IPQA Officer

Drlogy; India; On-site; INR 400,000 - 600,000; Full time

Job summary

Drlogy is seeking a detail-oriented IPQA Officer responsible for monitoring in-process quality assurance activities in India. The officer will ensure compliance with GMP and pharmaceutical quality standards while skilled in documentation review, line clearance, and other quality monitoring tasks.

The ideal candidate will possess a strong background in supporting production quality and maintaining regulatory compliance within pharmaceutical environments. Responsibilities include conducting line clearance, reviewing records, and participating in audits.

Qualifications

• Skilled in process inspections and quality monitoring.
• Experienced in supporting production quality in pharmaceutical manufacturing.
• Knowledge of regulatory compliance within the pharmaceutical industry.

Responsibilities

• Monitor manufacturing operations for GMP compliance.
• Conduct line clearance before production and packaging activities.
• Review batch manufacturing and packaging records accurately.
• Perform in-process quality assurance checks regularly.
• Ensure adherence to SOPs and pharmaceutical quality standards.

Skills

Detail-oriented

GMP compliance

Documentation review

Line clearance

Deviation handling

Quality monitoring

Job description

Overview

Detail-oriented IPQA Officer responsible for monitoring in-process quality assurance activities and ensuring compliance with GMP and pharmaceutical quality standards. Skilled in process inspections, documentation review, line clearance, deviation handling, and quality monitoring. Experienced in supporting production quality and maintaining regulatory compliance within pharmaceutical manufacturing environments.

Responsibilities

• Monitor manufacturing operations for GMP compliance.
• Conduct line clearance before production and packaging activities.
• Review batch manufacturing and packaging records accurately.
• Perform in-process quality assurance checks regularly.
• Ensure adherence to SOPs and pharmaceutical quality standards.
• Investigate deviations and support corrective action implementation.
• Coordinate with production and QC teams for quality-related issues.
• Maintain IPQA documentation and compliance records effectively.
• Monitor environmental and operational compliance standards.
• Participate in audits and regulatory inspection activities.
• Verify equipment cleaning and production readiness procedures.
• Support CAPA and change control management activities.
• Conduct GMP and quality awareness training sessions.
• Ensure compliance with safety and operational procedures.
• Contribute to continuous improvement initiatives within QA operations.