Officer/Sr. Officer-QA (Documentation)

institute logo

Officer/Sr. Officer-QA (Documentation)

work outline icon1 - 3 Years of Experiencerupess outline iconNot disclosed time outline iconFull Time

Stallion Laboratories Pvt Ltd

time outline iconAhmedabad, Gujarat, India

Posted on 31-10-2025

1 Vacancy

Description

  • Ensure that all manufacturing processes comply with cGMP, GLP, and regulatory standards.
  • Conduct in-process checks, line clearance, and batch record review.
  • Monitor documentation accuracy and ensure timely completion of QA records.
  • Perform deviation, change control, and CAPA (Corrective and Preventive Action) management.
  • Coordinate with production, QC, and warehouse teams for quality-related activities.
  • Assist in internal and external audits, including regulatory inspections.
  • Review and approve SOPs, validation protocols, and quality reports.
  • Ensure proper implementation of quality systems and maintain product traceability.
  • Train employees on quality policies, GMP, and hygiene practices.

Category

Pharmaceuticals

Functional Area

Pharma Quality Assurance (QA)

Key Skills

Good Communication SkillsAttention to DetailDecision-Making SkillsProblem Solving Skills

Aggregated job.

Learn more