Technical Assistant -Quality Assurance

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

Job summary

Drlogy is looking for a Technical Assistant - Executive - Quality Assurance to support QA activities at Torrent Pharma, Ahmedabad. This role requires qualifications such as M.Sc, M.Pharm, B.Sc, or B.Pharm, along with 1–5 years of quality assurance experience.

The ideal candidate will ensure compliance with quality systems and regulations, perform documentation reviews, and assist in maintaining GMP standards. Key responsibilities include supporting line clearances, conducting audits, and coordinating with various teams for quality adherence.

Qualifications

• 1–5 years of quality assurance experience is required.
• Strong understanding of quality systems and compliance.
• Proficiency in documentation practices.

Responsibilities

• Support QA activities related to manufacturing and compliance.
• Perform line clearance and shop floor compliance checks.
• Review batch manufacturing and packing records.
• Support internal audits and regulatory inspection readiness.
• Prepare QA reports and compliance trackers.

Skills

Quality assurance experience

GMP regulations

Documentation review

Deviations handling

Education

M.Sc, M.Pharm, B.Sc, or B.Pharm

Job description

The Technical Assistant - Executive - Quality Assurance will support QA activities, shop floor compliance, documentation review, line clearance, deviation support, batch record review, and quality system compliance at Torrent Pharma, Ahmedabad. This requires M.Sc, M.Pharm, B.Sc, or B.Pharm qualification with 1–5 years of quality assurance experience.

Responsibilities

• Support QA activities related to manufacturing, packaging, documentation, and compliance.
• Perform or assist in line clearance, in-process checks, shop floor compliance checks, and area verification.
• Review batch manufacturing records, batch packing records, logbooks, checklists, and quality documents.
• Support handling of deviations, change controls, CAPA, complaints, and quality events under senior guidance.
• Coordinate with production, packaging, QC, warehouse, engineering, and quality teams.
• Monitor GMP, GDP, data integrity, hygiene, and documentation practices on the shop floor.
• Prepare QA reports, compliance trackers, review observations, and documentation updates.
• Report documentation gaps, process deviations, quality issues, or SOP non-compliance promptly.
• Support internal audits, regulatory inspection readiness, and compliance improvement activities.
• Maintain confidentiality and accuracy of quality records and batch documents.
• Follow approved SOPs, quality systems, and pharmaceutical compliance requirements.
• Ensure smooth, compliant, and quality-focused QA support.