Careers

Career Openings

★ We have established a long-term mechanism for the introduction, reserve, evaluation, supervision, and guarantee of high-quality and high-level scientific and technological talents, built specialized research facilities, and attracted more talents to carry out scientific research and development, ensuring that talents are attracted, retained, and well utilized.

★ Organize employee training and learning based on their job sequence and job level. By providing refined and targeted training courses, individuals can enhance their abilities, improve work performance, promote the improvement of professional ethics, and achieve career development.

★ Provide comprehensive protection for employees' medical, food, accommodation, and transportation needs, making their work comfortable and life happy

 

Careers

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On-site QA Job Responsibilities

On-site QA Job Responsibilities

1

Negotiable

2025-05-07

1. Responsible for quality supervision of each batch of drug production and inspection process; communicate with CMO in time for tracking and rectification of problems found during inspection; 2. Participate in dealing with deviations, changes, returns, etc. during the production process; 3. Audit product process protocols, batch production records (blank), process/cleaning validation programs and reports; 4. Audit batch production records, batch inspection records, complete product release audit, batch file archiving; 5. Participate in CMO, material supplier site quality audit; 6. Draft quality agreements for commissioned production of pharmaceutical products, check the design of printed packaging materials and other text content information; 7. Responsible for product annual quality review report data collection and audit; 8. Participate in the collection and audit of B license additions; participate in GMP compliance checks. Qualifications 1. Bachelor degree or above in pharmacy related majors; 2. 2 years and above working experience in sterile preparation, engaged in QA or production management related work; 3. Familiar with drug administration law, drug production supervision and management methods, GMP, MAH related laws and regulations; 4. Adapt to business trip, work conscientiously and responsibly, and be good at communication with the outside.

Submit Resume

On-site QA Job Responsibilities

On-site QA Job Responsibilities

2

Negotiable

2025-05-07

1. Responsible for quality supervision of each batch of drug production and inspection process; communicate with CMO in time for tracking and rectification of problems found during inspection; 2. Participate in dealing with deviations, changes, returns, etc. during the production process; 3. Audit product process protocols, batch production records (blank), process/cleaning validation programs and reports; 4. Audit batch production records, batch inspection records, complete product release audit, batch file archiving; 5. Participate in CMO, material supplier site quality audit; 6. Draft quality agreements for commissioned production of pharmaceutical products, check the design of printed packaging materials and other text content information; 7. Responsible for product annual quality review report data collection and audit; 8. Participate in the collection and audit of B license additions; participate in GMP compliance checks. Qualifications 1. Bachelor degree or above in pharmacy related majors; 2. 2 years and above working experience in sterile preparation, engaged in QA or production management related work; 3. Familiar with drug administration law, drug production supervision and management methods, GMP, MAH related laws and regulations; 4. Adapt to business trip, work conscientiously and responsibly, and be good at communication with the outside.

Submit Resume