About Vita Green Group 
Vita Green stands at the forefront of the health supplements industry, committed to enhancing well-being through innovative research and cutting-edge solutions. Our GMP and HACCP-certified facilities ensure top-tier quality control at every step—from sourcing premium raw materials to advanced R&D—guaranteeing excellence in every product.  

With a diverse portfolio of established brands and over 150 products, we are continually expanding and reaching markets worldwide. At Vita Green, we uphold the highest standards, paving the way for a healthier future.  

Position Overview​ 

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. 

Requirements

What You’ll Be Doing​ 

• 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. 

Who We’re Looking For 

• 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.

Benefits

Why Join Us 

We value your professional and personal growth – fostering a positive work culture is our priority. Here, you’ll find more than just a job, you’ll discover a genuine opportunity to thrive. 

• Be part of a forward-thinking company dedicated to health and wellness.  

• Engage in pioneering projects that push the boundaries of innovation. 

• Opportunities for professional growth and development. 

• Generous leave policies, including paid annual leave, birthday leave, and other special leaves 

• Free and convenient shuttles from various locations. 

• Collaborate with a talented and diverse team. 

• Attractive staff purchase discount from your first day at work. 

And more!!! 

Vita Green Pharmaceutical (H.K.) Limited is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.  

Join us in our mission to make a positive impact on wellness around the world!