Registered Pharmacist | GMP Compliance | Quality & Ops | Tai Po Site at Vita Green Health Product Company Limited

Tai Po District, Hong Kong, China -

Full Time

Start Date

Immediate

Expiry Date

21 Dec, 25

Salary

0.0

Posted On

22 Sep, 25

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

GMP Compliance, Quality Control, Pharmaceutical Manufacturing, Attention To Detail, Organizational Skills, Communication Skills, Interpersonal Skills, Regulatory Compliance, Problem Solving, Team Collaboration, Adaptability, Training, Documentation, Auditing, Process Improvement

Industry

Retail

Description

Ready to shape the future of Health and Wellness? At Vita Green, we are all about creating a healthier, happier world, and we want you to be part of it! 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 continually expand and reach markets worldwide. At Vita Green, we uphold the highest standards, paving the way for a healthier future. Position Overview We are looking for a motivated and detail-oriented Registered Pharmacist to join our team for GMP Compliance Project. This role offers an exceptional opportunity for a newly registered pharmacist to gain hands-on experience and build a strong foundation in pharmaceutical manufacturing and quality control. Under the guidance of experienced Authorized Persons (APs) and industry professionals, you will play a critical role in ensuring compliance with Good Manufacturing Practice (GMP) standards at our Tai Po site, with free shuttle services provided for convenience. Key Competencies to Develop In-depth 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 support and eventually lead audits, inspections, and batch certifications. What You'll Be Doing Assist in ensuring that pharmaceutical products are manufactured and checked in compliance with GMP standards. Support the Authorized Person (AP) in certifying and releasing batches of pharmaceutical products, ensuring adherence to 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 day-to-day manufacturing and quality assurance activities, learning to identify and resolve issues effectively. Undergo structured training on regulatory compliance, GMP principles, and pharmaceutical production. Who We're Looking For Education: Must be a Registered Pharmacist in Hong Kong (or eligible for registration). Skills & Attributes: Strong interest in pharmaceutical manufacturing, quality control, and regulatory compliance. Excellent attention to detail and organizational skills. Strong communication and interpersonal skills for effective collaboration within a team. Eager to learn and adapt to a fast-paced, highly regulated environment. Why Join Us Training & Development This role is designed to provide structured training and hands-on experience. Supervised by experienced APs, you will gain practical exposure to GMP pharmaceutical manufacturing and quality assurance processes. Training programs will include: Fundamentals of GMP principles and their application in manufacturing and quality control. Understanding regulatory requirements of the Pharmacy and Poisons Board of Hong Kong. Preparation for potential future registration as an Authorized Person (AP). 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. Fun working culture with challenges to learn and grow together Rapid growth opportunities for strong performers Competitive benefits package with staff purchase discount to experience our quality products Enjoy different special leaves Casual wear every day to enjoy your work and flexible working schedule Chance to work on cutting-edge technology projects And More! Vita Green Health Products Co., Ltd. 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! #LI-EY1

Responsibilities

Assist in ensuring that pharmaceutical products are manufactured and checked in compliance with GMP standards. Support the Authorized Person in certifying and releasing batches of pharmaceutical products, ensuring adherence to registered particulars.