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QA Executive

Pharmaceuticals Punjab 3 yrs exp

Job Description

Key Responsibilities

- Prepare, review, revise and control QA documents as per cGMP and regulatory requirements.

- Review Batch Manufacturing Records (BMR), Batch Packing Records (BPR), logbooks and analytical documentation.

- Handle deviations, incidents, CAPA, change controls and root-cause investigations.

- Prepare and revise SOPs, formats, protocols and other quality-system documents.

- Manage document issuance, retrieval, archival, version control and record retention.

- Conduct shop-floor monitoring, line clearance and in-process compliance checks.

- Support equipment qualification, process validation and cleaning-validation activities.

- Review calibration, preventive-maintenance and qualification records.

- Ensure compliance with data-integrity requirements and ALCOA+ principles.

- Participate in internal, customer and regulatory audits and support closure of audit observations.

- Coordinate with Production, QC, Warehouse and Engineering departments on quality-related matters.

- Conduct or coordinate cGMP and SOP training and maintain training records.

- Ensure timely completion and closure of all assigned quality-system activities.

Candidate Profile

- Must have 3–5 years of QA experience in an API manufacturing facility.

- Strong knowledge of cGMP documentation and pharmaceutical quality systems.

- Hands-on experience with deviations, CAPA, change controls, investigations and batch-record review.

- Familiarity with regulatory standards such as WHO-GMP, ICH, USFDA or EU-GMP.

Minimum QualificationB.Pharm / M.Pharm / B.Sc. / M.Sc.

Experience Level (Years)3 - 5

LocationPunjab

Area of WorkQA

Salary Range (In LPA)3 - 4.5

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