三威
职业
职位空缺
★ 我们建立了长期引进、储备、评价、监督、保障高素质高层次科技人才的机制，建设了专门的研究设施，吸引更多人才从事科学研究和开发，确保人才引得进、留得住、用得好。
★ 根据员工的岗位序列和职级组织员工培训和学习。通过提供精细化、有针对性的培训课程，使个人能力得到提升，工作绩效得到提高，促进职业道德的提升，实现职业发展。
★ 为员工的医疗、食宿、交通等方面提供全面的保障，让员工工作舒心，生活开心
职位招聘
职位
工作地点
招聘人数
薪资
时间
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.
On-site QA Job Responsibilities
On-site QA Job Responsibilities
2
Negotiable
2025-05-07
暂无岗位要求信息
