Quality Control- Formulation

7 - 10 years

0 - 2 Lacs

Posted:4 days ago| Platform: Naukri logo

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Job Type

Full Time

Job Description

Qualification: B.Sc(Chemistry)/M.Sc(Chemistry)

Experience: 7-10 years

Position: Sr. Executive/Asst. Manager

Role & responsibilities

  • Work planning related to Raw Material, Finish Product, In-Process, Packing Material and Miscellaneous Sample.
  • Review of Analytical data, protocols, and reports.
  • Prepare and review of specification, standard test procedure,Analytical Record Data sheet and analytical method validation protocol and reports which is in line with pharmacopoeia and ICH guideline.
  • Supervise the analyst for sampling, testing and instrument/equipment handling.
  • Handling of Investigation of System Suitability Failures, OOS,OOC, OOT, Deviation,CAPA, RCI and decision making with QA and other department.
  • Prepare and review of study protocols, calibration reports, stability reports, all document related to quality control department and analytical data related to commercial and stability batches.
  • To observe, execute and comply Good Laboratory Practices (GLP), GMP & Good Documentation practices (GDP).
  • Conduct SOPs and Protocol training for all quality personnel and guidelines updation.
  • Assure readiness of site for regulatory agency inspections\internal audits and appropriate implementation of corrective actions regarding observations made by the agencies\internal audit teams

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