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Cipla Ltd

Analytical QA Associate I

Posted Today

Job Description

  • Reviewing and confirming the compliance related to raw materials, in­process and finished product analytical documents.
  • Monitoring and ensuring of current Good Laboratory Practices (cGLP) followed by laboratory personnel during routine operation to ensure adherence to procedure.
  • Verifying the laboratory chemicals/reagents, standards for completeness of the labels against standard operating procedures (SOPs).
  • Review of laboratory audit trials during data review against standard operating procedures (SOPs).
  • Coordinating with the Analytical Laboratory Teams to arrange required documents to cross functional teams.
  • Maintaining all the incoming documents with proper tracking, recording, storage and archival of the documents.
  • Reviewing and identifying the gaps within the system during routine monitoring and informing the supervisor of necessary improvements in the identified areas.
  • Actively participating in review of data related to laboratory investigations and incidents and ensuring proper compliance.
  • Performing other departmental and cross-functional projects and assignments given by the manager/supervisor.
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