立即应征

不指定
0年工作经验

职位描述

Job Responsibilities:

1. The establishment and maintenance of product technology transfer and process improvement management systems comply with product registration and GMP regulations;

2. Organize product technology transfer and production process improvements;

3. Responsible for organizing and executing the trial production of new products and testing new processes ;

4. Review process regulations, approve production records, and other production technical documents;

5. Review records of deviations, changes, etc., related to process technology;

6. The establishment and maintenance of the process verification and cleaning management system comply with GMP requirements;

7. Review process verification and cleaning verification plans and reports, and supervise verification implementation according to preset schemes;

8. Coordinate the implementation of various verification tasks, risk assessments, and SOP implementations;

9. Other tasks assigned by superiors.

Job Requirements:

1. Bachelor's degree or higher, majoring in pharmacy, pharmaceutics, pharmaceutical engineering, or related fields;

2. Proficient listening, speaking, reading, and writing skills in Chinese and English; familiarity with Cantonese is preferred;

3. Over 8 years of production or R&D experience in large or reputable pharmaceutical companies, including 3+ years of experience in pilot scale-up and technology transfer;

4. Proficient in solid dosage, semi-solid, and liquid process technologies, as well as technology transfer requirements;

5. Familiarity with GMP requirements and industry guidelines related to validation.

6. Strong organizational, coordination, and communication skills; possess solid English reading and writing abilities, demonstrate strong execution capabilities, and effectively handle work pressure.


工作种类
工作地区 不指定

有关招聘公司
Bright Future Pharmaceutical Laboratories Ltd