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Banner image for Brilliant Pharmaceuticals 成都倍特药业股份有限公司
Job Type   /   Job Level
Full-time   /   Senior Executive
Company Location
Hong Kong
职位来源于智联招聘。

岗位职责:

  • 根据生产计划,制定现场QA工作的日常安排和管理;
  • 负责关键工艺运行情况和关键生产过程参数(CPPs)的验证;
  • 根据不同剂型的生产过程,规范化现场QA工作流程和操作步骤;
  • 制定设施、厂房、公用设施和仓库的审核计划,并审查其实施情况;
  • 制定现场质量控制相关的SOP;
  • 定期对现场质量控制人员进行培训和评估;
  • 为生产人员在执行偏差、变更和CAPA过程中提供支持;
  • 负责生产记录的审核;
  • 协助进行产品质量审核;
  • 领导交办的其他工作。
  • According to the production schedule of each process, arrange the schedule of production QA periodically.
  • Verify the operation of critical processes and the critical process parameters (CPPs)
  • Standardize the workflow and operation steps of on-site QA according to each process of different dosage form.
  • Prepare facility, premises, utilities and warehouse inspection plan and review the implementation.
  • Prepare related SOP for on-site QA.
  • Training and assessment on-site QA periodically
  • Provide support for production personnel in the execution of deviation, change control and CAPA
  • Review batch processing records.
  • Assist in product quality review.
  • Other assignment of QA Manager.

任职要求:

  • 本科以上学历,药学/理学/应用科学相关专业;
  • 3年以上QA部门经验;
  • 熟悉口服固体、口服液和乳膏剂型;
  • 熟悉PIC/S或者GMP要求;
  • 英语书面精通,口语能进行常规交流,会讲普通话或广东话;
  • 熟悉EXCEL、word、PPT等办公软件。
  • Bachelors degree or above in Science / Applied Science/ Pharmaceutical Study or equivalent.
  • Above 3 years work experience in QA department.
  • Familiar with oral solid, oral liquid and cream dosage forms.
  • Familiar with PIC/S GMP requirement.
  • Fluent in spoken and written English, Cantonese or Putonghua.
  • Goods computer skill in words, power points, excels.

以担保或任何理由索要财物,扣押证照,均涉嫌违法。
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