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- Bright Future Pharmaceutical Laboratories LimitedHong Kong
- Conduct laboratory testing (routine test and stability study) and prepare analytical documents.
- This role involves laboratory testing including routine tests…
- Bright Future Pharmaceutical Laboratories LimitedHong Kong
- Responsible for following up on QA/QC related matters for the new project.
- Establish and maintain the quality management system of Chinese medicines, and ensure…
- Bright Future Pharmaceutical Laboratories LimitedHong Kong
- Oversee daily operations on the production floor, coordinating on-site resources to ensure production schedules are met.
- Bright Future Pharmaceutical Laboratories LimitedHong Kong
- Oversee daily operations on the production floor, coordinating on-site resources to ensure production schedules are met.
- Bright Future Pharmaceutical Laboratories LimitedHong Kong
- You will be responsible for the maintenance and management of all facilities such as air conditioners, air compressors, and boilers per design performance…
- Bright Future Pharmaceutical Laboratories LimitedHong Kong
- Prepare the layout and designs of new facilities, production systems and utilities, according to user requirement specifications and latest GMP requirements.
- Bright Future Pharmaceutical Laboratories LimitedHong Kong
- In charge of production management to fulfill GMP requirement, such as production on site management, facility and equipment management as well as documentation…
Job Post Details
QC Analyst
Job details
Pay information not provided
Full-time
Hong Kong
Full job description
Bright Future Group
Headquarters in Hong Kong, Bright Future Group is a leading pharmaceutical company committed to developing affordable and reliable generic medical solutions, and bringing brighter life better future to people’s lives all over the world since 1993. Today, we are the largest GMP certified pharmaceutical manufacturer in Hong Kong. With years of development, we have also established our subsidiary plants in Mainland China, USA and Germany. Pursuing its long-term corporate vision, more than 7,000 employees dedicate themselves in the research and development, manufacturing and commercialization of more than 160 generic medicines and health supplements worldwide. We focus on the treatment of disorders for patients in dermatology, orthopedics, respiratory, pediatrics, geriatric and gynecology. Bright Future Group has a strong international R&D team in Hong Kong, New York in US as well as Haikou and Suzhou in China to support our pipeline. We strive to our commitment and continue to expand our product portfolio to make a significant contribution locally and globally.
To facilitate our rapid growth in pharmaceutical business, we now invite high caliber talents with progressive career prospects to join us as follows.
www.brightfuture.com.hk
About the role
This role involves laboratory testing including routine tests and stability studies, preparation of analytical documents, and method validation of raw materials and finished products. You will conduct OOS investigations and CAPA activities as per PIC/s requirements.
Key responsibilities
Conduct laboratory testing (routine test and stability study) and prepare analytical documents
Perform method validation of raw materials and finished products
Conduct OOS investigation and CAPA activities as per PIC/s requirement
About you
Bachelor degree or above in chemistry or related fields
Experience in operating analytical instruments, such as HPLC/GC, is a plus
Fresh graduates and IANG are also welcomed
Full-time
Headquarters in Hong Kong, Bright Future Group is a leading pharmaceutical company committed to developing affordable and reliable generic medical solutions, and bringing brighter life better future to people’s lives all over the world since 1993. Today, we are the largest GMP certified pharmaceutical manufacturer in Hong Kong. With years of development, we have also established our subsidiary plants in Mainland China, USA and Germany. Pursuing its long-term corporate vision, more than 7,000 employees dedicate themselves in the research and development, manufacturing and commercialization of more than 160 generic medicines and health supplements worldwide. We focus on the treatment of disorders for patients in dermatology, orthopedics, respiratory, pediatrics, geriatric and gynecology. Bright Future Group has a strong international R&D team in Hong Kong, New York in US as well as Haikou and Suzhou in China to support our pipeline. We strive to our commitment and continue to expand our product portfolio to make a significant contribution locally and globally.
To facilitate our rapid growth in pharmaceutical business, we now invite high caliber talents with progressive career prospects to join us as follows.
www.brightfuture.com.hk
About the role
This role involves laboratory testing including routine tests and stability studies, preparation of analytical documents, and method validation of raw materials and finished products. You will conduct OOS investigations and CAPA activities as per PIC/s requirements.
Key responsibilities
Conduct laboratory testing (routine test and stability study) and prepare analytical documents
Perform method validation of raw materials and finished products
Conduct OOS investigation and CAPA activities as per PIC/s requirement
About you
Bachelor degree or above in chemistry or related fields
Experience in operating analytical instruments, such as HPLC/GC, is a plus
Fresh graduates and IANG are also welcomed
Full-time
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