Johnson & Johnson Careers

Associate Manager, Supplier Quality Management

Shanghai, China
Quality (Eng)

Job Description

Requisition ID: 1805647512W

·         Day-to-day supervision on implementation of the approved standard procedures related to material & warehouse management.

·         Participation in supplier/material selection and qualification activities.

·         Plan, conduct supplier audit using a risk-based approach against the J&J quality requirement. Evaluate and monitor the supplier’s MAP and its progress.

·         Work very closely with other departments to improve overall supplier’s quality performance and establish best practices to ensure supplier/material management fully comply with current GMP, and J&J quality standards.

·         Supervision and improvement material quality with the process of quarterly and annual review and common continuous improvement tools (e.g., Lean, DMAIIC, SPC)

·         Do evaluation and control for any change request from supplier’s end based on risk assessment methodology

·         Problem solving through NC/CAPA system to identify root cause and assess action taken from suppliers for material quality issues as a coordinator in required time period.

·         Work with the head of SQM to design and deploy SQE2/TA project to continuously improve the quality performance in key suppliers. 

·         Work with site strategic sourcing team to update supplier ownership list and ensure exact information reflected to the updated list.

·         Participate in process improvement projects and initiatives

·         Support ASPAC COE ONE activities.

Comply with the rules and regulations of company, EHS, and HCC  

·         A minimum bachelor degree, major in relevant science (e.g. pharmacy, chemistry, chemical engineering, microbiology, food technology)

Work Experience

·         A minimum of 5 years working in QA function in pharmaceutical industry


·         Strong communicator, and good team work with others

·         Good spoken and written English.

·         Good understanding on Chinese GMP and other regulations in China, cGMP, PIC/S and ICH knowledge preferred.

·         Experience in auditing and health authority inspections desirable.

·         High energy level; positive attitude; works well under stress

·         Problem solving and action planning facilitation skills

Primary Location
Shanghai Johnson & Johnson Pharmaceuticals, Ltd. (7048)
Job Function
Quality (Eng)
Requisition ID