Technical Assistant - Quality Control

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

Job summary

Drlogy is seeking a Technical Assistant - Executive - Quality Control in Ahmedabad, India. The role involves supporting QC laboratory testing, sample analysis, and ensuring compliance with GMP and GLP standards.

Candidates should possess a degree in M.Sc, M.Pharm, B.Sc, or B.Pharm along with 1–5 years of experience in quality control. The position also requires handling laboratory equipment and maintaining documentation. This is an essential role within the quality control department.

Qualifications

• 1–5 years of experience in quality control.
• Strong knowledge of GMP, GLP, GDP, and data integrity.
• Experience with laboratory safety practices.

Responsibilities

• Perform testing of raw materials and finished products.
• Prepare sample records and analytical reports accurately.
• Support instrument calibration and verification activities.
• Report deviations or abnormal results promptly.

Skills

Quality control testing

GMP compliance

GLP compliance

Analytical procedures

Education

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

Tools

Laboratory equipment

Job description

The Technical Assistant - Executive - Quality Control will support QC laboratory testing, sample analysis, documentation, instrument handling, quality control records, and GMP / GLP compliance at Torrent Pharma, Ahmedabad. This requires M.Sc, M.Pharm, B.Sc, or B.Pharm qualification with 1–5 years of quality control experience.

• Perform or support testing of raw materials, in-process samples, finished products, stability samples, and packaging materials.
• Handle QC instruments, laboratory equipment, reagents, standards, and analytical procedures as per SOP.
• Prepare sample records, test worksheets, analytical reports, logbooks, and QC documentation accurately.
• Follow GLP, GMP, GDP, data integrity, laboratory safety, and quality control standards.
• Support instrument calibration, verification, maintenance, and cleaning activities.
• Report OOS, OOT, deviations, abnormal results, instrument issues, or sample-related concerns promptly.
• Coordinate with QA, production, warehouse, packaging, and laboratory team members.
• Maintain proper labeling, storage, handling, and disposal of chemicals, reagents, and samples.
• Support stability studies, method execution, documentation review, and QC compliance activities.
• Maintain laboratory cleanliness, safety, and discipline.
• Participate in audits, inspections, and quality improvement activities when required.
• Ensure accurate, reliable, and compliant quality control testing support.