Quality Assurance Junior Officer to Assistant Manager

Drlogy; Vadodara; On-site; INR 300,000 - 500,000; Full time

Job summary

Drlogy is seeking a Quality Assurance Junior Officer to Assistant Manager in Vadodara, India. The selected candidate will be responsible for implementing quality systems, monitoring GMP compliance, and ensuring adherence to pharmaceutical regulatory standards. Key duties include reviewing manufacturing records, conducting quality checks, participating in audits, and training employees on quality procedures. This role is crucial to maintaining high standards in the pharmaceutical industry with opportunities for growth into management.

Qualifications

• Experience in monitoring manufacturing and quality processes to ensure GMP compliance.
• Ability to implement and maintain quality assurance systems and documentation.
• Proficient in conducting line clearance and in-process quality checks.

Responsibilities

• Monitor manufacturing and quality processes to ensure GMP compliance.
• Review batch manufacturing and packaging records for accuracy and completeness.
• Coordinate deviation investigations and corrective preventive action activities.
• Participate in internal audits and support regulatory inspections.

Skills

GMP compliance

Quality Assurance systems

Deviation investigations

Regulatory guidelines

Quality checks

Internal audits

Training

Job description

Quality Assurance Junior Officer to Assistant Manager

Dedicated Quality Assurance professional responsible for implementing quality systems, monitoring GMP compliance, and ensuring adherence to pharmaceutical regulatory standards.

• Monitor manufacturing and quality processes to ensure GMP compliance.
• Review batch manufacturing and packaging records for accuracy and completeness.
• Implement and maintain quality assurance systems and documentation.
• Coordinate deviation investigations and corrective preventive action activities.
• Ensure compliance with SOPs, regulatory guidelines, and quality standards.
• Conduct line clearance and in-process quality checks during production.
• Participate in internal audits and support regulatory inspections.
• Maintain change control, CAPA, and quality management documentation.
• Coordinate with production, QC, and engineering teams for compliance activities.
• Monitor environmental and operational compliance within manufacturing areas.
• Prepare quality reports and maintain audit readiness documentation.
• Train employees on GMP, SOPs, and quality system procedures.
• Investigate non-conformance issues and recommend process improvements.
• Support implementation of risk assessment and quality improvement initiatives.
• Ensure timely closure of quality observations and compliance gaps.