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Executive-QC

Piramal Pharma·Navi Mumbai, Mumbai

Pay not statedJunior levelFull-time
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About the role

Responsible for sampling and analysis of in-process, intermediate, stability, and hold-time study samples using UV and HPLC as per SOPs Prepare stability protocols and reports, maintain cGMP-compliant documentation, support deviation and OOS investigations, and perform other assigned QC activities Perform analysis of in-process, intermediate, stability, and hold-time study samples

What you'll do

  • Responsible for sampling and analysis of in-process, intermediate, stability, and hold-time study samples using UV and HPLC as per SOPs
  • Prepare stability protocols and reports, maintain cGMP-compliant documentation, support deviation and OOS investigations, and perform other assigned QC activities
  • Perform analysis of in-process, intermediate, stability, and hold-time study samples
  • Conduct UV and HPLC analysis as per SOPs and in-house procedures
  • Handle charging and withdrawal of stability samples

What you need

  • 1–3 years in mechanical & production
  • HPLC
  • SOP writing
  • GMP
  • Any graduate

What you get

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