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Qualification:BTech/MSc/MTech Biotechnology

Experience: 2-3 years

No of position: 01
 

Job Description:

  1. To assign and updating of equipment identification numbers, Instrument No. and Qualification document numbers
  2. Preparation of validation/qualification protocols and taking follow up for approval of prepared protocols
  3. Execution of qualification/validation activities
  4. To participate in internal trainings and external trainings
  5. To participate in self-inspection and external inspection
  6. Helping in archival of documents
  7. Taking evaluation comments from cross functional departments in Qualification documents
  8. Participate in all qualification activities
  9. Pre and post calibration for qualification activities
  10. To prepare and review of quality assurance SOPs
  11. To review all type of GMP documents from various department like SOP’s and validation protocol.
  12. Data logger and probe installation to the system
  13. Perform the Pure steam Quality test as per schedule
  14. To updating Qualification status label for HVAC and other equipment
  15. Coordination, execution and document review of CSV
  16. Responsible for any other responsibility provided by HOD

Send your resumes to murali.mohan@kemwellpharma.com
Please share the resumes on or before 17/05/2019

Bengaluru,India

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