHO YOU ARE

• University graduate or above in pharmacy or related major
• 5 years and above in quality department, or experience for implementation of qualification and validation
• Proven time management and communication skills.  
• High degree of autonomy in tasks, but team-worker and good skills in cross-functional work relationships
• GMP/regulations, Pharmaceutics and qualification/ validation related
• Knowledge of GMP standards and related national / international regulations and guidelines.
• Knowledge of production process and quality control.
• Good at computer operation.
• Fluent Spoken and good written English.

YOUR APPLICATION

If your background and personal experience fit this profile, please send us your complete application at www.career.bayer.cn If you have any recommendations, please kindly send mail to cnreferral@bayer.com
 

Location:                   

China : BeiJing : BeiJing 

Division:

Pharmaceuticals 

Reference Code:

347302