QA Officer | Validation | Supplements & Pharmaceuticals | GMP | Free Shuttle

You will be at the center of ensuring equipment, processes, and systems remain in a validated state. In this role, you will design and execute validation protocols in accordance with GMP, PIC/s, and other relevant regulatory standards, lead testing and data documentation, and collaborate cross-functionally to ensure compliance and operational reliability. Join us to make a direct impact on quality and continuous improvement within a dynamic pharmaceutical GMP environment. 

• →Design and execute validation protocols — including IQ/OQ/PQ, process, and cleaning — in line with GMP standards. 

• →Lead testing, data collection, and documentation to ensure accuracy and full compliance. 

• →Collaborate closely with Manufacturing, Engineering and other teams to plan and implement validation activities. 

• →Proactively identify and address validation risks, deviations, and non-conformances, supporting root cause analysis and corrective/preventive actions. 

• →Maintain validation lifecycle documentation and support audit readiness. 

• Bachelor’s degree in Quality Management, Pharmaceutical Sciences, or a related technical field; advanced degree is a plus. 

• Minimum of 1 years of hands-on experience in validation within a regulated GMP environment, with a focus on Equipment & System, Cleaning, and Process Validation is preferred. 

• Practical knowledge of validation lifecycle and protocol execution; familiarity with PIC/s GMP standards is preferred but not mandatory. 

• Strong technical documentation skills, with the ability to analyze validation data and support compliance in audit settings. 

• Fluency in English and Chinese to thrive in our regional operations.