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

> Vita Green Health Product Company Limited · Tai Po Industrial Estate, China · Full-time · Posted 2026-03-02

**Workplace:** on_site

**Department:** QA

## Description

**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!_

## Apply

[Apply at Vita Green Health Product Company Limited](https://apply.workable.com/vita-green/j/B38E2049F6/apply)

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