Trainee or Assistant - QA IPQA

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

Job summary

Drlogy in Hyderabad is seeking a Dedicated Trainee or Assistant - QA IPQA responsible for supporting in-process quality assurance activities. This role includes monitoring compliance with GMP and ensuring pharmaceutical quality standards.

The ideal candidate should be skilled in documentation, line clearance, and quality inspections while supporting production quality and operational compliance within pharmaceutical manufacturing environments.

Qualifications

• Skilled in documentation review and process monitoring.
• Experienced in supporting production quality compliance.
• Strong understanding of GMP and pharmaceutical quality standards.

Responsibilities

• Support monitoring of manufacturing operations for GMP compliance.
• Conduct line clearance before production and packaging activities.
• Perform in-process quality assurance checks regularly.
• Report deviations and support corrective action implementation.
• Participate in audits and regulatory inspection activities.

Skills

Documentation review

Line clearance

Process monitoring

Quality inspections

GMP compliance

Job description

Dedicated Trainee or Assistant - QA IPQA responsible for supporting in-process quality assurance activities and ensuring compliance with GMP and pharmaceutical quality standards. Skilled in documentation review, line clearance, process monitoring, and quality inspections. Experienced in supporting production quality and operational compliance within pharmaceutical manufacturing environments.

• Support monitoring of 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.
• Report deviations and support corrective action implementation.
• Coordinate with production and QC teams for quality support.
• 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 activities for staff.
• Ensure compliance with safety and operational procedures.
• Contribute to continuous improvement initiatives within QA operations.