What will be your key responsibilities?

• Drive the implementation of GMP on-site in compliance with the Mars GMP/ GHP standard, including GMP for production/ engineering and contractor, etc.
• Document control system management including the Nexus system.
• Develop the quality system training material and training plan and follow the implement
• CAPA system follow up to make sure all CAPA are not overdue.
• Prepare the management review report material.
• Verify the system procedure and regulation requirement compliance in process.
• Coordinate change management assessment in site level.
• Complete any other projects assigned by QA Manager.

What can you expect from Mars?

• Work with over 130,000 like-minded and talented Associates, all guided by The Five Principles.
• Join a purpose driven company, where we’re striving to build the world we want tomorrow, today.
• Best-in-class learning and development support from day one, including access to our in-house Mars University.
• An industry competitive salary and benefits package, including company bonus.