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Sr Executive / Assistant Manager - QA (IVD)

Promea Therapeutics·Hyderabad

Pay not statedSenior levelFull-time

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About the role

Responsible for preparation of Quality Documents such as SMF, Quality Policy etc. Responsible for review and compilation of Deviations, Incidents, Change Control and Root Cause Analysis. Responsible for review and proper implementation of CAPA. Responsible for conducting and preparation of Self-inspection reports.

What you'll do

  • Responsible for implementation of cGMP in the plant
  • Responsible for review of SOPs
  • Responsible for preparation of Quality Documents such as SMF, Quality Policy etc
  • Responsible for review and compilation of Deviations, Incidents, Change Control and Root Cause Analysis
  • Responsible for review and proper implementation of CAPA

What you need

  • SOP writing
  • GMP
  • Root cause analysis
  • Any graduate

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