Quality Assurance

Drlogy; Nagpur District; On-site; INR 300,000 - 400,000; Full time

Job summary

Drlogy is looking for a Quality Assurance professional to support GMP compliance and quality system activities. This role involves reviewing batch records, handling deviations, and ensuring documentation and production activities meet SOPs and GMP standards.

The ideal candidate will be a fresher or have up to 2 years of experience with a qualification in D.Pharm, B.Pharm, or M.Pharm. The position is based in Nagpur District, Maharashtra, and requires coordination with various teams to address quality concerns and compliance.

Qualifications

• Freshers or candidates with 0–2 years of experience are welcome.

Responsibilities

• Support quality assurance activities related to manufacturing and documentation.
• Review batch manufacturing and packing records under guidance.
• Assist in deviation and change control documentation.

Education

D.Pharm or B.Pharm or M.Pharm

Job description

The Quality Assurance will support GMP compliance, documentation review, batch record checking, deviation handling, audit preparation, SOP compliance, and quality system activities at Lupin, Nagpur. This role is suitable for freshers or candidates with 0–2 years of experience and requires D.Pharm, B.Pharm, or M.Pharm qualification.

Responsibilities

• Support quality assurance activities related to manufacturing, packaging, documentation, and compliance.
• Review batch manufacturing records, batch packing records, logbooks, and quality documents under guidance.
• Ensure production and quality activities are performed as per approved SOPs and GMP standards.
• Assist in deviation, change control, CAPA, incident, and investigation documentation.
• Support line clearance, area checks, process verification, and shop floor compliance activities.
• Participate in internal audits, documentation checks, and quality system follow-ups.
• Maintain proper documentation as per Good Documentation Practices and data integrity requirements.
• Coordinate with production, QC, warehouse, engineering, and regulatory teams when required.
• Report non-compliance, documentation gaps, or quality concerns to seniors promptly.
• Support SOP preparation, revision, training records, and compliance tracking.
• Follow safety, hygiene, and pharma quality standards at all times.
• Ensure quality-focused, compliant, and disciplined QA support.