Quality Staff

Drlogy; Mumbai; On-site; INR 300,000 - 450,000; Full time

Job summary

Drlogy in Mumbai is seeking a Quality Staff member responsible for supporting quality control and assurance activities. The role includes sample testing, documentation review, and compliance monitoring. Candidates should have a B.Pharm or M.Sc with 1–2 years of experience in the pharmaceutical industry.

Responsibilities involve operating analytical instruments, supporting quality checks, and maintaining laboratory disciplines to ensure adherence to GMP and GLP standards. This position offers a crucial opportunity to contribute to pharmaceutical quality operations.

Qualifications

• 1–2 years of experience in quality control or assurance.
• Proficient in operating analytical instruments and laboratory equipment.
• Excellent documentation and compliance skills.

Responsibilities

• Support quality control testing of raw materials and products.
• Assist in maintaining laboratory equipment and instruments.
• Prepare test-related documentation and reagents.

Skills

Knowledge of GMP

Documentation practices

Laboratory discipline

Pharmaceutical quality standards

Education

B.Pharm or M.Sc qualification

Job description

The Quality Staff will be responsible for supporting quality control and quality assurance activities, including sample testing, documentation review, analytical support, compliance monitoring, and quality system maintenance at Ciron Drugs, Mumbai. This requires B.Pharm or M.Sc qualification with 1–2 years of experience, knowledge of GMP, GLP, documentation practices, laboratory discipline, and pharmaceutical quality standards.

• Support quality control testing of raw materials, in-process samples, finished products, and stability samples.
• Assist in operating analytical instruments and laboratory equipment as per approved SOPs.
• Prepare reagents, standards, solutions, worksheets, and test‑related documentation.
• Review batch records, logbooks, analytical records, and quality documents when assigned.
• Follow GMP, GLP, GDP, safety, data integrity, and documentation compliance requirements.
• Report OOS, OOT, deviations, abnormal results, or quality observations to seniors promptly.
• Support calibration, maintenance, qualification, and troubleshooting of quality instruments.
• Coordinate with production, QA, QC, warehouse, engineering, and regulatory teams when required.
• Assist in line clearance, in‑process checks, sampling, and shop‑floor quality monitoring.
• Maintain sample registers, QC records, logbooks, controlled formats, and quality trackers.
• Support deviation, change control, CAPA, audit readiness, and investigation documentation.
• Ensure proper handling of chemicals, reference standards, samples, and laboratory materials.
• Maintain cleanliness and proper arrangement of quality control or quality assurance work areas.
• Participate in internal audits, training, and quality improvement activities.
• Contribute to accurate, compliant, and reliable pharmaceutical quality operations.