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职位介绍

  • Perform in-process monitoring of all production activities at defined intervals.
  • Perform physical testing of all products as per BMR/BPR requirements.
  • Check the batch files of all the in-process batches.
  • Ensure instruments of IPC Laboratory are calibrated as per defined frequency.
  • Collect the retention, stability and validation samples of the released products as per plan, when required.
  • Perform GMP audits of various production areas and report the deviations.
  • Maintain all analytical records in logbooks and designated worksheets.
  • Verification of Line Clearance process as per defined procedure.
  • Review and checking of analytical data before approval of batch for next processing stage.
  • Support to release the Batches in dMERP.

Qualification & experience:

  • Pharm D. or MSc (Chemistry or Microbiology) & 1 to 3 years experience in pharmaceutical industry

工作详细内容

全部职位:
1 发布
工作时间:
早班
工作类型:
性别:
没有偏好
最低学历:
Pharm-D
学位头衔:
Pharm D. or MSc (Chemistry or Microbiology)
职位等级:
入门级
经验:
1年 - 3年 (Pharm-D, pharmaceutical Lab)
在之前申请:
Jul 03, 2021
发布日期:
Jun 02, 2021
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