RESPONSIBILITYS

1. Able to independently complete drug preparation prescription screening, process research and optimization, and realize the transformation to pilot and large-scale production;

2. Responsible for the experimental implementation of drug preparation research and development for FDA, EMEA, and CFDA, record original data in Chinese and English and draft relevant application materials for drug preparation development;

3. Review the relevant research results of the project, including but not limited to product registration information, original data, maps, etc.; cooperate to complete the technical and regulatory compliance confirmation work involved in product registration.  

4. Training and guidance of subordinate employees.

REQUIREMENTS

1. Master degree or above, more than 3 years of relevant work experience, major in pharmacy, pharmacy, biochemistry and other related majors;

2. Have a strong pharmaceutical foundation and certain experience in drug preparation research and development, familiar with the requirements and regulations of drug research and development at home and abroad;

3. Able to draft and review research and development reports in Chinese and English;

4. Have rich drug preparation theory and experience, and be proficient in the use and daily maintenance of drug preparation equipment;

5. Have excellent professional ethics, professionalism and teamwork spirit; 6. Good team management ability and communication and coordination ability;

7. Have innovative spirit and strong stress resistance.

8. Those with ICH and FDA new drug registration experience are preferred.

Leader of Drug Perparation Project

RESPONSIBILITYS

1. Independently conduct literature search and develop synthesis process routes;

2. Able to independently design and optimize the synthesis route of target molecules; participate in product quality improvement and process technology improvement, and solve difficult problems in the project;

3. Responsible for the experimental implementation of API research and development for FDA, EMEA, and CFDA, record original data in Chinese and English, and draft relevant application materials for API development;

4. Review the relevant research results completed by the project, including but not limited to product registration information, original data, maps, etc.; cooperate to complete the technical and regulatory compliance confirmation work involved in product registration.

REQUIREMENTS

1. Major: Master degree or above in organic chemistry, synthesis and other related majors;

2. Have rich experience in organic synthesis theory and practice, and be familiar with the requirements and regulations of domestic and foreign drug development;

3. Be able to draft and review R&D reports in Chinese and English;

4. Have innovative spirit and strong stress resistance.

5. Those with ICH and FDA new drug registration experience are preferred.

BENEFITS

1. Five social insurances and one housing fund, living allowance, rental allowance;

2. Enjoy statutory holidays, paid annual leave, marriage leave, maternity leave, paternity leave, breastfeeding leave, bereavement leave, etc. stipulated by the state;

3. Year-end bonus, stock option incentives, annual physical examination, team building travel, etc.;

4. According to the work performance of employees in the company, those with excellent assessments can be promoted and receive salary increases, and annual salary increases, etc.;

5. Basic salary + various allowances + performance bonuses + project allowances + year-end bonuses + annual evaluation bonuses.

Drug Synthesis Researcher