Quality Operations Specialist

5 - 8 years

3 - 7 Lacs

Posted:-1 days ago| Platform: Naukri logo

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Job Type

Full Time

Job Description

  • Reporting to Zentiva Italy Quality & Compliance Manager, the Quality Operations Specialist will take lead responsibility for Product Quality Reviews (PQR) review completion for the cases in which Zentiva France is marketing authorization holder (MAH).
  • Responsible to meet the established schedule in completing the reviews of PQRs.
  • For each evaluated PQR the Quality Operations Specialist will ensure that the traceability of the evaluation (report) is always available (document crated, approved/signed and properly archived) according to Zentiva Italy procedures.
  • Responsible for flagging /escalating to the Zentiva Italy Quality & Compliance Manager any delays on time.
  • Prepares trends analysis and KPI on PQR review process.
  • Responsible for ensuring the maintenance of a up to date document for tracking of PQRs review operations and will support Zentiva Italy Quality & Compliance Manager in the preparation of periodic reporting of the PQRs review. The tracking document shall permit to Zentiva Italy to identify PQRs evaluated as to be improved or which are not meeting the requested quality standards.
  • Responsible for calculating PQRs review KPIs on monthly basis.
  • Responsible for the extraction and data compilation of analytical, manufacturing (including deviations, complaints, and change requests) from appropriate IT tools (Quality Forward, Share/DrugTrack, eDMS) and regulatory data (HA commitments, variations).
  • Responsible for collecting stability data and reports for product-related evaluations. (e.g. compliance investigations, divestitures, product transfers, validation. etc.).
  • Responsible for scheduling meetings with the transversal functions in case clarifications are needed or to determine and assign follow-up action items, if required.
  • Support the PQR review related deviation investigations.
  • CAPA plan follow-up on PQR related issues with transversal functions and CMO if required, communicate with CMOs, as required.
  • Participate to inspections.
  • Where requested, support the Zentiva Italy Quality & Compliance Manager in the review of Qualification status of the Zentiva Italy third parties such as suppliers (Risk assessments update, Quality Agreements update), and Zentiva entities (Quality Agreement update).
  • Where requested, support the Zentiva Italy Quality & Compliance Manager in the management of incoming batch controls, including quarantine arrivals and related scraps communication to the Italian Health authority.

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