Quality Assurance Officer
1 day ago
**Job description**:
**Key Responsibilities**:
- Ensure adherence to cGMP, GLP, and data integrity principles in all QA-related activities.
- Manage document control — issuance, review, retrieval, and archiving of controlled documents (SOPs, protocols, logbooks, etc.).
- Participate in internal audits, self-inspections, and regulatory audits.
- Handle deviations, change controls, CAPA, and incident investigations.
- Coordinate with production, QC, and warehouse teams to ensure compliance with company and regulatory standards.
- Monitor and review calibration and qualification records of equipment and instruments.
- Support vendor qualification, training programs, and quality risk management activities.
- Maintain records for product quality reviews (PQRs) and validation documentation.
- Assist in ensuring audit readiness and continuous improvement of the quality management system (QMS).
- B.Pharm / M.Pharm / B.Sc. / M.Sc. in Pharmaceutical Sciences, Chemistry, or related field.
- 0-2 years of experience in QA activities within a pharmaceutical manufacturing plant.
- Strong understanding of cGMP, ICH, WHO, and regulatory guidelines.
- Experience in documentation, deviation management, and QMS modules.
- Good communication, analytical, and organizational skills.
- Proficiency in MS Office and knowledge of electronic documentation systems (if applicable).
**Job Type**:
- Full-time, Permanent
**Benefits**:
- Provident Fund
- Professional growth opportunities
**Job Types**: Full-time, Permanent
Pay: ₹10,000.00 - ₹46,026.38 per month
Work Location: In person
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