Posted:2 hours ago| Platform: GlassDoor logo

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Work Mode

On-site

Job Type

Full Time

Job Description

Qualifications:

  • B.Sc. / M.Sc. in Chemistry or B.Pharm / M.Pharm.
  • 6–8 years of relevant experience in Quality Assurance in a pharmaceutical manufacturing environment.

Key Responsibilities:

  • Review and approve analytical data, batch records, specifications, and test methods to ensure compliance with cGMP and internal quality standards.
  • Lead investigations into deviations, out-of-specification (OOS) results, and non-conformances.
  • Support change control processes, CAPA implementation, and risk assessments.
  • Participate in internal and external audits; assist with regulatory inspections.
  • Review and maintain QA documentation including SOPs, validation protocols, and certificates of analysis.
  • Collaborate cross-functionally with QC, manufacturing, and regulatory teams to ensure quality objectives are met.
  • Provide mentorship and QA guidance to team members and junior staff.
  • Strong knowledge of GMP, ICH guidelines, and relevant regulatory standards

Job Types: Full-time, Permanent

Pay: Up to ₹40,000.00 per month

Benefits:

  • Health insurance
  • Life insurance
  • Provident Fund

Work Location: In person

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