About the job
Are you ready to make a significant impact in the Health and Wellness sector?
At Vita Green, we strive to create a healthier and happier world, and we invite you to be a part of this mission!
About Vita Green Group
Vita Green leads the health supplements industry, dedicated to enhancing well-being through innovative research and state-of-the-art solutions. Our GMP and HACCP-certified facilities guarantee top-tier quality control at every stage—from sourcing high-quality raw materials to advanced research and development, ensuring excellence in every product.
With a diverse portfolio of well-established brands and over 150 products, we are continuously expanding our reach to global markets. At Vita Green, we uphold the highest standards, paving the way for a healthier future.
Position Overview
We are seeking a motivated and detail-oriented Registered Pharmacist to join our team for a GMP Compliance Project. This role presents an exceptional opportunity for a newly registered pharmacist to acquire hands-on experience and establish a solid foundation in pharmaceutical manufacturing and quality control. Under the mentorship of experienced Authorized Persons (APs) and industry professionals, you will play a vital role in ensuring compliance with Good Manufacturing Practice (GMP) standards at our Tai Po site, with complimentary shuttle services available for your convenience.
Key Competencies to Develop
- Comprehensive understanding of GMP principles and compliance requirements.
- Practical experience in pharmaceutical manufacturing and quality control processes.
- Familiarity with Hong Kong pharmaceutical laws and administrative processes.
- Ability to assist and eventually lead audits, inspections, and batch certifications.
Your Responsibilities
- Assist in ensuring that pharmaceutical products are manufactured and evaluated in accordance with GMP standards.
- Support the Authorized Person (AP) in certifying and releasing batches of pharmaceutical products, ensuring compliance with registered particulars.
- Gain practical exposure to quality control processes, including sampling, analysis, and documentation.
- Assist in the preparation, review, and maintenance of Standard Operating Procedures (SOPs), batch records, and validation protocols.
- Participate in GMP audits, process improvements, and compliance activities as directed by the AP or senior management.
- Develop a working knowledge of pharmaceutical laws, regulations, and administrative procedures in Hong Kong.
- Support daily manufacturing and quality assurance activities, learning to identify and resolve issues effectively.

