Assistant Manager - Quality Control

0 years

0 Lacs

Posted:6 days ago| Platform: Linkedin logo

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Work Mode

On-site

Job Type

Full Time

Job Description


  • Oversee and manage QC activities for finished dosage formulations, raw materials, in-process, and stability samples.
  • Ensure compliance with

    cGMP, GLP, and regulatory guidelines (USFDA, EUGMP, etc.)

    in all QC operations.
  • Supervise and guide the QC team in chemical, instrumental (HPLC, GC, UV, Dissolution, IR, etc.), and microbiological testing.
  • Review and approve analytical reports, specifications, SOPs, and COAs.
  • Coordinate with QA, Production, and R&D departments to ensure timely release of materials and products.
  • Handle OOS/OOT investigations, deviations, CAPA, and ensure root cause analysis with effective implementation.
  • Monitor stability studies and prepare data for regulatory submissions.
  • Ensure calibration, qualification, and maintenance of laboratory instruments.
  • Conduct training for QC staff to enhance skills and compliance culture.
  • Support audits (regulatory and customer) and ensure timely closure of observations.

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