Senior / Production Officer (Temporary Role - 3-month contract) | GMP | Tai Po

Senior / Production Officer (Temporary Role - 3-month contract) | GMP | Tai Po Add expected salary to your profile for insights Ready to shape the future of Health and Wellness? AtVita 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 seeking a meticulous and experienced Senior Production Officer to join our team on a temporary 3‑month contract. In this critical role, you will be a key support to the Production Manager, ensuring the smooth, compliant, and efficient execution of our daily manufacturing operations. The ideal candidate is a proactive professional with a strong foundation in GMP, exceptional attention to detail, and a commitment to maintaining the highest standards of quality and documentation. What You'll Be Doing Operational Coordination: Assist the Production Manager in organizing and coordinating the daily activities of the Production Department to meet output targets. Documentation Management & Compliance: Prepare, review, and maintain critical documentation, including Batch Production Records (BPRs), Validation/Qualification protocols, and Standard Operating Procedures (SOPs) to ensure full compliance. GMP & Quality Assurance: Ensure all production processes and workflows strictly adhere to current Good Manufacturing Practice (GMP) guidelines and internal quality policies. Conduct routine monitoring of records and logbooks for accuracy and completeness. Systems & Hygiene Oversight: Assist in the development, implementation, and maintenance of the production documentation system. Monitor production equipment and cleanroom hygiene according to approved GMP procedures. Training Support: Participate in the induction and on‑the‑job training of new and existing production staff to uphold operational standards. Who We're Looking For Experience: Minimum of 3 years of hands‑on experience in a production or manufacturing environment within the pharmaceutical, biotechnology, or related regulated industry (GMP). Knowledge: Solid understanding and practical experience with GMP requirements, documentation practices (BPRs, SOPs), and quality systems. Experience with validation/qualification processes is a strong plus. Skills: Excellent organizational and coordination skills. Strong attention to detail and a commitment to accuracy in documentation. Effective communication and interpersonal skills. Ability to work independently and as part of a team in a fast‑paced environment. 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. 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. Equal Opportunity Employer 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 #J-18808-Ljbffr