Technician, Continuous Improvement
Genzyme
Shenzhen
6天前
  • Ke'y Requirement and Responsibility :
  • Management of documentation and record : Draft document on quality and update and train them; Manage and following up the lifecycle of all documents in Bulk .
  • Management of records in Bulk, including distributing, reviewing and archiving.

  • Training and personnel qualification : Initial departmental training plan, new employee training plan, cross-position training plan, maintain employee training content, ensure employees participate in the required training in a timely manner, collect training records generated by training.
  • Statistics, analysis and electronic management of the generated data, archiving all training materials at the end of the year;
  • management of personnel qualification and sampling authorization, reminder prior to expiration of authorization, coordination of re-authorization training until re-authorization is obtained.

  • Sample management : Set up a sample plan to manage samples delivery, samples storage and refrigerator. To ensure the supply of red blood cell.
  • Management of department administrative work .
  • GMP and HSE self-inspection : Inspect the workshop activities to ensure GMP compliance and make them continuous improvement.
  • To administrate the department safety committee. Work with the HSE department to regularly summarize safety inspection information.

    Actively implement the energy-saving plan.

  • Others : Backup for production activity and support the work of other departments. Participate in production, validation and team work when necessary, complete temporary work assigned by leaders.
  • Specific degree, duration of experience (Required to hold the job) : College degree or above is required, at least 2 years working experience on related filed, good knowledge in the fields of bio-chemistry, bio-process, microbiology, virology and physical-chemistry.

    Key technical competencies and soft skills : Good practice for procedure and instructions. Familiar with various pharmaceutical laws and regulations, e.

    g. : GMP / Pharmacopeia. Good practice for analysis and organization capacity. Be earnest rigorous for work. Proficiency in office software, like : Word, Excel, Power-point etc.

    At Sanofi diversity and inclusion is foundational to how we operate and embedded in our Core Values. We recognize to truly tap into the richness diversity brings we must lead with inclusion and have a workplace where those differences can thrive and be leveraged to empower the lives of our colleagues, patients and customers.

    We respect and celebrate the diversity of our people, their backgrounds and experiences and provide equal opportunity for all.

    申请
    添加至收藏
    从收藏夹中删除
    申请
    邮箱地址
    通过点击 "继续", 我 同意neuvoo处理我的信息数据, 并给我发送电子邮件提醒 详见neuvoo 隐私政策 。我可以在任何时候取消订阅。
    继续
    申请表