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Dedicated to the development of products for early diagnosis of human

Guangzhou Huangpu District Guangdong No.8 Biotechnology Information No.8 Xi Bao Sheng Wu Xue No.9 He Gan Acids No.10 Sheng Wu Xin Xi Xue No.10 Nucleic Acids No.11 Genetic Engineering No.11 Clinical Diagnostics No.12 Genes Detection No.13 Diagnostics Products No.15 Sheng Wu Yi Xue No.18 Kang Shuai Lao No.61 Cheng Guo Zhuan Chemical 科技型中小企业 AAA级信用企业 市科技型中小企业 发明专利 软件著作权 国家发明专利

Gese Biotechnology qa jobs (salary & requirements)

Gese Biotechnology qa salary range: 6K - 15K, where 100% of positions earn ¥6-15K
Gese Biotechnology qa salary range: 6K-15K, the most positions earn 6-8K, based on 2 related positions in the past year, as of 2026-11-10
¥6-15K
100% of positions earn

Note: the average salary is analyzed based on job postings published by the company. We recommend reviewing it together with position type, education, region and experience.

Gese Biotechnology qa salary changes over the years

Note: the data depends on salary samples of online job postings in the corresponding years and does not fully represent the actual situation within the company. For reference only.

Education requirements: 大专 is the most common

What education does Gese Biotechnology require for qa positions? 大专占比最多,占50%,本科占50%

Salary by education

Gese Biotechnology qa salaries by education: 大专 ¥7.0K, 本科 ¥12.5K.

Gese Biotechnology qa hiring regions: mainly 广州

In which cities does Gese Biotechnology have offices for qa positions? The main distribution is as follows: 广州 accounts for 100%. Click this module to view the proportions of other cities, based on job postings in the past year. For reference only.

Gese Biotechnology qa hiring trends over the years

Gese Biotechnology qa changes in hiring volume over the years

What does Gese Biotechnology qa do

Based on related job postings of Gese Biotechnology in the past year
  • 质量(QA)主管

    广州-黄埔区 | 3-5年 | 本科以上 | 2026-04-27
    10000-15000
    岗位职责:
    1、体系搭建:负责GMP质量体系与研发质量管理体系(GMP-like) 的建立、维护与优化,制定分级文件管理规范。
    2、验证管理:审核工艺/清洁/设备验证方案及报告;参与研发阶段仪器确认、方法验证及数据可靠性审查。
    3、现场监控:对生产现场进行GMP合规监控;定期巡查研发实验室,监督实验记录规范性、原始数据完整性及试剂使用合规性。
    4、质量要素:管理偏差、变更、CAPA、OOS/OOT及质量风险,覆盖研发异常调查至生产全流程。
    5、批记录与放行:审核研发批、中试批及GMP批记录,参与物料与产品放行监督。
    6、审计迎检:组织研发内部自查及GMP自检,对接官方审计与客户稽查。
    7、培训管理:分层级开展GMP及研发数据规范性培训。
    8、其他:上级交办的其他质量相关工作。
    岗位要求:
    1、教育背景:医学、药学、生物学等相关专业本科及以上学历或中级职称。
    2、工作经验:5年以上生物医药质量管理经验;兼具研发实验室(GLP/GMP-like) 与GMP生产质量管理经验者优先。
    3、专业技能:精通GMP及ICH法规,熟悉生物药研发与生产流程,具备验证、偏差调查及数据分析能力。
    4、综合能力:跨部门沟通协调能力强,能平衡创新与合规,具备独立解决问题及团队管理能力。
    More
  • QA专员(质量体系方向)

    广州-黄埔区 | 不限经验 | 大专以上 | 2026-09-30
    5-7千 򀀩

广州 qa salary

More
How much does 广州 qa pay? 10-15K is the most common

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