Sr. Officer QA (Documentation)

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Sr. Officer QA (Documentation)

work outline icon0 - 5 Years of Experiencerupess outline iconNot disclosed time outline iconFull Time

Ipca Laboratories Limited

time outline iconJorethang, Sikkim, India

Posted on 03-12-2024

142 Views

1 Vacancy

Description

  • Conduct in-process quality checks and inspections to ensure compliance with GMP and SOPs.
  • Review batch production records, deviation reports, and other quality documents for accuracy.
  • Assist in preparing, reviewing, and updating Standard Operating Procedures (SOPs) and quality policies.
  • Monitor and document quality-related activities, ensuring compliance with regulatory standards.
  • Investigate quality incidents, deviations, and complaints, and recommend corrective actions.
  • Coordinate with production, QC, and warehouse teams to ensure seamless quality practices.
  • Participate in internal audits and support external regulatory inspections.
  • Oversee the release of raw materials, intermediates, and finished products after quality clearance.
  • Maintain records of non-conformance, corrective actions, and quality metrics for reporting purposes.

Category

Pharmaceuticals

Key Skills

CommunicationProblem solvingAttention to DetailDecision Making

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