Assistant General Manager QA Validation

13 - 18 years

20 - 25 Lacs

Posted:1 hour ago| Platform: Naukri logo

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Job Type

Full Time

Job Description

  • Responsible to review and execution of qualification document related Equipment, Facility and Utility like Plant equipment, HVAC, Water system and Compressed air system.
  • Responsible to review and execution of Re-Qualification document.
  • Responsible to co-ordinate with manufacturing personnel for respective qualification / validation / Re-qualification activity form timely completion of activity.
  • Responsible for preparation, review and execution of risk assessment related tEquipment, System, Facility and Process.
  • Responsible for preparation and review of validation master plan tensure execution of activity.
  • Responsible for preparation of cleaning validation protocol and compilation and review of cleaning validation report.
  • Responsible t0 conduct sampling activity as per the approved cleaning validation protocol.
  • Responsible for preparation of process validation protocol and compilation and review of process validation report.
  • Responsible for preparation of packaging validation protocol and compilation and review of packaging validation report.
  • To co-ordination with Quality control or Micro department for sample preparation and testing for cleaning validation, Equipment, Utilities and System qualification / validation / re-qualification study.
  • Responsible to prepare and reviewed SOPs for process validation, Cleaning Validation and Qualification.
  • Responsible to impart training of validation/qualification for equipment/system /utilities/process.
  • Responsible to review of change control to evaluate validation requirement.
  • Responsible to review of deviation and laboratory OOS related to validation.
  • Responsible to check c-GMP compliance.

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Amneal Pharmaceuticals logo
Amneal Pharmaceuticals

Pharmaceutical Manufacturing

Bridgewater New Jersey

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