QA Documentation Officer

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QA Documentation Officer

work outline icon2 - 5 Years of Experiencerupess outline iconNot disclosed time outline iconFull Time

Stallion Laboratories Pvt Ltd

time outline iconBavla, Gujarat, India

Posted on 17-11-2025

1 Vacancy

Description

  • Manage controlled documents including SOPs, BMRs, BPRs, and validation protocols.
  • Review production and QC records to ensure regulatory and GMP compliance before batch release.
  • Maintain document control systems and ensure timely distribution and archival.
  • Prepare and update documentation as per change controls and regulatory requirements.
  • Ensure adherence to ALCOA+ principles in all data and document-related activities.
  • Support the documentation needs of QA, QC, and production teams during audits.
  • Conduct periodic reviews and version control of documents to ensure accuracy.
  • Maintain electronic documentation systems and ensure data integrity.

Category

Pharmaceuticals

Functional Area

Pharma Quality Assurance (QA)

Preferred Education

MSc (Master of Science)MPharm (Master Of Pharmacy)BPharm (Bachelor Of Pharmacy)

Key Skills

Attention to DetailCommunicationTeam WorkProblem Solving

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