Executive or Senior Officer - IPQA

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

Job summary

Drlogy is seeking a detail-oriented Executive/Senior Officer - IPQA to oversee in-process quality assurance activities, ensuring compliance with GMP and pharmaceutical standards. The candidate will be responsible for monitoring production quality and supporting regulatory compliance within pharmaceutical manufacturing environments.

The role requires experience in process inspections, documentation review, and deviation handling. Duties include conducting line clearances, reviewing batch records, and coordinating with QC teams to maintain high-quality standards.

Qualifications

• Experience in in-process quality assurance activities.
• Strong knowledge of GMP and pharmaceutical quality standards.
• Proven skills in documentation review and line clearance.

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.

Skills

Attention to detail

GMP compliance knowledge

Process inspections

Deviation handling

Quality monitoring

Job description

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

• 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.