Posted:1 day ago| Platform: Foundit logo

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Work Mode

On-site

Job Type

Full Time

Job Description

  • To assist in preparation, issuance, review, and control of SOPs, BMRs, and controlled documents.
  • To support documentation of deviations, change controls, CAPA, and incidents in line with QMS.
  • To ensure compliance with cGMP, QMS, and regulatory requirements during all QA activities.
  • To participate in internal audits, self-inspections, and regulatory inspections.
  • To follow ALCOA+ principles (Attributable, Legible, Contemporaneous, Original, Accurate, plus Complete, Consistent, Enduring, Available) in all documentation practices.
  • To maintain and update QA logbooks, training records, calibration records, and archives.
  • To support qualification, validation, and calibration documentation as per GMP guidelines.
  • To assist in vendor qualification processes and related documentation.
  • To participate in EHS (Environment, Health Safety) initiatives and ensure workplace safety compliance.
  • To report any deviations, incidents, and unsafe practices immediately to supervisors.
  • To contribute to continuous improvement initiatives related to QMS, GMP, and safety standards.
  • To support stability study documentation and ensure adherence to data integrity requirements.

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Piramal Pharma Limited logo
Piramal Pharma Limited

Pharmaceuticals

Mumbai

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